3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1986686&form=6&db=m Prevalence of Mycobacterium avium complex in respiratory specimens from AIDS and non-AIDS patients in a San Francisco hospital. diagnostic usage,ongoing research,unassigned 1,2,0 3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2305441&form=6&db=m Red cell transfusion therapy for anemia in patients with AIDS and ARC: incidence, associated factors, and outcome. causal interaction,unassigned 2,0 3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2345428&form=6&db=m Renal involvement in patients infected with HIV: experience at San Francisco General Hospital. diagnostic usage,ongoing research,unassigned 1,2,0 3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3777686&form=6&db=m Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization. causal interaction,therapeutic application,unassigned 4,2,0 3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9735689&form=6&db=m Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Acquired Immunodeficiency Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23607844&form=6&db=m A strange new disease in San Francisco:a brief history of the city and its response to the HIV/AIDS epidemic. unassigned - 3.1.2.12 Adenocarcinoma of Lung http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21596165&form=6&db=m Activity-based proteomics: Identification of ABHD11 and ESD activities as potential biomarkers for human lung adenocarcinoma. ongoing research,unassigned 1,0 3.1.2.12 Agranulocytosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10503166&form=6&db=m A placebo-controlled trial of the immune modulator, lentinan, in HIV-positive patients: a phase I/II trial. causal interaction,therapeutic application,unassigned 1,2,0 3.1.2.12 Alzheimer Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19717305&form=6&db=m Synthesis of organophosphates with fluorine-containing leaving groups as serine esterase inhibitors with potential for Alzheimer disease therapeutics. causal interaction,therapeutic application,unassigned 4,4,0 3.1.2.12 Amyloidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2068530&form=6&db=m Fibril amyloid enhancing factor (FAEF)-accelerated amyloidosis in the hamster is not dependent on serine esterase activity and mononuclear phagocytosis. unassigned - 3.1.2.12 Amyloidosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2860918&form=6&db=m Activities of lysosomal enzymes and levels of serum amyloid A (SAA) in blood plasma of hamsters during casein induction of AA-amyloidosis. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Anaphylaxis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=84487&form=6&db=m Diisopropylfluorophosphate-evoked inhibition of anaphylactic histamine release from human skin: decrease of the inhibition by storing the skin specimens. unassigned - 3.1.2.12 Anaphylaxis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6224392&form=6&db=m Characterization of two strains of selectively bred guinea-pigs. I. Skin transplantation experiments and screening for erythrocyte enzyme polymorphism. diagnostic usage,ongoing research,unassigned 3,1,0 3.1.2.12 Anaphylaxis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10503166&form=6&db=m A placebo-controlled trial of the immune modulator, lentinan, in HIV-positive patients: a phase I/II trial. causal interaction,therapeutic application,unassigned 1,2,0 3.1.2.12 Aniridia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6298811&form=6&db=m Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories. causal interaction,diagnostic usage,unassigned 2,2,0 3.1.2.12 Bone Resorption http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3342254&form=6&db=m Inhibition of bone resorption in vitro by serine-esterase inhibitors. ongoing research,unassigned 2,0 3.1.2.12 Carcinogenesis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3508413&form=6&db=m [Retinoblastoma and esterase D II. The oncogenesis of retinoblastoma and the phenotype of esterase D] diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Carcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=686669&form=6&db=m The esterase D polymorphism in patients with diabetes or carcinoma of the bladder and a matched sample of non-donor controls. causal interaction,diagnostic usage,ongoing research,unassigned 2,2,4,0 3.1.2.12 Carcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11092615&form=6&db=m Expression of acute and late-stage inflammatory antigens, c-fms, CSF-1, and human monocytic serine esterase 1, in tumor-associated macrophages of renal cell carcinomas. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,3,0 3.1.2.12 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11884245&form=6&db=m Differential inhibition of hepatic, pancreatic, and plasma fatty acid ethyl ester synthase by tri-o-tolylphosphate in rats. ongoing research,unassigned 2,0 3.1.2.12 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33206527&form=6&db=m Potential Regulatory Role of Human-Carboxylesterase-1 Glycosylation in Liver Cancer Cell Growth. diagnostic usage,unassigned 3,0 3.1.2.12 Carcinoma, Renal Cell http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11092615&form=6&db=m Expression of acute and late-stage inflammatory antigens, c-fms, CSF-1, and human monocytic serine esterase 1, in tumor-associated macrophages of renal cell carcinomas. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,3,0 3.1.2.12 Cholera http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1646113&form=6&db=m Interleukin 2 counteracts the inhibition of cytotoxic T lymphocytes by cholera toxin in vitro and in vivo. ongoing research,therapeutic application,unassigned 3,1,0 3.1.2.12 Cholera http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1828826&form=6&db=m Lack of target cell participation in cytotoxic T lymphocyte-mediated lysis. unassigned - 3.1.2.12 Colonic Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2297043&form=6&db=m Colonic aberrant crypts in azoxymethane-treated F344 rats have decreased hexosaminidase activity. causal interaction,unassigned 3,0 3.1.2.12 Communicable Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9735689&form=6&db=m Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Diabetic Nephropathies http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18588510&form=6&db=m Renal oxidative stress and nitric oxide production in streptozotocin-induced diabetic nephropathy in rats: the possible modulatory effects of garlic (Allium sativum L.). causal interaction,diagnostic usage,therapeutic application,unassigned 4,1,2,0 3.1.2.12 Digestive System Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7184301&form=6&db=m [Acid phosphatase activity and non-specific esterase D of alpha-naphthyl acetate in the lymphocytes of patients with digestive system neoplasms after surgical treatment] diagnostic usage,unassigned 2,0 3.1.2.12 Endometriosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9102363&form=6&db=m [Genetic aspects of endometriosis: features of the distribution of polymorphic gene frequencies] diagnostic usage,ongoing research,unassigned 2,1,0 3.1.2.12 Foot-and-Mouth Disease http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27267271&form=6&db=m Esterase D enhances type I interferon signal transduction to suppress foot-and-mouth disease virus replication. ongoing research,unassigned 1,0 3.1.2.12 Gardner Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3991240&form=6&db=m Benign epithelial polyps of the stomach. causal interaction,unassigned 3,0 3.1.2.12 Glioblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2838156&form=6&db=m A human glioblastoma line with karyotypic nullisomy 13 containing several chromosome 13-specific sequences. ongoing research,therapeutic application,unassigned 2,1,0 3.1.2.12 Granuloma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6609969&form=6&db=m Fibroblast stimulation in schistosomiasis. V. Egg granuloma macrophages spontaneously secrete a fibroblast-stimulating factor. ongoing research,therapeutic application,unassigned 2,1,0 3.1.2.12 Hematologic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9735689&form=6&db=m Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Hepatitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2115090&form=6&db=m Mechanism of killing by virus-induced cytotoxic T lymphocytes elicited in vivo. ongoing research,therapeutic application,unassigned 3,1,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1679032&form=6&db=m Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan. ongoing research,unassigned 2,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2563776&form=6&db=m Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis. causal interaction,diagnostic usage,ongoing research,unassigned 1,2,2,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3164702&form=6&db=m Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3456572&form=6&db=m A sialic acid-specific O-acetylesterase in human erythrocytes: possible identity with esterase D, the genetic marker of retinoblastomas and Wilson disease. diagnostic usage,ongoing research,unassigned 1,2,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3459695&form=6&db=m Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method. diagnostic usage,ongoing research,unassigned 2,1,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3462698&form=6&db=m Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3474893&form=6&db=m Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. causal interaction,ongoing research,unassigned 2,1,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3856863&form=6&db=m Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus. causal interaction,unassigned 1,0 3.1.2.12 Hepatolenticular Degeneration http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8432554&form=6&db=m Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease. causal interaction,diagnostic usage,ongoing research,therapeutic application 1,1,4,1 3.1.2.12 Hydatidiform Mole http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6453910&form=6&db=m [Polymorphic studies of the etiological mechanism of hydatidiform mole using phosphoglucomutase-1 and esterase D] unassigned - 3.1.2.12 Hypertension http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20739164&form=6&db=m Potential of garlic and its active constituent, S-allyl cysteine, as antihypertensive and cardioprotective in presence of captopril. unassigned - 3.1.2.12 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2610220&form=6&db=m Infection of the health-care worker by HIV and other blood-borne viruses: risks, protection, and education. unassigned - 3.1.2.12 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9263127&form=6&db=m Inhibition of tryptase TL2 from human T4+ lymphocytes and inhibition of HIV-1 replication in H9 cells by recombinant aprotinin and bikunin homologues. ongoing research,unassigned 2,0 3.1.2.12 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10481961&form=6&db=m Paediatric nosocomial urinary tract infection at a regional hospital. ongoing research,unassigned 1,0 3.1.2.12 Influenza, Human http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9820488&form=6&db=m Selective induction of CD8+ cytotoxic T lymphocyte effector function by staphylococcus enterotoxin B. ongoing research,therapeutic application,unassigned 2,1,0 3.1.2.12 Influenza, Human http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28437488&form=6&db=m The novel carboxylesterase 1 variant c.662A>G may decrease the bioactivation of oseltamivir in humans. therapeutic application,unassigned 4,0 3.1.2.12 Leprosy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=162080&form=6&db=m Genetic markers and leprosy in South African negroes: Part II. Erythrocyte enzyme polymorphisms. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,1,0 3.1.2.12 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=448121&form=6&db=m IgE mediated triggering of rat basophil leukemia cells: lack of evidence for serine esterase activation. ongoing research,unassigned 3,0 3.1.2.12 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2497282&form=6&db=m Demonstration of the increase in serine esterase-positive T cells in hairy-cell leukemia patients undergoing alpha-interferon therapy. causal interaction,therapeutic application,unassigned 3,1,0 3.1.2.12 Leukemia, Myeloid, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24085543&form=6&db=m Esterase D and gamma 1 actin level might predict results of induction therapy in patients with acute myeloid leukemia without and with maturation. causal interaction,diagnostic usage,therapeutic application,unassigned 4,3,2,0 3.1.2.12 Lymphadenopathy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1806183&form=6&db=m [In situ production and possible role of interleukins in clinical immunopathology] unassigned - 3.1.2.12 Lymphocytosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2036661&form=6&db=m Lymphocyte activation and serine-esterase induction following recombinant interleukin-2 infusion for lymphomas and acute leukaemias. causal interaction,unassigned 2,0 3.1.2.12 Lymphoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2522906&form=6&db=m T-cell activation. I. Evidence for a functional linkage between class I MHC antigens and the Tc-Ti complex. ongoing research,unassigned 3,0 3.1.2.12 Migraine Disorders http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7553809&form=6&db=m Genetic markers: association study in migraine. causal interaction,unassigned 1,0 3.1.2.12 Nasopharyngeal Carcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15995522&form=6&db=m Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma. causal interaction,diagnostic usage,therapeutic application,unassigned 2,4,3,0 3.1.2.12 Neoplasm Metastasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21596165&form=6&db=m Activity-based proteomics: Identification of ABHD11 and ESD activities as potential biomarkers for human lung adenocarcinoma. ongoing research,unassigned 1,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2115090&form=6&db=m Mechanism of killing by virus-induced cytotoxic T lymphocytes elicited in vivo. ongoing research,therapeutic application,unassigned 3,1,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2596526&form=6&db=m Esterase D assay in Brazilian retinoblastoma families. diagnostic usage,ongoing research,unassigned 2,2,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2878716&form=6&db=m Chromosome 13 instability and esterase D expression in an osteosarcoma cell line. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,4,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3164261&form=6&db=m Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastoma. causal interaction,diagnostic usage,ongoing research,therapeutic application 4,3,2,1 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3471703&form=6&db=m A null allele of esterase D is a marker for genetic events in retinoblastoma formation. diagnostic usage,ongoing research,unassigned 1,3,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3666787&form=6&db=m Antibody-dependent tumour cytolysis by human neutrophils: effect of synthetic serine esterase inhibitors and substrates. ongoing research,therapeutic application,unassigned 2,1,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6336308&form=6&db=m Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6823558&form=6&db=m Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. ongoing research,therapeutic application,unassigned 4,1,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6877367&form=6&db=m Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma. causal interaction,unassigned 4,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7184301&form=6&db=m [Acid phosphatase activity and non-specific esterase D of alpha-naphthyl acetate in the lymphocytes of patients with digestive system neoplasms after surgical treatment] diagnostic usage,unassigned 2,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8058730&form=6&db=m Immunotherapy with anti-CD3 monoclonal antibodies and recombinant interleukin 2: stimulation of molecular programs of cytotoxic killer cells and induction of tumor regression. therapeutic application,unassigned 2,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11069717&form=6&db=m Cationic lipid gene transfer of an IL-2 transgene leads to activation of natural killer cells in a SCID mouse human tumor xenograft. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15995522&form=6&db=m Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma. causal interaction,diagnostic usage,therapeutic application,unassigned 2,4,3,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25221997&form=6&db=m Compound A398, a novel podophyllotoxin analogue: cytotoxicity and induction of apoptosis in human leukemia cells. ongoing research,unassigned 4,0 3.1.2.12 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32757998&form=6&db=m Phytochemical Profile, and Antiproliferative and Proapoptotic Effects of Pouteria ramiflora (Mart.) Radlk. Leaf Extract, and Its Synergism with Cisplatin in HepG2 Cells. causal interaction,ongoing research,unassigned 1,4,0 3.1.2.12 Obesity http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16355479&form=6&db=m An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study. diagnostic usage,therapeutic application,unassigned 3,1,0 3.1.2.12 Osteosarcoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2878716&form=6&db=m Chromosome 13 instability and esterase D expression in an osteosarcoma cell line. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,4,0 3.1.2.12 Otosclerosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34471729&form=6&db=m Personalized Proteomics for Precision Diagnostics in Hearing Loss: Disease-Specific Analysis of Human Perilymph by Mass Spectrometry. unassigned - 3.1.2.12 Pneumonia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3777686&form=6&db=m Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization. causal interaction,therapeutic application,unassigned 4,2,0 3.1.2.12 Pneumonia, Pneumocystis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3777686&form=6&db=m Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization. causal interaction,therapeutic application,unassigned 4,2,0 3.1.2.12 Psoriasis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=903165&form=6&db=m Esterase D phenotypes in psoriasis vulgaris, atopic diseases and healthy controls. diagnostic usage,ongoing research,unassigned 2,3,0 3.1.2.12 Respiratory Insufficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3777686&form=6&db=m Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization. causal interaction,therapeutic application,unassigned 4,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1679032&form=6&db=m Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan. ongoing research,unassigned 2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1819032&form=6&db=m A genetic study of retinoblastoma. diagnostic usage,ongoing research,unassigned 4,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1886375&form=6&db=m [Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients] diagnostic usage,ongoing research,unassigned 3,4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1992447&form=6&db=m Molecular definition in a somatic cell hybrid of a specific 2:13 translocation breakpoint in childhood rhabdomyosarcoma. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2227145&form=6&db=m Old syndromes and new cytogenetics. causal interaction,therapeutic application,unassigned 4,1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2297043&form=6&db=m Colonic aberrant crypts in azoxymethane-treated F344 rats have decreased hexosaminidase activity. causal interaction,unassigned 3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2587027&form=6&db=m Esterase D analysis in familial retinoma and retinoblastoma. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2596526&form=6&db=m Esterase D assay in Brazilian retinoblastoma families. diagnostic usage,ongoing research,unassigned 2,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2630183&form=6&db=m Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma. diagnostic usage,therapeutic application,unassigned 1,1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2781416&form=6&db=m Assignment of retinoblastoma susceptibility gene to mouse chromosome 14. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2878716&form=6&db=m Chromosome 13 instability and esterase D expression in an osteosarcoma cell line. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2901396&form=6&db=m Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma. causal interaction,diagnostic usage,ongoing research,unassigned 1,4,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3032521&form=6&db=m Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridization. diagnostic usage,ongoing research,unassigned 2,1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3164261&form=6&db=m Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastoma. causal interaction,diagnostic usage,ongoing research,therapeutic application 4,3,2,1 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3164702&form=6&db=m Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3346019&form=6&db=m A "new" allele of esterase D in a retinoblastoma family. therapeutic application,unassigned 3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3377648&form=6&db=m Association of autism, retinoblastoma, and reduced esterase D activity. causal interaction,unassigned 2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3456572&form=6&db=m A sialic acid-specific O-acetylesterase in human erythrocytes: possible identity with esterase D, the genetic marker of retinoblastomas and Wilson disease. diagnostic usage,ongoing research,unassigned 1,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3462698&form=6&db=m Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3462714&form=6&db=m Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. causal interaction,ongoing research,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3462728&form=6&db=m Purification, biochemical characterization, and biological function of human esterase D. diagnostic usage,ongoing research,unassigned 1,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3471703&form=6&db=m A null allele of esterase D is a marker for genetic events in retinoblastoma formation. diagnostic usage,ongoing research,unassigned 1,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3472646&form=6&db=m A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31). unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3502696&form=6&db=m De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma. causal interaction,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3508412&form=6&db=m [Retinoblastoma and esterase D. I. The esterase D activity of RBC of retinoblastoma patients] diagnostic usage,unassigned 3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3508413&form=6&db=m [Retinoblastoma and esterase D II. The oncogenesis of retinoblastoma and the phenotype of esterase D] diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3587887&form=6&db=m Activity of red cell esterase D in 50 cases of retinoblastoma patients and their family members. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3653883&form=6&db=m Familial retinoblastoma (mother and son) with 13q14 deletion. diagnostic usage,unassigned 2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3679214&form=6&db=m Interstitial deletion of chromosome 13 involving the region 13q14. causal interaction,therapeutic application,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3813643&form=6&db=m The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions. causal interaction,diagnostic usage,unassigned 2,4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3823889&form=6&db=m Human retinoblastoma susceptibility gene: cloning, identification, and sequence. ongoing research,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3862370&form=6&db=m Accuracy of detection of the retinoblastoma gene by esterase D linkage. causal interaction,diagnostic usage,ongoing research,unassigned 2,1,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3864729&form=6&db=m A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3943870&form=6&db=m Deletions of the esterase D locus from a survey of 200 retinoblastoma patients. therapeutic application,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=4091103&form=6&db=m [Clinical features and red cell esterase D in retinoblastoma over a 23-year period] ongoing research,unassigned 3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6126695&form=6&db=m Retinoblastoma and esterase D. diagnostic usage,ongoing research,unassigned 4,4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6159813&form=6&db=m Human gene mapping, genetic linkage, and clinical applications. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6298811&form=6&db=m Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories. causal interaction,diagnostic usage,unassigned 2,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6336308&form=6&db=m Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6500578&form=6&db=m Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3). therapeutic application,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6642986&form=6&db=m Esterase D studies in human retinoblastoma. ongoing research,unassigned 4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6716423&form=6&db=m Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus. diagnostic usage,ongoing research,unassigned 3,2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6731533&form=6&db=m Linkage of genes for human esterase D and hereditary retinoblastoma. ongoing research,unassigned 4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6731544&form=6&db=m Esterase D and hereditary retinoblastoma. ongoing research,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6823558&form=6&db=m Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. ongoing research,therapeutic application,unassigned 4,1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6877367&form=6&db=m Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma. causal interaction,unassigned 4,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6885050&form=6&db=m Low incidence of deletion of the esterase D locus in retinoblastoma patients. causal interaction,diagnostic usage,unassigned 3,3,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7116321&form=6&db=m Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis. therapeutic application,unassigned 1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7327583&form=6&db=m Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D. causal interaction,therapeutic application,unassigned 3,1,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7375916&form=6&db=m Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. diagnostic usage,unassigned 2,0 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8410043&form=6&db=m Geographic variations in Wilson's disease. unassigned - 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8432554&form=6&db=m Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease. causal interaction,diagnostic usage,ongoing research,therapeutic application 1,1,4,1 3.1.2.12 Retinoblastoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19126594&form=6&db=m Crystal structure of human esterase D: a potential genetic marker of retinoblastoma. diagnostic usage,therapeutic application,unassigned 3,1,0 3.1.2.12 Rhabdomyosarcoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2630183&form=6&db=m Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma. diagnostic usage,therapeutic application,unassigned 1,1,0 3.1.2.12 s-formylglutathione hydrolase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3943870&form=6&db=m Deletions of the esterase D locus from a survey of 200 retinoblastoma patients. therapeutic application,unassigned 1,0 3.1.2.12 Sarcoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2878716&form=6&db=m Chromosome 13 instability and esterase D expression in an osteosarcoma cell line. causal interaction,diagnostic usage,ongoing research,unassigned 2,3,4,0 3.1.2.12 Sexually Transmitted Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11465906&form=6&db=m Soft tissue infections among injection drug users--San Francisco, California, 1996-2000. causal interaction,diagnostic usage,unassigned 4,1,0 3.1.2.12 Splenic Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9735689&form=6&db=m Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients. causal interaction,diagnostic usage,unassigned 1,2,0 3.1.2.12 Thrombosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=939568&form=6&db=m The red blood cell esterase D polymorphism in Europe and Asia. therapeutic application,unassigned 1,0 3.1.2.12 Tongue Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15995522&form=6&db=m Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma. causal interaction,diagnostic usage,therapeutic application,unassigned 2,4,3,0 3.1.2.12 Tonsillar Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15995522&form=6&db=m Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma. causal interaction,diagnostic usage,therapeutic application,unassigned 2,4,3,0 3.1.2.12 Trisomy 13 Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=511174&form=6&db=m Expression of esterase D and other gene markers in trisomy 13. causal interaction,diagnostic usage,ongoing research,unassigned 1,3,1,0 3.1.2.12 Trisomy 13 Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2377566&form=6&db=m [Gene-dosage effect of esterase D enzyme on erythrocytes in a patient with Patau's syndrome] ongoing research,unassigned 2,0 3.1.2.12 Trisomy 13 Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3560513&form=6&db=m Determination of esterase D (EsD) genotype in cases with trisomy 13. diagnostic usage,unassigned 2,0 3.1.2.12 Trisomy 13 Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8213811&form=6&db=m Overexpression of esterase D in kidney from trisomy 13 fetuses. causal interaction,diagnostic usage,ongoing research,unassigned 3,1,2,0 3.1.2.12 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25408994&form=6&db=m In situ characterization of mycobacterial growth inhibition by lytic enzymes expressed in vectorized E. coli. ongoing research,therapeutic application,unassigned 2,1,0 3.1.2.12 Urinary Tract Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10481961&form=6&db=m Paediatric nosocomial urinary tract infection at a regional hospital. ongoing research,unassigned 1,0 3.1.2.12 Uveitis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18552983&form=6&db=m Proteomic surveillance of retinal autoantigens in endogenous uveitis: implication of esterase D and brain-type creatine kinase as novel autoantigens. causal interaction,diagnostic usage,unassigned 3,3,0