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57篇 您的检索式:作者名="Wrighton SA"
    题名 作者 年代 出处 被引量
1The human drug metabolizing cytochromes P450显示文摘Wrighton SA VandenBranden M Ring BJ 1996J Pharmacokinet Biopharm1996,24,5:1
2Intronic polymorphism in CYP3A4 affects hepatic expression and response to statin drugs显示文摘Wang D Guo Y Wrighton SA 2011Pharmacogenomics J2011,11,4:1
3Intronic polymorphism in CYP3A4affects hepatic expression and response to statin drugs 显示文摘Wang D Guo Y Wrighton SA 2011Pharmacogenomics2011,11,4:1
4The human drug metabolizing cytochrome P450显示文摘Wrighton SA Van der Branden M Ring BJ 1996J Pharmacokinet Biopharm1996,24,5:1
5Comparison of human and monkey peptide transporters: PEPT1 and PEPT2 显示文摘Zhang EY Emerick RM Pak YA Wrighton SA Hillgren KM 2004Mol Pharm2004,1,3:1
6Metabolism and disposition of the thienopyridine antiplatelet drugs ticlopidine, clopidogrel, and prasugrel in humans显示文摘FARID NA KURIHARA A WRIGHTON SA 2010J Clin Pharm2010,50,2:1
7The human hepatic cytochromesP450 involved in drug metabolism显示文摘Wrighton SA Stevens JC 1992Critical Reviews inToxicology1992,22,:1
8Isolation and characterization of human liver cytochrome P450 2C 19: correlation between 2C19 and S-mephenytoin 4'-hydroxylation显示文摘Wrighton SA Stevens JC Becker GW 1993Arch Bioehem Biophys1993,306,1:1
9Isolation andcharacterization of human liver cytochrome P450 2C19: correlation between 2C19 and S-mephenytoin 4r-hydroxyl- ation显示文摘Wrighton SA Stevens JC Becket GW 1993Arch Bioehem Biophys1993,306,1:1
10Isolation and characterization of human liver cytochrome P450 2C19:correlation between 2C19 and S-mephenytoin 4'-hydroxylation显示文摘Wrighton SA Stevens JC Becker GW 1993Arch Biochem Biophys1993,306,1:1
11Physiological approaches to the prediction of drug-drug interactions in study populations显示文摘CHIEN JY MOHUTSKY MA WRIGHTON SA 2003Curr Drug Metab2003,4,5:1
12Isolation and characterization of human liver eytoehrome P4502C19 : corre- lation between 2C19 and S- mephenytoin 4' hydroxylation 显示文摘WRIGHTON SA STEVENS JC BECKER GW 1993Arch Biochem Biophys1993,306,1:1
13The role of he- patic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism显示文摘Fisher MB Paine MF Strelevitz T J Wrighton SA 2001Drug Metab Rev2001,33,34:1
14The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism显示文摘Fisher MB Paine MF Strelevitz TJ Wrighton SA 2001Drug Metab Rev2001,33,34:1
15Studies on the expression and metabolic capabilities of human liver cytochrome P450 Ⅲ A5 (HLp3)显示文摘Wrighton SA Brian WR Sari MA 1990Mol Pharmacol1990,38,2:1
16Application of in silico approaches to predicting drug-drug Interactions显示文摘Ekins S Wrighton SA 2001Pharmacol Toxicol Methods2001,45,:1
17The human drug metabolizing cytochromes 17450 显示文摘Wrighton SA vardonbradon M Ring BJ 1996J pharmacokinet Biopharm1996,24,5:1
18Studies on the expression and metabolic capabilities of human liver cytochrome P4503A5(HLp3)显示文摘Wrighton SA Brian WR Sari MA 1990Mol Pharmacol1990,38,2:1
19The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism显示文摘Fisher MB Paine MF Strelevitz TJ Wrighton SA 2001Drug Metab Rev2001,33,34:1
20Studies on the expression and metabolic capabilities of human liver cytochrome P450m A5(HLP3)显示文摘Wrighton SA Brian WR Sari MA 1990Mol Pharmacol1990,38,2:1
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