Herbal Medicines and Drugs Interactions: Cytochrome P450 Responsibility. [PDF]
Shanaida M +7 more
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Expression and function of CYP enzymes and hepatobiliary transporters in an improved long-term sandwich culture hepatocyte model. [PDF]
Pacsuta J +6 more
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DDIapp-A Web-Based Application for Static Drug-Drug Interaction Assessment. [PDF]
Watase H +5 more
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Towards Personalized Chemotherapy in Gastrointestinal Cancers: Prospective Analysis of Pharmacogenetic Variants in a Russian Cohort. [PDF]
Fedorinov D +9 more
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Protein Levels of 16 Cytochrome P450s and 2 Carboxyl Esterases Using Absolute Quantitative Proteomics: CYP2C9 and CYP3A4 Are the Most Abundant Isoforms in Human Liver and Intestine, Respectively. [PDF]
Grangeon A +5 more
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IV-EVE: EVE for Injection-ADME, Pharmacokinetic and Toxicological Evaluation for Novel Deciparticle EVE Formulation. [PDF]
Chang WH +7 more
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Green Sensitive Derivative Emission Spectrofluorimetry for the Estimation of Repaglinide and Febuxostat Simultaneously in Dosage Forms and Spiked Human Plasma. [PDF]
Marie AA, Roshdy A.
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In Vitro Inhibitory Effects and Molecular Mechanism of Four Theaflavins on Isozymes of CYP450 and UGTs. [PDF]
Hu L +11 more
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CYP2C8 polymorphism among the Portuguese
Clinical Chemistry and Laboratory Medicine, 2006AbstractCytochrome P450 2C8 (CYP2C8) is a polymorphic phase I drug-metabolising enzyme involved in the metabolism of a wide variety of xenobiotics, as well as a proposed player in the regulation of vascular tone. Polymorphisms in this gene may have an impact on the metabolism of therapeutic drugs such as paclitaxel and verapamil. In this report we have
Isa Cavaco, Vera Ribeiro
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