Polymorphism in drug conjugation in man: is it a factor of concern in drug toxicity or efficacy?-Reference-Cited by-同舟云学术

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Polymorphism in drug conjugation in man: is it a factor of concern in drug toxicity or efficacy?

Published:1995-02 Issue:1 Volume:3 Page:57-59
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Mulder Gerard J.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference22 articles.

1. Genetic heterogeneity of the human glutathione transferases: a complex of gene families;Board;Pharmacol. Ther.,1990

2. UDP-glucuronosyltransferases;Burchell,1992

3. Risk factors for isoniazid (INH)-induced liver dysfunction;Dickinson;J. Clin. Gastroenterol.,1981

4. The genetic polymorphism of debrisoquine/sparteine metabolism — clinical aspects;Eichelbaum,1992

5. Amino acid conjugation;Hutt,1990

Cited by 2 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. The Detoxification Limitation Hypothesis: Where Did it Come From and Where is it Going?;Journal of Chemical Ecology;2006-05-23

2. Genetic Polymorphisms of HumanN-Acetyltransferase, Cytochrome P450, Glutathione-S-Transferase, and Epoxide Hydrolase Enzymes: Relevance to Xenobiotic Metabolism and Toxicity;Critical Reviews in Toxicology;1999-01

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