Glucuronidation of drugs in humanized UDP ‐glucuronosyltransferase 1 mice: Similarity with glucuronidation in human liver microsomes
Author:
Affiliation:
1. School of Pharmacy Kitasato University 5‐9‐1 Shirokane Minato‐ku Tokyo 108‐8641 Japan
2. Laboratory of Environmental Toxicology Department of Pharmacology University of California San Diego La Jolla California
Publisher
Wiley
Subject
General Pharmacology, Toxicology and Pharmaceutics,Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prp2.2
Reference39 articles.
1. High-performance liquid chromatography method for determination of N-glucuronidation of 4-aminobiphenyl by mouse, rat, and human liver microsomes
2. S-Naproxen and desmethylnaproxen glucuronidation by human liver microsomes and recombinant human UDP-glucuronosyltransferases (UGT): role of UGT2B7 in the elimination of naproxen
3. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
4. A Humanized UGT1 Mouse Model Expressing the UGT1A1*28 Allele for Assessing Drug Clearance by UGT1A1-Dependent Glucuronidation
5. Tissue-specific, Inducible, and Hormonal Control of the Human UDP-Glucuronosyltransferase-1 (UGT1) Locus
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