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Publications

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Comprehensive substrate characterization of 22 antituberculosis drugs for multiple solute carrier (SLC) uptake transporters, in vitro (cPMTb)
Antimicrob Agents Chemother. 27;62(9):e00512-18 / 2018.08 [LINK]
Identification and characterization of amiodarone metabolites in rats using UPLC-ESI-QTOFMS-based untargeted metabolomics approach (cPMTb)
J Toxicol Environ Health A. 81(12):481-492 / 2018.05 [LINK]
Pharmacokinetic comparison of a fixed-dose combination versus concomitant administration of fimasartan, amlodipine, and rosuvastatin using partial replicated design in healthy adult subjects (cPMTb)
Drug Des Devel Ther. 8:12:1157-1164 / 2018.05 [LINK]
Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical endpoints - Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC) (cPMTb)
Am Heart J. 198:152-159 / 2018.04 [LINK]
Identification of novel CYP4F2 genetic variants exhibiting decreased catalytic activity in the conversion of arachidonic acid to 20-hydroxyeicosatetraenoic acid (20-HETE) (cPMTb)
Prostaglandins Leukot Essent Fatty Acids. 131:6-13 / 2018.04 [LINK]
CYP2C19 poor metabolizer is associated with clinical outcome of clopidogrel therapy in acute myocardial infarction but not stable angina. (BMRC, PRCDM)
Circ Cardiovasc Genet. 6(5):514-21 / 2013.10 [LINK]
2013-International
Identification of cytochrome P450s involved in the metabolism of arachidonic acid in human platelets. (BMRC, PRCDM)
Prostaglandins Leukot Essent Fatty Acids. 89(4):227-34 / 2013.09 [LINK]
2013-International
Impact of the CYP2C19*17 polymorphism on the clinical outcome of clopidogrel therapy in Asian patients undergoing percutaneous coronary intervention. (PRCDM)
Pharmacogenet Genomics. 23(10):558-62 / 2013.10 [LINK]
2013-International
Single nucleotide polymorphisms in SULT1A1 and SULT1A2 in a Korean population. (BMRC, PRCDM)
Drug Metab Pharmacokinet. 28(4):372-7 / 2013.05 [LINK]
2013-International
Glucuronidation of a sarpogrelate active metabolite is mediated by UDP-glucuronosyltransferases 1A4, 1A9, and 2B4. (BMRC)
Drug Metab Dispos. 41(8):1529-37 / 2013.08 [LINK]
2013-International