CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
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Hydroxylation index of omeprazole in relation to CYP2C19 polymorphism and sex in a healthy Iranian populationInactive alleles of cytochrome P450 2C19 may be positively selected in human evolutionHelicobacter pylori virulence genes and host genetic polymorphisms as risk factors for peptic ulcer diseaseCYP2C9 variants as a risk modifier of NSAID-related gastrointestinal bleeding: a case-control study.Genotype and allele frequency of CYP2C19*17 in a healthy Iranian populationEffects of Genetic Polymorphisms of Cytochrome P450 Enzymes and MDR1 Transporter on Pantoprazole Metabolism and Helicobacter pylori Eradication.Genotyping of CYP2C19 polymorphisms and its clinical validation in the ethnic Arab population.CYP2C9, CYPC19 and CYP2D6 gene profiles and gene susceptibility to drug response and toxicity in Turkish population.Tumour necrosis factor-alpha polymorphism increases risk of nonvariceal upper gastrointestinal bleeding among patients taking proton pump inhibitors.The prognostic value of CYP2C subfamily genes in hepatocellular carcinoma.
P2860
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P2860
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@en
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@nl
type
label
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@en
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@nl
prefLabel
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@en
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease.
@nl
P2093
P2860
P50
P356
P1476
CYP2C19*17 gain-of-function polymorphism is associated with peptic ulcer disease
@en
P2093
P2860
P304
P356
10.1038/CLPT.2012.215
P407
P577
2012-10-26T00:00:00Z