Disease on EC 1.1.1.1 - alcohol dehydrogenase

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DISEASE
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4-aminobutyrate-2-oxoglutarate transaminase deficiency
Clinical aspects of the disorders of GABA metabolism in children.
Disorders of GABA metabolism: SSADH and GABA-transaminase deficiencies.
Abdominal Pain
Varicella in immunocompromised children. Incidence of abdominal pain and organ involvement.
Abducens Nerve Diseases
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Acalculous Cholecystitis
Disseminated visceral varicella zoster virus presenting with the constellation of colonic pseudo-obstruction, acalculous cholecystitis and syndrome of inappropriate ADH secretion.
Acidosis
Cytoplasmic acidosis as a determinant of flooding intolerance in plants.
Ethylene glycol or methanol intoxication: which antidote should be used, fomepizole or ethanol?
Fomepizole fails to prevent progression of acidosis in 2-butoxyethanol and ethanol coingestion.
Forgoing the Folate?-Contemporary Recommendations for Methanol Poisoning and Evidence Review.
Functional characterization of transmembrane intracellular pH regulators and mechanism of alcohol-induced intracellular acidosis in human umbilical cord blood stem cell-like cells.
Intravenous 4-methylpyrazole as an antidote for diethylene glycol and triethylene glycol poisoning: a case report.
Methanol and ethylene glycol poisonings. Mechanism of toxicity, clinical course, diagnosis and treatment.
Not only students can express alcohol dehydrogenase: goldfish can too!
Poisoning with 1-propanol and 2-propanol.
The 'gap' in the 'plasma osmolar gap'.
[Acute poisoning with industrial products]
[Effect of artificial hibernation state on intensity of metabolic processes in rabbits]
[Ethylene glycol intoxication. Important differential diagnosis in comatose patients with metabolic acidosis]
[Severe ethylene glycol poisoning treated wtih fomepizole (4-methylpyrazole)]
[Toxic alcohol poisonings].
Acidosis, Respiratory
[The changes on plasma aldosterone concentration during acute respiratory acidosis in dogs. The relationship to renin-angiotensin system and electrolyte metabolism (author's transl)]
Acquired Immunodeficiency Syndrome
[Inadequate ADH secretion syndrome associated with acquired immunodeficiency syndrome]
[The inappropriate antidiuretic hormone secretion syndrome associated with cryptococcal meningitis in a patient with the acquired immunodeficiency syndrome]
Acromegaly
Diagnosis and treatment of pituitary disease.
ACTH Syndrome, Ectopic
Paraneoplastic syndromes in olfactory neuroblastoma.
Syndrome of inappropriate antidiuretic hormone secretion and ectopic ACTH production in small cell lung carcinoma.
Acute Coronary Syndrome
Alcohol drinking habits, alcohol dehydrogenase genotypes and risk of acute coronary syndrome.
Acute Kidney Injury
ADH effects in development of ischemic acute renal failure.
Renal excretion of antidiuretic hormone in healthy subjects and patients with renal failure.
Addison Disease
Seizure in a normal marrow donor: Addison's disease unmasked.
[Role of ADH in the pathogenesis of hyponatremia in a case of primary adrenal insufficiency (author's transl)]
Adenocarcinoma
A novel short-chain alcohol dehydrogenase from rats with retinol dehydrogenase activity, cyclically expressed in uterine epithelium.
A rare case of ectopic antidiuretic hormone-producing pancreatic adenocarcinoma: new diagnostic approach.
Adrenocorticotropin, calcitonin, and antidiuretic hormone as tumor markers in patients with bronchogenic carcinoma of various histological types.
Alcohol dehydrogenase 3 and risk of esophageal and gastric adenocarcinomas.
Aldehyde Dehydrogenase 1B1 as a Modulator of Pancreatic Adenocarcinoma.
Aldehyde dehydrogenase activity selects for lung adenocarcinoma stem cells dependent on notch signaling.
Changes in the pattern of aldehyde dehydrogenase activity in primary and metastatic adenocarcinomas of the human colon.
Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human large bowel: association of the functional polymorphisms of ADH and ALDH genes with hemorrhoids and colorectal cancer.
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
High expression of octamer-binding transcription factor 4A, prominin-1 and aldehyde dehydrogenase strongly indicates involvement in the initiation of lung adenocarcinoma resulting in shorter disease-free intervals.
Identification of a methylcholanthrene-induced aldehyde dehydrogenase in a human breast adenocarcinoma cell line exhibiting oxazaphosphorine-specific acquired resistance.
Identification of the class-3 aldehyde dehydrogenases present in human MCF-7/0 breast adenocarcinoma cells and normal human breast tissue.
Inhibitory effect of PPAR? on NR0B1 in tumorigenesis of lung adenocarcinoma.
Intrinsic cellular resistance to oxazaphosphorines exhibited by a human colon carcinoma cell line expressing relatively large amounts of a class-3 aldehyde dehydrogenase.
Mammographic-histopathologic correlation of large-core needle biopsies of the breast.
Phenolic antioxidant-induced overexpression of class-3 aldehyde dehydrogenase and oxazaphosphorine-specific resistance.
Prostate adenocarcinoma producing syndrome of inappropriate secretion of antidiuretic hormone.
Syndrome of inappropriate secretion of ADH (SIADH) following cisplatin administration in a pulmonary adenocarcinoma patient with a malignant pleural effusion.
[Antidiuretic hormone in patients with bronchial carcinoma (author's transl)]
[Changes in hormonal and biochemical parameters in gastric adenocarcinoma]
[Dynamic study on plasma antidiuretic hormone before and after surgery for lung cancers]
Adenocarcinoma, Mucinous
Altered mucin expression is a field change that accompanies mucinous (colloid) breast carcinoma histogenesis.
Mucin extravasation in breast core biopsies--clinical significance and outcome correlation.
Adenoma
Alcohol consumption, alcohol dehydrogenase 3 polymorphism, and colorectal adenomas.
Altered Expression of Multiple Genes Involved in Retinoic Acid Biosynthesis in Human Colorectal Cancer.
Atypical ductal hyperplasia and ductal carcinoma in situ of the breast associated with perineural invasion.
Colorectal adenoma stem-like cell populations: Associations with adenoma characteristics and metachronous colorectal neoplasia.
DNA methyltransferase and alcohol dehydrogenase: gene-nutrient interactions in relation to risk of colorectal polyps.
Lack of Influence of the ADH1B Arg47His Genetic Polymorphism on Risk of Colorectal Adenoma in Middle-aged Japanese Men.
Methylenetetrahydrofolate reductase, alcohol dehydrogenase, diet, and risk of colorectal adenomas.
The tumor suppressor adenomatous polyposis coli and caudal related homeodomain protein regulate expression of retinol dehydrogenase L.
Adenomatous Polyposis Coli
The tumor suppressor adenomatous polyposis coli and caudal related homeodomain protein regulate expression of retinol dehydrogenase L.
The zebrafish retinol dehydrogenase, rdh1l, is essential for intestinal development and is regulated by the tumor suppressor adenomatous polyposis coli.
Adenomatous Polyps
DNA methyltransferase and alcohol dehydrogenase: gene-nutrient interactions in relation to risk of colorectal polyps.
Adrenal Insufficiency
A Rare Mechanism of Hyponatremia in HIV Disease.
Hormonal responses upon return of spontaneous circulation after cardiac arrest: a retrospective cohort study.
Isolated ACTH deficiency and primary hypothyroidism: volume-dependent elevation of antidiuretic hormone secretion in the presence of hyponatremia.
University of Miami Division of Clinical Pharmacology Therapeutic Rounds: the water-intolerant patient and perioperative hyponatremia.
[Acute symptomatic hyponatremia in a 70-year-old patient. Insufficient ADH secretion syndrome]
[Constantly negative clearances of free water (inappropriate secretion of paraneoplastic ADH (antidiuretic hormone), adrenal insufficiency, cranial injury)]
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
AIDS-Associated Nephropathy
Induction of Retinol Dehydrogenase 9 Expression in Podocytes Attenuates Kidney Injury.
Airway Obstruction
Association between the aldehyde dehydrogenase 2*2 allele and smoking-related chronic airway obstruction in a Japanese general population: a pilot study.
Alagille Syndrome
Acquired right diaphragmatic hernia following pediatric living donor orthotopic liver transplantation.
[Ocular anomalies in Alagille's syndrome]
alcohol dehydrogenase deficiency
4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism.
4-Hydroxybutyric aciduria associated with catheter usage: A diagnostic pitfall in the identification of SSADH deficiency.
A boy with a severe phenotype of succinic semialdehyde dehydrogenase deficiency.
A case of acute onset succinic semialdehyde dehydrogenase deficiency: neuroimaging findings and literature review.
A case of succinic semialdehyde dehydrogenase deficiency with status epilepticus and rapid regression.
A ketogenic diet rescues the murine succinic semialdehyde dehydrogenase deficient phenotype.
Aberrant GABA(A) receptor-mediated inhibition in cortico-thalamic networks of succinic semialdehyde dehydrogenase deficient mice.
Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome.
Absence seizures in succinic semialdehyde dehydrogenase deficient mice: a model of juvenile absence epilepsy.
Acute and long-term pituitary insufficiency in traumatic brain injury: a prospective single-centre study.
Aldehyde dehydrogenase deficiency as cause of facial flushing reaction to alcohol in Japanese.
Aldehyde dehydrogenase deficiency, flush patterns and prevalence of alcoholism: an interethnic comparison.
ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural chinese sample.
Altered cerebral glucose and acetate metabolism in succinic semialdehyde dehydrogenase-deficient mice: evidence for glial dysfunction and reduced glutamate/glutamine cycling.
Altered PGE2 production by glomeruli and papilla of rats with hereditary diabetes insipidus.
Basis of aldehyde dehydrogenase deficiency in Orientals: immunochemical studies.
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.
Circadian distribution of generalized tonic-clonic seizures associated with murine succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism.
Clinical aspects of the disorders of GABA metabolism in children.
Clinical spectrum of succinic semialdehyde dehydrogenase deficiency.
Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity.
D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?
Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiency.
Defects in GABA metabolism affect selective autophagy pathways and are alleviated by mTOR inhibition.
Detection of aldehyde dehydrogenase deficiency in Chachi Indians, Ecuador.
Determination of the GABA analogue succinic semialdehyde in urine and cerebrospinal fluid by dinitrophenylhydrazine derivatization and liquid chromatography-tandem mass spectrometry: Application to SSADH deficiency.
Diabetes insipidus secondary to Langerhans' cell histiocytosis: is radiation therapy indicated?
Differential corneal sensitivity to ultraviolet light among inbred strains of mice. Correlation of ultraviolet B sensitivity with aldehyde dehydrogenase deficiency.
Disordered control of thirst in hypothalamic-pituitary sarcoidosis.
Ecogenetic and pharmacogenetic studies in Hungary.
Ecogenetic studies in Atacameño Indians.
Effect of ADH II deficiency on the intracellular redox homeostasis in Zymomonas mobilis.
Effect of aldehyde dehydrogenase deficiency on ethanol elimination after peroral or intravenous administrations.
Effect of gene dosage on single-cell hippocampal electrophysiology in a murine model of SSADH deficiency (gamma-hydroxybutyric aciduria).
Effects of 1,4-butanediol administration on oxidative stress in rat brain: study of the neurotoxicity of gamma-hydroxybutyric acid in vivo.
Effects of lithium on water intake and renal concentrating ability in rats with vasopressin-deficient diabetes insipidus (Brattleboro strain).
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice).
Epilepsy in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism.
Ethanol patch test for low Km aldehyde dehydrogenase deficiency.
Evidence for oxidative stress in tissues derived from succinate semialdehyde dehydrogenase-deficient mice.
Evidence of redox imbalance in a patient with succinic semialdehyde dehydrogenase deficiency.
Eye Findings on Vigabatrin and Taurine Treatment in Two Patients with Succinic Semialdehyde Dehydrogenase Deficiency.
Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity.
Fatty aldehyde dehydrogenase is up-regulated by polyunsaturated fatty acid via peroxisome proliferator-activated receptor alpha and suppresses polyunsaturated fatty acid-induced endoplasmic reticulum stress.
Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenase.
GABAB-ergic motor cortex dysfunction in SSADH deficiency.
Gamma-hydroxybutyric acid induces oxidative stress in cerebral cortex of young rats.
Gamma-hydroxybutyric aciduria: a biochemist's education from a heritable disorder of GABA metabolism.
Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH).
Genotypes for aldehyde dehydrogenase deficiency and alcohol sensitivity. The inactive ALDH2(2) allele is dominant.
Hepatic lipid profiling of deer mice fed ethanol using (1)H and (31)P NMR spectroscopy: A dose-dependent subchronic study.
Histochemical localization of aldehyde dehydrogenase in the respiratory tract of the Fischer-344 rat.
Hypothalamic dysfunction after chemotherapy.
Ichthyosis, mental retardation, and asymptomatic spasticity. A new neurocutaneous syndrome with normal fatty alcohol:NAD+ oxidoreductase activity.
Impaired growth hormone secretion in patients operated for pituitary adenomas.
Incidence and Geographic Distribution of Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency.
Incomplete Sjögren-Larsson syndrome in two Japanese siblings.
Increased guanidino species in murine and human succinate semialdehyde dehydrogenase (SSADH) deficiency.
Inherited disorders of GABA metabolism.
Inherited disorders of gamma-aminobutyric acid metabolism and advances in ALDH5A1 mutation identification.
Inherited disorders of neurotransmitters in children and adults.
Kidney and liver function in rats during the edema following constriction of thoracic inferior vena cava with and without adrenalectomy or hypophysectomy.
Liver-directed adenoviral gene transfer in murine succinate semialdehyde dehydrogenase deficiency.
Low serum urea level in dehydrated patients with central diabetes insipidus.
Low-Km aldehyde dehydrogenase deficiency does not influence the elevation of blood pressure by alcohol.
Lymphocytic panhypophysitis: its clinical features in Japanese cases.
Manganese superoxide dismutase and aldehyde dehydrogenase deficiency increase mitochondrial oxidative stress and aggravate age-dependent vascular dysfunction.
Mannitol osmolar clearance in diabetes insipidus of children.
Metabolic basis of ethanol-induced cytotoxicity in recombinant HepG2 cells: role of nonoxidative metabolism.
Monitoring of 4-hydroxybutyric acid levels in body fluids during vigabatrin treatment in succinic semialdehyde dehydrogenase deficiency.
Murine succinate semialdehyde dehydrogenase deficiency.
Mutation analysis and prenatal diagnosis in a Chinese family with succinic semialdehyde dehydrogenase and a systematic review of the literature of reported ALDH5A1 mutations.
Mutation analysis in a patient with succinic semialdehyde dehydrogenase deficiency: a compound heterozygote with 103-121del and 1460T > A of the ALDH5A1 gene.
Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency.
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.
Neurodevelopmental pattern of succinic semialdehyde dehydrogenase deficiency (gamma-hydroxybutyric aciduria).
Neuropsychiatric morbidity in adolescent and adult succinic semialdehyde dehydrogenase deficiency patients.
Night-time polyuria and urine hypo-osmolality in enuretics identified by nocturnal sequential urine sampling--do they represent a subset of relative ADH-deficient subjects?
Partial ADH deficiency vs endogenous fluid overload in hypotonic polyuria.
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase.
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency.
Plasma leptin levels in male patients with idiopathic central diabetes insipidus.
Polysomnographic abnormalities in succinic semialdehyde dehydrogenase (SSADH) deficiency.
Population genetic and family studies on aldehyde dehydrogenase deficiency and alcohol sensitivity.
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses.
Proton magnetic resonance spectroscopy findings and clinical effects of montelukast sodium in a case with Sjögren-Larsson syndrome.
Proton MR spectroscopy in succinic semialdehyde dehydrogenase deficiency.
Quantitation of gamma-hydroxybutyric acid in dried blood spots: feasibility assessment for newborn screening of succinic semialdehyde dehydrogenase (SSADH) deficiency.
Radiochromium conservation and distribution in diuretic states.
Rapid and sensitive detection of urinary 4-hydroxybutyric acid and its related compounds by gas chromatography-mass spectrometry in a patient with succinic semialdehyde dehydrogenase deficiency.
Redox-switch modulation of human SSADH by dynamic catalytic loop.
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiency.
Seizures in a boy with succinic semialdehyde dehydrogenase deficiency treated with vigabatrin (gamma-vinyl-GABA).
Selective involvement of the globus pallidus and dentate nucleus in succinic semialdehyde dehydrogenase deficiency.
Sensory integration intervention: Historical concepts, treatment strategies and clinical experiences in three patients with succinic semialdehyde dehydrogenase (SSADH) deficiency.
Sjögren-Larsson syndrome. Deficient activity of the fatty aldehyde dehydrogenase component of fatty alcohol:NAD+ oxidoreductase in cultured fibroblasts.
Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patients.
Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.
Sleep disorders in succinic semialdehyde dehydrogenase deficiency: a family report.
Sodium-induced elevation of blood pressure in the anephric state.
SSADH deficiency in an adult: Venturing outside of the diagnostic box and inside of the registry.
SSADH deficiency leads to elevated extracellular GABA levels and increased GABAergic neurotransmission in the mouse cerebral cortex.
SSADH deficiency possibly associated with enzyme activity-reducing SNPs.
Status epilepticus in mice deficient for succinate semialdehyde dehydrogenase: GABAA receptor-mediated mechanisms.
Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoforms.
Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses.
Succinic semialdehyde dehydrogenase deficiency: GABAB receptor-mediated function.
Symptoms of gonadal dysfunction are more predictive of hypopituitarism than nonspecific symptoms in screening for pituitary dysfunction following moderate or severe traumatic brain injury.
Synthesis of Drosophila melanogaster alcohol dehydrogenase in yeast.
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.
The effects of a ketogenic diet on ATP concentrations and the number of hippocampal mitochondria in Aldh5a1(-/-) mice.
The flushing syndrome after ethanol intake caused by aldehyde dehydrogenase deficiency in Orientals.
The influence of Adh function on ethanol preference and tolerance in adult Drosophila melanogaster.
The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family.
Therapeutic concepts in succinate semialdehyde dehydrogenase (SSADH; ALDH5a1) deficiency (gamma-hydroxybutyric aciduria). Hypotheses evolved from 25 years of patient evaluation, studies in Aldh5a1-/- mice and characterization of gamma-hydroxybutyric acid pharmacology.
Therapeutic intervention in mice deficient for succinate semialdehyde dehydrogenase (gamma-hydroxybutyric aciduria).
Transient reduction in the posterior pituitary bright signal preceding water intoxication in a malnourished child.
Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria).
Unusual delayed onset of diabetes insipidus following closed head trauma. Case report.
Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency.
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiency.
[Diagnostic value of the determination of blood urea in dehydrated patients with and without central diabetes insipidus]
[Polyuria]
[Succinic semialdehyde dehydrogenase deficiency].
Alcohol-Related Disorders
Genetic alcohol sensitivity regulated by ALDH2 and ADH1B polymorphisms is strongly associated with depression and anxiety in Japanese employees.
Plasma alcohol dehydrogenase in normal and alcoholic individuals.
aldehyde dehydrogenase (nad+) deficiency
Effects of ALDH2 genotype, PPI treatment and L-cysteine on carcinogenic acetaldehyde in gastric juice and saliva after intragastric alcohol administration.
Alkalosis
Hormonal disturbances of fluid-electrolyte metabolism under altitude exposure in man.
Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.
Role of tolvaptan in the management of hyponatremia in patients with lung and other cancers: current data and future perspectives.
Altitude Sickness
Hormonal disturbances of fluid-electrolyte metabolism under altitude exposure in man.
Alzheimer Disease
6-benzothiazolyl ureas, thioureas and guanidines are potent inhibitors of ABAD/17?-HSD10 and potential drugs for Alzheimer's disease treatment: Design, synthesis and in vitro evaluation.
ABAD: a potential therapeutic target for Abeta-induced mitochondrial dysfunction in Alzheimer's disease.
Amyloid-? as a Modulator of Synaptic Plasticity.
Crystal structure of human ABAD/HSD10 with a bound inhibitor: implications for design of Alzheimer's disease therapeutics.
Disruption of the retinoid signalling pathway causes a deposition of amyloid beta in the adult rat brain.
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Identification of Human ABAD Inhibitors for Rescuing A?-Mediated Mitochondrial Dysfunction.
Identification of small-molecule inhibitors of the Abeta-ABAD interaction.
Increased brain protein levels of carbonyl reductase and alcohol dehydrogenase in Down syndrome and Alzheimer's disease.
Mitochondrial dysfunction and Alzheimer's disease: role of amyloid-beta peptide alcohol dehydrogenase (ABAD).
Role of ADH1B rs1229984 and ALDH2 rs671 gene polymorphisms in the development of Alzheimer's disease.
Amebiasis
Cloning and expression of a putative alcohol dehydrogenase gene of Entamoeba histolytica and its application to immunological examination.
Amnesia
ADH and related peptides: effect of pre- or posttraining treatment on puromycin amnesia.
Amyloidosis
An autopsy case of macroglobulinemia complicated with syndrome of inappropriate secretion of ADH (SIADH) like hyponatremia, hypopituitarism and AL amyloidosis.
Androgen-Insensitivity Syndrome
Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome.
More about X-linked testicular feminization of the mouse as a noninducible(is)mutation of a regulatory locus: 5-alpha-androstan-3-alpha-17-beta-diol as the true inducer of kidney alcohol dehydrogenase and beta-glucuronidase.
Anemia, Macrocytic
Blood Leukocyte Counts and Genetic Polymorphisms of Alcohol Dehydrogenase-1B and Aldehyde Dehydrogenase-2 in Japanese Alcoholic Men.
Aneurysm
The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the wall of abdominal aortic aneurysms.
Aneurysm, Ruptured
SIADH after subarachnoid hemorrhage and craniotomy.
Anuria
Renal function and fluid therapy in high risk infants.
Aortic Aneurysm
The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the wall of abdominal aortic aneurysms.
Aortic Aneurysm, Abdominal
The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the wall of abdominal aortic aneurysms.
Arrhythmias, Cardiac
A study of autonomic cardiovascular reflexes in elderly patients with pneumonia.
Arthritis
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Ascorbic Acid Deficiency
Relation between hepatic alcohol dehydrogenase activity and the ascorbic acid in leucocytes of patients with liver disease.
Asthma
Antidiuretic hormone in acute asthma in children: effects of medication on serum levels and clinical course.
Ataxia
A histochemical study of the distribution of aldehyde dehydrogenase activity in brain structures of rats with genetically different alcohol-related behaviour.
Clinical aspects of the disorders of GABA metabolism in children.
Ethylene glycol poisoning in three dogs: Importance of early diagnosis and role of hemodialysis as a treatment option.
Inherited disorders of neurotransmitters in children and adults.
The X-ray crystal structure of Escherichia coli succinic semialdehyde dehydrogenase; structural insights into NADP+/enzyme interactions.
Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency.
Atherosclerosis
Atherosclerosis progression in patients with autosomal dominant hypercholesterolemia in clinical practice.
Carotid atherosclerotic plaques: proteomics study after a low-abundance protein enrichment step.
Effects of aldehyde dehydrogenase genotypes on carotid atherosclerosis.
[Aldolase and -glycerolphosphate and 3-phosphoglycerol aldehyde dehydrogenase activity of rabbit muscles in experimental atherosclerosis]
Atrial Fibrillation
Genetic variations of aldehyde dehydrogenase 2 and alcohol dehydrogenase 1B are associated with the etiology of atrial fibrillation in Japanese.
Atypical Squamous Cells of the Cervix
Protein degradation during yeast sporulation. Enzyme and cytochrome patterns.
Autoimmune Diseases
Proteomic surveillance of putative new autoantigens in thyroid orbitopathy.
Autonomic Dysreflexia
Nocturnal polyuria and antidiuretic hormone levels in spinal cord injury.
Bacterial Infections
Transcriptional profiling of indica rice cultivar IET8585 (Ajaya) infected with bacterial leaf blight pathogen Xanthomonas oryzae pv oryzae.
Bacteriuria
Frequency and distribution of uropathogenic Escherichia coli adhesins: a clinical correlation over 2,000 cases.
Bartter Syndrome
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome.
Functional activities of mutant calcium-sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia.
Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.
The renal tubular defect of Bartter's syndrome.
Biliary Atresia
Continuous increase of alcohol dehydrogenase activity along the liver plate in normal and cirrhotic human livers.
Birth Injuries
[Neuro-MR-findings in primary panhypopituitarism]
Blepharospasm
Primary Whipple's disease of the brain: characterization of the clinical syndrome and molecular diagnosis.
Blindness
Ethylene glycol or methanol intoxication: which antidote should be used, fomepizole or ethanol?
RDH12, a retinol dehydrogenase causing Leber's congenital amaurosis, is also involved in steroid metabolism.
Bone Diseases, Metabolic
Bone formation in alcohol-induced osteopenia is associated with elevated p21 expression in bone marrow cells in aldehyde dehydrogenase 2-disrupted mice.
Bradycardia
Pretreatment of CD-1 mice with 4-methylpyrazole blocks toxicity from the gamma-hydroxybutyrate precursor, 1,4-butanediol.
Brain Death
Changes in hepatic microcirculation and histomorphology in brain-dead organ donors: an experimental study in rats.
Morphological and functional alterations of the hypothalamic-pituitary system in brain death with long-term bodily living.
Prolonged hemodynamic maintenance by the combined administration of vasopressin and epinephrine in brain death: a clinical study.
[Examination of ADH in a case of brain death]
[Hormone evaluation in brain death]
[Organ preservation with the combination of vasopressin and catecholamine in brain dead donors]
[Preservation of homeostasis following the onset of brain death]
Brain Diseases
Immunological and endocrinological abnormalities in paraneoplastic disorders with involvement of the autonomic nervous system.
Sleep disorders in succinic semialdehyde dehydrogenase deficiency: a family report.
Triphasic AVP secretion in encephalopathy.
[Paraneoplastic limbic encephalopathy, inappropriate ADH secretion and recurrent subclinical epileptic seizures. Clinical, anatomo-pathological and metabolic correlations by positron emission tomography]
Brain Edema
Increased intracranial pressure is associated with elevated cerebrospinal fluid ADH levels in closed-head injury.
Brain Injuries
A subpopulation of endothelial progenitor cells with low aldehyde dehydrogenase activity attenuates acute ischemic brain injury in rats.
Brain Neoplasms
Aldehyde dehydrogenase activity in xenografted human brain tumor in nude mice. Preliminary results in human glioma biopsies.
Chronic demeclocycline therapy in the syndrome of inappropriate ADH secretion due to brain tumor.
Disulfiram modulates stemness and metabolism of brain tumor initiating cells in atypical teratoid/rhabdoid tumors.
Identification of brain tumour initiating cells using the stem cell marker aldehyde dehydrogenase.
The activity of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the sera of patients with brain cancer.
The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in brain cancer.
The diagnostic value of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) measurement in the sera of patients with brain tumor.
Breast Carcinoma In Situ
Atypical ductal hyperplasia and atypia of uncertain significance in core biopsies from mammographically detected lesions: correlation with excision diagnosis.
Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow-up biopsies.
Comparison of the diagnostic accuracy of a vacuum-assisted percutaneous intact specimen sampling device to a vacuum-assisted core needle sampling device for breast biopsy: initial experience.
Epithelial lesions in prophylactic mastectomy specimens from women with BRCA mutations.
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Fourteen-gauge needle core biopsy of mammographically evident radial scars: is excision necessary?
Histology after lumpectomy in women with epithelial atypia on stereotactic vacuum-assisted breast biopsy.
Pathologic High-risk Lesions, Diagnosis and Management.
Significance of flat epithelial atypia on mammotome core needle biopsy: Should it be excised?
The histologic spectrum of apocrine breast proliferations: a comparative study of morphology and DNA content by image analysis.
The role of chemoprevention in modifying the risk of breast cancer in women with atypical breast lesions.
Underestimation of atypical ductal hyperplasia at MRI-guided 9-gauge vacuum-assisted breast biopsy.
Vacuum-assisted biopsy diagnosis of atypical ductal hyperplasia and patient management.
Breast Diseases
Extent of atypical hyperplasia stratifies breast cancer risk in 2 independent cohorts of women.
Understanding the premalignant potential of atypical hyperplasia through its natural history: a longitudinal cohort study.
Breast Neoplasms
A cluster of microcalcifications: women with high risk for breast cancer versus other women.
A common coding variant in CASP8 is associated with breast cancer risk.
Aberrant BLID expression is associated with breast cancer progression.
Accuracy of screening mammography in women with a history of lobular carcinoma in situ or atypical hyperplasia of the breast.
Activity of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the sera of patients with breast cancer.
Alcohol dehydrogenase 1B (ADH1B) genotype, alcohol consumption and breast cancer risk by age 50 years in a German case-control study.
Alcohol dehydrogenase 3 genotype modification of the association of alcohol consumption with breast cancer risk.
Alcohol dehydrogenase genetic polymorphisms, low-to-moderate alcohol consumption, and risk of breast cancer.
Alcohol metabolism, alcohol intake, and breast cancer risk: a sister-set analysis using the Breast Cancer Family Registry.
Alcohol, genetics and risk of breast cancer in the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial.
Alcohol-induced breast cancer: a proposed mechanism.
Aldehyde dehydrogenase 1-positive cells in axillary lymph node metastases after chemotherapy as a prognostic factor in patients with lymph node-positive breast cancer.
Aldehyde Dehydrogenase Activity of Breast Cancer Stem Cells is Primarily Due to Isoform ALDH1A3 and Its Expression is Predictive of Metastasis.
Aldehyde dehydrogenase activity of breast cancer stem cells is primarily due to isoform ALDH1A3 and its expression is predictive of metastasis.
Analysis of breast cancer progression using principal component analysis and clustering.
Analysis of loss of heterozygosity on chromosome 11q13 in atypical ductal hyperplasia and in situ carcinoma of the breast.
Analysis of p53 mutations in cells taken from paraffin-embedded tissue sections of ductal carcinoma in situ and atypical ductal hyperplasia of the breast.
Appropriate management of atypical ductal hyperplasia diagnosed by stereotactic core needle breast biopsy.
Aromatase expression in atypical ductal hyperplasia in women.
Atypical Ductal Hyperplasia at the Margin of Lumpectomy Performed for Early Stage Breast Cancer: Is there Enough Evidence to Formulate Guidelines?
Atypical Ductal Hyperplasia Bordering on Ductal Carcinoma In Situ: Interobserver Variability and Outcomes in 105 Cases.
Atypical ductal hyperplasia of the breast diagnosed by 11-gauge directional vacuum-assisted biopsy.
Atypical hyperplastic lesions of the female breast. A long-term follow-up study.
Bilateral atypical ductal hyperplasia, an incidental finding in gynaecomastia--case report and literature review.
Breast cancer risk by extent and type of atypical hyperplasia: An update from the Nurses' Health Studies.
Breast cancer risk factors in younger and older women.
Breast cancer risk of lobular-based hyperplasia after biopsy: "ductal" pattern lesions.
Breast carcinoma presenting with inappropriate ADH secretion.
Chromosomal Alterations in Pure Nonneoplastic Breast Lesions: Implications for Breast Cancer Progression.
Class I alcohol dehydrogenase is highly expressed in normal human mammary epithelium but not in invasive breast cancer: implications for breast carcinogenesis.
Clinicopathologic analysis of breast lesions associated with multiple papillomas.
Combination Twist1 and CA15-3 in axillary lymph nodes for breast cancer prognosis.
Diagnostic value of vacuum-assisted breast biopsy for breast carcinoma: a meta-analysis and systematic review.
Distribution of aldehyde dehydrogenase 1-positive stem cells in benign mammary tissue from women with and without breast cancer.
Down-regulation of vitamin D receptor in mammospheres: implications for vitamin D resistance in breast cancer and potential for combination therapy.
Ductal Carcinoma in situ and related lesions of the breast: recent advances in pathology practice.
Early dysregulation of cell adhesion and extracellular matrix pathways in breast cancer progression.
Elimination of ALDH+ breast tumor initiating cells by docosahexanoic acid and/or gamma tocotrienol through SHP-1 inhibition of Stat3 signaling.
Epidermal growth factor/heat shock protein 27 pathway regulates vasculogenic mimicry activity of breast cancer stem/progenitor cells.
ER81 Expression in Breast Cancers and Hyperplasia.
Expression of aldehyde dehydrogenase after neoadjuvant chemotherapy is associated with expression of hypoxia-inducible factors 1 and 2 alpha and predicts prognosis in locally advanced breast cancer.
Expression of epithelial-mesenchymal transition-related markers in triple-negative breast cancer: ZEB1 as a potential biomarker for poor clinical outcome.
Expression pattern and methylation of estrogen receptor ? in breast intraductal proliferative lesions.
Frequency and upgrade rates of atypical ductal hyperplasia diagnosed at stereotactic vacuum-assisted breast biopsy: 9-versus 11-gauge.
Genetic mutations and expression of p53 in non-invasive breast lesions.
HER2 as a prognostic factor in breast cancer.
High aldehyde dehydrogenase activity enhances stem cell features in breast cancer cells by activating hypoxia-inducible factor-2?
High aldehyde dehydrogenase and expression of cancer stem cell markers selects for breast cancer cells with enhanced malignant and metastatic ability.
Hsp27 participates in the maintenance of breast cancer stem cells through regulation of epithelial-mesenchymal transition and nuclear factor-?B.
Human 21T breast epithelial cell lines mimic breast cancer progression in vivo and in vitro and show stage-specific gene expression patterns.
Immunohistochemical analysis of aldehyde dehydrogenase isoforms and their association with estrogen-receptor status and disease progression in breast cancer.
Immunohistochemical analysis of Metadherin in proliferative and cancerous breast tissue.
Immunohistochemical study of matrix metalloproteinase 9 and tissue inhibitor of matrix metalloproteinase 1 in benign and malignant breast tissue--strong expression in intraductal carcinomas of the breast.
Inhibition of aldehyde dehydrogenase (ALDH) activity reduces chemotherapy and radiation resistance of stem-like ALDH(hi)CD44 (+) human breast cancer cells.
Inhibition of heat shock protein (Hsp) 27 potentiates the suppressive effect of Hsp90 inhibitors in targeting breast cancer stem-like cells.
Interaction between ADH1C Arg(272)Gln and alcohol intake in relation to breast cancer risk suggests that ethanol is the causal factor in alcohol related breast cancer.
Interaction between alcohol dehydrogenase II gene, alcohol consumption, and risk for breast cancer.
Interaction of the effects of alcohol drinking and polymorphisms in alcohol-metabolizing enzymes on the risk of female breast cancer in Japan.
Is surgical excision necessary for atypical ductal hyperplasia of the breast diagnosed by Mammotome?
Kinetic modelling of the role of the aldehyde dehydrogenase enzyme and the breast cancer resistance protein in drug resistance and transport.
Lack of association of ADH1C genotype with breast cancer susceptibility in Caucasian population: A pooled analysis of case-control studies.
Let-7c blocks estrogen-activated Wnt signaling in induction of self-renewal of breast cancer stem cells.
Lobular neoplasia on core-needle biopsy--clinical significance.
LOH analyses of premalignant and malignant lesions of human breast: frequent LOH in 8p, 16q, and 17q in atypical ductal hyperplasia.
Long-Term Safety of Observation in Selected Women Following Core Biopsy Diagnosis of Atypical Ductal Hyperplasia.
Loss of heterozygosity and microsatellite instability in epithelial hyperplasia of the breast.
Loss of the Timp gene family is sufficient for the acquisition of the CAF-like cell state.
Loss of WISP2/CCN5 in estrogen-dependent MCF7 human breast cancer cells promotes a stem-like cell phenotype.
Lung-Derived Factors Mediate Breast Cancer Cell Migration through CD44 Receptor-Ligand Interactions in a Novel Ex Vivo System for Analysis of Organ-Specific Soluble Proteins.
Luteolin inhibits progestin-dependent angiogenesis, stem cell-like characteristics, and growth of human breast cancer xenografts.
Magnitude and laterality of breast cancer risk according to histologic type of atypical hyperplasia: results from the Nurses' Health Study.
miR-199a-5p confers tumor-suppressive role in triple-negative breast cancer.
NF-kappa?-inducing kinase regulates stem cell phenotype in breast cancer.
Nicotine increases cancer stem cell population in MCF-7 cells.
NOTCH-induced aldehyde dehydrogenase 1A1 deacetylation promotes breast cancer stem cells.
PHLDA1 expression is controlled by an estrogen receptor-NF?B-miR-181 regulatory loop and is essential for formation of ER+ mammospheres.
Possible Prognostic Role of HER2/Neu in Ductal Carcinoma In Situ and Atypical Ductal Proliferative Lesions of the Breast.
PPAR? maintains ERBB2-positive breast cancer stem cells.
Predictive factors for breast cancer in patients diagnosed atypical ductal hyperplasia at core needle biopsy.
Predictors of breast cancer development in a high-risk population.
Preferential antitumor effect of the Src inhibitor dasatinib associated with a decreased proportion of aldehyde dehydrogenase 1-positive cells in breast cancer cells of the basal B subtype.
Preventive medical services not covered by public health insurance at Daiko Medical Center in Japan, 2004-2011.
Rates of atypical ductal hyperplasia have declined with less use of postmenopausal hormone treatment: findings from the Breast Cancer Surveillance Consortium.
Retroviral-infection increases tumorigenic potential of MDA-MB-231 breast carcinoma cells by expanding an aldehyde dehydrogenase (ALDH1) positive stem-cell like population.
Risk factors in alcohol associated breast cancer: alcohol dehydrogenase polymorphism and estrogens.
Role of deregulated microRNAs in breast cancer progression using FFPE tissue.
Role of microRNAs in the Regulation of Breast Cancer Stem Cells.
Silencing NOTCH signaling causes growth arrest in both breast cancer stem cells and breast cancer cells.
Stand-Sit Microchip for High-Throughput, Multiplexed Analysis of Single Cancer Cells.
Stem cell biomarker ALDH1A1 in breast cancer shows an association with prognosis and clinicopathological variables that is highly cut-off dependent.
Stem cell marker aldehyde dehydrogenase 1-positive breast cancers are characterized by negative estrogen receptor, positive human epidermal growth factor receptor type 2, and high Ki67 expression.
Stereotactic and sonographic large-core biopsy of nonpalpable breast lesions: results of the Radiologic Diagnostic Oncology Group V study.
Stereotactic breast biopsy of atypical ductal hyperplasia and ductal carcinoma in situ lesions: improved accuracy with directional, vacuum-assisted biopsy.
Subsequent Breast Cancer Risk Following Diagnosis of Atypical Ductal Hyperplasia on Needle Biopsy.
Targeting aberrant expression of Notch-1 in ALDH(+) cancer stem cells in breast cancer.
Targeting the HER/EGFR/ErbB Family to Prevent Breast Cancer.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in breast cancer.
The Alcohol Dehydrogenase 1C(rs698) Genotype and Breast Cancer: A Meta-analysis.
The discordance between primary breast cancer lesions and pulmonary metastatic lesions in expression of aldehyde dehydrogenase 1-positive cancer cells.
The expression and significance of insulin-like growth factor-1 receptor and its pathway on breast cancer stem/progenitors.
The expression of aldehyde dehydrogenase family in breast cancer.
The management of lobular neoplasia identified on percutaneous core breast biopsy.
The role of chemoprevention in modifying the risk of breast cancer in women with atypical breast lesions.
The Status of STAT3 and STAT5 in Human Breast Atypical Ductal Hyperplasia.
Understanding the premalignant potential of atypical hyperplasia through its natural history: a longitudinal cohort study.
Vacuum-assisted biopsy diagnosis of atypical ductal hyperplasia and patient management.
Women with familial risk for breast cancer have an increased frequency of aldehyde dehydrogenase expressing cells in breast ductules.
Xenografts in zebrafish embryos as a rapid functional assay for breast cancer stem-like cell identification.
[Atypical ductal hyperplasia and atypical epithelial proliferation of ductal type]
[Follow-up study of benign breast diseases]
[The cancer stem cell: the breast cancer driver]
Bronchial Hyperreactivity
Immunoglobulin E Sensitization to Cross-Reactive Carbohydrate Determinants: Epidemiological Study of Clinical Relevance and Role of Alcohol Consumption.
Bronchial Spasm
Elevated plasma antidiuretic hormone levels in status asthmaticus.
Bronchiolitis
Water, electrolyte, and endocrine homeostasis in infants with bronchiolitis.
Brucellosis
The Syndrome of Inappropriate Secretion of Anti-Diuretic Hormone (SIADH) and Brucellosis.
Burkitt Lymphoma
Relapse of central nervous system Burkitt's lymphoma presenting as Guillain-Barre syndrome and syndrome of inappropriate ADH secretion.
Calcinosis
A cluster of microcalcifications: women with high risk for breast cancer versus other women.
Absence of Residual Microcalcifications in Atypical Ductal Hyperplasia Diagnosed via Stereotactic Vacuum-Assisted Breast Biopsy: Is Surgical Excision Obviated?
Atypical ductal hyperplasia diagnosis by directional vacuum-assisted stereotactic biopsy of breast microcalcifications. Considerations for surgical excision.
Atypical lobular hyperplasia or lobular carcinoma in situ at core-needle breast biopsy.
Extent and histologic pattern of atypical ductal hyperplasia present on core needle biopsy specimens of the breast can predict ductal carcinoma in situ in subsequent excision.
Factors associated with upgrading to malignancy at surgery of atypical ductal hyperplasia diagnosed on core biopsy.
Flat epithelial atypia on core needle biopsy, must we surgically excise?
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Is surgical biopsy mandatory in case of atypical ductal hyperplasia on 11-gauge core needle biopsy? A retrospective study of 300 patients.
Mammographic-histopathologic correlation of large-core needle biopsies of the breast.
Minimizing underestimation rate of microcalcifications excised via vacuum-assisted breast biopsy: a blind study.
Scoring system for predicting malignancy in patients diagnosed with atypical ductal hyperplasia at ultrasound-guided core needle biopsy.
The value of dynamic contrast enhanced breast MRI in mammographically detected bi-rads 5 microcalcifications.
Canavan Disease
Effects of ethanol and of alcohol dehydrogenase inhibitors on the reduction of N-acetylaspartate levels of brain in mice in vivo: a search for substances that may have therapeutic value in the treatment of Canavan disease.
Candidiasis
Proteomics-based identification of novel Candida albicans antigens for diagnosis of systemic candidiasis in patients with underlying hematological malignancies.
Candidiasis, Vulvovaginal
Alcohol dehydrogenase I expression correlates with CDR1, CDR2 and FLU1 expression in Candida albicans from patients with vulvovaginal candidiasis.
Carcinogenesis
A gene-gene interaction between ALDH2 Glu487Lys and ADH2 His47Arg polymorphisms regarding the risk of colorectal cancer in Japan.
Activity of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the sera of patients with breast cancer.
ADH1B: From alcoholism, natural selection, and cancer to the human phenome.
Alcohol and cancer: an overview with special emphasis on the role of acetaldehyde and cytochrome P450 2E1.
Alcohol and colorectal cancer: the role of alcohol dehydrogenase 1C polymorphism.
Alcohol and pancreatic cancer.
Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) in the cancer diseases.
Alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) activity in the sera of patients with gastric cancer.
Alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) activity in the sera of patients with pancreatic cancer.
Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms.
Changes in aldehyde dehydrogenase during rat urinary bladder carcinogenesis.
Class I alcohol dehydrogenase is highly expressed in normal human mammary epithelium but not in invasive breast cancer: implications for breast carcinogenesis.
Cyclin D1 expression in ductal carcinoma in situ, atypical ductal hyperplasia and usual ductal hyperplasia: an immunohistochemical study.
Dietary iron enhances the tumor rate in dimethylhydrazine-induced colon carcinogenesis in mice.
Dioxin receptor regulates aldehyde dehydrogenase to block melanoma tumorigenesis and metastasis.
ER81 Expression in Breast Cancers and Hyperplasia.
Genetic mutations and expression of p53 in non-invasive breast lesions.
Glutathione-S-transferase, alcohol dehydrogenase and aldehyde reductase activities during diethylnitrosamine-carcinogenesis in rat liver.
Immunohistochemical analysis of Metadherin in proliferative and cancerous breast tissue.
Kinetic properties of alcohol dehydrogenase in hepatocellular carcinoma and normal tissues of rat.
Lack of Influence of the ADH1B Arg47His Genetic Polymorphism on Risk of Colorectal Adenoma in Middle-aged Japanese Men.
Oral cancer and polymorphism of ethanol metabolising genes.
Role of deregulated microRNAs in breast cancer progression using FFPE tissue.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in breast cancer.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in cervical cancer.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in renal cell carcinoma.
The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in brain cancer.
The Activity of Class I, II, III, and IV Alcohol Dehydrogenase (ADH) Isoenzymes and Aldehyde Dehydrogenase (ALDH) in Esophageal Cancer.
The activity of class I, II, III, and IV alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in liver cancer.
The activity of class I, II, III, and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in colorectal cancer.
The activity of class I, II, III, and IV of alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in pancreatic cancer.
The activity of class I, III, and IV of alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in gastric cancer.
[Alcohol dehydrogenase and aldehyde dehydrogenase as tumour markers and factors intensifying carcinogenesis in colorectal cancer]
[Alcohol dehydrogenase and aldehyde dehydrogenase as tumour markers and factors intensifying carcinogenesis in liver cancer]
[Alcohol dehydrogenase and aldehyde dehydrogenase in malignant diseases--Part II]
Carcinoid Tumor
[Endocrine crises]
Carcinoma
A case of oat cell carcinoma of the lung associated with ectopic production of ADH, neurophysin and ACTH.
A single nucleotide polymorphism in the alcohol dehydrogenase 7 gene (alanine to glycine substitution at amino acid 92) is associated with the risk of squamous cell carcinoma of the head and neck.
Aberrant BLID expression is associated with breast cancer progression.
ACTH, ADH, and calcitonin concentrations as markers of response and relapse in small-cell carcinoma of the lung.
ADH1B and ALDH2 are associated with metachronous SCC after endoscopic submucosal dissection of esophageal squamous cell carcinoma.
ADH1B and ALDH2 polymorphisms and their associations with increased risk of squamous cell carcinoma of the head and neck in the Korean population.
Adrenocorticotropin, calcitonin, and antidiuretic hormone as tumor markers in patients with bronchogenic carcinoma of various histological types.
Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) as candidates for tumor markers in patients with pancreatic cancer.
Alcohol dehydrogenase 3 and risk of esophageal and gastric adenocarcinomas.
Alcohol dehydrogenase 3 and risk of squamous cell carcinomas of the head and neck.
Alcohol dehydrogenase 3 genotype is not associated with risk of squamous cell carcinoma of the oral cavity and pharynx.
Alcohol flushing, alcohol and aldehyde dehydrogenase genotypes, and risk for esophageal squamous cell carcinoma in Japanese men.
Aldehyde dehydrogenase 1/epidermal growth factor receptor coexpression is characteristic of a highly aggressive, poor-prognosis subgroup of high-grade serous ovarian carcinoma.
Aldehyde dehydrogenase activities in hepatocyte nodules and hepatocellular carcinomas from Wistar rats.
Aldehyde dehydrogenase activity in cancer stem cells from canine mammary carcinoma cell lines.
Aldehyde dehydrogenase activity is a cancer stem cell marker of tongue squamous cell carcinoma.
All radial scars/complex sclerosing lesions seen on breast screening mammograms should be excised.
All-trans retinoic acid targets gastric cancer stem cells and inhibits patient-derived gastric carcinoma tumor growth.
Altered mucin expression is a field change that accompanies mucinous (colloid) breast carcinoma histogenesis.
Amplification of Her-2/neu gene in Her-2/neu-overexpressing and -nonexpressing breast carcinomas and their synchronous benign, premalignant, and metastatic lesions detected by FISH in archival material.
Analysis of loss of heterozygosity on chromosome 11q13 in atypical ductal hyperplasia and in situ carcinoma of the breast.
Appropriate management of atypical ductal hyperplasia diagnosed by stereotactic core needle breast biopsy.
Association between ADH1B and ADH1C polymorphisms and the risk of head and neck squamous cell carcinoma.
Association of breast cancer with the finding of atypical ductal hyperplasia at core breast biopsy.
Atypical ductal hyperplasia and atypia of uncertain significance in core biopsies from mammographically detected lesions: correlation with excision diagnosis.
Atypical ductal hyperplasia at margin of breast biopsy--is re-excision indicated?
Atypical ductal hyperplasia diagnosed at stereotactic breast biopsy: improved reliability with 14-gauge, directional, vacuum-assisted biopsy.
Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow-up biopsies.
Atypical Ductal Hyperplasia in Directional Vacuum-Assisted Biopsy of Breast Microcalcifications: Considerations for Surgical Excision.
Atypical ductal hyperplasia of the breast diagnosed by 11-gauge directional vacuum-assisted biopsy.
Atypical ductal hyperplasia: can some lesions be defined as probably benign after stereotactic 11-gauge vacuum-assisted biopsy, eliminating the recommendation for surgical excision?
BMP-2 inhibits tumor-initiating ability in human renal cancer stem cells and induces bone formation.
Breast papillomas with atypical ductal hyperplasia: a clinicopathologic study.
Calcification retrieval at stereotactic, 11-gauge, directional, vacuum-assisted breast biopsy.
Can mammographic findings help discriminate between atypical ductal hyperplasia and ductal carcinoma in situ after needle core biopsy?
Cancer stem cells in head and neck squamous cell carcinoma: a review.
Cancerization of lobules and atypical ductal hyperplasia adjacent to ductal carcinoma in situ of the breast.
Carcinogenetic impact of ADH1B and ALDH2 genes on squamous cell carcinoma risk of the esophagus with regard to the consumption of alcohol, tobacco and betel quid.
Carcinostatic effect of aliphatic aldehydes and aldehyde dehydrogenase activity in Ehrlich carcinoma, Sarcoma 180, and Yoshida AH 130 hepatoma.
Chromosomal Alterations in Pure Nonneoplastic Breast Lesions: Implications for Breast Cancer Progression.
Cisplatin induces bmi-1 and enhances the stem cell fraction in head and neck cancer.
Core biopsy of the breast with atypical ductal hyperplasia: a probabilistic approach to reporting.
Detoxification of cyclophosphamide by human aldehyde dehydrogenase isozymes.
Early Breast Cancer Precursor Lesions: Lessons Learned from Molecular and Clinical Studies.
Ectopic ADH production before clinical recognition of small cell carcinoma of the lung.
Electron microscopic sub-classification of small cell carcinoma of the lung.
Endometrial carcinoma and its precancerous lesions related with glandular cystic hyperplasia.
Esophageal squamous cell carcinoma and ALDH2 and ADH1B polymorphisms in Chinese females.
Expression of cyclins in ductal hyperplasia, atypical ductal hyperplasia and ductal carcinoma in situ of the breast.
Extent and histologic pattern of atypical ductal hyperplasia present on core needle biopsy specimens of the breast can predict ductal carcinoma in situ in subsequent excision.
Factors associated with upgrading to malignancy at surgery of atypical ductal hyperplasia diagnosed on core biopsy.
Fine-needle aspiration cytology of ductal hyperplasia with and without atypia and ductal carcinoma in situ.
Flat epithelial atypia on breast needle core biopsy: a retrospective study with clinical-pathological correlation.
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Frequencies of ADH1C alleles and genotypes in a Turkish head and neck cancer population.
Frequency and upgrade rates of atypical ductal hyperplasia diagnosed at stereotactic vacuum-assisted breast biopsy: 9-versus 11-gauge.
Genetic modulation of ADH1B and ALDH2 polymorphisms with regard to alcohol and tobacco consumption for younger aged esophageal squamous cell carcinoma diagnosis.
Genetic polymorphism and activities of human colon alcohol and aldehyde dehydrogenases: no gender and age differences.
Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males.
Genetic Polymorphisms of ADH1C and CYP2E1 and Risk of Oral Squamous Cell Carcinoma.
Genetic polymorphisms of alcohol and aldehyde dehydrogenases, and drinking, smoking and diet in Japanese men with oral and pharyngeal squamous cell carcinoma.
Genomic instability demonstrates similarity between DCIS and invasive carcinomas.
Glutathione, glutathione S-transferase alpha and pi, and aldehyde dehydrogenase content in relationship to drug resistance in ovarian cancer.
Head and Neck Squamous Cell Carcinoma Metabolism Draws on Glutaminolysis, and Stemness Is Specifically Regulated by Glutaminolysis via Aldehyde Dehydrogenase.
Hormonal polypeptides and amine metabolites in small cell carcinoma of the lung, with special reference to stage and subtypes.
Identification of a subpopulation of nasopharyngeal carcinoma cells with cancer stem-like cell properties by high aldehyde dehydrogenase activity.
Immunohistochemical analysis of Metadherin in proliferative and cancerous breast tissue.
Immunohistochemical study of matrix metalloproteinase 9 and tissue inhibitor of matrix metalloproteinase 1 in benign and malignant breast tissue--strong expression in intraductal carcinomas of the breast.
Immunological and endocrinological abnormalities in paraneoplastic disorders with involvement of the autonomic nervous system.
Impact of alcohol dehydrogenase gene 4 polymorphisms on esophageal squamous cell carcinoma risk in a Chinese population.
In silico analysis of differential gene expressions in biliary stricture and hepatic carcinoma.
Inappropriate ADH secretion caused by oat cell carcinoma and relieved by lung resection.
Increasing chromosome 1 copy number parallels histological progression in breast carcinogenesis.
Interactive effects of lifetime alcohol consumption and alcohol and aldehyde dehydrogenase polymorphisms on esophageal cancer risks.
Intrinsic cellular resistance to oxazaphosphorines exhibited by a human colon carcinoma cell line expressing relatively large amounts of a class-3 aldehyde dehydrogenase.
Is surgical excision necessary for focal atypical ductal hyperplasia found at stereotactic vacuum-assisted breast biopsy?
Laryngeal cancer risk in Caucasians is associated with alcohol and tobacco consumption but not modified by genetic polymorphisms in class I alcohol dehydrogenases ADH1B and ADH1C, and glutathione-S-transferases GSTM1 and GSTT1.
Long term clinical follow-up of atypical ductal hyperplasia and lobular carcinoma in situ in breast core needle biopsies.
Long-Term Safety of Observation in Selected Women Following Core Biopsy Diagnosis of Atypical Ductal Hyperplasia.
Loss of heterozygosity and microsatellite instability in epithelial hyperplasia of the breast.
Mammographic-histopathologic correlation of large-core needle biopsies of the breast.
Mammotome core biopsy for mammary microcalcification: analysis of 160 biopsies from 142 women with surgical and radiologic followup.
Mean corpuscular volume and ADH1C genotype in white patients with alcohol-associated diseases.
Minimal change nephrotic syndrome revealing solid tumors.
Minimizing underestimation rate of microcalcifications excised via vacuum-assisted breast biopsy: a blind study.
Neurophysins as markers of vasopressin and oxytocin release. A study in carcinoma of the lung.
Papillary lesions of the breast with and without atypical ductal hyperplasia: can we accurately predict benign behavior from core needle biopsy?
Polymorphism in ADH and MTHFR genes in oral squamous cell carcinoma of Indians.
Polymorphisms in metabolizing enzymes and the risk of head and neck squamous cell carcinoma in the Slavic population of the central Europe.
Predicting cancer on excision of atypical ductal hyperplasia.
Rapid isolation of tissue-specific genes from rat kidney.
Risk of head and neck cancer and the alcohol dehydrogenase 3 genotype.
Role of biological markers and probes in lung carcinomas.
Significance of flat epithelial atypia on mammotome core needle biopsy: Should it be excised?
Single-marker identification of head and neck squamous cell carcinoma cancer stem cells with aldehyde dehydrogenase.
Stem cell markers aldehyde dehydrogenase type 1 and nestin expressions in renal cell cancer.
Stereotactic and sonographic large-core biopsy of nonpalpable breast lesions: results of the Radiologic Diagnostic Oncology Group V study.
Stereotactic breast biopsy: an audit of 18 months at BreastScreen Auckland.
Stereotactic vacuum-assisted breast biopsy in 2874 patients: a multicenter study.
Stereotactic, automated, large-core needle biopsy of nonpalpable breast lesions: false-negative and histologic underestimation rates after long-term follow-up.
Strong interaction between the effects of alcohol consumption and smoking on oesophageal squamous cell carcinoma among individuals with ADH1B and/or ALDH2 risk alleles.
Syndrome of inappropriate ADH secretion and diplopia: oat cell (small cell) rectal carcinoma metastatic to the central nervous system.
Syndrome of inappropriate secretion of anti-diuretic hormone (SIADH) produced by an adenocarcinoma of the colon. Report of one case.
Tag single nucleotide polymorphisms of alcohol-metabolizing enzymes modify the risk of upper aerodigestive tract cancers: HapMap database analysis.
Targeting cancer initiating cells by promoting cell differentiation and restoring chemosensitivity via dual inactivation of STAT3 and src activity using an active component of antrodia cinnamomea mycelia.
Thalamic degeneration, dementia, and seizures. Inappropriate ADH secretion associated with bronchogenic carcinoma.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in renal cell carcinoma.
The activity of class I, II, III, and IV alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in liver cancer.
The ADH1C polymorphism modifies the risk of squamous cell carcinoma of the head and neck associated with alcohol and tobacco use.
The aldehyde dehydrogenase enzyme 7A1 is functionally involved in prostate cancer bone metastasis.
The biology of head and neck cancer stem cells.
The Diagnostic Value of Alcohol Dehydrogenase (ADH) Isoenzymes and Aldehyde Dehydrogenase (ALDH) Measurement in the Sera of Colorectal Cancer Patients.
The diagnostic value of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) measurement in the sera of patients with brain tumor.
The syndrome of inappropriate antidiuretic hormone secretion with carcinoma of the tongue.
The tumor suppressor adenomatous polyposis coli and caudal related homeodomain protein regulate expression of retinol dehydrogenase L.
Timing of critical genetic changes in human breast disease.
Tumor initiating cells: Development and critical characterization of a model derived from the A431 carcinoma cell line forming spheres in suspension.
Tumor markers in patients with lung cancer.
Two cases of multiple hormone-producing small cell carcinoma of the lung: coexistence of tumor ADH, ACTH, and beta-MSH.
Underestimation of atypical ductal hyperplasia at sonographically guided core biopsy of the breast.
[A case of postoperative hyponatremia caused by Sheehan syndrome associated with lung carcinoma]
[A case of small cell carcinoma of the ureter with SIADH-like symptoms]
[Atypical ductal hyperplasia of the breast. Its diagnostic imaging and the role of percutaneous needle biopsy with a 14-gauge needle]
[Biological characteristics of cells expressing high level of aldehyde dehydrogenase subpopulation in tongue squamous cell carcinoma Tca8113 cell line].
[Cysts of the mammary gland--surgical behavior and treatment].
[Double paraneoplastic syndrome and anaplastic carcinoma of the lung. ADH and ACTH levels in the tumoral tissue (author's transl)]
[Ductal hyperplasia and ductal carcinoma in situ. Definition--classification--differential diagnosis]
[Dynamic study on plasma antidiuretic hormone before and after surgery for lung cancers]
[Ectopic production of ADH and ACTH by the oat cell carcinoma of the lung (author's transl)]
[Investigation of the hypoosmolal syndrome in carcinomas of the lung (author's transl)]
[Lung carcinoma with inappropriate ADH secretion and Eaton-Lambert syndrome]
[Pathological characterization of atypical ductal hyperplasia of the breast]
[Pulmonary carcinoma with inappropriate ADH and ACTH secretion]
[Syndrome of inappropriate ADH secretion (SIADH) in small-cell bronchus carcinoma]
[Systematic evaluation of 8 arginine vasopressin and neurophysins plasma levels in 10 patients with oat cells carcinoma of the lung (author's transl)]
Carcinoma, Bronchogenic
Ectopic ADH production before clinical recognition of small cell carcinoma of the lung.
Plasma arginine vasopressin in the syndrome of antidiuretic hormone excess associated with bronchogenic carcinoma.
Thalamic degeneration, dementia, and seizures. Inappropriate ADH secretion associated with bronchogenic carcinoma.
Vasopressin and hypertension in man.
[Antidiuretic hormone in patients with bronchial carcinoma (author's transl)]
Carcinoma, Ductal
AgNOR analysis of atypical ductal hyperplasia and intraductal carcinoma of the breast.
Analysis of breast cancer progression using principal component analysis and clustering.
Analysis of p53 mutations in cells taken from paraffin-embedded tissue sections of ductal carcinoma in situ and atypical ductal hyperplasia of the breast.
Association of breast cancer with the finding of atypical ductal hyperplasia at core breast biopsy.
Atypical ductal hyperplasia at margin of breast biopsy--is re-excision indicated?
Atypical ductal hyperplasia diagnosis by directional vacuum-assisted stereotactic biopsy of breast microcalcifications. Considerations for surgical excision.
Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow-up biopsies.
Atypical ductal hyperplasia of the breast diagnosed by 11-gauge directional vacuum-assisted biopsy.
Atypical ductal hyperplasia of the breast: clonal proliferation with loss of heterozygosity on chromosomes 16q and 17p.
Borderline atypical ductal hyperplasia/low-grade ductal carcinoma in situ on breast needle core biopsy should be managed conservatively.
Can mammographic findings help discriminate between atypical ductal hyperplasia and ductal carcinoma in situ after needle core biopsy?
Chromosomal Alterations in Pure Nonneoplastic Breast Lesions: Implications for Breast Cancer Progression.
Comparison of immunohistochemical staining in breast papillary neoplasms of cytokeratin 5/6 and p63 in core needle biopsies and surgical excisions.
Core biopsy of the breast with atypical ductal hyperplasia: a probabilistic approach to reporting.
Diagnosis of Columnar Cell Lesions and Atypical Ductal Hyperplasia by Ultrasound-Guided Core Biopsy: Findings Associated with Underestimation of Breast Carcinoma.
Early Breast Cancer Precursor Lesions: Lessons Learned from Molecular and Clinical Studies.
Elucidating encounters of atypical ductal hyperplasia arising in gynaecomastia.
Evidence of chromosomal alterations in pure usual ductal hyperplasia as a breast carcinoma precursor.
Expression of cyclins in ductal hyperplasia, atypical ductal hyperplasia and ductal carcinoma in situ of the breast.
Extent and histologic pattern of atypical ductal hyperplasia present on core needle biopsy specimens of the breast can predict ductal carcinoma in situ in subsequent excision.
Flat epithelial atypia on breast needle core biopsy: a retrospective study with clinical-pathological correlation.
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Genetic mutations and expression of p53 in non-invasive breast lesions.
HER2 as a prognostic factor in breast cancer.
Immunohistochemical analysis of cancer stem cell markers in invasive breast carcinoma and associated ductal carcinoma in situ: relationships with markers of tumor hypoxia and microvascularity.
Immunohistochemical staining for cyclin D1 and Ki-67 aids in the stratification of atypical ductal hyperplasia diagnosed on breast core biopsy.
Increased expression of centrosomal alpha, gamma-tubulin in atypical ductal hyperplasia and carcinoma of the breast.
Increasing chromosome 1 copy number parallels histological progression in breast carcinogenesis.
Is the upgrade rate of atypical ductal hyperplasia diagnosed by core needle biopsy of calcifications different for digital and film-screen mammography?
Lobular neoplasia on core needle biopsy does not require excision.
Mammary ductoscopy and follow-up avoid unnecessary duct excision in patients with pathologic nipple discharge.
Mammographic-histopathologic correlation of large-core needle biopsies of the breast.
Mild ductal atypia after large-core needle biopsy of the breast: is surgical excision always necessary?
Papillary lesions of the breast with and without atypical ductal hyperplasia: can we accurately predict benign behavior from core needle biopsy?
Progesterone receptor A and B isoforms in the human breast and its disorders.
RNA-Seq of human breast ductal carcinoma in situ models reveals aldehyde dehydrogenase isoform 5A1 as a novel potential target.
Significance of flat epithelial atypia on mammotome core needle biopsy: Should it be excised?
Stereotactic and sonographic large-core biopsy of nonpalpable breast lesions: results of the Radiologic Diagnostic Oncology Group V study.
The diagnosis and management of pre-invasive breast disease: ductal carcinoma in situ (DCIS) and atypical ductal hyperplasia (ADH)--current definitions and classification.
The histologic spectrum of apocrine breast proliferations: a comparative study of morphology and DNA content by image analysis.
The management of lobular neoplasia identified on percutaneous core breast biopsy.
The role of molecular biomarkers for predicting adjacent breast cancer of Atypical Ductal Hyperplasia diagnosed on core biopsy.
Underestimation of atypical ductal hyperplasia at MRI-guided 9-gauge vacuum-assisted breast biopsy.
Understanding the premalignant potential of atypical hyperplasia through its natural history: a longitudinal cohort study.
[Role of cytokeratin expression in differential diagnosis of intraductal proliferative lesions of breast]
Carcinoma, Hepatocellular
Ability of different hepatoma cells to metabolize 4-hydroxynonenal.
Alcohol dehydrogenase 3, glutathione S-transferase M1 and T1 polymorphisms, alcohol consumption and hepatocellular carcinoma (Italy).
Alcohol Drinking Mediates the Association between Polymorphisms of ADH1B and ALDH2 and Hepatitis B-Related Hepatocellular Carcinoma.
Aldehyde dehydrogenase (ALDH2) activity in hepatoma cells is reduced by an adenoviral vector coding for an ALDH2 antisense mRNA.
Aldehyde dehydrogenase 2 polymorphism for development to hepatocellular carcinoma in East Asian alcoholic liver cirrhosis.
Aldehyde dehydrogenase 3 expression is decreased by clofibrate via PPAR gamma induction in JM2 rat hepatoma cell line.
Aldehyde dehydrogenase activities in hepatocyte nodules and hepatocellular carcinomas from Wistar rats.
Aldehyde dehydrogenase activity in a rat hepatoma.
Aldehyde dehydrogenase in 2-acetamidofluorene-induced rat hepatomas. Ontogeny and evidence that the new isoenzymes are not due to normal gene de-repression.
Aldehyde dehydrogenase in 2-acetylaminofluorene-induced rat hepatomas. Characterization of antigens recognized by anti-hepatoma aldehyde dehydrogenase sera.
Antisense oligonucleotides against aldehyde dehydrogenase 3 inhibit hepatoma cell proliferation by affecting MAP kinases.
Benzaldehyde: NADP aldehyde dehydrogenase activity in hepatocyte nodules, hepatocellular carcinomas and drug-induced rat liver.
Carcinostatic effect of aliphatic aldehydes and aldehyde dehydrogenase activity in Ehrlich carcinoma, Sarcoma 180, and Yoshida AH 130 hepatoma.
Cellular steatosis in ethanol oxidizing-HepG2 cells is partially controlled by the transcription factor, early growth response-1.
Characteristics and aldehyde dehydrogenase activity of four rat hepatoma cell lines produced by diethylnitrosamine-phenobarbital treatment.
Characterization of a nonhepatic alcohol dehydrogenase from rat hepatocellular carcinoma and stomach.
Characterization of alcohol dehydrogenase from cultured rat hepatoma (HTC) cells.
Characterization of aldehyde dehydrogenase from HTC rat hepatoma cells.
Chronic ethanol intake impairs insulin signaling in rats by disrupting Akt association with the cell membrane. Role of TRB3 in inhibition of Akt/protein kinase B activation.
Comparison of expression of aldehyde dehydrogenase 3 and CYP1A1 in dominant and recessive aryl hydrocarbon hydroxylase-deficient mutant mouse hepatoma cells.
Corticosterone induces rat liver alcohol dehydrogenase mRNA but not enzyme protein or activity.
Cytochemical detection of a class 3 aldehyde dehydrogenase in human hepatocellular carcinoma.
Diamine oxidase activity in regenerating rat liver and in 4-dimethylaminoazobenzene-induced and Yoshida AH 130 hepatomas.
Differential regulation of the alcohol dehydrogenase 1B (ADH1B) and ADH1C genes by DNA methylation and histone deacetylation.
Disulfiram eradicates tumor-initiating hepatocellular carcinoma cells in ROS-p38 MAPK pathway-dependent and -independent manners.
Dose-dependent inhibition of cell proliferation induced by lipid peroxidation products in rat hepatoma cells after enrichment with arachidonic acid.
Effect of ethanol on lipoprotein secretion in two human hepatoma cell lines, HepG2 and Hep3B.
Effect of phenobarbital and 3-methylcholanthrene on aldehyde dehydrogenase activity in cultures of HepG2 cells and normal human hepatocytes.
Elevated glutathione level does not protect against chronic alcohol mediated apoptosis in recombinant human hepatoma cell line VL-17A over-expressing alcohol metabolizing enzymes - Alcohol dehydrogenase and Cytochrome P450 2E1.
Epithelial Mesenchymal Transition and Hedgehog Signaling Activation are Associated with Chemoresistance and Invasion of Hepatoma Subpopulations.
Establishment of a recombinant hepatic cell line stably expressing alcohol dehydrogenase.
Ethanol induces fatty acid synthesis pathways by activation of sterol regulatory element-binding protein (SREBP).
Ethanol-induced inhibition of liver cell function: I. Effect of ethanol on hormone stimulated hepatocyte DNA synthesis and the role of ethanol metabolism.
Expression of differentiated functions in hepatoma cell hybrids. VI. Extinction and re-expression of liver alcohol dehydrogenase.
Expression of the tumor aldehyde dehydrogenase phenotype during 2-acetylaminofluorene-induced rat hepatocarcinogenesis.
Expression of tumor-associated aldehyde dehydrogenase gene in rat hepatoma cell lines.
Fatty aldehyde dehydrogenase is up-regulated by polyunsaturated fatty acid via peroxisome proliferator-activated receptor alpha and suppresses polyunsaturated fatty acid-induced endoplasmic reticulum stress.
Formation and export of the glutathione conjugate of 4-hydroxy-2, 3-E-nonenal (4-HNE) in hepatoma cells.
Genetic polymorphisms of ALDH2 and ADH2 are not associated with risk of hepatocellular carcinoma among East Asians.
Hormonal and chemical influences on the expression of class 2 aldehyde dehydrogenases in rat H4IIEC3 and human HuH7 hepatoma cells.
Immunohistochemical detection of tumour-associated aldehyde dehydrogenase in formalin-fixed rat and mouse normal liver and hepatomas.
Increased oxidative stress and toxicity in ADH and CYP2E1 overexpressing human hepatoma VL-17A cells exposed to high glucose.
Inducible (class 3) aldehyde dehydrogenase from rat hepatocellular carcinoma and 2,3,7,8-tetrachlorodibenzo-p-dioxin-treated liver: distant relationship to the class 1 and 2 enzymes from mammalian liver cytosol/mitochondria.
Induction of alcohol dehydrogenase activity and mRNA in hepatoma cells by dexamethasone.
Induction of class 3 aldehyde dehydrogenase in the mouse hepatoma cell line Hepa-1 by various chemicals.
Inhibition of alcohol dehydrogenase blocks enhanced Gi-protein expression following ethanol treatment in experimental hepatocellular carcinoma in vitro.
Inhibition of class-3 aldehyde dehydrogenase and cell growth by restored lipid peroxidation in hepatoma cell lines.
Kinetic properties of alcohol dehydrogenase in hepatocellular carcinoma and normal tissues of rat.
Knock down of GCN5 histone acetyltransferase by siRNA decreases ethanol-induced histone acetylation and affects differential expression of genes in human hepatoma cells.
Mitochondrial morphology and dynamics in hepatocytes from normal and ethanol-fed rats.
Molecular Links between Alcohol and Tobacco Induced DNA Damage, Gene Polymorphisms and Patho-physiological Consequences: A Systematic Review of Hepatic Carcinogenesis.
Molecular mechanisms of alcoholic fatty liver: role of sterol regulatory element-binding proteins.
New data on kinetics of lipid peroxidation in experimental hepatomas and preneoplastic nodules.
Oxidative metabolism of 4-hydroxy-2,3-nonenal during diethyl-nitrosamine-induced carcinogenesis in rat liver.
Promoters for the human alcohol dehydrogenase genes ADH1, ADH2, and ADH3: interaction of CCAAT/enhancer-binding protein with elements flanking the ADH2 TATA box.
Promyelocytic leukemia protein induces arsenic trioxide resistance through regulation of aldehyde dehydrogenase 3 family member A1 in hepatocellular carcinoma.
Properties of aldehyde dehydrogenas from chemically-induced rat hepatomas and normal rat liver.
Properties of serum alcohol dehydrogenase in Nigerians with primary hepatoma.
Proteomic alterations of the variants of human aldehyde dehydrogenase isozymes correlate with hepatocellular carcinoma.
Purification and catalytic properties of liver alcohol dehydrogenase isoenzymes in patients with hepatoma in Nigeria.
Purification and immunochemical characterization of aldehyde dehydrogenase from 2-acetylaminofluorene-induced rat hepatomas.
Regulation of 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible expression of aldehyde dehydrogenase in hepatoma cells.
Regulation of aldehyde dehydrogenase activity in five rat hepatoma cell lines.
Regulation of gene expression of class I alcohol dehydrogenase by glucocorticoids.
Role of aldehyde dehydrogenase activity in cyclophosphamide metabolism in rat hepatoma cell lines.
Role of aldehyde metabolizing enzymes in mediating effects of aldehyde products of lipid peroxidation in liver cells.
Sequential 2-acetylaminofluorene--phenobarbital exposure induces a cytosolic aldehyde dehydrogenase during rat hepatocarcinogenesis.
Subcellular distribution and properties of aldehyde dehydrogenase from 2-acetylaminofluorene-induced rat hepatomas.
Superinduction of 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible expression of aldehyde dehydrogenase by the inhibition of protein synthesis.
The class I alcohol dehydrogenase gene is glucocorticoid-responsive in the rat hepatoma microcell hybrid cell line, 11-3.
The novel aldehyde dehydrogenase gene, ALDH5, encodes an active aldehyde dehydrogenase enzyme.
The subcellular distribution and properties of aldehyde dehydrogenase of hepatoma AH-130.
Toxicity of ethanol and acetaldehyde in hepatocytes treated with ursodeoxycholic or tauroursodeoxycholic acid.
trans activation of human alcohol dehydrogenase gene expression in hepatoma cells by C/EBP molecules bound in a novel arrangement just 5' and 3' to the TATA box.
Use of an "acetaldehyde clamp" in the determination of low-KM aldehyde dehydrogenase activity in H4-II-E-C3 rat hepatoma cells.
Viability of cells in ethanol. Role of alcohol dehydrogenase.
Carcinoma, Intraductal, Noninfiltrating
17 beta-Hydroxysteroid dehydrogenase type 1 and type 2 in ductal carcinoma in situ and intraductal proliferative lesions of the human breast.
A study of the role of Notch1 and JAG1 gene methylation in development of breast cancer.
A unique proteolytic fragment of alpha1-antitrypsin is elevated in ductal fluid of breast cancer patient.
A useful immunohistochemical approach to evaluate intraductal proliferative lesions of the breast and to predict their prognosis.
Aberrant BLID expression is associated with breast cancer progression.
Absence of Residual Microcalcifications in Atypical Ductal Hyperplasia Diagnosed via Stereotactic Vacuum-Assisted Breast Biopsy: Is Surgical Excision Obviated?
Accuracy of 11-gauge vacuum-assisted core biopsy of mammographic breast lesions.
Accuracy of percutaneous core biopsy of isolated breast microcalcifications identified by mammography. Experience with a vacuum-assisted large-core biopsy device.
Accuracy of stereotactic vacuum-assisted breast biopsy with a 10-gauge hand-held system.
AgNOR analysis of atypical ductal hyperplasia and intraductal carcinoma of the breast.
All radial scars/complex sclerosing lesions seen on breast screening mammograms should be excised.
Altered mucin expression is a field change that accompanies mucinous (colloid) breast carcinoma histogenesis.
Amplification of Her-2/neu gene in Her-2/neu-overexpressing and -nonexpressing breast carcinomas and their synchronous benign, premalignant, and metastatic lesions detected by FISH in archival material.
Analysis of breast cancer progression using principal component analysis and clustering.
Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci.
Analysis of p53 mutations in cells taken from paraffin-embedded tissue sections of ductal carcinoma in situ and atypical ductal hyperplasia of the breast.
Aromatase expression in atypical ductal hyperplasia in women.
Association of breast cancer with the finding of atypical ductal hyperplasia at core breast biopsy.
Atypical ductal hyperplasia and atypia of uncertain significance in core biopsies from mammographically detected lesions: correlation with excision diagnosis.
Atypical ductal hyperplasia and ductal carcinoma in situ of the breast associated with perineural invasion.
Atypical ductal hyperplasia at margin of breast biopsy--is re-excision indicated?
Atypical Ductal Hyperplasia at the Margin of Lumpectomy Performed for Early Stage Breast Cancer: Is there Enough Evidence to Formulate Guidelines?
Atypical Ductal Hyperplasia Bordering on Ductal Carcinoma In Situ: Interobserver Variability and Outcomes in 105 Cases.
Atypical ductal hyperplasia diagnosis by directional vacuum-assisted stereotactic biopsy of breast microcalcifications. Considerations for surgical excision.
Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow-up biopsies.
Atypical ductal hyperplasia of the breast diagnosed by 11-gauge directional vacuum-assisted biopsy.
Atypical Ductal Hyperplasia of the Breast Diagnosed by Ultrasonographically Guided Core Needle Biopsy.
Atypical ductal hyperplasia of the breast: clonal proliferation with loss of heterozygosity on chromosomes 16q and 17p.
Atypical lobular hyperplasia or lobular carcinoma in situ at core-needle breast biopsy.
bcl-2 expression in the spectrum of preinvasive breast lesions.
Biomarkers in early breast neoplasia.
Borderline atypical ductal hyperplasia/low-grade ductal carcinoma in situ on breast needle core biopsy should be managed conservatively.
Breast carcinogenesis. Transition from hyperplasia to invasive lesions.
Breast Lesion Excision Sample (BLES Biopsy) Combining Stereotactic Biopsy and Radiofrequency: Is it a Safe and Accurate Procedure in Case of BIRADS 4 and 5 Breast Lesions?
Breast papillomas with atypical ductal hyperplasia: a clinicopathologic study.
Calcification retrieval at stereotactic, 11-gauge, directional, vacuum-assisted breast biopsy.
Can mammographic findings help discriminate between atypical ductal hyperplasia and ductal carcinoma in situ after needle core biopsy?
Cancerization of lobules and atypical ductal hyperplasia adjacent to ductal carcinoma in situ of the breast.
Cell polarity, epithelial-mesenchymal transition, and cell-fate decision gene expression in ductal carcinoma in situ.
Chromosomal Alterations in Pure Nonneoplastic Breast Lesions: Implications for Breast Cancer Progression.
Comparative features of carcinoma in situ and atypical ductal hyperplasia of the breast on fine-needle aspiration biopsy specimens.
Comparison of immunohistochemical staining in breast papillary neoplasms of cytokeratin 5/6 and p63 in core needle biopsies and surgical excisions.
Comparison of the diagnostic accuracy of a vacuum-assisted percutaneous intact specimen sampling device to a vacuum-assisted core needle sampling device for breast biopsy: initial experience.
Computerized Classification of Intraductal Breast Lesions using Histopathological Images.
Consistency achieved by 23 European pathologists from 12 countries in diagnosing breast disease and reporting prognostic features of carcinomas. European Commission Working Group on Breast Screening Pathology.
Core biopsy of the breast with atypical ductal hyperplasia: a probabilistic approach to reporting.
Cyclin D1 and associated proteins in mammary ductal carcinoma in situ and atypical ductal hyperplasia.
Cyclin D1 expression in ductal carcinoma in situ, atypical ductal hyperplasia and usual ductal hyperplasia: an immunohistochemical study.
D2-40: an additional marker for myoepithelial cells of breast and the precaution in interpreting tumor lymphovascular invasion.
Diagnosis of Columnar Cell Lesions and Atypical Ductal Hyperplasia by Ultrasound-Guided Core Biopsy: Findings Associated with Underestimation of Breast Carcinoma.
Diagnostic underestimation of atypical ductal hyperplasia and ductal carcinoma in situ at percutaneous core needle and vacuum-assisted biopsies of the breast in a Brazilian reference institution.
Diagnostic value of vacuum-assisted breast biopsy for breast carcinoma: a meta-analysis and systematic review.
Discrepancies in the diagnosis of intraductal proliferative lesions of the breast and its management implications: results of a multinational survey.
Downregulation of gelsolin correlates with the progression to breast carcinoma.
Ductal carcinoma in situ and atypical ductal hyperplasia of the breast diagnosed at stereotactic core biopsy.
Ductal Carcinoma in situ and related lesions of the breast: recent advances in pathology practice.
Ductal carcinoma in situ of the breast. Heterogeneity of individual lesions.
Early Breast Cancer Precursor Lesions: Lessons Learned from Molecular and Clinical Studies.
Early dysregulation of cell adhesion and extracellular matrix pathways in breast cancer progression.
Elucidating encounters of atypical ductal hyperplasia arising in gynaecomastia.
ER81 Expression in Breast Cancers and Hyperplasia.
Estrogen Receptor and Cytokeratin 5 Are Reliable Markers to Separate Usual Ductal Hyperplasia From Atypical Ductal Hyperplasia and Low-Grade Ductal Carcinoma In Situ.
Evidence of chromosomal alterations in pure usual ductal hyperplasia as a breast carcinoma precursor.
Experience in large-core needle biopsy in the diagnosis of 1431 breast lesions.
Expression of c-erbB-2 oncogene and p53 tumor suppressor gene in benign and malignant breast tissue: correlation with proliferative activity and prognostic index.
Expression of centrosomal tubulins associated with DNA ploidy in breast premalignant lesions and carcinoma.
Expression of cyclins in ductal hyperplasia, atypical ductal hyperplasia and ductal carcinoma in situ of the breast.
Expression of ER, Ki-67 and CylinD1 in the Pre-cancerous Breast of Chinese Patients.
Expression pattern and methylation of estrogen receptor ? in breast intraductal proliferative lesions.
Extent and histologic pattern of atypical ductal hyperplasia present on core needle biopsy specimens of the breast can predict ductal carcinoma in situ in subsequent excision.
Fine-needle aspiration cytology of ductal hyperplasia with and without atypia and ductal carcinoma in situ.
Flat epithelial atypia on breast needle core biopsy: a retrospective study with clinical-pathological correlation.
Flat epithelial atypia on core needle biopsy, must we surgically excise?
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Four quadrant fine needle aspiration cytology of non-palpable benign proliferative breast lesions.
Fourteen-gauge needle core biopsy of mammographically evident radial scars: is excision necessary?
Frequency and upgrade rates of atypical ductal hyperplasia diagnosed at stereotactic vacuum-assisted breast biopsy: 9-versus 11-gauge.
Genetic changes at specific stages of breast cancer progression detected by comparative genomic hybridization.
Genetic mutations and expression of p53 in non-invasive breast lesions.
Genomic instability demonstrates similarity between DCIS and invasive carcinomas.
HER2 as a prognostic factor in breast cancer.
Histologic correlation of image-guided core biopsy with excisional biopsy of nonpalpable breast lesions.
Histologic work-up of non-palpable breast lesions classified as probably benign at initial mammography and/or ultrasound (BI-RADS category 3).
Histopathologic analysis of atypical lesions in image-guided core breast biopsies.
Histopathological alterations during breast carcinogenesis in a rat model induced by 7,12-Dimethylbenz (a) anthracene and estrogen-progestogen combinations.
Hsp90 in the continuum of breast ductal carcinogenesis: Evaluation in precursors, preinvasive and ductal carcinoma lesions.
Human 21T breast epithelial cell lines mimic breast cancer progression in vivo and in vitro and show stage-specific gene expression patterns.
Hypoxia and metabolic phenotypes during breast carcinogenesis: expression of HIF-1alpha, GLUT1, and CAIX.
Image-guided procedures for breast masses.
Immunohistochemical analysis of Metadherin in proliferative and cancerous breast tissue.
Immunohistochemical evaluation of c-erbB-2 oncogene expression in ductal carcinoma in situ and atypical ductal hyperplasia of the breast.
Immunohistochemical staining for cyclin D1 and Ki-67 aids in the stratification of atypical ductal hyperplasia diagnosed on breast core biopsy.
Immunohistochemical studies of early breast cancer evolution.
Immunohistochemical study of matrix metalloproteinase 9 and tissue inhibitor of matrix metalloproteinase 1 in benign and malignant breast tissue--strong expression in intraductal carcinomas of the breast.
Impact of concurrent proliferative high-risk lesions on the risk of ipsilateral breast carcinoma recurrence and contralateral breast carcinoma development in patients with ductal carcinoma in situ treated with breast-conserving therapy.
Increased expression of centrosomal alpha, gamma-tubulin in atypical ductal hyperplasia and carcinoma of the breast.
Increasing chromosome 1 copy number parallels histological progression in breast carcinogenesis.
Indeterminate calcification and clustered cystic lesions are strongly predictive of the presence of mucocele-like tumor of the breast: a report of six cases.
Is the upgrade rate of atypical ductal hyperplasia diagnosed by core needle biopsy of calcifications different for digital and film-screen mammography?
Lobular carcinoma in situ or atypical lobular hyperplasia at core-needle biopsy: is excisional biopsy necessary?
Lobular neoplasia on core needle biopsy does not require excision.
Lobulocentricity of breast hypersecretory hyperplasia with cytologic atypia: infrequent association with carcinoma in situ.
Long term clinical follow-up of atypical ductal hyperplasia and lobular carcinoma in situ in breast core needle biopsies.
Loss of co-ordinate expression of progesterone receptors A and B is an early event in breast carcinogenesis.
Magnetic resonance imaging-guided breast biopsy in lesions not visualized by mammogram or ultrasound.
Mammary ductoscopy and follow-up avoid unnecessary duct excision in patients with pathologic nipple discharge.
Mammographic-histopathologic correlation of large-core needle biopsies of the breast.
Mammotome core biopsy for mammary microcalcification: analysis of 160 biopsies from 142 women with surgical and radiologic followup.
Mild ductal atypia after large-core needle biopsy of the breast: is surgical excision always necessary?
Minimizing underestimation rate of microcalcifications excised via vacuum-assisted breast biopsy: a blind study.
miRNAs as potential biomarkers in early breast cancer detection following mammography.
MR-Guided vacuum biopsy of 206 contrast-enhancing breast lesions.
Mucin extravasation in breast core biopsies--clinical significance and outcome correlation.
Mucocele-like lesions of the breast: a benign cause for indeterminate or suspicious mammographic microcalcifications.
Mucocele-like lesions of the breast: a long-term follow-up study.
Multicenter evaluation of the breast lesion excision system, a percutaneous, vacuum-assisted, intact-specimen breast biopsy device.
NUCKS overexpression in breast cancer.
Nuclear cytometric changes in breast carcinogenesis.
Nuclear morphometry in columnar cell lesions of the breast: is it useful?
Numerical abnormalities of chromosomes 7, 18, and x in precancerous breast disease defined by fluorescent in situ hybridization.
Oestrogen receptor expression in the normal and pre-cancerous breast.
p53 nuclear accumulation and ERalpha expression in ductal hyperplasia of breast in a cohort of 215 Chinese women.
P63 and cytokeratin8/18 expression in breast, atypical ductal hyperplasia, ductal carcinoma in situ and invasive duct carcinoma.
Papillary lesions of the breast at percutaneous core-needle biopsy.
Papillary lesions of the breast with and without atypical ductal hyperplasia: can we accurately predict benign behavior from core needle biopsy?
Pathologic and biologic response to preoperative endocrine therapy in patients with ER-positive ductal carcinoma in situ.
Pathological criteria and practical issues in papillary lesions of the breast - a review.
Personal experience of ultrasound-guided 14-gauge core biopsy of breast tumor.
Possible Prognostic Role of HER2/Neu in Ductal Carcinoma In Situ and Atypical Ductal Proliferative Lesions of the Breast.
Predictive factors for breast cancer in patients diagnosed atypical ductal hyperplasia at core needle biopsy.
Prevalence and classification of spontaneous mammary intraepithelial lesions in dogs without clinical mammary disease.
Progesterone receptor A and B isoforms in the human breast and its disorders.
Prognostic significance of reactivation of telomerase in breast core biopsy specimens.
Rates of atypical ductal hyperplasia have declined with less use of postmenopausal hormone treatment: findings from the Breast Cancer Surveillance Consortium.
Retinoic acid receptor and retinoid X receptor in ductal carcinoma in situ and intraductal proliferative lesions of the human breast.
Review of 125 SiteSelect stereotactic large-core breast biopsy procedures.
RNA-Seq of human breast ductal carcinoma in situ models reveals aldehyde dehydrogenase isoform 5A1 as a novel potential target.
Role of deregulated microRNAs in breast cancer progression using FFPE tissue.
Role of RNA binding protein HuR in ductal carcinoma in situ of the breast.
Significance of flat epithelial atypia on mammotome core needle biopsy: Should it be excised?
Spontaneous feline mammary intraepithelial lesions as a model for human estrogen receptor- and progesterone receptor-negative breast lesions.
Spontaneous mammary intraepithelial lesions in dogs--a model of breast cancer.
Stereotactic and sonographic large-core biopsy of nonpalpable breast lesions: results of the Radiologic Diagnostic Oncology Group V study.
Stereotactic breast biopsy of atypical ductal hyperplasia and ductal carcinoma in situ lesions: improved accuracy with directional, vacuum-assisted biopsy.
Stereotactic breast biopsy: an audit of 18 months at BreastScreen Auckland.
Stereotactic vacuum-assisted breast biopsy in 2874 patients: a multicenter study.
Subareolar Sclerosing Ductal Hyperplasia.
Surgical follow-up and clinical presentation of 142 breast papillary lesions diagnosed by ultrasound-guided core-needle biopsy.
Targeting the HER/EGFR/ErbB Family to Prevent Breast Cancer.
The diagnosis and management of pre-invasive breast disease: ductal carcinoma in situ (DCIS) and atypical ductal hyperplasia (ADH)--current definitions and classification.
The histologic spectrum of apocrine breast proliferations: a comparative study of morphology and DNA content by image analysis.
The management of lobular neoplasia identified on percutaneous core breast biopsy.
The role of chemoprevention in modifying the risk of breast cancer in women with atypical breast lesions.
The role of molecular biomarkers for predicting adjacent breast cancer of Atypical Ductal Hyperplasia diagnosed on core biopsy.
The significance of extracellular mucin in breast fine needle aspiration specimens.
The use of Au@SiO2 shell-isolated nanoparticle-enhanced Raman spectroscopy for human breast cancer detection.
The value of dynamic contrast enhanced breast MRI in mammographically detected bi-rads 5 microcalcifications.
Thymidine kinase 1 expression in atypical ductal hyperplasia significantly differs from usual ductal hyperplasia and ductal carcinoma in situ: A useful tool in tumor therapy management.
Timing of critical genetic changes in human breast disease.
Tubular carcinoma and grade 1 (well-differentiated) invasive ductal carcinoma: comparison of flat epithelial atypia and other intra-epithelial lesions.
Underestimation of atypical ductal hyperplasia at MRI-guided 9-gauge vacuum-assisted breast biopsy.
Underestimation of malignancy of atypical ductal hyperplasia diagnosed on 11-gauge stereotactically guided Mammotome breast biopsy: an Asian breast screen experience.
Underestimation Rate at MR Imaging-guided Vacuum-assisted Breast Biopsy: A Multi-Institutional Retrospective Study of 1509 Breast Biopsies.
Understanding the premalignant potential of atypical hyperplasia through its natural history: a longitudinal cohort study.
Upregulation of focal adhesion kinase (FAK) expression in ductal carcinoma in situ (DCIS) is an early event in breast tumorigenesis.
Vacuum-assisted breast biopsy: The value and limitations of cores with microcalcifications.
Value of cytokeratin 5/6 immunostaining using D5/16 B4 antibody in the spectrum of proliferative intraepithelial lesions of the breast. A comparative study with 34betaE12 antibody.
When is a diagnosis of sclerosing adenosis acceptable at core biopsy?
[Breast calcifications with percutaneous vacuum-assisted biopsy diagnosis of malignancy or atypical hyerplasia: correlations with surgical findings]
[Clonality of the peripheral papilloma and cancerous cells of breast]
[Ductal hyperplasia and ductal carcinoma in situ. Definition--classification--differential diagnosis]
[Evaluation of atypical ductal hyperplasia]
[Pathological characterization of atypical ductal hyperplasia of the breast]
[Role of cytokeratin expression in differential diagnosis of intraductal proliferative lesions of breast]
[Sonographically guided core needle biopsy of the breast: technique, accuracy and indications]
[The role of stereotactic 11G vacuum biopsy for clarification of BI-RADS IV findings in mammography]
[Vacuum-assisted biopsy and wire localization for the diagnosis of non-palpable breast lesions]
[Value of CK5/6, CK14, ER and PR detection in differential diagnosis of intraductal proliferative lesions of the breast].
Carcinoma, Lobular
Atypical ductal hyperplasia and atypia of uncertain significance in core biopsies from mammographically detected lesions: correlation with excision diagnosis.
Atypical ductal hyperplasia in breast core needle biopsies. Correlation of size of the lesion, complete removal of the lesion, and the incidence of carcinoma in follow-up biopsies.
Comparison of the diagnostic accuracy of a vacuum-assisted percutaneous intact specimen sampling device to a vacuum-assisted core needle sampling device for breast biopsy: initial experience.
Epithelial lesions in prophylactic mastectomy specimens from women with BRCA mutations.
Flat epithelial atypia with and without atypical ductal hyperplasia: to re-excise or not. Results of a 5-year prospective study.
Fourteen-gauge needle core biopsy of mammographically evident radial scars: is excision necessary?
Histology after lumpectomy in women with epithelial atypia on stereotactic vacuum-assisted breast biopsy.
Immunohistochemical evaluation of c-erbB-2 oncogene expression in ductal carcinoma in situ and atypical ductal hyperplasia of the breast.
Lobular neoplasia on core needle biopsy does not require excision.
Pathologic High-risk Lesions, Diagnosis and Management.
Significance of flat epithelial atypia on mammotome core needle biopsy: Should it be excised?
The histologic spectrum of apocrine breast proliferations: a comparative study of morphology and DNA content by image analysis.
The role of chemoprevention in modifying the risk of breast cancer in women with atypical breast lesions.
Underestimation of atypical ductal hyperplasia at MRI-guided 9-gauge vacuum-assisted breast biopsy.
Vacuum-assisted biopsy diagnosis of atypical ductal hyperplasia and patient management.
Carcinoma, Mucoepidermoid
Over-expression of glutathione S-transferases, DT-diaphorase and an apparently tumour-specific cytosolic class-3 aldehyde dehydrogenase by Warthin tumours and mucoepidermoid carcinomas of the human parotid gland.
Carcinoma, Non-Small-Cell Lung
Blocking the epithelial-to-mesenchymal transition pathway abrogates resistance to anti-folate chemotherapy in lung cancer.
Carcinoma, Renal Cell
BMP-2 inhibits tumor-initiating ability in human renal cancer stem cells and induces bone formation.
Stem cell markers aldehyde dehydrogenase type 1 and nestin expressions in renal cell cancer.
The activity of class I, II, III and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in renal cell carcinoma.
The diagnostic significance of serum alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase activity in renal cell cancer patients.
Carcinoma, Small Cell
A case of oat cell carcinoma of the lung associated with ectopic production of ADH, neurophysin and ACTH.
Ectopic ADH production before clinical recognition of small cell carcinoma of the lung.
Electron microscopic sub-classification of small cell carcinoma of the lung.
Hormonal polypeptides and amine metabolites in small cell carcinoma of the lung, with special reference to stage and subtypes.
Inappropriate ADH secretion caused by oat cell carcinoma and relieved by lung resection.
Neurophysins as markers of vasopressin and oxytocin release. A study in carcinoma of the lung.
Tumor markers in patients with lung cancer.
Two cases of multiple hormone-producing small cell carcinoma of the lung: coexistence of tumor ADH, ACTH, and beta-MSH.
[Ectopic production of ADH and ACTH by the oat cell carcinoma of the lung (author's transl)]
[Systematic evaluation of 8 arginine vasopressin and neurophysins plasma levels in 10 patients with oat cells carcinoma of the lung (author's transl)]
Carcinoma, Squamous Cell
A single nucleotide polymorphism in the alcohol dehydrogenase 7 gene (alanine to glycine substitution at amino acid 92) is associated with the risk of squamous cell carcinoma of the head and neck.
ADH1B and ALDH2 are associated with metachronous SCC after endoscopic submucosal dissection of esophageal squamous cell carcinoma.
ADH1B and ALDH2 polymorphisms and their associations with increased risk of squamous cell carcinoma of the head and neck in the Korean population.
Alcohol dehydrogenase 3 and risk of esophageal and gastric adenocarcinomas.
Alcohol dehydrogenase 3 and risk of squamous cell carcinomas of the head and neck.
Alcohol dehydrogenase 3 genotype is not associated with risk of squamous cell carcinoma of the oral cavity and pharynx.
Alcohol flushing, alcohol and aldehyde dehydrogenase genotypes, and risk for esophageal squamous cell carcinoma in Japanese men.
Aldehyde dehydrogenase activity is a cancer stem cell marker of tongue squamous cell carcinoma.
Association between ADH1B and ADH1C polymorphisms and the risk of head and neck squamous cell carcinoma.
Cancer stem cells in head and neck squamous cell carcinoma: a review.
Carcinogenetic impact of ADH1B and ALDH2 genes on squamous cell carcinoma risk of the esophagus with regard to the consumption of alcohol, tobacco and betel quid.
Esophageal squamous cell carcinoma and ALDH2 and ADH1B polymorphisms in Chinese females.
Frequencies of ADH1C alleles and genotypes in a Turkish head and neck cancer population.
Genetic modulation of ADH1B and ALDH2 polymorphisms with regard to alcohol and tobacco consumption for younger aged esophageal squamous cell carcinoma diagnosis.
Genetic polymorphisms in cytochrome P4502E1, alcohol and aldehyde dehydrogenases and the risk of esophageal squamous cell carcinoma in Gansu Chinese males.
Genetic Polymorphisms of ADH1C and CYP2E1 and Risk of Oral Squamous Cell Carcinoma.
Genetic polymorphisms of alcohol and aldehyde dehydrogenases, and drinking, smoking and diet in Japanese men with oral and pharyngeal squamous cell carcinoma.
Head and Neck Squamous Cell Carcinoma Metabolism Draws on Glutaminolysis, and Stemness Is Specifically Regulated by Glutaminolysis via Aldehyde Dehydrogenase.
Impact of alcohol dehydrogenase gene 4 polymorphisms on esophageal squamous cell carcinoma risk in a Chinese population.
Interactive effects of lifetime alcohol consumption and alcohol and aldehyde dehydrogenase polymorphisms on esophageal cancer risks.
Polymorphism in ADH and MTHFR genes in oral squamous cell carcinoma of Indians.
Polymorphisms in metabolizing enzymes and the risk of head and neck squamous cell carcinoma in the Slavic population of the central Europe.
Risk of head and neck cancer and the alcohol dehydrogenase 3 genotype.
Single-marker identification of head and neck squamous cell carcinoma cancer stem cells with aldehyde dehydrogenase.
Strong interaction between the effects of alcohol consumption and smoking on oesophageal squamous cell carcinoma among individuals with ADH1B and/or ALDH2 risk alleles.
Tag single nucleotide polymorphisms of alcohol-metabolizing enzymes modify the risk of upper aerodigestive tract cancers: HapMap database analysis.
Targeting cancer initiating cells by promoting cell differentiation and restoring chemosensitivity via dual inactivation of STAT3 and src activity using an active component of antrodia cinnamomea mycelia.
The ADH1C polymorphism modifies the risk of squamous cell carcinoma of the head and neck associated with alcohol and tobacco use.
The biology of head and neck cancer stem cells.
The syndrome of inappropriate antidiuretic hormone secretion with carcinoma of the tongue.
[Antidiuretic hormone in patients with bronchial carcinoma (author's transl)]
[Biological characteristics of cells expressing high level of aldehyde dehydrogenase subpopulation in tongue squamous cell carcinoma Tca8113 cell line].
[Dynamic study on plasma antidiuretic hormone before and after surgery for lung cancers]
Cardiac Output, Low
Possible role of juxtaglomerular apparatus in low cardiac output syndrome and multiple organ failure: modulation by high sodium load.
Cardiomegaly
Cardiac overexpression of alcohol dehydrogenase exacerbates cardiac contractile dysfunction, lipid peroxidation, and protein damage after chronic ethanol ingestion.
Cardiac overexpression of alcohol dehydrogenase exacerbates chronic ethanol ingestion-induced myocardial dysfunction and hypertrophy: role of insulin signaling and ER stress.
Cardiomyopathies
Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia.
[The status of the ethanol-oxidizing enzyme systems in fatal alcohol poisonings]
Cardiomyopathy, Alcoholic
Acetaldehyde and alcoholic cardiomyopathy: lessons from the ADH and ALDH2 transgenic models.
Overexpression of alcohol dehydrogenase exacerbates ethanol-induced contractile defect in cardiac myocytes.
Cardiovascular Diseases
Alcohol consumption, genetic variants in alcohol deydrogenases, and risk of cardiovascular diseases: a prospective study and meta-analysis.
Alcohol Dehydrogenase Protects against Endoplasmic Reticulum Stress-Induced Myocardial Contractile Dysfunction via Attenuation of Oxidative Stress and Autophagy: Role of PTEN-Akt-mTOR Signaling.
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Influence of alcohol dehydrogenase 1C polymorphism on the alcohol-cardiovascular disease association (from the Framingham Offspring Study).
The association of ADH and ALDH gene variants with alcohol drinking habits and cardiovascular disease risk factors.
Carotid Artery Diseases
Effects of aldehyde dehydrogenase genotypes on carotid atherosclerosis.
Cataract
Aldehyde dehydrogenase, aldose reductase, and free radical scavengers in cataract.
Anti-chaperone betaA3/A1(102-117) peptide interacting sites in human alphaB-crystallin.
NADPH-oxidising activity in lens and erythrocytes in diabetic and nondiabetic patients with cataract.
Significance of interactions of low molecular weight crystallin fragments in lens aging and cataract formation.
The transcripts of zeta-crystallin, a lens protein related to the alcohol dehydrogenase family, are altered in a guinea-pig hereditary cataract.
Central Nervous System Diseases
Hyponatremia in a nursing home population.
Inflammasome activation by cell volume regulation and inflammation-associated hyponatremia: A vicious cycle.
[Serum Na abnormality and disturbance of ADH secretion--with special reference to the central nervous system diseases]
Cerebral Hemorrhage
A study of serum antidiuretic hormone and atrial natriuretic peptide levels in a series of patients with intracranial disease and hyponatremia.
Cerebral Infarction
A study of serum antidiuretic hormone and atrial natriuretic peptide levels in a series of patients with intracranial disease and hyponatremia.
A subpopulation of endothelial progenitor cells with low aldehyde dehydrogenase activity attenuates acute ischemic brain injury in rats.
Alcohol dehydrogenase 2 variant is associated with cerebral infarction and lacunae.
Cerebral Palsy
Adeno-associated virus vectors are able to restore fatty aldehyde dehydrogenase-deficiency. Implications for gene therapy in Sjogren-Larsson syndrome.
Chemical and Drug Induced Liver Injury
Serum activities of classes I and II alcohol dehydrogenases in toxic liver damage.
[Molecular mechanisms of metabolic adaptation in pathological changed liver during toxic hepatitis ]
Chickenpox
Disseminated visceral varicella zoster virus presenting with the constellation of colonic pseudo-obstruction, acalculous cholecystitis and syndrome of inappropriate ADH secretion.
Varicella in immunocompromised children. Incidence of abdominal pain and organ involvement.
[Probable ADH inappropriate secretion syndrome in varicella]
Cholangiocarcinoma
ALDH1A3, the Major Aldehyde Dehydrogenase Isoform in Human Cholangiocarcinoma Cells, Affects Prognosis and Gemcitabine Resistance in Cholangiocarcinoma Patients.
Transforming growth factor-?1-induced epithelial-mesenchymal transition generates ALDH-positive cells with stem cell properties in cholangiocarcinoma.
Cholera
Expression of the Vibrio cholerae gene encoding aldehyde dehydrogenase is under control of ToxR, the cholera toxin transcriptional activator.
PGE2, forskolin, and cholera toxin interactions in modulating NaCl transport in mouse mTALH.
PGE2, forskolin, and cholera toxin interactions in rabbit cortical collecting tubule.
Prevention of alpha 2-adrenergic inhibition on ADH action by pertussis toxin in rabbit CCT.
[ADH and cAMP receptor binding in the kidney medulla of mice insensitive to ADH]
Cholestasis
Effects of high taurocholate load on activities of hepatic alcohol metabolizing enzymes.
Cholestasis, Intrahepatic
Serum alcohol dehydrogenase, an indicator of intrahepatic cholestasis.
Choline Deficiency
Changes in aldehyde dehydrogenase occurring during rat hepatocarcinogenesis induced by ethionine combined with dietary choline deficiency.
Chorea
A case of acute onset succinic semialdehyde dehydrogenase deficiency: neuroimaging findings and literature review.
Cleft Lip
Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.
Cleft Palate
Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia.
Cluster Headache
Cluster Headache is Associated With the Alcohol Dehydrogenase 4 (ADH4) Gene.
Cocarcinogenesis
Alcohol dehydrogenase in the human colon and rectum.
Gastrointestinal alcohol dehydrogenase.
Colonic Neoplasms
Activities of cytosolic aldehyde dehydrogenase isozymes in colon cancer: determination using selective, fluorimetric assays.
Aldehyde dehydrogenase-expressing colon stem cells contribute to tumorigenesis in the transition from colitis to cancer.
Human colon cancer stem cells are enriched by insulin-like growth factor-1 and are sensitive to figitumumab.
Resistance factors in colon cancer tissue and the adjacent normal colon tissue: glutathione S-transferases alpha and pi, glutathione and aldehyde dehydrogenase.
STAT3 signaling pathway is necessary for cell survival and tumorsphere forming capacity in ALDH?/CD133? stem cell-like human colon cancer cells.
The impact of inflammatory lipid mediators on colon cancer-initiating cells.
Colonic Pseudo-Obstruction
Disseminated visceral varicella zoster virus presenting with the constellation of colonic pseudo-obstruction, acalculous cholecystitis and syndrome of inappropriate ADH secretion.
Colorectal Neoplasms
A novel polymorphism rs1329149 of CYP2E1 and a known polymorphism rs671 of ALDH2 of alcohol metabolizing enzymes are associated with colorectal cancer in a southwestern Chinese population.
Alcohol and colorectal cancer: the role of alcohol dehydrogenase 1C polymorphism.
Alcohol consumption, alcohol dehydrogenase 1C (ADH1C) genotype, and risk of colorectal cancer in the Netherlands Cohort Study on diet and cancer.
Alcohol consumption, alcohol dehydrogenase 3 polymorphism, and colorectal adenomas.
Alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) activity in the sera of patients with colorectal cancer.
Alcohol dehydrogenase 3 genotype is not predictive for risk of colorectal cancer.
Alcohol dehydrogenase and aldehyde dehydrogenase gene polymorphisms, alcohol intake and the risk of colorectal cancer in the European Prospective Investigation into Cancer and Nutrition study.
Alcohol dehydrogenase and aldehyde dehydrogenase polymorphisms and colorectal cancer: the Fukuoka Colorectal Cancer Study.
Alcohol dehydrogenase, iron containing, 1 promoter hypermethylation associated with colorectal cancer differentiation.
Alcohol drinking and colorectal cancer in Japanese: a pooled analysis of results from five cohort studies.
Alcohol induces cell proliferation via hypermethylation of ADHFE1 in colorectal cancer cells.
Altered Expression of Multiple Genes Involved in Retinoic Acid Biosynthesis in Human Colorectal Cancer.
Association of ADH1B Arg47His and ALDH2 Glu487Lys polymorphisms with risk of colorectal cancer and their interaction with environmental factors in a Chinese population.
Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human large bowel: association of the functional polymorphisms of ADH and ALDH genes with hemorrhoids and colorectal cancer.
Impact of multiple Alcohol Dehydrogenase gene polymorphisms on risk of laryngeal, esophageal, gastric and colorectal cancers in Chinese Han population.
Meta-analysis of the ADH1B and ALDH2 polymorphisms and the risk of colorectal cancer in East Asians.
Polymorphisms in alcohol metabolism genes ADH1B and ALDH2, alcohol consumption and colorectal cancer.
Polymorphisms of alcohol dehydrogenase 2 and aldehyde dehydrogenase 2 and colorectal cancer risk in Chinese males.
Resistance factors in colon cancer tissue and the adjacent normal colon tissue: glutathione S-transferases alpha and pi, glutathione and aldehyde dehydrogenase.
Role of epoxide hydrolase, NAD(P)H:quinone oxidoreductase, cytochrome P450 2E1 or alcohol dehydrogenase genotypes in susceptibility to colorectal cancer.
The activity of class I, II, III, and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in colorectal cancer.
The Diagnostic Value of Alcohol Dehydrogenase (ADH) Isoenzymes and Aldehyde Dehydrogenase (ALDH) Measurement in the Sera of Colorectal Cancer Patients.
[Alcohol dehydrogenase and aldehyde dehydrogenase as tumour markers and factors intensifying carcinogenesis in colorectal cancer]
[Role of alcohol-metabolizing enzymes gene polymorphisms and environmental exposure on colorectal cancer: a case-only study].
Coma
Pretreatment of CD-1 mice with 4-methylpyrazole blocks toxicity from the gamma-hydroxybutyrate precursor, 1,4-butanediol.
Triethylene glycol poisoning treated with intravenous ethanol infusion.
Vasopressin: deficiency, excess and the syndrome of inappropriate antiduretic hormone secretion.
[Central pontine myelinolysis following severe hyponatremia]
Communicable Diseases
Histoplasmosis associated with a bamboo bonfire--Arkansas, October 2011.
Cone-Rod Dystrophies
Toll-like receptor 3 is required for development of retinopathy caused by impaired all-trans-retinal clearance in mice.
Congenital Abnormalities
[Neurogenic hypernatremia with adipsia and cerebral malformations in a child with ectrodactyly-ectodermal dysplasia-cleft lip-palate syndrome]
Corneal Opacity
A genetic basis for corneal sensitivity to ultraviolet light among recombinant SWXJ inbred strains of mice.
[Ocular anomalies in Alagille's syndrome]
Coronary Artery Disease
Association of genetic polymorphisms in ADH and ALDH2 with risk of coronary artery disease and myocardial infarction: a meta-analysis.
Circulating progenitor cells can be reliably identified on the basis of aldehyde dehydrogenase activity.
Genetic variation in aldehyde dehydrogenase 2 and the effect of alcohol consumption on cholesterol levels.
Joint effects of eNOS gene T-786C and ADH2 Arg47His polymorphisms on the risk of premature coronary artery disease.
[Association analysis of gene polymorphism in alcohol metabolizing enzymes with risk for coronary atherosclerosis]
Coronary Disease
Alcohol consumption, alcohol dehydrogenase and risk of coronary heart disease in the MONICA/KORA-Augsburg cohort 1994/1995-2002.
Alcohol dehydrogenase type 1C (ADH1C) variants, alcohol consumption traits, HDL-cholesterol and risk of coronary heart disease in women and men: British Women's Heart and Health Study and Caerphilly cohorts.
Exploring causal associations between alcohol and coronary heart disease risk factors: findings from a Mendelian randomization study in the Copenhagen General Population Study.
Genetic variation in alcohol dehydrogenase 1C and the beneficial effect of alcohol intake on coronary heart disease risk in the Second Northwick Park Heart Study.
Is ADH1C genotype relevant for the cardioprotective effect of alcohol?
[The status of the ethanol-oxidizing enzyme systems in fatal alcohol poisonings]
Cough
[Coughs and a loss of appetite (thoracic radiography and serum sodium and ADH levels): (lung cancer--ADH producing type--)]
Cranial Nerve Diseases
Overdosage with vincristine.
Craniocerebral Trauma
Antidiuretic hormone release in the bovine: values at rest, and evidence for sex differences under stressful conditions including severe hemorrhage.
Increased intracranial pressure is associated with elevated cerebrospinal fluid ADH levels in closed-head injury.
Unusual delayed onset of diabetes insipidus following closed head trauma. Case report.
Craniopharyngioma
[A case of postoperative craniopharyngioma with hypernatremia. The mechanisms of ADH and atrial natriuretic peptide (ANP) releases]
[Diabetes insipidus and inappropriate ADH secretion in the postoperative period of a craniopharyngioma]
Cryptorchidism
[Expression changes of aldehyde dehydrogenase 1A1 in rat cryptorchidism and normal testis].
Cushing Syndrome
Ectopic hormone production by tumours. Clinical aspects.
Effect of exogenous glucocorticoid on osmotically stimulated antidiuretic hormone secretion and on water reabsorption in man.
Multiple pituitary hormone abnormalities, fever, behavioral problems, seizures and apnoic spells in a 6-year old girl.
[Paraneoplastic endocrine syndromes]
Cutis Laxa
Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1.
Cystic Fibrosis
Inappropriate secretion of ADH as a cause of hyponatremia in cystic fibrosis.
Cystitis
Frequency and distribution of uropathogenic Escherichia coli adhesins: a clinical correlation over 2,000 cases.
Cysts
Synthesis of pyruvate: ferredoxin oxidoreductase and alcohol dehydrogenase E enzymes during Giardia intestinalis excystation.
Transcription of metabolic enzyme genes during the excystation of Giardia lamblia.
[Cysts of the mammary gland--surgical behavior and treatment].
d-lactate dehydrogenase deficiency
Genetic and physiological analysis of the lethal effect of L-(+)-lactate dehydrogenase deficiency in Streptococcus mutans: complementation by alcohol dehydrogenase from Zymomonas mobilis.
Decompression Sickness
Eye lens zeta-crystallin relationships to the family of "long-chain" alcohol/polyol dehydrogenases. Protein trimming and conservation of stable parts.
Deficiency Diseases
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase.
Dehydration
A case of diabetic non-ketotic hyperosmolar coma with an increase with plasma 3-hydroxybutyrate.
A case of hypopituitarism with diabetes insipidus and loss of thirst. Role of antidiuretic hormone and angiotensin II in the control of urine flow and osmolality.
A question of balance--dehydration in the elderly.
A systems biology approach reveals major metabolic changes in the thermoacidophilic archaeon Sulfolobus solfataricus in response to the carbon source L-fucose versus D-glucose.
Abscisic acid induces the alcohol dehydrogenase gene in Arabidopsis.
Adaptation to water depletion in the newborn rat--immunocytochemical localization of aquaporin-2.
Aldosterone and ADH response to heat and dehydration in cattle.
An assessment of posterior pituitary function in patients with Sheehan's syndrome.
ANF-induced modulation of ADH-release in the rabbit and Pekin duck.
Angiotensin II inhibits ADH-stimulated cAMP: role on O2- and transport-related oxygen consumption in the loop of Henle.
Cloning of an aquaporin homologue present in water channel containing endosomes of toad urinary bladder.
Copeptin as a marker for arginine-vasopressin/antidiuretic hormone secretion in the diagnosis of paraneoplastic syndrome of inappropriate ADH secretion.
Dehydration, antidiuretic hormone and the intravenous urogram.
Differential interactions of promoter elements in stress responses of the Arabidopsis Adh gene.
Dissociation between antidiuretic response and renal medullary cyclic AMP levels in the rat.
Dissociation of renin and aldosterone during dehydration: studies in a case of diabetes insipidus and adipsia.
Downregulation of Klotho expression by dehydration.
Dual effects of antidiuretic hormone on urinary prostaglandin E2 excretion in man.
Effect of dehydration on stimulation of ADH release by heterologous renin infusions in conscious dogs.
Effects of dehydration on body fluid regulated by ADH and aldosterone in swamp buffaloes and Friesian cows.
Effects of intracerebroventricular administration of atrial natriuretic peptide (ANP) on blood pressure, heart rate and plasma ADH and corticosterone levels in normal and dehydrated rabbits.
Effects of osmolality and antidiuretic hormone on prostaglandin synthesis by renal papilla. Study in Brattleboro rats with diabetes insipidus.
Effects of water deprivation on immunoreactive angiotensin II levels in plasma, cerebroventricular perfusate and hypothalamus of the rat.
Ethylene glycol poisoning in three dogs: Importance of early diagnosis and role of hemodialysis as a treatment option.
High antidiuretic hormone levels and hyponatremia in children with gastroenteritis.
Influence of renal denervation on urine concentration in awake and anaesthetized dogs.
Influence of season on plasma antidiuretic hormone, angiotensin II, aldosterone and plasma renin activity in young volunteers.
Inhibition of ADH release in the rat by narcotic antagonists.
Intra-specific variations in expression of stress-related genes in beech progenies are stronger than drought-induced responses.
Intracerebroventricular administration of atrial natriuretic peptide prevents increase of plasma ADH, aldosterone and corticosterone levels in restrained conscious dehydrated rabbits.
Low serum urea level in dehydrated patients with central diabetes insipidus.
Low Temperature Induces the Accumulation of Alcohol Dehydrogenase mRNA in Arabidopsis thaliana, a Chilling-Tolerant Plant.
Organic osmolytes in inner medulla of Brattleboro rat: effects of ADH and dehydration.
Physiological and behavioral basis for the successful adaptation of goats to severe water restriction under hot environmental conditions.
Plasma antidiuretic hormone (ADH) concentrations in cattle, during various water and feed regimes.
Polyuria and imparied ADH release following medial preoptic lesioning in the rat.
Profound hyponatraemia following an idiosyncratic reaction to diuretics.
Recovery of ADH activity in the urine of goats under normal and stimulated conditions.
Reversal of ethanol induced body dehydration with prolonged consumption in rats.
Serum antidiuretic hormone is elevated in relation to the increase in average total body transepidermal water loss in severe atopic dermatitis.
Suppression of ADH during water immersion in normal man.
Temperature and water loss affect ADH activity and gene expression in grape berry during postharvest dehydration
Temperature and water loss affect ADH activity and gene expression in grape berry during postharvest dehydration.
The aging kidney.
The effect of dehydration and repeated water loading on the supraoptic-neurohypophyseo-neurosecretory system and the ADH content of the neurohypophysis in the rat.
The toxicokinetics of 1,3-butylene glycol versus ethanol in the treatment of ethylene glycol poisoning.
Thirst and hydration: physiology and consequences of dysfunction.
Transcription factor veracity: is GBF3 responsible for ABA-regulated expression of Arabidopsis Adh?
Ultrastructural effects of anteroventral third ventricle lesions on supraoptic nuclei and neural lobes of rats.
Urinary concentrating ability during dehydration in the absence of vasopressin.
[A patient with meningeal carcinomatosis accompanied by a small pituitary metastatic lesion from gastric cancer who developed cerebral salt wasting syndrome]
[Diagnostic value of the determination of blood urea in dehydrated patients with and without central diabetes insipidus]
[Increased plasma antidiuretic hormone in the presence of hyponatremia in primary hypothyroidism]
[Measurement of antidiuretic hormone and plasma renin activity in desert rodents]
[Syndrome of inappropriate ADH secretion (SIADH) induced by pramipexole in a patient with Parkinson's disease]
[The determination of the ethanol elimination rate in the blood based on its concentration in the exhaled air].
Dementia
Thalamic degeneration, dementia, and seizures. Inappropriate ADH secretion associated with bronchogenic carcinoma.
Dental Caries
The role of aldehyde dehydrogenase and hsp70 in suppression of white spot syndrome virus replication at high temperature.
Dermatitis
[Polymorphisms of aldehyde and alcohol dehydrogenase genes associated with susceptibility to trichloroethylene-induced medicamentosa-like dermatitis]
Dermatitis, Contact
Safety evaluation of topical applications of ethanol on the skin and inside the oral cavity.
Diabetes Complications
Chlorpropamide-alcohol flushing, aldehyde dehydrogenase activity, and diabetic complications.
Effects of chlorpropamide and alcohol on aldehyde dehydrogenase activity and blood acetaldehyde concentration.
[Pathophysiological analysis of diabetes mellitus and complications from the urine of diabetic patients]
Diabetes Insipidus
A heterologous radioimmunoassay for arginine vasopressin.
Abnormal water turnover associated with hypothalamic obesity.
Adaptation of the rat kidney to altered water intake and urine concentration.
ADH-associated pathologies. Diabetes insipidus and syndrome of inappropriate ADH.
Alobar holoprosencephaly with diabetes insipidus and neuronal migration disorder.
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS AND AMERICAN COLLEGE OF ENDOCRINOLOGY DISEASE STATE CLINICAL REVIEW: POSTOPERATIVE MANAGEMENT FOLLOWING PITUITARY SURGERY.
An assessment of posterior pituitary function in patients with Sheehan's syndrome.
Antidiuretic action of prolactin in the rat with diabetes insipidus.
Beta-adrenergic (isoproterenol) regulation of antidiuretic hormone.
Bioassay of ADH on the experimental diabetes insipidus rats with a study on the ADH level in normal human plasma.
Boxing as a sport activity associated with isolated GH deficiency.
Captopril (SQ 14225) depresses drinking and aldosterone in rats lacking vasopressin.
Chlorpropamide-induced hyponatremia.
Clinical guidelines for management of diabetes insipidus and syndrome of inappropriate antidiuretic hormone secretion after pituitary surgery.
Clonidine-induced diuresis in the rat: evidence for a renal site of action.
Competing interests in a lung cancer with metastasis to the pituitary gland: syndrome of inappropriate ADH secretion versus diabetes insipidus.
Diabetes insipidus and ADH regulation.
Diabetes insipidus in children.
Diabetes insipidus.
Diagnosis and treatment of pituitary disease.
Disordered control of thirst in hypothalamic-pituitary sarcoidosis.
Dose-dependent stimulation of renal prostaglandin synthesis by deamino-8-D-arginine vasopressin in rats with hereditary diabetes insipidus.
Effect of long- and short-term antidiuretic hormone availability on internephron heterogeneity in the adult rat.
Effect of potassium loading on prostaglandin E2 and F2 alpha excretion in the Brattleboro rat.
Effects of osmolality and antidiuretic hormone on prostaglandin synthesis by renal papilla. Study in Brattleboro rats with diabetes insipidus.
Endocrine crises. Diabetes insipidus.
Endocrine manifestations of critical illness in the child.
Essential hypernatraemia, antidiuretic hormone and neurophysin secretion: response to chlorpropamide.
Hedgehog signaling: endocrine gland development and function.
Hypothalamo-pituitary dysfunction in patients with chronic subdural hematoma.
If ADH goes out of balance. Diabetes insipidus.
Influence of chronic ADH treatment on adenylate cyclase and ATPase activity in distal nephron segments of diabetes insipidus Brattleboro rats.
Intrarenal distribution of blood flow in diabetes insipidus: role of ADH.
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Lithium: ADH antagonism and ADH independent action in rats with diabetes insipidus.
MRI of ectopic posterior pituitary bright spot with large adenomas: appearances and relationship to transient postoperative diabetes insipidus.
NADH-dependent prostaglandin E2-9-ketoreductase activity and prostaglandin synthesis in the Brattleboro rat kidney: effects of the antidiuretic hormone.
Neuroendocrine abnormalities in patients with traumatic brain injury.
Neuroendocrine dysfunction in the acute phase of traumatic brain injury.
Pathophysiologic and pharmacologic alterations in the release and action of ADH.
Plasma ADH in normal Long-Evans rats and in Long-Evans rats heterozygous and homozygous for hypothalamic diabetes insipidus.
Prognostic factors for impaired plasma sodium homeostasis after transsphenoidal surgery.
Regulation of water intake.
Salt and water imbalance following pituitary surgery.
Selective ADH-induced hypertrophy of the medullary thick ascending limb in Brattleboro rats.
Sensitivity to ADH of normal and diabetes insipidus rats.
Sialadenosis of the major salivary glands in a patient with central diabetes insipidus--implications of aquaporin water channels in the pathomechanism of sialadenosis.
Stimulation of tubular reabsorption of magnesium and calcium by antidiuretic hormone in conscious rats. Study in Brattleboro rats with hereditary hypothalamic diabetes insipidus.
The effects of antidiuretic hormone and state of potassium balance on the renin-angiotensin system in rats with diabetes insipidus.
Transient Diabetes Insipidus Following Cardiopulmonary Bypass.
Triphasic AVP secretion in encephalopathy.
Up-regulation of renal adenylate cyclase-coupled vasopressin receptors after chronic administration of vasopressin antagonists to rats.
Water and sodium disorders following surgical excision of pituitary region tumours.
[Abnormal sweat test in patient with Diabetes Insipidus unresponsive to ADH]
[Arhinencephaly detected by a pitressin-sensitive diabetes insipidus]
[Case reports of disturbances of effective osmolality regulation in disorders of the central nervous system]
[Cerebral salt loss as Schwartz-Bartter-syndrome in childhood (author's transl)]
[Changes in water metabolism of rats with diabetes insipidus under treatment with clofibrate, with or without ADH]
[Comparative action of carbamazepine and clofibrate in diabetes insipidus. Study of 7 cases]
[Demonstration of serum ADH activities in hypophysectomy patients with polyuria and polydipsia and subjects with diabetes insipidus under the influence of an antidiuretically active psychotropic antiepilepticum (5-carbamyl-5-H-dibenzo-(b,f)azepin=Tegretal)]
[Diabetes insipidus after surgery of intracranial arterial aneurysms--with special reference to the human ADH and aldosterone secretion (author's transl)]
[Diabetes insipidus and adipsic hypernatremia in a patient with a craniopharyngioma]
[Diabetes insipidus and inappropriate ADH secretion in the postoperative period of a craniopharyngioma]
[Diabetes insipidus in pregnancy--a case report].
[Discrepant excretion volume (DV); a new nomogram for clinical diagnosis and treatment of diabetes insipidus and inappropriate secretion of ADH in neurosurgical patients (author's transl)]
[Drug-related disorders of water and electrolyte metabolism]
[Hormonal diseases after traumatic brain injury]
[Idiopathic diabetes insipidus. Changes of thyroid function before and after treatment with ADH]
[Plasma renin activity in vasopressin-sensitive diabetes insipidus and changes in the same produced by clofibrate, carbamazepine and exogenous ADH]
[Polyuria]
[Polyuropolydipsic syndromes]
[Posttraumatic hypopituitarism]
[Radioimmunoassay for human plasma 8-arginine-vasopressin (author's transl)]
[Studies on diabetes insipidus in children. I. Sensitivity to ADH]
[The diagnostic value of the determination of cyclic 3',5'-adenosine monophosphate (cAMP) in urine]
[The effect of clofibrate on fluid metabolism in hypothalamic and ADH resistant diabetes insipidus]
[Transient diabetes insipidus following removal of a medullary thyroid carcinoma (author's transl)]
Diabetes Insipidus, Nephrogenic
Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus.
Demeclocycline treatment in the syndrome of inappropriate antidiuretic hormone secretion.
Newly symptomatic central diabetes insipidus in ESRD with adult polycystic kidney disease following intracranial hemorrhage: the first reported case.
Pathophysiologic and pharmacologic alterations in the release and action of ADH.
Response to ADH in nephrogenic diabetes insipidus type 2.
Severe bladder dysfunction in a family with ADH receptor gene mutation responsible for X-linked nephrogenic diabetes insipidus.
[Hormonal dysnatremia].
Diabetes Insipidus, Neurogenic
Endocrine crises. Diabetes insipidus.
Evidence for permanent enhancement of residual ADH induced by antidiuretic agents (chlorpropamide, carbamazepine, clofibrate) in patients with pituitary diabetes insipidus.
Head trauma as a possible cause of central diabetes insipidus in a cat.
Inappropriate secretion of ADH and central diabetes insipidus are related to antiphospholipid antibodies in SLE--case report and review of the literature.
Mannitol osmolar clearance in diabetes insipidus of children.
Newly symptomatic central diabetes insipidus in ESRD with adult polycystic kidney disease following intracranial hemorrhage: the first reported case.
Transient diabetes insipidus following Escherichia coli meningitis complicated by ventriculoperitoneal shunt.
[Polyuropolydipsic syndromes]
Diabetes Mellitus
Aldehyde dehydrogenase activity and large vessel disease in diabetes mellitus. A preliminary study.
Chlorpropamide-induced ADH release, hyponatremia and central pontine myelinolysis in diabetes mellitus.
[Aldehyde dehydrogenase 2(ALDH2) gene polymorphism in NIDDM patients with chronic renal failure]
[Endocrine crises]
Diabetes Mellitus, Experimental
The effect of experimental diabetes on liver alcohol dehydrogenase activity in rats.
Diabetes Mellitus, Type 1
Fatty aldehyde dehydrogenase: potential role in oxidative stress protection and regulation of its gene expression by insulin.
Diabetes Mellitus, Type 2
Alcohol consumption and type 2 diabetes: influence of genetic variation in alcohol dehydrogenase.
Association of aldehyde dehydrogenase with inheritance of NIDDM.
Differential Effect of Initiating Moderate Red Wine Consumption on 24-h Blood Pressure by Alcohol Dehydrogenase Genotypes: Randomized Trial in Type 2 Diabetes.
Downregulation of the acetyl-CoA metabolic network in adipose tissue of obese diabetic individuals and recovery after weight loss.
Hypoglycemic drugs induce antioxidant aldehyde dehydrogenase activity and remain high in patients with glycemic control in type 2 diabetes.
[Aldehyde dehydrogenase 2(ALDH2) gene polymorphism in NIDDM patients with chronic renal failure]
Diabetic Neuropathies
A case of syndrome of inappropriate secretion of antidiuretic hormone associated with diabetes mellitus.
Possible involvement of hypersecretion of ADH in hyponatremia in a diabetic patient complicated with severe neuropathy.
Diphtheria
Comparative immunogenicity of conjugates composed of the Staphylococcus aureus type 8 capsular polysaccharide bound to carrier proteins by adipic acid dihydrazide or N-succinimidyl-3-(2-pyridyldithio)propionate.
Preparation and testing of a Haemophilus influenzae Type b/Hepatitis B surface antigen conjugate vaccine.
Diplopia
Syndrome of inappropriate ADH secretion and diplopia: oat cell (small cell) rectal carcinoma metastatic to the central nervous system.
Down Syndrome
Increased brain protein levels of carbonyl reductase and alcohol dehydrogenase in Down syndrome and Alzheimer's disease.
Reduced aldehyde dehydrogenase levels in the brain of patients with Down syndrome.
Duodenal Ulcer
Polymorphism of alcohol and aldehyde dehydrogenase genes and alcoholic cirrhosis in Chinese patients.
Relation between hepatic alcohol dehydrogenase activity and the ascorbic acid in leucocytes of patients with liver disease.
Dupuytren Contracture
Common Variants of the ALDH2 and DHDH Genes and the Risk of Dupuytren's Disease.
Dyskinesias
Extrapyramidal disorders: a possible underlying mechanism.
Dyslipidemias
Molecular basis of autosomal dominant hypercholesterolemia: assessment in a large cohort of hypercholesterolemic children.
Dyspnea
Update: hydrogen cyanamide-related illnesses--Italy, 2002-2004.
Empyema
Inappropriate secretion of ADH in empyema.
Empyema, Subdural
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Encephalitis
HYPONATREMIA WITH HERPES SIMPLEX ENCEPHALITIS. POSSIBLE RELATIONSHIP OF LIMBIC LESIONS AND ADH SECRETION.
Severe hyponatremia caused by syndrome of inappropriate secretion of antidiuretic hormone developed as initial manifestation of human herpesvirus-6-associated acute limbic encephalitis after unrelated bone marrow transplantation.
Encephalitis, Herpes Simplex
HYPONATREMIA WITH HERPES SIMPLEX ENCEPHALITIS. POSSIBLE RELATIONSHIP OF LIMBIC LESIONS AND ADH SECRETION.
Encephalocele
Basal encephaloceles with morning glory syndrome, and progressive hormonal and visual disturbances: case report and review of the literature.
Endolymphatic Hydrops
Changes in immunostaining of cochleas with experimentally induced endolymphatic hydrops.
Serum antidiuretic hormone levels in patients with unilateral Meniere's disease.
Endometrial Neoplasms
Clinical translation for endometrial cancer stem cells hypothesis.
IL6/JAK1/STAT3 Signaling Blockade in Endometrial Cancer Affects the ALDHhi/CD126+ Stem-like Component and Reduces Tumor Burden.
The activity of class I, II, III, and IV alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase in endometrial cancer.
The diagnostic value of alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase measurement in the sera of patients with endometrial cancer.
Endotoxemia
The effect of endotoxin on alcohol dehydrogenase (ADH) activity in the serum of ethanol intoxicated rats.
Enuresis
Antidiuretic hormone levels and polyuria in spinal cord injury. A preliminary report.
Antidiuretic hormone regulation in patients with primary nocturnal enuresis.
Evaluation of antidiuretic hormone before and after long-term treatment with desmopressin in a group of enuretic children.
Nocturnal polyuria and antidiuretic hormone levels in spinal cord injury.
[Endocrine theory of idiopathic nocturnal enuresis]
Eosinophilia
[A case of pulmonary infiltration with eosinophilia (PIE) syndrome associated with syndrome of inappropriate secretion of ADH (SIADH) in the elderly patient]
Epidermal Cyst
[Cysts of the mammary gland--surgical behavior and treatment].
Epilepsy
Clinical aspects of the disorders of GABA metabolism in children.
Inherited disorders of neurotransmitters in children and adults.
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency.
Status epilepticus in mice deficient for succinate semialdehyde dehydrogenase: GABAA receptor-mediated mechanisms.
Therapeutic concepts in succinate semialdehyde dehydrogenase (SSADH; ALDH5a1) deficiency (gamma-hydroxybutyric aciduria). Hypotheses evolved from 25 years of patient evaluation, studies in Aldh5a1-/- mice and characterization of gamma-hydroxybutyric acid pharmacology.
Vomiting attack with ACTH and ADH discharge improves startle epilepsy.
[Paraneoplastic limbic encephalopathy, inappropriate ADH secretion and recurrent subclinical epileptic seizures. Clinical, anatomo-pathological and metabolic correlations by positron emission tomography]
Epilepsy, Absence
Aberrant GABA(A) receptor-mediated inhibition in cortico-thalamic networks of succinic semialdehyde dehydrogenase deficient mice.
Absence seizures in succinic semialdehyde dehydrogenase deficient mice: a model of juvenile absence epilepsy.
Plasticity of postsynaptic, but not presynaptic, GABAB receptors in SSADH deficient mice.
Epilepsy, Generalized
Epilepsy in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism.
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency.
Erythema
Coding and non-coding polymorphisms in alcohol dehydrogenase alters protein expression and alcohol-associated erythema.
Substrate specificity of human cutaneous alcohol dehydrogenase and erythema provoked by lower aliphatic alcohols.
[Associations between ALDH2 and ADH1B Genotypes and Ethanol-Induced Cutaneous Erythema in Young Japanese Women].
Esophageal Neoplasms
A variant allele of ADH1B and ALDH2, is associated with the risk of esophageal cancer.
ADH1B Arg47His Polymorphism Is Associated with Esophageal Cancer Risk in High-Incidence Asian Population: Evidence from a Meta-Analysis.
Alcohol and aldehyde dehydrogenase gene polymorphisms influence susceptibility to esophageal cancer in Japanese alcoholics.
Alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase activity in the sera of patients with esophageal cancer.
Alcohol flushing, alcohol and aldehyde dehydrogenase genotypes, and risk for esophageal squamous cell carcinoma in Japanese men.
ALDH2 and CYP2E1 genotypes, urinary acetaldehyde excretion and the health consequences in moderate alcohol consumers.
Association between alcohol dehydrogenase-2 gene polymorphism and esophageal cancer risk: a meta-analysis.
CD14 promoter polymorphism in Chinese alcoholic patients with cirrhosis of liver and acute pancreatitis.
Combination of ADH1B*2/ALDH2*2 polymorphisms alters acetaldehyde-derived DNA damage in the blood of Japanese alcoholics.
Esophageal cancer tumorspheres involve cancer stem-like populations with elevated aldehyde dehydrogenase enzymatic activity.
Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk.
Genes encoding enzymes involved in ethanol metabolism.
Genetic polymorphisms of ADH2 and ALDH2 association with esophageal cancer risk in southwest China.
Genetic Variant of Single-Nucleotide Polymorphism Is Associated with Risk of Esophageal Squamous Cell Carcinoma.
Identifying genetic variation for alcohol dependence.
Impact of Multiple Alcohol Dehydrogenase Gene Polymorphisms on Risk of Upper Aerodigestive Tract Cancers in a Japanese Population.
Interactive effects of lifetime alcohol consumption and alcohol and aldehyde dehydrogenase polymorphisms on esophageal cancer risks.
Meta-analysis of ADH1B and ALDH2 polymorphisms and esophageal cancer risk in China.
Polymorphisms of alcohol dehydrogenase-2 and aldehyde dehydrogenase-2 and esophageal cancer risk in Southeast Chinese males.
Relationship between genetic polymorphisms of ALDH2 and ADH1B and esophageal cancer risk: a meta-analysis.
Single nucleotide polymorphisms of ADH1B, ADH1C and ALDH2 genes and esophageal cancer: A population-based case-control study in china.
The Activity of Class I, II, III, and IV Alcohol Dehydrogenase (ADH) Isoenzymes and Aldehyde Dehydrogenase (ALDH) in Esophageal Cancer.
The alcohol dehydrogenase isoenzyme (ADH IV) as a candidate tumour marker of esophageal cancer.
[Fluctuation in plasma ADH levels during and after surgery of esophageal cancer]
[Genetic polymorphisms of ADH1B and ALDH-2 associated with risk of esophageal cancer: a meta-analysis].
Essential Tremor
Alcohol dehydrogenase 2 genotype and allelic variants are not associated with the risk for essential tremor.
Euthyroid Sick Syndromes
Hormonal response in sepsis.
Eye Diseases
Classical dendritic cells mediate fibrosis directly via the retinoic acid pathway in severe eye allergy.
Eye Diseases, Hereditary
Primary structure of human 11-cis retinol dehydrogenase and organization and chromosomal localization of the corresponding gene.
Fanconi Anemia
Molecular Portrait of Metastasis-Competent Circulating Tumor Cells in Colon Cancer Reveals the Crucial Role of Genes Regulating Energy Metabolism and DNA Repair.
Fatty Liver
Genetic Association and Gene-Gene Interaction Reveal Genetic Variations in ADH1B, GSTM1 and MnSOD Independently Confer Risk to Alcoholic Liver Diseases in India.
Limited Excessive Voluntary Alcohol Drinking Leads to Liver Dysfunction in Mice.
Liver lipid disposal following t-butanol administration to rats.
Rat strain differences in susceptibility to alcohol-induced chronic liver injury and hepatic insulin resistance.
Fatty Liver, Alcoholic
Hepatic lipid profiling of deer mice fed ethanol using (1)H and (31)P NMR spectroscopy: A dose-dependent subchronic study.
Favism
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Fetal Alcohol Spectrum Disorders
A hypothetical mechanism for fetal alcohol syndrome involving ethanol inhibition of retinoic acid synthesis at the alcohol dehydrogenase step.
Alcohol dehydrogenase 1B genotype and fetal alcohol syndrome: a HuGE minireview.
Catalytic efficiency of human alcohol dehydrogenases for retinol oxidation and retinal reduction.
Contribution to first-pass metabolism of ethanol and inhibition by ethanol for retinol oxidation in human alcohol dehydrogenase family--implications for etiology of fetal alcohol syndrome and alcohol-related diseases.
Effect of alcohol on the heart and cardiac metabolism.
Genetic polymorphisms: impact on the risk of fetal alcohol spectrum disorders.
Kinetic mechanism of human class IV alcohol dehydrogenase functioning as retinol dehydrogenase.
Retinoic acid synthesis in mouse embryos during gastrulation and craniofacial development linked to class IV alcohol dehydrogenase gene expression.
Retinoids and the alcohol dehydrogenase gene family.
The role of alcohol dehydrogenase in retinoic acid homeostasis and fetal alcohol syndrome.
Fetal Growth Retardation
Fetal ADH2*3, maternal alcohol consumption, and fetal growth.
Intrauterine growth restriction affects the proteomes of the small intestine, liver, and skeletal muscle in newborn pigs.
Fibroadenoma
Atypical ductal hyperplasia and atypia of uncertain significance in core biopsies from mammographically detected lesions: correlation with excision diagnosis.
Expression of c-erbB-2 oncogene and p53 tumor suppressor gene in benign and malignant breast tissue: correlation with proliferative activity and prognostic index.
Is the "blooming sign" a promising additional tool to determine malignancy in MR mammography?
Loss of heterozygosity and microsatellite instability in epithelial hyperplasia of the breast.
No elevation in long-term breast carcinoma risk for women with fibroadenomas that contain atypical hyperplasia.
Gastritis
13C-ethanol breath test reveals impaired alcohol metabolism in patients with Helicobacter pylori infection.
Alcohol dehydrogenase activities in the human gastric mucosa: effects of Helicobacter pylori infection, sex, age, and the part of the stomach.
Effects of Helicobacter pylori infection and gastritis on gastric alcohol dehydrogenase activity.
Ethylene glycol poisoning in three dogs: Importance of early diagnosis and role of hemodialysis as a treatment option.
Helicobacter infection and gastric ethanol metabolism.
The effect of gastritis on human gastric alcohol dehydrogenase activity and ethanol metabolism.
Gastritis, Atrophic
Acetaldehyde as a common denominator and cumulative carcinogen in digestive tract cancers.
Age and bioavailability of alcohol.
Ethanol metabolism in the gastrointestinal tract and its possible consequences.
Gastric emptying and first-pass metabolism of ethanol in elderly subjects with and without atrophic gastritis.
Survival of yogurt-containing organisms and Lactobacillus gasseri (ADH) and their effect on bacterial enzyme activity in the gastrointestinal tract of healthy and hypochlorhydric elderly subjects.
Gastroenteritis
High antidiuretic hormone levels and hyponatremia in children with gastroenteritis.
Genetic Diseases, Inborn
Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene.
Hypothesis of demodicidosis rosacea flushing etiopathogenesis.
Proton magnetic resonance spectroscopy findings and clinical effects of montelukast sodium in a case with Sjögren-Larsson syndrome.
[Sjogren-Larsson syndrome: two cases with delayed diagnosis]
Giant Cell Arteritis
[Inappropriate ADH secretion syndrome and hypereosinophilia in Horton disease with stenosis of the subclavian arteries]
Glioblastoma
A study of serum antidiuretic hormone and atrial natriuretic peptide levels in a series of patients with intracranial disease and hyponatremia.
Aldehyde dehydrogenase 1A1--a new mediator of resistance to temozolomide in glioblastoma.
Aldehyde dehydrogenase and HSP90 co-localize in human glioblastoma biopsy cells.
Hypoxia upregulates aldehyde dehydrogenase isoform 1 (ALDH1) expression and induces functional stem cell characteristics in human glioblastoma cells.
Retinoid resistance and multifaceted impairment of retinoic acid synthesis in glioblastoma.
Suppressing Glioblastoma Stem Cell Function by Aldehyde Dehydrogenase Inhibition with Chloramphenicol or Disulfiram as a New Treatment Adjunct: An Hypothesis.
Glioma
Aldehyde dehydrogenase activity in xenografted human brain tumor in nude mice. Preliminary results in human glioma biopsies.
Cyclopamine-mediated hedgehog pathway inhibition depletes stem-like cancer cells in glioblastoma.
Inappropriate ADH secretion with unique features in a child with a hypothalamic glioma.
Glucose Intolerance
Cardiac overexpression of alcohol dehydrogenase exacerbates chronic ethanol ingestion-induced myocardial dysfunction and hypertrophy: role of insulin signaling and ER stress.
Endothelial Progenitor Cell Levels Predict Future Physical Function: An Exploratory Analysis From the VA Enhanced Fitness Study.
Involvement of AMPK in alcohol dehydrogenase accentuated myocardial dysfunction following acute ethanol challenge in mice.
The association of alcohol and alcohol metabolizing gene variants with diabetes and coronary heart disease risk factors in a white population.
Granulomatosis with Polyangiitis
[A case of Wegener's granulomatosis associated with the syndrome of inappropriate secretion of ADH]
Guillain-Barre Syndrome
Relapse of central nervous system Burkitt's lymphoma presenting as Guillain-Barre syndrome and syndrome of inappropriate ADH secretion.
Head and Neck Neoplasms
Association between aldehyde dehydrogenase gene polymorphisms and the phenomenon of field cancerization in patients with head and neck cancer.
Association of aldehyde dehydrogenase 2 gene polymorphism with multiple oesophageal dysplasia in head and neck cancer patients.
Changes in human serum alcohol dehydrogenase activity during retinoic acid treatment of cancer patients.
Frequencies of ADH1C alleles and genotypes in a Turkish head and neck cancer population.
Head and Neck Squamous Cell Carcinoma Metabolism Draws on Glutaminolysis, and Stemness Is Specifically Regulated by Glutaminolysis via Aldehyde Dehydrogenase.
Pooled analysis of alcohol dehydrogenase genotypes and head and neck cancer: a HuGE review.
Risk of head and neck cancer and the alcohol dehydrogenase 3 genotype.
Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium.
The interplay between alcohol consumption, oral hygiene, ALDH2, and ADH1B in the risk of head and neck cancer.
Head Injuries, Closed
Increased intracranial pressure is associated with elevated cerebrospinal fluid ADH levels in closed-head injury.
Headache
Effect of surgery and radiotherapy on visual and endocrine function in nonfunctioning pituitary adenomas.
The expression of succinate semialdehyde dehydrogenase in the caudal part of the spinal trigeminal nucleus is down-regulated after electrical stimulation of the dura mater surrounding the superior sagittal sinus in conscious rats.
Hearing Loss
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Menière's disease in congenital nephrogenic diabetes insipidus: report of two twins.
Heart Arrest
Hormonal responses upon return of spontaneous circulation after cardiac arrest: a retrospective cohort study.
The efficacy of rewarming with a portable and percutaneous cardiopulmonary bypass system in accidental deep hypothermia patients with hemodynamic instability.
[Utility of vasopressin in cardiopulmonary resuscitation]
Heart Diseases
(13) C magnetic resonance spectroscopic imaging of hyperpolarized [1-(13) C, U-(2) H5 ] ethanol oxidation can be used to assess aldehyde dehydrogenase activity in vivo.
Gene-environment interaction and its impact on coronary heart disease risk.
Plasma ADH levels during heart surgery.
Validation of a commercially available enzyme immunoassay for measurement of plasma antidiuretic hormone concentration in healthy dogs and assessment of plasma antidiuretic hormone concentration in dogs with congestive heart failure.
Heart Failure
Antidiuretic hormone in congestive heart failure.
High plasma antidiuretic hormone in patients with cardiac failure: influence of age.
Hyponatremia: manifestations and treatment.
Hyponatremia: Mechanisms and Newer Treatments.
Neurohumoral activation during exercise in congestive heart failure.
Plasma ADH level in patients with chronic congestive heart failure.
Tolvaptan.
Validation of a commercially available enzyme immunoassay for measurement of plasma antidiuretic hormone concentration in healthy dogs and assessment of plasma antidiuretic hormone concentration in dogs with congestive heart failure.
[Acute poisoning with industrial products]
[Correlation of hyponatremia with plasma renin activity, antidiuretic hormone and brain natriuretic peptide in chronic heart failure]
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
[Hyponatremia: etiopathogenetic observations in the personal experiences]
[Hyponatremic syndrome.]
[Significance of ADH in the pathogenesis of edema in heart failure]
[Symposium on pathophysiology of congestive heart failure. 3. Plasma ADH levels in congestive heart failure (author's transl)]
[Syndrome of inappropriate ADH secretion (SIADH) induced by pramipexole in a patient with Parkinson's disease]
Hematoma, Subdural
Inappropriate release of ADH in subdural hematoma.
Hemorrhoids
Expression pattern, ethanol-metabolizing activities, and cellular localization of alcohol and aldehyde dehydrogenases in human large bowel: association of the functional polymorphisms of ADH and ALDH genes with hemorrhoids and colorectal cancer.
Hepatitis
Alcohol dehydrogenase (ADH) activity in the sera of patients during the course of viral hepatitis.
Alcohol dehydrogenase - physiological and diagnostic Importance.
Alcohol Drinking Mediates the Association between Polymorphisms of ADH1B and ALDH2 and Hepatitis B-Related Hepatocellular Carcinoma.
Blockade of Retinol Metabolism Protects T Cell-Induced Hepatitis by Increasing Migration of Regulatory T Cells.
Effect of liver disorders on ethanol elimination and alcohol and aldehyde dehydrogenase activities in liver and erythrocytes.
Human serum alcohol dehydrogenase isoenzymes as a markers of liver injury during viral hepatitis.
Immunohistochemical staining of cancer stem cell markers in hepatocellular carcinoma.
Isoenzymes of class I and II alcohol dehydrogenase in chronic hepatitis.
Measurement of serum alcohol dehydrogenase activity at different pH-values during the course of viral hepatitis in children.
Serum alcohol dehydrogenase activity in liver diseases.
Serum class I and II alcohol dehydrogenase activity during the course of viral hepatitis.
[Alcohol dehydrogenase interference in clinical chemical laboratory tests]
[Alcoholic liver damage in rats: histological and histochemical findings of an one year trial (author's transl)]
[Comparative analysis of the effects of alcoholism and opium addiction on liver function]
[Glutamic dehydrogenase and alcohol dehydrogenase of blood in various conditions of experimental hepatic necrosis: hepatitis due to MHV-3 virus, acute poisoning due to carbon tetrachloride.]
Hepatitis B
A case-control study on male hepatocellular carcinoma based on hospital and community controls.
Analysis of naturally processed human histocompatibility leukocyte antigen class I-bound peptides from hepatocellular carcinoma tissues in vivo.
Controlled fed-batch fermentation of recombinant Saccharomyces cerevisiae to produce hepatitis B surface antigen.
Synthesis and assembly of hepatitis B virus surface antigen particles in yeast.
Hepatitis B, Chronic
Alcohol Drinking Mediates the Association between Polymorphisms of ADH1B and ALDH2 and Hepatitis B-Related Hepatocellular Carcinoma.
Aldehyde dehydrogenase 2 polymorphism for development to hepatocellular carcinoma in East Asian alcoholic liver cirrhosis.
Hepatitis C
Effects of alcohol intake and low Km aldehyde dehydrogenase on hepatic function in a high hepatitis C virus-prevalent Japanese island population.
Hepatitis, Alcoholic
Acute alcoholic hepatitis and cellular Th1 immune responses to alcohol dehydrogenase.
Effect of liver disorders on ethanol elimination and alcohol and aldehyde dehydrogenase activities in liver and erythrocytes.
[Genetic susceptibility to the development of acute alcoholic hepatitis: role of genetic mutations in dehydrogenase alcohol, aldehyde dehydrogenase and cytochrome P450 2E1]
Hepatitis, Chronic
Hepatic alcohol and aldehyde dehydrogenases in liver disease.
Influence of liver disease on hepatic alcohol and aldehyde dehydrogenases.
Isoenzymes of class I and II alcohol dehydrogenase in chronic hepatitis.
Hepatoblastoma
Immunohistochemical staining of cancer stem cell markers in hepatocellular carcinoma.
Hepatolenticular Degeneration
Alcohol dehydrogenase: a target of humoral autoimmune response in liver disease.
Herpes Labialis
Invasive Meningococcal Infection: Analysis of 110 cases from a Tertiary Care Centre in North East India.
Herpes Zoster
Disseminated visceral varicella zoster virus presenting with the constellation of colonic pseudo-obstruction, acalculous cholecystitis and syndrome of inappropriate ADH secretion.
Identification of differentially expressed ovarian genes during primary and early secondary oocyte growth in coho salmon, Oncorhynchus kisutch.
Retinoic acid and alcohol/retinol dehydrogenase in the mouse adrenal gland: a potential endocrine source of retinoic acid during development.
Sodium fluoride-induced changes in the hypothalamic neurosecretory system of the spotted owlet, Athene brama Temminck.
Syndrome of Inappropriate Secretion of Antidiuretic Hormone Associated with Localized Herpes Zoster Ophthalmicus.
Histoplasmosis
Histoplasmosis associated with a bamboo bonfire--Arkansas, October 2011.
HIV Infections
Presentation and outcome of tuberculous meningitis in adults in the province of Castellon, Spain: a retrospective study.
Hodgkin Disease
Reactive oxygen species and aldehyde dehydrogenase activity in Hodgkin lymphoma cells.
Holoprosencephaly
Hedgehog signaling: endocrine gland development and function.
Hydrocephalus
Hypodipsia and hypernatremia in congenital hydrocephalus.
[Alteration of atrial natriuretic peptide and cyclic GMP in cerebrospinal fluid in canine kaolin-induced hydrocephalus]
Hyperaldosteronism
Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome.
Plasma antidiuretic hormone levels in patients with normal and low renin essential hypertension, and secondary hypertension.
Water, electrolyte, and endocrine homeostasis in infants with bronchiolitis.
[Hemosorption in the treatment of patients with ischemic heart disease and drug-resistant stenocardia]
Hypercalcemia
Calcium-prostaglandin interaction on the action of antidiuretic hormone in the dog.
Paraneoplastic syndromes in olfactory neuroblastoma.
Syndromes that Link the Endocrine System and Genitourinary Tract.
Hypercholesterolemia
Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia.
Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes.
Molecular basis of autosomal dominant hypercholesterolemia: assessment in a large cohort of hypercholesterolemic children.
Molecular characterization of Polish patients with familial hypercholesterolemia: novel and recurrent LDLR mutations.
Molecular genetic background of an autosomal dominant hypercholesterolemia in the Czech Republic.
Mutational analysis of the LDL receptor and APOB genes in Mexican individuals with autosomal dominant hypercholesterolemia.
The p.Leu167del mutation in APOE gene causes autosomal dominant hypercholesterolemia by down-regulation of LDL receptor expression in hepatocytes.
Hyperglycemia
Interaction between high-fat diet and alcohol dehydrogenase on ethanol-elicited cardiac depression in murine myocytes.
Syndromes that Link the Endocrine System and Genitourinary Tract.
Hyperinsulinism
[SIADH and hypoglycemia in pulmonary microcytoma]
Hyperkalemia
[Thiazide diuretics for hypertensive treatment induced severe hyponatremia with consciousness disturbance in two elderly cases]
Hyperlipoproteinemia Type II
Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes.
Mutational analysis of the LDL receptor and APOB genes in Mexican individuals with autosomal dominant hypercholesterolemia.
Mutations in STAP1 Are Associated With Autosomal Dominant Hypercholesterolemia.
Premature coronary heart disease and autosomal dominant hypercholesterolemia: Increased risk in women with LDLR mutations.
The molecular basis of familial hypercholesterolemia in Lebanon: Spectrum of LDLR mutations and role of PCSK9 as a modifier gene.
Update of the molecular basis of familial hypercholesterolemia in The Netherlands.
Hypernatremia
A question of balance--dehydration in the elderly.
Antidiuretic hormone infusion reduces taurine and NaCl-induced hypernatremia in the rat.
Carbamazepine-induced hyponatremia in a patient with partial central diabetes insipidus.
Essential hypernatraemia, antidiuretic hormone and neurophysin secretion: response to chlorpropamide.
HYPERNATREMIA AND COPEPTIN LEVELS IN THE ELDERLY HOSPITALIZED PATIENT.
Hypodipsia and hypernatremia in congenital hydrocephalus.
Hypodipsia-hypernatremia syndrome.
Hypothalamic hypernatremia due to volume--dependent ADH release, and its treatment with carbamazepine and clofibrate.
Regulation of water intake.
Role of vasopressin in rats with bilateral ureteral obstruction.
Sodium disturbances frequently encountered in a neurologic intensive care unit.
Volume receptor control of ADH release in essential hypernatremia.
[A case of postoperative craniopharyngioma with hypernatremia. The mechanisms of ADH and atrial natriuretic peptide (ANP) releases]
[A case of severe hypernatremia complicated with rhabdomyolysis]
[Arhinencephaly detected by a pitressin-sensitive diabetes insipidus]
[Hypernatremia due to hypothalamic tumor: ADH response to changes in plasma osmolality]
[Hyponatremia--with comments on hypernatremia]
[Neurogenic hypernatremia caused by a teratoma on the supraoptic region (author's transl)]
[Neurogenic hypernatremia syndrome in children]
[Neurogenic hypernatremia with adipsia and cerebral malformations in a child with ectrodactyly-ectodermal dysplasia-cleft lip-palate syndrome]
[Palliative therapy in cancer. 4. Palliation of the symptoms from a malignant tumor. (2)]
Hyperphosphatemia
Calcilytic Ameliorates Abnormalities of Mutant Calcium-Sensing Receptor (CaSR) Knock-In Mice Mimicking Autosomal Dominant Hypocalcemia (ADH).
Hyperprolactinemia
Diagnosis and treatment of pituitary disease.
Neuroendocrine abnormalities in patients with traumatic brain injury.
[A case of multiple sclerosis with galactorrhea-amenorrhea syndrome]
Hypersensitivity
Effects of genetic polymorphisms in alcohol-metabolizing enzymes on alcohol hypersensitivity and alcohol-related health problems in orientals.
GAGA factor-dependent transcription and establishment of DNase hypersensitivity are independent and unrelated events in vivo.
Genetic determinants of both ethanol and acetaldehyde metabolism influence alcohol hypersensitivity and drinking behaviour among Scandinavians.
Spontaneous resolution of diabetes insipidus after pituitary stalk sectioning during surgery for large craniopharyngioma. Endocrinological evaluation and clinical implications for surgical strategy.
[Interactions between ethanol and histamine]
[Pathobiochemistry of alcoholism]
Hypertension
Angiotensin II and Anti Diuretic Hormone Exert Synergistic Effects on Thick Ascending Limb Transport in Spontaneously Hypertensive Rats.
Effect of alcohol and aldehyde dehydrogenase gene polymorphisms on alcohol-associated hypertension: the Guangzhou Biobank Cohort Study.
Effects of furosemide-induced plasma volume reduction on plasma antidiuretic hormone in normal and hypertensive subjects.
Evidence against a vasopressor role of ADH in malignant DOC-salt hypertension.
Hypertension in dogs during antidiuretic hormone and hypotonic saline infusion.
Idiopathic, sustained, inappropriate secretion of ADH with associated hypertension and thirst.
Interaction between high-fat diet and alcohol dehydrogenase on ethanol-elicited cardiac depression in murine myocytes.
Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia.
Nerve blocks in the critical care environment.
Overdosage with vincristine.
Paraneoplastic syndromes in olfactory neuroblastoma.
Plasma and urinary ADH levels in patients with essential hypertension.
Plasma antidiuretic hormone levels in patients with normal and low renin essential hypertension, and secondary hypertension.
Syndromes that Link the Endocrine System and Genitourinary Tract.
The neurohypophysis.
The role of the renin-angiotensin system in arterial hypertension in hypercorticism.
Urinary anti diuretic hormone level in essential hypertension.
Urinary excretion of digoxin-like factor (DLF) and ADH during DOCA-salt and Goldblatt 2 kidney-1 clip hypertension development.
Vasopressor role of ADH in the pathogenesis of malignant DOC hypertension.
Volume receptors in guinea pig labyrinth: relevance with respect to ADH and Na control.
[Responses of antidiuretic hormone (ADH) and atrial natriuretic polypeptide (ANP) to hypertonic saline infusion in essential hypertensive patients and normotensive subjects]
[The vasopressor role of ADH in the maintenance of blood pressure in experimentally hypertensive rats (author's transl)]
Hypertension, Malignant
Plasma antidiuretic hormone levels in patients with normal and low renin essential hypertension, and secondary hypertension.
Hypertension, Renal
Plasma antidiuretic hormone levels in patients with normal and low renin essential hypertension, and secondary hypertension.
Hypertension, Renovascular
Plasma antidiuretic hormone levels in patients with normal and low renin essential hypertension, and secondary hypertension.
Hyperthyroidism
Diagnosis and treatment of pituitary disease.
Effects of thyroxine on the expression of alcohol dehydrogenase in rat liver and kidney.
Hypertriglyceridemia
Individual susceptibility to alcoholic pancreatitis: still an enigma.
Hypertrophy, Left Ventricular
[Increase by ANP and ADH of the duration of activation and deactivation of the cardiopulmonary baroreceptor reflex: modification in the presence of left ventricular hypertrophy]
Hyperventilation
[Plasma ANP levels and its relation to electrolyte and water regulation in neurosurgical intensive care patients]
Hypervitaminosis A
The eye and nutrition
[Alcohol dehydrogenase system in the pigment epithelium of the rat retina. Normal, hypo- and hypervitaminosis A]
[The eye and nutrition]
Hypoalbuminemia
[Antidiuretic hormone in severe cases of atopic dermatitis]
Hypocalcemia
A novel activating mutation in calcium-sensing receptor gene associated with a family of autosomal dominant hypocalcemia.
Calcilytic Ameliorates Abnormalities of Mutant Calcium-Sensing Receptor (CaSR) Knock-In Mice Mimicking Autosomal Dominant Hypocalcemia (ADH).
CASR gene activating mutations in two families with autosomal dominant hypocalcemia.
CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
Epigenetic regulation of microRNAs controlling CLDN14 expression as a mechanism for renal calcium handling.
Functional activities of mutant calcium-sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia.
Mutational Analysis of the Adaptor Protein 2 Sigma Subunit (AP2S1) gene: Search for Autosomal Dominant Hypocalcemia Type 3 (ADH3).
[Activating mutations of calcium-sensing receptor cause insufficient secretion of parathyroid hormone]
[Familial hypoparathyroidism due to activating mutations in the calcium-sensing receptor gene]
Hypoglycemia
High antidiuretic hormone levels and hyponatremia in children with gastroenteritis.
Modification of water and electrolyte metabolism during head-down tilting by hypoglycemia in men.
N1-alkyl-substituted derivatives of chlorpropamide as inhibitors of aldehyde dehydrogenase.
Neuroendocrine abnormalities in patients with traumatic brain injury.
Pathogenesis and treatment of alcoholic liver disease: progress over the last 50 years.
[Mechanisms of spontaneous hypoglycaemia in the adult (author's transl)]
[Paraneoplastic endocrine syndromes]
[Pituitary coma.]
[SIADH and hypoglycemia in pulmonary microcytoma]
Hypokalemia
Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome.
Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.
Role of tolvaptan in the management of hyponatremia in patients with lung and other cancers: current data and future perspectives.
Hypokinesia
[The water-salt balance and renal function in space flights and in model experiments]
Hyponatremia
A case of hyponatremia in panhypopituitarism caused by the primary empty sella syndrome.
A case of non-SIADH-induced hyponatremia in depression after treatment with reboxetine.
A rare case of ectopic antidiuretic hormone-producing pancreatic adenocarcinoma: new diagnostic approach.
A Rare Mechanism of Hyponatremia in HIV Disease.
Acute hyponatremic encephalopathy after a cerebrovascular accident.
An autopsy case of macroglobulinemia complicated with syndrome of inappropriate secretion of ADH (SIADH) like hyponatremia, hypopituitarism and AL amyloidosis.
Anaplastic small cell carcinoma of the larynx.
Antidiuretic hormone and renal function after water loading in patients with cirrhosis of the liver.
Antidiuretic hormone excess.
Case of inappropriate ADH syndrome: hyponatremia due to polyethylene glycol bowel preparation.
Causes of hyponatremia in the Departments of Internal Medicine and Neurosurgery.
Cerebral salt wasting syndrome in a patient with a pituitary adenoma.
Cerebral salt wasting syndrome.
Cerebral salt-wasting syndrome. We need better proof of its existence.
Chlorpropamide-induced ADH release, hyponatremia and central pontine myelinolysis in diabetes mellitus.
Clinical Analysis of Hyponatremia in Acute Craniocerebral Injury.
Development of an experimental model to study the pathophysiology of cerebral salt wasting following subarachnoid hemorrhage.
Effect of adjunctive cortisol on serum sodium in a polydipsic hyponatremic schizophrenic patient.
Elevation of plasma atrial natriuretic peptide in a neurosurgical patient with the syndrome of inappropriate secretion of antidiuretic hormone--case report.
Endocrine manifestations of critical illness in the child.
Evidence in hyponatremia related to inappropriate secretion of ADH that V1 receptor stimulation contributes to the increase in renal uric acid clearance.
Failure of intravenous fluid therapies to decrease serum sodium levels in elderly hospitalized patients.
Fatal hyponatremia and other metabolic disturbances associated with psychotropic drug polypharmacy.
Frequency and significance of electrolyte abnormalities in pneumonia.
Giant intrasellar carotid aneurysm - an unusual cause of panhypopituitarism.
Hypertension in dogs during antidiuretic hormone and hypotonic saline infusion.
Hyponatremia and hypernatremia: disorders of water balance.
Hyponatremia and natriuresis following subarachnoid hemorrhage in a monkey model.
HYPONATREMIA AND THE SYNDROME OF INAPPROPRIATE SECRETION OF ANTIDIURETIC HORMONE (SIADH).
Hyponatremia in a neonate of a cocaine abusing mother.
Hyponatremia in a nursing home population.
Hyponatremia in cirrhosis: pathophysiology and management.
Hyponatremia in hospitalized critically ill children: current concepts.
Hyponatremia in intracranial disorders.
Hyponatremia in small cell lung cancer. Mechanisms not involving inappropriate ADH secretion.
Hyponatremia in the rat in the absence of positive water balance.
Hyponatremia resulting from arginine vasopressin receptor 2 gene mutation.
HYPONATREMIA WITH HERPES SIMPLEX ENCEPHALITIS. POSSIBLE RELATIONSHIP OF LIMBIC LESIONS AND ADH SECRETION.
Hyponatremia with increased plasma antidiuretic hormone in a case of hypothyroidism.
Hyponatremia: manifestations and treatment.
Hyponatremia: Mechanisms and Newer Treatments.
Hyponatremic encephalopathy after excessive water ingestion prior to pelvic ultrasound: neuroimaging findings.
Hyponatremic seizure associated with acute respiratory infection.
Inappropriate secretion of ADH as a cause of hyponatremia in cystic fibrosis.
Inappropriate secretion of antidiuretic hormone and hyponatremia in severe falciparum malaria.
Inappropriate secretion of antidiuretic hormone in isolated adrenocorticotropin deficiency.
Inflammasome activation by cell volume regulation and inflammation-associated hyponatremia: A vicious cycle.
Long-term outcomes in a family with nephrogenic syndrome of inappropriate antidiuresis.
Low-dose tolvaptan for the treatment of hyponatremia in the syndrome of inappropriate ADH secretion (SIADH).
Management of euvolemic hyponatremia attributed to SIADH in the hospital setting.
Management of sodium abnormalities in patients with CNS disease.
Multiple metabolic abnormalities in a patient with the syndrome of inappropriate antidiuresis.
Multiple pituitary hormone abnormalities, fever, behavioral problems, seizures and apnoic spells in a 6-year old girl.
Normal osmotic threshold for vasopressin release in the hyponatremia of hypothyroidism.
Paroxetine-induced hyponatremia in the elderly due to the syndrome of inappropriate secretion of antidiuretic hormone (SIADH).
Pathogenesis and diagnosis of hyponatremia.
Patient With Severe Hyponatremia Caused by Adrenal Insufficiency Due to Ectopic Posterior Pituitary Lobe and Miscommunication Between Hypothalamus and Pituitary: A Case Report.
Plasma arginine vasopressin response to water load during labor.
Plasma concentrations of brain natriuretic peptide in patients with subarachnoid hemorrhage.
Possible involvement of hypersecretion of ADH in hyponatremia in a diabetic patient complicated with severe neuropathy.
Posthysteroscopic hyponatremia: evidence for a multifactorial cause.
Proton pump inhibitors and the kidney: critical review.
Quantification and predictors of plasma volume expansion from mannitol treatment.
Release of antidiuretic hormone during mass-induced elevation of intracranial pressure.
Role of antidiuretic hormone in hyponatremia in patients with isolated adrenocorticotropic hormone deficiency.
Severe hyponatremia associated with the combined use of thiazide diuretics and selective serotonin reuptake inhibitors.
SIADH and other hyponatremic disorders: diagnosis and therapeutic problems.
SIADH associated with prostate cancer.
Sodium disturbances frequently encountered in a neurologic intensive care unit.
Syndrome of inappropriate antidiuresis in small-cell lung cancer. Classification and effect of tumor regression.
Syndrome of inappropriate secretion of anti-diuretic hormone (SIADH) produced by an adenocarcinoma of the colon. Report of one case.
Syndrome of Inappropriate Secretion of Antidiuretic Hormone Associated with Localized Herpes Zoster Ophthalmicus.
Syndrome of inappropriate secretion of antidiuretic hormone in nasopharynx carcinoma.
Syndrome of recurrent increased secretion of antidiuretic hormone following multiple doses of vincristine.
The charted and the uncharted waters of hyponatremia.
The hyponatremia of exercise.
The syndrome of inappropriate antidiuretic hormone secretion associated with chemotherapy for hypopharyngeal cancer.
The syndrome of inappropriate secretion of antidiuretic hormone in the pharyngeal flap operation.
Therapeutic efficacy of non-peptide ADH antagonist OPC-31260 in SIADH rats.
Tolvaptan.
Urea for management of the syndrome of inappropriate secretion of ADH: A systematic review.
Urinary arginine vasopressin in asthma: consideration of fluid therapy.
Vaptans are not the mainstay of treatment in hyponatremia: perhaps not yet.
Vasopressin: deficiency, excess and the syndrome of inappropriate antiduretic hormone secretion.
Very delayed hyponatremia after surgery and radiotherapy for a pituitary macroadenoma.
Voriconazole-associated salt-losing nephropathy.
Water metabolism in diabetes mellitus.
["Polydipsia, intermittent hyponatremia and psychoses" syndrome: a diagnosis and therapeutic management of a case]
[A 25-year-old patient with colonic pseudo-obstruction, hyponatremia, hypertension, and diffuse pain]
[A study of plasma atrial natriuretic peptide, antidiuretic hormone and aldosterone levels in a series of patients with intracranial disease and hyponatremia]
[Acute myelomonocytic leukemia complicated with syndrome of inappropriate secretion of antidiuretic hormone, nephrotic syndrome, and hemophagocytic syndrome]
[Acute symptomatic hyponatremia in a 70-year-old patient. Insufficient ADH secretion syndrome]
[An interesting case of pituitary apoplexy showing abnormality in water-electrolyte before and after surgery]
[Aquaretic drugs--a new therapeutic principle in treatment of hyponatremia?]
[Case of hyponatremia resulting from inappropriate secretion of ADH]
[Cerebral salt loss as Schwartz-Bartter-syndrome in childhood (author's transl)]
[Changes in antidiuretic hormone (ADH) in liver cirrhosis with resistant ascites]
[Clinical case. Severe hyponatremia associated with inappropriate ADH syndrome]
[Correlation of hyponatremia with plasma renin activity, antidiuretic hormone and brain natriuretic peptide in chronic heart failure]
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
[Ectopic hormone secretion by neuroendocrine tumors.]
[Hormonal dysnatremia].
[Hypo-osmolar hyponatremia as the chief symptom in hypothyroidism]
[Hyponatremia and syndrome of inappropriate ADH secretion (SIADH)].
[Hyponatremia in cirrhosis with ascites]
[Hyponatremia in Duchenne muscular dystrophy on mechanical ventilation]
[Hyponatremia in isolated deficiency of adrenocorticotropic hormone: role of a decrease in aldosterone secretion independent of antidiuretic hormone excess]
[Hyponatremia in patients with subarachnoid hemorrhage]
[Hyponatremia in the aged person]
[Hyponatremia secondary to inappropriate antidiuretic hormone secretion]
[Hyponatremia with high plasma ANP level--report of two cases with emphasis on the pathophysiology of cerebral salt wasting]
[Hyponatremia.]
[Hyponatremia: etiopathogenetic observations in the personal experiences]
[Hyponatremic syndrome.]
[Inappropriate ADH secretion caused by alcohol withdrawal: a rare cause of hyponatremia]
[Inappropriate ADH secretion-induced hyponatremia and associated with paroxetine use]
[Increased plasma antidiuretic hormone in the presence of hyponatremia in primary hypothyroidism]
[Lambert-Eaton myasthenic syndrome with acute respiratory failure associated with small cell lung cancer]
[Pathogenesis of hyponatremia observed in the treatment of acute subarachnoid hemorrhage]
[Pathophysiology of dehydration]
[Role of ADH in the pathogenesis of hyponatremia in a case of primary adrenal insufficiency (author's transl)]
[Serum ANP and ADH after subarachnoid hemorrhage and hyponatremia]
[Severe hyponatremia and comatose state during colonoscopy preparation.]
[Severe idiopathic hyponatremia caused by ADH inappropriate secretion in the elderly]
[Severe peripheral neuropathy, cardiac hypofunction, and syndrome of inappropriate secretion of antidiuretic hormone (SIADH) in a patient with Churg-Strauss syndrome]
[Syndrome of inappropriate ADH secretion (SIADH) in small-cell bronchus carcinoma]
[Syndrome of inappropriate ADH secretion (SIADH) induced by pramipexole in a patient with Parkinson's disease]
[Syndrome of inappropriate secretion of anti-diuretic hormone associated with limbic encephalitis due to herpes simplex virus infection--a case report]
[The clinical study of hyponatremia in the elderly. Part Three. Plasma ADH secretion in dilutional hyponatremia]
[Three cases of respiratory failure of collagen diseases accompanied by syndrome of inappropriate secretion of antidiuretic hormone (SIADH)]
[Valproate related syndrome of inappropriate secretion of antidiuretic hormone (SIADH)--a case report]
[Vasopressin receptor antagonists: the vaptans].
Hypoparathyroidism
A family of autosomal dominant hypocalcemia with an activating mutation of calcium-sensing receptor gene.
Calcilytic Ameliorates Abnormalities of Mutant Calcium-Sensing Receptor (CaSR) Knock-In Mice Mimicking Autosomal Dominant Hypocalcemia (ADH).
Hormonal disturbances in visceral leishmaniasis (kala-azar).
Identification of a G-Protein Subunit-?11 Gain-of-Function Mutation, Val340Met, in a Family with Autosomal Dominant Hypocalcemia Type 2 (ADH2).
[Endocrine crises]
Hypophosphatemia
Effect of phosphate depletion on vasopressin secretion and kidney tissue vasopressin concentration in rats.
Hypophosphatemia, Familial
Demeclocycline-induced phosphate diabetes in a patient with inappropriate ADH secretion and systemic sarcoidosis.
Hypopituitarism
An assessment of posterior pituitary function in patients with Sheehan's syndrome.
An autopsy case of macroglobulinemia complicated with syndrome of inappropriate secretion of ADH (SIADH) like hyponatremia, hypopituitarism and AL amyloidosis.
Hypothalamic encephalitis with bradycardia.
Hypotension
Arterial hypotension at elevated plasma levels of Na+, ADH and AII in ducks with high chronic salt intake.
Fomepizole fails to prevent progression of acidosis in 2-butoxyethanol and ethanol coingestion.
Haematocrit, leukocyte and platelet counts and the severity of the ovarian hyperstimulation syndrome.
Overdosage with vincristine.
Stimulation of cardiac receptors with veratrum alkaloids inhibits ADH secretion.
Update: hydrogen cyanamide-related illnesses--Italy, 2002-2004.
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
[Effect of various fluids on plasma concentrations of ADH and angiotensin II during hemorrhagic hypotension in dogs (author's transl)]
[Hemodynamic and endocrine responses to prostaglandin E1 induced hypotension during enflurane anesthesia in surgical patients--evaluation by transesophageal echocardiography]
Hypotension, Orthostatic
A case of syndrome of inappropriate secretion of antidiuretic hormone associated with diabetes mellitus.
A study of autonomic cardiovascular reflexes in elderly patients with pneumonia.
Possible involvement of hypersecretion of ADH in hyponatremia in a diabetic patient complicated with severe neuropathy.
[A case of Shy-Drager syndrome complicated with syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and incomplete paralysis of bilateral vocal cords]
Hypothalamic Neoplasms
[Hypernatremia due to hypothalamic tumor: ADH response to changes in plasma osmolality]
Hypothyroidism
1,1-Dichloroethylene hepatotoxicity: hypothyroidism decreases metabolism and covalent binding but not injury in the rat.
Diagnosis and treatment of pituitary disease.
Hypothalamic dysfunction after chemotherapy.
Hypothalamo-pituitary dysfunction in patients with chronic subdural hematoma.
Isolated ACTH deficiency and primary hypothyroidism: volume-dependent elevation of antidiuretic hormone secretion in the presence of hyponatremia.
Masking of central diabetes insipidus and hypogonadotrophic hypogonadism by germ cell tumour in suprasellar--pineal region.
Normal osmotic threshold for vasopressin release in the hyponatremia of hypothyroidism.
Thyroxine treatment induces upregulation of renin-angiotensin-aldosterone system due to decreasing effective plasma volume in patients with primary myxoedema.
University of Miami Division of Clinical Pharmacology Therapeutic Rounds: the water-intolerant patient and perioperative hyponatremia.
[Acute symptomatic hyponatremia in a 70-year-old patient. Insufficient ADH secretion syndrome]
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
[Endocrine crises]
[Increased plasma antidiuretic hormone in the presence of hyponatremia in primary hypothyroidism]
Hypoxia, Brain
Histological distribution of class III alcohol dehydrogenase in human brain.
Renal function in brain dead patients with respect to transplantation.
Ichthyosis
Adeno-associated virus vectors are able to restore fatty aldehyde dehydrogenase-deficiency. Implications for gene therapy in Sjogren-Larsson syndrome.
Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome.
Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene.
Ichthyosis, mental retardation, and asymptomatic spasticity. A new neurocutaneous syndrome with normal fatty alcohol:NAD+ oxidoreductase activity.
Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome.
Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patients.
Inappropriate ADH Syndrome
A case of non-SIADH-induced hyponatremia in depression after treatment with reboxetine.
A case of SIADH induced by mizoribin administration.
A case of syndrome of inappropriate secretion of antidiuretic hormone (SIADH) with low plasma concentrations of antidiuretic hormone.
Adenocarcinoma of the prostate with ectopic antidiuretic hormone production: a case report.
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS AND AMERICAN COLLEGE OF ENDOCRINOLOGY DISEASE STATE CLINICAL REVIEW: POSTOPERATIVE MANAGEMENT FOLLOWING PITUITARY SURGERY.
Anti-aquaporin-4 antibody-positive neuromyelitis optica presenting with syndrome of inappropriate antidiuretic hormone secretion as an initial manifestation.
Antidiuretic hormone excess.
Antidiuretic principle in malignant tumor extracts from patients with inappropriate ADH syndrome.
Case of inappropriate ADH syndrome: hyponatremia due to polyethylene glycol bowel preparation.
Correction of an inappropriate ADH syndrome by tumor resection.
Defects in osmoregulation of vasopressin secretion. A report of four cases.
Diabetes insipidus secondary to penetrating spinal cord trauma: case report and literature review.
Haloperidol-induced syndrome of inappropriate secretion of antidiuretic hormone.
How to recognize and treat the inappropriate ADH syndrome.
Hyponatraemia and the inappropriate ADH syndrome in pneumonia.
Hyponatraemia in premature babies and following surgery in older children.
Hyponatremia in the postoperative craniofacial pediatric patient population: a connection to cerebral salt wasting syndrome and management of the disorder.
Imaging of the sella in the syndrome of inappropriate secretion of antidiuretic hormone.
Inappropriate antidiuretic hormone syndrome in craniofacial surgery.
Is it cerebral or renal salt wasting?
Management of euvolemic hyponatremia attributed to SIADH in the hospital setting.
Management of the syndrome of inappropriate secretion of antidiuretic hormone.
Miliary tuberculosis presenting with hyponatremia and thrombocytopenia.
Occult pulmonary malignancy in syndrome of inappropriate ADH secretion with normal ADH levels.
Pathophysiologic and pharmacologic alterations in the release and action of ADH.
Pharmacologic studies in Bartter's syndrome: effect of DDAVP and indomethacin on renal concentrating operation. Part II.
Phase I trial of intravenous vinzolidine (LY 104208) given on a biweekly dosing schedule.
Postoperative assessment of the patient after transsphenoidal pituitary surgery.
Seizure in a normal marrow donor: Addison's disease unmasked.
SIADH: a case review.
Syndrome of inappropriate antidiuretic hormone secretion and ectopic ACTH production in small cell lung carcinoma.
Syndrome of inappropriate antidiuretic hormone secretion associated with acute myeloid leukemia with multilineage dysplasia.
Syndrome of inappropriate antidiuretic hormone secretion in children following spinal fusion.
Syndrome of inappropriate secretion of anti-diuretic hormone (SIADH) produced by an adenocarcinoma of the colon. Report of one case.
Syndrome of inappropriate secretion of antidiuretic hormone (SIADH) in a patient with multiple sclerosis.
Syndrome of Inappropriate Secretion of Antidiuretic Hormone Associated with Localized Herpes Zoster Ophthalmicus.
Syndrome of inappropriate secretion of antidiuretic hormone in elderly patients with rheumatoid arthritis associated with infections: report of two cases.
Syndrome of recurrent increased secretion of antidiuretic hormone following multiple doses of vincristine.
The syndrome of inappropriate ADH secretion secondary to vinblastine-bleomycin therapy.
The syndrome of inappropriate antidiuretic hormone secretion (SIADH): pathophysiologic mechanisms in solute and volume regulation.
The syndrome of inappropriate antidiuretic hormone secretion associated with chemotherapy for hypopharyngeal cancer.
The syndrome of inappropriate secretion of antidiuretic hormone and fluid restriction in meningitis--how strong is the evidence?
Therapeutic efficacy of non-peptide ADH antagonist OPC-31260 in SIADH rats.
Tolvaptan.
Two cases of MND/ALS developing the syndrome of inappropriate secretion of antidiuretic hormone.
Urinary antidiuretic hormone in polyuric disorders and in inappropriate ADH syndrome.
Urinary retention as a cause of hyponatremia in an elderly man.
Varicella in immunocompromised children. Incidence of abdominal pain and organ involvement.
[A 25-year-old patient with colonic pseudo-obstruction, hyponatremia, hypertension, and diffuse pain]
[A case of postoperative hyponatremia caused by Sheehan syndrome associated with lung carcinoma]
[A case of Shy-Drager syndrome complicated with syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and incomplete paralysis of bilateral vocal cords]
[A case of SIADH without ectopic production of ADH from neoplasm, associated with superior vena cava syndrome caused by metastatic mediastinal tumor of pancreatic cancer]
[Acute intermittent porphyria and inappropriate ADH syndrome]
[An interesting case of pituitary apoplexy showing abnormality in water-electrolyte before and after surgery]
[Clinical case. Severe hyponatremia associated with inappropriate ADH syndrome]
[Current considerations in syndrome of inappropriate secretion of antidiuretic hormone/syndrome of inappropriate antidiuresis].
[Disorders of the osmoregulation of vasopressin in the inappropriate ADH syndrome]
[Hyponatremia in cancer patients].
[Important points in diagnosis and therapy: inappropriate ADH syndrome]
[Inappropriate ADH syndrome (Schwartz-Bartter syndrome) in porphyria]
[Inappropriate ADH syndrome and other toxic effects in the course of childhood ALL treated with vincristine]
[Inappropriate ADH syndrome in a patient with acute intermittent porphyria]
[Inappropriate ADH syndrome]
[Inappropriate secretion of antidiuretic hormone: true and false Schwartz-Bartter syndrome. Apropos of 2 cases]
[Inhibition of prostaglandins in the syndrome of inappropriate secretion of antidiuretic hormone (SIADH)]
[Lennert's lymphoma associated with the syndrome of inappropriate secretion of antidiuretic hormone and autoimmune hemolytic anemia]
[Paraneoplastic endocrine syndromes]
[Progress in diagnosis and treatment of kidney diseases. IV. Abnormalities of renal tubular functions. 2. Inappropriate ADH syndrome]
[Small-cell lung carcinoma with hyponatremia]
[Syndrome of inappropriate ADH secretion (SIADH) in small-cell bronchus carcinoma]
[Syndrome of inappropriate ADH secretion (SIADH) induced by pramipexole in a patient with Parkinson's disease]
[Syndrome of inappropriate secretion of anti-diuretic hormone associated with limbic encephalitis due to herpes simplex virus infection--a case report]
[The effect of vasopressin analogs on water metabolism]
[The use of carbamazepine in the treatment of secondary ADH deficit: on a letter titled SIADH and carbamazepine]
[Valproate related syndrome of inappropriate secretion of antidiuretic hormone (SIADH)--a case report]
Infection
A sensitive, colorimetric, microtitre assay for alcohol dehydrogenase in standard endoscopic gastric biopsies.
Alcohol dehydrogenase (ADH) isoenzyme activity in the sera of patients with Helicobacter pylori infection.
Alcohol dehydrogenase 1 of barley modulates susceptibility to the parasitic fungus Blumeria graminis f.sp. hordei.
Alcohol dehydrogenase activities in the human gastric mucosa: effects of Helicobacter pylori infection, sex, age, and the part of the stomach.
Alcohol dehydrogenase: an autoantibody target in patients with alcoholic liver disease.
Alcohol metabolism in Helicobacter pylori-infected stomach.
Case of inappropriate ADH syndrome: hyponatremia due to polyethylene glycol bowel preparation.
Cochliobolus lunatus down-regulates proteome at late stage of colonization and transiently alters StNPR1 expression in Solanum tuberosum L.
Detection of candidal antigens in autoimmune polyglandular syndrome type I.
Development of disease-resistant rice by pathogen-responsive expression of WRKY45.
Effect of Helicobacter pylori infection on the activity of class I, III and IV alcohol dehydrogenase in the human stomach.
Effects of Helicobacter pylori infection and gastritis on gastric alcohol dehydrogenase activity.
Evaluation of alcohol metabolism in humans using the non-invasive [C]-ethanol breath test - influence of gender, Helicobacter pylori infection and polymorphism of alcohol-oxidizing enzymes.
Helicobacter infection and gastric ethanol metabolism.
Helicobacter pylori infection decreases gastric alcohol dehydrogenase activity and first-pass metabolism of ethanol in man.
HSV-2 infection of dendritic cells amplifies a highly susceptible HIV-1 cell target.
Hyponatremic seizure associated with acute respiratory infection.
Inactivation of aldehyde dehydrogenase by a putative metabolite of cefamandole. Re: K.J. Freundt et al. Infection 13 (1985) 91.
Infection of barley with the parasitic fungus Blumeria graminis f.sp. hordei results in the induction of HvADH1 and HvADH2.
Influence of age, sex, and Helicobacter pylori infection before and after eradication on gastric alcohol dehydrogenase activity.
Nocturnal polyuria and antidiuretic hormone levels in spinal cord injury.
Structure and regulation of the Candida albicans ADH1 gene encoding an immunogenic alcohol dehydrogenase.
Syndrome of Inappropriate Secretion of Antidiuretic Hormone Associated with Localized Herpes Zoster Ophthalmicus.
Syndrome of inappropriate secretion of antidiuretic hormone in elderly patients with rheumatoid arthritis associated with infections: report of two cases.
The Adh adhesin domain is required for trimeric autotransporter Apa1-mediated Actinobacillus pleuropneumoniae adhesion, autoaggregation, biofilm formation and pathogenicity.
The alcohol dehydrogenase isoenzyme alcohol dehydrogenase IV as a candidate marker of Helicobacter pylori infection.
The syndrome of inappropriate secretion of antidiuretic hormone associated with cleft palate: report of a case and review of the literature.
Trigger factor of Streptococcus suis is involved in stress tolerance and virulence.
[Alcoholic liver disease]
[Characteristics of endogenous intoxication in children with Helicobacter pylori-associated gastroduodenal diseases]
[Helicobacter pylori alcohol dehydrogenase (HPADH)--characteristics and role in the pathogenesis of diseases associated with Helicobacter pylori infection]
Infectious Mononucleosis
Polyradiculoneuritis and inappropriate ADH secretion in infectious mononucleosis.
Infertility, Male
The rf2 nuclear restorer gene of male-sterile T-cytoplasm maize.
Inflammatory Bowel Diseases
Dysplastic lesions in inflammatory bowel disease show increased positivity for the stem cell marker aldehyde dehydrogenase.
Inflammatory Breast Neoplasms
Aldehyde dehydrogenase 1-positive cancer stem cells mediate metastasis and poor clinical outcome in inflammatory breast cancer.
Influenza, Human
Application of MOLMAP approach for QSAR modeling of various biological activities using substituent electronic descriptors.
Induction of glutathione-dependent formaldehyde dehydrogenase activity in Escherichia coli and Hemophilus influenza.
Influenza viral (A/WSN/33) hemagglutinin is expressed and glycosylated in the yeast Saccharomyces cerevisiae.
Insulin Resistance
Acute ethanol-mediated insulin resistance in the rat: the role of ethanol oxidation.
Alcohol-induced disruption of endocrine signaling.
Cardiac overexpression of alcohol dehydrogenase exacerbates chronic ethanol ingestion-induced myocardial dysfunction and hypertrophy: role of insulin signaling and ER stress.
FALDH reverses the deleterious action of oxidative stress induced by lipid peroxidation product 4-hydroxynonenal on insulin signaling in 3T3-L1 adipocytes.
Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES).
[Reappraisal of perioperative fluid therapy in children]
Intellectual Disability
Adeno-associated virus vectors are able to restore fatty aldehyde dehydrogenase-deficiency. Implications for gene therapy in Sjogren-Larsson syndrome.
Drosophila Torsin Protein Regulates Motor Control and Stress Sensitivity and Forms a Complex with Fragile-X Mental Retardation Protein.
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.
Essential hypernatraemia, antidiuretic hormone and neurophysin secretion: response to chlorpropamide.
Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome.
Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene.
Ichthyosis, mental retardation, and asymptomatic spasticity. A new neurocutaneous syndrome with normal fatty alcohol:NAD+ oxidoreductase activity.
Inherited disorders of neurotransmitters in children and adults.
Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiency.
Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.
Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome.
Succinic semialdehyde dehydrogenase deficiency: GABAB receptor-mediated function.
Intestinal Obstruction
Clinical evaluation of serum alcohol dehydrogenase activity in horses with acute intestinal obstruction.
Intestinal Pseudo-Obstruction
Overdosage with vincristine.
Phase I trial of intravenous vinzolidine (LY 104208) given on a biweekly dosing schedule.
Intracranial Hemorrhages
The efficacy of rewarming with a portable and percutaneous cardiopulmonary bypass system in accidental deep hypothermia patients with hemodynamic instability.
Intracranial Hypertension
Release of antidiuretic hormone during mass-induced elevation of intracranial pressure.
The syndrome of inappropriate secretion of antidiuretic hormone and fluid restriction in meningitis--how strong is the evidence?
Invasive Fungal Infections
In vivo Hypoxia and a Fungal Alcohol Dehydrogenase Influence the Pathogenesis of Invasive Pulmonary Aspergillosis.
Invasive Pulmonary Aspergillosis
In vivo Hypoxia and a Fungal Alcohol Dehydrogenase Influence the Pathogenesis of Invasive Pulmonary Aspergillosis.
Iron Overload
Hyperinsulinemia shifted energy supply from glucose to ketone bodies in early nonalcoholic steatohepatitis from high-fat high-sucrose diet induced Bama minipigs.
Keratoconus
Analysis of corneal aldehyde dehydrogenase patterns in pathologic corneas.
Identification of a G-Protein Subunit-?11 Gain-of-Function Mutation, Val340Met, in a Family with Autosomal Dominant Hypocalcemia Type 2 (ADH2).
Marked reduction of alcohol dehydrogenase in keratoconus corneal fibroblasts.
Ketosis
A case of diabetic non-ketotic hyperosmolar coma with an increase with plasma 3-hydroxybutyrate.
Poisoning with 1-propanol and 2-propanol.
Kidney Diseases
Emerging roles for retinoids in regeneration and differentiation in normal and disease states.
Induction of Retinol Dehydrogenase 9 Expression in Podocytes Attenuates Kidney Injury.
[Progress in diagnosis and treatment of kidney diseases. IV. Abnormalities of renal tubular functions. 2. Inappropriate ADH syndrome]
Kidney Failure, Chronic
Antidiuretic hormone in end-stage renal disease.
Effect of haemodialysis on plasma ADH levels, plasma renin activity and plasma aldosterone levels in patients with end-stage renal disease.
Effect of isoosmolar volume reduction during hemofiltration on plasma antidiuretic hormone in patients with chronic renal failure.
Newly symptomatic central diabetes insipidus in ESRD with adult polycystic kidney disease following intracranial hemorrhage: the first reported case.
Renal excretion of antidiuretic hormone in healthy subjects and patients with renal failure.
[Aldehyde dehydrogenase 2(ALDH2) gene polymorphism in NIDDM patients with chronic renal failure]
Kidney Neoplasms
Alcohol dehydrogenase and aldehyde dehydrogenase in malignant neoplasms.
The diagnostic significance of serum alcohol dehydrogenase isoenzymes and aldehyde dehydrogenase activity in renal cell cancer patients.
Korsakoff Syndrome
Alcohol and aldehyde dehydrogenase genotypes in Korsakoff syndrome.
l-lactate dehydrogenase deficiency
Genetic and physiological analysis of the lethal effect of L-(+)-lactate dehydrogenase deficiency in Streptococcus mutans: complementation by alcohol dehydrogenase from Zymomonas mobilis.
Lambert-Eaton Myasthenic Syndrome
Immunological and endocrinological abnormalities in paraneoplastic disorders with involvement of the autonomic nervous system.
[Eaton-Lambert syndrome with ADH and ACTH producing lund cancer--a case report (author's transl)]
[Lung carcinoma with inappropriate ADH secretion and Eaton-Lambert syndrome]
Language Development Disorders
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.
Redox-switch modulation of human SSADH by dynamic catalytic loop.
Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency.
Laryngeal Neoplasms
ADH1B and CDH1 polymorphisms predict prognosis in male patients with non-metastatic laryngeal cancer.
Aldehyde dehydrogenase isoform 1 (ALDH1) expression as a predictor of radiosensitivity in laryngeal cancer.
Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms.
Laryngeal cancer risk in Caucasians is associated with alcohol and tobacco consumption but not modified by genetic polymorphisms in class I alcohol dehydrogenases ADH1B and ADH1C, and glutathione-S-transferases GSTM1 and GSTT1.
[Distribution of alcohol dehydrogenase (ADH1C) genotypes in subjects with tobacco smoke-associated laryngeal cancer]
Leigh Disease
Leigh Syndrome Caused by the MT-ND5 m.13513G>A Mutation: A Case Presenting with WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia.
Leiomyoma
All-trans-retinoic acid mediates changes in PI3K and retinoic acid signaling proteins of leiomyomas.
Leishmaniasis, Visceral
Hyponatremia in visceral leishmaniasis.
Leprosy
Inappropriate ADH secretion in a patient with leprosy.
Lethargy
A case of acute onset succinic semialdehyde dehydrogenase deficiency: neuroimaging findings and literature review.
Hypodipsia-hypernatremia syndrome.
Leukemia
Aldehyde dehydrogenase activity among primary leukemia cells is associated with stem cell features and correlates with adverse clinical outcome.
Association of Acute Myeloid Leukemia's Most Immature Phenotype with Risk Groups and Outcomes.
Effect of 4-(diethylamino)benzaldehyde on ethanol metabolism in mice.
Enhanced expressions of glucose-6-phosphate dehydrogenase and cytosolic aldehyde dehydrogenase and elevation of reduced glutathione level in cyclophosphamide-resistant human leukemia cells.
Extended flow cytometry characterization of normal bone marrow progenitor cells by simultaneous detection of aldehyde dehydrogenase and early hematopoietic antigens: implication for erythroid differentiation studies.
Heterogeneity of leukemia stem cell candidates at diagnosis of acute myeloid leukemia and their clinical significance.
In vitro selection for K562 cells with higher retrovirally mediated copy number of aldehyde dehydrogenase class-1 and higher resistance to 4-hydroperoxycyclophosphamide.
Promyelocytic leukemia protein induces arsenic trioxide resistance through regulation of aldehyde dehydrogenase 3 family member A1 in hepatocellular carcinoma.
Role of aldehyde dehydrogenase in cyclophosphamide-resistant L1210 leukemia.
Structure and expression of the cytosolic aldehyde dehydrogenase gene in cyclophosphamide-resistant murine leukemia L1210 cells.
Syndrome of inappropriate secretion of ADH after administration of intrathecal chemotherapy in acute promyelocytic leukemia with empty sella of pituitary gland.