UDP‐Glucuronosyltransferase 1A6: Structural, Functional, and Regulatory Aspects

Author:

Walter Bock Karl,Köhle Christoph

Publisher

Elsevier

Reference81 articles.

1. An alternative promoter contributes to tissue‐ and inducer‐specific expression of the rat UDP‐glucuronosyltransferase 1A6 gene;Auyeung;Toxicol. Appl. Pharmacol.,2001

2. Quinol diglucuronides are predominant conjugated metabolites found in bile of rats following intratracheal instillation of benzo(a)pyrene;Bevan;Carcinogenesis,1992

3. Paracetamol glucuronidation by recombinant rat and human phenol UDP‐glucuronosyltransferases;Bock;Biochem. Pharmacol.,1993

4. Mono‐ and diglucuronide formation from chrysene and benzo(a)pyrene phenols by 3‐methylcholanthrene‐inducible phenol UDP‐glucuronosyltransferase (UGT1A1);Bock;Mol. Pharmacol.,1992

5. Induction of rat hepatic UDP‐glucuronosyltransferases by dietary ethoxyquin;Bock;Naunyn‐Schmiedeberg's Arch. Pharmacol.,1980

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