Rabbit as an animal model to predict CYP3A-mediated drug-drug interactions

被引：0

作者：

Chauret, N ^{[1
]}

Sleno, L ^{[1
]}

Silva, J ^{[1
]}

Houle, R ^{[1
]}

Day, S ^{[1
]}

Nicoll-Griffith, DA ^{[1
]}

机构：

[1] Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada

来源：

CYTOCHROMES P450, BIOCHEMISTRY, BIOPHYSICS AND DRUG METABOLISM | 2003年

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：157 / 162

页数：6

共 8 条

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[2]

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[3]

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[4]

Lin JH, 1997, PHARMACOL REV, V49, P403

[5]

*MED EC CO INC, 1999, PHYS REF DESK MAN

[6]

Nicoll-Griffith DA, 2001, DRUG METAB DISPOS, V29, P159

[7] An overview of current cytochrome P450 technology for assessing the safety and efficacy of new materials [J].

Parkinson, A .

TOXICOLOGIC PATHOLOGY, 1996, 24 (01) :45-57

[8]

SILVA JM, 2001, IN VITRO MODELS STUD

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