Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
about
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brainMercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activitySegregation and linkage studies of plasma dopamine-beta-hydroxylase (DBH), erythrocyte catechol-O-methyltransferase (COMT), and platelet monoamine oxidase (MAO): possible linkage between the ABO locus and a gene controlling DBH activityA Multi-scale Computational Platform to Mechanistically Assess the Effect of Genetic Variation on Drug Responses in Human Erythrocyte MetabolismThe complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria.Neurobehavioral evidence for changes in dopamine system activity during adolescence.Schizophrenia: genetic tools for unraveling the nature of a complex disorderA hotspot of inactivation: The A22S and V108M polymorphisms individually destabilize the active site structure of catechol O-methyltransferase.Association of COMT Val158Met polymorphism and breast cancer risk: an updated meta-analysisMethyl conjugation in uraemia: catechol-O-methyltransferase.Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.structured exploratory data analysis (SEDA) for determining mode of inheritance of quantitative traits. II. simulation studies on the effect of ascertaining families through high-valued probandsStructured exploratory data analysis (SEDA) for determining mode of inheritance of quantitative traits. I. Simulation studies on the effect of background distributions.Application of the major gene index and offspring-between-parents function to dermatoglyphic fingertip variables.Major locus analysis for quantitative traits.Elevated dehydroepiandrosterone sulfate levels as the reproductive phenotype in the brothers of women with polycystic ovary syndrome.Insulin resistance in the sisters of women with polycystic ovary syndrome: association with hyperandrogenemia rather than menstrual irregularity.Molecular genetic mechanisms of allelic specific regulation of murine Comt expressionA review on experimental and clinical genetic associations studies on fear conditioning, extinction and cognitive-behavioral treatment.Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder.Therapygenetics: Using genetic markers to predict response to psychological treatment for mood and anxiety disorders.Evidence for a genetic basis for hyperandrogenemia in polycystic ovary syndrome.Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms.Catechol-O-methyltransferase: characteristics, polymorphisms and role in breast cancerEffect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancerDopamine pathway is highly diverged in primate species that differ markedly in social behavior.Inheritance of low serum immunoglobulin DBrain white matter structure and COMT gene are linked to second-language learning in adults.Decreased catecholamine degradation associates with shock and kidney injury after cardiac surgery.Comprehensive interrogation of CpG island methylation in the gene encoding COMT, a key estrogen and catecholamine regulator.Pharmacogenomics and adverse drug reactions in children.An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.Inhibitors of catechol-O-methyltransferase sensitize mice to painThe COMT-polymorphism is not associated with the incidence of acute kidney injury after cardiac surgery - a prospective cohort study.
P2860
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P2860
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
description
1977 nî lūn-bûn
@nan
1977 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի մարտին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@ast
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@en
type
label
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@ast
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@en
prefLabel
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@ast
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@en
P2860
P1476
Inheritance of low erythrocyte catechol-o-methyltransferase activity in man
@en
P2093
Raymond FA
P2860
P304
P407
P577
1977-03-01T00:00:00Z