Alteration of the Function of the UDP-Glucuronosyltransferase 1A Subfamily by Cytochrome P450 3A4: Different Susceptibility for UGT Isoforms and UGT1A1/7 Variants

Author:

Ishii Yuji,Koba Hiroki,Kinoshita Kousuke,Oizaki Toshiya,Iwamoto Yuki,Takeda Shuso,Miyauchi Yuu,Nishimura Yoshio,Egoshi Natsuki,Taura Futoshi,Morimoto Satoshi,Ikushiro Shin’ichi,Nagata Kiyoshi,Yamazoe Yasushi,Mackenzie Peter I.,Yamada Hideyuki

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference52 articles.

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4. Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

5. Differential and Special Properties of the Major Human UGT1-encoded Gastrointestinal UDP-glucuronosyltransferases Enhance Potential to Control Chemical Uptake

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