Monogenic control of variations in antipyrine metabolite formation. New polymorphism of hepatic drug oxidation.
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 76 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. An indirect approach to imply trade-off shapes: population level patterns in resistance suggest a decreasingly costly resistance mechanism in a model insect system;Journal of Evolutionary Biology;2006-03
2. Polymorphism in dinuclear Cu(II) compounds – polymorphism caused by different degrees of hydration: the structures of [Cu(HL)]2Cl24H2O (I), [Cu(HL)]2Cl2·2H2O (II), [Cu(HL)]2)(NO3)2·4H2O (III), [Cu(HL)]2)(NO3)2·2H2O (IV) and [Cu(HL)]2)(ClO4)2·2H2O (V) (HL=[(3-aminopropyl)-di-(2-hydroxopropyl)]amine anion). Counterion control of the crystallization pathway. Part 11;Inorganica Chimica Acta;2004-03
3. Determination of drug-metabolizing enzyme activity in vivo : pharmacokinetic and statistical issues;Xenobiotica;1998-01
4. Inhibition and induction of human cytochrome P450 (CYP) enzymes;Xenobiotica;1998-01
5. Influence of Oral Contraceptive Use and Cigarette Smoking, Alone and Together, on Antipyrine Pharmacokinetics;The Journal of Clinical Pharmacology;1997-05
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