Insights into the substrate specificity, inhibitors, regulation, and polymorphisms and the clinical impact of human cytochrome P450 1A2.
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Pharmacological approaches to the challenge of treatment-resistant depressionHuman Cytochrome P450 1A1 Structure and Utility in Understanding Drug and Xenobiotic MetabolismCytochrome P450 1A2 Metabolizes 17β-Estradiol to Suppress Hepatocellular CarcinomaComputational and in vitro studies on the inhibitory effects of herbal compounds on human cytochrome P450 1A2.Structure, function, regulation and polymorphism and the clinical significance of human cytochrome P450 1A2.CYP1A2 polymorphism -1545C > T (rs2470890) is associated with increased side effects to clozapine.Phospholipase D: enzymology, functionality, and chemical modulationPharmGKB summary: very important pharmacogene information for CYP1A2.CYP1A2--a novel genetic marker for early aromatase inhibitor response in the treatment of breast cancer patientsCaffeine Cytochrome P450 1A2 Metabolic Phenotype Does Not Predict the Metabolism of Heterocyclic Aromatic Amines in Humans.Population pharmacokinetics of dolutegravir in HIV-infected treatment-naive patients.The Impact of CYP1A2 and CYP2E1 Genes Polymorphism on Theophylline ResponseDevelopment and validation of an HPLC-UV method for the simultaneous determination of the antipsychotics clozapine, olanzapine and quetiapine, several beta-blockers and their metabolites.Selective Inhibition of Bakuchicin Isolated from Psoralea corylifolia on CYP1A in Human Liver MicrosomesExtreme sensitivity and the practical implications of risk assessment thresholds.Gene expression and immunochemical localization of major cytochrome P450 drug-metabolizing enzymes in bovine nasal olfactory and respiratory mucosa.Proper heat shock pretreatment reduces acute liver injury induced by carbon tetrachloride and accelerates liver repair in mice.A Comparison of the In Vitro Inhibitory Effects of Thelephoric Acid and SKF-525A on Human Cytochrome P450 Activity.In vitro analysis of factors influencing CYP1A2 expression as potential determinants of interindividual variation.Gene polymorphisms involved in triptans pharmacokinetics and pharmacodynamics in migraine therapy.Factors affecting interindividual differences in clozapine response: a review and case report.Substrate selectivity of drug-metabolizing cytochrome P450s predicted from crystal structures and in silico modeling.Cytochrome P450 variations in different ethnic populations.Challenges in exploring the cytochrome P450 system as a source of variation in canine drug pharmacokinetics.Pharmacogenomics of anti-platelet and anti-coagulation therapy.Female gender as a susceptibility factor for drug-induced liver injury.Blood pressure in relation to coffee and caffeine consumption.Oral antineoplastic agent interactions with medicinal plants and food: an issue to take into account.Combination analysis in genetic polymorphisms of drug-metabolizing enzymes CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A5 in the Japanese population.Lack of effect of smoking status on axitinib pharmacokinetics in patients with non-small-cell lung cancer.Systematical analysis of impacts of heat stress on the proliferation, apoptosis and metabolism of mouse hepatocyte.Quantitative Prediction of Drug Interactions Caused by CYP1A2 Inhibitors and Inducers.Co-expression of active human cytochrome P450 1A2 and cytochrome P450 reductase on the cell surface of Escherichia coli.Does "smoker's paradox" exist in clopidogrel-treated Turkish patients with acute coronary syndrome.Impact of smoking status on clinical outcomes after successful chronic total occlusion intervention: Korean national registry of CTO intervention.The genetic profiles of CYP1A1, CYP1A2 and CYP2E1 enzymes as susceptibility factor in xenobiotic toxicity in Turkish population.Genetic polymorphisms of cytochrome P450-1A2 (CYP1A2) among EmiratisGenetic polymorphism analysis of the drug-metabolizing enzyme CYP1A2 in a Uyghur Chinese population: a pilot study.Metabolism of the anthelmintic drug niclosamide by cytochrome P450 enzymes and UDP-glucuronosyltransferases: metabolite elucidation and main contributions from CYP1A2 and UGT1A1.The expression, induction and pharmacological activity of CYP1A2 are post-transcriptionally regulated by microRNA hsa-miR-132-5p.
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Insights into the substrate specificity, inhibitors, regulation, and polymorphisms and the clinical impact of human cytochrome P450 1A2.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 10 July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@en
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@nl
type
label
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@en
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@nl
prefLabel
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@en
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@nl
P2093
P2860
P1433
P1476
Insights into the substrate sp ...... of human cytochrome P450 1A2.
@en
P2093
Li-Ping Yang
Shu-Feng Zhou
Zhi-Wei Zhou
P2860
P2888
P304
P356
10.1208/S12248-009-9127-Y
P407
P577
2009-07-10T00:00:00Z
P5875
P6179
1004902101