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Disease on EC 3.1.21.4 - type II site-specific deoxyribonuclease

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Abetalipoproteinemia
Genetic exclusion of apo-B gene in recessive abetalipoproteinemia.
Abortion, Habitual
The contribution of Hind III C>G PAI-1 gene polymorphism in etiology of recurrent miscarriages.
Abortion, Spontaneous
Alleles and haplotypes of the estrogen receptor alpha gene are associated with an increased risk of spontaneous abortion.
Evaluation of PvuII and XbaI polymorphisms in the estrogen receptor alpha gene (ESR1) in relation to menstrual cycle timing and reproductive parameters in post-menopausal women.
The contribution of Hind III C>G PAI-1 gene polymorphism in etiology of recurrent miscarriages.
Abscess
Elevated serum antibody response to toxin A following splenic abscess due to Clostridium difficile.
Molecular characterization of Mycobacterium massiliense and Mycobacterium bolletii in isolates collected from outbreaks of infections after laparoscopic surgeries and cosmetic procedures.
Achondroplasia
FGFR3 gene mutation (Gly380Arg) with achondroplasia and i(21q) Down syndrome: phenotype-genotype correlation.
Nonrandom association of a type II procollagen genotype with achondroplasia.
Acidosis, Lactic
Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation.
Acquired Immunodeficiency Syndrome
A computer assisted method for the determination of restriction enzyme recognifion sites.
A fifth human cytomegalovirus glycoprotein B genotype.
Adenovirus isolates from urine of patients with acquired immunodeficiency syndrome.
Analysis of antigenically intermediate strains of subgenus B and D adenoviruses from AIDS patients.
Characterization of cytomegalovirus isolates from patients with AIDS by DNA restriction analysis.
Distribution of type D retrovirus sequences in tissues of macaques with simian acquired immune deficiency and retroperitoneal fibromatosis.
DNA subtypes and fluconazole susceptibilities of Candida albicans isolates from the oral cavities of patients with AIDS.
Genomic polymorphism, growth properties, and immunologic variations in human herpesvirus-6 isolates.
Human immunodeficiency virus isolates from asymptomatic homosexual men and from AIDS patients have distinct biologic and genetic properties.
Molecular biological characterization of adenovirus DNA.
Molecular characterization of human T-cell leukemia (lymphotropic) virus type III in the acquired immune deficiency syndrome.
Molecular cloning of AIDS-associated retrovirus.
Molecular comparison of retroviruses associated with human and simian AIDS.
Restriction endonuclease mapping of adenovirus 35, a type isolated from immunocompromised hosts.
Acute Chest Syndrome
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.
Adenocarcinoma
A rapid and reliable enzyme immunoassay PCR-based screening method to identify EBV-carrying gastric carcinomas.
Association of tumor necrosis factor genetic polymorphism with chronic atrophic gastritis and gastric adenocarcinoma in Chinese Han population.
Beta-Catenin mutations in a mouse model of inflammation-related colon carcinogenesis induced by 1,2-dimethylhydrazine and dextran sodium sulfate.
Biochemical and cytogenetic studies of human lung cancers.
Coexpression of gonadotropic hormones and their corresponding FSH- and LH/CG-receptors in the human prostate.
Colonic adenocarcinomas rapidly induced by the combined treatment with 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and dextran sodium sulfate in male ICR mice possess beta-catenin gene mutations and increases immunoreactivity for beta-catenin, cyclooxygenase-2 and inducible nitric oxide synthase.
Detection of acquired provirus sequences in mammary tumors from low-expressor, low-risk mice.
Effect of p53 polymorphism on the susceptibility of cervical cancer.
Epstein-Barr virus plays little role in cervical carcinogenesis in Korean women.
ERBB2 amplifications in esophageal adenocarcinoma.
Human gastric adenocarcinoma cathepsin B: isolation and sequencing of full-length cDNAs and polymorphisms of the gene.
Proviral unit II of endogenous mouse mammary tumour virus is selectively amplified and expressed in C57B1/10 mammary tumours induced by non-viral carcinogens.
Relationships between c-Ki-ras mutations, HPV types, and prognostic indicators in invasive endocervical adenocarcinomas.
Repair of ionizing radiation induced DNA double-strand breaks (dsb) at the c-myc locus in comparison to the overall genome.
Adenocarcinoma of Lung
Activated protooncogenes in human lung tumors from smokers.
Amylase mRNA transcripts in normal tissues and neoplasms: the implication of different expressions of amylase isogenes.
DNA double-strand breaks activate ATM independent of mitochondrial dysfunction in A549 cells.
Adenoma
Abnormalities of the human growth hormone gene and protooncogenes in some human pituitary adenomas.
Analysis of the TSH receptor gene structure in various thyroid disorders: DNA from thyroid adenomas can have large insertions or deletions.
Clonal analysis of focal nodular hyperplasia of the liver.
Downregulation of CD44v6 in colorectal carcinomas is associated with hypermethylation of the CD44 promoter region.
INK4a-ARF alterations in liver cell adenoma.
Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population.
Loss of heterozygosity of p53 gene and p53 protein expression in human colorectal carcinomas.
No rearrangement of c-mos in salivary gland pleomorphic adenomas with 8q12 aberrations.
PCR-SSCP analysis of the promoter region of the renin gene in patients with aldosterone-producing adenomas.
Promoter region methylation does not account for the frequent loss of expression of the Fas gene in colorectal carcinoma.
Adenoma, Liver Cell
INK4a-ARF alterations in liver cell adenoma.
Adenoma, Oxyphilic
Absence of HinfI Restriction Abnormalities in Renal Oncocytoma Mitochondrial DNA.
Adenomatous Polyposis Coli
Alternatively spliced adenomatous polyposis coli (APC) gene transcripts that delete exons mutated in attenuated APC.
Adenomyosis
Assessment of hypermethylated DNA in two promoter regions of the estrogen receptor alpha gene in human endometrial diseases.
Oestrogen receptor-alpha gene polymorphism is associated with endometriosis, adenomyosis and leiomyomata.
Adenoviridae Infections
Assessment of genetic variability among subspecies b1 human adenoviruses for molecular epidemiology studies.
Genomic variation of adenovirus type 5 isolates recovered from bone marrow transplant recipients.
Adrenal Hyperplasia, Congenital
PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module.
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.
African Swine Fever
A gene homologous to topoisomerase II in African swine fever virus.
A set of African swine fever virus tandem repeats shares similarities with SAR-like sequences.
African swine fever virus DNA: deletions and additions during adaptation to growth in monkey kidney cells.
African swine fever virus DNA: restriction endonuclease cleavage patterns of wild-type, Vero cell-adapted and plaque-purified virus.
African swine fever virus encodes a CD2 homolog responsible for the adhesion of erythrocytes to infected cells.
African swine fever virus encodes a DNA ligase.
African swine fever virus EP153R open reading frame encodes a glycoprotein involved in the hemadsorption of infected cells.
Characterization of pathogenic and non-pathogenic African swine fever virus isolates from Ornithodoros erraticus inhabiting pig premises in Portugal.
Characterization of the african swine fever virus protein p49: a new late structural polypeptide.
Genes homologous to ubiquitin-conjugating proteins and eukaryotic transcription factor SII in African swine fever virus.
Genetic diversity of African swine fever virus isolates from soft ticks (Ornithodoros moubata) inhabiting warthog burrows in Zambia.
Genetic variation of African swine fever virus: variable regions near the ends of the viral DNA.
Genome analysis of African swine fever virus isolated in Italy in 1983.
Mapping and sequence of the gene coding for protein p72, the major capsid protein of African swine fever virus.
Molecular cloning and restriction enzyme mapping of an African swine fever virus isolate from Malawi.
Molecular cloning of African swine fever virus DNA.
Multigene families in African swine fever virus: family 505.
Proteolytic processing in African swine fever virus: evidence for a new structural polyprotein, pp62.
Replication of African swine fever virus DNA in infected cells.
Restriction site map of African swine fever virus DNA.
Sequence and characterization of the major early phosphoprotein p32 of African swine fever virus.
Variable regions on the genome of Malawi isolates of African swine fever virus.
Aggressive Periodontitis
No association with HLA-DQB1 in European Caucasians with early-onset periodontitis.
Unique intronic variations of HLA-DQ beta gene in early-onset periodontitis.
Albuminuria
Association between polymorphisms of the atrial natriuretic peptide gene and proteinuria: a population-based study.
Polymorphisms in the hANP (human atrial natriuretic peptide) gene, albuminuria, and hypertension.
Relationship among urinary albumin excretion rate, lipoprotein lipase PvuII polymorphism and plasma fibrinogen in type 2 diabetic patients.
Alexander Disease
[Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease]
alpha 1-Antitrypsin Deficiency
Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease.
Restriction enzyme MaeIII for prenatal diagnosis of alpha 1-antitrypsin deficiency.
alpha-Thalassemia
alpha thalassemia in black populations.
Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.
Alpha-thalassemia in Saudi Arabia: deletion pattern.
Alpha-thalassemia in two Mediterranean populations.
Alpha-thalassemia incidence in southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind Hospital.
Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
Concomitant inheritance of alpha-thalassemia in beta 0- thalassemia/Hb E disease.
Dysfunctional alpha-globin gene in hemoglobin H disease in blacks. A dinucleotide deletion produces a frameshift and a termination codon.
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis.
Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
Gene probes: application to prenatal and postnatal diagnosis of genetic disease.
Genetic and molecular diversity in nondeletion Hb H disease.
Hematological evaluation of patients with various combinations of alpha-thalassemia.
High prevalence of alpha-thalassemia among individuals with microcytosis and hypochromia without anemia.
Interaction of chromosomes bearing 1, 2 or 3 alpha-globin genes in an American black family with alpha-thalassemia.
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
Prenatal diagnosis of alpha-thalassemia by polymerase chain reaction and dual restriction enzyme analysis.
Prenatal diagnosis of thalassemia: experiences at the Shanghai Children's Hospital.
Structural analysis of the alpha-globin gene cluster in two Chinese families with alpha-thalassemias.
The 3' untranslated regions of the duplicated human alpha-globin genes are unexpectedly divergent.
The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.
The molecular basis of HbH disease in Taiwan.
The prevalence of avascular necrosis in sickle cell anemia: correlation with alpha-thalassemia.
The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacks.
The xerocytosis of Hb SC disease.
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
[Detection of alpha-thalassemias in patients with microcytic hypochromic anemia or microcytosis by restriction endonuclease mapping]
Alveolar Bone Loss
Association of gene polymorphisms for plasminogen activators with alveolar bone loss.
Alzheimer Disease
A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping or DNA sequencing. V. Analysis of case/control sampling designs: Alzheimer's disease and the apoprotein E locus.
A HindIII polymorphism detected by the cDNA encoding amyloid beta protein of Alzheimer's disease.
Association of estrogen receptor alpha (ESR1) PvuII and XbaI polymorphisms with sporadic Alzheimer's disease and their effect on apolipoprotein E concentrations.
Association study between Alzheimer's disease and restriction fragment length polymorphisms at the human amyloid beta protein gene locus.
Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease.
DNA polymorphisms of apolipoprotein B and angiotensin I-converting enzyme genes and relationships with lipid levels in Italian patients with vascular dementia or Alzheimer's disease.
Editing for an AMPA receptor subunit RNA in prefrontal cortex and striatum in Alzheimer's disease, Huntington's disease and schizophrenia.
Estrogen receptor 1 PvuII and XbaI polymorphisms and susceptibility to Alzheimer's disease: a meta-analysis.
Estrogen receptor ? gene polymorphisms and risk of Alzheimer's disease: evidence from a meta-analysis.
Familial Alzheimer's disease (FAD): co-segregation between alleles at the D21S11 DNA marker and the FAD gene in a particular pedigree.
Lipoprotein Lipase HindIII Intronic Polymorphism in a Subset of Iranian Patients with Late-Onset Alzheimer's Disease.
Low frequency of the APP 670/671 mutation in familial Alzheimer's disease in Sweden.
Meta-analysis of PvuII, XbaI variants in ESR1 gene and the risk of Alzheimer's disease: the regional European difference.
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's disease.
Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease.
Screening for the APP codon 670/671 mutations in Alzheimer's disease.
Screening of the mis-sense mutation producing the 717Val-->Ile substitution in the amyloid precursor protein in Japanese familial and sporadic Alzheimer's disease.
Study of restriction fragment length polymorphism in the cystatin C gene of elderly patients with dementia and aged Down's syndrome patients.
The H+ allele of the lipoprotein lipase (LPL) HindIII intronic polymorphism and the risk for sporadic late-onset Alzheimer's disease.
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease.
[An association analysis of apolipoprotein E genotypes with Alzheimer's disease in Chinese population]
Ameloblastoma
Analysis of amelogenin gene (AMGX, AMGY) expression in ameloblastoma.
Epigenetic regulation of matrix metalloproteinase expression in ameloblastoma.
Amyloidosis
A specific test for transthyretin 122 (Val----Ile), based on PCR-primer-introduced restriction analysis (PCR-PIRA): confirmation of the gene frequency in blacks.
Frequency and genetic background of the position 122 (Val----Ile) variant transthyretin gene in the black population.
Amyloidosis, Familial
Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences.
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Androgen-Insensitivity Syndrome
An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndrome.
Deletion of the steroid-binding domain of the human androgen receptor gene in one family with complete androgen insensitivity syndrome: evidence for further genetic heterogeneity in this syndrome.
Anemia
A decade of screening in the hemoglobinopathies: is a national program to prevent sickle cell anemia possible?
Amplification of a beta-haemoglobin sequence in individual human oocytes and polar bodies.
Antenatal diagnosis of sickle-cell anaemia by means of DNA restriction analysis.
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications.
Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis.
Frequency of haplotypes in the beta globin gene cluster in a selected sample of the mexican population.
Gene probes: application to prenatal and postnatal diagnosis of genetic disease.
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.
Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
Recombinant DNA technology and laboratory medicine.
The use of restriction endonucleases in the prenatal diagnosis of hemoglobinopathies.
Anemia, Hemolytic
[Molecular-genetic studies of carrier stage of glucose-6-phosphate dehydrogenase deficiency]
Anemia, Hypochromic
Viromes of Ten Alfalfa Plants in Australia Reveal Diverse Known Viruses and a Novel RNA Virus.
[Detection of alpha-thalassemias in patients with microcytic hypochromic anemia or microcytosis by restriction endonuclease mapping]
[The molecular basis of HbH disease in a Japanese girl]
Anemia, Sickle Cell
A decade of screening in the hemoglobinopathies: is a national program to prevent sickle cell anemia possible?
Amplification of a beta-haemoglobin sequence in individual human oocytes and polar bodies.
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications.
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.
Frequency of haplotypes in the beta globin gene cluster in a selected sample of the mexican population.
Gene probes: application to prenatal and postnatal diagnosis of genetic disease.
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.
Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability.
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
Recombinant DNA technology and laboratory medicine.
Restriction endonuclease analysis of DNA in sickle cell lesions among tribals of Bihar, Madhya Pradesh, Gujarat & Rajasthan.
The use of restriction endonucleases in the prenatal diagnosis of hemoglobinopathies.
Anencephaly
A human autosomal phosphoglycerate kinase locus maps near the HLA cluster.
Aneurysm
Cellular, enzymatic, and genetic factors in the pathogenesis of abdominal aortic aneurysms.
Surgical Treatment of Middle Cerebral Artery Aneurysms: Aneurysm Location and Size Ratio as Risk Factors for Neurologic Worsening and Ischemic Complications.
Angina, Stable
[Connection of HindIII-polymorphism in the lipoprotein lipase gene with myocardial infarct and life span in elderly ischemic heart disease patients]
Angiomatosis, Bacillary
Characterization of a novel Rochalimaea species, R. henselae sp. nov., isolated from blood of a febrile, human immunodeficiency virus-positive patient.
Anthrax
[A species-specific DNA probe for identifying toxic strains of anthrax pathogens]
Antiphospholipid Syndrome
Association of HLA-DM polymorphism with the production of antiphospholipid antibodies.
Aortic Aneurysm, Abdominal
Genetic variants of collagen III and abdominal aortic aneurysm.
Aphakia
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.
Arteritis
Detection of equine arteritis virus (EAV) by polymerase chain reaction (PCR) and differentiation of EAV strains by restriction enzyme analysis of PCR products.
Arthritis
Characteristics of a novel lentivirus derived from South African sheep with pulmonary adenocarcinoma (jaagsiekte).
Comparison of avian Chlamydia psittaci isolates by restriction endonuclease analysis and serovar-specific monoclonal antibodies.
Comparison of Chlamydia psittaci isolates by restriction endonuclease and DNA probe analyses.
HLA in ankylosing spondylitis: is HLA-B27 the only MHC gene involved in disease pathogenesis?
Polymorphism in the LMP2 gene influences susceptibility to extraspinal disease in HLA-B27 positive individuals with ankylosing spondylitis.
Arthritis, Psoriatic
Arthritis in patients with psoriasis is associated with an immunoglobulin gene polymorphism.
Arthritis, Rheumatoid
A minority of patients with rheumatoid arthritis show a dominant rearrangement of T-cell receptor beta chain genes in synovial lymphocytes.
Association between EcoRI fragment-length polymorphism of the immunoglobulin lambda variable 8 (IGLV8) gene family with rheumatoid arthritis and systemic lupus erythematosus.
Lack of correlation between BglII RFLP in the human interleukin 6 gene and rheumatoid arthritis.
Plasminogen activator inhibitor-1 C/G polymorphism in relation to plasma levels in rheumatoid arthritis.
Polymerase chain reaction-based genotyping for allotypic markers of immunoglobulin kappa shows allelic association of Km with kappa variable segment.
Polymorphism and expression of the galactosyltransferase-associated protein kinase gene in normal individuals and galactosylation-defective rheumatoid arthritis patients.
The association of DNA variants at or near the IgH locus with rheumatoid arthritis.
aspartate transaminase deficiency
Cloning and nucleotide sequencing of Rhizobium meliloti aminotransferase genes: an aspartate aminotransferase required for symbiotic nitrogen fixation is atypical.
Aspartylglucosaminuria
Aspartylglycosaminuria in the Finnish population: identification of two point mutations in the heavy chain of glycoasparaginase.
Aspergillosis
Comparison of three typing methods for clinical and environmental isolates of Aspergillus fumigatus.
DNA typing of epidemiologically-related isolates of Aspergillus fumigatus.
Asthma
Association between genetic variants of mast-cell chymase and eczema.
Correlation between polymorphisms in the glucocorticoid receptor gene NR3C1 and susceptibility to asthma in a Chinese population from the Henan Province.
Effect of glucocorticoid receptor gene polymorphisms on asthma phenotypes.
Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.
[Screening specific allergens of allergic asthma from DNA expression library of humulus pollen]
Astrocytoma
Expression and characterization of the bovine histamine H1 receptor in cDNA-transfected C6 astroglioma cells.
ICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.
Ataxia
A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia.
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Ataxia Telangiectasia
Analysis of mutations caused by DNA double-strand breaks produced by a restriction enzyme in shuttle vector plasmids propagated in ataxia telangiectasia cells.
Focus-formation of replication protein A, activation of checkpoint system and DNA repair synthesis induced by DNA double-strand breaks in Xenopus egg extract.
Response of ataxia telangiectasia cells to restriction endonuclease induced DNA double-strand breaks: I. Cytogenetic characterization.
Atherosclerosis
ApoA-I related DNA polymorphism in humans with coronary heart disease.
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population.
Association of LPL gene variant and LDL, HDL, VLDL cholesterol and triglyceride levels with ischemic stroke and its subtypes.
Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden.
Common DNA polymorphisms at the lipoprotein lipase gene. Association with severity of coronary artery disease and diabetes.
CR1 genotype and haplotype involvement in coronary artery disease: the pivotal role of hypertension and dyslipidemia.
DNA polymorphisms of the apolipoprotein B gene (XbaI, EcoRI, and MspI RFLPs) in Norwegians at risk of atherosclerosis and healthy controls.
Estrogen receptor ? genetic variants and the risk of stroke in a South Indian population from Andhra Pradesh.
Evaluation of high sensitive C-reactive protein and 5-10 methylenetetrahydrofolate reductase genotype in japanese young adults.
HindIII DNA polymorphism in the lipoprotein lipase gene and plasma lipid phenotypes and carotid artery atherosclerosis.
Interactive effect of the p53 gene and cigarette smoking on coronary artery disease.
Lipoprotein lipase gene polymorphisms: associations with myocardial infarction and lipoprotein levels, the ECTIM study. Etude Cas Témoin sur l'Infarctus du Myocarde.
Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS).
Lipoprotein lipase locus and progression of atherosclerosis in coronary-artery bypass grafts.
The effect of hormone replacement therapy on atherosclerotic severity in relation to ESR1 genotype in postmenopausal women.
Variation in the apolipoprotein B gene and development of type 2 diabetes mellitus.
Variation of apolipoprotein B gene is associated with myocardial infarction and lipoprotein levels in Danes.
[Connection of polymorphic alleles of the gene cluster AI/CIII/AIV with disturbed lipid metabolism]
Bacteremia
An endemic strain of Staphylococcus haemolyticus colonizing and causing bacteremia in neonatal intensive care unit patients.
Association between the A/A genotype at the lymphotoxin-alpha+250 site and increased mortality in children with positive blood cultures.
Genomic variations among Bartonella henselae isolates derived from naturally infected cats.
Klebsiella typing: pulsed-field gel electrophoresis (PFGE) in comparison with O:K-serotyping.
Recurrent Staphylococcus aureus bacteremia.
Bacterial Infections
Characterization of four lytic transducing bacteriophages of luminescent Vibrio harveyi isolated from shrimp (Penaeus monodon) hatcheries.
Molecular epidemiology of bacterial infections.
Molecular genetic analysis of Actinobacillus actinomycetemcomitans epidemiology.
Basal Cell Nevus Syndrome
A missense mutation in PTCH2 underlies dominantly inherited NBCCS in a Chinese family.
Beckwith-Wiedemann Syndrome
Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome.
beta-Thalassemia
Abnormal globin gene structure and expression in beta-thalassemia.
Alpha globin gene triplication in severe heterozygous beta thalassemia.
Analysis of globin gene structure in patients with beta thalassemia by restriction endonuclease mapping.
Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemia.
Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis.
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis.
Gene probes: application to prenatal and postnatal diagnosis of genetic disease.
Heterogeneity of DNA deletion in gamma delta beta-thalassemia.
High incidence of the CD8/9 (+G) beta 0-thalassemia mutation in Spain.
Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin.
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Molecular basis of beta-thalassemia in Japan: heterogeneity and origins of mutations.
Molecular basis of beta-thalassemia in Turkey: detection of rare mutations by direct sequencing.
Molecular characterization of beta-thalassemia in Syria.
Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia.
Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites.
Prenatal diagnosis of thalassemia: experiences at the Shanghai Children's Hospital.
Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic origin.
The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes.
The entire beta-globin gene cluster is deleted in a form of gamma delta beta-thalassemia.
The molecular basis of beta-thalassemia in Turkey.
The peculiar spectrum of beta-thalassemia genes in Tunisia.
Utility of the polymerase chain reaction (PCR) for prenatal diagnosis of genetic disease.
Birdshot Chorioretinopathy
A 1.4-kb BamHI restriction fragment of genomic DNA correlates with the birdshot retinochoroidopathy susceptibility gene.
Bluetongue
Characterization of an Indian bluetongue virus isolate by RT-PCR and restriction enzyme analysis of the VP-7 gene sequence.
Identification of bluetongue virus VP6 protein as a nucleic acid-binding protein and the localization of VP6 in virus-infected vertebrate cells.
Restriction enzyme analysis of VP7 gene of Indian isolates of bluetongue virus.
Bone Diseases, Metabolic
A novel polymorphism in the promoter region for the human osteocalcin gene: the possibility of a correlation with bone mineral density in postmenopausal Japanese women.
Estrogen receptor (ER) gene polymorphism may predict the bone mineral density response to raloxifene in postmenopausal women on chronic hemodialysis.
PvuII and XbaI polymorphisms of the estrogen receptor gene and bone mineral density in a Bulgarian population sample.
The importance of polymorphic variants of collagen 1A2 gene (COL1A2) in the development of osteopenia and osteoporosis in postmenopausal women.
[PvuII genetic polymorphism of estrogen receptor alpha in the group of postmenopausal women with osteopenia and osteoporosis]
Bone Resorption
Vitamin-D receptor genotype does not predict bone mineral density, bone turnover, and growth in prepubertal children.
Border Disease
Genetic identification of pestivirus strain Frijters as a border disease virus from pigs.
Brain Diseases
Detection frequency of human herpesviruses-6A, -6B, and -7 genomic sequences in central nervous system DNA samples from post-mortem individuals with unspecified encephalopathy.
High prevalence of Helicobacter pylori infection in cohabiting children. Epidemiology of a cluster, with special emphasis on molecular typing.
Brain Neoplasms
Measurement of O-6-methylguanine-DNA methyltransferase activity using oligonucleotides and restriction enzyme in human brain tumors.
Molecular biology of brain tumors.
[Analysis of DNA damage induced by nitrosourea derivatives in rat brain tumor cells using a sequencing procedure]
Breast Diseases
Selected estrogen receptor 1 and androgen receptor gene polymorphisms in relation to risk of breast cancer and fibrocystic breast conditions among Chinese women.
Breast Neoplasms
A cytochrome P4502E1 genetic polymorphism and tobacco smoking in breast cancer.
A functional polymorphism of the tumor necrosis factor receptor-II gene associated with the survival and relapse prediction of breast carcinoma.
A multigenic study on breast cancer risk associated with genetic polymorphisms of ER Alpha, COMT and CYP19 gene in BRCA1/BRCA2 negative Shanghai women with early onset breast cancer or affected relatives.
A single point mutation responsible for c-mos polymorphism in cancer patients.
A truncated cyclin D1 gene encodes a stable mRNA in a human breast cancer cell line.
Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy.
Analysis of the ERalpha germline PvuII marker in breast cancer risk.
Analysis of the PvuII restriction fragment-length polymorphism and exon structure of the estrogen receptor gene in breast cancer and peripheral blood.
Analysis of the R72P polymorphism of the TP53 gene in patients with invasive ductal breast carcinoma.
Apolipoprotein A1 -75 G/A and +83 C/T polymorphisms: susceptibility and prognostic implications in breast cancer.
Association between ER? gene Pvu II polymorphism and breast cancer susceptibility: A meta-analysis.
Association Between ESR1 PvuII, XbaI, and P325P Polymorphisms and Breast Cancer Susceptibility: A Meta-Analysis.
Association between restriction fragment length polymorphism of the L-myc gene and lung metastasis in human breast cancer.
Association of estrogen receptor alpha (ER?) gene polymorphisms with endometrial thickness and lipid profile in women with breast cancer treated with aromatase inhibitors.
Association of FokI and PvuII polymorphisms with breast cancer staging and survival among Caucasian women: a prospective study.
Association of PvuII and XbaI polymorphisms on estrogen receptor alpha (ESR1) gene to changes into serum lipid profile of post-menopausal women: Effects of aging, body mass index and breast cancer incidence.
Characterization of sequences related to the mouse mammary tumor virus that are specific to MCF-7 breast cancer cells.
Close proximity of c-erbA2 and c-erbA-beta genes on the short arm of chromosome 3.
Detection of mammary tumor virus env gene-like sequences in human breast cancer.
Detection of metastatic breast cancer by beta-hCG polymerase chain reaction.
EcoRI polymorphism of the metastasis-suppressor gene NME1 in Mexican patients with breast cancer.
Epidermal growth factor genetic variation, breast cancer risk, and waiting time to onset of disease.
Epigenetic reversion of breast carcinoma phenotype is accompanied by changes in DNA sequestration as measured by AluI restriction enzyme.
Estrogen receptor alpha gene polymorphisms and breast cancer risk.
Estrogen receptor alpha gene polymorphisms and breast cancer risk: a case-control study with meta-analysis combined.
Estrogen receptor alpha polymorphisms and postmenopausal breast cancer risk.
Estrogen receptor polymorphisms in tamoxifen-treated women with breast cancer.
Estrogen receptor-alpha gene (T/C) Pvu II polymorphism in endometriosis and uterine fibroids.
Genetic polymorphims of estrogen receptor alpha -397 PvuII (T>C) and -351 XbaI (A>G) in a portuguese population: prevalence and relation with breast cancer susceptibility.
Genetic polymorphisms in the estrogen receptor alpha gene and risk of breast cancer: results from the Shanghai Breast Cancer Study.
Genetic variation in the tumor necrosis factor-alpha promoter region and in the stress protein hsp70-2: susceptibility and prognostic implications in breast carcinoma.
Hypermethylation of HpaII recognition sequences within the 5' coding region of the estrogen receptor gene is not associated with estrogen receptor negativity in primary breast tumours.
Identification, cloning and characterization of two N-acetylgalactosamine binding lectins from the albumen gland of Helix pomatia .
Immunohistochemical expression of p53 in breast carcinoma is associated with the intron 1 BglII polymorphism of the p53 gene.
Interaction between alcohol dehydrogenase II gene, alcohol consumption, and risk for breast cancer.
Joint effects of the CYP1A1 MspI, ERalpha PvuII, and ERalpha XbaI polymorphisms on the risk of breast cancer: results from a population-based case-control study in Shanghai, China.
Leptin and leptin receptor polymorphisms are associated with increased risk and poor prognosis of breast carcinoma.
Menopausal status modifies breast cancer risk associated with ESR1 PvuII and XbaI polymorphisms in Asian women: a HuGE review and meta-analysis.
MMTV-associated transcription factor binding sites increase nm23-H1 metastasis suppressor gene expression in human breast carcinoma cell lines.
Polymorphism in mtDNA control region of Mizo-Mongloid Breast Cancer samples as revealed by PCR-RFLP analysis.
Polymorphism in the tumor necrosis factor-alpha promotor region and in the heat shock protein 70 genes associated with malignant tumors.
Polymorphisms in ER-alpha gene interact with estrogen receptor status in breast cancer survival.
Polymorphisms in the DNA repair gene XRCC1, breast cancer risk, and response to radiotherapy.
Polymorphisms in the estrogen receptor alpha gene and mammographic density.
Possibilities of a viral etiology for human breast cancer. A review.
Presence of an allelic EcoRI restriction fragment of the c-mos locus in leukocyte and tumor cell DNAs of breast cancer patients.
Progesterone receptor gene restriction fragment length polymorphisms in human breast tumors.
Prognostic Significance of ESR1 Amplification and ESR1 PvuII, CYP2C19*2, UGT2B15*2 Polymorphisms in Breast Cancer Patients.
Promoter Methylation Status of Breast Cancer Susceptibility Gene 1 and 17 Beta Hydroxysteroid Dehydrogenase Type 1 Gene in Sporadic Breast Cancer Patients.
PvuII polymorphism of estrogen receptor-? gene in breast cancer.
Restriction endonuclease fingerprinting enhanced conformation sensitive gel electrophoresis (REF-CSGE) in the analysis of BRCA1 exon 11 mutations in a high-risk breast cancer cohort.
Selected estrogen receptor 1 and androgen receptor gene polymorphisms in relation to risk of breast cancer and fibrocystic breast conditions among Chinese women.
Silencing of the mammary-derived growth inhibitor (MDGI) gene in breast neoplasms is associated with epigenetic changes.
Structural changes in DNA of human breast carcinoma.
The estrogen receptor alpha gene and breast cancer risk (The Netherlands).
The variant T allele of PvuII in ESR1 gene is a prognostic marker in early breast cancer survival.
Vitamin D receptor polymorphisms (FokI, BsmI) and breast cancer risk: association replication in two case-control studies within French Canadian population.
[Analysis of the association of inherited predisposition to breast cancer with c-Ha-ras-1 oncogene alleles]
[Construction of the eukaryotic expression vector of human syk and its effect on MHC-I expression of human breast cancer cells.]
[Genetic variation in pro-inflammatory cytokines (interleukin-1beta, interleukin-1alpha and interleukin-6) associated with the aggressive forms, survival, and relapse prediction of breast carcinoma.]
[The XbaI and PvuII gene polymorphisms of the estrogen receptor alpha gene in Chinese women with breast cancer]
Bronchiectasis
Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease.
Bronchiolitis
Molecular epidemiology and clinical presentation of human adenovirus infections in Kansas City children.
Bronchitis
A new typing method for the avian infectious bronchitis virus using polymerase chain reaction and restriction enzyme fragment length polymorphism.
Bronchitis, Chronic
Effect of glucocorticoid receptor gene polymorphisms on asthma phenotypes.
Pneumocystis jiroveci isolates with dihydropteroate synthase mutations in patients with chronic bronchitis.
Bronchopulmonary Dysplasia
No association between TAP1 DpnII polymorphism and bronchopulmonary dysplasia.
Brucellosis
Interferon-? receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region.
Brucellosis, Bovine
Restriction endonuclease analysis of Brucella abortus.
Burkitt Lymphoma
Characterization of the major Epstein-Barr virus-specific RNA in Burkitt lymphoma-derived cells.
Clonality and methylation status of the Epstein-Barr virus (EBV) genomes in in vivo-infected EBV-carrying chronic lymphocytic leukemia (CLL) cell lines.
Epstein-Barr virus latent gene transcription in nasopharyngeal carcinoma cells: coexpression of EBNA1, LMP1, and LMP2 transcripts.
Epstein-Barr virus nuclear antigen (EBNA): size polymorphism of EBNA 1.
Identification of transcribed regions of Epstein-Barr virus DNA in Burkitt lymphoma-derived cells.
Interferon regulatory factor 2 represses the Epstein-Barr virus BamHI Q latency promoter in type III latency.
Interferon regulatory factor 7 is induced by Epstein-Barr virus latent membrane protein 1.
Methylation of discrete sites within the enhancer region regulates the activity of the Epstein-Barr virus BamHI W promoter in Burkitt lymphoma lines.
Methylation of transcription factor binding sites in the Epstein-Barr virus latent cycle promoter Wp coincides with promoter down-regulation during virus-induced B-cell transformation.
Somatic mutation and transcriptional deregulation of myc in endemic Burkitt's lymphoma disease: heptamer-nonamer recognition mistakes?
Structural analyses of the Epstein-Barr virus BamHI A transcripts.
The Epstein-Barr virus (EBV) nuclear antigen 1 BamHI F promoter is activated on entry of EBV-transformed B cells into the lytic cycle.
The Epstein-Barr virus BamHI F promoter is an early lytic promoter: lack of correlation with EBNA 1 gene transcription in group 1 Burkitt's lymphoma cell lines.
Transfection of lymphoblastoid cells using DNA-loaded reconstituted Sendai virus envelopes: expression of transfected DNA and selection of transfected cells.
Up regulation of the Epstein-Barr virus (EBV)-encoded membrane protein LMP in the Burkitt's lymphoma line Daudi after exposure to n-butyrate and after EBV superinfection.
Campylobacter Infections
Campylobacter spp. in New Zealand raw sheep liver and human campylobacteriosis cases.
Candidemia
Clustering of Candida infections in the neonatal intensive care unit: concurrent emergence of multiple strains simulating intermittent outbreaks.
Carcinogenesis
An analysis of the polymorphisms of the GLUT1 gene in urothelial cell carcinomas of the bladder and its correlation with p53, Ki67 and GLUT1 expressions.
CD59 silencing via retrovirus-mediated RNA interference enhanced complement-mediated cell damage in ovary cancer.
Epstein--Barr virus gene polymorphisms in Chinese Hodgkin's disease cases and healthy donors: identification of three distinct virus variants.
Epstein-Barr Virus miR-BART17-5p Promotes Migration and Anchorage-Independent Growth by Targeting Kruppel-Like Factor 2 in Gastric Cancer.
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.
Methylation of the alphafetoprotein gene in cell populations isolated from rat livers during carcinogenesis.
Polymorphisms of xenobiotic metabolizing genes in oropharyngeal carcinoma.
Relative enhancer activity and transforming potential of authentic human papillomavirus type 6 genomes from benign and malignant lesions.
Sequence variations of Epstein-Barr virus-encoded BARF1 gene in nasopharyngeal carcinomas and healthy donors from southern and northern China.
Vitamin D and cancer.
Carcinoid Tumor
Two prohormones for gastrin-releasing peptide are encoded by two mRNAs differing by 19 nucleotides.
Carcinoma
A single point mutation responsible for c-mos polymorphism in cancer patients.
A submicroscopic homozygous deletion at the D3S3 locus in a cell line isolated from a small cell lung carcinoma.
Abnormal restriction pattern of PIP gene associated with human primary prostate cancers.
Abnormal structure of the canine oncogene, related to the human c-yes-1 oncogene, in canine mammary tumor tissue.
An analysis of the polymorphisms of the GLUT1 gene in urothelial cell carcinomas of the bladder and its correlation with p53, Ki67 and GLUT1 expressions.
Association of -1171 promoter polymorphism of matrix metalloproteinase-3 with increased risk for oral cancer.
c-Ha-ras BamHI RFLP in human urothelial tumors and point mutations in hot codons.
c-myc oncogene alterations in human thyroid carcinomas.
Can Different Thyroid Tumor Types Be Distinguished by Polymerase Chain Reaction-Based K-ras Mutation Detection?
Cell-specific ribosomal DNA spacer variability in human urothelial carcinoma cultures.
CG island methylation changes near the GSTP1 gene in prostatic carcinoma cells detected using the polymerase chain reaction: a new prostate cancer biomarker.
Characterization of a transcriptional promoter of human papillomavirus 18 and modulation of its expression by simian virus 40 and adenovirus early antigens.
Characterization of the tumor-associated 38-kd protein of herpes simplex virus type 2.
Cloning and analysis of integrated hepatitis virus sequences from a human hepatoma cell line.
Detection of human papillomavirus in vulval carcinoma using semi-nested PCR and restriction enzyme typing: a rapid and sensitive technique.
Differential methylation of the c-H-ras gene in normal mouse cells and during skin tumour progression.
DNA hypermethylation on multiple CpG islands associated with increased DNA methyltransferase DNMT1 protein expression during multistage urothelial carcinogenesis.
Effect of p53 polymorphism on the susceptibility of cervical cancer.
Epstein-Barr virus infection in carcinoma of the salivary gland.
Epstein-Barr virus plays little role in cervical carcinogenesis in Korean women.
Expression of beta-human chorionic gonadotropin genes in renal cell cancer and benign renal disease tissues.
Expression of the Epstein-Barr virus BamHI A fragment in nasopharyngeal carcinoma: evidence for a viral protein expressed in vivo.
Free cottontail rabbit papillomavirus DNA persists in warts and carcinomas of infected rabbits and in cells in culture transformed with virus or viral DNA.
Frequent ras gene mutations in squamous cell cervical cancer.
Genetic polymorphisms of estrogen receptor alpha, CYP19, catechol-O-methyltransferase are associated with familial prostate carcinoma risk in a Japanese population.
Glutathione S-transferase and cytochrome P450 genotypes as risk factors for laryngeal carcinoma.
H-ras protooncogene mutations in human thyroid neoplasms.
H19-DMR allele-specific methylation analysis reveals epigenetic heterogeneity of CTCF binding site 6 but not of site 5 in head-and-neck carcinomas: a pilot case-control analysis.
HLA class II antigen expression in human papillomavirus-associated cervical cancer.
Host Gene Expression Is Regulated by Two Types of Noncoding RNAs Transcribed from the Epstein-Barr Virus BamHI A Rightward Transcript Region.
HSV-2-induced tumorigenicity in HPV16-immortalized human genital keratinocytes.
Human papillomavirus DNA in cutaneous primary and metastasized squamous cell carcinomas from patients with epidermodysplasia verruciformis.
Hypermethylation of the tumor necrosis factor receptor superfamily 6 (APT1, Fas, CD95/Apo-1) gene promoter at rel/nuclear factor kappaB sites in prostatic carcinoma.
Identification of a tumor-specific methylation site in the Wilms tumor suppressor gene.
Increased hTR expression during transition from adenoma to carcinoma is not associated with promoter methylation.
Integration and methylation of shope papilloma virus DNA in the transplantable Vx2 and Vx7 rabbit carcinomas.
Methylation at the CpG doublet in equine adenovirus genome.
Methylation of CpG sites in exon 2 of the bcl-2 gene occurs in colorectal carcinoma.
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Mouse and human ornithine decarboxylase genes. Methylation polymorphism and amplification.
MUC2 gene suppression in human colorectal carcinomas and their metastases: in vitro evidence of the modulatory role of DNA methylation.
Polymerase chain reaction detection and restriction enzyme typing of human papillomavirus in cervical carcinoma.
Polymorphisms of xenobiotic metabolizing genes in oropharyngeal carcinoma.
Possible role for human papillomavirus 16 in squamous cell carcinoma of the finger.
Pretreatment with restriction enzyme or bovine serum albumin for effective PCR amplification of Epstein-Barr virus DNA in DNA extracted from paraffin-embedded gastric carcinoma tissue.
Promoter region methylation does not account for the frequent loss of expression of the Fas gene in colorectal carcinoma.
Regulation of ornithine decarboxylase gene expression in mouse epidermis and epidermal tumors during two-stage tumorigenesis.
Silencing of the E-cadherin invasion-suppressor gene by CpG methylation in human carcinomas.
Structural analyses of the Epstein-Barr virus BamHI A transcripts.
Synthesis, mutagenicity, binding to pBR 322 DNA and antitumour activity of platinum(II) complexes with ethambutol.
The association between estrogen receptor alpha polymorphisms and the risk of prostate cancer in Slovak population.
The Harvey ras 1 gene is activated in papillomavirus-associated carcinomas of the upper alimentary canal in cattle.
Transforming genes in human tumors.
Tumor-specific demethylation of heterochromatic repetitive DNA in gastrointestinal cancer.
[Construction and expression of human IL-8 sense or antisense eukaryotic expression vectors.]
[Deletion of OPCML gene and promoter methylation in ovarian epithelial carcinoma]
[Detection of human papillomavirus and herpesvirus genotypes in biopsy specimens from cervical carcinoma by PCR-endonuclease cleavage]
[Loss of Ha-ras alleles in DNA from gastric carcinoma tissue of Chinese individuals]
[Methylation of the putative tumor suppressor gene, RASSF1A, in primary cervical tumors]
[Restriction enzyme mismatch polymerase chain reaction in the demonstration of Ki-ras-oncogene mutation in carcinoma of the pancreas]
[Structural organization of the human p53 gene. I. Molecular cloning of the human p53 gene]
[Study on Ha-ras RFLPs in gastric carcinoma and normal tissue DNAs of Chinese individuals]
[The relation between prognosis and amplification of the c-erB-2 (HER-2/neu) proto-oncogene in ovarian carcinomas]
Carcinoma, Embryonal
Characterization of a mutant polyoma that expresses in F9 embryonal carcinoma cells: morphology, tumorigenicity, and restriction enzyme analysis.
Distribution and DNA methylation of a repetitive promoter sequence cloned from mouse embryonal carcinoma cells.
Molecular characterization of extrachromosomal circular DNAs from an embryonal carcinoma cell line induced to differentiate into neuron-like cells in vitro.
Carcinoma, Hepatocellular
Abnormal expression of hepatoma specific gamma-glutamyl transferase and alteration of gamma-glutamyl transferase gene methylation status in patients with hepatocellular carcinoma.
Aflatoxin sufferer and p53 gene mutation in hepatocellular carcinoma.
Analysis of integrated hepatitis B virus DNA and cellular flanking sequences cloned from a hepatocellular carcinoma.
Analysis of the cellular origin of hepatocellular carcinoma by p53 genotype.
Apolipoprotein B genetic polymorphisms in several human hepatoma derived liver cell lines.
Association between estrogen receptor 1 (ESR1) genetic variations and cancer risk: a meta-analysis.
Base sequences of highly repetitive components in nuclear DNAs from rat liver and rat-ascites hepatoma.
Binding affinities of highly repetitive DNA components for a nuclear scaffold protein from rat-ascites hepatoma cells.
Chicken embyro lethal orphan (CELO) virus DNA present in hamster cell lines derived from CELO-induced hepatomas.
Covalent modification and repressed transcription of a gene in hepatoma cells.
Defective hepatitis B virus DNA molecules detected in a stable integration pattern in a hepatoma cell line, and in induced tumours and derived cell lines.
Detection of a progression-linked DNA restriction fragment in rat hepatoma cells probed with a hexokinase cDNA.
Establishment of mice model with human viral hepatitis B.
Expression of calcium-binding protein regucalcin mRNA in hepatoma cells.
Fowl Adenovirus-Based Vaccine Platform.
Glucose metabolism in cancer. Evidence that demethylation events play a role in activating type II hexokinase gene expression.
Hepatocellular carcinoma in Richardson's ground squirrels (Spermophilus richardsonii): evidence for association with hepatitis B-like virus infection.
Hypomethylation of c-myc and epidermal growth factor receptor genes in human hepatocellular carcinoma and fetal liver.
Modifications in alpha 2u globulin gene structure, transcription, and mRNA translation in hepatomas.
Molecular and functional analysis of glutamine uptake in human hepatoma and liver-derived cells.
Mutations in the p53 gene at codon 249 are rare in squamous-cell carcinoma of the head and neck.
No Association between Catalase Gene Polymorphism and Gastric Carcinoma and Hepatocellular Carcinoma in Koreans.
P53 codon 249 mutation in hepatocellular carcinomas from Nigeria.
P53 mutations may be related to tumor invasiveness of human hepatocellular-carcinoma in china.
Point mutation, allelic loss and increased methylation of c-Ha-ras gene in human hepatocellular carcinoma.
Regulation and expression of carbamyl phosphate synthetase I mRNA in developing rat liver and Morris hepatoma 5123D.
Regulation of microsomal, xenobiotic epoxide hydrolase messenger RNA in persistent hepatocyte nodules and hepatomas induced by chemical carcinogens.
[Differences in expression and functional organization of the rat tyrosine aminotransferase gene in two lines of Morris hepatoma, 8994 and 7777]
[Establishment of AFP promoter operated murine IL-1beta recombinant vector and its expression in H22 cells.]
[Induction of specific humoral immune response in mice by recombinant mutant HBV s gene vaccine]
[Research on promoter region methylation status of tumor repressor gene P16 in human hepatocellular carcinoma by using methylation sensitive restriction enzyme and semi-nested PCR assay]
[The relation between p53 mutations and tumor invasiveness of human hepatocellular carcinoma]
Carcinoma, Lewis Lung
Synthesis, mutagenicity, binding to pBR 322 DNA and antitumour activity of platinum(II) complexes with ethambutol.
Carcinoma, Non-Small-Cell Lung
Association of EcoRI polymorphism of the metastasis-suppressor gene NME1 with susceptibility to and severity of non-small cell lung cancer.
Association of estrogen receptor ? gene PvuII and XbaI polymorphisms with non-small cell lung cancer.
Carcinoma, Papillary
Can Different Thyroid Tumor Types Be Distinguished by Polymerase Chain Reaction-Based K-ras Mutation Detection?
Carcinoma, Renal Cell
Aberrant promoter methylation of the ABCG2 gene in renal carcinoma.
c-Ha-ras BamHI RFLP in human urothelial tumors and point mutations in hot codons.
Expression of beta-human chorionic gonadotropin genes in renal cell cancer and benign renal disease tissues.
Identification of a tumor-specific methylation site in the Wilms tumor suppressor gene.
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Carcinoma, Squamous Cell
Cytotoxicity of restriction enzyme-induced DNA strand breaks in radiosensitive and radioresistant human tumor cell lines.
Epstein-Barr virus plays little role in cervical carcinogenesis in Korean women.
Frequent ras gene mutations in squamous cell cervical cancer.
H19-DMR allele-specific methylation analysis reveals epigenetic heterogeneity of CTCF binding site 6 but not of site 5 in head-and-neck carcinomas: a pilot case-control analysis.
HSV-2-induced tumorigenicity in HPV16-immortalized human genital keratinocytes.
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas.
Possible role for human papillomavirus 16 in squamous cell carcinoma of the finger.
[Methylation of the putative tumor suppressor gene, RASSF1A, in primary cervical tumors]
Carcinoma, Transitional Cell
Cell-specific ribosomal DNA spacer variability in human urothelial carcinoma cultures.
DNA hypermethylation on multiple CpG islands associated with increased DNA methyltransferase DNMT1 protein expression during multistage urothelial carcinogenesis.
Methylation at the CpG doublet in equine adenovirus genome.
Cardiomyopathies
A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathy.
Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.
Cardiovascular Diseases
Association of estrogen receptor-alpha gene polymorphisms with cardiac autonomic nervous activity in healthy young Japanese males.
Association of lipase lipoprotein polymorphisms with myocardial infarction and lipid levels.
Association of the apolipoprotein B gene polymorphisms with essential hypertension in Northern Chinese Han population.
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
ESR1 gene polymorphisms PvuII (rs2234693T>C) and XbaI (rs9340799A>G) may not be directly correlated with cardiovascular disease risk.
MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Variation in the apolipoprotein B gene and development of type 2 diabetes mellitus.
Carotid Artery Diseases
Polymorphisms XbaI (rs693) and EcoRI (rs1042031) of the ApoB gene are associated with carotid plaques but not with carotid intima-media thickness in patients with diabetes mellitus type 2.
Carotid Stenosis
IL-6 promoter polymorphism increased risks of recurrent stroke in the young patients with moderate internal carotid artery stenosis.
Cat-Scratch Disease
Predominance of two Bartonella henselae variants among cat-scratch disease patients in the Netherlands.
Celiac Disease
An HLA-D region restriction fragment length polymorphism associated with celiac disease.
Hemochromatosis gene mutations and iron metabolism in celiac disease.
Cerebral Hemorrhage
A study of ER? PvuII polymorphism in female patients with acute stroke: no associations with disease severity and early outcome.
Cerebral Infarction
Polymorphisms of the lipoprotein lipase gene are associated with atherosclerotic cerebral infarction in the Chinese.
Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
[Association of estrogen receptor gene polymorphism with cerebral infarction, a case-control study]
Cerebrovascular Disorders
Association of estrogen receptor-alpha gene polymorphisms with stroke risk in patients with metabolic syndrome.
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Dyslipidemia: Genetics, lipoprotein lipase and HindIII polymorphism.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
Cervical Intraepithelial Neoplasia
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas.
Chagas Disease
Characterization of Trypanosoma cruzi isolates from Paraguay, using restriction enzyme analysis of kinetoplast DNA.
Strains and clones of Trypanosoma cruzi can be characterized by pattern of restriction endonuclease products of kinetoplast DNA minicircles.
Chancroid
Molecular characterization of Haemophilus ducreyi by ribosomal DNA fingerprinting.
Charcot-Marie-Tooth Disease
X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.
Chickenpox
Analysis of varicella-zoster virus DNAs of clinical isolates by endonuclease HpaI.
Characterization of human varicella-zoster virus DNA.
Comparative analysis of the restriction endonuclease profiles of the Dumas and Singapore strains of varicella-zoster virus.
Differentiation of oka varicella vaccine strain from wild varicella-zoster virus strains isolated from vaccinees and household contact.
Genome differences among varicella-zoster viruses isolated in Thailand.
Identification and analysis of the simian varicella virus thymidine kinase gene.
Molecular epidemiology of live, attenuated varicella virus vaccine in children with leukemia and in normal adults.
Nationwide distribution of varicella-zoster virus clades in China.
Simian varicella virus DNA shares homology with human varicella-zoster virus DNA.
The simian varicella virus and varicella zoster virus genomes are similar in size and structure.
Varicella zoster virus DNA exists as two isomers.
Viral isolates derived from simian varicella epizootics are genetically related but are distinct from other primate herpesviruses.
VZV Molecular Epidemiology.
Cholangiocarcinoma
Detection of c-Ki-ras mutations in bile samples from patients with pancreatic and biliary cancers.
Expression of nuclear factor kappa B in hepatitis C virus core gene transfected cholangiocarcinoma cells.
Cholecystolithiasis
[The relationship between the C589T polymorphism of IL-4 gene and cholelithiasis]
Cholelithiasis
Association of lipoprotein receptor, receptor-associated protein, and metabolizing enzyme gene polymorphisms with gallstone disease: A case-control study.
[Polymorphism at cholesteryl ester transfer protein gene loci in patients with gallstone]
[Relationship among the XhaI and EcoRI locus polymorphisms of apolipoprotein B gene, serum lipid metabolism and gallstone disease]
Cholera
A study of the use of multilocus enzyme electrophoresis as a typing tool in fowl cholera outbreaks.
Characterisation of Pasteurella multocida isolated from fowl cholera outbreaks on turkey farms.
Characterization of avian strains of Pasteurella multocida by restriction endonuclease and amplified fragment length polymorphism.
Differentiation of field isolates of Pasteurella multocida serotype 3,4 from live vaccine strain by genotypic characterization.
Gene fusion of cholera toxin B subunit and HBV PreS2 epitope and the antigenicity of fusion protein.
Persistence of cholera in the United States: isolation of Vibrio cholerae O1 from a patient with diarrhea in Maryland.
Persistence of plasmids, cholera toxin genes, and prophage DNA in classical Vibrio cholerae O1.
Phenotypic and genotypic characters of isolates of Pasteurella multocida obtained from back-yard poultry and from two outbreaks of avian cholera in avifauna in Denmark.
Recombinant nontoxinogenic Vibrio cholerae strains as attenuated cholera vaccine candidates.
Transmission of Pasteurella multocida on California turkey premises in 1988-89.
[Application of pulse-field gel electrophoresis analysis in the source-tracking of cholera epidemics]
[Phenotypic and molecular features of Vibrio cholerae isolated in Chile, Peru and Bolivia. Comparison with environmental reservoirs]
Chordoma
Cytogenetic, telomere, and telomerase studies in five surgically managed lumbosacral chordomas.
Choriocarcinoma
Segregation patterns of polymorphic restriction sites of the gene encoding the alpha subunit of human chorionic gonadotropin in trophoblastic disease.
Structural analysis of the polymorphic 3' region of the human chorionic gonadotropin-alpha gene in normal placenta and choriocarcinoma cells.
Choroideremia
Cloning of the breakpoints of a deletion associated with choroidermia.
Chronic Periodontitis
Association between Estrogen Receptor-? Gene XbaI and PvuII Polymorphisms and Periodontitis Susceptibility: A Meta-Analysis.
Transmission of Actinobacillus actinomycetemcomitans in families of adult periodontitis patients.
Classical Swine Fever
Classical swine fever virus: discrimination between vaccine strains and European field viruses by restriction endonuclease cleavage of PCR amplicons.
Genetic grouping of classical swine fever virus by restriction fragment length polymorphism of the E2 gene.
Cleft Lip
Genetic variation in transforming growth factor alpha: possible association of BamHI polymorphism with bilateral sporadic cleft lip and palate.
Interaction Effect of RsaI and BamHI Polymorphisms of TGF?, BMP2 and BMP4 on the Occurrence of Non-Syndromic Cleft Lip and Palate in Iranian Patients.
Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome.
TGF?/HinfI Polymorphisms Contribute to Nonsyndromic Cleft Lip and Palate in Turkish Patients.
[Analysis between transforming growth factor beta3 gene sfaNI polymorphism variant and non-syndromic cleft lip with or without cleft palate in people of Uygur's nationality and Han's in Xinjiang].
Cleft Palate
[Analysis between transforming growth factor beta3 gene sfaNI polymorphism variant and non-syndromic cleft lip with or without cleft palate in people of Uygur's nationality and Han's in Xinjiang].
Coinfection
Characterization of high-growth reassortant influenza A viruses generated in MDCK cells cultured in serum-free medium.
Competition between wild-type and a marked recombinant baculovirus (Spodoptera exigua nucleopolyhedrovirus) with enhanced speed of action in insect larvae.
Detection of human papillomavirus DNA in genital warts, cervical dysplasias and neoplasias.
Detection of mixed Leishmania infections in dogs from an endemic area in southeastern Brazil.
Epstein-Barr virus intrastrain recombination in oral hairy leukoplakia.
Evaluation of a Restriction Fragment Length Enzyme Assay for Differentiation of Haemoproteus and Plasmodium Across a Standard Region of the Mitochondrial Genome.
Genetic evidence for coinfection of honey bees by acute bee paralysis and Kashmir bee viruses.
High-level recombination specific to polyomavirus genomes targeted to the integration-transformation pathway.
Identification of a novel Lymantria dispar nucleopolyhedrovirus mutant that exhibits abnormal polyhedron formation and virion occlusion.
Intermolecular recombination of the herpes simplex virus type 1 genome analysed using two strains differing in restriction enzyme cleavage sites.
Intra-specific and inter-specific recombination of tortricid-specific granuloviruses during co-infection in insect larvae.
Molecular differentiation of bovine sarcocysts.
Molecular evidence and sequence analysis of a natural reassortant between cucumber mosaic virus subgroup IA and II strains.
Phenotypic and genetic analysis of Lymantria dispar nucleopolyhedrovirus few polyhedra mutants: mutations in the 25K FP gene may be caused by DNA replication errors.
Rad51 and Rad52 are involved in homologous recombination of replicating herpes simplex virus DNA.
Recombination in adenovirus. I. Analysis of recombinant viruses under non-selective conditions.
Colitis
Cloning and expression of genes for lysozyme and a 20-kDal protein of colitis bacteriophage.
Identification and expression of the 20 kd structural protein gene of colitis bacteriophage.
Colitis, Ulcerative
Lack of an association between polymorphisms of the T-cell receptor alpha-chain and ulcerative colitis.
The C/C(-13910) and G/G(-22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel disease.
The C/C_????? and G/G_????? Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease.
Colonic Neoplasms
Down-regulation of PIK3CG, a catalytic subunit of phosphatidylinositol 3-OH kinase, by CpG hypermethylation in human colorectal carcinoma.
Osteopontin knockdown suppresses the growth and angiogenesis of colon cancer cells.
Colorectal Neoplasms
A novel approach for rapid screening of mitochondrial D310 polymorphism.
Evidence for an association between compound heterozygosity for germ line mutations in the hemochromatosis (HFE) gene and increased risk of colorectal cancer.
Loss of heterozygosity of p53 gene and p53 protein expression in human colorectal carcinomas.
Restriction enzyme analysis of mitochondrial DNA in colorectal tumours.
Vitamin D receptor start codon polymorphism and colorectal cancer risk: effect modification by dietary calcium and fat in Singapore Chinese.
[Methylation status of p16 gene in colorectal carcinoma and normal colonic mucosa]
[Polymorphism of vitamin D receptor Fok I and colorectal cancer risk in Chinese]
Communicable Diseases
Application of a quantitative algorithm to restriction endonuclease analysis of Aujeszky's disease (pseudorabies) virus from a geographically localized outbreak.
Laboratory aspects of clinically significant rapidly growing mycobacteria.
[High homology of plasmids carrying class II restriction modification systems, EcoRV isoschizomers, and their prevalence in natural Escherichia coli strains]
Condylomata Acuminata
Rearrangements of the upstream regulatory region of human papillomavirus type 6 can be found in both Buschke-Löwenstein tumours and in condylomata acuminata.
Conjunctivitis
Antigenic and restriction endonuclease analyses of new adenovirus types 19 and 37 causing acute conjunctivitis.
Comparison of Chlamydia psittaci isolates by restriction endonuclease and DNA probe analyses.
Genome analysis of adenovirus type 3 isolated in Japan.
Genome analysis with restriction endonucleases recognizing 4- or 5-base pair sequences of adenovirus type.
Genome type analysis of Brazilian adenovirus strains of serotypes 1,2,3,5, and 7 collected between 1976 and 1995.
Genome typing of adenovirus strains isolated from conjunctivitis in Japan, Australia, and the Philippines.
Genomic comparison of adenovirus type 3 isolates from patients with acute conjunctivitis in Japan, Australia, and the Philippines.
Identification of a conjunctivitis-associated gene locus from the virulence plasmid of Yersinia enterocolitica.
Molecular epidemiology of adenoviral conjunctivitis in Sapporo, Japan, and Manila, the Philippines.
Molecular epidemiology of adenovirus conjunctivitis in Glasgow 1981-1991.
[Studies on new adenovirus types of subgenus D causing conjunctivitis--antigenic and restriction endonuclease analysis of adenovirus types 19 and 37]
Contracture
Detection of a novel ryanodine receptor subtype 1 mutation (R328W) in a malignant hyperthermia family by sequencing of a leukocyte transcript.
Corneal Ulcer
Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis--a case report of corneal ulcer.
Coronary Artery Disease
A common variant of the angiotensinogen gene and the risk of coronary artery disease in a German population.
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci.
APO B gene polymorphisms and coronary artery disease: a meta-analysis.
Apolipoprotein B, apolipoprotein E, and angiotensin-converting enzyme polymorphisms in 2 Italian populations at different risk for coronary artery disease and comparison of allele frequencies among European populations.
Apolipoproteins B and E, and angiotensin I-converting enzyme (ACE) genetic polymorphisms in Italian women with coronary artery disease (CAD) and their relationships with plasma lipid and apolipoprotein levels.
Association between HaeIII polymorphism of scavenger receptor class B type I gene and plasma HDL-cholesterol concentration.
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population.
Association of glucocorticoid receptor gene NR3C1 genetic variants with angiographically documented coronary artery disease and its risk factors.
Association of lipoprotein lipase gene polymorphisms with coronary artery disease.
Association of lipoprotein lipase Hind III and Ser 447 Ter polymorphisms with dyslipidemia in Asian Indians.
Association of PvuII polymorphism in the lipoprotein lipase gene with the coronary artery disease in Macedonian population.
Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden.
Associations for lipoprotein lipase and peroxisome proliferator-activated receptor-gamma gene and coronary artery disease in an Indian population.
Common DNA polymorphisms at the lipoprotein lipase gene. Association with severity of coronary artery disease and diabetes.
Common variants in the lipoprotein lipase gene in Brazil: association with lipids and angiographically assessed coronary atherosclerosis.
CR1 genotype and haplotype involvement in coronary artery disease: the pivotal role of hypertension and dyslipidemia.
DNA polymorphisms of the lipoprotein lipase gene and their association with coronary artery disease in the saudi population.
Does the EcoRI polymorphism in the human apolipoprotein B gene affect the binding of low density lipoprotein to the low density lipoprotein receptor?
Estrogen receptor ? gene PvuII polymorphism and coronary artery disease: a meta-analysis of 21 studies.
Functional significance of lipoprotein lipase HindIII polymorphism associated with the risk of coronary artery disease.
Genetic markers in coronary artery disease in a Russian population.
Genetic variability on adiponectin gene affects myocardial infarction risk: The role of endothelial dysfunction.
Human lipoprotein lipase HindIII polymorphism in young patients with myocardial infarction.
Identification of a BamHI Polymorphism for the Urokinase Gene Associated with Symptomatic Coronary Artery Disease.
Interactive effect of the p53 gene and cigarette smoking on coronary artery disease.
Lipoprotein lipase gene polymorphism and lipid profile in coronary artery disease.
Lipoprotein lipase gene PvuII polymorphism serum lipids and risk for coronary artery disease: meta-analysis.
Lipoprotein lipase HindIII polymorphism influences HDL-cholesterol levels in statin-treated patients with coronary artery disease.
Polymorphism of the methionine synthase gene : association with homocysteine metabolism and late-onset vascular diseases in the Japanese population.
Polymorphisms of the lipoprotein lipase gene and premature atherosclerosis.
Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
Relationship between two estrogen receptor-alpha gene polymorphisms and angiographic coronary artery disease.
Restriction fragment length polymorphisms in the apo B gene in relation to coronary artery disease.
Seven DNA polymorphisms at the candidate genes of atherosclerosis in Brazilian women with angiographically documented coronary artery disease.
The Association of Lipoprotein Lipase Genes, HindIII and S447X Polymorphisms With Coronary Artery Disease in Shiraz City.
The poliovirus receptor related 2 (PRR2) and apolipoprotein E genes and coronary heart disease.
Variation of apolipoprotein B gene is associated with myocardial infarction and lipoprotein levels in Danes.
[Association of estrogen receptor gene polymorphism with cerebral infarction, a case-control study]
[The genetic application for Japanese patients with coronary artery diseases using restriction fragment length polymorphisms (RFLPs) of apolipoprotein gene]
[XbaI polymorphism of apolipoprotein B gene in a Tunisian population: alleles frequencies and relationship with plasma lipid parameters]
Coronary Disease
Apolipoprotein B gene DNA polymorphisms are associated with macro- and microangiopathy in non-insulin-dependent diabetes mellitus.
Apolipoprotein B Gene Polymorphisms and Dyslipidemia in HIV Infected Adult Zimbabweans.
Apolipoprotein B gene polymorphisms are associated with lipid levels in men of South Asian descent.
Association between apolipoprotein B EcoRI poly?mor?phisms and coronary heart disease : A meta-analysis.
Characterization of apolipoprotein E genetic variations in Taiwanese: association with coronary heart disease and plasma lipid levels.
Correlation between polymorphisms in the estrogen receptor ? gene and coronary heart disease: A meta-analysis.
CYP11B2 gene polymorphism among coronary heart disease patients and blood donors in Malaysia.
DNA polymorphisms at the lipoprotein lipase gene are associated with macroangiopathy in type 2 (non-insulin-dependent) diabetes mellitus.
Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart disease.
LDL-R AvaII and NcoI polymorphisms: an indirect risk factor for coronary heart disease among a Mendelian population of Delhi, India.
Lipoprotein lipase gene variants and progression of nephropathy in hypercholesterolaemic patients with type 2 diabetes.
Lipoprotein lipase gene variants and risk of coronary disease: a quantitative analysis of population-based studies.
Polymorphisms in the lipoprotein lipase gene and their associations with plasma lipid concentrations in 40-year-old Danish men.
Polymorphisms of apolipoprotein B gene in relation to coronary heart disease in Chinese Han nationality.
Restriction fragment length polymorphisms of apolipoprotein B gene in Chinese population with coronary heart disease.
[Relation between insulin resistance and A1166C molecular variant of type 1 angiotensin II receptor gene in patients with coronary heart disease]
Coronary Stenosis
PON1 L55M polymorphism is not a predictor of coronary atherosclerosis either alone or in combination with Q192R polymorphism in an Italian population.
Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis.
Six lipoprotein lipase gene polymorphisms, lipid profile and coronary stenosis in a Tunisian population.
Cough
Three candidate genes and angiotensin-converting enzyme inhibitor-related cough: a pharmacogenetic analysis.
Cowpox
Characteristics of four cowpox virus isolates from Norway and Sweden.
Characterization of orthopoxviruses isolated from man and animals in Germany.
Conservation and variation in Orthopoxvirus genome structure.
Cowpox virus infection in an 11-year-old girl.
Generalized fatal Cowpox virus infection in a cat with transmission to a human contact case.
Genomic characterization of a poxvirus isolated from a child.
Restriction endonuclease analysis of red cowpox virus and its white pock variant.
Sequence alterations within and downstream of the A-type inclusion protein genes allow differentiation of Orthopoxvirus species by polymerase chain reaction.
Sequence of terminal regions of cowpox virus DNA: arrangement of repeated and unique sequence elements.
Tandemly repeated sequences are present at the ends of the DNA of raccoonpox virus.
The genome structure of cowpox virus white pock variants.
The second-largest subunit of the poxvirus RNA polymerase is similar to the corresponding subunits of procaryotic and eucaryotic RNA polymerases.
Crohn Disease
DNA polymorphism in Mycobacterium paratuberculosis, "wood pigeon mycobacteria," and related mycobacteria analyzed by field inversion gel electrophoresis.
Lack of an association between polymorphisms of the T-cell receptor alpha-chain and ulcerative colitis.
The C/C(-13910) and G/G(-22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel disease.
The C/C_????? and G/G_????? Genotypes for Adult-type Hypolactasia are not Associated with Inflammatory Bowel Disease.
Cross Infection
A new methicillin- and gentamicin-resistant Staphylococcus aureus in Dublin: molecular genetic analysis.
Molecular epidemiology of methicillin-resistant Staphylococcus aureus in Ilorin, Nigeria.
Nosocomial herpetic infections in a pediatric intensive care unit.
Nosocomial infection with Candida albicans in a pancreatic transplant recipient investigated by means of restriction enzyme analysis.
The clinical microbiology laboratory as an aid in infection control. The application of molecular techniques in epidemiologic studies of methicillin-resistant Staphylococcus aureus.
Use of molecular methods to characterize Moraxella catarrhalis strains in a suspected outbreak of nosocomial infection.
[Analysis of genome-type, serovar and antibiotic susceptibility of Pseudomonas aeruginosa isolated in Beijing Hospital China in 1991 to 1993]
[Analysis of the metallo-beta-lactamase gene in multidrug-resistant Pseudomonas aeruginosa isolated at Showa University Hospital]
[Ribosomal DNA fingerprinting analysis of Enterobacter cloacae isolated from an outbreak of nosocomial infection]
Cryptosporidiosis
Genotyping human and bovine isolates of Cryptosporidium parvum by polymerase chain reaction-restriction fragment length polymorphism analysis of a repetitive DNA sequence.
Cystic Fibrosis
A HinfI polymorphism in the cystic fibrosis gene CFTR.
Cross-infections with Pseudomonas aeruginosa in patients with cystic fibrosis attending the Warsaw Centre.
Cystic fibrosis mutation frequencies in upstate New York.
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus.
Molecular epidemiology of Burkholderia cepacia in two Australian cystic fibrosis centres.
Mutation analysis of Western Australian families affected by cystic fibrosis.
Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomes.
R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzyme digestion.
Restriction enzyme and Southern hybridization analyses of Pseudomonas aeruginosa strains from patients with cystic fibrosis.
Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations.
ScrfI restriction fragment length polymorphism at the D7S23 locus (probe pKM. 19), closely linked to cystic fibrosis.
T cell receptor beta chain polymorphisms are associated with cystic fibrosis.
Utility of the polymerase chain reaction (PCR) for prenatal diagnosis of genetic disease.
XV-2c/KM19 haplotypes analysis of cystic fibrosis patients from western Mexico.
Cysts
Detection and differentiation of Entamoeba histolytica and Entamoeba dispar isolates in clinical samples by PCR.
DNA methylation pattern during the encystment of Physarum flavicomum.
DNA Restriction Fragment Length Polymorphism in Races of the Soybean Cyst Nematode, Heterodera glycines.
Genetic diversity in Echinococcus shiquicus from the plateau pika (Ochotona curzoniae) in Darlag County, Qinghai, China.
Molecular detection of Sarcocystis species in slaughtered sheep by PCR-RFLP from south-western of Iran.
Cytomegalovirus Infections
Molecular epidemiology of cytomegalovirus infections associated with bone marrow transplantation.
No evidence of hospital-acquired cytomegalovirus infection in a pregnant pediatric nurse using restriction endonuclease analysis.
Deafness
Frequency of c.35delG Mutation in
[Mutations analysis in a pedigree with maternally inherited sensorineural hearing loss]
Death, Sudden, Cardiac
Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family.
Decompression Sickness
C.EcoO109I, a regulatory protein for production of EcoO109I restriction endonuclease, specifically binds to and bends DNA upstream of its translational start site.
Non-cognate enzyme-DNA complex: structural and kinetic analysis of EcoRV endonuclease bound to the EcoRI recognition site GAATTC.
Peculiarities of the interaction of the restriction endonuclease BspD6I with DNA containing its recognition site.
Regulation of DNA methylation using different tensions of double strands constructed in a defined DNA nanostructure.
Role of protein-induced bending in the specificity of DNA recognition: crystal structure of EcoRV endonuclease complexed with d(AAAGAT) + d(ATCTT).
Sequence-dependent bending in plasmid pUC19.
Simultaneous DNA binding, bending, and base flipping: evidence for a novel M.EcoRI methyltransferase-DNA complex.
Tension-dependent DNA cleavage by restriction endonucleases: two-site enzymes are "switched off" at low force.
Unwinding and hydrodynamic flow linear dichroism characteristics of supercoiled DNA covalently modified with two isomeric methylchrysene diol epoxides of different biological activities.
Dehydration
Macromolecular hydration changes associated with BamHI binding and catalysis.
delta-Thalassemia
Delta +-thalassemia in Sardinia.
Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis.
Dementia
DNA polymorphisms of apolipoprotein B and angiotensin I-converting enzyme genes and relationships with lipid levels in Italian patients with vascular dementia or Alzheimer's disease.
Estrogen receptor ? polymorphism is associated with dementia in a Brazilian cohort.
Variations in estrogen receptor alpha gene and risk of dementia, and brain volumes on MRI.
Dementia, Vascular
DNA polymorphisms of apolipoprotein B and angiotensin I-converting enzyme genes and relationships with lipid levels in Italian patients with vascular dementia or Alzheimer's disease.
Dengue
A PCR-restriction enzyme technique for determining dengue virus subgroups within serotypes.
Detection and identification of dengue-1 virus in clinical samples by a nested-PCR followed by restriction enzyme digestion of amplicons.
Infectious RNA transcripts from full-length dengue virus type 2 cDNA clones made in yeast.
Restriction enzyme analysis of American region dengue viruses.
Variation in dengue type 2 viruses isolated in Bangkok during 1980.
[Construction and identification of genomic cDNA subclones of dengue 2 virus NGC strain]
Dental Caries
Use of polymerase chain reaction techniques and sodium dodecyl sulfate-polyacrylamide gel electrophoresis for differentiation of oral Lactobacillus species.
Dental Plaque
Evidence for the occurrence of the same strain of Campylobacter pylori in the stomach and dental plaque.
Microbiological evidence of Helicobacter pylori from dental plaque in dyspeptic patients.
Dermatitis
Molecular typing of a BHV-4 (bovine herpesvirus 4) field isolate.
Dermatitis, Contact
DNA double strand breaks in epidermal cells cause immune suppression in vivo and cytokine production in vitro.
Diabetes Complications
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Diabetes Insipidus
[Identification of a new mutation (CysII6Gly) in a family with neurogenic diabetes insipidus]
Diabetes Mellitus
Analysis of the insulin-sensitive phosphodiesterase 3B gene in type 2 diabetes.
Apolipoprotein B gene variants are involved in the determination of blood glucose and lipid levels in patients with non-insulin dependent diabetes mellitus.
Association of Estrogen Receptor ? Genes PvuII and XbaI Polymorphisms with Type 2 Diabetes Mellitus in the Inpatient Population of a Hospital in Southern Iran.
Association of HaeIII single nucleotide polymorphisms in the SLC2A1 gene with risk of diabetic nephropathy; Evidence from Kurdish patients with type 2 diabetes mellitus.
Association of lipoprotein lipase and apolipoprotein C-III genes polymorphism with acute myocardial infarction in diabetic patients.
Association Study between BGLAP Gene HindIII Polymorphism and Type 2 Diabetes Mellitus Development in Ukrainian Population.
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Associations of Estrogen Receptor Alpha Gene Polymorphisms with Type 2 Diabetes Mellitus and Metabolic Syndrome: A Systematic Review and Meta-Analysis.
Estrogen receptor alpha gene polymorphism associated with type 2 diabetes mellitus and the serum lipid concentration in Chinese women in Guangzhou.
MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Polymorphisms XbaI (rs693) and EcoRI (rs1042031) of the ApoB gene are associated with carotid plaques but not with carotid intima-media thickness in patients with diabetes mellitus type 2.
The E-selectin S128R polymorphism is not a risk factor for coronary artery disease in patients with diabetes mellitus type 2.
The heparan sulfate proteoglycan gene polymorphism: association with type 2 diabetic nephropathy in Chinese.
The HindIII polymorphism in the lipoprotein lipase gene predicts type 2 diabetes risk among Chinese adults.
Three mutant insulins in man.
[Association of estrogen receptor gene polymorphism with cerebral infarction, a case-control study]
[The association of HincII/low density lipoprotein receptor (LDLR) restriction fragment length polymorphism (RFLP) with diabetes mellitus and its lipid phenotype with PCR gene amplification]
Diabetes Mellitus, Type 1
2'-5' oligoadenylate synthetase and its relationship to HLA and genetic markers of insulin-dependent diabetes mellitus.
Association and sibpair analysis for the HLA, Gm, Km, and insulin polymorphisms in multiplex IDDM families.
Association of HLA-DR phenotypes and T-lymphocyte-receptor beta-chain-region RFLP with IDDM in Japanese.
Characterization of three HLA-DR beta genes isolated from an HLA-DR 3/4 insulin-dependent diabetic patient.
DNA polymorphisms in the ACE gene, serum ACE activity and the risk of nephropathy in insulin-dependent diabetes mellitus.
DQ beta restriction fragment length polymorphism in insulin dependent diabetes mellitus.
DQA1 restriction fragment length polymorphisms and insulin-dependent diabetes mellitus: a BglII fragment labels a subset of B8,DR3 haplotypes uniquely associated with insulin-dependent diabetes mellitus.
Genetic variation of a collagen IV alpha 1-chain gene polymorphism in Danish insulin-dependent diabetes mellitus (IDDM) patients: lack of association to nephropathy and proliferative retinopathy.
Gestational diabetes mellitus is associated with HLA-DQ beta-chain DNA endonuclease fragments.
HLA and insulin-dependent diabetes: an overview.
HLA-D region beta-chain DNA endonuclease fragments differ between HLA-DR identical healthy and insulin-dependent diabetic individuals.
Interaction between T cell receptor beta chain and immunoglobulin heavy chain region genes in susceptibility to insulin-dependent diabetes mellitus.
Lack of association between the heparan sulfate proteoglycan gene polymorphism and diabetic nephropathy in Japanese NIDDM with proliferative diabetic retinopathy.
Molecular cloning of a polymorphic DNA endonuclease fragment associates insulin-dependent diabetes mellitus with HLA-DQ.
Nephropathy in type 1 diabetes: a manifestation of insulin resistance and multiple genetic susceptibilities? Further evidence from the Pittsburgh Epidemiology of Diabetes Complication Study.
Polymorphic restriction endonuclease sites linked to the HLA-DR alpha gene: localization and use as genetic markers of insulin-dependent diabetes.
Specific genomic markers for the HLA-DQ subregion discriminate between DR4+ insulin-dependent diabetes mellitus and DR4+ seropositive juvenile rheumatoid arthritis.
The genetics of type I and type II diabetes: analysis by recombinant DNA methodology.
The polymorphism linked to the human insulin gene: its lack of association with either IDDM or NIDDM in Japanese.
Viruses as a triggering factor of type 1 diabetes and genetic markers related to the susceptibility to the virus-associated diabetes.
Diabetes Mellitus, Type 2
An analysis of amplified insulin gene products in diabetics of Indian origin.
Analysis of the insulin-sensitive phosphodiesterase 3B gene in type 2 diabetes.
Association of Estrogen Receptor ? Genes PvuII and XbaI Polymorphisms with Type 2 Diabetes Mellitus in the Inpatient Population of a Hospital in Southern Iran.
Association of HaeIII single nucleotide polymorphisms in the SLC2A1 gene with risk of diabetic nephropathy; Evidence from Kurdish patients with type 2 diabetes mellitus.
Association of monocyte chemoattractant protein-1 (MCP-1) 2518A/G polymorphism with proliferative diabetic retinopathy in Korean type 2 diabetes.
Association of the HindIII and S447X polymorphisms in LPL gene with hypertension and type 2 diabetes in Mexican families.
Association Study between BGLAP Gene HindIII Polymorphism and Type 2 Diabetes Mellitus Development in Ukrainian Population.
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Associations of Estrogen Receptor Alpha Gene Polymorphisms with Type 2 Diabetes Mellitus and Metabolic Syndrome: A Systematic Review and Meta-Analysis.
BglII gene polymorphism of the alpha2beta1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetes.
DNA polymorphisms at the lipoprotein lipase gene are associated with macroangiopathy in type 2 (non-insulin-dependent) diabetes mellitus.
DNA polymorphisms of the insulin receptor gene in Japanese subjects with non-insulin-dependent diabetes mellitus.
Estrogen receptor alpha gene polymorphism associated with type 2 diabetes mellitus and the serum lipid concentration in Chinese women in Guangzhou.
Estrogen receptor alpha gene polymorphisms are associated with type 2 diabetes and fasting glucose in male subjects.
Hep-G2 glucose transporter gene polymorphism in Caucasian, black, Hispanic and Japanese patients with NIDDM.
Lack of association between the heparan sulfate proteoglycan gene polymorphism and diabetic nephropathy in Japanese NIDDM with proliferative diabetic retinopathy.
Lipoprotein lipase gene variants and progression of nephropathy in hypercholesterolaemic patients with type 2 diabetes.
Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
Molecular biology of islet amyloid polypeptide.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Polymorphisms at the GLUT2 (beta-cell/liver) glucose transporter gene and non-insulin-dependent diabetes mellitus (NIDDM): analysis in affected pedigree members.
Relationship among urinary albumin excretion rate, lipoprotein lipase PvuII polymorphism and plasma fibrinogen in type 2 diabetic patients.
Relationship between TaqIB cholesteryl ester transfer protein gene polymorphism and macrovascular complications in Japanese patients with type 2 diabetes.
Relationship of LDLR gene polymorphism and NIDDM in Chinese.
The heparan sulfate proteoglycan gene polymorphism: association with type 2 diabetic nephropathy in Chinese.
The HindIII polymorphism in the lipoprotein lipase gene predicts type 2 diabetes risk among Chinese adults.
The islet amyloid polypeptide gene and non-insulin-dependent diabetes mellitus in south Indians.
The peroxisome proliferator activated receptorgamma2 (PPARgamma2) Pro12Ala variant: lack of association with type 2 diabetes in obese and non obese Tunisian patients.
Variation in the apolipoprotein B gene and development of type 2 diabetes mellitus.
Vitamin D and estrogen receptor gene polymorphisms in type 2 diabetes mellitus and in android type obesity.
[Glycogen synthase gene-glycogen synthase gene in Japanese patients with NIDDM]
[Sulfonylurea receptor gene polymorphism is associated with non-insulin dependent diabetes mellitus in Chinese population]
[The relationship between angiotensin II type 1 receptor gene and coronary heart disease, hypertension and diabetes mellitus in Chinese]
Diabetes, Gestational
Relationship between a lipoprotein lipase gene polymorphism in placental tissue and insulin resistance in patients with gestational diabetes mellitus.
Diabetic Nephropathies
Association of HaeIII single nucleotide polymorphisms in the SLC2A1 gene with risk of diabetic nephropathy; Evidence from Kurdish patients with type 2 diabetes mellitus.
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Genetic variation around the collagen IV 1a gene locus and proliferative retinopathy in type 2 diabetes mellitus.
Genetic variation of a collagen IV alpha 1-chain gene polymorphism in Danish insulin-dependent diabetes mellitus (IDDM) patients: lack of association to nephropathy and proliferative retinopathy.
Lack of association between the heparan sulfate proteoglycan gene polymorphism and diabetic nephropathy in Japanese NIDDM with proliferative diabetic retinopathy.
Diabetic Retinopathy
An aldose reductase intragenic polymorphism associated with diabetic retinopathy.
BglII gene polymorphism of the alpha2beta1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetes.
Genetic Variants (rs869109213 and rs2070744) Of the eNOS Gene and BglII in the ?2 Subunit of the ?2?1 Integrin Gene and Diabetic Retinopathy.
Genetic variation around the collagen IV 1a gene locus and proliferative retinopathy in type 2 diabetes mellitus.
Genetic variation of a collagen IV alpha 1-chain gene polymorphism in Danish insulin-dependent diabetes mellitus (IDDM) patients: lack of association to nephropathy and proliferative retinopathy.
The Role of Genetic Variants (rs869109213 and rs2070744) Of the eNOS Gene and BglII in the ?2 Subunit of the ?2?1 Integrin Gene in Diabetic Retinopathy in a Tunisian Population.
Diphtheria
Cloned diphtheria toxin fragment A is expressed from the tox promoter and exported to the periplasm by the SecA apparatus of Escherichia coli K12.
Complete nucleotide sequence and characterization of the 5'-flanking region of mammalian elongation factor 2 gene.
Construction of an epitope vector utilising the diphtheria toxin B-subunit.
Effective targeted cytotoxicity of neuroblastoma cells.
Epidemiology of diphtheria: polypeptide and restriction enzyme analysis in comparison with conventional phage typing.
Genetic construction, expression, and melanoma-selective cytotoxicity of a diphtheria toxin-related alpha-melanocyte-stimulating hormone fusion protein.
Identification of deoxyribonucleic acid restriction fragments of beta-converting corynebacteriophages that carry the gene for diphtheria toxin.
Down Syndrome
Study of restriction fragment length polymorphism in the cystatin C gene of elderly patients with dementia and aged Down's syndrome patients.
[Study of polymorphism in human rRNA gene clusters. Population and familial analysis of basic types of RFLP]
Duodenal Ulcer
Genetic heterogeneity of combined gastric and duodenal ulcers detected by pepsinogen C gene polymorphism.
Pepsinogen C gene polymorphisms associated with gastric body ulcer.
Dwarfism, Pituitary
Genetic analysis of familial isolated growth hormone deficiency type I.
Growth characteristics and response to growth hormone therapy in patients with hypochondroplasia: genetic linkage of the insulin-like growth factor I gene at chromosome 12q23 to the disease in a subgroup of these patients.
Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?
Long-lasting catch-up growth under bio-methionyl growth hormone treatment in an infant with isolated growth hormone deficiency type 1A.
Prevalence of human growth hormone-1 gene deletions among patients with isolated growth hormone deficiency from different populations.
[Use of growth hormone genes for the diagnosis of the disease of dwarfism]
Dysentery
Evaluation of pulsed-field gel electrophoresis for typing of Shigella dysenteriae type 1.
Typing of Treponema hyodysenteriae by restriction endonuclease analysis.
Dysentery, Bacillary
Molecular epidemiology of Shigella infections: plasmid profiles, serotype correlation, and restriction endonuclease analysis.
Dyslipidemias
Association of lipoprotein lipase Hind III and Ser 447 Ter polymorphisms with dyslipidemia in Asian Indians.
Association of polymorphisms at restriction enzyme recognition sites of apolipoprotein B and E gene with dyslipidemia in children undergoing primary nephrotic syndrome.
CR1 genotype and haplotype involvement in coronary artery disease: the pivotal role of hypertension and dyslipidemia.
Dyslipidemia: Genetics, lipoprotein lipase and HindIII polymorphism.
Effect of gene polymorphisms on lipoprotein levels in patients with dyslipidemia of metabolic syndrome.
Genetic association of APOB polymorphisms with variation in serum lipid profile among the Kuwait population.
Lipoprotein lipase gene polymorphisms and risks of childhood obesity in Chinese preschool children.
PAI-1 haplogenotype confers genetic susceptibility for obesity and hypertriglyceridemia in Mexican children.
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
Dystonic Disorders
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia.
Echinococcosis
Genetic Identification of Echinococcus granulosus Isolates in Hamadan, Western Iran.
MHC-DRB1/DQB1 Gene Polymorphism and Its Association with Resistance/Susceptibility to Cystic Echinococcosis in Chinese Merino Sheep.
Ecthyma, Contagious
Comparison of contagious ecthyma virus genomes by restriction endonucleases.
Ectromelia
Conservation and variation in Orthopoxvirus genome structure.
Further characterization of the biological and pathogenic properties of erythromelalgia-related poxviruses.
Genomic characterization of a poxvirus isolated from a child.
Eczema
Association between genetic variants of mast-cell chymase and eczema.
Embolic Stroke
Estrogen receptor ? genetic variants and the risk of stroke in a South Indian population from Andhra Pradesh.
Encephalitis
Characteristics of a novel lentivirus derived from South African sheep with pulmonary adenocarcinoma (jaagsiekte).
Comparative genome mapping of bovine encephalitis herpesvirus, bovine herpesvirus 1, and buffalo herpesvirus.
DNA restriction enzyme analysis of a bovine herpesvirus 1 strain isolated from encephalitis in Hungary.
DNA restriction enzyme analysis of viruses isolated from cerebrospinal fluid and brain-biopsy tissue in a patient with herpes simplex encephalitis.
Genetic differentiation of Murray Valley encephalitis virus in Australia and Papua New Guinea.
Herpes simplex encephalitis: analysis of a cluster of cases by restriction endonuclease mapping of virus isolates.
Molecular characterization of a caprine adenovirus.
Molecular epidemiology and pathogenesis of ruminant herpesviruses including bovine, buffalo and caprine herpesviruses l and bovine encephalitis herpesvirus.
Restriction endonuclease analysis of bovine herpesvirus type 1 isolates from calves with fatal encephalitis: comparison with vaccine virus.
Restriction endonuclease analysis of Hungarian bovine herpesvirus isolates from different clinical forms of IBR, IPV and encephalitis.
Temporal cluster of herpes simplex encephalitis: investigation by restriction endonuclease cleavage of viral DNA.
The molecular epidemiology of equine herpesvirus 1 (equine abortion virus) in Australasia 1975 to 1989.
Encephalitis, Herpes Simplex
DNA restriction enzyme analysis of viruses isolated from cerebrospinal fluid and brain-biopsy tissue in a patient with herpes simplex encephalitis.
Herpes simplex encephalitis: analysis of a cluster of cases by restriction endonuclease mapping of virus isolates.
Temporal cluster of herpes simplex encephalitis: investigation by restriction endonuclease cleavage of viral DNA.
Variable restriction endonuclease sites of herpes simplex virus type 1 isolates from encephalitic, facial and genital lesions and ganglia.
Encephalomyelitis
Comparison of Chlamydia psittaci isolates by restriction endonuclease and DNA probe analyses.
Molecular epidemiology and pathogenesis of some equine herpesvirus type 1 (equine abortion virus) and type 4 (equine rhinopneumonitis virus) isolates.
Encephalomyelitis, Eastern Equine
Coupled PCR-restriction enzyme analysis for rapid identification of structural gene relationships among strains of eastern equine encephalitis virus.
Endocarditis
Genetic heterogeneity among isolates of Coxiella burnetii.
Endometrial Neoplasms
Association of MDM2 SNP309 and TP53 Arg72Pro polymorphisms with risk of endometrial cancer.
Association of mismatch repair deficiency with PTEN frameshift mutations in endometrial cancers and the precursors in a Japanese population.
Estrogen receptor alpha (ER-alpha) gene polymorphism in patients from the Lodz region of Poland with sporadic endometrial cancer.
Estrogen receptor alpha gene polymorphisms and endometrial cancer risk.
Genetic polymorphism of PRKCDBP is associated with an increased risk of endometrial cancer.
Genetic polymorphisms in the estrogen receptor-? gene and the risk of endometrial cancer: A meta-analysis.
Endometriosis
Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates.
Association between oestrogen receptor alpha (ESR1) gene polymorphisms and endometriosis: a meta-analysis of 24 case-control studies.
Estrogen receptor dinucleotide repeat polymorphism is associated with minimal or mild endometriosis.
Estrogen receptor gene polymorphisms are associated with recurrence of endometriosis.
Estrogen receptor-alpha gene (T/C) Pvu II polymorphism in endometriosis and uterine fibroids.
Estrogen receptor-alpha gene PvuII (T/C) and XbaI (A/G) polymorphisms and endometriosis risk: A meta-analysis.
Evaluation of clinical parameters and estrogen receptor alpha gene polymorphisms for patients with endometriosis.
Oestrogen receptor-alpha gene polymorphism is associated with endometriosis, adenomyosis and leiomyomata.
Polymorphisms in the estrogen receptor beta gene but not estrogen receptor alpha gene affect the risk of developing endometriosis in a Japanese population.
PvuII and XbaI in Estrogen Receptor 1 (ESR1) Polymorphisms and Susceptibility to Endometriosis Risk.
Endophthalmitis
Reliability of nested polymerase chain reaction in the diagnosis of bacterial endophthalmitis.
Enteritis
Application of serotyping and chromosomal restriction endonuclease digest analysis in investigating a laboratory-acquired case of Campylobacter jejuni enteritis.
Canine parvovirus: relationship to wild-type and vaccine strains of feline panleukopenia virus and mink enteritis virus.
Comparison of canine parvovirus with mink enteritis virus by restriction site mapping.
Comparison of isolates of canine parvovirus by restriction enzyme analysis, and vaccine efficacy against field strains.
Differentiation of avian adenovirus type-II strains by restriction endonuclease fingerprinting.
Differentiation of Salmonella enteritidis and S. typhimurium by plasmid profile analysis and restriction endonuclease analysis of chromosomal DNA.
Investigation of a Campylobacter jejuni outbreak by serotyping and chromosomal restriction endonuclease analysis.
Investigation of zoonotically acquired Campylobacter jejuni enteritis with serotyping and restriction endonuclease DNA analysis.
Enzootic Bovine Leukosis
Bovine leukosis virus: recloning of specific DNA fragments.
Detection, purification, and characterization of two species of covalently closed circular proviral DNA molecules of bovine leukemia virus.
Leukemogenesis by bovine leukemia virus: proviral DNA integration and lack of RNA expression of viral long terminal repeat and 3' proximate cellular sequences.
Molecular cloning of covalently closed circular DNA of bovine leukemia virus.
Restriction endonuclease mapping of linear unintegrated proviral DNA of bovine leukemia virus.
Transmission and propagation in cell culture of virus produced by cells transfected with an infectious molecular clone of bovine leukemia virus.
Epididymitis
Characterisation of Histophilus ovis and related organisms by restriction endonuclease analysis.
Epilepsies, Myoclonic
Identification of point mutations by mispairing PCR as exemplified in MERRF disease.
Epilepsy
A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocysteinemia in epileptic patients receiving anticonvulsants.
Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy.
Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review.
New wave of research in the epilepsies.
RNA editing (R/G site) and flip-flop splicing of the AMPA receptor subunit GluR2 in nervous tissue of epilepsy patients.
The new wave of research in the epilepsies.
Epilepsy, Temporal Lobe
RNA editing (R/G site) and flip-flop splicing of the AMPA receptor subunit GluR2 in nervous tissue of epilepsy patients.
Epstein-Barr Virus Infections
Epstein-Barr virus infected lymphoepithelial carcinomas of the salivary gland in the Russia-Asia area: a clinicopathologic study of 160 cases.
Epstein-Barr virus plays little role in cervical carcinogenesis in Korean women.
Identification of an Epstein-Barr virus glycoprotein which is antigenically homologous to the varicella-zoster virus glycoprotein II and the herpes simplex virus glycoprotein B.
Interferon regulatory factor 2 represses the Epstein-Barr virus BamHI Q latency promoter in type III latency.
Interferon regulatory factor 7 is induced by Epstein-Barr virus latent membrane protein 1.
Low cell dosage of lymphoblastoid human cell lines EBV(+) is associated to chronic hepatitis in a minority of inoculated Nu/Nu mice.
Terminal Repeat Analysis of EBV Genomes.
The Epstein-Barr virus BARF1 gene encodes a novel, soluble colony-stimulating factor-1 receptor.
Esophageal Neoplasms
Presence of an EcoRI RFLP of the c-mos locus in normal and tumor tissue of esophageal cancer patients.
Essential Hypertension
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives.
Association of the apolipoprotein B gene polymorphisms with essential hypertension in Northern Chinese Han population.
Frequency of renin gene restriction fragment length polymorphism in hypertensives with a genetic predisposition to hypertension.
Polymorphisms in the hANP (human atrial natriuretic peptide) gene, albuminuria, and hypertension.
Significant relationships of plasma lipids and body mass index with polymorphisms at the linked low-density-lipoprotein receptor gene and insulin receptor gene loci (19p13.2) in essential hypertensive patients.
The -174 G/C polymorphism of the interleukin-6 gene promoter and essential hypertension in an elderly Italian population.
[Association between angiotensin II type I receptor gene and human essential hypertension]
[Association between AvaII exon 13 polymorphism at the LDL receptor gene different and serum lipid levels in normotensives and essential hypertensives in Shanghai]
Exanthema
Genomic polymorphism, growth properties, and immunologic variations in human herpesvirus-6 isolates.
Molecular pathogenesis of equine coital exanthema (ECE): temperature sensitivity (TS) and restriction endonuclease (RE) fragment profiles of several field isolates.
Molecular pathogenesis of equine coital exanthema: restriction endonuclease digestions of EHV-3 DNA and indications of a unique XbaI cleavage site.
Oestrogen receptor {alpha} gene polymorphisms in systemic lupus erythematosus.
Eye Infections
Restriction endonuclease analysis of adenovirus isolates from sporadic and epidemic ocular infections: experience in a clinical laboratory.
Factor XII Deficiency
Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme.
Fanconi Anemia
EcoRI RFLP in the Fanconi anaemia complementation group C gene (FACC).
Fasciitis, Necrotizing
Emergence and spread of a new clone of M type 1 group A Streptococcus coincident with the increase in invasive diseases in Japan.
Fatigue Syndrome, Chronic
Genomic polymorphism, growth properties, and immunologic variations in human herpesvirus-6 isolates.
Feline Panleukopenia
Antigenic and genomic comparisons of some feline parvovirus subspecies strains.
Canine parvovirus: relationship to wild-type and vaccine strains of feline panleukopenia virus and mink enteritis virus.
Feline panleukopenia virus replicates in cells in which cellular DNA synthesis is blocked.
No evidence for a role of modified live virus vaccines in the emergence of canine parvovirus.
Fibroadenoma
Clonal analysis of fibroadenoma and phyllodes tumor of the breast.
Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development.
[Analysis of the association of inherited predisposition to breast cancer with c-Ha-ras-1 oncogene alleles]
Fibrocystic Breast Disease
[The clinical significance of pvuii polymorphism estradiol receptor alpha gene to improve diagnosis of proliferative forms of benign breast dysplasia].
Fibroma
Detection of beta-catenin mutations in paraffin-embedded sporadic desmoid-type fibromatosis by mutation-specific restriction enzyme digestion (MSRED): an ancillary diagnostic tool.
Sequence and analysis of a portion of the genomes of Shope fibroma virus and malignant rabbit fibroma virus that is important for viral replication in lymphocytes.
Sequence and analysis of the BamHI "D" fragment of Shope fibroma virus: comparison with similar regions of related poxviruses.
Fibromatosis, Aggressive
Telomere length in familial adenomatous polyposis-associated desmoids.
Fibrosarcoma
Frequent activation of c-kis as a transforming gene in fibrosarcomas induced by methylcholanthrene.
Structure of the c-Ki-ras gene in a rat fibrosarcoma induced by 1,8-dinitropyrene.
Fluorosis, Dental
Association of COL1A2 (PvuII) gene polymorphism with risk and severity of dental fluorosis - A case control study.
COL1A2 gene polymorphisms (Pvu II and Rsa I), serum calciotropic hormone levels, and dental fluorosis.
The association between osteocalcin gene polymorphism and dental fluorosis among children exposed to fluoride in People's Republic of China.
Foodborne Diseases
Comparison of methods for discrimination between strains of Listeria monocytogenes from epidemiological surveys.
Restriction endonuclease analysis, DNA relatedness and phenotypic characterization of Campylobacter jejuni and Camp. coli isolates involved in food-borne disease.
Restriction endonuclease PshAI from Plesiomonas shigelloides with the novel recognition site 5'-GACNN/NNGTC.
Species identification of ciguatoxin-carrying grouper implicated in food poisoning.
The enterotoxin gene (cpe) of Clostridium perfringens can be chromosomal or plasmid-borne.
[Application of pulse-field gel electrophoresis analysis in source-tracking of food-borne disease caused by Vibrio parahaemolyticus]
Foot-and-Mouth Disease
Detection of foot-and-mouth disease virus from culture and clinical samples by reverse transcription-PCR coupled to restriction enzyme and sequence analysis.
Rapid detection and characterization of foot-and-mouth disease virus by restriction enzyme and nucleotide sequence analysis of PCR products.
[Construction and functional characterization of a monocistronic replicon based on the HCV genotype 2a promotor].
Fowlpox
A rapid method for identifying the thymidine kinase genes of avipoxviruses.
Characterization of avipoxviruses from wild birds in Norway.
Comparison of field and vaccine strains of Australian fowlpox viruses.
Comparison of the locations of homologous fowlpox and vaccinia virus genes reveals major genome reorganization.
Fowlpox virus encodes a protein related to human deoxycytidine kinase: further evidence for independent acquisition of genes for enzymes of nucleotide metabolism by different viruses.
Gene translocations in poxviruses: the fowlpox virus thymidine kinase gene is flanked by 15 bp direct repeats and occupies the locus which in vaccinia virus is occupied by the ribonucleotide reductase large subunit gene.
Genetic and antigenic differences between fowlpox and quailpox viruses.
Insertional inactivation of a fowlpox virus homologue of the vaccinia virus F12L gene inhibits the release of enveloped virions.
Nucleotide sequence analysis of a 10.5 kbp HindIII fragment of fowlpox virus: relatedness to the central portion of the vaccinia virus HindIII D region.
Partial transcriptional mapping of the fowlpox virus genome and analysis of the EcoRI L fragment.
Restriction endonuclease mapping of the fowlpox virus genome.
Sequence analysis of an 11.2 kilobase, near-terminal, BamHI fragment of fowlpox virus.
Similar genetic organization between a region of fowlpox virus DNA and the vaccinia virus HindIII J fragment despite divergent location of the thymidine kinase gene.
Tandem repeated sequences within the terminal region of the fowlpox virus genome.
[Detection of fowlpox in chickens and turkeys in Germany].
Fragile X Syndrome
Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis.
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome.
Molecular studies of the fragile X syndrome.
Friedreich Ataxia
Large Interruptions of GAA Repeat Expansion Mutations in Friedreich Ataxia Are Very Rare.
Fructose Intolerance
Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations.
The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.
Fucosidosis
Characterization of EcoRI mutation in fucosidosis patients: a stop codon in the open reading frame.
Fungemia
Kodamaea ohmeri isolates from patients in a university hospital: identification, antifungal susceptibility, and pulsed-field gel electrophoresis analysis.
Gallbladder Neoplasms
Association between estrogen receptor 1 (ESR1) genetic variations and cancer risk: a meta-analysis.
Gallstones
Complement receptor 1 (A3650G RsaI and intron 27 HindIII) polymorphisms and risk of gallbladder cancer in north Indian population.
[Relationship among the XhaI and EcoRI locus polymorphisms of apolipoprotein B gene, serum lipid metabolism and gallstone disease]
Gastritis
Absence of Helicobacter pylori high tetracycline resistant 16S rDNA AGA926-928TTC genotype in gastric biopsy specimens from dyspeptic patients of a city in the interior of Sao Paulo, Brazil.
Evaluation of global genome methylation in gastritis lesion and its correlation with clinicopatological findings.
Gastroenteritis
High Frequency Of Cultivable Human Subgroup F Adenoviruses In Stool Samples From An Italian Paediatric Population Admitted To Hospital With Acute Gastroenteritis.
Prevalence and characterization of enteric adenoviruses in the South of Ireland.
Gaucher Disease
Gene rearranagement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene.
Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher disease.
Molecular screening of Japanese patients with Gaucher disease: phenotypic variability in the same genotypes.
Mutation analysis of 28 Gaucher disease patients: the Australasian experience.
Structure and linkage relationships of the region containing the human L-type pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genes.
The facile detection of 1505G-->A in Gaucher patients with different phenotypes.
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease.
Genetic Diseases, Inborn
Detection of single base substitutions in total genomic DNA.
Genetic diseases: diagnosis by restriction endonuclease analysis.
Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification.
Recombinant DNA technology and laboratory medicine.
Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.
The rare intracellular RET mutation p.Ser891Ala in an apparently sporadic medullary thyroid carcinoma: a case report and review of the literature.
Genital Diseases
Biological and biochemical comparison of bovid herpesvirus-4 strains.
Glaucoma
OPTN gene: profile of patients with glaucoma from India.
The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma.
Glaucoma, Open-Angle
The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma.
Glioblastoma
Effect of changes in the CD44 gene on tumour cell invasion in gliomas.
In Silico Enhanced Restriction Enzyme Based Methylation Analysis of the Human Glioblastoma Genome Using Agilent 244K CpG Island Microarrays.
Glioma
Analysis of glial fibrillary acidic protein gene methylation in human malignant gliomas.
Coamplification of simple repetitive DNA fingerprint fragments and the EGFR gene in human gliomas.
DNA lability induced by nimustine and ramustine in rat glioma cells.
Identification of cytochromes P450 1A2, 2A1, 2C7, 2E1 in rat glioma C6 cell line by RT-PCR and specific restriction enzyme digestion.
Identification of Retinol Binding Protein 1 Promoter Hypermethylation in Isocitrate Dehydrogenase 1 and 2 Mutant Gliomas.
In vitro damage of isolated DNA from two brain tumor cell lines induced by a water-soluble antitumor nitrosourea.
Measurement of O-6-methylguanine-DNA methyltransferase activity using oligonucleotides and restriction enzyme in human brain tumors.
Restriction endonuclease recognition and southern hybridization of bromodeoxyuridine-substituted genomic DNA.
Glomerulonephritis
Streptokinase gene variable region classification in streptococci: lack of correlation with post-streptococcal glomerulonephritis.
Glomerulonephritis, Membranous
A DQA1 allele is strongly associated with idiopathic membranous nephropathy.
Glucose Intolerance
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
[Common mutation analysis for patients found in Tianjin area with glucose-6-phosphate dehydrogenase deficiency]
[Glucose-6-phosphate dehydrogenase gene mutations in She nationality, Fujian province]
Glucosephosphate Dehydrogenase Deficiency
[Common mutation analysis for patients found in Tianjin area with glucose-6-phosphate dehydrogenase deficiency]
[Glucose-6-phosphate dehydrogenase gene mutations in She nationality, Fujian province]
Glycogen Storage Disease
Prenatal diagnosis of glycogen storage disease type Ia by restriction enzyme digestion.
Goiter
Clonal analysis of solitary follicular nodules in the thyroid.
Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population.
Granuloma Inguinale
A colorimetric detection system for Calymmatobacterium granulomatis.
Granulomatous Disease, Chronic
Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.
Graves Disease
A polymorphism within the vitamin D-binding protein gene is associated with Graves' disease but not with Hashimoto's thyroiditis.
A thyroid hormone receptor beta gene polymorphism associated with Graves' disease.
Analysis of mutations in exon 1 of the human thyrotropin receptor gene: high frequency of the D36H and P52T polymorphic variants.
Analysis of the TSH receptor gene structure in various thyroid disorders: DNA from thyroid adenomas can have large insertions or deletions.
Association of HLA antigen and restriction fragment length polymorphism of T cell receptor beta-chain gene with Graves' disease and Hashimoto's thyroiditis.
C4A gene deletion: association with Graves' disease.
Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family.
Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population.
Linkage of HLA-DR beta specific restriction fragment length polymorphisms with Graves' disease.
Restriction enzyme analysis of HLA class II DR beta genes in patients with Graves' disease.
Head and Neck Neoplasms
Rflp analysis of the L-myc oncogene in head and neck-cancer - relationship study with susceptibility and disease progression.
The characteristics of human papillomavirus DNA in head and neck cancers and papillomas.
[Immunohistologic and molecular genetic studies of the effect of glutathione-S-transferases on the development of squamous epithelial carcinomas in the area of the head-neck]
Hearing Loss
Audiological and genetic features of the mtDNA mutations.
New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss.
Heart Diseases
Frequency and genetic background of the position 122 (Val----Ile) variant transthyretin gene in the black population.
Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family.
The lipoprotein lipase gene HindIII polymorphism is associated with lipid levels in early-onset type 2 diabetic patients.
Heart Failure
Epigenetic silencing of TIMP4 in heart failure.
Hemangioma
Use of X-Chromosome Inactivation Pattern to Analyze the Clonality of 14 Female Cases of Kaposi Sarcoma.
Hemangiosarcoma
Molecular analysis of clonality in Kaposi's sarcoma.
Hematologic Neoplasms
Restriction fragment length polymorphism of bcr in Japanese patients with hematological malignancies.
Hematuria
Identification of a single base insertion in the COL4A5 gene in Alport syndrome.
Hemochromatosis
Confirmation of two major polyarticular osteoarthritis (POA) phenotypes - differentiation on the basis of joint topography.
Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.
Genotyping as a diagnostic aid in genetic haemochromatosis.
HLA class I gene polymorphism in genetic hemochromatosis.
Hemoglobinopathies
Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping.
Prenatal diagnosis of hemoglobinopathies by restriction endonuclease analysis: pregnancies at risk for sickle cell anemia and S--O Arab disease.
Prenatal diagnosis of hemoglobinopathies: evaluation of techniques for analysing globin-chain synthesis in blood samples obtained by fetoscopy.
Hemoglobinuria
Polymorphism of the complement receptor 1 gene correlates with hematological response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria.
Hemoglobinuria, Paroxysmal
Polymorphism of the complement receptor 1 gene correlates with hematological response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria.
Hemophilia A
A directed search for mutations in hemophilia A using restriction enzyme analysis and denaturing gradient gel electrophoresis. A study of seven exons in the factor VIII gene of 170 cases.
A new HindIII restriction fragment length polymorphism in the hemophilia A locus.
Application of Indirect Linkage Analysis for Carrier Detection of Hemophilia A in Kurdistan Region of Iraq: Usefulness of Intron 18 BclI T>A, Intron 19 HindIII C>T, and IVS7 nt27 G>A Markers.
Detection of Hemophilia A Carriers in Azeri Turkish Population of Iran: Usefulness of HindIII and BclI markers.
Determination of haemophilia A carrier status from hair samples using polymerase chain reaction technique.
Factor VIII gene mutations and RFLP analysis in hemophilia A.
Factor VIII gene polymorphisms in the Asian Indian population.
HindIII polymorphism in carrier detection of hemophilia A in India: a new primer design.
Inversion mutation analysis in hemophilia a by restriction enzyme analysis and southern blotting.
Polymorphisms associated with the FVIII and FIX genes in the Turkish population.
Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia A.
Screening for nonsense mutations in patients with severe hemophilia A can provide rapid, direct carrier detection.
Screening of intron 1 inversion and three intragenic factor VIII gene polymorphisms in Pakistani hemophilia A families.
Severe Hemophilia A in a Male Old English Sheep Dog with a C?T Transition that Created a Premature Stop Codon in Factor VIII.
The Chapel Hill hemophilia A dog colony exhibits a factor VIII gene inversion.
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI.
Use of denaturing gradient gel electrophoresis to detect point mutations in the factor VIII gene.
[Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: a new marker for the hemophilia A carrier detection]
[Assessment of the frequency of finding polymorphic alleles of the human X-chromosome locus DXS52 in the Muscovite population]
[Detection of carriers of hemophilia A by testing for HindIII polymorphism in the factor VIII gene by PCR]
[Detection of hemophilia A carriers by testing polymorphic Bcl I and HINDIII sites using the PCR method with internal splitting control]
[Molecular genetic study of the factor VIII gene in families from Bashkir with hemophilia A]
[Significance of BclI and HindIII Polymorphism Detection in Genetic Diagnosis of Familial Hemophilia A.]
Hemophilia B
Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism.
Molecular defects in haemophilia B: detection by direct restriction enzyme analysis.
Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status.
Hemorrhagic Fever with Renal Syndrome
Dobrava virus as a new Hantavirus: evidenced by comparative sequence analysis.
Isolation of a Puumala-like virus from Mus musculus captured in Yugoslavia and its association with severe hemorrhagic fever with renal syndrome.
Hemorrhagic Septicemia
Clonality and virulence traits of Escherichia coli associated with haemorrhagic septicaemia in turkeys.
Restriction endonuclease analysis using Hhal and Hpall to discriminate among group B Pasteurella multocida associated with haemorrhagic septicaemia.
Hemorrhagic Stroke
Association between Lipoprotein Lipase Polymorphism and the Risk of Stroke: A Meta-analysis.
Hepatitis
Characterization of an avian adenovirus associated with inclusion body hepatitis in day-old turkeys.
Detection of human cytomegalovirus DNA in liver biopsies from patients with cytomegalovirus-related liver disease.
Genetic manipulation of equine arteritis virus using full-length cDNA clones: separation of overlapping genes and expression of a foreign epitope.
Genotyping of mouse hepatitis virus strains by restriction endonuclease analysis of amplified nucleocapsid protein genes.
Hepatocellular carcinoma in Richardson's ground squirrels (Spermophilus richardsonii): evidence for association with hepatitis B-like virus infection.
Isolation and characterization of an adenovirus associated with inclusion body hepatitis in psittacine birds.
Molecular characterization of highly virulent fowl adenoviruses associated with outbreaks of inclusion body hepatitis.
SpEDIT: A fast and efficient CRISPR/Cas9 method for fission yeast.
State of hepatitis B virus DNA in hepatocytes of patients with hepatitis B surface antigen-positive and -negative liver diseases.
The use of PCR combined with restriction enzyme analysis to characterize fowl adenovirus field isolates from northern India.
Virion DNA of ground squirrel hepatitis virus: structural analysis and molecular cloning.
Hepatitis A
[Construction of the plant expression vector with hepatitis a capsid protein fusion gene and genetic transformation of Citrus. Sinensis Osbeck.]
Hepatitis B
A clone of hepatitis B virus (subtype adr) DNA with a new HindIII site.
A molecularly cloned hepatitis B virus produced in vitro is infectious in a chimpanzee.
Analysis of integrated hepatitis B virus DNA and cellular flanking sequences cloned from a hepatocellular carcinoma.
Association of PvuII and XbaI polymorphisms in estrogen receptor alpha gene with the risk of hepatitis B virus infection in the Guangxi Zhuang population.
Characterization and biological properties of a hepatitis B virus isolated from a patient without hepatitis B virus serologic markers.
Characterization of restriction endonuclease maps of hepatitis B viral DNAs.
Cloning and analysis of integrated hepatitis virus sequences from a human hepatoma cell line.
Cloning simulation in the cage environment.
Construction and identification of Complex DNA vaccine of hepatitis B and Toxoplasma gondii.
Defective hepatitis B virus DNA molecules detected in a stable integration pattern in a hepatoma cell line, and in induced tumours and derived cell lines.
Detection of hepatitis B virus DNA in hepatocellular carcinoma: methylation of integrated viral DNA.
Distribution of hepatitis B virus genotypes and its association with severity of liver disease in patients with chronic hepatitis B in uttar pradesh, India.
DNA cloned from the ayw subtype of hepatitis B virus.
Efficient amplification with NASBA of hepatitis B virus, herpes simplex virus and methicillin resistant Staphylococcus aureus DNA.
Enhanced specificity of real-time PCR for measurement of hepatitis B virus cccDNA using restriction endonuclease and plasmid-safe ATP-dependent DNase and selective primers.
Evaluation of transcriptional efficiency of hepatitis B virus covalently closed circular DNA by reverse transcription-PCR combined with the restriction enzyme digestion method.
Expression and secretion of hepatitis B viral surface antigen in E. coli.
Genome of hepatitis B virus: restriction enzyme cleavage and structure of DNA extracted from Dane particles.
Identification and characterization of intrahepatic hepatitis B virus DNA in HBsAg-seronegative patients with chronic liver disease and hepatocellular carcinoma in Taiwan.
Identification of the hepatitis B virus factor that inhibits expression of the beta interferon gene.
Integration pattern of hepatitis B virus DNA sequences in human hepatoma cell lines.
Novel RNA family structure of hepatitis B virus expressed in human cells, using a helper-free adenovirus vector.
Nucleotide sequence of a cloned duck hepatitis B virus genome: comparison with woodchuck and human hepatitis B virus sequences.
Nucleotide sequence of the gene coding for the major protein of hepatitis B virus surface antigen.
Prevalence of precore-defective mutant of hepatitis B virus in HBV carriers.
Rapid screening for bacterial colonies harbouring tandem hepatitis B virus sequences by an oligonucleotide probe.
Restriction endonuclease cleavage map and location of unique features of the DNA of hepatitis B virus, subtype adw2.
Restriction endonuclease mapping of the hepatitis B viral genome isolated from Taiwan.
Restriction map of the hepatitis B virus DNA cloned in Escherichia coli.
Stable expression of the hepatitis B virus surface antigen containing pre-S2 protein in mouse cells using a bovine papillomavirus vector.
Strain analysis of hepatitis B virus on the basis of restriction endonuclease analysis of polymerase chain reaction products.
Synthesis of hepatitis B virus e antigen in E. coli.
Tissue preferential expression of the hepatitis B virus (HBV) surface antigen gene in two lines of HBV transgenic mice.
Trans-complementation of the C gene of human and the P gene of woodchuck hepadnaviruses.
Transcription of the human beta interferon gene is inhibited by hepatitis B virus.
[Enhancement of a hepatitis B DNA vaccine potency using aluminum phosphate in mice]
[Expression of 12 antibody escape mutants of hepatitis B virus surface antigen gene in mammalian cell by using an Epstein-Barr based vector]
[Genotyping of hepatitis B virus by restriction enzyme analysis]
[The comparative mapping of virion and cloned DNA of the hepatitis B virus]
Hepatitis B, Chronic
Hepatitis B virus carriers without precore mutations in hepatitis B e antigen-negative stage show more severe liver damage.
Interleukin-10 promoter polymorphism predicts initial response of chronic hepatitis B to interferon alfa.
Hepatitis C
Electrochemical detection of hepatitis C virus based on site-specific DNA cleavage of BamHI endonuclease.
Electrochemical detection of hepatitis C virus with signal amplification using BamHI endonuclease and horseradish peroxidase-encapsulated nanogold hollow spheres.
Hepatitis C virus-specific DNA sequences in human DNA: differentiation by means of restriction enzyme analysis at the DNA level in healthy, anti-HCV-negative individuals.
Identification of numerous hepatitis C virus genotypes in Montreal, Canada.
Magnetic bead/capture DNA/glucose-loaded nanoliposomes for amplifying the glucometer signal in the rapid screening of hepatitis C virus RNA.
Survey of major genotypes and subtypes of hepatitis C virus using RFLP of sequences amplified from the 5' non-coding region.
Ultrasensitive and selective electrochemical identification of hepatitis C virus genotype 1b based on specific endonuclease combined with gold nanoparticles signal amplification.
[Detection of Hepatitis C Virus by Reverse Transcription-loop Mediated Isothermal Amplification].
[Hepatitis c virus genotype research by ABC programs of 5'-NCR restriction endonuclease digestion]
Hepatitis E
Genotyping of hepatitis E virus in clinical specimens by restriction endonuclease analysis.
Identification of hepatitis E virus in clinical specimens: amplification of hydroxyapatite-purified virus RNA and restriction endonuclease analysis.
[Genotyping of hepatitis E virus by PCR combining with single restriction endonuclease analysis]
Herpes Genitalis
Analysis of DNA from recurrent genital herpes simplex virus isolates by restriction endonuclease digestion.
Demonstration of either endogenous recurrence or exogenous reinfection by restriction endonuclease cleavage analysis of herpes simplex virus from patients with recrudescent genital herpes.
Lack of evidence for intertypic recombinants in the pathogenesis of recurrent genital infections with herpes simplex virus type 1.
Molecular biology in viral diagnosis: restriction enzyme analysis of viruses from recurrent genital herpes infections.
Restriction endonuclease analysis of deoxyribonucleic acid (DNA) from genital herpes simplex virus type 2 isolates in Thailand.
Restriction enzyme analysis of herpes simplex virus isolates from known contacts of patients with genital herpes.
Herpes Simplex
A comparative analysis of restriction enzyme digests of the DNA of herpes simplex virus isolated from genital and facial lesions.
A cosmid-based system for constructing mutants of herpes simplex virus type 1.
A lambda library of Herpes simplex virus type 1 (KOS) DNA fragments obtained by partial digestion with Sau3A.
A miniaturised and simplified technique for typing and subtyping herpes simplex virus.
A rapid method for restriction endonuclease analysis of DNA from herpes simplex virus type 2.
A simple and practical method for typing and strain differentiation of herpes simplex virus using infected cell DNAs.
A tandem repeat sequence found in a heterogeneous fragment of UL of herpes simplex virus type 1.
Amplification by host cell factors of a sequence contained within the herpes simplex virus 1 genome.
An ICP6::lacZ insertional mutagen is used to demonstrate that the UL52 gene of herpes simplex virus type 1 is required for virus growth and DNA synthesis.
An in vitro ligation and transfection system for inserting DNA sequences into the latency-associated transcripts (LATs) gene of herpes simplex virus type 1.
Analysis of DNA of defective herpes simplex virus type 1 by restriction endonuclease cleavage and nucleic acid hybridization.
Analysis of genomic polymorphism among herpes simplex virus type 2 isolates from four areas of Japan and three other countries.
Analysis of intrastrain recombination in herpes simplex virus type 1 strain 17 and herpes simplex virus type 2 strain HG52 using restriction endonuclease sites as unselected markers and temperature-sensitive lesions as selected markers.
Anatomy of herpes simplex virus DNA VII. alpha-RNA is homologous to noncontiguous sites in both the L and S components of viral DNA.
Anatomy of herpes simplex virus DNA: strain differences and heterogeneity in the locations of restriction endonuclease cleavage sites.
BamI, KpnI, and SalI restriction enzyme maps of the DNAs of herpes simplex virus strains Justin and F: occurrence of heterogeneities in defined regions of the viral DNA.
Biochemical transformation of mouse cells by a purified fragment of marmoset herpesvirus DNA.
Cell-specific selection of mutants of a herpes simplex virus recombinant carrying deletions.
Characterization of a major late herpes simplex virus type 1 mRNA.
Characterization of coliphage lambda hybrids carrying DNA fragments from Herpes simplex virus type 1 defective interfering particles.
Characterization of herpes simplex viral DNA using 3H-thymidine and restriction enzyme digestion analysis.
Characterization of mRNAs that map in the BglII N fragment of the herpes simplex virus type 2 genome.
Characterization of the tumor-associated 38-kd protein of herpes simplex virus type 2.
Cloning and restriction endonuclease mapping of herpes simplex virus type-1 strains H129 and +GC.
Cloning of reiterated and nonreiterated herpes simplex virus 1 sequences as BamHI fragments.
Cloning of the active thymidine kinase gene of herpes simplex virus type 1 in Escherichia coli K-12.
Comparative analysis of herpes simplex virus type 1 mutants that are defective in fusion function by using restriction endonuclease.
Comparison of a commercial ELISA system with restriction endonuclease analysis for typing herpes simplex virus.
Comparison of four methods for typing low-passage herpes simplex virus isolates.
Comparison of restriction endonuclease profiles of DNA from local herpes simplex virus type 2 (HSV-2) strains.
Comparison of the bovine herpesvirus 1 gI gene and the herpes simplex virus type 1 gB gene.
Concurrent oral and genital infection with an identical strain of herpes simplex virus type 1. Restriction endonuclease analysis.
Construction and characterization of a recombinant plasmid encoding the gene for the thymidine kinase of Herpes simplex type 1 virus.
Demonstration of circularization of herpes simplex virus DNA following infection using pulsed field gel electrophoresis.
Demonstration of either endogenous recurrence or exogenous reinfection by restriction endonuclease cleavage analysis of herpes simplex virus from patients with recrudescent genital herpes.
Demonstration of exogenous genital reinfection with herpes simplex virus type 2 by restriction endonuclease fingerprinting of viral DNA.
Detailed analysis of the portion of the herpes simplex virus type 1 genome encoding glycoprotein C.
Detailed characterization of an apparently unspliced beta herpes simplex virus type 1 gene mapping in the interior of another.
Detailed characterization of the mRNA mapping in the HindIII fragment K region of the herpes simplex virus type 1 genome.
Detection of herpes simplex virus-specific DNA sequences in latently infected mice and in humans.
Detection of viral DNA and RNA by in situ hybridization.
Determination of the coding capacity of the BamHI DNA fragment B of apathogenic Herpes simplex virus type 1 strain HFEM by DNA nucleotide sequence analysis.
Different sizes of restriction endonuclease fragments from the terminal repetitions of the herpes simplex virus type 1 genome latent in trigeminal ganglia of mice.
Direction of synthesis of the message for a 35 000 polypeptide of herpes simplex virus type 2.
Discrimination between twenty isolates of herpesvirus simiae (B virus) by restriction enzyme analysis of the viral genome.
DNA amplification and neoplastic transformation mediated by a herpes simplex DNA fragment containing cell-related sequences.
DNA restriction enzyme analysis of digital and genital isolates of herpes simplex virus from three patients.
DNA sequence and genetic content of the HindIII l region in the short unique component of the herpes simplex virus type 2 genome: identification of the gene encoding glycoprotein G, and evolutionary comparisons.
DNA-mediated gene transfer in Chinese hamster ovary cells: clonal variation in transfer efficiency.
Does restriction enzyme analysis reveal changes in herpes simplex virus DNA after latency in mouse ganglia?
Down-regulation of keratin 14 gene expression after v-Ha-ras transfection of human papillomavirus-immortalized human cervical epithelial cells.
Efficient amplification with NASBA of hepatitis B virus, herpes simplex virus and methicillin resistant Staphylococcus aureus DNA.
Enhanced rate of conversion or recombination of markers within a region of unique sequence in the herpes simplex virus genome.
Expression of human immunodeficiency virus type 1 gag gene using genetically engineered herpes simplex virus type 1 recombinants.
Expression of transferred thymidine kinase genes is controlled by methylation.
Functional expression of the Herpes simplex virus thymidine kinase gene in Escherichia coli K-12.
Genetic analysis of herpes simplex virus type 1 isolates from recurrent lesions and clinical reinfections.
Genital recurrent infection occurring 6 months after meningitis due to the same herpes simplex virus type 2 (HSV-2) strain evidence by restriction endonuclease analysis.
Genome differences among field isolates and vaccine strains of pseudorabies virus.
Genome variations in herpes simplex virus type 2 strains isolated in Japan and Sweden.
Genomic comparison of herpes simplex virus type 1 isolates from Japan, Sweden and Kenya.
Genomic variation among herpes simplex virus type 1 strains: virus DNA analysis of isolates from Saudi patients.
Geographical distribution of the herpes simplex virus type 1 BgKL variant in Japan suggests gradual dispersion of the virus from Shikoku Island to the other Islands.
Herpes simplex virus glycoprotein D is sufficient to induce spontaneous pH-independent fusion in a cell line that constitutively expresses the glycoprotein.
Herpes simplex virus mRNA species mapping in EcoRI fragment I.
Herpes simplex virus thymidine kinase transcripts are absent from both nucleus and cytoplasm during infection in the presence of cycloheximide.
Herpes simplex virus type 1 Angelotti and a defective viral genotype: analysis of genome structures and genetic relatedness by DNA-DNA reassociation kinetics.
Herpes simplex virus type 1 deletion variants 1714 and 1716 pinpoint neurovirulence-related sequences in Glasgow strain 17+ between immediate early gene 1 and the 'a' sequence.
Herpes simplex virus type 1 HindIII fragment L encodes spliced and complementary mRNA species.
Herpes simplex virus type 1 restriction fragment polymorphism determined using southern hybridization.
Herpes simplex virus type 1 that exhibits herpes simplex virus type 2 sensitivity to (E)-5-(2-bromovinyl)-2'-deoxyuridine.
High-frequency transfer of cloned herpes simplex virus type 1 sequences to mammalian cells by protoplast fusion.
Homogeneity and diversity of genome polymorphism in a set of herpes simplex virus type 1 strains classified as the same genotypic group.
Hybrid plasmids containing an active thymidine kinase gene of Herpes simplex virus 1.
Identification and characterization of pseudorabies virus glycoprotein gM as a nonessential virion component.
Identification and mapping of two polypeptides encoded within the herpes simplex virus type 1 thymidine kinase gene sequences.
Identification and nucleotide sequence of the glycoprotein gB gene of equine herpesvirus 4.
Identification and typing of herpes simplex virus types 1 and 2 by monoclonal antibodies, sensitivity to the drug (E)-5-(2-bromovinyl)-2'-deoxyuridine, and restriction endonuclease analysis of viral DNA.
Identification of a virus-specific polypeptide associated with a transforming fragment (BglII-N) of herpes simplex virus type 2 DNA.
Identification of an Epstein-Barr virus-coded thymidine kinase.
Identification of five new variable restriction sites in HSV-1 DNA.
Identification of proteins encoded by a fragment of herpes simplex virus type 2 DNA that has transforming activity.
Immortalization of rabbit vascular smooth muscle cells after transfection with a fragment of the BglII N region of herpes simplex virus type 2 DNA.
Improved sensitivity of restriction endonuclease analysis of herpes simplex virus type 2 DNA with polyacrylamide gradient gel electrophoresis.
In vitro and in vivo transcription initiation sites on the TK-encoding BamHI Q fragment of HSV-1 DNA.
In vitro transcription of herpes simplex virus genes: identification of a new initiation site and second intervening sequence in the immediate-early RNA-5 gene.
Induction of mutations in bacteria by a fragment of DNA from herpes simplex virus type 1.
Initial Characterization of the Epstein?Barr Virus BSRF1 Gene Product.
Insertion of DNA sequences at a unique restriction enzyme site engineered for vector purposes into the genome of herpes simplex virus type 1.
Insertion sites for recombinant vaccinia virus construction: effects on expression of a foreign protein.
Intermolecular recombination of the herpes simplex virus type 1 genome analysed using two strains differing in restriction enzyme cleavage sites.
Intracellular transport of herpes simplex virus gD occurs more rapidly in uninfected cells than in infected cells.
Is ribonucleotide reductase the transforming function of herpes simplex virus 2?
Isolation and characterisation of herpes simplex virus type 1 mutants which fail to induce dUTPase activity.
Isolation and characterization of herpes simplex virus type 1 host range mutants defective in viral DNA synthesis.
Isolation of herpes simplex virus type 1 during first attack of multiple sclerosis.
Isolation of restriction endonuclease site deletion mutants of herpes simplex virus.
Large-scale rearrangement of homologous regions in the genomes of HCMV and EBV.
Latent herpes simplex virus type 1 DNA contains two copies of the virion DNA joint region.
Latex and vinyl examination gloves. Quality control procedures and implications for health care workers.
Localization and comparative nucleotide sequence analysis of the transforming domain in herpes simplex virus DNA containing repetitive genetic elements.
Localization of the coding region for a 35000 Dalton polypeptide on the genome of herpes simplex virus type 2.
Localization of the thymidine kinase gene of herpes simplex virus type 2 (333).
Method for induction of mutations in physically defined regions of the herpes simplex virus genome.
Molecular cloning of herpes simplex virus type 2 DNA.
Nosocomial herpetic infections in a pediatric intensive care unit.
Nucleotide sequence and characterization of the Marek's disease virus homologue of glycoprotein B of herpes simplex virus.
Organization of the left-hand end of the herpes simplex virus type 2 BglII N fragment.
Organotropism of latent herpes simplex virus type 1 is correlated to the presence of a 1.5 kb RNA transcript mapped within the BamHI DNA fragment B (0.738 to 0.809 map units).
Physical map of the origin of defective DNA in herpes simplex virus type 1 DNA.
Physical mapping of drug resistance mutations defines an active center of the herpes simplex virus DNA polymerase enzyme.
Physical mapping of temperature-sensitive mutations of herpes simplex virus type 1 using cloned restriction endonuclease fragments.
Physical mapping of the herpes simplex virus type 2 nuc- lesion affecting alkaline exonuclease activity by using herpes simplex virus type 1 deletion clones.
Promiscuous trans activation of gene expression by an Epstein-Barr virus-encoded early nuclear protein.
Proteins containing only half of the coding information of early region 1b of adenovirus are functional in human cells transformed with the herpes simplex virus type 1 thymidine kinase gene and adenovirus type 2 DNA.
Pseudorabies virus and equine herpesvirus 1 share a nonessential gene which is absent in other herpesviruses and located adjacent to a highly conserved gene cluster.
Quantitative analysis of genomic polymorphism of herpes simplex virus type 1 strains from six countries: studies of molecular evolution and molecular epidemiology of the virus.
Rapid detection of cytomegalovirus in clinical specimens by using biotinylated DNA probes and analysis of cross-reactivity with herpes simplex virus.
Recurrent intraoral herpes simplex virus infection.
Regulation of herpesvirus macromolecular synthesis. VIII. The transcription program consists of three phases during which both extent of transcription and accumulation of RNA in the cytoplasm are regulated.
Reliable identification of herpes simplex viruses by DNA restriction endonuclease analysis with EcoRI.
Replacement of glycoprotein B gene in the herpes simplex virus type 1 strain ANGpath DNA by that originating from nonpathogenic strain KOS reduces the pathogenicity of recombinant virus.
Rescue of a tk-plasmid from transgenic mice reveals its episomal transmission.
Restriction endonuclease analysis of deoxyribonucleic acid (DNA) from genital herpes simplex virus type 2 isolates in Thailand.
Restriction endonuclease analysis of DNA from genital isolates of herpes simplex virus type 2.
Restriction endonuclease analysis of herpes simplex virus from recrudescent lesions, from latent infection and during passage in the skin and nervous system of mice.
Restriction endonuclease cleavage analysis of herpes simplex virus isolates obtained from three pairs of siblings.
Restriction endonuclease cleavage analysis of herpes simplex virus type 2 from Chiang Mai, Thailand and Okinawa, Japan.
Restriction endonuclease cleavage of DNA obtained from herpes simplex isolates of two patients with bilateral herpetic disease.
Restriction endonuclease digestion analysis of DNA from viruses isolated from different sites of two fatal cases of herpes simplex virus type-1 infection.
Restriction endonuclease fingerprinting of herpes simplex virus DNA: a novel epidemiological tool applied to a nosocomial outbreak.
Restriction endonuclease patterns of herpes simplex virus DNA: application to diagnosis and molecular epidemiology.
Restriction endonuclease patterns of herpes simplex virus DNA: subtyping of HSV-1 and HSV-2 strains from genital and nongenital lesions.
Restriction endonucleases recognizing DNA sequences of four base pairs facilitate differentiation of herpes simplex virus type 1 strains.
Restriction enzyme analysis and herpes simplex infections.
Restriction enzyme analysis of herpes simplex virus isolates from known contacts of patients with genital herpes.
Restriction enzyme fragment length polymorphisms of amplified herpes simplex virus type-1 DNA provide epidemiologic information.
Retention and expression of the left end subfragment of the herpes simplex virus type 2 BglII N DNA fragment do not correlate with tumorigenic conversion of NIH 3T3 cells.
Retention of herpes simplex virus type II sequences in bglII n-transformed cells after co-transfection with a selectable marker.
RNAs transcribed from a 3.6-kilobase SmaI fragment of the short unique region of the herpes simplex virus type 1 genome.
Sequence arrangement in herpes simplex virus type 1 DNA: identification of terminal fragments in restriction endonuclease digests and evidence for inversions in redundant and unique sequences.
Sequence Arrangement in Herpes Simplex Virus Type 1 DNA: Identification of Terminal Fragments in Restriction Endonuclease Digests and Evidence for Inversions in Redundant and Unique Sequences.
Seroepidemiology of herpes simplex virus and restriction endonuclease cleavages analysis of herpes simplex virus type 2 in Okinawa.
Simplified method for typing herpes simplex virus by restriction endonuclease analysis.
Stability of the cloned 'joint region' of herpes simplex virus DNA.
Stable expression in mouse cells of nuclear neoantigen after transfer of a 3.4-megadalton cloned fragment of Epstein-Barr virus DNA.
Structure and function of herpesvirus genomes. II. EcoRl, Sbal, and HindIII endonuclease cleavage sites on herpes simplex virus.
Structure and origin of defective genomes contained in serially passaged herpes simplex virus type 1 (Justin).
Structure of replicating herpes simplex virus DNA.
Structure of the joint region and the termini of the DNA of herpes simplex virus type 1.
Terminal fragments of herpes simplex virus DNA produced by restriction endonuclease.
The BamHI fragment 9 of pseudorabies virus contains genes homologous to the UL24, UL25, UL26, and UL 26.5 genes of herpes simplex virus type 1.
The cervical tumor-associated antigen (ICP-10/AG-4) is encoded by the transforming region of the genome of herpes simplex virus type 2.
The herpes simplex virus type 1 BgKL variant, unlike the BgOL variant, shows a higher association with orolabial infection than with infections at other sites, supporting the variant-dispersion-replacement hypothesis.
The heterogenous regions in herpes simplex virus 1 DNA.
The left border of the genomic inversion of pseudorabies virus contains genes homologous to the UL46 and UL47 genes of herpes simplex virus type 1, but no UL45 gene.
The polypeptide and the DNA restriction enzyme profiles of spontaneous isolates of herpes simplex virus type 1 from explants of human trigeminal, superior cervical and vagus ganglia.
The pseudorabies virus gII gene is closely related to the gB glycoprotein gene of herpes simplex virus.
The virulence-determining genomic BamHI fragment 4 of pseudorabies virus contains genes corresponding to the UL15 (partial), UL18, UL19, UL20, and UL21 genes of herpes simplex virus and a putative origin of replication.
Three mutants of herpes simplex virus type 2: one lacking the genes US10, US11 and US12 and two in which Rs has been extended by 6 kb to 0.91 map units with loss of Us sequences between 0.94 and the Us/TRs junction.
trans-activation and autoregulation of gene expression by the immediate-early region 2 gene products of human cytomegalovirus.
Transcription analysis and sequence of the putative murine cytomegalovirus DNA polymerase gene.
Transcription and translation of the herpes simplex virus type 1 thymidine kinase gene after microinjection into Xenopus laevis oocytes.
Transcription from the BamHI J fragment of herpes simplex virus type 1 (KOS).
Transcription of herpes simplex virus genes in vivo: overlap of a late promoter with the 3' end of the early thymidine kinase gene.
Transcriptional control of the equine herpesvirus 1 immediate early gene.
Transformation of hamster embryo fibroblasts by a specific fragment of the herpes simplex virus genome.
Transformation of NIH 3T3 cells by herpes simplex type 2 BglII n fragment and sub-fragments is independent from induction of mutation at the HPRT locus.
Transformation of rodent cells by a cloned DNA fragment of herpes simplex virus type 2.
Transmission of herpes simplex virus infection via lacrimal canaliculi.
Typing of clinical herpes simplex virus isolates with mouse monoclonal antibodies to herpes simplex virus types 1 and 2: comparison with type-specific rabbit antisera and restriction endonuclease analysis of viral DNA.
Typing of herpes simplex virus by capture biotin-streptavidin enzyme-linked immunosorbent assay and comparison with restriction endonuclease analysis and immunofluorescence method using monoclonal antibodies.
Typing of herpes simplex virus isolates with monoclonal antibodies and by nucleic acid spot hybridization.
Use of site-directed mutagenesis to generate a herpes simplex virus type 1 strain 17+ mutant lacking seven HindIII restriction endonuclease cleavage sites.
Utility of restriction fragment analysis for typing herpes simplex virus amplicons following PCR of targets in the DNA polymerase gene.
Variable restriction endonuclease sites of herpes simplex virus type 1 isolates from encephalitic, facial and genital lesions and ganglia.
[Analysis of herpes simplex virus DNA using restriction endonucleases]
[Detection of herpes simplex virus by DNA-DNA hybridization method]
[Evaluation of molecular hybridization tests and DNA restriction enzyme analysis for the detection and typing of herpes simplex virus (HSV)]
[Molecular-epidemiological and phylogenic analysis of herpes simplex virus type 1 from seven areas in Japan]
[Restriction endonuclease study of interstrain differences in the DNA of herpes simplex virus type 1]
[The DNA restriction enzyme analyses of herpes simplex virus type 1 isolates from cases of ocular herpes]
[Typing of herpes simplex viral strains using restriction endonuclease XhoI]
Herpes Zoster
Analysis of varicella-zoster virus DNAs of clinical isolates by endonuclease HpaI.
Characterization of human varicella-zoster virus DNA.
Comparative analysis of the restriction endonuclease profiles of the Dumas and Singapore strains of varicella-zoster virus.
Genome differences among varicella-zoster viruses isolated in Thailand.
Identification and analysis of the simian varicella virus thymidine kinase gene.
Nationwide distribution of varicella-zoster virus clades in China.
Restriction endonuclease analysis of viral DNA from a patient with bilateral herpes zoster lesions.
The simian varicella virus and varicella zoster virus genomes are similar in size and structure.
Varicella zoster virus DNA exists as two isomers.
VZV Molecular Epidemiology.
[Influence of combined microinjection of gene engineering construct and endonuclease on preimplantation development of mouse embryos in vitro]
Hodgkin Disease
Co-expression of Epstein-Barr virus latent membrane protein and vimentin in "aggressive" histological subtypes of Hodgkin's disease.
Increased frequency of the S allele of the L-myc oncogene in non-Hodgkin's lymphoma.
HTLV-II Infections
Differential diagnosis of HTLV-I and HTLV-II infections by restriction enzyme analysis of 'nested' PCR products.
Huntington Disease
Counting CAG repeats in the Huntington's disease gene by restriction endonuclease EcoP15I cleavage.
Editing for an AMPA receptor subunit RNA in prefrontal cortex and striatum in Alzheimer's disease, Huntington's disease and schizophrenia.
Molecular diagnosis of Huntington's disease in Mexican patients by polymerase chain reaction.
Predictive testing for Huntington's disease with use of a linked DNA marker.
Some developments on the affected-pedigree-member method of linkage analysis.
Studies of a DNA marker (G8) genetically linked to Huntington disease in British families.
Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families.
[Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique]
Hydatidiform Mole
Complete hydatidiform moles combine maternal mitochondria with a paternal nuclear genome.
PTEN promoter methylation and protein expression in normal early placentas and hydatidiform moles.
The human chorionic gonadotrophin alpha subunit gene in gestational trophoblastic disease. 1. Restriction fragment length polymorphisms in hydatidiform moles.
Hydatidiform Mole, Invasive
PTEN promoter methylation and protein expression in normal early placentas and hydatidiform moles.
Hydrops Fetalis
Alpha-globin gene organisation and prenatal diagnosis of alpha-thalassaemia in Chinese.
First-trimester prenatal diagnosis of severe alpha-thalassemia.
Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
Hyperaldosteronism
Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expression.
Hypercholesterolemia
Lipid-lowering response of the HMG-CoA reductase inhibitor fluvastatin is influenced by polymorphisms in the low-density lipoprotein receptor gene in Brazilian patients with primary hypercholesterolemia.
Screening for mutations in the LDL receptor gene and apolipoprotein B-100 gene in 218 patients with severe hypercholesterolemia.
[The relation of polymorphism of low-density lipoprotein receptor gene with serum cholesterol levels]
Hyperemia
Endothelial function and insulin resistance in early postmenopausal women with cardiovascular risk factors: importance of ESR1 and NOS3 polymorphisms.
Hyperglycinemia, Nonketotic
Partial structure of the human H-protein gene.
Hyperinsulinism
Familial hyperinsulinemia due to a structurally abnormal insulin. Definition of an emerging new clinical syndrome.
Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome.
Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings.
Hyperlipidemias
Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia.
Associations of the ABCA1 and LPL Gene Polymorphisms With Lipid Levels in a Hyperlipidemic Population.
Comparison of lipid profiles in relation to APOB EcoRI polymorphism in obese children with hyperlipidemia.
Relationship between plasma HDL subclasses distribution and lipoprotein lipase gene HindIII polymorphism in hyperlipidemia.
Restriction isotyping of apolipoprotein E R145C in type III hyperlipoproteinemia.
The influence of lipoprotein lipase gene variation on postprandial lipoprotein metabolism.
Hyperlipoproteinemia Type I
A newly identified heterozygous lipoprotein lipase gene mutation (Cys239-->stop/TGC972-->TGA; LPLobama) in a patient with primary type IV hyperlipoproteinemia.
Apolipoprotein C-II deficiency syndrome due to apo C-IIHamburg: clinical and biochemical features and HphI restriction enzyme polymorphism.
Detection of familial LPL deficiency by PvuII RFLP.
Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency.
Heterozygous apolipoprotein C-II deficiency: lipoprotein and apoprotein phenotype and RsaI restriction enzyme polymorphism in the Apo C-IIPadova kindred.
Hyperlipoproteinemia Type II
A new missense mutation (Cys297-->Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste).
A three-allelic polymorphic system in exon 12 of the LDL receptor gene is highly informative for segregation analysis of familial hypercholesterolemia in the Spanish population.
Diagnosis of familial hypercholesterolemia using DNA haplotype analysis in three large families with two hyperlipidemic parents.
Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect.
Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia.
Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.
Prenatal diagnosis of familial hypercholesterolemia caused by the "Lebanese" mutation at the low density lipoprotein receptor locus.
Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia.
Hyperlipoproteinemias
A newly identified heterozygous lipoprotein lipase gene mutation (Cys239-->stop/TGC972-->TGA; LPLobama) in a patient with primary type IV hyperlipoproteinemia.
Hypersensitivity
A mutant approach and molecular strategy to study fungal cell walls.
Active transcription of the human FASL/CD95L/TNFSF6 promoter region in T lymphocytes involves chromatin remodeling: role of DNA methylation and protein acetylation suggest distinct mechanisms of transcriptional repression.
Analyzing the contributions of chromatin structure in nuclear hormone receptor activated transcription in vivo.
Assaying chromatin structure and remodeling by restriction enzyme accessibility.
Deletions in the r-determinant mer region of plasmid R100-1 selected for loss of mercury hypersensitivy.
Estrogen Induces Estrogen-related Receptor {alpha} Gene Expression and Chromatin Structural Changes in Estrogen Receptor (ER)-positive and ER-negative Breast Cancer Cells.
HindIII liposomes suppress delayed-type hypersensitivity responses in vivo and induce epidermal IL-10 in vitro.
Identification of Simian virus 40 promoter DNA sequences capable of conferring restriction endonuclease hypersensitivity.
Preferential accessibility of the yeast his3 promoter is determined by a general property of the DNA sequence, not by specific elements.
Probabilistic regulation of IL-4 production in Th2 cells: accessibility at the Il4 locus.
Proteasomal inhibition enhances glucocorticoid receptor transactivation and alters its subnuclear trafficking.
Radiosensitive Chinese hamster irs2 cells show enhanced chromosomal sensitivity to ionizing radiation and restriction endonuclease induced blunt-ended double-strand breaks.
Steroid hormone receptor status defines the MMTV promoter chromatin structure in vivo.
[IL4RA gene polymorphism (Q576R) is associated with higher total IgE levels in Spanish patients with family history of atopy]
Hypertension
A 5-year follow-up study of 3 polymorphisms in the human glucocorticoid receptor gene in relation to obesity, hypertension, and diabetes.
Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus.
Association of the HindIII and S447X polymorphisms in LPL gene with hypertension and type 2 diabetes in Mexican families.
Five polymorphisms in gene candidates for cardiovascular disease in Afro-Brazilian individuals.
Frequency in hypertensives of alleles for a RFLP associated with the renin gene.
Gender-specific effect of estrogen receptor-1 gene polymorphisms in coronary artery disease and its angiographic severity in Chinese population.
HpaII polymorphism in the atrial natriuretic peptide gene and hypertension.
Polymorphisms in the hANP (human atrial natriuretic peptide) gene, albuminuria, and hypertension.
RAAS polymorphisms alter the acute blood pressure response to aerobic exercise among men with hypertension.
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
[Association between angiotensin II type I receptor gene and human essential hypertension]
[Association of estrogen receptor gene polymorphism with cerebral infarction, a case-control study]
Hypertension, Malignant
The renin gene in patients with malignant hypertension and raised plasma renin activity.
Hyperthyroidism
Changes in plasma low-density lipoprotein (LDL)- and high-density lipoprotein cholesterol in hypo- and hyperthyroid patients are related to changes in free thyroxine, not to polymorphisms in LDL receptor or cholesterol ester transfer protein genes.
Thyroid hormone-, carbohydrate, and age-dependent regulation of a methylation site in the hepatic S14 gene.
Hypertriglyceridemia
Gender-related relation between metabolic syndrome and S447X and HindIII polymorphisms of lipoprotein lipase gene in northern Iran.
Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese.
Isolation and characterization of cDNA clones corresponding to two different human apoC-III alleles.
Single-strand conformational polymorphisms (SSCP): studies of the genetic polymorphisms of exon 4 of apolipoprotein C III.
Structure and polymorphic map of human lipoprotein lipase gene.
Hypoparathyroidism
Parathyroid hormone gene polymorphism and sporadic idiopathic hypoparathyroidism.
Hypopituitarism
Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe.
Hypospadias
Genetic polymorphisms of ESR1 and ESR2 that may influence estrogen activity and the risk of hypospadias.
hypoxanthine phosphoribosyltransferase deficiency
Carrier detection of partial hypoxanthine-guanine phosphoribosyltransferase deficiency by analysis with BamHI restriction fragment length polymorphisms and oligonucleotide probes.
Idiopathic Pulmonary Fibrosis
[Association between genetic polymorphism of erythrocyte CR1 and the susceptibility of idiopathic pulmonary fibrosis].
IgA Deficiency
Detection of IgA heavy chain constant region genes in IgA deficient donors: evidence against gene deletions.
IgA Vasculitis
The CD18 AvaII polymorphic site not associated with Henoch-Schonlein purpura.
Impetigo
DNA heterogeneity of Staphylococcus aureus strains evaluated by SmaI and SgrAI pulsed-field gel electrophoresis in patients with impetigo.
Streptokinase gene polymorphism in group A streptococci isolated from Ethiopian children with various disease manifestations.
Infections
A bacteriophage nucleus-like compartment shields DNA from CRISPR nucleases.
A cluster of neonatal herpes simplex infections without mucocutaneous manifestations.
A molecularly cloned hepatitis B virus produced in vitro is infectious in a chimpanzee.
A poxvirus-encoded uracil DNA glycosylase is essential for virus viability.
Absence of significant membrane localization of the proteins coded by the ilvGEDAC genes of Escherichia coli K-12.
Agrobacterium infections in humans: experience at one hospital and review.
Amphotropic proviral envelope sequences are absent from the Mus germ line.
An institutional outbreak of Salmonella enteritidis in Singapore.
An orthopoxvirus serpinlike gene controls the ability of infected cells to fuse.
An outbreak of Mycoplasma synoviae infection in North Carolina turkeys: comparison of isolates by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and restriction endonuclease analysis.
Analysis of an outbreak of variably methicillin-resistant Staphylococcus aureus with chromosomal RFLPs and mec region probes.
Analysis of clonal relationships among isolates of Shigella sonnei by different molecular typing methods.
Anatomy of herpes simplex virus DNA VII. alpha-RNA is homologous to noncontiguous sites in both the L and S components of viral DNA.
Antimicrobial susceptibility of Listeria monocytogenes isolated from food and clinical cases in Navarra, Spain.
Application of restriction endonuclease analysis and genetic probes in the epidemiology of Yersinia enterocolitica infection.
Application of restriction endonuclease analysis of chromosomal DNA in the study of Staphylococcus aureus colonization in continuous ambulatory peritoneal dialysis patients.
Aspects of the ecology of phlebotomine sand flies (Diptera: Psychodidae) in the Private Natural Heritage Reserve Sanctuary Caraça.
Association of PvuII and XbaI polymorphisms in estrogen receptor alpha gene with the risk of hepatitis B virus infection in the Guangxi Zhuang population.
Association of vaccinia virus-expressed adenovirus E3-19K glycoprotein with class I MHC and its effects on virulence in a murine pneumonia model.
ATP-dependent restriction enzymes.
Atypical myxomatosis--virus isolation, experimental infection of rabbits and restriction endonuclease analysis of the isolate.
BK virus renal infection in a patient with the acquired immunodeficiency syndrome.
Camelpox: epidemiology, diagnosis and control measures.
Campylobacter jejuni infection within a laboratory animal production unit.
Cervical human papillomavirus infection in Tunisian women.
Changes in the restriction endonuclease patterns of four modified-live infectious bovine rhinotracheitis virus (IBRV) vaccines after one passage in host animal.
Characterisation of Histophilus ovis and related organisms by restriction endonuclease analysis.
Characterisation of regulatory sequences at the Epstein-Barr virus BamHI W promoter.
Characterization of cytotoxicity and R-plasmid in Salmonella krefeld.
Characterization of pathogenic and non-pathogenic African swine fever virus isolates from Ornithodoros erraticus inhabiting pig premises in Portugal.
Characterization of prototype and clinically defined strains of Streptococcus suis by genomic fingerprinting.
Characterization of Streptococcus pneumoniae ophthalmic, systemic & commensal isolates by pulsed-field gel electrophoresis & ribotyping.
Characterization of the temporal accumulation of minute virus of mice replicative intermediates.
Characterization of three proteins expressed from the virulence region of plasmid pSDL2 in Salmonella dublin.
Circulating Hypermethylated RASSF1A as a Molecular Biomarker for Diagnosis of Hepatocellular Carcinoma
Clinical Mycoplasma gallisepticum infection in multiplier breeder and meat turkeys caused by F strain: identification by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, restriction endonuclease analysis, and the polymerase chain reaction.
Clonal analysis of the integration and expression of endogenous avian retroviral DNA acquired by exogenous viral infection.
Cloning and restriction endonuclease mapping of herpes simplex virus type-1 strains H129 and +GC.
Comparative evaluation of three commercial software packages for analysis of DNA polymorphism patterns.
Comparative genomics analysis of Clostridium difficile epidemic strain DH/NAP11/106.
Comparative studies of strains of infectious bovine rhinotracheitis virus isolated from latently infected calves.
Comparative study of two strains of Bovid herpesvirus-4.
Comparison between serological classification and auxotyping in the analysis of Neisseria gonorrhoeae infections.
Comparison of camelpox viruses isolated in Dubai.
Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustular vulvovaginitis virus strains by restriction endonuclease analysis.
Complete genotyping of mucosal human papillomavirus using a restriction fragment length polymorphism analysis and an original typing algorithm.
Complete sequence of a new bipartite begomovirus infecting Sida sp. in Northeastern Brazil.
Computer matching of oligonucleotide patterns on electrophoretic gels: an application to the epidemiology of cytomegalovirus.
Concurrent oral and genital infection with an identical strain of herpes simplex virus type 1. Restriction endonuclease analysis.
Congenital cytomegalovirus infection.
Cowpox virus in a 12-year-old boy: rapid identification by an orthopoxvirus-specific polymerase chain reaction.
CpaA Is a Glycan-Specific Adamalysin-like Protease Secreted by Acinetobacter baumannii That Inactivates Coagulation Factor XII.
Cytomegalovirus and blood transfusion.
Cytomegalovirus infection in sex partners: evidence for sexual transmission.
Decrease of hypervirulent Clostridium difficile PCR ribotype 027 in the Netherlands.
Decreased cure and increased recurrence rates for Clostridium difficile infection caused by the epidemic C. difficile BI strain.
Definitive differentiation between single and mixed mycobacterial infections in red deer (Cervus elaphus) by a combination of duplex amplification of p34 and f57 sequences and Hpy188I enzymatic restriction of duplex amplicons.
Detection and strain differentiation of feline calicivirus in conjunctival swabs by RT-PCR of the hypervariable region of the capsid protein gene.
Detection of bovine herpesvirus 4 (BoHV-4) DNA in the cell fraction of milk of dairy cattle with history of BoHV-4 infection.
Detection of varicella zoster virus DNA and viral antigen in human cornea after herpes zoster ophthalmicus.
Diagnosis of mycobacterial infections by PCR and restriction enzyme digestion.
Disseminated Nocardia beijingensis Infection in an Immunocompetent Patient.
Diversity of naturally occurring Epstein-Barr virus revealed by nucleotide sequence polymorphism in hypervariable domains in the BamHI K and N subgenomic regions.
DNA analysis in the study of fungal infections in the immunocompromised host.
DNA-dependent RNA polymerase subunits encoded within the vaccinia virus genome.
Early acquisition of cytomegalovirus infection.
Epidemic Clostridium difficile strains demonstrate increased competitive fitness compared to nonepidemic isolates.
Epidemiologic investigation of nosocomial outbreak of methicillin-resistant Staphylococcus aureus by plasmid pattern analysis.
Epidemiological analysis of a methicillin-resistant Staphylococcus aureus outbreak using restriction fragment length polymorphisms of genomic DNA.
Epidemiology of molluscum contagiosum using genetic analysis of the viral DNA.
Epidemiology of Staphylococcus aureus infections in patients on hemodialysis.
Epstein-Barr virus intrastrain recombination in oral hairy leukoplakia.
Epstein-Barr virus replicative gene transcription during de novo infection of human thymocytes: simultaneous early expression of BZLF-1 and its repressor RAZ.
Epstein-Barr virus small nuclear RNAs are not expressed in permissively infected cells in AIDS-associated leukoplakia.
Equine herpesvirus genomes: heterogeneity of naturally occurring type 4 isolates and of a type 1 isolate after heterologous cell passage.
Escalating Plasmodium falciparum antifolate drug resistance mutations in Macha, rural Zambia.
Evaluation of methods for epidemiologic typing of group A streptococci.
Evidence for the Asiatic origin of endogenous AKR-type murine leukemia proviruses.
Experimental in vivo generation of intertypic recombinant strains of HSV in the mouse.
Experimental infection of bulls with a genital isolate of bovine herpesvirus-4 and reactivation of latent virus with dexamethasone.
Expression of the gene encoding the adenovirus DNA terminal protein precursor in productively infected and transformed cells.
Eye infections due to Listeria monocytogenes in three cows and one horse.
First Report on Natural Infection of Paeonia tenuifolia by 'Candidatus Phytoplasma solani' in Serbia.
Further characterization of the biological and pathogenic properties of erythromelalgia-related poxviruses.
gamma 2-Thymidine kinase chimeras are identically transcribed but regulated a gamma 2 genes in herpes simplex virus genomes and as beta genes in cell genomes.
Gene replacement with linear DNA fragments in wild-type Escherichia coli: enhancement by Chi sites.
Genetic and antigenic characterisation of elongation factor Tu from Mycoplasma mycoides subsp. mycoides SC.
Genetic characterization of high-level gentamicin-resistant strains of Enterococcus faecalis in Iran.
Genetic diversity of rRNA operons of unrelated Streptococcus agalactiae strains isolated from cerebrospinal fluid of neonates suffering from meningitis.
Genetic heterogeneity of M type 3 group A streptococci causing severe infections in Tayside, Scotland.
Genetic relationship between thirteen genome types of adenovirus 11, 34, and 35 with different tropisms.
Genetic variability and molecular typing of Shigella sonnei strains isolated in Canada.
Genetically modified filamentous phage as bactericidal agents: a pilot study.
Genital recurrent infection occurring 6 months after meningitis due to the same herpes simplex virus type 2 (HSV-2) strain evidence by restriction endonuclease analysis.
Genome differences among varicella-zoster viruses isolated in Thailand.
Genome localization of simian virus 40 RNA species.
Genotypes of merozoite surface protein 2 of Plasmodium falciparum in Tanzania.
Genotyping and genetic diversity of Arcobacter butzleri by amplified fragment length polymorphism (AFLP) analysis.
Genotyping of Canadian hepatitis C virus isolates by PCR.
Grouping of Salmonella enterica serotype Montevideo strains by ribotyping and IS200 profiling.
Guinea pig cytomegalovirus immediate-early transcription.
Hepatocellular carcinoma in Richardson's ground squirrels (Spermophilus richardsonii): evidence for association with hepatitis B-like virus infection.
High-frequency switching in Candida strains isolated from vaginitis patients.
Homologous recombination of adenovirus DNA in mammalian cells: enhanced recombination following UV-irradiation of the virus.
Host range expansion of Autographa californica nuclear polyhedrosis virus (NPV) following recombination of a 0.6-kilobase-pair DNA fragment originating from Bombyx mori NPV.
Host range of two multiple nucleopolyhedroviruses isolated from Spodoptera litura
Hyperacetylation and differential deacetylation of histones H4 and H3 define two distinct classes of acetylated SV40 chromosomes early in infection.
Identification of a Mycobacterium tuberculosis gene that enhances mycobacterial survival in macrophages.
Identification of a proviral genome associated with avian myeloblastic leukemia.
Identification of Epstein-Barr virus genes expressed during the early phase of virus replication and during lymphocyte immortalization.
Identification of murine helicobacters by PCR and restriction enzyme analyses.
Identification of the crayfish plague fungus Aphanomyces astaci by polymerase chain reaction and restriction enzyme analysis.
Identifying the RNA polymerases that synthesize specific transcripts of the Autographa californica nuclear polyhedrosis virus.
In vitro characterization of a biologically active molecular clone of HIV-2NIH-Z containing a nef deletion and expressing a full-length transmembrane protein.
In vivo and in vitro reactivation of latent pseudorabies virus in pigs born to vaccinated sows.
In vivo recombination of cauliflower mosaic virus DNA.
Inactivation of restriction endonuclease bamNx after infection with phage phi NR2.
Incidence of human papillomavirus 16 and 18 infection and p53 mutation in patients with oral squamous cell carcinoma in Japan.
Increased expression of Borrelia burgdorferi vlsE in response to human endothelial cell membranes.
Integration of the BALB/c ecotropic provirus into the colony-stimulating factor-1 growth factor locus in a myc retrovirus-induced murine monocyte tumor.
Intracellular forms of adenovirus DNA. V. Viral DNA sequences in hamster cells abortively infected and transformed with human adenovirus type 12.
Intramolecular recombination enables the formation of hepatitis B virus (HBV) cccDNA in mice after HBV genome transfer using recombinant AAV vectors.
Isolation of recombinant DNA clones carrying complete integrated proviruses of Moloney murine leukemia virus.
JC polyomavirus infection in candidates for kidney transplantation living in the Brazilian Amazon region.
Lack of surface receptors not restriction-modification system determines F4 phage resistance in Streptococcus bovis II/1.
Linear diffusion of the restriction endonuclease EcoRV on DNA is essential for the in vivo function of the enzyme.
Locations of bacteriophage T4 origins of replication.
Low tumorigenicity of canine cells transformed by the human cytomegalovirus.
Mapping bovine herpesvirus type 1 latency-related RNA in trigeminal ganglia of latently infected rabbits.
Mapping of adenovirus type 5 temperature-sensitive mutations by marker rescue in enhanced double DNA infections.
Membrane morphogenesis from cloned fragments of bacteriophage PM2 DNA that contain the sp6.6 gene.
Methylation of milk-borne and genetically transmitted mouse mammary tumor virus proviral DNA.
Model of Epstein-Barr virus infection of human thymocytes: expression of viral genome and impact on cellular receptor expression in the T-lymphoblastic cell line, HPB-ALL.
Molecular biology in viral diagnosis: restriction enzyme analysis of viruses from recurrent genital herpes infections.
Molecular Characterization of a Prevalent Ribocluster of Methicillin-Sensitive Staphylococcus aureus from Orthopedic Implant Infections. Correspondence with MLST CC30.
Molecular characterization of canine parvovirus-2 variants circulating in Tunisia.
Molecular cloning and physical characterization of a chromosomal hemolysin from Escherichia coli.
Molecular determination of infection source of a sporadic Legionella pneumonia case associated with a hot spring bath.
Molecular differentiation of bovine sarcocysts.
Molecular diversity of turncurtoviruses in Iran.
Molecular epidemiologic study of an outbreak of Salmonella typhimurium infection at a newborn nursery.
Molecular epidemiology of adenovirus acute lower respiratory infections of children in the south cone of South America (1991-1994).
Molecular epidemiology of cytomegalovirus infections in premature twin infants and their mother.
Molecular epidemiology of cytomegalovirus: a study of factors affecting transmission among children at three day-care centers.
Molecular epidemiology of Legionella species by restriction endonuclease and alloenzyme analysis.
Molecular epidemiology of live, attenuated varicella virus vaccine in children with leukemia and in normal adults.
Molecular epidemiology of Proteus mirabilis infections of the catheterized urinary tract.
Molecular epizootiologic studies of equine herpesvirus-1 infections by restriction endonuclease fingerprinting of viral DNA.
Molecular evidence for single Wolbachia infections among geographic strains of the flour beetle Tribolium confusum.
Molecular genetic analysis of a vaccinia virus gene with an essential role in DNA replication.
Molecular subtyping and characterization of bovine and human Streptococcus agalactiae isolates.
Moraxella (Branhamella) catarrhalis: restriction enzyme analysis typing with HinfI, HaeIII and PstI.
Natural history of perinatal cytomegaloviral infection.
Nosocomial herpetic infections in a pediatric intensive care unit.
Nuclear processing of viral high-molecular-weight RNA in cells infected with herpes simplex virus type 1.
Overlapping sets of viral RNAs reflect the array of polypeptides in the EcoRI J and N fragments (map positions 81.2 to 85.0) of the Autographa californica nuclear polyhedrosis virus genome.
Pathology, diagnosis and epidemiology of the rodent Helicobacter infection.
Persistent Epstein-Barr virus infection in a human T-cell line: unique program of latent virus expression.
Persistent infection with herpes simplex virus type 1 in an Ia antigen-positive murine macrophage cell line.
Physical map of the origin of defective DNA in herpes simplex virus type 1 DNA.
Polyoma virus has three late mRNA's: one for each virion protein.
Prevalence of Trichomonas spp. in domestic pigeons in Shandong Province, China, and genotyping by restriction fragment length polymorphism.
Psoralen-cross-linking study of the organization of intracellular adenovirus nucleoprotein complexes.
Purification of the gene 0.3 protein of bacteriophage T7, an inhibitor of the DNA restriction system of Escherichia coli.
Rapid chromatin remodeling of Toll-like receptor 2 promoter during infection of macrophages with Mycobacterium avium.
Rapid identification of herpesvirus simiae (B virus) DNA from clinical isolates in nonhuman primate colonies.
Regulator-dependent temporal dynamics of a restriction-modification system's gene expression upon entering new host cells: single-cell and population studies.
Restriction endonuclease activity induced by NC-1A virus infection of a Chlorella-like green alga.
Restriction endonuclease analysis of plasmid DNA of Yersinia pseudotuberculosis infections in Shimane Prefecture, Japan.
Restriction endonuclease analysis of the genome of two Italian caprine herpesvirus 1 strains.
Restriction endonuclease analysis of the pseudorabies (Aujeszky's disease) virus before and after serial passage in vivo and in vitro.
Restriction endonuclease analysis of virulence plasmids for molecular epidemiology of Yersinia pseudotuberculosis infections.
Restriction endonuclease digestion analysis of DNA from viruses isolated from different sites of two fatal cases of herpes simplex virus type-1 infection.
Restriction endonuclease mapping of adenovirus 35, a type isolated from immunocompromised hosts.
Restriction endonuclease mapping of unintegrated proviral DNA of Kirsten murine sarcoma virus.
Restriction endonuclease patterns of herpes simplex virus DNA: subtyping of HSV-1 and HSV-2 strains from genital and nongenital lesions.
Restriction enzyme accessibility and RNA polymerase localization on transcriptionally active SV40 minichromosomes isolated late in infection.
Restriction enzyme analysis (REA) of group A streptococcal (GAS) M-serotypes 1, 3, and 28. A comparison of isolates from severe systemic infections (SSI) and from uncomplicated pharyngitis (UP): epidemiologic and pathogenetic implications.
Restriction enzyme analysis and herpes simplex infections.
Restriction enzyme analysis of cytomegalovirus DNA to study transmission of infection.
Restriction fragment length polymorphisms of 16S rDNA and of whole rRNA genes (ribotyping) of Streptococcus iniae strains from the United States and Israel.
Roles of RuvC and RecG in phage lambda red-mediated recombination.
S-gene sequences and genotype-related restriction sites in hepatitis B virus carriers in Turkey.
Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes.
Selective lack of antibody to a component of EB nuclear antigen in patients with chronic active Epstein-Barr virus infection.
Sensitive detection of canine parvovirus DNA by the nested polymerase chain reaction.
Septicaemic pasteurellosis in free-range pigs associated with an unusual biovar 13 of Pasteurella multocida.
Sequence analysis of the gene encoding the Chlamydia pneumoniae DnaK protein homolog.
Sequence and characterization of the major early phosphoprotein p32 of African swine fever virus.
SP1 and AP-1 elements direct chromatin remodeling in SV40 chromosomes during the first 6 hours of infection.
Streptococcus suis infection in northern Thailand.
Structure and expression of the vaccinia virus gene which prevents virus-induced breakdown of RNA.
Temporal regulation of murine cytomegalovirus transcription and mapping of viral RNA synthesized at immediate early times after infection.
Terminal Repeat Analysis of EBV Genomes.
The bacteriophage T4 dexA gene: sequence and analysis of a gene conditionally required for DNA replication.
The detection of Alcelaphine herpesvirus-1 DNA by in situ hybridization of tissues from rabbits affected with malignant catarrhal fever.
The Epstein-Barr virus (EBV) nuclear antigen 1 BamHI F promoter is activated on entry of EBV-transformed B cells into the lytic cycle.
The Escherichia coli prr region encodes a functional type IC DNA restriction system closely integrated with an anticodon nuclease gene.
The impact of environmental Pseudomonas aeruginosa genotypes on skin infections in occupational saturation diving systems.
The interaction of Escherichia coli core RNA polymerase with specificity-determining subunits derived from unmodified and SP82-modified Bacillus subtilis RNA polymerase.
The role of a rapid diagnostic test (adenovirus immune dot-blot) in the control of an outbreak of adenovirus type 8 keratoconjunctivitis.
The three major immediate-early transcripts of bovine herpesvirus 1 arise from two divergent and spliced transcription units.
The use of plasmid profiles and nucleic acid probes in epidemiologic investigations of foodborne, diarrheal diseases.
The use of polymerase chain reaction for the detection and speciation of bacterial bone and joint infection in children.
Therapeutic management of Mycobacterium avium subspecies paratuberculosis infection with complete resolution of symptoms and disease in a patient with advanced inflammatory bowel syndrome.
Transcription from the BamHI J fragment of herpes simplex virus type 1 (KOS).
Transcription of adenoviral genetic information in isolated nuclei. Characterization of viral RNA sequences synthesized in vitro.
Transcription of overlapping sets of RNAs from the genome of Autographa californica nuclear polyhedrosis virus: a novel method for mapping RNAs.
Transcriptome analyses of cells carrying the Type II Csp231I restriction-modification system reveal cross-talk between two unrelated transcription factors: C protein and the Rac prophage repressor.
Transcripts from the Epstein-Barr virus BamHI A fragment are detectable in all three forms of virus latency.
Transfer of recombinant plasmids containing the gene for DpnII DNA methylase into strains of Streptococcus pneumoniae that produce DpnI or DpnII restriction endonucleases.
Transmission of fluconazole-resistant Candida albicans between patients with AIDS and oropharyngeal candidiasis documented by pulsed-field gel electrophoresis.
Transplacental toxoplasmosis in a wild southern sea otter (Enhydra lutris nereis).
Tumor necrosis factor genetic polymorphisms correlate with infections after liver transplantation. NEMC TNF Study Group. New England Medical Center Tumor Necrosis Factor.
Two "early" mRNA species in adenovirus type 2-transformed rat cells.
Typing of Pseudomonas aeruginosa from hospitalized patients: a comparison of susceptibility and biochemical profiles with genotype.
Use of molecular tools to distinguish Entamoeba histolytica and Entamoeba dispar infection among the aborigines in Cameron Highlands.
Use of PCR-restriction fragment length polymorphism for the identification of zoonotic mycobacteriosis in zebrafish caused by Mycobacterium abscessus and Mycobacterium chelonae.
Use of restriction endonuclease analysis of plasmids and pulsed-field gel electrophoresis to investigate outbreaks of methicillin-resistant Staphylococcus aureus infection.
Use of the P167 recombinant antigen for serodiagnosis of Helicobacter bilis.
Using transposon Tn5 insertions to sequence bacteriophage T4 gene 11.
Vaccinia virus gene D12L encodes the small subunit of the viral mRNA capping enzyme.
Vaccinia virus gene D8 encodes a virion transmembrane protein.
[25S intron analysis followed by restriction enzyme digestion performed for genotyping Candida albicans isolates].
[A molecular epidemiological study on the relationship between the polymorphism of GSTP1 and susceptibility to gastric cancer in northern Chinese]
[Analysis of genome types of adenovirus type 7 isolated in Fukuoka Prefecture in 1996]
[Cloning of hsa-miR-148a and construction of its retroviral expression vector]
[Expression of recombinated canine factor VIII in vitro mediated by lentiviral vector]
[Gene technology in medical microbiology--epidemiology and diagnosis]
[MRSA infection]
[Multi-drug resistance of serovar E strains in clinically isolated Pseudomonas aeruginosa and analysis of genome pattern]
[PFGE analysis of Mycobacterium kansasii isolates in Okayama Prefecture]
[Polymerase chain reaction (PCR) for detection of BLV provirus-- a practical complement for BLV diagnosis?]
Infectious Bovine Rhinotracheitis
Bovine herpesvirus 1: differentiation of IBR- and IPV-viruses and identification and functional role of their major immunogenic components.
Changes in the restriction endonuclease patterns of four modified-live infectious bovine rhinotracheitis virus (IBRV) vaccines after one passage in host animal.
Characterization of bovine herpesviruses isolated from six sheep and four goats by restriction endonuclease analysis and radioimmunoprecipitation.
Comparative studies of strains of infectious bovine rhinotracheitis virus isolated from latently infected calves.
Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustular vulvovaginitis virus strains by restriction endonuclease analysis.
Genomic heterogeneities in bovine herpesvirus type 1 viral isolates: a major variant selected from a field isolate.
Investigation of possible vaccine-induced epizootics of infectious bovine rhinotracheitis, using restriction endonuclease analysis of viral DNA.
Molecular cloning of DNA from a bovine herpesvirus 1 strain isolated in Hungary.
Restriction endonuclease analysis of herpesviruses isolated from two peninsular bighorn sheep (Ovis canadensis cremnobates).
Restriction endonuclease patterns of bovine herpesvirus type 1 isolated from bovine mammary glands.
[Infectious bovine rhinotracheitis virus (bovine herpesvirus l): biochemical aspects]
Infectious Mononucleosis
Marmoset lymphoblastoid cells transformed by NPC-KT-derived Epstein-Barr virus which possesses transforming and superinfecting characteristics.
Infertility
CORRELATIONS BETWEEN POLYMORPHISMS OF ESTROGEN 1, VITAMIN D RECEPTORS AND HORMONAL PROFILE IN INFERTILE MEN.
Evaluation of in vitro fertilization parameters and estrogen receptor alpha gene polymorphisms for women with unexplained infertility.
Male-sterile chicory cybrids obtained by intergeneric protoplast fusion.
Polymorphism analysis in estrogen receptors alpha and beta genes and their association with infertile population in Pakistan.
The CC-allele of the PvuII polymorphic variant in intron 1 of the ?-estrogen receptor gene is significantly more prevalent among infertile women at risk of premature ovarian aging.
Infertility, Male
Association of polymorphisms in the estrogen receptors alpha, and beta (ESR1, ESR2) with the occurrence of male infertility and semen parameters.
Engineered selective plant male sterility through pollen-specific expression of the EcoRI restriction endonuclease.
Influence of the XbaI polymorphism in the estrogen receptor-? gene on human spermatogenic defects.
Influenza in Birds
Rapid pathotyping of recent H5N1 highly pathogenic avian influenza viruses and of H5 viruses with low pathogenicity by RT-PCR and restriction enzyme cleavage pattern (RECP).
Influenza, Human
A double-stranded RNA-inducible fish gene homologous to the murine influenza virus resistance gene Mx.
A ligation and restriction enzyme independent cloning technique: an alternative to conventional methods for cloning hard-to-clone gene segments in the influenza reverse genetics system.
An efficient and rapid influenza gene cloning strategy for reverse genetics system.
Analysis of influenza A H3N2 strains isolated in England during 1995-1996 using polymerase chain reaction restriction.
Cloning DNA sequences from influenza viral RNA segments.
Expression of the influenza virus haemagglutinin in insect cells by a baculovirus vector.
Gene analysis of reassortant influenza virus by RT-PCR followed by restriction enzyme digestion.
New procedure for the production of influenza virus-specific double-stranded DNA's.
Simplified recombinational approach for influenza A virus reverse genetics.
The influenza virus haemagglutinin gene: cloning and characterisation of a double-stranded DNA copy.
[Efficient soluble expression and purification of influenza A nucleoprotein in Escherichia coli].
[Preparation of armored RNA containing M gene of influenza H3N2]
Insulin Resistance
Altered expression and function of the insulin receptor in a family with lipoatrophic diabetes.
Association of Estrogen Receptor ? Gene Polymorphism and its Expression with Gestational Diabetes Mellitus.
Association of lipoprotein lipase gene variation with the physiological components of the insulin-resistance syndrome in the population of the San Luis Valley, Colorado.
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
The apoB-100 gene EcoRI polymorphism influences the relationship between features of the insulin resistance syndrome and the hyper-apoB and dense LDL phenotype in men.
[Correlation of FABP2-A54T polymorphism and the metabolic syndrome in Maros County of Romania]
Insulinoma
Nucleotide sequence and analysis of the mouse SPC3 promoter region.
Intellectual Disability
Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy.
Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.
Rare variants in the promoter of the fragile X syndrome gene (FMR1).
Intracranial Hemorrhage, Hypertensive
HindIII Polymorphism in the Lipoprotein Lipase Gene and Hypertensive Intracerebral Hemorrhage in the Chinese Han Population.
Iritis
Polymorphism in an HLA linked proteasome gene influences phenotypic expression of disease in HLA-B27 positive individuals.
Iron Deficiencies
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis.
Iron Overload
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient.
Ischemic Stroke
A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease.
Association between Lipoprotein Lipase Polymorphism and the Risk of Stroke: A Meta-analysis.
Association of BglII Polymorphism in ITGA2 and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients ?2 Gene Polymorphism in ?2?1 Integrin and eNOS Gene Variants and Stroke.
Association of estrogen receptor-alpha gene polymorphisms with stroke risk in patients with metabolic syndrome.
Association of LPL gene variant and LDL, HDL, VLDL cholesterol and triglyceride levels with ischemic stroke and its subtypes.
Estrogen receptor alpha (ESR1) PvuII and XbaI gene polymorphisms in ischemic stroke in a Hungarian population.
Gene polymorphism of platelet glycoprotein I balpha in Chinese patients with large- and small-artery subtypes of ischemic stroke.
Genetic variation in the promoter region of the beta-fibrinogen gene is associated with ischemic stroke in a Japanese population.
Prevalence of the prothrombin G20210A mutation among ischemic stroke patients.
The HindIII and PvuII polymorphisms of lipoprotein lipase (LPL) gene reduce the risk of ischemic stroke (IS): A meta-analysis.
Joint Diseases
Contamination of Marek's disease vaccine suspensions with Enterococcus faecalis and its possible role in amyloid arthropathy.
Keratitis
An outbreak of keratitis caused by Mycobacterium immunogenum.
Differentiation of Acanthamoeba strains from infected corneas and the environment by using restriction endonuclease digestion of whole-cell DNA.
Keratitis, Herpetic
Analysis of HSV isolated from patients with unilateral and bilateral herpetic keratitis.
Transmission of herpes simplex virus infection via lacrimal canaliculi.
Keratoconjunctivitis
Genetic characterisation of adenovirus type 8 isolated in Hiroshima city over a 15 year period.
Genome typing of adenovirus strains isolated from conjunctivitis in Japan, Australia, and the Philippines.
New genome type of adenovirus serotype 19 causing nosocomial infections of epidemic keratoconjunctivitis in Japan.
Restriction endonuclease cleavage analysis of adenovirus type 8: two new subtypes from patients with epidemic keratoconjunctivitis in Sapporo, Japan.
The changing etiology of epidemic keratoconjunctivitis: antigenic and restriction enzyme analyses of adenovirus types 19 and 37 isolated over a 10-year period.
Keratosis, Seborrheic
Clonal nature of seborrheic keratosis demonstrated by using the polymorphism of the human androgen receptor locus as a marker.
Kidney Failure, Chronic
Aldosterone Synthase Gene (CYP11B2) Polymorphism in Korean End-Stage Renal Disease Patients on Hemodialysis.
Association between oestrogen receptor alpha gene polymorphism and mortality in female end-stage renal disease patients.
Interleukin-1 receptor antagonist gene polymorphism affects the progression of chronic renal failure.
Latent Infection
5' Coding and regulatory region sequence divergence with conserved function of the Epstein-Barr virus LMP2A homolog in herpesvirus papio.
Characterization of Epstein-Barr virus recombinants with deletions of the BamHI C promoter.
Does restriction enzyme analysis reveal changes in herpes simplex virus DNA after latency in mouse ganglia?
Early stage of Epstein-Barr virus lytic infection leading to the "starry sky" pattern formation in endemic Burkitt lymphoma.
Expression of herpes simplex virus type 2 latency-associated transcript in neurons and nonneurons.
IRF-7, a new interferon regulatory factor associated with Epstein-Barr virus latency.
Isolation and characterization of HSV-1 DNA from trigeminal ganglion neurons during suppressed infection in vitro.
Restriction endonuclease analysis of herpes simplex virus from recrudescent lesions, from latent infection and during passage in the skin and nervous system of mice.
Transcriptional expression of RPMS1 in nasopharyngeal carcinoma and its oncogenic potential.
Virus reactivation in pigs latently infected with a thymidine kinase negative vaccine strain of pseudorabies virus.
Lecithin Cholesterol Acyltransferase Deficiency
Restriction enzyme analysis of the apolipoprotein A-I gene in fish eye disease and Tangier disease.
Leg Ulcer
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.
Legionnaires' Disease
Molecular epidemiology of Legionella pneumophila serogroup 1.
Phenotypic variation amongst genotypically homogeneous Legionella pneumophila serogroup 1 isolates: implications for the investigation of outbreaks of Legionnaires' disease.
Leigh Disease
Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency.
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Leiomyoma
Analysis of estrogen and progesterone receptor gene polymorphisms in leiomyoma.
Assessment of hypermethylated DNA in two promoter regions of the estrogen receptor alpha gene in human endometrial diseases.
Association study between catechol-O-methyltransferase polymorphisms and uterine leiomyomas in a Japanese population.
Clonal determination of uterine leiomyomas by analyzing differential inactivation of the X-chromosome-linked phosphoglycerokinase gene.
Estrogen receptor-alpha gene (T/C) Pvu II polymorphism in endometriosis and uterine fibroids.
Oestrogen receptor alpha PvuII polymorphism and uterine fibroid incidence in Caucasian women.
Leiomyomatosis
Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosis.
Leishmaniasis
Investigation of natural infection of Phlebotomine (Diptera: Psychodidae) by Leishmania in Tunisian endemic regions.
Schizodeme and zymodeme characterization of Leishmania in the investigation of foci of visceral and cutaneous leishmaniasis.
Leishmaniasis, Cutaneous
Diagnosis of cutaneous leishmaniasis and species discrimination of parasites by PCR and hybridization.
Evaluation of PCR-RFLP (based on ITS-1 and HaeIII) for the detection of Leishmania species, using Greek canine isolates and Jordanian clinical material.
Schizodeme and zymodeme characterization of Leishmania in the investigation of foci of visceral and cutaneous leishmaniasis.
Leishmaniasis, Visceral
Genetic heterogeneity among visceral and post-Kala-Azar dermal leishmaniasis strains from eastern India.
Leprosy
A species-specific repetitive sequence in Mycobacterium leprae DNA.
Genetic variations at the T cell receptor gamma locus in circulating peripheral blood mononuclear cells of clinically categorised leprosy patients.
Leprosy, Multibacillary
Genetic variations at the T cell receptor gamma locus in circulating peripheral blood mononuclear cells of clinically categorised leprosy patients.
Leptospirosis
[A molecular epidemiological investigation on Leptospira interrogans serovar hebdomadis and australia in China]
Leukemia
A BglII RFLP demonstrated for the Il-3 gene in normal human blood cells and leukemias.
A case of acute monocytic leukemia with t(11;17) involving a rearrangement of MLL-1 and a region proximal to the RARA gene.
A deletion mutation in the 5' part of the pol gene of Moloney murine leukemia virus blocks proteolytic processing of the gag and pol polyproteins.
A restriction fragment length polymorphism for human topoisomerase II: possible relationship to drug-resistance.
A single point mutation responsible for c-mos polymorphism in cancer patients.
Abelson murine leukemia virus: molecular cloning of infectious integrated proviral DNA.
Acquisition of proviral DNA of mouse mammary tumor virus in thymic leukemia cells from GR mice.
Adaptation of a retrovirus as a eucaryotic vector transmitting the herpes simplex virus thymidine kinase gene.
Breakpoint clustering in t(4;11)(q21;q23) acute leukemia.
Characterization and partial nucleotide sequence of endogenous type C retrovirus segments in human chromosomal DNA.
Cloning and analysis of reverse transcript P160 genomes of Abelson murine leukemia virus.
Cloning and characterization of an envelope-specific probe from xenotropic murine leukemia proviral DNA.
Cloning and expression of uridine/cytidine kinase cDNA from human fibrosarcoma cells.
Cloning of the rat endogenous helper leukemia virus DNA sequence and expression of the helper activity encoded by the cloned DNA sequence in normal rat kidney cells by microinjection.
Comparative restriction endonuclease maps of proviral DNA of the primate type C simian sarcoma-associated virus and gibbon ape leukemia virus group.
Comparison of the restriction endonuclease maps of unintegrated proviral DNAs from four xenotropic murine leukemia viruses.
DNA polymorphism 5' to the JH region of the human immunoglobulin heavy chain gene and immunoglobulin gene rearrangements in leukemia.
Dual-probe electrochemical DNA biosensor based on the "Y" junction structure and restriction endonuclease assisted cyclic enzymatic amplification for detection of double-strand DNA of PML/RAR? related fusion gene.
Easy detection of all T cell receptor gamma (TCRG) gene rearrangements by Southern blot analysis: recommendations for optimal results.
Endogenous xenotropic murine leukemia virus-related sequences map to chromosomal regions encoding mouse lymphocyte antigens.
env-Related leukemogenic genes (gp55 genes) of two closely related polycythemic strains of Friend spleen focus-forming virus possess different recombination points with an endogenous mink cell focus-forming virus env gene.
Evidence for the Asiatic origin of endogenous AKR-type murine leukemia proviruses.
Genetic mapping of the amphotropic murine leukemia virus receptor on mouse chromosome 8.
Genomic hypomethylation in neoplastic cells from dogs with malignant lymphoproliferative disorders.
Heteroduplex analysis using flow cytometric microbead assays to detect deletions, insertions, and single-strand lesions.
Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia.
Identification by transfection of transforming sequences in DNA of human T-cell leukemias.
Identification of the avian myeloblastosis virus genome. I. Identification of restriction endonuclease fragments associated with acute myeloblastic leukemia.
Inactivation of p16 gene in leukemia.
Inhibition of DNA restriction enzyme digestion by anthracyclines.
Insertion of long interspersed repeated elements at the Igh (immunoglobulin heavy chain) and Mlvi-2 (Moloney leukemia virus integration 2) loci of rats.
Isolation of recombinant DNA clones carrying complete integrated proviruses of Moloney murine leukemia virus.
Karyotypic changes identified by HaeIII restriction endonuclease banding in a patient with M2 acute non-lymphoblastic leukemia.
Lack of class I H-2 antigens in cells transformed by radiation leukemia virus is associated with methylation and rearrangement of H-2 DNA.
Molecular cloning and characterization of a leukemia-inducing myeloproliferative sarcoma virus and two of its temperature-sensitive mutants.
Molecular cloning and characterization of murine leukemia virus-related DNA sequences from C3H/HeN mouse DNA.
Molecular cloning of 19p13 breakpoint region in infantile leukemia with t(11;19)(q23;p13) translocation.
Molecular cloning of Friend mink cell focus-inducing virus: identification of mink cell focus-inducing virus-like messages in normal and transformed cells.
Molecular cloning of infectious integrated murine leukemia virus DNA from infected mouse cells.
Molecular cloning of osteoma-inducing replication-competent murine leukemia viruses from the RFB osteoma virus stock.
Molecular cloning of Snyder-Theilen feline leukemia and sarcoma viruses: comparative studies of feline sarcoma virus with its natural helper virus and with Moloney murine sarcoma virus.
Multiple integration sites for Moloney murine leukemia virus in productively infected mouse fibroblasts.
Mutations in gag proteins P12 and P15 of Moloney murine leukemia virus block early stages of infection.
Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus.
RAS mutations in pediatric leukemias with MLL gene rearrangements.
Rauscher murine leukemia virus: molecular cloning of infectious integrated proviral DNA.
Restriction endonuclease cleavage of linear and closed circular murine leukemia viral DNAs: discovery of a smaller circular form.
Restriction endonuclease mapping of ecotropic murine leukemia viral DNAs: size and sequence heterogeneity of the long terminal repeat.
Restriction endonuclease mapping of unintegrated viral DNA of B- and N-tropic BALB/c murine leukemia virus.
Restriction enzyme analysis of partially transformation-defective mutants of acute leukemia virus MC29.
Reversal of Fv-1 host range by in vitro restriction endonuclease fragment exchange between molecular clones of N-tropic and B-tropic murine leukemia virus genomes.
SMX-1 virus-induced inhibition of ecotropic and recombinant proviral sequence amplification in thymuses of AKR mice.
Southern blot patterns, frequencies, and junctional diversity of T-cell receptor-delta gene rearrangements in acute lymphoblastic leukemia.
Structure of the FBJ murine osteosarcoma virus genome: molecular cloning of its associated helper virus and the cellular homolog of the v-fos gene from mouse and human cells.
The methylation status of the major breakpoint cluster region in human leukemia cells, including Philadelphia chromosome-positive cells, is linked to the lineage of hematopoietic cells.
The rapid detection of clonal T-cell proliferations in patients with lymphoid disorders.
Use of the polymerase chain reaction to detect hypermethylation in the calcitonin gene. A new, sensitive approach to monitor tumor cells in acute myelogenous leukemia.
Variation in the number of copies and in the genomic organization of ecotropic murine leukemia virus proviral sequences in sublines of AKR mice.
[Detection of hypermethylation of p15 gene in patients with acute leukemia by polymerase chain reaction]
[Detection of nucleotide sequences specific for retroviruses in Saccharomyces cells]
[Hypermethylation of the calcitonin gene as molecular genetic marker in detecting minimal residual disease of leukemia]
[Prokaryotic expression and purification of moloney murine leukemia virus reverse transcriptase and verification of the activity]
Leukemia, Erythroblastic, Acute
A structurally abnormal erythropoietin receptor gene in a human erythroleukemia cell line.
Cloning of the complete Ly-6E.1 gene and identification of DNase I hypersensitive sites corresponding to expression in hematopoietic cells.
Dimethyl sulfoxide affects the amount of extrachromosomal spleen focus-forming virus DNA in murine erythroleukemia cells.
Erythropoietin receptor mRNA expression in human endothelial cells.
Hydrodynamic studies on defined heterochromatin fragments support a 30-nm fiber having six nucleosomes per turn.
Physical properties of a genomic condensed chromatin fragment.
Rate of replication of the murine immunoglobulin heavy-chain locus: evidence that the region is part of a single replicon.
Regulatory factors specific for adult and embryonic globin genes may govern their expression in erythroleukemia cells.
Restriction endonuclease mapping of globin genomic regions of HEL (human erythroleukemia) line.
Restriction endonuclease sensitivity of DNA containing globin genes in different murine erythroleukemia cell lines.
Structural organization and DNA methylation patterning within the mouse L1 family.
The beta-major and beta-minor globin genes in murine erythroleukemia cells replicate during the same early interval of the S phase.
The temporal order of replication of murine immunoglobulin heavy chain constant region sequences corresponds to their linear order in the genome.
Leukemia, Lymphocytic, Chronic, B-Cell
Absence of Kirsten-ras oncogene activation in B-cell chronic lymphocytic leukemia.
Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia.
Leukemia, Lymphoid
Possible new genetic marker for human lymphoid leukemias as detected by ribosomal protein S14 cDNA.
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Acceleration of chronic myeloid leukemia correlates with calcitonin gene hypermethylation.
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ.
Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia.
Methylation of the major breakpoint cluster region (M-bcr) in Philadelphia-positive CML.
Multiple restriction enzyme digests are required to rule out polymorphism in the molecular diagnosis of chronic myeloid leukemia.
Novel restriction fragment length polymorphisms in the cellular oncogene SEA.
P53 tumor suppressor gene in chronic myelogenous leukemia: a sequential study.
Presence of cell lineage-specific hypomethylated sites in the major breakpoint cluster region.
[Hypermethylation of the calcitonin gene as molecular genetic marker in detecting minimal residual disease of leukemia]
Leukemia, Myeloid, Acute
A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo.
Analysis of proto-oncogenes in acute myeloid leukemia: loss of heterozygosity for the Ha-ras gene.
Bone marrow transplantation monitoring by DNA analysis.
Clonal analysis in acute myeloid leukemia by polymerase chain reaction.
Distribution of 11q23 breakpoints within the MLL breakpoint cluster region in de novo acute leukemia and in treatment-related acute myeloid leukemia: correlation with scaffold attachment regions and topoisomerase II consensus binding sites.
DNA polymorphism 5' to the JH region of the human immunoglobulin heavy chain gene and immunoglobulin gene rearrangements in leukemia.
Identification of the avian myeloblastosis virus genome. I. Identification of restriction endonuclease fragments associated with acute myeloblastic leukemia.
Mutations within the FLR exon of NF1 are rare in myelodysplastic syndromes and acute myelocytic leukemias.
The methylation status of the major breakpoint cluster region in human leukemia cells, including Philadelphia chromosome-positive cells, is linked to the lineage of hematopoietic cells.
Leukemia, Promyelocytic, Acute
Dual-probe electrochemical DNA biosensor based on the "Y" junction structure and restriction endonuclease assisted cyclic enzymatic amplification for detection of double-strand DNA of PML/RAR? related fusion gene.
Leukemia-Lymphoma, Adult T-Cell
Comparison of a human T-cell lymphotropic virus type I strain from cerebrospinal fluid of a Jamaican patient with tropical spastic paraparesis with a prototype human T-cell lymphotropic virus type I.
DNA methylation and expression of HLA-DR alpha.
Leukodystrophy, Globoid Cell
Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients.
Leukoencephalopathies
Comparison of infectious JC virus DNAs cloned from human brain.
Comparison of JC and BK human papovaviruses with simian virus 40: DNA homology studies.
Genetic characterization of JC virus Tokyo-1 strain, a variant oncogenic in rodents.
Naturally occurring and passage-induced variation in the genome of JC virus.
Leukoencephalopathy, Progressive Multifocal
Comparison of infectious JC virus DNAs cloned from human brain.
Comparison of JC and BK human papovaviruses with simian virus 40: DNA homology studies.
Genetic characterization of JC virus Tokyo-1 strain, a variant oncogenic in rodents.
Naturally occurring and passage-induced variation in the genome of JC virus.
Leukopenia
Genomic polymorphism, growth properties, and immunologic variations in human herpesvirus-6 isolates.
Leukoplakia, Hairy
Coinfection with multiple strains of the Epstein-Barr virus in human immunodeficiency virus-associated hairy leukoplakia.
Epstein-Barr virus intrastrain recombination in oral hairy leukoplakia.
Lichen Planus, Oral
Association of vdr, cyp27b1, cyp24a1 and mthfr gene polymorphisms with oral lichen planus risk.
lipoprotein lipase deficiency
Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency.
Listeriosis
Characterization by DNA restriction endonuclease analysis of Listeria monocytogenes strains related to the Swiss epidemic of listeriosis.
Comparison of methods for discrimination between strains of Listeria monocytogenes from epidemiological surveys.
Dairy farm reservoir of Listeria monocytogenes sporadic and epidemic strains.
Eye infections due to Listeria monocytogenes in three cows and one horse.
Molecular epidemiological survey of Listeria monocytogenes in seafoods and seafood-processing plants.
Molecular epidemiology and cluster analysis of human listeriosis cases in three U.S. states.
Liver Cirrhosis
Association of restriction fragment-length polymorphisms in the alcohol dehydrogenase 2 gene with alcoholic brain atrophy.
Ethanol-inducible cytochrome P4502E1: genetic polymorphism, regulation, and possible role in the etiology of alcohol-induced liver disease.
Liver Cirrhosis, Alcoholic
Association between polymorphisms of ethanol-metabolizing enzymes and susceptibility to alcoholic cirrhosis in a Korean male population.
Liver Cirrhosis, Biliary
Collagen type Ialpha1 and vitamin D receptor gene polymorphisms and bone mass in primary biliary cirrhosis.
Vitamin D receptor, oestrogen receptor-alpha gene and interleukin-1 receptor antagonist gene polymorphisms in Hungarian patients with primary biliary cirrhosis.
Liver Diseases
Association between polymorphisms of ethanol-metabolizing enzymes and susceptibility to alcoholic cirrhosis in a Korean male population.
Liver Diseases, Alcoholic
Polymorphism at the P450IIE1 locus is not associated with alcoholic liver disease in Caucasian men.
Liver Neoplasms
CYP2D6 genes and risk of liver cancer.
[Hepatitis C virus RNA in tumor tissues of Chinese liver cancer patients]
Liver Neoplasms, Experimental
Amplified DNA of the Novikoff hepatoma nucleolus is arranged in a 7.3-kilobase tandem repeat.
Cloning and characterization of a highly reiterated 5.8-kilobase pair nucleolar EcoRI DNA fragment found in Novikoff hepatoma ascites cells.
Cloning and characterization of a Novikoff hepatoma ribosomal DNA-fragment containing the initiation site of transcription.
Low Tension Glaucoma
OPTN gene: profile of patients with glaucoma from India.
Lung Diseases
Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC.
Lung Injury
Caspase inhibitor zVAD-fmk protects against acute pancreatitis-associated lung injury via inhibiting inflammation and apoptosis.
Resistin-like molecule-? causes lung injury in rats with acute pancreatitis by activating the PI-3K/Akt-NF-?B pathway and promoting inflammatory cytokine release.
Lung Neoplasms
A new polymorphism (Ser362Thr) of the L-myc gene is not associated with lung adenocarcinoma risk and prognosis.
Amplification and expression of the c-myc oncogene in human lung cancer cell lines.
Amylase mRNA transcripts in normal tissues and neoplasms: the implication of different expressions of amylase isogenes.
Association of EcoRI polymorphism of the metastasis-suppressor gene NME1 with susceptibility to and severity of non-small cell lung cancer.
Association of estrogen receptor ? gene PvuII and XbaI polymorphisms with non-small cell lung cancer.
Close correlation between restriction fragment length polymorphism of the L-MYC gene and metastasis of human lung cancer to the lymph nodes and other organs.
Determination of the allelic frequencies of an L-myc and a p53 polymorphism in human lung cancer.
Expression of MAGE gene family in lung cancers.
Human debrisoquine hydroxylase gene polymorphisms in cancer patients and controls.
Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method.
Identification of genetically high risk individuals to lung cancer by DNA polymorphisms of the cytochrome P450IA1 gene.
Inhibitory effects of syk transfection on lung cancer cell invasion.
Lung cancer, race, and a CYP1A1 genetic polymorphism.
Meta-analysis suggests association of L-myc EcoRI polymorphism with cancer prognosis.
Methylation patterns in human androgen receptor gene and clonality analysis.
Racial variation in the distribution of Ha-ras-1 alleles.
Restriction fragment length polymorphism analysis of the L-myc gene locus in a case-control study of lung cancer.
Studies of the L-myc DNA polymorphism and relation to metastasis in Norwegian lung cancer patients.
The FHIT gene 3p14.2 is abnormal in lung cancer.
[RelE toxin protein of Mycobacterium tuberculosis induces growth inhibition of lung cancer A-549 cell]
[Silencing effect study of Akt2-siRNA aimed at lung cancer cell NCI-H446.]
Lupus Erythematosus, Systemic
Association between EcoRI fragment-length polymorphism of the immunoglobulin lambda variable 8 (IGLV8) gene family with rheumatoid arthritis and systemic lupus erythematosus.
Association of HLA-DM polymorphism with the production of antiphospholipid antibodies.
Association of the oestrogen receptor alpha gene polymorphisms with disease onset in systemic lupus erythematosus.
CR1 polymorphism in hydralazine-induced systemic lupus erythematosus: DNA restriction fragment length polymorphism.
Distribution of the HindIII restriction fragment length polymorphism among patients with systemic lupus erythematosus with different concentrations of CR1.
Plasminogen activator inhibitor-1 polymorphisms (-844 G>A and HindIII C>G) in systemic lupus erythematosus: association with clinical variables.
Lyme Disease
Characterization of Borrelia burgdorferi isolates by restriction endonuclease analysis and DNA hybridization.
Comparison of Borrelia isolated from UK foci of Lyme disease.
Conservation of gene arrangement and an unusual organization of rRNA genes in the linear chromosomes of the Lyme disease spirochaetes Borrelia burgdorferi, B. garinii and B. afzelii.
Correlation of plasmids with infectivity of Borrelia burgdorferi sensu stricto type strain B31.
Molecular and immunological characterization of the p83/100 protein of various Borrelia burgdorferi sensu lato strains.
Lymphadenopathy
Clinical importance of extraordinary integration patterns of human T-cell lymphotropic virus type I proviral DNA in adult T-cell leukemia/lymphoma.
Lymphatic Metastasis
Human papillomavirus 16 exhibits a similar integration pattern in primary squamous cell carcinoma of the penis and in its metastasis.
Silencing of CD44 expression in prostate cancer by hypermethylation of the CD44 promoter region.
Lymphocytic Choriomeningitis
The development of multiple expression vectors for high level synthesis of eukaryotic proteins: expression of LCMV-N and AcNPV polyhedrin protein by a recombinant baculovirus.
Lymphogranuloma Venereum
Characterization of Chlamydia DNA by restriction endonuclease cleavage.
DNA fingerprinting of Chlamydia trachomatis by use of ribosomal RNA, oligonucleotide and randomly cloned DNA probes.
Lymphoma
A Ki-1-positive cell line expressing Epstein-Barr virus antigens, established from a child with Ki-1-positive lymphoma.
cdc25 cell cycle-activating phosphatases and c-myc expression in human non-Hodgkin's lymphomas.
Chromosomal translocation t(1;22) and sis oncogene variant with gene amplification in a case of atypical malignant lymphoma.
Clinical usefulness of serum EBV DNA levels of BamHI W and LMP1 for Nasal NK/T-cell lymphoma.
Clonal analysis of untreated non-Hodgkin's lymphoma utilizing immunoglobulin gene rearrangement and immunophenotype.
Epstein-Barr virus nuclear antigen 2 (EBNA2) gene deletion is consistently linked with EBNA3A, -3B, and -3C expression in Burkitt's lymphoma cells and with increased resistance to apoptosis.
Expression of Epstein-Barr virus in cutaneous T-cell lymphoma including mycosis fungoides.
Gene amplification in methotrexate-resistant mouse cells. IV. Different DNA sequences are amplified in different resistant lines.
Genomic hypomethylation in neoplastic cells from dogs with malignant lymphoproliferative disorders.
Human homologue of Moloney leukemia virus integration-4 locus (MLVI-4), located 20 kilobases 3' of the myc gene, is rearranged in multiple myelomas.
Human T-cell leukemia virus I provirus and antibodies in a captive gorilla with non-Hodgkin's lymphoma.
Integration and expression of MCF-13 provirus in MCF-13-induced lymphomas.
Integration patterns of HTLV-I provirus in relation to the clinical course of ATL: frequent clonal change at crisis from indolent disease.
MYC rearrangements in histologically progressed follicular lymphomas.
N-methyl-N-nitrosourea-induced T-lymphomas of AKR/J mice contain somatically acquired ecotropic-like murine leukemia proviruses.
Regulation of mouse mammary tumor virus env transcriptional activator initiated mammary tumor virus superantigen transcripts in lymphomas of SJL/J mice: role of Ikaros, demethylation, and chromatin structural change in the transcriptional activation of mammary tumor virus superantigen.
Restriction enzyme analysis of mouse cellular type C viral DNA: emergence of new viral sequences in spontaneous AKR/J lymphomas.
Small deletions occur in highly conserved regions of the LAZ3/BCL6 major translocation cluster in one case of non-Hodgkin's lymphoma without 3q27 translocation.
Structural organization and DNA methylation patterning within the mouse L1 family.
Triplication of one chromosome No. 15 with an altered c-myc containing EcoRI fragment and elimination of the normal homologue in a T-cell lymphoma line of AKR origin (TIKAUT).
[Establishment of AFP promoter operated murine IL-1beta recombinant vector and its expression in H22 cells.]
[Fibronectin gene polymorphisms and clinical manifestations of mixed cryoglobulinemic syndrome: increased risk of lymphoma associated to MspI DD and HaeIII AA genotypes]
Lymphoma, Large B-Cell, Diffuse
Cloning and characterization of cDNAs encoding the epsilon-subunit of eukaryotic initiation factor-2B from rabbit and human.
Lymphoma, Non-Hodgkin
Allelic variation of the c-raf-1 proto-oncogene in human lymphoma and leukemia.
Immunoglobulin and T-cell receptor genes in thymomas: genotypic evidence supporting the nonneoplastic nature of the lymphocytic component.
Increased frequency of the S allele of the L-myc oncogene in non-Hodgkin's lymphoma.
Polymorphism in the tumor necrosis factor-alpha promotor region and in the heat shock protein 70 genes associated with malignant tumors.
Restriction fragment length polymorphism of the L-myc oncogene in non-Hodgkin's lymphoma patients from India.
The EcoRI RFLP of c-mos in patients with non-Hodgkin's lymphoma and acute lymphoblastic leukemia, compared to geriatric and non-geriatric controls.
Lymphoma, T-Cell
Lymphomatoid papulosis: ultrastructural, immunohistochemical and gene analytical studies.
Mouse mammary tumor proviruses from a T-cell lymphoma are associated with the retroposon L1Md.
The rapid detection of clonal T-cell proliferations in patients with lymphoid disorders.
Triplication of one chromosome No. 15 with an altered c-myc containing EcoRI fragment and elimination of the normal homologue in a T-cell lymphoma line of AKR origin (TIKAUT).
Lymphoma, T-Cell, Peripheral
Epstein-Barr virus (EBV) gene expression in EBV-positive peripheral T-cell lymphomas.
Macular Degeneration
Association of CFH Y402H Polymorphism with Both Forms of Advanced Age-Related Macular Degeneration in Turkish Patients.
Idiopathic and radiation-induced ocular telangiectasia: the involvement of the ATM gene.
Malaria
A circular DNA in malaria parasites encodes an RNA polymerase like that of prokaryotes and chloroplasts.
An assay for the identification of Plasmodium simium infection for diagnosis of zoonotic malaria in the Brazilian Atlantic Forest.
Analysis of DNA from various species and strains of malaria parasites by restriction endonuclease fingerprinting.
Erythrocyte CR1 expression level does not correlate with a HindIII restriction fragment length polymorphism in Africans; implications for studies on malaria susceptibility.
Malaria: use of restriction endonuclease digestion and mutation-specific PCR for antifolate resistance isolate detection.
Population differentiation of the malaria vector Anopheles aquasalis using mitochondrial DNA.
The four ribosomal DNA units of the malaria parasite Plasmodium berghei. Identification, restriction map, and copy number analysis.
[A comparative restriction analysis of the DNA of strains of the malarial parasite sensitive and resistant to chloroquine]
Malignant Catarrh
Diagnosis of malignant catarrhal fever by polymerase chain reaction amplification of alcelaphine herpesvirus 1 sequence.
Prevalence of antibodies to alcelaphine herpesvirus-1 and nucleic acid hybridization analysis of viruses isolated from captive exotic ruminants.
Marek Disease
Cell culture amplification of a defective Marek's disease virus.
Characterization of the gene encoding herpesvirus of turkeys gp57-65: comparison to Marek's disease virus gp57-65 and herpes simplex virus glycoprotein C.
Comparative studies on Marek's disease virus and herpesvirus of turkey DNAs.
Complex assembly, crystallization and preliminary X-ray crystallographic analysis of the chicken MHC class I molecule BF2*1501.
DNA sequence and organization of genes in a 5.5 kbp EcoRI fragment mapping in the short unique segment of Marek's disease virus (strain RB1B).
Gene arrangement and RNA transcription of the BamHI fragments K and M2 within the non-oncogenic Marek's disease virus serotype 2 unique long genome region.
Genome analysis of Marek's disease virus strain CVI-988: effect of cell culture passage on the inverted repeat regions.
Genomic expansion of Marek's disease virus DNA is associated with serial in vitro passage.
Identification and characterization of a Marek's disease virus gene homologous to glycoprotein L of herpes simplex virus.
Methylation of Marek's disease virus DNA in chicken T-lymphoblastoid cell lines.
Nucleotide sequence and characterization of the Marek's disease virus homologue of glycoprotein B of herpes simplex virus.
Partial restriction map of Marek's disease virus DNA.
Restriction endonuclease analysis of Marek's disease virus DNA and homology between strains.
Restriction endonuclease analysis of Marek's disease virus DNA: differentiation of viral strains and determination of passage history.
Restriction endonuclease analysis of the genomes of virulent and avirulent Marek's disease viruses.
Restriction enzyme map of herpesvirus of turkey DNA and its collinear relationship with Marek's disease virus DNA.
Structural analysis and transcriptional mapping of the Marek's disease virus gene encoding pp38, an antigen associated with transformed cells.
Structure of Marek's disease virus DNA: detailed restriction enzyme map.
Structure of the Marek's disease virus BamHI-H gene family: genes of putative importance for tumor induction.
The restriction endonuclease map of Marek's disease virus (MDV) serotype 2 and collinear relationship among three serotypes of MDV.
Mastitis
A comparative study of Staphylococcus aureus strains isolated from bovine subclinical mastitis during 1952-1956 and 1992.
Bovine Staphylococcus aureus mastitis: strain recognition and dynamics of infection.
Genetic variations among Mycoplasma bovis strains isolated from Danish cattle.
Identification and antimicrobial resistance of Streptococcus uberis and Streptococcus parauberis isolated from bovine milk samples.
Molecular characterization and combined genotype association study of bovine cluster of differentiation 14 gene with clinical mastitis in crossbred dairy cattle.
Polymorphism of exon 2 of BoLA-DRB3 gene and its relationship with somatic cell score in Beijing Holstein cows.
Restriction endonuclease fingerprinting of genomic DNA of Staphylococcus species of bovine origin.
Subtyping of Streptococcus uberis by DNA amplification fingerprinting.
The upper respiratory tract is a natural reservoir of haemolytic Mannheimia species associated with ovine mastitis.
Mastocytosis
Demonstration that mast cells, T cells, and B cells bearing the activating kit mutation D816V occur in clusters within the marrow of patients with mastocytosis.
Mastocytosis, Systemic
Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia.
Measles
Absence of paramyxovirus RNA in cultures of pagetic bone cells and in pagetic bone.
Megalencephaly
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Melanoma
Combination Therapy of Novel Oncolytic Adenovirus with Anti-PD1 Resulted in Enhanced Anti-Cancer Effect in Syngeneic Immunocompetent Melanoma Mouse Model.
Correlation of growth capacity of cells in hard agarose with successful transfection by the activated c-Ha-ras oncogene and in vivo proliferative capacity at metastatic sites.
Detection of Aberrant TERT Promoter Methylation by Combined Bisulfite Restriction Enzyme Analysis for Cancer Diagnosis.
Differential expression of HLA class I and II antigens in primary and metastatic melanomas.
DNA damage enhances melanogenesis.
Harvey-ras oncogene restriction fragment alleles in familial melanoma kindreds.
In situ hybridization analysis of interstitial C-heterochromatin in marker chromosomes of two human melanomas.
Loss of polymorphic restriction fragments of class I and class II MHC genes in a malignant melanoma.
Metastatic potential of cloned murine melanoma cells transfected with activated c-Ha-ras.
Migration patterns in pulsed-field electrophoresis of DNA restriction fragments from log-phase mammalian cells after irradiation and incubation for repair.
Phenotypic changes and loss of melanoma-specific endogenous C-type retroviruses in BL6 melanoma cells transfected with the H-2Kb gene.
Search for genes critical for the early and/or late events in carcinogenesis: studies in Xiphophorus (Pisces, Teleostei).
Synthesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole-pyrrolo[2,1-c][1,4]benzodiazepine conjugates.
v-erbB related sequences in Xiphophorus that map to melanoma determining Mendelian loci and overexpress in a melanoma cell line.
Variants Fok1 and Bsm1 on VDR are associated with the melanoma risk: evidence from the published epidemiological studies.
Vitamin D receptor FokI, BsmI, TaqI, ApaI, and EcoRV polymorphisms and susceptibility to melanoma: a meta-analysis.
Vitamin D receptor polymorphisms and melanoma.
Vitamin D receptor polymorphisms and the risk of cutaneous melanoma: a systematic review and meta-analysis.
Melanoma, Experimental
Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1).
MELAS Syndrome
Comparison of European systemic piscine and amphibian iridoviruses with epizootic haematopoietic necrosis virus and frog virus 3.
Melioidosis
Comparison of Pseudomonas pseudomallei from humans, animals, soil and water by restriction endonuclease analysis.
Ribotyping and DNA macrorestriction analysis of isolates of Burkholderia pseudomallei from cases of melioidosis in Malaysia.
Stability of strain genotypes of Burkholderia pseudomallei from patients with single and recurrent episodes of melioidosis.
Meningioma
Analysis of cell cycle regulators: p16INK4A, pRb, and CDK4 in low- and high-grade meningiomas.
Expression of c-sis and c-fos genes in human meningiomas and neurinomas.
Meningitis
Characterization of an anonymous molecular marker strongly linked to Escherichia coli strains causing neonatal meningitis.
Characterization of epidemic and nonepidemic Neisseria meningitidis serogroup A strains from Sudan and Sweden.
Diagnosis of partially treated culture-negative bacterial meningitis using 16S rRNA universal primers and restriction endonuclease digestion.
DNA fingerprinting in the epidemiology of African serogroup A Neisseria meningitidis.
Genital recurrent infection occurring 6 months after meningitis due to the same herpes simplex virus type 2 (HSV-2) strain evidence by restriction endonuclease analysis.
Phylogenetic analysis of Escherichia coli strains causing neonatal meningitis suggests horizontal gene transfer from a predominant pool of highly virulent B2 group strains.
Virulence patterns of Escherichia coli K1 strains associated with neonatal meningitis.
Meningitis, Bacterial
Diagnosis of partially treated culture-negative bacterial meningitis using 16S rRNA universal primers and restriction endonuclease digestion.
Meningococcal Infections
Clonal distribution of invasive Neisseria meningitidis isolates from the Norwegian county of Telemark, 1987 to 1995.
Differentiation of B15 strains of Neisseria meningitidis by DNA restriction endonuclease fingerprinting.
Effect of the Factor V Leiden mutation on the severity of meningococcal disease.
Evaluation of porB PCR-amplicon restriction endonuclease analysis as a method to determine porB variable-region sequences in nonserotypeable meningococci.
PCR amplicon restriction endonuclease analysis of the chromosomal dhps gene of Neisseria meningitidis: a method for studying spread of the disease-causing strain in contacts of patients with meningococcal disease.
Strain differentiation of Neisseria meningitidis by small-fragment restriction endonuclease analysis (SF-REA).
Use of antigenic markers and genomic fingerprinting to study epidemiology of meningococcal disease.
Menkes Kinky Hair Syndrome
An EcoRV polymorphism at the ovine Menkes disease locus (ATP7A).
MERRF Syndrome
Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome.
Identification of point mutations by mispairing PCR as exemplified in MERRF disease.
Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review.
Mesothelioma
Identification of a tumor-specific methylation site in the Wilms tumor suppressor gene.
Metabolic Diseases
Advanced aging phenotype is revealed by epigenetic modifications in rat liver after in utero malnutrition.
Metabolic Syndrome
Analysis of the Association of Preeclampsia with Polymorphisms of the INS, INSR and IRS1 Genes in Mexican Women.
Association of MicroRNA-146a rs2910164 Gene Polymorphism with Metabolic Syndrome.
Associations of Estrogen Receptor Alpha Gene Polymorphisms with Type 2 Diabetes Mellitus and Metabolic Syndrome: A Systematic Review and Meta-Analysis.
Corrigendum to "Gender-related relation between metabolic syndrome and S447X and HindIII polymorphisms of lipoprotein lipase gene in northern Iran" [Gene 706 (2019) 13-18].
Effect of gene polymorphisms on lipoprotein levels in patients with dyslipidemia of metabolic syndrome.
Estrogen receptor ? is not a candidate gene for metabolic syndrome in Caucasian elderly subjects.
Gender-related relation between metabolic syndrome and S447X and HindIII polymorphisms of lipoprotein lipase gene in northern Iran.
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
The association of lipoprotein lipase PvuII polymorphism and niacin intake in the prevalence of metabolic syndrome: a KMSRI-Seoul study.
The gene-diet interaction, LPL PvuII and HindIII and carbohydrate, on the criteria of metabolic syndrome: KMSRI-Seoul Study.
Methemoglobinemia
[Arginine-glutamine replacement at residue 57 of NADH-cytochrome b5 reductase in Chinese hereditary methemoglobinemia]
Migraine Disorders
Role of the oestrogen receptor (ESR1 PvuII and ESR1 325 C-->G) and progesterone receptor (PROGINS) polymorphisms in genetic susceptibility to migraine in a North Indian population.
Mitochondrial Diseases
Accurate detection and quantitation of heteroplasmic mitochondrial point mutations by pyrosequencing.
False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites.
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Mitochondrial Encephalomyopathies
Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation.
Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation.
Mitochondrial Myopathies
Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.
Duplications of mitochondrial DNA in mitochondrial myopathy.
PCR amplification using a single cell allows the detection of the mtDNA lesion associated with Leber's hereditary optic neuropathy.
Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy.
Mitral Valve Prolapse
Lack of association between perlecan gene intron 6 BamHI polymorphism and risk of mitral valve prolapse in Taiwan Chinese.
Molluscum Contagiosum
Analysis of molluscum contagiosum virus genomes isolated in Japan.
Analysis of the genome of molluscum contagiosum virus by restriction endonuclease analysis and molecular cloning.
Characterisation by restriction mapping of three subtypes of molluscum contagiosum virus.
Characterization and physical mapping of Molluscum contagiosum virus DNA and location of a sequence capable of encoding a conserved domain of epidermal growth factor.
Determination of the position of the boundaries of the terminal repetitive sequences within the genome of molluscum contagiosum virus type 1 by DNA nucleotide sequence analysis.
Epidemiology of molluscum contagiosum using genetic analysis of the viral DNA.
Genomic characterization of Molluscum contagiosum virus type 1: identification of the repetitive DNA sequences in the viral genome.
Molecular epidemiology of Australian isolates of molluscum contagiosum.
Molluscum contagiosum: characterization of viral DNA and clinical features.
[Heterogeneity of restriction enzyme cleavage pattern of molluscum contagiosum virus DNA]
[Molecular epidemiological study of molluscum contagiosum]
Monkeypox
Comparison of white pock (h) mutants of monkeypox virus with parental monkeypox and with variola-like viruses isolated from animals.
Conservation and variation in Orthopoxvirus genome structure.
Evidence for recent genetic variation in monkeypox viruses.
Orthopoxvirus DNA: a comparison of restriction profiles and maps.
Mouth Neoplasms
Genetic Polymorphisms of ADH1C and CYP2E1 and Risk of Oral Squamous Cell Carcinoma.
Restriction fragment length polymorphisms of the human N-myc gene in normal healthy individuals and oral cancer patients in India.
Multiple Endocrine Neoplasia
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.
Multiple Endocrine Neoplasia Type 2a
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families.
Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue.
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.
Genotype-phenotype correlation of patients with multiple endocrine neoplasia type 2 in Japan.
High prevalence of the C634Y mutation in the RET proto-oncogene in MEN 2A families in Spain.
Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.
Multiple Endocrine Neoplasia Type 2b
Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue.
Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.
Presence of the 918 mutation in the RET proto-oncogene in a Mexican patient with multiple endocrine neoplasia type 2B.
Multiple Myeloma
Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia.
Multiple Sclerosis
Association between the -844 G>A, HindIII C>G, and 4G/5G PAI-1 Polymorphisms and Susceptibility to Multiple Sclerosis in Western Mexican Population.
Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis.
Estrogen receptor gene polymorphism and multiple sclerosis in Japanese patients: interaction with HLA-DRB1*1501 and disease modulation.
Mitochondrial tRNA(Gln) and tRNA(Thr) gene variants in Parkinson's disease.
Multiple sclerosis and HLA class II susceptibility and resistance genes.
The Impact of Five VDR Polymorphisms on Multiple Sclerosis Risk and Progression: a Case-Control and Genotype-Phenotype Study.
Tumor necrosis factor beta NcoI polymorphism is associated with inflammatory and metabolic markers in multiple sclerosis patients.
Mumps
Differentiation of the mumps vaccine strains from the wild viruses by the nucleotide sequences of the P gene.
Isolation and characterization of mumps virus strains in a mumps outbreak with a high incidence of aseptic meningitis.
Muscle Weakness
Facioscapulohumeral Muscular Dystrophy: A Multicenter Study on Hearing Function.
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
Muscular Diseases
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia.
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy.
Muscular Dystrophies
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.
Muscular Dystrophy, Duchenne
A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?
Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.
Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
RFLP for HindIII at the Duchenne muscular dystrophy gene.
Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy.
Muscular Dystrophy, Facioscapulohumeral
Clinical predominance of proximal upper limb weakness in CMT1A syndrome.
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis.
Facioscapulohumeral muscular dystrophy with chromosome 9p deletion.
Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.
Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.
Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.
The Clinical Features of Facioscapulohumeral Muscular Dystrophy Associated With Borderline (>/=35 kb) 4q35 EcoRI Fragments.
Muscular Dystrophy, Oculopharyngeal
Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13.
Mycosis Fungoides
HTLV-I-related retroviral markers in Hungarian patients with mycosis fungoides.
Myelodysplastic Syndromes
Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction.
Hypermethylation of the calcitonin gene in the myelodysplastic syndromes.
myeloperoxidase deficiency
Aberrant restriction endonuclease digests of DNA from subjects with hereditary myeloperoxidase deficiency.
Myeloproliferative Disorders
Detection of methylated ABL1 promoter in philadelphia-negative myeloproliferative disorders.
Myocardial Infarction
APO B gene polymorphisms and coronary artery disease: a meta-analysis.
Apolipoprotein B, apolipoprotein E, and angiotensin-converting enzyme polymorphisms in 2 Italian populations at different risk for coronary artery disease and comparison of allele frequencies among European populations.
Association between genetic variation in the Y chromosome and hypertension in myocardial infarction patients.
Association of lipase lipoprotein polymorphisms with myocardial infarction and lipid levels.
Association of lipoprotein lipase and apolipoprotein C-III genes polymorphism with acute myocardial infarction in diabetic patients.
Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden.
Fibrinogen polymorphisms are not associated with the risk of myocardial infarction.
Genetic variation at the beta-fibrinogen locus in relation to plasma fibrinogen concentrations and risk of myocardial infarction. The ECTIM Study.
Human lipoprotein lipase HindIII polymorphism in young patients with myocardial infarction.
Lipoprotein lipase gene HindIII polymorphism and risk of myocardial infarction in South Indian population.
Lipoprotein lipase gene polymorphism, cholesterol subfractions and myocardial infarction in large samples of the general population.
Lipoprotein lipase gene polymorphisms: associations with myocardial infarction and lipoprotein levels, the ECTIM study. Etude Cas Témoin sur l'Infarctus du Myocarde.
Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS).
MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus.
Plasminogen activator inhibitor-1 C/G polymorphism in relation to plasma levels in rheumatoid arthritis.
Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis.
[Connection of HindIII-polymorphism in the lipoprotein lipase gene with myocardial infarct and life span in elderly ischemic heart disease patients]
[Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers]
[HindIII polymorphism of lipoprotein lipase gene and risk of myocardial infarction]
Myocardial Ischemia
[HindIII DNA-polymorphism of lipoprotein lipase gene in elderly patients with ischemic heart disease]
Myoclonic Epilepsies, Progressive
A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3.
Myopia, Degenerative
[Studies of the association of pathological myopia in Chinese patients with HLA alleles]
Myotonic Dystrophy
Expansion of CTG repeat in myotonin protein kinase gene on Alu(ins)-HinfI-I background in a myotonic dystrophy patient from India. Mutations in brief no. 210. Online.
[Allelic polymorphism and analysis of haplotypes of the muscle protein kinase genes and haplotype analysis in residents of northwestern Russia and patients with myotonic dystrophy]
Myxoma
Characterization, molecular cloning, and physical mapping of the Shope fibroma virus genome.
Cloning and molecular characterization of the myxoma virus genome.
GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma.
Leporine acquired immune deficiency disease.
Sequence mapping of the Californian MSW strain of Myxoma virus.
Nasopharyngeal Carcinoma
An Epstein-Barr virus protein interacts with Notch.
Analysis of Epstein-Barr virus BamHI F DNA fragment in nude mouse-passaged nasopharyngeal carcinoma tissues.
Analysis of Epstein-Barr virus DNA in nude mouse-passaged nasopharyngeal carcinoma tissues.
Anticancer activity of recombinant Siva1 protein in human nasopharyngeal carcinoma cell line CNE-2.
Circulating Epstein-Barr virus microRNAs BART7-3p and BART13-3p as novel biomarkers in nasopharyngeal carcinoma.
Effects of Dicer1 targeted by EBV-miR-BART6-5p on biological properties and radiosensitivity of nasopharyngeal carcinoma.
Epstein--Barr virus gene polymorphisms in Chinese Hodgkin's disease cases and healthy donors: identification of three distinct virus variants.
Expression of the Epstein-Barr virus BamHI A fragment in nasopharyngeal carcinoma: evidence for a viral protein expressed in vivo.
Identification and mapping of Epstein-Barr virus early antigens and demonstration of a viral gene activator that functions in trans.
Identification of a novel protein encoded by the BamHI A region of the Epstein-Barr virus.
Interferon regulatory factor 2 represses the Epstein-Barr virus BamHI Q latency promoter in type III latency.
Isolation and sequencing of the Epstein-Barr virus BNLF-1 gene (LMP1) from a Chinese nasopharyngeal carcinoma.
Novel transcription from the Epstein-Barr virus terminal EcoRI fragment, DIJhet, in a nasopharyngeal carcinoma.
Sequence variation in the Epstein-Barr virus latent membrane protein 1.
Structural analyses of the Epstein-Barr virus BamHI A transcripts.
The association of genomic variation of Epstein-Barr virus BamHI F fragment with the proliferation of nasopharyngeal carcinoma.
The role of miRNAs and EBV BARTs in NPC.
Transcriptional expression of RPMS1 in nasopharyngeal carcinoma and its oncogenic potential.
Transcripts from the Epstein-Barr virus BamHI A fragment are detectable in all three forms of virus latency.
[Analysis of Epstein-Barr virus with BamHI "f" variant and XhoI-loss of LMP1 gene in nasopharyngeal carcinoma]
[Construction of eukaryotic expression vector encoding human nasopharyngeal carcinoma anti-idiotype antibody single chain fragment gene G22 and its expression.]
[Investigation of EB virus DNA BamHI W fragment, EBNA-2 types and EBNA expression in benign and malignant nasopharyngeal biopsies]
[No point mutation of the 2.8 kb EcORI fragment of the nasopharyngeal carcinoma transforming gene TX in nasopharyngeal carcinoma]
[Studies on c-myc gene expression and p16 gene inactivation in nasopharyngeal carcinoma]
Nasopharyngitis
Epstein-Barr virus DNA in nasopharyngeal biopsies.
[Investigation of EB virus DNA BamHI W fragment, EBNA-2 types and EBNA expression in benign and malignant nasopharyngeal biopsies]
Neoplasm Metastasis
Activated protooncogenes in human lung tumors from smokers.
Amplifications of both c-Ki-ras with a point mutation and c-myc in a primary pancreatic cancer and its metastatic tumors in lymph nodes.
EcoRI polymorphism of the metastasis-suppressor gene NME1 in Mexican patients with breast cancer.
Human papillomavirus 16 exhibits a similar integration pattern in primary squamous cell carcinoma of the penis and in its metastasis.
Human papillomavirus DNA in normal, metaplastic, preneoplastic and neoplastic epithelia of the cervix uteri.
Human papillomavirus type 16 in an oral squamous carcinoma and its metastasis.
Silencing of CD44 expression in prostate cancer by hypermethylation of the CD44 promoter region.
Neoplasms
A case of simultaneous multiple gastric cancers with p53 gene mutation.
A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.
A defective, rearranged Epstein-Barr virus genome in EBER-negative and EBER-positive Hodgkin's disease.
A Ki-1-positive cell line expressing Epstein-Barr virus antigens, established from a child with Ki-1-positive lymphoma.
A MboII polymorphism in exon 11 of the human MDM2 gene occuring in normal blood donors and in soft tissue sarcoma patients: an indication for an increased cancer susceptibility?
A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees.
A sensitive mutation-specific screening technique for GNAS1 mutations in cases of fibrous dysplasia: the first report of a codon 227 mutation in bone.
A simple reverse transcriptase PCR assay to distinguish EBNA1 gene transcripts associated with type I and II latency from those arising during induction of the viral lytic cycle.
A single missense mutation in codon 918 of the RET proto-oncogene in sporadic medullary thyroid carcinomas.
A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancers.
A truncated cyclin D1 gene encodes a stable mRNA in a human breast cancer cell line.
Abnormal expression of the ATM and TP53 genes in sporadic breast carcinomas.
Absence of HinfI Restriction Abnormalities in Renal Oncocytoma Mitochondrial DNA.
Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue.
Accumulation of genetic defects during astrocytoma progression.
Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma.
Activated H-ras oncogenes in human kidney tumors.
Activation of related transforming genes in mouse and human mammary carcinomas.
Allelic methylation bias of the RARB2 tumor suppressor gene promoter in cancer.
Allelic variation of the c-raf-1 proto-oncogene in human lymphoma and leukemia.
Alterations in DNA sequence and RNA transcription of the Bam HI-H fragment accompany attenuation of oncogenic Marek's disease herpesvirus.
Alterations in the structural gene and the expression of p53 in rat liver tumors induced by aflatoxin B1.
Alterations in the U3 region of the long terminal repeat of an infectious thymotropic type B retrovirus.
Alterations of acquired mouse mammary tumor virus DNA during mammary tumorigenesis in BALB/cfC3H mice.
Altered mouse mammary tumor virus transcript synthesis in T-cell lymphoma cells.
Amplification of a specific set of intracisternal A-particle genes in a mouse plasmacytoma.
Amplifications of both c-Ki-ras with a point mutation and c-myc in a primary pancreatic cancer and its metastatic tumors in lymph nodes.
Amplified DNA of the Novikoff hepatoma nucleolus is arranged in a 7.3-kilobase tandem repeat.
Amplified ribosomal RNA genes in a rat hepatoma cell line are enriched in 5-methylcytosine.
Amylase mRNA transcripts in normal tissues and neoplasms: the implication of different expressions of amylase isogenes.
An association of polymorphism of DNA repair genes XRCC1 and XRCC3 with colorectal cancer.
An avaII restriction fragment length polymorphism in the insulin-like growth factor II gene and the occurrence of smooth muscle tumors.
Analysis of clonality by amplification of short tandem repeats. Carcinomas of the female reproductive tract.
Analysis of clonality in archival tissues by polymerase chain reaction amplification of PGK-1.
Analysis of Epstein-Barr virus infection in nasopharyngeal biopsies from a group at high risk of nasopharyngeal carcinoma.
Analysis of glial fibrillary acidic protein gene methylation in human malignant gliomas.
Analysis of radon-associated squamous cell carcinomas of the lung for a p53 gene hotspot mutation.
Analysis of the ERalpha germline PvuII marker in breast cancer risk.
Analysis of the PvuII restriction fragment-length polymorphism and exon structure of the estrogen receptor gene in breast cancer and peripheral blood.
Anticancer and Cytotoxic activities of [Cu(C6H16N2O2)2][Ni(CN)4] and [Cu(C6H16N2O2)Pd(CN)4] Cyanidometallate Compounds on HT29, HeLa, C6 and Vero Cell Lines.
Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.
Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer.
Association of estrogen receptor ? PvuII and XbaI polymorphisms with prostate cancer susceptibility and risk stratification: a meta-analysis from case-control studies.
Association of FokI and PvuII polymorphisms with breast cancer staging and survival among Caucasian women: a prospective study.
Association of lipoprotein lipase gene polymorphism with risk of prostate cancer in a Japanese population.
Biological activity of polyoma viral DNA in mice and hamsters.
Bovine papillomavirus DNA in neoplastic and nonneoplastic tissues obtained from horses with and without sarcoids in the western United States.
c-Ha-ras BamHI RFLP in human urothelial tumors and point mutations in hot codons.
Can Different Thyroid Tumor Types Be Distinguished by Polymerase Chain Reaction-Based K-ras Mutation Detection?
CD4+, but not CD8+, T cells from mammary tumor-bearing mice have a down-regulated production of IFN-gamma: role of phosphatidyl serine.
Central-nervous-system lymphoma related to Epstein-Barr virus.
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region.
Characterization of AKR murine leukemia virus sequences in AKR mouse substrains and structure of integrated recombinant genomes in tumor tissues.
Characterization of BK virus variants rescued from human tumours and tumour cell lines.
Characterization of endogenous and exogenous mouse mammary tumor virus proviral DNA with site-specific molecular clones.
Characterization of integrated human papillomavirus type 11 DNA in primary and metastatic tumors from a renal transplant recipient.
Characterization of sequences related to the mouse mammary tumor virus that are specific to MCF-7 breast cancer cells.
Characterization of the DIM series of BALB/c preneoplasms for mouse mammary tumor virus-mediated oncogenesis.
Characterization of variants in the promoter of EBV gene BZLF1 in normal donors, HIV-positive patients and in AIDS-related lymphomas.
Chorionic gonadotropin synthesis by human tumor cell lines: examination of subunit accumulation, steady-state levels of mRNA, and gene structure.
Chromatin organization measured by AluI restriction enzyme changes with malignancy and is regulated by the extracellular matrix and the cytoskeleton.
Circulating Epstein-Barr virus microRNAs miR-BART7 and miR-BART13 as biomarkers for nasopharyngeal carcinoma diagnosis and treatment.
Circulating Hypermethylated RASSF1A as a Molecular Biomarker for Diagnosis of Hepatocellular Carcinoma
Clonal analysis of focal nodular hyperplasia of the liver.
Clonal analysis of human gynecologic cancers by means of the polymerase chain reaction.
Clonal origin of adenovirus type 12-induced hamster tumors: nonspecific chromosomal integration sites of viral DNA.
Cloning and characterization of a Novikoff hepatoma ribosomal DNA-fragment containing the initiation site of transcription.
Cloning and physical mapping of Yaba monkey tumor virus DNA.
Cloning of deleted sequences (CODE): A genomic subtraction method for enriching and cloning deleted sequences.
Common proviral integration region on mouse chromosome 7 in lymphomas and myelogenous leukemias induced by Friend murine leukemia virus.
Common proviral integration sites in C57BL mouse lymphomas induced by radiation leukemia virus and absence of novel virus-related sequences in radiogenic lymphoma DNA.
Comparison of endogenous murine leukemia virus proviral organization and RNA expression in 3-methylcholanthrene-induced and spontaneous thymic lymphomas in RF and AKR mice.
Comparison of Epstein-Barr viral DNAs in Burkitt lymphoma biopsy cells and in cells clonally transformed in vitro.
Comparison of the polymerase chain reaction and Southern blot analysis in detecting and typing human papilloma virus deoxyribonucleic acid in tumors of the lower female genital tract.
Concerted DNA rearrangements in Moloney murine leukemia virus-induced thymomas: a potential synergistic relationship in oncogenesis.
Correlation of DNA hypomethylation with expression of carcinoembryonic antigen in human colon carcinoma cells.
Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposis.
Cytokine polymorphic analyses indicate ethnic differences in the allelic distribution of interleukin-2 and interleukin-6.
Dehydroepiandrosterone activates mutant androgen receptors expressed in the androgen-dependent human prostate cancer xenograft CWR22 and LNCaP cells.
Demethylation of a repetitive DNA sequence in human cancers.
Detection of Aberrant TERT Promoter Methylation by Combined Bisulfite Restriction Enzyme Analysis for Cancer Diagnosis.
Detection of acquired provirus sequences in mammary tumors from low-expressor, low-risk mice.
Detection of c-Ki-ras mutations in bile samples from patients with pancreatic and biliary cancers.
Detection of Epstein-Barr virus (EBV) in hepatocellular carcinoma tissue: a novel EBV latency characterized by the absence of EBV-encoded small RNA expression.
Detection of genomic alterations in carcinogen-induced mouse liver tumors by DNA fingerprint analysis.
Detection of hepatitis B virus DNA in hepatocellular carcinoma: methylation of integrated viral DNA.
Detection of herpes simplex virus type-2 DNA restriction fragments in human cervical carcinoma tissue.
Detection of metastatic breast cancer by beta-hCG polymerase chain reaction.
Detection of retrovirus sequences in budgerigars with tumours.
Detection of somatic changes in human renal cell carcinomas with oligonucleotide probes specific for simple repeat motifs.
Detection, cloning and characterisation of papillomaviral DNA present in sarcoid tumours of Equus asinus.
Determination of the level of DNA modification with cisplatin by catalytic hydrogen evolution at mercury-based electrodes.
Different imprinting status of IGF-2 in epithelial ovarian tumors.
Differential methylation of the c-H-ras gene in normal mouse cells and during skin tumour progression.
Distinct DNA methylation profiles between adenocarcinoma and squamous cell carcinoma of human uterine cervix.
Distinct helper virus requirements for Abelson murine leukemia virus-induced pre-B- and T-cell lymphomas.
Distinctive differences in DNA double-strand break repair between normal urothelial and urothelial carcinoma cells.
DNA alterations in human oral squamous cell carcinomas detected by restriction landmark genomic scanning.
DNA fragments of altered electrophoretic mobility in leukemia samples can arise from double-strand DNA breaks at nuclease hypersensitive sites of active genes.
DNA hypermethylation at the D17S5 locus in non-small cell lung cancers: its association with smoking history.
DNA hypermethylation at the D17S5 locus is associated with gastric carcinogenesis.
DNA methylation and expression of HLA-DR alpha.
DNA methylation and hepatocarcinogenesis in rats fed a choline-devoid diet.
Do highly oncogenic group A human adenoviruses cause human cancer? Analysis of human tumors for adenovirus 12 transforming DNA sequences.
EBV miR-BART10-3p Promotes Cell Proliferation and Migration by Targeting DKK1.
EcoRI polymorphism of the L-myc gene in gastric cancer patients.
Effect of budesonide on the methylation and mRNA expression of the insulin-like growth factor 2 and c-myc genes in mouse lung tumors.
Effect of methylation on expression of microinjected genes.
Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphism.
Enhancement of anti-tumour immunity in syngeneic mice after MHC class II gene transfection.
Episomal simian virus 40 genomes in human brain tumors.
Epstein-Barr virus DNA in nasopharyngeal biopsies.
Epstein-Barr virus infected lymphoepithelial carcinomas of the salivary gland in the Russia-Asia area: a clinicopathologic study of 160 cases.
Epstein-Barr virus infections and DNA hybridization studies in posttransplantation lymphoma and lymphoproliferative lesions: the role of primary infection.
Epstein-Barr virus miR-BART20-5p regulates cell proliferation and apoptosis by targeting BAD.
Epstein-Barr virus plays no role in the tumorigenesis of small-cell carcinoma of the lung.
Epstein-Barr virus transcription in nasopharyngeal carcinoma.
Epstein-Barr virus-encoded Bcl-2 homologue functions as a survival factor in Wp-restricted Burkitt lymphoma cell line P3HR-1.
Esophageal squamous cell carcinomas arising in patients from a high-risk area of North China lack an association with Epstein-Barr virus.
ESR1 PvuII (rs2234693 T>C) polymorphism and cancer susceptibility: Evidence from 80 studies.
Establishment and characterization of an epithelioid sarcoma cell line with an autocrine response to interleukin-6.
Estrogen receptor alpha (ER-alpha) gene polymorphism in patients from the Lodz region of Poland with sporadic endometrial cancer.
Estrogen receptor expression in human breast cancer associated with an estrogen receptor gene restriction fragment length polymorphism.
Evaluation of the risk of lymphomagenesis in xenografts by the PCR-based detection of EBV BamHI W region in patient cancer specimens.
Evidence against a tumour-specific EcoRI RFLP of the c-mos locus.
Expression and amplification of the HER-2/neu (c-erbB-2) protooncogene in epithelial ovarian tumors and cell lines.
Expression and methylation of the Blym gene in human tumor cell lines.
Expression of c-sis and c-fos genes in human meningiomas and neurinomas.
Expression of early viral gene products in adenovirus type 12-infected and -transformed cells.
Expression of EBV-encoded oncogenes and EBV-like virions in multiple canine tumors.
Expression of Epstein-Barr virus (EBV) DNA and cloned DNA fragments in human lymphocytes following Sendai virus envelope-mediated gene transfer.
Expression of plant tumor-specific proteins in minicells of Escherichia coli: a fusion protein of lysopine dehydrogenase with chloramphenicol acetyltransferase.
Expression of the Epstein-Barr virus BamHI A fragment in nasopharyngeal carcinoma: evidence for a viral protein expressed in vivo.
Expression profile of microRNAs in Epstein-Barr virus-infected AGS gastric carcinoma cells.
Extensive DNA methylation spanning the Rb promoter in retinoblastoma tumors.
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.
Extent of DNA methylation in human tumor cells.
Extra DNA in the T region of crown gall Ti-plasmid pTiA66.
Extrachromosomal deer fibromavirus DNA in deer fibromas and virus-transformed mouse cells.
Fluorescent conjugated polymer-based FRET technique for detection of DNA methylation of cancer cells.
FRA7G extends over a broad region: coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites.
Free cottontail rabbit papillomavirus DNA persists in warts and carcinomas of infected rabbits and in cells in culture transformed with virus or viral DNA.
Frequency of BRAF T1796A mutation in papillary thyroid carcinoma relates to age of patient at diagnosis and not to radiation exposure.
Frequent alterations of specific reiterated DNA sequence abundances in human cancer.
Frequent c-Ha-ras gene mutations in rat mammary carcinomas induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine.
Frequent mutations of the beta-catenin gene in mouse colon tumors induced by azoxymethane.
Gene expression of tumor necrosis factor alpha and interferon gamma in the lungs of Mycoplasma pulmonis-infected mice.
Genetic alterations in thyroid carcinomas and adenomas detected by restriction landmark genomic scanning.
Genetic analysis using genomic representations.
Genetic and epigenetic alterations of steroidogenic factor?1 in ovarian tumors.
Genetic heterogeneity of prostatic carcinoma-derived cell lines as emphasized by DNA fingerprinting.
Genetic mapping of endogenous mouse mammary tumor viruses: locus characterization, segregation, and chromosomal distribution.
Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck.
Genetic predisposition to pre-B lymphomas in SL/Kh strain mice.
Genetic sequences that predispose to retinoblastoma and osteosarcoma.
Genomic DNA analysis of the estrogen receptor gene in breast cancer.
Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma.
Genotypic and phenotypic characterization of the histoblood group ABO(H) in primary bladder tumors.
Genotyping of mouse hepatitis virus strains by restriction endonuclease analysis of amplified nucleocapsid protein genes.
H-ras protooncogene mutations in human thyroid neoplasms.
H-ras-1 restriction fragment length polymorphism in normal individuals and oral cancer patients in India.
Harvey-ras oncogene restriction fragment alleles in familial melanoma kindreds.
herg1b expression as a potential specific marker in pediatric acute myeloid leukemia patients with HERG 897K/K genotype.
High frequency of mas oncogene activation detected in the NIH3T3 tumorigenicity assay.
Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development.
Host Gene Expression Is Regulated by Two Types of Noncoding RNAs Transcribed from the Epstein-Barr Virus BamHI A Rightward Transcript Region.
Human papillomavirus (HPV) in head and neck cancer. An association of HPV 16 with squamous cell carcinoma of Waldeyer's tonsillar ring.
Human papillomavirus 16 exhibits a similar integration pattern in primary squamous cell carcinoma of the penis and in its metastasis.
Human papillomavirus DNA in cutaneous primary and metastasized squamous cell carcinomas from patients with epidermodysplasia verruciformis.
Human papillomavirus DNA in normal, metaplastic, preneoplastic and neoplastic epithelia of the cervix uteri.
Human papillomavirus type 16 DNA in genital tumours: a pathological and molecular analysis.
Human papillomavirus type 16 in an oral squamous carcinoma and its metastasis.
Human papillomavirus type 6 associated Buschke-Loewenstein tumor (giant condyloma acuminatum).
Human-tumor-derived cell lines contain common and different transforming genes.
Identification of a novel protein encoded by the BamHI A region of the Epstein-Barr virus.
Identification of a rearrangement in the 5' upstream region of the poly(ADP-ribose) polymerase pseudogene on chromosome 13 in Ewing's sarcoma cells.
Identification of a unique mouse mammary tumor virus in the BALB/cNIV mouse strain.
Identification of Epstein-Barr virus RK-BARF0-interacting proteins and characterization of expression pattern.
Identification of Retinol Binding Protein 1 Promoter Hypermethylation in Isocitrate Dehydrogenase 1 and 2 Mutant Gliomas.
Identification of transcribed regions of Epstein-Barr virus DNA in Burkitt lymphoma-derived cells.
Imbalanced MHC class II molecule expression at surface of murine B cell lymphomas.
Immunohistochemical expression of p53 in breast carcinoma is associated with the intron 1 BglII polymorphism of the p53 gene.
Immunotypic and genotypic characterization of non-Hodgkin's lymphomas of the ovary.
In Silico Enhanced Restriction Enzyme Based Methylation Analysis of the Human Glioblastoma Genome Using Agilent 244K CpG Island Microarrays.
Increased bcl-2 protein levels in prostatic adenocarcinomas are not associated with rearrangements in the 2.8 kb major breakpoint region or with p53 protein accumulation.
Increased DNA methyltransferase 1 (DNMT1) protein expression correlates significantly with poorer tumor differentiation and frequent DNA hypermethylation of multiple CpG islands in gastric cancers.
Increased expression of myc-related oncogene mRNA characterizes most BALB/c plasmacytomas induced by pristane or Abelson murine leukemia virus.
Increased hTR expression during transition from adenoma to carcinoma is not associated with promoter methylation.
Induction of a latent herpes simplex virus from a rat tumour initiated by herpes simplex virus-transformed cells.
Induction of angiosarcoma by a c-erbB transducing virus.
Infrequent MDM2 gene amplification and absence of gross WAF1 gene alterations in nasopharyngeal carcinoma.
Inhibition of DNA restriction enzyme digestion by anthracyclines.
Insulin-like growth factor II in uterine smooth-muscle tumors: maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata.
Integrated human papillomavirus type 16 and loss of heterozygosity at 11q22 and 18q21 in an oral carcinoma and its derivative cell line.
Kappa immunoglobulin light chain polymorphisms and survival after allogeneic transplantation for B-cell malignancies: a potential graft-vs-leukaemia target.
L-myc proto-oncogene alleles and susceptibility to hepatocellular carcinoma.
Leukemogenesis by bovine leukemia virus: proviral DNA integration and lack of RNA expression of viral long terminal repeat and 3' proximate cellular sequences.
Linker insertion mutants of simian virus 40 large T antigen that show trans-dominant interference with wild-type large T antigen map to multiple sites within the T-antigen gene.
Loss of a c-H-ras-1 allele and aggressive human primary breast carcinomas.
Loss of allelic heterozygosity at the harvey ras locus in human oral carcinomas.
Loss of E-cadherin expression resulting from promoter hypermethylation in oral tongue carcinoma and its prognostic significance.
Loss of heterozygosity in non-tumoral tissue in two children with Beckwith-Wiedemann syndrome.
Loss of heterozygosity of p53 gene and p53 protein expression in human colorectal carcinomas.
Loss of imprinting of insulin-like growth factor 2 is associated with increased risk of lymph node metastasis and gastric corpus cancer.
Low frequency of p53 gene mutation in tumors induced by aflatoxin B1 in nonhuman primates.
Lymphoma-type adult T-cell leukaemia-lymphoma with a bulky cutaneous tumour showing multiple human T-lymphotropic virus-1 DNA integration.
Measurement of O6-alkylguanine-DNA alkyltransferase activity in human cells and tumor tissues by restriction endonuclease inhibition.
Mechanism of activation of human ras genes cloned from a gastric adenocarcinoma and a pancreatic carcinoma cell line.
Mechanism of H-ras oncogene activation in mouse squamous carcinoma induced by an alkylating agent.
Meta-analysis suggests association of L-myc EcoRI polymorphism with cancer prognosis.
Methylation and amplification of mouse mammary tumor virus DNA in normal, premalignant, and malignant cells of GR/A mice.
Methylation and expression of rat kappa-casein gene in normal and neoplastic rat mammary gland.
Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms' tumours.
Methylation of cottontail rabbit papillomavirus DNA and tissue-specific expression in transgenic rabbits.
Methylation of CpG sites in exon 2 of the bcl-2 gene occurs in colorectal carcinoma.
Mitochondrial DNA copy number changes in human gliomas.
Mitotic abnormalities leading to cancer predisposition and progression.
Molecular analysis of breaks in BCL-1 proto-oncogene in B-cell lymphomas with abnormalities of 11q13.
Molecular characterization of size and copy number of the human insulin gene in transfected rat islet tumor cell clones.
Molecular cloning of equine herpesvirus type 1 DNA: analysis of standard and defective viral genomes and viral sequences in oncogenically transformed cells.
Molecular cloning of feline leukemia provirus genomes integrated in the feline large granular lymphoma cells.
Molecular cloning, characterization, and genetic mapping of an endogenous murine mammary tumor virus proviral unit I of C3H/He mice.
Molecular genetics of human cancer predisposition and progression.
Mouse and human ornithine decarboxylase genes. Methylation polymorphism and amplification.
Mouse mammary tumor proviruses from a T-cell lymphoma are associated with the retroposon L1Md.
Multiple chromosomal rearrangements in a spontaneously arising t(6;7) rat immunocytoma juxtapose c-myc and immunoglobulin heavy chain sequences.
Mutation affecting the 12th amino acid of the c-Ha-ras oncogene product occurs infrequently in human cancer.
Mutation of the p53 gene precedes aneuploid clonal divergence in colorectal carcinoma.
MYCL genotypes and loss of heterozygosity in non-small-cell lung cancer.
N-myc gene amplification and other prognosis-associated factors in neuroblastoma.
Next-generation sequencing is highly sensitive for the detection of beta-catenin mutations in desmoid-type fibromatoses.
nm23-H1 expression and disease recurrence after surgical resection of small hepatocellular carcinoma.
Non-covalent conjugates between cationic polyamino acids and GdIII chelates: a route for seeking accumulation of MRI-contrast agents at tumor targeting sites.
Novel point mutations and allele loss at the RET locus in sporadic medullary thyroid carcinomas.
Number and location of mouse mammary tumor virus proviral DNA in mouse DNA of normal tissue and of mammary tumors.
Oestrogen receptor (ESR) polymorphisms and breast cancer susceptibility.
Oestrogen receptor gene structure and function in breast cancer.
On the mechanism of retrovirus-induced avian lymphoid leukosis: deletion and integration of the proviruses.
Oncogenicity of simian virus 40 deletion mutants that induce altered 17-kilodalton t-proteins.
Organization and expression of mouse mammary tumor virus sequences in normal and neoplastic C3Hf/HeSed mouse tissues.
Organomegaly and tumors in transgenic mice with targeted expression of HpaII methyltransferase in smooth muscle cells.
Patterns of chromosomal breakpoint locations in Burkitt's lymphoma: relevance to geography and Epstein-Barr virus association.
Patterns of DNA methylation and gene expression in human tumor cell lines.
Persistence and expression of Marek's disease virus DNA in tumour cells and peripheral nerves studied by in situ hybridization.
Persistent Epstein-Barr virus infection in a human T-cell line: unique program of latent virus expression.
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas.
Point mutation, allelic loss and increased methylation of c-Ha-ras gene in human hepatocellular carcinoma.
Polyclonal anti-colorectal cancer Fab phage display library selected in one round using density gradient centrifugation to separate antigen-bound and free phage.
Polymerase chain reaction amplification and in situ hybridization for the detection of human B-lymphotropic virus.
Polymorphism in the P2X7 receptor gene and survival in chronic lymphocytic leukaemia.
Polymorphism of the stress protein HSP70-2 gene is associated with the susceptibility to the nasopharyngeal carcinoma.
Polymorphisms of Epstein-Barr virus BHRF1 gene, a homologue of bcl-2.
Polymorphisms of mitochondrial DNAs in Norway rats (Rattus norvegicus): cleavage site variations and length polymorphism of restriction fragments.
Polymorphisms of xenobiotic metabolizing genes in oropharyngeal carcinoma.
Polyoma large tumor antigen is not required for tumorigenesis mediated by viral DNA.
Potentiation of cisplatin-induced antiproliferative and apoptotic activities by the antiarrhythmic drug procainamide hydrochloride.
Presence of an allelic EcoRI restriction fragment of the c-mos locus in leukocyte and tumor cell DNAs of breast cancer patients.
Presence of an EcoRI RFLP of the c-mos locus in normal and tumor tissue of esophageal cancer patients.
Primary mesenteric tumor of adult T-cell leukemia/lymphoma: report of a case.
Problem-solving test: analysis of DNA damage recognizing proteins in yeast and human cells.
Promoter methylation of cancer-related genes in gastric carcinoma.
Promoter Methylation Status of Breast Cancer Susceptibility Gene 1 and 17 Beta Hydroxysteroid Dehydrogenase Type 1 Gene in Sporadic Breast Cancer Patients.
Proteins encoded by Agrobacterium tumefaciens Ti plasmid DNA (T-DNA) in crown gall tumors.
Proviral unit II of endogenous mouse mammary tumour virus is selectively amplified and expressed in C57B1/10 mammary tumours induced by non-viral carcinogens.
Pulsed field gel electrophoresis on frozen tumour tissue sections.
Rapid acquisition of entire DNA polymerase gene of a novel herpesvirus from green turtle fibropapilloma by a genomic walking technique.
Rearrangement of c-myc gene in rapidly induced avian lymphoid leukosis tumors.
Rearrangements of c-myc and c-abl genes in tumour cells in Burkitt's lymphoma.
Rearrangements of the upstream regulatory region of human papillomavirus type 6 can be found in both Buschke-Löwenstein tumours and in condylomata acuminata.
Recurrent germline mutations in BRCA1 and BRCA2 genes in high risk families in Israel.
Relationship of oestrogen receptor alpha gene polymorphisms with risk for benign prostatic hyperplasia and prostate cancer in Chinese men.
Relevance of environmental alkylating agents to repair protein O6-alkylguanine-DNA alkyltransferase: determination of individual and collective repair capacities of O6-methylguanine.
Repression of MLH1 and MGMT genes in colon mucosa adjacent to implanted cancer in athymic mouse.
Resistance of tumor-derived DNA to restriction enzyme digestion.
Restriction endonuclease analysis of mitochondrial DNA from virus-transformed, tumor and control cells of human, hamster and avian origin. Sequence conservation and intraspecific variation.
Restriction endonuclease and nucleotide sequence analyses of molecularly cloned unintegrated avian tumor virus DNA: structure of large terminal repeats in circle junctions.
Restriction endonuclease map of endogenous mouse mammary tumor virus loci in GR, DBA, and NFS mice.
Restriction endonuclease mapping of the proviral DNA of the exogenous RIII murine mammary tumor virus.
Restriction endonuclease studies of hyperplastic outgrowth lines from BALB/cfC3H mouse hyperplastic mammary nodules.
Restriction enzyme sites on the avian RNA tumor virus genome.
Restriction enzymes in the analysis of genetic alterations responsible for cancer progression.
Restriction fragment length polymorphism (RFLP) analysis in the TNF genes of patients with systemic lupus erythematosus (SLE).
Restriction fragment length polymorphisms of the human N-myc gene in normal healthy individuals and oral cancer patients in India.
RFLP analysis in the TNF-beta gene and the susceptibility to alloreactive NK cells in Behçet's disease.
Role of BRCA1, HSD17B1 and HSD17B2 methylation in breast cancer tissue.
Search for HSV DNA in genital, cerebral and labial tumors.
Search for human papillomavirus, herpes simplex virus and c-myc oncogene in human genital tumors.
Selected nuclear LINE elements with mitochondrial-DNA-like inserts are more plentiful and mobile in tumor than in normal tissue of mouse and rat.
Sequence variations of Epstein-Barr virus-encoded BARF1 gene in nasopharyngeal carcinomas and healthy donors from southern and northern China.
Sequences homologous to two separate transforming regions of herpes simplex virus DNA are linked in two human genital tumors.
Severity of respiratory syncytial virus disease related to type and genotype of virus and to cytokine values in nasopharyngeal secretions.
Shope papilloma virus DNA is extensively methylated in non-virus-producing neoplasms.
Simple repeat sequence in Epstein-Barr virus DNA is transcribed in latent and productive infections.
Simultaneously arising Ly-1(CD5) B cell lymphomas have identical expressed IgH and kappa-genes but different nonproductive heavy chain rearrangements.
Somatic DNA alterations in breast carcinomas of different lymph-node status by DNA fingerprint analyses.
Some tumors of the bladder are polyclonal in origin.
Specifically unmethylated cytidylic-guanylate sites in Herpesvirus saimiri DNA in tumor cells.
Structural alterations in the 5' region of the BCL2 gene in follicular lymphomas with BCL2-MBR or BCL2-MCR rearrangements.
Structural analysis and transcriptional mapping of the Marek's disease virus gene encoding pp38, an antigen associated with transformed cells.
Structure of the activated c-raf-1 gene from human stomach cancer.
T-DNA and opine synthetic loci in tumors incited by Agrobacterium tumefaciens A281 on soybean and alfalfa plants.
T-DNA from Agrobacterium Ti plasmid is in the nuclear DNA fraction of crown gall tumor cells.
T-DNA of a crown gall tumor is organized in nucleosomes.
TALENs Construction: Slowly but Surely.
The adenovirus type 12 - mouse cell system: permissivity and analysis of integration patterns of viral DNA in tumor cells.
The BamHI restriction fragment length polymorphism detected in the c-Ha-ras locus of human skin tumors.
The detection of JC viral genome in owl monkey tumors.
The effects of estrogen on prolactin gene methylation in normal and neoplastic rat pituitary tissues.
The Epstein-Barr Virus BART microRNAs target the pro-apoptotic protein Bim.
The exogenous form of Jaagsiekte retrovirus is specifically associated with a contagious lung cancer of sheep.
The FHIT gene 3p14.2 is abnormal in lung cancer.
The mechanism underlying hypaconitine-mediated alleviation of pancreatitis-associated lung injury through up-regulating aquaporin-1/TNF-?.
The prevalence of different human papillomavirus types and p53 mutations in laryngeal carcinomas: is there a reciprocal relationship?
The rate of the 6174delT founder Jewish mutation in BRCA2 in patients with non-colonic gastrointestinal tract tumours in Israel.
The repair fidelity of restriction enzyme-induced double strand breaks in plasmid DNA correlates with radioresistance in human tumor cell lines.
The use of molecular probes to distinguish new primary tumors from recurrent tumors in gynecologic malignancies.
The variant T allele of PvuII in ESR1 gene is a prognostic marker in early breast cancer survival.
Transcription of the Epstein-Barr virus gene EBNA-1 from different promoters in nasopharyngeal carcinoma and B-lymphoblastoid cells.
Transcription of the simian virus 40 genome in DNA-transformed murine teratocarcinoma stem cells.
Transcriptional expression of RPMS1 in nasopharyngeal carcinoma and its oncogenic potential.
Transcripts from the Epstein-Barr virus BamHI A fragment are detectable in all three forms of virus latency.
Transforming activity of DNA from rat liver tumors induced by the carcinogen methyl(acetoxymethyl)nitrosamine.
Transforming potential is detectable in arteriosclerotic plaques of young animals.
Translocation t(12;16)(q13;p11) in myxoid liposarcoma of a child and implication of the human int-1 gene in tumorigenesis.
Tumor necrosis factor beta NcoI polymorphism is associated with inflammatory and metabolic markers in multiple sclerosis patients.
Tumor necrosis factor genetic polymorphisms correlate with infections after renal transplantation.
Tumor progression stage: specific losses of heterozygosity.
Tumorigenesis of Epstein-Barr virus-positive epithelial cell lines derived from gastric tissues in the SCID mouse.
Two identical active X chromosomes in human mammary carcinoma cells.
Two rearranged immunoglobulin kappa light chain genes in one mouse myeloma.
Unique long terminal repeat U3 sequences distinguish exogenous jaagsiekte sheep retroviruses associated with ovine pulmonary carcinoma from endogenous loci in the sheep genome.
Variable-sized free episomes of Shope papilloma virus DNA are present in all non-virus-producing neoplasms and integrated episomes are detected in some.
Viral DNA in bursal lymphomas induced by avian leukosis viruses.
Viral DNA integration patterns of primary SV40 tumors.
Vitamin D and cancer.
Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria.
X-chromosomal inactivation analysis of uterine leiomyomas reveals a common clonal origin of different tumor nodules in some multiple leiomyomas.
[Activated c-raf-1 gene from human stomach cancer]
[Clonality detection of cervical cancer and cervical intraepithelial neoplasia by human androgen receptor gene analysis]
[Deletion of OPCML gene and promoter methylation in ovarian epithelial carcinoma]
[Endogenous MMTV in the normal mammary gland and in dimethylanthracene-induced mammary cancer in BALB/c mice]
[Expression of Epstein-Barr virus A73 gene in nasopharyngeal carcinoma tissues and its subcellular location]
[Methylation of the putative tumor suppressor gene, RASSF1A, in primary cervical tumors]
[Research on promoter region methylation status of tumor repressor gene P16 in human hepatocellular carcinoma by using methylation sensitive restriction enzyme and semi-nested PCR assay]
[Sensitive detection of K-ras oncogene codon 12 mutations by nested PCR using mismatched primers and selective digestion of non-mutated PCR fragments with restriction enzyme]
[Structural organization of the human p53 gene. I. Molecular cloning of the human p53 gene]
[Study on Ha-ras RFLPs in gastric carcinoma and normal tissue DNAs of Chinese individuals]
[The construction of recombinant AAV vector expressing HSVtk gene controlled by Tet-On and the detection of its activity]
[The relevance of molecular biology studies in the genetic counselling of argentine retinoblastoma families]
[Transfection of a plasmid with a retrovirus promoter: distribution of sequences in the genome of induced tumors]
Nephritis, Hereditary
Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient.
Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosis.
Nephrolithiasis
A HindIII Polymorphism of Fibronectin Gene Is Associated With Nephrolithiasis.
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
Nephrotic Syndrome
Association of polymorphisms at restriction enzyme recognition sites of apolipoprotein B and E gene with dyslipidemia in children undergoing primary nephrotic syndrome.
Neuroblastoma
A 5'-CG-3'-rich region in the promoter of the transcriptionally frequently silenced RET protooncogene lacks methylated cytidine residues.
A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees.
Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue.
Amplification of IMR-32 clones 8, G21, and N-myc in human neuroblastoma xenografts.
Characterization of N-myc amplification units in human neuroblastoma cells.
Cyclic AMP regulation of pro-vasoactive intestinal polypeptide/PHM-27 synthesis in human neuroblastoma cells.
Neuroectodermal Tumors
Conservation of repeated DNA sequences in aneuploid human tumor cells.
Neurofibroma
Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1.
Neurofibromatoses
A BglII RFLP near the human neurofibromatosis type 1 (NF1) gene.
A novel and very peculiar HincII polymorphism in the 5' region of the human neurofibromatosis type 1 (NF1) gene.
Two novel mutations in exons 19a and 20 and a BsaBI [correction of BsaI] polymorphism in a newly characterized intron of the neurofibromatosis type 1 gene.
Neurofibromatosis 1
A BglII RFLP near the human neurofibromatosis type 1 (NF1) gene.
A novel and very peculiar HincII polymorphism in the 5' region of the human neurofibromatosis type 1 (NF1) gene.
Two novel mutations in exons 19a and 20 and a BsaBI [correction of BsaI] polymorphism in a newly characterized intron of the neurofibromatosis type 1 gene.
Neuromyelitis Optica
Neuromyelitis optica (Devic's syndrome): no association with the primary mitochondrial DNA mutations found in Leber hereditary optic neuropathy.
Newcastle Disease
Identification and subgrouping of pigeon type Newcastle disease virus strains by restriction enzyme cleavage site analysis.
Lentogenic field isolates of Newcastle disease virus isolated in Canada and Hungary are identical with the vaccine type used in the region.
Newcastle disease outbreaks in recent years in western Europe were caused by an old (VI) and a novel genotype (VII).
Occurrence of genotypes IV, V, VI and VIIa in Newcastle disease outbreaks in Germany between 1939 and 1995.
Pathotyping of Newcastle disease viruses by RT-PCR and restriction enzyme analysis.
Positive identification of Newcastle disease virus vaccine strains and detection of contamination in vaccine batches by restriction site analysis of the matrix protein gene.
Restriction Enzyme Analysis of Tissue Culture-adapted Velogenic Newcastle Disease Virus.
Simple Differentiation of Avirulent and Virulent Strains of Avian Paramyxovirus Serotype-1 (Newcastle Disease Virus) by PCR and Restriction Endonuclease Analysis in Japan.
The occurrence of five major Newcastle disease virus genotypes (II, IV, V, VI and VIIb) in Bulgaria between 1959 and 1996.
Thrombocytopenia in Newcastle disease: haematological evaluation and histological study of bone marrow.
Two novel genetic groups (VIIb and VIII) responsible for recent Newcastle disease outbreaks in Southern Africa, one (VIIb) of which reached Southern Europe.
[Construction and identification of recombinant fowlpox virus for expressing haemagglutinin-neuraminidase glycoprotein of Newcastle disease virus strain F48E8]
Obesity
A 5-year follow-up study of 3 polymorphisms in the human glucocorticoid receptor gene in relation to obesity, hypertension, and diabetes.
ApoB-100 gene EcoRI polymorphism. Relations to plasma lipoprotein changes associated with abdominal visceral obesity.
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives.
Cross-sectional study of a microsatellite marker in the low density lipoprotein receptor gene in obese normotensives.
Genetic variation in the stress protein hsp70-2 gene is highly associated with obesity.
Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese.
Lipoprotein lipase gene polymorphisms and risks of childhood obesity in Chinese preschool children.
No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects.
PAI-1 haplogenotype confers genetic susceptibility for obesity and hypertriglyceridemia in Mexican children.
Polymorphism in exon 6 of the dopamine D(2) receptor gene (DRD2) is associated with elevated blood pressure and personality disorders in men.
Relationship of metabolic syndrome and its components with -844 G/A and HindIII C/G PAI-1 gene polymorphisms in Mexican children.
Variation in the apolipoprotein B gene and development of type 2 diabetes mellitus.
Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease.
Vitamin D and estrogen receptor gene polymorphisms in type 2 diabetes mellitus and in android type obesity.
[XbaI polymorphism of apolipoprotein B gene in a Tunisian population: alleles frequencies and relationship with plasma lipid parameters]
Obesity, Abdominal
ApoB-100 gene EcoRI polymorphism. Relations to plasma lipoprotein changes associated with abdominal visceral obesity.
Effects of a liquid high-fat meal on postprandial lipid metabolism in type 2 diabetic patients with abdominal obesity.
The lipoprotein lipase HindIII polymorphism modulates plasma triglyceride levels in visceral obesity.
Onychomycosis
Detection and differentiation of causative fungi of onychomycosis using PCR amplification and restriction enzyme analysis.
Investigation of a cluster of Candida albicans invasive Candidiasis in a neonatal intensive care unit by pulsed-field gel electrophoresis.
Opportunistic Infections
Disseminated Nocardia beijingensis Infection in an Immunocompetent Patient.
Optic Atrophy
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy.
Optic Atrophy, Hereditary, Leber
Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.
Mitochondrial DNA mutations in multiple sclerosis.
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
PCR amplification using a single cell allows the detection of the mtDNA lesion associated with Leber's hereditary optic neuropathy.
Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy.
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy.
[DNA diagnosis of Leber's hereditary optic neuropathy]
Optic Nerve Diseases
Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.
Mitochondrial DNA mutations in multiple sclerosis.
PCR amplification using a single cell allows the detection of the mtDNA lesion associated with Leber's hereditary optic neuropathy.
Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy.
[DNA diagnosis of Leber's hereditary optic neuropathy]
Ornithine Carbamoyltransferase Deficiency Disease
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiency.
New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.
Osteitis Deformans
Detection of Exon 8 mutations in sqstm1/p62 gene by mutation-specific restriction enzyme digestion: a sensitive screening for Paget disease of bone.
Osteoarthritis
Association between estrogen receptor-alpha gene PvuII and XbaI polymorphisms and osteoarthritis risk: a meta-analysis.
Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosis.
Polymorphisms in the gene encoding estrogen receptor alpha are associated with osteoarthritis in Han Chinese women.
Osteoarthritis, Knee
Association of ESR? Gene Pvu II T>C, XbaI A>G and BtgI G>A Polymorphisms with Knee Osteoarthritis Susceptibility: A Systematic Review and Meta-Analysis Based on 22 Case-Control Studies.
Genetic estrogen receptor alpha gene PvuII polymorphism in susceptibility to knee osteoarthritis in a Chinese Han population: A southern Jiangsu study.
Osteogenesis Imperfecta
Genetic counselling and prenatal diagnosis of osteogenesis imperfecta caused by paternal mosaicism.
Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.
Osteonecrosis
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia.
Osteopetrosis
Sequences in the gag-pol-5'env region of avian leukosis viruses confer the ability to induce osteopetrosis.
Osteoporosis
Association of estrogen receptor alpha gene polymorphisms and lifestyle factors with calcaneal quantitative ultrasound and osteoporosis in postmenopausal Vietnamese women.
Association of estrogen receptor-alpha gene Pvull polymorphisms with the effect of calcium supplementation on skeletal development in Chinese pubertal girls.
BsmI vitamin D receptor genotypes influence the efficacy of antiresorptive treatments in postmenopausal osteoporotic women. A 1-year multicenter, randomized and controlled trial.
Correlation between vitamin D receptor genotypes and bone mineral density in Japanese patients with osteoporosis.
ESR1 Gene Variants Are Predictive of Osteoporosis in Female Patients with Crohn's Disease.
Estrogen receptor (ER) gene polymorphism may predict the bone mineral density response to raloxifene in postmenopausal women on chronic hemodialysis.
Estrogen receptor-alpha gene (T/C) Pvu II polymorphism in endometriosis and uterine fibroids.
Evaluation of ER? and VDR gene polymorphisms in relation to bone mineral density in Turkish postmenopausal women.
Lack of association between estrogen receptor genotypes and bone mineral density, fracture history, or muscle strength in elderly women.
Lack of association between the HindIII RFLP of the osteocalcin (BGP) gene and bone mineral density (BMD) in healthy pre- and postmenopausal Chinese women.
Lack of association between vitamin D receptor genotypes and osteoporosis in Koreans.
PvuII and XbaI polymorphisms of the estrogen receptor gene and bone mineral density in a Bulgarian population sample.
Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan.
The importance of polymorphic variants of collagen 1A2 gene (COL1A2) in the development of osteopenia and osteoporosis in postmenopausal women.
[PvuII genetic polymorphism of estrogen receptor alpha in the group of postmenopausal women with osteopenia and osteoporosis]
Osteoporosis, Postmenopausal
Early postmenopausal bone loss is associated with PvuII estrogen receptor gene polymorphism in Finnish women: effect of hormone replacement therapy.
Osteosarcoma
Correlation of growth capacity of cells in hard agarose with successful transfection by the activated c-Ha-ras oncogene and in vivo proliferative capacity at metastatic sites.
Expression and nature of the alkaline phosphatase gene in cultured osteosarcoma cells.
FBJ murine osteosarcoma virus: identification and molecular cloning of biologically active proviral DNA.
Homozygous deletion within the retinoblastoma gene in a native osteosarcoma specimen of a patient cured of a retinoblastoma of both eyes.
Methylation status of the retinoblastoma gene (RB1) in osteosarcoma: no evidence for hypermethylation.
Otitis Media
Carriage of multiple ribotypes of non-encapsulated Haemophilus influenzae in aboriginal infants with otitis media.
Turnover of nonencapsulated Haemophilus influenzae in the nasopharynges of otitis-prone children.
Otosclerosis
Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis.
Ovarian Neoplasms
Amplification of the C-erbB-2(HER-2/neu) proto-oncogene in ovarian carcinomas.
Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer.
Association of ER-? gene PvuII polymorphism with ovarian cancer.
Rates of Jewish ancestral mutations in BRCA1 and BRCA2 in borderline ovarian tumors.
Overweight
Estrogen receptor ? is not a candidate gene for metabolic syndrome in Caucasian elderly subjects.
Lipoprotein lipase gene variation is associated with adipose tissue lipoprotein lipase activity, and lipoprotein lipid and glucose concentrations in overweight postmenopausal women.
Pancreatic Neoplasms
Detection of c-Ki-ras mutations in bile samples from patients with pancreatic and biliary cancers.
Significance of MUC2 gene methylation detection in pancreatic cancer diagnosis.
Pancreatitis
Association of the HindIII Lipoprotein Lipase Gene Polymorphism with the Development of the Non-Biliary Acute Pancreatitis: a Pilot Study.
Pancreatitis, Acute Necrotizing
Mapping of a serotype specific epitope of the major capsid protein VP2 of infectious pancreatic necrosis virus.
Pancreatitis, Chronic
Significance of MUC2 gene methylation detection in pancreatic cancer diagnosis.
Papilloma
Analysis of the structure of human papilloma virus DNA.
Cloning and characterization of a papillomavirus associated with papillomas and carcinomas in the European harvest mouse (Micromys minutus).
Differential methylation of the c-H-ras gene in normal mouse cells and during skin tumour progression.
Free cottontail rabbit papillomavirus DNA persists in warts and carcinomas of infected rabbits and in cells in culture transformed with virus or viral DNA.
Heterogeneity of human papilloma viruses.
HLA class II antigen expression in human papillomavirus-associated cervical cancer.
Immunology of human warts.
Inducible expression of the human interferon beta 1 gene linked to a bovine papilloma virus DNA vector and maintained extrachromosomally in mouse cells.
Integration and methylation of shope papilloma virus DNA in the transplantable Vx2 and Vx7 rabbit carcinomas.
Introduction of cloned human papillomavirus genomes into mouse cells and expression at the RNA level.
Loss of critical palindromic transgene promoter sequence in chemically induced Tg.AC mouse skin papillomas expressing transgene-derived mRNA.
Mastomys natalensis papilloma virus (MnPV), the causative agent of epithelial proliferations: characterization of the virus particle.
Molecular cloning and characterization of human papilloma virus DNA derived from a laryngeal papilloma.
Parapoxvirus papillomatosis in the muskoxen (Ovibos moschatus): genetical differences between the virus causing new outbreak in a vaccinated herd, the vaccine virus and a local orf virus.
Partial characterization of viral DNA from human genital warts (Condylomata acuminata).
Plurality of genital human papillomaviruses: characterization of two new types with distinct biological properties.
Regulation of ornithine decarboxylase gene expression in mouse epidermis and epidermal tumors during two-stage tumorigenesis.
Seroepidemiological studies of human papilloma virus (HPV-1) infections.
Shope papilloma virus DNA is extensively methylated in non-virus-producing neoplasms.
Structure, DNaseI hypersensitivity and expression of integrated papilloma virus in the genome of HeLa cells.
Viral etiology of juvenile- and adult-onset squamous papilloma of the larynx.
Paramyxoviridae Infections
Cloning and gene assignment of mRNAs of human parainfluenza virus 3.
Construction in vitro of mutants of simian virus 40: insertion of a poly(dA-dT) segment at the Hemophilus parainfluenza II restriction endonuclease cleavage site.
Paraplegia
Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients.
Parasitemia
Theileria sergenti and T. buffeli: polymerase chain reaction-based marker system for differentiating the parasite species from infected cattle blood and infected tick salivary gland.
[Studies on diagnosis of falciparum malaria based on amplifying specific SSUrDNA fragment with nested PCR]
Paratuberculosis
A cloned DNA probe for the detection of Mycobacterium paratuberculosis.
A method for purification and characterisation of Mycobacterium avium subsp. paratuberculosis from the intestinal mucosa of sheep with Johne's disease.
Analysis of restriction endonuclease fragment patterns of DNA from Mycobacterium paratuberculosis.
Characterization by restriction endonuclease analysis and DNA hybridization using IS900 of bovine, ovine, caprine and human dependent strains of Mycobacterium paratuberculosis isolated in various localities.
Characterization of ovine strains of Mycobacterium paratuberculosis by restriction endonuclease analysis and DNA hybridization.
Definitive differentiation between single and mixed mycobacterial infections in red deer (Cervus elaphus) by a combination of duplex amplification of p34 and f57 sequences and Hpy188I enzymatic restriction of duplex amplicons.
DNA polymorphism in Mycobacterium paratuberculosis, "wood pigeon mycobacteria," and related mycobacteria analyzed by field inversion gel electrophoresis.
Effect of IS900 gene of Mycobacterium paratuberculosis on Mycobacterium smegmatis.
High genetic diversity among Mycobacterium avium subsp. paratuberculosis strains from German cattle herds shown by combination of IS900 restriction fragment length polymorphism analysis and mycobacterial interspersed repetitive unit-variable-number tandem-repeat typing.
Identification of two groups of Mycobacterium paratuberculosis strains by restriction endonuclease analysis and DNA hybridization.
Isolation and analysis of restriction endonuclease digestive patterns of chromosomal DNA from Mycobacterium paratuberculosis and other Mycobacterium species.
Molecular epidemiology of Types I/III strains of Mycobacterium avium subspecies paratuberculosis isolated from goats and cattle.
Mycobacteria distenct from Mycobacterium avium subsp. paratuberculosis isolated from the faeces of ruminants possess IS900-like sequences detectable IS900 polymerase chain reaction: implications for diagnosis.
Paratuberculosis in farmed deer: case reports and DNA characterization of isolates of Mycobacterium paratuberculosis.
Presence of Mycobacterium avium subspecies paratuberculosis in suspensions of ovine trichostrongylid larvae produced in faecal cultures artificially contaminated with the bacterium.
Rapid differentiation of Mycobacterium avium and M. paratuberculosis by PCR and restriction enzyme analysis.
Rapid identification of mycobacteria from AIDS patients by capillary electrophoretic profiling of amplified SOD gene.
Restriction endonuclease analysis of various strains of Mycobacterium paratuberculosis isolated from cattle.
Standardisation of restriction fragment length polymorphism analysis for Mycobacterium avium subspecies paratuberculosis.
Suspicion of Mycobacterium avium subsp. paratuberculosis transmission between cattle and wild-living red deer (Cervus elaphus) by multitarget genotyping.
Unique genotypes of Mycobacterium avium subsp. paratuberculosis strains of Type III.
Parkinson Disease
Absence of the mitochondrial A7237T mutation in Parkinson's disease.
Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease.
Gender difference in the interaction of smoking and monoamine oxidase B intron 13 genotype in Parkinson's disease.
High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease.
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.
The EcoRV genetic polymorphism of human monoamine oxidase type A is not associated with Parkinson's disease and does not modify the effect of smoking on Parkinson's disease.
[Relationship between the Fnu4HI site polymorphism of monoamine oxidase A gene and Parkinson's disease]
Parkinsonian Disorders
Absence of the mitochondrial A7237T mutation in Parkinson's disease.
Pasteurella Infections
The molecular epidemiology of four outbreaks of porcine pasteurellosis.
Pediatric Obesity
Lipoprotein lipase gene polymorphisms and risks of childhood obesity in Chinese preschool children.
Pemphigus
Detection of disease-specific restriction fragment length polymorphisms in pemphigus vulgaris linked to the DQw1 and DQw3 alleles of the HLA-D region.
Peptic Ulcer
Absence of Helicobacter pylori high tetracycline resistant 16S rDNA AGA926-928TTC genotype in gastric biopsy specimens from dyspeptic patients of a city in the interior of Sao Paulo, Brazil.
PCR-based restriction pattern typing of the vacA gene provides evidence for a homogeneous group among Helicobacter pylori strains associated with peptic ulcer disease.
TGFB1 gene polymorphisms: their relevance in the susceptibility to Helicobacter pylori-related diseases.
Periapical Granuloma
DNA Methylation of MMP9 Is Associated with High Levels of MMP-9 Messenger RNA in Periapical Inflammatory Lesions.
Periodontal Diseases
Association of gene polymorphisms for plasminogen activators with alveolar bone loss.
Periodontal Pocket
Host-related genotypic heterogeneity of Porphyromonas gingivalis strains in the beagle dog.
Periodontitis
Association between Estrogen Receptor-? Gene XbaI and PvuII Polymorphisms and Periodontitis Susceptibility: A Meta-Analysis.
IL-1 gene polymorphism and periodontal status of HIV Brazilians on highly active antiretroviral therapy.
Microflora and bacterial DNA restriction enzyme analysis in young adults with periodontitis.
Peripheral Arterial Disease
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
DNA polymorphisms of the gene for apolipoprotein B in patients with peripheral arterial disease.
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus.
Study of DNA polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster in patients with peripheral arterial disease.
Peripheral Nervous System Diseases
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus.
Peritonitis
Staphylococcus aureus colonization and infection in patients on continuous ambulatory peritoneal dialysis.
Persistent Infection
Antigenic and restriction enzyme analysis of isolates of Campylobacter fetus subsp venerealis recovered from persistently infected cattle.
Pharyngitis
Comparison of emm typing and ribotyping with three restriction enzymes to characterize clinical isolates of Streptococcus pyogenes.
Comparison of epidemic and endemic group G streptococci by restriction enzyme analysis.
Emergence and spread of a new clone of M type 1 group A Streptococcus coincident with the increase in invasive diseases in Japan.
Genotyping of group A streptococcus by various molecular methods.
M.SpyI, a DNA methyltransferase encoded on a mefA chimeric element, modifies the genome of Streptococcus pyogenes.
Restriction enzyme analysis (REA) of group A streptococcal (GAS) M-serotypes 1, 3, and 28. A comparison of isolates from severe systemic infections (SSI) and from uncomplicated pharyngitis (UP): epidemiologic and pathogenetic implications.
Phenylketonurias
Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria.
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene.
Rapid mutation screening of phenylketonuria by polymerase chain reaction-linked restriction enzyme assay and direct sequence of the phenylalanine hydroxylase gene: clinical application in northern Japan and northern China.
Two distinct mutations at a single BamHI site in phenylketonuria.
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.
Phyllodes Tumor
Clonal analysis of fibroadenoma and phyllodes tumor of the breast.
Phytoplasma Disease
Detection and identification of aster yellows (16SrI) phytoplasma in peach trees in Jordan by RFLP analysis of PCR-amplified products (16S rDNAs).
Detection and Molecular Characterization of Two Little Leaf Phytoplasma Strains Associated with Pepper and Tomato Diseases in Guanajuato and Sinaloa, Mexico
Detection and Molecular Characterization of Two Little Leaf Phytoplasma Strains Associated with Pepper and Tomato Diseases in Guanajuato and Sinaloa, Mexico.
First Report of a 16SrI-B Group Phytoplasma Associated with a Yellows-Type Disease Affecting Tomato Plants in the Baja California Peninsula of Mexico.
First Report of a 16SrI-C Group Phytoplasma Associated With a Yellows-Type Disease Affecting Willow Plants in China.
First Report of a Member of Aster Yellows Phytoplasma Group and of Clover Proliferation Phytoplasma Group Associated with Onion in Texas.
First report of an aster yellows subgroup 16Sr-I-B phytoplasma infecting chayote in Costa Rica.
First Report of an Aster Yellows Subgroup 16SrI-B Phytoplasma Infecting Chayote in Costa Rica.
First Report of Paulownia Witches'-Broom Phytoplasma in China.
First Report of Phytoplasmas Associated with the Degeneration Syndrome of Artichoke in Catalonia (Spain).
First Report of Phytoplasmas in Soybean, Alfalfa, and Lupinus sp. in Lithuania.
First report of phytoplasmas in soybean, alfalfa, and Lupinus sp. in Lithuania.
First Report of Virus and Phytoplasma Pathogens Associated with Yellow Leaf Syndrome of Sugarcane in Cuba.
First report of virus and phytoplasma pathogens associated with yellow leaf syndrome of sugarcane in Cuba.
First Report of Yucca Phyllody Associated with 16SrI-A Phytoplasmas in Texas.
Identification of a phytoplasma causing yellows of Monarda.
Molecular Identification and Classification of Strawberry Phylloid Fruit Phytoplasma in Group 16SrI, New Subgroup.
Niger Seed (Guizotia abyssinica), a New Host of ‘Candidatus Phytoplasma asteris' in Iran
Sequence and RFLP analysis of the elongation factor Tu gene used in differentiation and classification of phytoplasmas.
The First Report of Stolbur Phytoplasma Associated with Phyllody of Calendula officinalis in Serbia.
Pituitary Neoplasms
Chromatin structure, transcription, and methylation of the prolactin gene domain in pituitary tumors of Fischer 344 rats.
Clinically nonfunctioning pituitary tumors are monoclonal in origin.
Plague
Identification of duck plague virus by polymerase chain reaction.
Identification of the crayfish plague fungus Aphanomyces astaci by polymerase chain reaction and restriction enzyme analysis.
[Construction of recombinant adenovirus vector of mouse keratinocyte growth factor.]
Plasmacytoma
Deletions are associated with somatic rearrangement of immunoglobulin heavy chain genes.
Evidence for somatic rearrangement of immunoglobulin genes coding for variable and constant regions.
Increased expression of myc-related oncogene mRNA characterizes most BALB/c plasmacytomas induced by pristane or Abelson murine leukemia virus.
Intervening sequences divide the gene for the constant region of mouse immunoglobulin mu chains into segments, each encoding a domain.
Non-immunoglobulin-associated DNA rearrangements in mouse plasmacytomas.
Structure of immunoglobulin gamma 2b heavy chain gene cloned from mouse embryo gene library.
Variable and constant parts of the immunoglobulin light chain gene of a mouse myeloma cell are 1250 nontranslated bases apart.
Pleuropneumonia
Diagnosis of contagious caprine pleuropneumonia by detection and identification of Mycoplasma capricolum subsp. capripneumoniae by PCR and restriction enzyme analysis.
Restriction endonuclease analysis and plasmid profiling of Actinobacillus pleuropneumoniae serotype 7 strains.
Pneumonia
Demonstration that Australian Pasteurella multocida isolates from sporadic outbreaks of porcine pneumonia are non-toxigenic (toxA-) and display heterogeneous DNA restriction endonuclease profiles compared with toxigenic isolates from herds with progressive atrophic rhinitis.
Determination of the number of tuf genes in Chlamydia trachomatis and Neisseria gonorrhoeae.
Herpes simplex virus pneumonia: clinical, virologic, and pathologic features in 20 patients.
Methylation-targeted specificity of the DNA binding proteins R.DpnI and MeCP2 studied by molecular dynamics simulations.
Molecular determination of infection source of a sporadic Legionella pneumonia case associated with a hot spring bath.
Molecular investigation of two novel bacteriophages of a facultative methylotroph, Raoultella ornithinolytica: first report of Raoultella phages.
[Adenovirus types 11 and 21: genome types and clinic features]
[Study on gene cloning of Chlamydial pneumonia CPn0308 and its endogenous localization]
Pneumonia, Pneumocystis
Pneumocystis jiroveci isolates with dihydropteroate synthase mutations in patients with chronic bronchitis.
Poliomyelitis
Analysis of the accumulation of mutants in Sabin attenuated polio vaccine viruses passaged in Vero cells.
Increased safety level of serotype 3 Sabin oral poliomyelitis vaccine lots by improved seed virus, and tissue culture and virus infection conditions.
Methods to Monitor Molecular Consistency of Oral Polio Vaccine.
The use of next generation sequencing for the quality control of live-attenuated polio vaccines.
Polycystic Kidney, Autosomal Dominant
Alpha thalassaemia: a potential source of error in DNA linkage studies for adult polycystic kidney disease.
No association of the TGF-beta1 gene polymorphisms with the renal progression in autosomal dominant polycystic kidney disease (ADPKD) patients.
[Gene diagnosis of adult polycystic kidney disease--linkage analysis between APKD gene and alpha-globin gene 3'HVR]
Polycystic Ovary Syndrome
Estrogen receptor ?lpha gene (ESR1) PvuII and XbaI polymorphisms are associated to metabolic and proinflammatory factors in polycystic ovary syndrome.
Estrogen receptor alpha gene PvuII polymorphism and polycystic ovary syndrome.
Polycythemia Vera
Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction.
Hypomethylation of ornithine decarboxylase gene and erb-A1 oncogene in human chronic lymphatic leukemia.
Polyneuropathies
Diagnostic radioimmunoassay and DNA-analysis in Swedish and Japanese patients with familial amyloidotic polyneuropathy. Homozygosity for the TTR met30 gene.
Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA.
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Polyomavirus Infections
Polymerase chain reaction assay for avian polyomavirus.
Porcine Reproductive and Respiratory Syndrome
Overexpression of BsoBI restriction endonuclease in E. coli, purification of the recombinant BsoBI, and identification of catalytic residues of BsoBI by random mutagenesis.
Posterior Tibial Tendon Dysfunction
ER? PvuII and XbaI polymorphisms in postmenopausal women with posterior tibial tendon dysfunction: a case control study.
Poxviridae Infections
Analysis of parapoxvirus genomes.
Prader-Willi Syndrome
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region.
Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).
Pre-Eclampsia
Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus.
Association between estrogen receptor alpha (ESR1) gene polymorphisms and severe preeclampsia.
Association between the estrogen receptor ? gene polymorphisms rs2234693 and rs9340799 and severe and mild pre-eclampsia: a meta-analysis.
ESR1 polymorphisms and risk of preeclampsia.
Estrogen Receptor Alpha (ESR1) Gene Polymorphisms in Pre-eclamptic Saudi Patients.
Genotype distribution of estrogen receptor alpha polymorphisms in pregnant women from healthy and preeclampsia populations and its relation to blood pressure levels.
Maternal and fetal single nucleotide polymorphisms in the epoxide hydrolase and gluthatione S-transferase P1 genes are not associated with pre-eclampsia in the Coloured population of the Western Cape, South Africa.
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Allelic variation of the c-raf-1 proto-oncogene in human lymphoma and leukemia.
Distribution of 11q23 breakpoints within the MLL breakpoint cluster region in de novo acute leukemia and in treatment-related acute myeloid leukemia: correlation with scaffold attachment regions and topoisomerase II consensus binding sites.
Integrated genetic and epigenetic analysis of childhood acute lymphoblastic leukemia.
Restriction endonuclease in situ digestion (REISD) and fluorescence in situ hybridization (FISH) as complementary methods to analyze chimerism and residual disease after bone marrow transplantation.
The EcoRI RFLP of c-mos in patients with non-Hodgkin's lymphoma and acute lymphoblastic leukemia, compared to geriatric and non-geriatric controls.
The methylation status of the major breakpoint cluster region in human leukemia cells, including Philadelphia chromosome-positive cells, is linked to the lineage of hematopoietic cells.
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
DNA methylation and expression of HLA-DR alpha.
Localization of the human CD59 gene by fluorescence in situ hybridization and pulsed-field gel electrophoresis.
Molecular analysis of T cell receptor V beta chain to detect leukemia cell clonality in patients by adaptor ligation-mediated polymerase chain reaction.
Primary Ovarian Insufficiency
Association between estrogen receptora gene (ESR1) PvuII (T/C) and XbaI (A/G) polymorphisms and premature ovarian failure risk: evidence from a meta-analysis.
Estrogen receptor-1 genetic polymorphisms for the risk of premature ovarian failure and early menopause.
Risk of premature ovarian failure is associated to the PvuII polymorphism at estrogen receptor gene ESR1.
Prolactinoma
Abnormalities of the human growth hormone gene and protooncogenes in some human pituitary adenomas.
Prostatic Hyperplasia
Association of lipoprotein lipase gene polymorphism with risk of prostate cancer in a Japanese population.
Prostatic Neoplasms
Association between an estrogen receptor alpha gene polymorphism and the risk of prostate cancer in black men.
Association between estrogen receptor 1 (ESR1) genetic variations and cancer risk: a meta-analysis.
Association between estrogen receptor alpha PvuII polymorphism and prostate cancer risk.
Association of estrogen receptor ? PvuII and XbaI polymorphisms with prostate cancer susceptibility and risk stratification: a meta-analysis from case-control studies.
Association of lipoprotein lipase gene polymorphism with risk of prostate cancer in a Japanese population.
Association of Polymorphisms in the VDR, CYP17 and SRD5A2 Genes and Prostate Cancer Among Lebanese Men
Dehydroepiandrosterone activates mutant androgen receptors expressed in the androgen-dependent human prostate cancer xenograft CWR22 and LNCaP cells.
Estrogen receptor alpha gene polymorphisms and risk of prostate cancer: a meta-analysis involving 18 studies.
Estrogen receptor alpha polymorphisms and the risk of prostate cancer development.
Lack of association between CYP17 Mspa1 polymorphism and prostate cancer risk: a meta-analysis of 14494 cases and 15971 controls.
Osteocalcin gene HindIII C/T polymorphism is a biomarker for prostate cancer and responsiveness to hormone therapy.
Phytoestrogen exposure, polymorphisms in COMT, CYP19, ESR1, and SHBG genes, and their associations with prostate cancer risk.
Preoperative serum DNA GSTP1 CpG island hypermethylation and the risk of early prostate-specific antigen recurrence following radical prostatectomy.
Role of genetic polymorphism of estrogen receptor-alpha gene and risk of prostate cancer in north Indian population.
Silencing of CD44 expression in prostate cancer by hypermethylation of the CD44 promoter region.
The association between estrogen receptor alpha polymorphisms and the risk of prostate cancer in Slovak population.
The rate of the founder Jewish mutations in BRCA1 and BRCA2 in prostate cancer patients in Israel.
Protein C Deficiency
Genetic analysis of protein C deficiency in nineteen Japanese families: five recurrent defects can explain half of the deficiencies.
Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations.
Six missense mutations associated with type I and type II protein C deficiency and implications obtained from molecular modelling.
Protein S Deficiency
Two new frequent dimorphisms in the protein S (PROS1) gene.
Proteinuria
Identification of a single base insertion in the COL4A5 gene in Alport syndrome.
Pseudorabies
A double-strand break in a herpesvirus genome stimulates targeted homologous recombination with exogenous, cloned viral sequences.
A necrotizing pneumonia in lambs caused by pseudorabies virus (Aujesky's disease virus).
A novel intergenic site for integration and expression of foreign genes in the genome of pseudorabies virus.
Analysis of pseudorabies virus glycoprotein gIII localization and modification by using novel infectious viral mutants carrying unique EcoRI sites.
Application of a quantitative algorithm to restriction endonuclease analysis of Aujeszky's disease (pseudorabies) virus from a geographically localized outbreak.
Biological evaluation of glycoproteins mapping to two distinct mRNAs within the BamHI fragment 7 of pseudorabies virus: expression of the coding regions by vaccinia virus.
Characterisation of Aujeszky's disease viruses isolated from domestic animals and from a wild boar (Sus scrofa) in Italy between 1972 and 1995.
Characterization of Japanese isolates of Aujeszky's disease virus by restriction endonuclease cleavage patterns, virulence in mice and thymidine kinase activity.
Characterization of pseudorabies viruses recently isolated in Japan by restriction endonuclease assay.
Characterization of the genes, including that encoding the viral proteinase, contained in BamHI restriction fragment 9 of the pseudorabies virus genome.
Characterization of virulent and attenuated strains of pseudorabies virus for thymidine kinase activity, virulence and restriction patterns.
Comparison of the genomes of pseudorabies (Aujeszky's disease) virus strains by restriction endonuclease analysis.
Deletions in the genomes of pseudorabies virus vaccine strains and existence of four isomers of the genomes.
Differentiation of pseudorabies (Aujeszky's disease) virus strains by restriction endonuclease analysis.
DNA restriction fragment length polymorphism among British isolates of Aujeszky's disease virus: use of the polymerase chain reaction to discriminate among strains.
Equine herpesvirus genomes: heterogeneity of naturally occurring type 4 isolates and of a type 1 isolate after heterologous cell passage.
Evaluation of field isolates of pseudorabies (Aujeszky's disease) virus as determined by restriction endonuclease analysis and hybridization.
Genome differences among field isolates and vaccine strains of pseudorabies virus.
Genotyping of the pseudorabies virus by multiplex PCR followed by restriction enzyme analysis.
Identification and characterization of pseudorabies virus glycoprotein gM as a nonessential virion component.
Identification and transcriptional analysis of pseudorabies virus UL6 to UL12 genes.
Isolation and characterization of Aujeszky's disease virus in captive brown bears from Italy.
Isolation, characterization, and physical mapping of a pseudorabies virus mutant containing antigenically altered gp50.
Mutations affecting the UL21 gene contribute to avirulence of pseudorabies virus vaccine strain Bartha.
Pseudorabies virus and equine herpesvirus 1 share a nonessential gene which is absent in other herpesviruses and located adjacent to a highly conserved gene cluster.
Pseudorabies virus displays variable numbers of a repeat unit adjacent to the 3' end of the glycoprotein gII gene.
Restriction endonuclease analysis of Aujeszky's disease (pseudorabies) virus DNA: comparison of Northern Ireland isolates and isolates from other countries.
Restriction endonuclease analysis of Aujeszky's disease viruses isolated in Japan.
Restriction endonuclease analysis of the pseudorabies (Aujeszky's disease) virus before and after serial passage in vivo and in vitro.
Silver staining of DNA restriction fragments for the ultrarapid identification of pseudorabies virus strains.
Some characteristics of four attenuated vaccine virus strains and a virulent strain of Aujeszky's disease virus.
Stability of the pseudorabies virus genome after in vivo serial passage.
Stability of virulent pseudorabies (Aujeszky's disease) viral genome after single passage through nonswine animal species.
The BamHI fragment 9 of pseudorabies virus contains genes homologous to the UL24, UL25, UL26, and UL 26.5 genes of herpes simplex virus type 1.
The BamHI J fragment (0.706 to 0.737 map units) of pseudorabies virus is transcriptionally active during viral replication.
The genotype of Aujeszky's disease viruses isolated in Argentina.
The left border of the genomic inversion of pseudorabies virus contains genes homologous to the UL46 and UL47 genes of herpes simplex virus type 1, but no UL45 gene.
The pseudorabies virus gII gene is closely related to the gB glycoprotein gene of herpes simplex virus.
The structure of the pseudorabies virus genome at the end of the inverted repeat sequences proximal to the junction with the short unique region.
The UL49.5 gene of pseudorabies virus codes for an O-glycosylated structural protein of the viral envelope.
The virulence-determining genomic BamHI fragment 4 of pseudorabies virus contains genes corresponding to the UL15 (partial), UL18, UL19, UL20, and UL21 genes of herpes simplex virus and a putative origin of replication.
Psittacosis
Comparison of Chlamydia psittaci isolates by restriction endonuclease and DNA probe analyses.
Psoriasis
Arthritis in patients with psoriasis is associated with an immunoglobulin gene polymorphism.
Polymorphisms in folate, pyrimidine, and purine metabolism are associated with efficacy and toxicity of methotrexate in psoriasis.
Puberty, Precocious
Analysis of the PvuII and XbaI polymorphisms in the estrogen receptor alpha gene in girls with central precocious puberty: a pilot study.
Association of estrogen receptor gene polymorphisms with human precocious puberty: a systematic review and meta-analysis.
Pulmonary Disease, Chronic Obstructive
Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.
Neither IL-1beta, IL-1 receptor antagonist, nor TNF-alpha polymorphisms are associated with susceptibility to COPD.
The cyclooxygenase-2-765C promoter polymorphism protects against the development of chronic obstructive pulmonary disease.
Transforming growth factor-beta1 genotype and susceptibility to chronic obstructive pulmonary disease.
Pulmonary Embolism
Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample.
Pulmonary Emphysema
Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease.
Purpura, Thrombocytopenic, Idiopathic
Interleukin-23R gene polymorphism in pediatric Egyptian patients with primary immune thrombocytopenia.
Pyoderma
Characterisation of Staphylococcus intermedius isolates from canine pyoderma and from healthy carriers by SDS-PAGE of exoproteins, immunoblotting and restriction endonuclease digest analysis.
Characterization of Staphylococcus intermedius from healthy dogs and cases of superficial pyoderma by DNA restriction endonuclease patterns.
Pyometra
Escherichia coli strains isolated from the uterus and urinary bladder of bitches suffering from pyometra: comparison by restriction enzyme digestion and pulsed-field gel electrophoresis.
Pyruvate Dehydrogenase Complex Deficiency Disease
Biochemical and molecular analysis of an X-linked case of Leigh syndrome associated with thiamin-responsive pyruvate dehydrogenase deficiency.
pyruvate kinase deficiency
Coexistence of alpha-thalassemia and a new pyruvate kinase variant: PK Fukien.
Rabies
A method for simultaneous detection and identification of Brazilian dog- and vampire bat-related rabies virus by reverse transcription loop-mediated isothermal amplification assay.
A molecular epidemiological study of rabies virus in central Ontario and western Quebec.
A reverse-transcription, loop-mediated isothermal amplification assay for detection of bovine ephemeral fever virus in the blood of infected cattle.
Differentiation of two rabies strains in Estonia with reference to recent Finnish isolates.
In vitro assessments of the genetic stability of a live recombinant human adenovirus vaccine against rabies.
Molecular epidemiology of enzootic rabies in California.
Molecular epidemiology of rabies epizootics in Texas.
Studies on antigenic and genomic properties of Brazilian rabies virus isolates.
Radicular Cyst
DNA Methylation of MMP9 Is Associated with High Levels of MMP-9 Messenger RNA in Periapical Inflammatory Lesions.
Rectal Neoplasms
Oestrogen and vitamin D receptor (VDR) genotypes and the expression of ErbB-2 and EGF receptor in human rectal cancers.
[Construction of eukaryotic expression vector encoding human nasopharyngeal carcinoma anti-idiotype antibody single chain fragment gene G22 and its expression.]
Renal Insufficiency
The heparan sulfate proteoglycan gene polymorphism: association with type 2 diabetic nephropathy in Chinese.
Respiratory Tract Infections
Genetic relationship between thirteen genome types of adenovirus 11, 34, and 35 with different tropisms.
Genotyping of Uruguayan Human adenovirus isolates collected between 1994 and 1998.
Moraxella (Branhamella) catarrhalis: restriction enzyme analysis typing with HinfI, HaeIII and PstI.
Restriction endonuclease analysis of bovine herpesvirus 1 DNA and nucleic acid homology between isolates.
Reticuloendotheliosis, Avian
Sites of integration of infectious DNA of avian reticuloendotheliosis viruses in different avian cellular DNAs.
Retinitis
Cytomegalovirus glycoprotein B groups associated with retinitis in AIDS.
Retinitis Pigmentosa
A NlaIII PCR/RFLP in an intron of the retinitis pigmentosa GTPase regulator gene (RPGR) on the canine X chromosome.
A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase beta-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa.
Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.
[Yeast artificial chromosome cloning and physical mapping of retinitis pigmentosa 3 (RP3) locus]
Retinoblastoma
A linkage analysis in two families with bilateral retinoblastoma.
Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13.
Extensive DNA methylation spanning the Rb promoter in retinoblastoma tumors.
Genetic sequences that predispose to retinoblastoma and osteosarcoma.
Homozygous deletion within the retinoblastoma gene in a native osteosarcoma specimen of a patient cured of a retinoblastoma of both eyes.
PCR-based detection of a polymorphic BamHI site in intron 1 of the human retinoblastoma (RB) gene.
The adenovirus type 12 - mouse cell system: permissivity and analysis of integration patterns of viral DNA in tumor cells.
Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families.
Rhabdomyosarcoma
Inhibition of the interferon-gamma/signal transducers and activators of transcription (STAT) pathway by hypermethylation at a STAT-binding site in the p21WAF1 promoter region.
Methylation alterations of the MyoD1 upstream region are predictive of subclassification of human rhabdomyosarcomas.
Rheumatic Fever
Streptokinase gene polymorphism in group A streptococci isolated from Ethiopian children with various disease manifestations.
Rhinitis
Association between genetic variants of mast-cell chymase and eczema.
Rhinitis, Allergic
Investigation of the genetic regulation in allergic rhinitis.
Rhinitis, Atrophic
Demonstration that Australian Pasteurella multocida isolates from sporadic outbreaks of porcine pneumonia are non-toxigenic (toxA-) and display heterogeneous DNA restriction endonuclease profiles compared with toxigenic isolates from herds with progressive atrophic rhinitis.
Molecular fingerprinting of Pasteurella multocida associated with progressive atrophic rhinitis in swine herds.
Rickets
Vitamin D receptor polymorphisms and nutritional rickets in Nigerian children.
Rickettsia Infections
Simple method to differentiate among Rickettsia species.
Rinderpest
Progress in the development of a heat-stable recombinant rinderpest vaccine using an attenuated vaccinia virus vector.
Rubella
Restriction endonuclease digestion eliminates product contamination in reverse transcribed polymerase chain reaction.
Reverse transcription and subsequent DNA amplification of rubella virus RNA.
Salmonella Infections
[Characteristics of the plasmid profile of inositol- and rhamnose- negative strains of Salmonella typhimurium]
Sarcoidosis
Analysis of gene polymorphisms in interleukin-10 and transforming growth factor-beta 1 in sarcoidosis.
Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patients.
Sarcoma
A MboII polymorphism in exon 11 of the human MDM2 gene occuring in normal blood donors and in soft tissue sarcoma patients: an indication for an increased cancer susceptibility?
Cloning of integrated Moloney sarcoma proviral DNA sequences in bacteriophage lambda.
Comparative analysis of the human and feline c-sis proto-oncogenes. Identification of 5' human c-sis coding sequences that are not homologous to the transforming gene of simian sarcoma virus.
DNA sequence of the viral and cellular src gene of chickens. 1. Complete nucleotide sequence of an EcoRI fragment of recovered avian sarcoma virus which codes for gp37 and pp60src.
Dual evolutionary origin for the rat genetic sequences of Harvey murine sarcoma virus.
Functional organization of the Harvey murine sarcoma virus genome.
Genome organization of retroviruses. III. Restriction endonuclease cleavage maps of mouse sarcoma virus double-stranded DNA synthesized in vitro.
Human DNA sequence homologous to the transforming gene (mos) of Moloney murine sarcoma virus.
Identification and molecular cloning of Moloney mouse sarcoma virus-specific sequences from uninfected mouse cells.
Identification of unintegrated forms of Kirsten murine sarcoma viral DNA and restriction endonuclease cleavage map of linear DNA.
In vitro methylation of specific regions of the cloned Moloney sarcoma virus genome inhibits its transforming activity.
Molecular cloning and comparative analyses of the genomes of simian sarcoma virus and its associated helper virus.
Molecular cloning of Snyder-Theilen feline leukemia and sarcoma viruses: comparative studies of feline sarcoma virus with its natural helper virus and with Moloney murine sarcoma virus.
Molecular cloning of the Harvey sarcoma virus closed circular DNA intermediates: initial structural and biological characterization.
onc sequences (v-fes) of Snyder-Theilen feline sarcoma virus are derived from noncontiguous regions of a cat cellular gene (c-fes).
Restriction endonuclease mapping of unintegrated proviral DNA of Kirsten murine sarcoma virus.
Restriction endonuclease mapping of unintegrated proviral DNA of Snyder-Theilen feline sarcoma virus: localization of sarcoma-specific sequences.
Sarcoma, Avian
Amino acid alterations within a highly conserved region of the Rous sarcoma virus src gene product pp60src inactivate tyrosine protein kinase activity.
Analysis of cellular integration sites in avian sarcoma virus infected duck embryo cells.
Analysis of integrated avian RNA tumor virus DNA in transformed chicken, duck and quail fibroblasts.
Assay of noninfectious fragments of DNA of avian leukosis virus-infected cells by marker rescue.
Comparison between the viral transforming gene (src) of recovered avian sarcoma virus and its cellular homolog.
Differences between cellular integration sites of transcribed and nontranscribed Rous sarcoma proviruses.
DNA sequence of the viral and cellular src gene of chickens. 1. Complete nucleotide sequence of an EcoRI fragment of recovered avian sarcoma virus which codes for gp37 and pp60src.
Integration of avian sarcoma virus DNA sequences in transformed mammalian cells.
Modification of avian sarcoma proviral DNA sequences in nonpermissive XC cells but not in permissive chicken cells.
Restriction endonuclease mapping of the DNA of Rous-associated virus O reveals extensive homology in structure and sequence with avian sarcoma virus DNA.
Restriction enzyme sites on the avian RNA tumor virus genome.
Role of 3'-end of viral genome in tumor heteroinduction by the avian sarcoma virus.
[Detection of nucleotide sequences specific for retroviruses in Saccharomyces cells]
[Fragments of linear unintegrated Rous sarcoma virus DNA, resulting from digestion with SmaI restriction endonuclease]
Sarcoma, Kaposi
HHV-8 is not a cofactor in the pathogenesis of environmentally induced malignant pleural mesothelioma.
Molecular characterization of human T-cell leukemia (lymphotropic) virus type III in the acquired immune deficiency syndrome.
Use of X-Chromosome Inactivation Pattern to Analyze the Clonality of 14 Female Cases of Kaposi Sarcoma.
Scabies
SsbI, an isoschizomer of HindIII isolated from Streptomyces scabies.
Scoliosis
Association between Estrogen Receptor Alpha Gene Polymorphisms and Susceptibility to Idiopathic Scoliosis in Bulgarian Patients: A Case-Control Study.
Association of ESR? XbaI A?>?G, ESR? PvuII T?>?C and ESR? AlwNI T?>?C Polymorphisms with the Risk of Developing Adolescent Idiopathic Scoliosis: A Systematic Review and Genetic Meta-analysis.
XbaI and PvuII polymorphisms of estrogen receptor 1 gene in females with idiopathic scoliosis: no association with occurrence or clinical form.
Scrapie
Natural scrapie in British sheep: breeds, ages and PrP gene polymorphisms.
Restriction fragment length polymorphisms of the scrapie-associated fibril protein (PrP) gene and their association with susceptibility to natural scrapie in British sheep.
Sepsis
Emergence and spread of a new clone of M type 1 group A Streptococcus coincident with the increase in invasive diseases in Japan.
Epidemiological typing of Candida albicans from bloodstream infections by restriction enzyme analysis.
Infant with two relapses of group B streptococcal sepsis documented by DNA restriction enzyme analysis.
Shock, Septic
Emergence and spread of a new clone of M type 1 group A Streptococcus coincident with the increase in invasive diseases in Japan.
Sickle Cell Trait
A beta-thalassemia lesion abolishes the same Mst II site as the sickle mutation.
Alpha globin gene number: population and restriction endonuclease studies.
Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin.
Restriction endonuclease analysis of DNA in sickle cell lesions among tribals of Bihar, Madhya Pradesh, Gujarat & Rajasthan.
Simian Acquired Immunodeficiency Syndrome
Distribution of type D retrovirus sequences in tissues of macaques with simian acquired immune deficiency and retroperitoneal fibromatosis.
Isolation of a new serotype of simian acquired immune deficiency syndrome type D retrovirus from Celebes black macaques (Macaca nigra) with immune deficiency and retroperitoneal fibromatosis.
Molecular comparison of retroviruses associated with human and simian AIDS.
Ultrastructural comparison of the retroviruses associated with human and simian acquired immunodeficiency syndromes.
Skin Neoplasms
Correlation of the clinical manifestations and gene mutations of Japanese xeroderma pigmentosum group A patients.
The GSTM1 null genotype confers an increased risk for solar keratosis development in an Australian Caucasian population.
Sleep Initiation and Maintenance Disorders
MAO-A gene polymorphisms are associated with major depression and sleep disturbance in males.
Small Cell Lung Carcinoma
A submicroscopic homozygous deletion at the D3S3 locus in a cell line isolated from a small cell lung carcinoma.
The FHIT gene 3p14.2 is abnormal in lung cancer.
Smallpox
Analysis of the nucleotide sequence of a 43 kbp segment of the genome of variola virus India-1967 strain.
Conservation and variation in Orthopoxvirus genome structure.
Nucleotide sequence analysis of variola virus HindIII M, L, I genome fragments.
One time intranasal vaccination with a modified vaccinia Tiantan strain MVTT(ZCI) protects animals against pathogenic viral challenge.
Orthopoxvirus DNA: a comparison of restriction profiles and maps.
[Comparative restriction enzyme analysis of the genome in variola virus strains from the Russian collection]
[Study of the structural-functional organization of the natural variola virus genome. I. Cloning HindIII- and XhoI-fragments of viral DNA and sequencing HindIII -M, -L, -I fragments]
[Study of the structure-activity organization of the variola virus genome. II. Analysis of the nucleotide sequence of the HindIII region (C,E,R,Q,K and H)-DNA fragments of the India-1967 strain]
Smooth Muscle Tumor
An avaII restriction fragment length polymorphism in the insulin-like growth factor II gene and the occurrence of smooth muscle tumors.
Soft Tissue Infections
Use of PCR-restriction fragment length polymorphism for the identification of zoonotic mycobacteriosis in zebrafish caused by Mycobacterium abscessus and Mycobacterium chelonae.
Spinal Dysraphism
A human autosomal phosphoglycerate kinase locus maps near the HLA cluster.
Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring.
Spinocerebellar Ataxias
The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).
Spondylarthropathies
HLA in ankylosing spondylitis: is HLA-B27 the only MHC gene involved in disease pathogenesis?
Non-association between 9.2 KB PvuII RFLP and seronegative spondyloarthropathies in Spain.
Spondylitis, Ankylosing
HLA in ankylosing spondylitis: is HLA-B27 the only MHC gene involved in disease pathogenesis?
Restriction fragment length polymorphism analysis in ankylosing spondylitis.
[PvuII restriction polymorphism of class I genes in ankylosing spondylarthritis. Absence of relation with the 9,2 kb band]
Spotted Fever Group Rickettsiosis
Comparison of serologic typing, sodium dodecyl sulfate-polyacrylamide gel electrophoresis protein analysis, and genetic restriction fragment length polymorphism analysis for identification of rickettsiae: characterization of two new rickettsial strains.
Genotypic and antigenic identification of two new strains of spotted fever group rickettsiae isolated from China.
Genotypic identification of three new strains of spotted fever group rickettsiae isolated in China.
Human and tick spotted fever group Rickettsia isolates from Israel: a genotypic analysis.
Nucleotide sequence of polymerase chain reaction product amplified from Rickettsia japonica DNA using Rickettsia rickettsii 190-kilodalton surface antigen gene primers.
Using PCR/RFLP to detect spotted fever group rickettsia in ticks and rodents collected in Ninghua, Fujian province.
[Detection of north-Asia tick-borne spotted fever in ticks and rodents along the Heilongjiang river-side by restriction fragment length polymorphism of PCR products]
Squamous Cell Carcinoma of Head and Neck
Association of -1171 promoter polymorphism of matrix metalloproteinase-3 with increased risk for oral cancer.
Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck.
Staphylococcal Infections
Use of restriction endonuclease analysis of plasmids and pulsed-field gel electrophoresis to investigate outbreaks of methicillin-resistant Staphylococcus aureus infection.
Starvation
Does dinophysis caudata (dinophyceae) have permanent plastids
Inititation and termination of chromosome replication in Escherichia coli subjected to amino acid starvation.
Regulation of the operon encoding ribonucleotide reductase: role of the negative sites in nrd repression.
steroid 21-monooxygenase deficiency
Prenatal diagnosis of 21-hydroxylase deficiency by RFLP analysis of the 21-hydroxylase, complement C4, and HLA class II genes.
[Detection of steroid 21-hydroxylase gene variation among normal Chinese and patients with congenital adrenal hyperplasia]
Stomach Neoplasms
Association of COX2 gene hypomethylation with intestinal type gastric cancer in samples of patients from northern Brazil.
DNA hypermethylation at the D17S5 locus is associated with gastric carcinogenesis.
EcoRI polymorphism of the L-myc gene in gastric cancer patients.
Epstein-Barr Virus miR-BART17-5p Promotes Migration and Anchorage-Independent Growth by Targeting Kruppel-Like Factor 2 in Gastric Cancer.
Expression of hypoxic marker CA IX is regulated by site-specific DNA methylation and is associated with the histology of gastric cancer.
Expression of tumor related gene NAG6 in gastric cancer and restriction fragment length polymorphism analysis.
Frequent overexpression, but not activation by point mutation, of ras genes in primary human gastric cancers.
Mechanism and clinical significance of cyclooxygenase-2 expression in gastric cancer.
Study on detection of mutation DNA fragment in gastric cancer by restriction endonuclease fingerprinting with capillary electrophoresis.
Zinc finger E-box binding factor 1 plays a central role in regulating Epstein-Barr virus (EBV) latent-lytic switch and acts as a therapeutic target in EBV-associated gastric cancer.
[A molecular epidemiological study on the relationship between the polymorphism of GSTP1 and susceptibility to gastric cancer in northern Chinese]
[Establishment of BGC-823/WTX-EGFP gastric cancer cell line stably expressing Wilms tumor gene on X chromosome.]
[Helicobacter pylori cytotoxin associated protein CagA regulates gastrin gene promoter activity].
Stomatitis
Analysis of parapoxvirus genomes.
Characterization of parapoxviruses circulating among wild Japanese serows (Capricornis crispus).
Physical characterization of a stomatitis papulosa virus genome: a cleavage map for the restriction endonucleases HindIII and EcoRI.
Stomatitis, Herpetic
Recurrent intraoral herpes simplex virus infection.
Streptococcal Infections
Comparison of epidemic and endemic group G streptococci by restriction enzyme analysis.
Molecular epidemiology of group B streptococcal infections: use of restriction endonuclease analysis of chromosomal DNA and DNA restriction fragment length polymorphisms of ribosomal RNA genes (ribotyping).
Stroke
A study of ER? PvuII polymorphism in female patients with acute stroke: no associations with disease severity and early outcome.
A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease.
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population.
Association between Lipoprotein Lipase Polymorphism and the Risk of Stroke: A Meta-analysis.
Association of BglII Polymorphism in ITGA2 and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients ?2 Gene Polymorphism in ?2?1 Integrin and eNOS Gene Variants and Stroke.
Association of estrogen receptor-alpha gene polymorphisms with stroke risk in patients with metabolic syndrome.
Association of LPL gene variant and LDL, HDL, VLDL cholesterol and triglyceride levels with ischemic stroke and its subtypes.
Estrogen receptor ? genetic variants and the risk of stroke in a South Indian population from Andhra Pradesh.
The -174G/C polymorphism of the interleukin 6 gene is a hallmark of lacunar stroke and not other ischemic stroke phenotypes.
TNF-alpha -308G/A and IL-6 -174 G/C polymorphisms in the Turkish pediatric stroke patients.
[Investigation of the association between the HindIII polymorphism of the LPL gene and the Taq1b polymorphism of the CETP gene with the risk of atherothrombotic stroke in the dwellers of Central Russia].
Stroke, Lacunar
The -174G/C polymorphism of the interleukin 6 gene is a hallmark of lacunar stroke and not other ischemic stroke phenotypes.
Subarachnoid Hemorrhage
Estrogen receptor alpha gene variant, PvuII (rs2234693), as a potential pharmacogenetic biomarker for aneurysmal subarachnoid hemorrhage in postmenopausal women.
Superinfection
Changes in the restriction endonuclease patterns of four modified-live infectious bovine rhinotracheitis virus (IBRV) vaccines after one passage in host animal.
Expression of superinfection immunity to bacteriophage phi 105 by Bacillus subtilis cells carrying a plasmic chimera of pUB110 and EcoRI fragment F of phi 105 DNA.
Hybrid plasmids containing an active thymidine kinase gene of Herpes simplex virus 1.
Recovery of herpes simplex virus genetic information from human trigeminal ganglion cells following superinfection with herpes simplex virus type 2 temperature-sensitive mutants.
Superinfection of a chimpanzee with a second strain of human immunodeficiency virus.
Tangier Disease
Restriction enzyme analysis of the apolipoprotein A-I gene in fish eye disease and Tangier disease.
Tardive Dyskinesia
Polymorphic drug metabolism in schizophrenic patients with tardive dyskinesia.
Tay-Sachs Disease
The frequency of Tay-Sachs disease causing mutations in the Brazilian Jewish population justifies a carrier screening program.
Telangiectasis
Idiopathic and radiation-induced ocular telangiectasia: the involvement of the ATM gene.
Tendinopathy
ER? PvuII and XbaI polymorphisms in postmenopausal women with posterior tibial tendon dysfunction: a case control study.
Tennis Elbow
The BstUI and DpnII Variants of the COL5A1 Gene Are Associated With Tennis Elbow.
Tension-Type Headache
Role of the oestrogen receptor (ESR1 PvuII and ESR1 325 C-->G) and progesterone receptor (PROGINS) polymorphisms in genetic susceptibility to migraine in a North Indian population.
Teratoma
Induced pluripotent stem cell line from an atopic dermatitis patient heterozygous for c.2282del4 mutation in filaggrin: KCLi001-A.
Induced pluripotent stem cell line heterozygous for p.R2447X mutation in filaggrin: KCLi002-A.
Induced pluripotent stem cell line heterozygous for p.R501X mutation in filaggrin: KCLi003-A.
Testicular Neoplasms
CpG island hypermethylation of cell-free circulating serum DNA in patients with testicular cancer.
Tetanus
The structural gene for tetanus neurotoxin is on a plasmid.
Thalassemia
A beta-thalassemia lesion abolishes the same Mst II site as the sickle mutation.
Beta thalassemia in Melanesia: association with malaria and characterization of a common variant (IVS-1 nt 5 G----C).
Gene analysis in delta beta and delta (0) thalassemia.
Overview of the beta thalassemias: genetic and clinical aspects.
Recombinant DNA technology and laboratory medicine.
Thrombocytopenia
An improved DNA-based identification of fetuses at risk for HPA-1a (PlA1) neonatal alloimmune thrombocytopenia.
Hypermethylation of p15 gene associated with an inferior poor long-term outcome in childhood acute lymphoblastic leukemia.
In vivo gene amplification in non-cancerous cells: cholinesterase genes and oncogenes amplify in thrombocytopenia associated with lupus erythematosus.
Thrombocytopenia, Neonatal Alloimmune
An improved DNA-based identification of fetuses at risk for HPA-1a (PlA1) neonatal alloimmune thrombocytopenia.
Thrombosis
Association of estrogen receptor-alpha genepolymorphisms with venous thrombosis.
Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis.
Factor VII and fibrinogen levels as risk factors for venous thrombosis. A case-control study of plasma levels and DNA polymorphisms--the Leiden Thrombophilia Study (LETS).
Fibrinogen polymorphisms TaqI, HaeIII and BclI are not associated with a higher risk of deep vein thrombosis.
Intraoperative Thrombophilia-Associated Thrombosis of Both Saphenous Veins during Harvesting for Coronary Artery Bypass Grafting.
Thymoma
Deregulation of the c-myc oncogene in virus-induced thymic lymphomas of AKR/J mice.
Distinct helper virus requirements for Abelson murine leukemia virus-induced pre-B- and T-cell lymphomas.
Immunoglobulin and T-cell receptor genes in thymomas: genotypic evidence supporting the nonneoplastic nature of the lymphocytic component.
Recombination between two integrated proviruses, one of which was inserted near c-myc in a retrovirus-induced rat thymoma: implications for tumor progression.
Specific integration of recombinant proviral sequences in ecotropic Gross virus-accelerated AKR thymomas.
Thyroid Diseases
Association of functional GITR gene polymorphisms related to expression of glucocorticoid-induced tumour necrosis factor-receptor (GITR) molecules with prognosis of autoimmune thyroid disease.
Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population.
Thyroid Neoplasms
Analysis of the TSH receptor gene structure in various thyroid disorders: DNA from thyroid adenomas can have large insertions or deletions.
Thyroiditis
A polymorphism within the vitamin D-binding protein gene is associated with Graves' disease but not with Hashimoto's thyroiditis.
Association of HLA antigen and restriction fragment length polymorphism of T cell receptor beta-chain gene with Graves' disease and Hashimoto's thyroiditis.
Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family.
Thyroiditis, Autoimmune
The tumor necrosis factor beta * 1 allele is linked significantly to HLA-DR8 in Koreans with atrophic autoimmune thyroiditis who are positive for thyrotropin receptor blocking antibody.
Thyroiditis, Subacute
Analysis of the TSH receptor gene structure in various thyroid disorders: DNA from thyroid adenomas can have large insertions or deletions.
Tics
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113].
Gender in obsessive-compulsive disorder: clinical and genetic findings.
Tonsillar Neoplasms
Human papillomavirus type 16 is episomal and a high viral load may be correlated to better prognosis in tonsillar cancer.
Tonsillitis
Streptokinase gene polymorphism in group A streptococci isolated from Ethiopian children with various disease manifestations.
Tooth Loss
Association of estrogen and vitamin D receptor gene polymorphisms with tooth loss and oral bone loss in Japanese postmenopausal women.
Trachoma
Characterization and sequence of a plasmid from the trachoma biovar of Chlamydia trachomatis.
DNA fingerprinting of Chlamydia trachomatis by use of ribosomal RNA, oligonucleotide and randomly cloned DNA probes.
[Restriction endonuclease analysis of Chlamydia trachomatis DNA]
Transfusion-Related Acute Lung Injury
Effect of rapamycin on early stage apoptosis of neutrophils in Sprague-Dawley rats with acute lung injury.
triacylglycerol lipase deficiency
Structure and polymorphic map of human lipoprotein lipase gene.
Trypanosomiasis, African
Isolation and characterization of kinetoplast DNA from bloodstream form of Trypanosoma brucei.
Tuberculosis
A genomic library-based amplification approach (GL-PCR) for the mapping of multiple IS6110 insertion sites and strain differentiation of Mycobacterium tuberculosis.
A report of tuberculosis in cats in New Zealand, and the examination of strains of Mycobacterium bovis by DNA restriction endonuclease analysis.
Alterations in the superoxide dismutase gene of an isoniazid-resistant strain of Mycobacterium tuberculosis.
Characterization of mycobacteria isolated from bovines by PRA-targetting hsp 65 gene region.
Chromosomal DNA fingerprint patterns produced with IS6110 as strain-specific markers for epidemiologic study of tuberculosis.
Cloning and B-cell-epitope mapping of MPT64 from Mycobacterium tuberculosis H37Rv.
Comparative assays of the rpoB gene for identification of Mycobacterium tuberculosis isolated from patients in Sudan.
Comparison of restriction fragment length polymorphism of Mycobacterium tuberculosis isolated from cerebrospinal fluid and sputum: a preliminary report.
Detection and species identification of mycobacteria in paraffin sections of lung biopsy specimens by the polymerase chain reaction.
Detection of isoniazid and rifampin resistance in Mycobacterium tuberculosis strains by single-strand conformation polymorphism analysis and restriction fragment length polymorphism.
Detection of Mycobacterium tuberculosis complex DNA by the polymerase chain reaction for rapid diagnosis of cutaneous tuberculosis.
Detection of Mycobacterium tuberculosis DNA with thermophilic strand displacement amplification and fluorescence polarization.
Development of a Novel PCR Restriction Analysis of the hsp65 Gene as a Rapid Method To Screen for the Mycobacterium tuberculosis Complex and Nontuberculous Mycobacteria in High-Burden Countries.
Differentiation of clinical Mycobacterium tuberculosis complex isolates by their GyrB polymorphism.
Differentiation of mycobacterial species by PCR-restriction analysis of DNA (342 base pairs) of the RNA polymerase gene (rpoB).
DNA restriction endonuclease analysis of Mycobacterium bovis and other members of the tuberculosis complex.
DNA restriction endonuclease analysis of Mycobacterium tuberculosis and Mycobacterium bovis BCG.
Evidence of transmission of tuberculosis by DNA fingerprinting.
Genetic polymorphisms among Mycobacterium tuberculosis isolates from patients with pulmonary tuberculosis in northern India.
Genetic relatedness among Mycobacterium tuberculosis and M. bovis.
Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain.
Genomic mutations in the katG, inhA and aphC genes are useful for the prediction of isoniazid resistance in Mycobacterium tuberculosis isolates from Kwazulu Natal, South Africa.
Host-mediated modification of PvuII restriction in Mycobacterium tuberculosis.
Identification of a restriction fragment length polymorphism associated with a deletion that maps in a transcriptionally active open-reading frame, orfX, in Mycobacterium tuberculosis Erdman.
Identification of an IS6110 insertion site in plcD, the unique phospholipase C gene of Mycobacterium bovis.
Influence of vitamin D deficiency and vitamin D receptor polymorphisms on tuberculosis among Gujarati Asians in west London: a case-control study.
Insertion element IS1081-associated restriction fragment length polymorphisms in Mycobacterium tuberculosis complex species: a reliable tool for recognizing Mycobacterium bovis BCG.
Isolation and restriction endonuclease analysis of mycobacterial DNA.
Limited variation of DNA fingerprints (IS6110 and IS1081) in Korean strains of Mycobacterium tuberculosis.
Molecular analysis of isoniazid resistance in Mycobacterium tuberculosis isolates recovered from South Korea.
Molecular Epidemiology of Mycobacterium tuberculosis Isolates in 100 Patients With Tuberculosis Using Pulsed Field Gel Electrophoresis.
Molecular epidemiology of tuberculosis in Austria.
Molecular evolution of Mycobacterium tuberculosis: phylogenetic reconstruction of clonal expansion.
Mycobacterium bovis infection in goats from the Northeast region of Brazil.
Mycobacterium tuberculosis infection within Warthin's tumor: report of two cases.
One-tube loop-mediated isothermal amplification combined with restriction endonuclease digestion and ELISA for colorimetric detection of resistance to isoniazid, ethambutol and streptomycin in Mycobacterium tuberculosis isolates.
PCR restriction fragment length polymorphism analysis (PRA)-algorithm targeting 644 bp Heat Shock Protein 65 (hsp65) gene for differentiation of Mycobacterium spp.
PCR-restriction fragment length polymorphism for rapid, low-cost identification of isoniazid-resistant Mycobacterium tuberculosis.
Preliminary studies on the detection ofMycobacterium avium-intracellulare complex using DNA probe from a clinical isolate.
Rapid detection and species identification of mycobacteria in paraffin-embedded tissues by polymerase chain reaction.
Rapid identification of Mycobacterium tuberculosis and Mycobacterium avium by polymerase chain reaction and restriction enzyme analysis within sigma factor regions.
Recent nosocomial transmission and genotypes of multidrug-resistant Mycobacterium tuberculosis.
Restriction endonuclease analysis as a solution for determining rifampin resistance mutations by automated DNA sequencing in heteroresistant Mycobacterium tuberculosis strains.
Restriction endonuclease analysis of total deoxyribonucleic acid of Mycobacterium tuberculosis H37RV (ATCC 27294) and of M. bovis (ATCC 19210).
Restriction fragment analysis of chromosomal DNA defines different strains of Mycobacterium tuberculosis.
Species-specific identification of Mycobacterium bovis by PCR.
Study of the gyrB gene polymorphism as a tool to differentiate among Mycobacterium tuberculosis complex subspecies further underlines the older evolutionary age of 'Mycobacterium canettii'.
The detection of mycobacterial DNA sequences in uncultured clinical specimens with cloned Mycobacterium tuberculosis DNA as probes.
The re-emergence of Mycobacterium bovis infection in brushtail possums (Trichosurus vulpecula) after localised possum eradication.
The susceptibility of Mycobacterium tuberculosis to isoniazid and the Arg-->Leu mutation at codon 463 of katG are not associated.
Tuberculosis in a New Zealand (Hooker's) sea lion (abstract).
Tuberculosis in captive seals: bacteriological studies on an isolate belonging to the Mycobacterium tuberculosis complex.
Typing Method for the QUB11a Locus of Mycobacterium tuberculosis: IS6110 Insertions and Tandem Repeat Analysis.
Use of restriction enzyme analysis of amplified DNA coding for the hsp65 gene and polymerase chain reaction with universal primer for rapid differentiation of mycobacterium species in the clinical laboratory.
[A micro-epidemic of tuberculosis in the South Moravia Region]
[Application of RFLP to typing strains of Mycobacterium tuberculosis]
[Construction and immunogenicity of DNA vaccine encoding secreted form of Ag85B protein of Mycobacterium tuberculosis]
[Establishment and application of a standard IS6110-RFLP method in the study of molecular genotyping analysis on Mycobacterium tuberculosis]
[Fingerprinting of mycobacterial DNA in the molecular epidemiology of tuberculosis]
[Human transmission of tuberculosis confirmed by DNA fingerprinting]
[Methodology of DNA fingerprinting and its application in identification of M. tuberculosis]
[Usefulness of polymerase chain reaction for the diagnosis of Bazin erythema induratum]
Tuberculosis, Bovine
Comparison of 45 variable number tandem repeat (VNTR) and two direct repeat (DR) assays to restriction endonuclease analysis for typing isolates of Mycobacterium bovis.
Geographic distribution of restriction types of Mycobacterium bovis isolates from brush-tailed possums (Trichosurus vulpecula) in New Zealand.
Tuberculosis, Pulmonary
Restriction enzyme analysis of the hsp65 gene in clinical isolates from patients suspected of having pulmonary tuberculosis in Teresina, Brazil.
Tuberous Sclerosis
An EcoRV polymorphism in exon 40 of the tuberous sclerosis 2 (TSC2) gene.
Tumor Virus Infections
African swine fever virus guanylyltransferase.
Characterization, molecular cloning, and physical mapping of the Shope fibroma virus genome.
Identification and DNA sequence of the large subunit of the capping enzyme from Shope fibroma virus.
Identification and DNA sequence of the Shope fibroma virus DNA topoisomerase gene.
Identification of a poxvirus gene encoding a uracil DNA glycosylase.
Physical characterization and molecular cloning of the Shope fibroma virus DNA genome.
Sequence and analysis of the BamHI "D" fragment of Shope fibroma virus: comparison with similar regions of related poxviruses.
Tumorigenic poxviruses: construction of the composite physical map of the Shope fibroma virus genome.
Turner Syndrome
Molecular diagnosis of Turner's syndrome.
Typhus, Epidemic Louse-Borne
A recombinant Rickettsia conorii vaccine protects guinea pigs from experimental boutonneuse fever and Rocky Mountain spotted fever.
Approaches to the molecular epidemiology of rickettsioses.
Differentiation among spotted fever group rickettsiae species by analysis of restriction fragment length polymorphism of PCR-amplified DNA.
Flying squirrel-associated Rickettsia prowazekii (epidemic typhus rickettsiae) characterized by a specific DNA fragment produced by restriction endonuclease digestion.
Tyrosinemias
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.
Urethritis
Genomic fingerprinting of penicillinase-producing strains of Neisseria gonorrhoeae in Valencia, Spain.
Restriction endonuclease analysis and ribotyping differentiate genital and nongenital strains of Bacteroides ureolyticus.
Urinary Bladder Neoplasms
Abnormal c-myc oncogene DNA methylation in human bladder cancer: possible role in tumor progression.
DNA hypermethylation on multiple CpG islands associated with increased DNA methyltransferase DNMT1 protein expression during multistage urothelial carcinogenesis.
Screening of human bladder tumors and urine sediments for the presence of H-ras mutations.
The human c-ras1H oncogene: a mutation in normal and neoplastic tissue from the same patient.
Urinary Tract Infections
Genetic relationship between thirteen genome types of adenovirus 11, 34, and 35 with different tropisms.
Molecular cloning and physical characterization of a chromosomal hemolysin from Escherichia coli.
Uterine Cervical Neoplasms
Cytoplasmic NANOG-positive stromal cells promote human cervical cancer progression.
Epstein-Barr virus plays little role in cervical carcinogenesis in Korean women.
Interleukin-10 promoter polymorphisms and cervical cancer risk in Korean women.
The DNA binding domain of a papillomavirus E2 protein programs a chimeric nuclease to cleave integrated human papillomavirus DNA in HeLa cervical carcinoma cells.
Uveitis, Anterior
Polymorphism in the LMP2 gene influences susceptibility to extraspinal disease in HLA-B27 positive individuals with ankylosing spondylitis.
Vaccinia
A human homolog of the vaccinia virus HindIII K4L gene is a member of the phospholipase D superfamily.
A poxvirus-derived vector that directs high levels of expression of cloned genes in mammalian cells.
A poxvirus-encoded uracil DNA glycosylase is essential for virus viability.
A single nucleotide substitution in the 5'-untranslated region of the vaccinia N2L gene is responsible for both alpha-amanitin-resistant and temperature-sensitive phenotypes.
A vaccinia virus isatin-beta-thiosemicarbazone resistance mutation maps in the viral gene encoding the 132-kDa subunit of RNA polymerase.
African swine fever virus guanylyltransferase.
An orthopoxvirus serpinlike gene controls the ability of infected cells to fuse.
Analysis of a large cluster of nonessential genes deleted from a vaccinia virus terminal transposition mutant.
Arrangement of late RNAs transcribed from a 7.1-kilobase EcoRI vaccinia virus DNA fragment.
Association of vaccinia virus-expressed adenovirus E3-19K glycoprotein with class I MHC and its effects on virulence in a murine pneumonia model.
Attenuated deletion mutant of vaccinia virus IHD-W recovered virulence by reinsertion of a terminal restriction fragment.
Biogenesis of poxviruses: mirror-image deletions in vaccinia virus DNA.
Biological evaluation of glycoproteins mapping to two distinct mRNAs within the BamHI fragment 7 of pseudorabies virus: expression of the coding regions by vaccinia virus.
Characteristics of four cowpox virus isolates from Norway and Sweden.
Characterization, molecular cloning, and physical mapping of the Shope fibroma virus genome.
Cleavage of vaccinia virus DNA by restriction endonuclease Bal I, Eco R1, Bam HI. Isolation of the natural cross-links.
Conservation and variation in Orthopoxvirus genome structure.
Conservation of gene structure and arrangement between vaccinia virus and orf virus.
Conserved TAAATG sequence at the transcriptional and translational initiation sites of vaccinia virus late genes deduced by structural and functional analysis of the HindIII H genome fragment.
Construction of chimeric vaccinia viruses by molecular cloning and packaging.
DNA sequence analysis of conserved and unique regions of swinepox virus: identification of genetic elements supporting phenotypic observations including a novel G protein-coupled receptor homologue.
Effect of in vitro mutations in a vaccinia virus early promoter region monitored by herpes simplex virus thymidine kinase expression in recombinant vaccinia virus.
Expression of cloned vaccinia virus DNA sequences introduced into animal cells.
Extension of the transcriptional and translational map of the left end of the vaccinia virus genome to 21 kilobase pairs.
Fine structure analysis and nucleotide sequence of the vaccinia virus thymidine kinase gene.
Fine structure marker rescue of temperature-sensitive mutations of vaccinia virus within a central conserved region of the genome.
Gene translocations in poxviruses: the fowlpox virus thymidine kinase gene is flanked by 15 bp direct repeats and occupies the locus which in vaccinia virus is occupied by the ribonucleotide reductase large subunit gene.
General method for production and selection of infectious vaccinia virus recombinants expressing foreign genes.
Genetic analysis of vaccinia virus Lister strain and its attenuated mutant LC16m8: production of intermediate variants by homologous recombination.
Genetic instability of vaccinia virus containing artificially duplicated genome regions.
Genetic map of the vaccinia virus HindIII D Fragment.
Genomic characterization of a poxvirus isolated from a child.
HindIII and Sst I restriction sites mapped on rabbit poxvirus and vaccinia virus DNA.
Host range selection of vaccinia recombinants containing insertions of foreign genes into non-coding sequences.
Identification and cloning of the fowlpox virus thymidine kinase gene using vaccinia virus.
Identification and DNA sequence of the large subunit of the capping enzyme from Shope fibroma virus.
Identification of the DNA sequences encoding the large subunit of the mRNA-capping enzyme of vaccinia virus.
Increased turnover of vaccinia virus-specific immediate early RNAs in interferon-treated chick embryo fibroblasts.
Insertion sites for recombinant vaccinia virus construction: effects on expression of a foreign protein.
Intermolecular duplexes formed from polyadenylylated vaccinia virus RNA.
Inverted terminal repeats in rabbit poxvirus and vaccinia virus DNA.
Involvement of spicules in the formation of vaccinia virus envelopes elucidated by a conditional lethal mutant.
Map positions of the 5' ends of eight mRNAs synthesized from the late genes in the vaccinia virus HindIII D fragment.
Mapping and nucleotide sequence of the vaccinia virus gene that encodes a 14-kilodalton fusion protein.
Mapping of a vaccinia host range sequence by insertion into the viral thymidine kinase gene.
Mapping the genomic location of the gene encoding alpha-amanitin resistance in vaccinia virus mutants.
Mapping thymidine kinase-deficient mutants of vaccinia virus by marker rescue with hybrid plasmid DNAs containing portions of the HindIII-J fragment of virus DNA.
Marker rescue of temperature-sensitive mutations of vaccinia virus WR: correlation of genetic and physical maps.
Molecular dissection of cis-acting regulatory elements from 5'-proximal regions of a vaccinia virus late gene cluster.
Multiple-cloning-site plasmids for the rapid construction of recombinant poxviruses.
Neutralizing epitope on penetration protein of vaccinia virus.
Non-essential genes in the vaccinia virus HindIII K fragment: a gene related to serine protease inhibitors and a gene related to the 37K vaccinia virus major envelope antigen.
Nucleotide sequence analysis of a 10.5 kbp HindIII fragment of fowlpox virus: relatedness to the central portion of the vaccinia virus HindIII D region.
Nucleotide sequence and genetic map of the 16-kb vaccinia virus HindIII D fragment.
Nucleotide sequence and molecular genetic analysis of the large subunit of ribonucleotide reductase encoded by vaccinia virus.
Nucleotide sequence and molecular genetic analysis of the vaccinia virus HindIII N/M region encoding the genes responsible for resistance to alpha-amanitin.
Nucleotide sequence and transcript organization of a region of the vaccinia virus genome which encodes a constitutively expressed gene required for DNA replication.
One time intranasal vaccination with a modified vaccinia Tiantan strain MVTT(ZCI) protects animals against pathogenic viral challenge.
Organization of RNA transcripts from a vaccinia virus early gene cluster.
Organization of six early transcripts synthesized from a vaccinia virus EcoRI DNA fragment.
Orthopoxvirus DNA: a comparison of restriction profiles and maps.
Phosphorylation of vaccinia virus core proteins during transcription in vitro.
Procedure for purification of intact DNA from vaccinia virus.
Purification and identification of a vaccinia virus-encoded intermediate stage promoter-specific transcription factor that has homology to eukaryotic transcription factor SII (TFIIS) and an additional role as a viral RNA polymerase subunit.
Resolution of vaccinia virus DNA concatemer junctions requires late-gene expression.
Restriction enzyme digests of rapidly renaturing fragments of vaccinia virus DNA.
Restriction enzyme mapping of vaccinia virus DNA.
Retroviral protease-like gene in the vaccinia virus genome.
Selective inhibition of protein synthesis by synthetic and vaccinia virus-core synthesized poly(riboadenylic acids).
Selective inhibition of viral gene expression as the mechanism of the antiviral action of PGA1 in vaccinia virus-infected cells.
Sequence analysis, expression, and deletion of a vaccinia virus gene encoding a homolog of profilin, a eukaryotic actin-binding protein.
Sequence and analysis of the BamHI "D" fragment of Shope fibroma virus: comparison with similar regions of related poxviruses.
Sequence and transcriptional analysis of the vaccinia virus HindIII I fragment.
Similar genetic organization between a region of fowlpox virus DNA and the vaccinia virus HindIII J fragment despite divergent location of the thymidine kinase gene.
Structure of the transcription initiation and termination sequences of seven early genes in the vaccinia virus HindIII D fragment.
Symmetrical arrangement of the heterologous regions of rabbit poxvirus and vaccinia virus DNA.
The second-largest subunit of the poxvirus RNA polymerase is similar to the corresponding subunits of procaryotic and eucaryotic RNA polymerases.
The vaccinia virus HindIII F fragment: nucleotide sequence of the left 6.2 kb.
The vaccinia virus HindIII K fragment encodes a novel protein belonging to the serpin superfamily.
Tn9 CAT gene contains a promoter for vaccinia virus transcription: implications for reverse-genetic techniques.
Transcription and translation mapping of the 13 genes in the vaccinia virus HindIII D fragment.
Transcriptional and translational analysis of a strongly expressed early region of the vaccinia virus genome.
Transcriptional and translational analysis of the vaccinia virus late gene L65.
Transcriptional and translational mapping of a 6.6-kilobase-pair DNA fragment containing the junction of the terminal repetition and unique sequence at the left end of the vaccinia virus genome.
Translation of reovirus RNA species m1 can initiate at either of the first two in-frame initiation codons.
Use of a restriction endonuclease in analyzing the genomes from two different strains of vaccinia virus.
Vaccinia keratouveitis manifesting as a masquerade syndrome.
Vaccinia virus gene D12L encodes the small subunit of the viral mRNA capping enzyme.
Vaccinia virus gene D8 encodes a virion transmembrane protein.
Vaccinia virus gene encoding a 30-kilodalton subunit of the viral DNA-dependent RNA polymerase.
Vaccinia virus host range genes.
Vaccinia virus morphogenesis is blocked by temperature-sensitive mutations in the F10 gene, which encodes protein kinase 2.
Vaccinia virus morphogenesis is interrupted when expression of the gene encoding an 11-kilodalton phosphorylated protein is prevented by the Escherichia coli lac repressor.
Vaccinia virus-encoded ribonucleotide reductase: sequence conservation of the gene for the small subunit and its amplification in hydroxyurea-resistant mutants.
Vaccinia virus-specific human CD4+ cytotoxic T-lymphocyte clones.
Variation in the HindIII restriction fragments of DNA from the Chinese Tian Tan strain of vaccinia virus.
[Analysis of vaccinia virus genome with restriction endonucleases EcoRI, BamHI, KpnI and HindIII]
[Cloning, sequencing and translation analysis of the Vaccinia virus LIVP HINDIII N genome fragment]
[Comparative restriction analysis of HindIII-F-fragments of DNA from 4 strains of vaccinia virus]
[Mapping of "nonessential" regions in the genome of vaccinia virus]
[Molecular-biological study of vaccinia virus genome. I. Cloning of vaccinia virus DNA fragments in bacterial vectors]
Vaginal Discharge
[25S intron analysis followed by restriction enzyme digestion performed for genotyping Candida albicans isolates].
Vascular Diseases
Genetics of the lipoprotein lipase gene and hypertriglyceridaemia.
Polymorphisms of the lipoprotein lipase gene are associated with atherosclerotic cerebral infarction in the Chinese.
Venous Thrombosis
Association of estrogen receptor-alpha genepolymorphisms with venous thrombosis.
Fibrinogen polymorphisms TaqI, HaeIII and BclI are not associated with a higher risk of deep vein thrombosis.
Frequency of the 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene in 35 cases of cerebral venous thrombosis.
Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease.
Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
Venous thrombosis in relation to fibrinogen and factor VII genes among African-Americans.
Viremia
A Novel Live Attenuated Vaccine Candidate Protects Against Heterologous Senecavirus A Challenge.
Virus Diseases
Activation of human herpesviruses 6 and 7 in patients with chronic fatigue syndrome.
Characterization of an Indian bluetongue virus isolate by RT-PCR and restriction enzyme analysis of the VP-7 gene sequence.
Cytomegalovirus glycoprotein B groups associated with retinitis in AIDS.
Expression of functional human interleukin-2 receptors in murine interleukin-3-dependent cells.
Expression of genes introduced into cells by retroviral infection is more efficient than that of genes introduced into cells by DNA transfection.
Genomic variation of adenovirus type 5 isolates recovered from bone marrow transplant recipients.
IL-3A virus infection of a Chlorella-like green alga induces a DNA restriction endonuclease with novel sequence specificity.
In vitro and in vivo transcription initiation sites on the TK-encoding BamHI Q fragment of HSV-1 DNA.
Mapping of genes in BamHI fragment M of Epstein-Barr virus DNA that may determine the fate of viral infection.
Presence of human papilloma virus types 16 and 18 in genital warts and cervical neoplasias.
Restriction endonuclease activity induced by NC-1A virus infection of a Chlorella-like green alga.
Restriction endonuclease activity induced by PBCV-1 virus infection of a Chlorella-like green alga.
Selective inhibition of viral gene expression as the mechanism of the antiviral action of PGA1 in vaccinia virus-infected cells.
Sequence arrangement of the 5' ends of simian virus 40 16S and 19S mRNAs.
Temporal cluster of herpes simplex encephalitis: investigation by restriction endonuclease cleavage of viral DNA.
The Need for Speed: Run-On Oligomer Filament Formation Provides Maximum Speed with Maximum Sequestration of Activity.
Topography of polyoma virus messenger RNA molecules.
Two forms of restriction enzyme HindIII.
Visna
Characteristics of a novel lentivirus derived from South African sheep with pulmonary adenocarcinoma (jaagsiekte).
Isolation and identification of a South African lentivirus from jaagsiekte lungs.
Molecular cloning of unintegrated visna viral DNA and characterization of frequent deletions in the 3' terminus.
Vitiligo
Analysis of the effect of endogenous viral genes in the Smyth line chicken model for autoimmune vitiligo.
Genetic association of the catalase gene (CAT) with vitiligo susceptibility.
von Willebrand Diseases
An infrequent DNA polymorphism associated with severe von Willebrand's disease.
Vulvovaginitis
Bovine herpesvirus 1: differentiation of IBR- and IPV-viruses and identification and functional role of their major immunogenic components.
Characterization of bovine herpesviruses isolated from six sheep and four goats by restriction endonuclease analysis and radioimmunoprecipitation.
Comparative study of two strains of Bovid herpesvirus-4.
Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustular vulvovaginitis virus strains by restriction endonuclease analysis.
Molecular cloning of DNA from a bovine herpesvirus 1 strain isolated in Hungary.
Warts
Analysis of the structure of human papilloma virus DNA.
Characterization of human papillomavirus 3 in warts of a renal allograft patient.
Detection and identification of human papillomavirus types isolated from Korean patients with flat warts.
Effect of oral aromatic retinoid (Ro 10-9359) on human papilloma virus-2-induced common warts.
Immunology of human warts.
Linkage of regression and malignant conversion of rabbit viral papillomas to MHC class II genes.
Molecular and biological characterization of cottontail rabbit papillomavirus variant DNA sequences integrated in the VX7 carcinoma.
Molecular cloning, refined physical map and heterogeneity of methylation sites of papilloma virus type 1a DNA.
Papillomaviruses with unusual restriction endonuclease profiles from bovine skin warts.
Whooping Cough
Antigenic analysis of Bordetella pertussis filamentous hemagglutinin with phage display libraries and rabbit anti-filamentous hemagglutinin polyclonal antibodies.
Bordetella parapertussis and Bordetella bronchiseptica contain transcriptionally silent pertussis toxin genes.
Cloning of the virulence regulatory (vir) locus of Bordetella pertussis and its expression in B. bronchiseptica.
Evidence for a DNA inversion system in Bordetella pertussis.
Identification of Bordetella pertussis in a critically ill human immunodeficiency virus-infected patient by direct genotypical analysis of Gram-stained material and discrimination from B. holmesii by using a unique recA gene restriction enzyme site.
Isolation of a repeated DNA sequence from Bordetella pertussis.
Phase variants of Bordetella bronchiseptica arise by spontaneous deletions in the vir locus.
Plasmid transfer to Bordetella pertussis: conjugation and transformation.
Strain variation among Bordetella pertussis isolates in finland, where the whole-cell pertussis vaccine has been used for 50 years.
The isolation of a restriction enzyme from Bordetella pertussis.
Validation of nested Bordetella PCR in pertussis vaccine trial.
[Isolation and purification of restriction endonuclease BpeI from Bordetella pertussis]
[Nucleotide sequence and properties of a transposon-like structure cloned from a Bordetella pertussis chromosome]
[Structural organization of a segment of chromosome, containing the vir gene of Bordetella pertussis]
Wilms Tumor
Allele frequency of HinfI restriction fragment length polymorphism (RFLP) and dinucleotide repeat polymorphism in the Wilms tumor gene (WT1) among the Japanese.
Avian nephroblastomas induced by a retrovirus (MAV-2) lacking oncogene. II. Search for common sites of proviral integration in tumour DNA.
HinfI polymorphism within the 3' untranslated region of the candidate Wilms tumour gene.
Localization of the human CD59 gene by fluorescence in situ hybridization and pulsed-field gel electrophoresis.
Mapping and characterization of 129 cosmids on human chromosome 11p.
[Increased expression of IGF-2 in tumor tissue of nephroblastoma]
Wound Infection
Restriction fragment analysis of a Candida tropicalis outbreak of sternal wound infections.
Xanthomatosis
Characterization of genetic markers in the 3' end of the apo B gene and their use in family and population studies.
Xeroderma Pigmentosum
Requirement of ATM in phosphorylation of the human p53 protein at serine 15 following DNA double-strand breaks.
Yersinia Infections
Application of restriction endonuclease analysis and genetic probes in the epidemiology of Yersinia enterocolitica infection.
Yersinia pseudotuberculosis Infections
Restriction endonuclease analysis of plasmid DNA of Yersinia pseudotuberculosis infections in Shimane Prefecture, Japan.
Restriction endonuclease analysis of virulence plasmids for molecular epidemiology of Yersinia pseudotuberculosis infections.