UDP-glucuronosyltransferases (UGTs) and their related metabolic cross-talk with internal homeostasis: A systematic review of UGT isoforms for precision medicine

Author:

Yang Na,Sun Runbin,Liao Xiaoying,Aa Jiye,Wang Guangji

Funder

National Natural Science Foundation of the People’s Republic of China

Project for Jiangsu Province Key Lab of Drug Metabolism and Pharmacokinetics

Key Technology Projects of China “Creation of New Drugs”

Publisher

Elsevier BV

Subject

Pharmacology

Reference193 articles.

1. UDP-glucuronosyltransferases and clinical drug-drug interactions;Kiang;Pharmacol. Ther.,2005

2. Assessment of UGT polymorphisms and neonatal jaundice;Bartlett;Semin. Perinatol.,2011

3. UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecan;Carlini;Clin. Cancer Res.,2005

4. Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity;Kitagawa;Pharmacogenet. Genom.,2005

5. Deletion polymorphism of UDP-glucuronosyltransferase 2B17 and risk of prostate cancer in African American and Caucasian men;Park;Cancer Epidemiol. Biomarkers Prev.,2006

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