Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature
Author:
Affiliation:
1. Pharmacy Department; Cross Cancer Institute; Edmonton AB Canada
2. Pharmacy Department; Foothills Medical Centre; Calgary AB Canada
3. Department of Oncology; Tom Baker Cancer Centre; University of Calgary; Calgary AB Canada
Publisher
Wiley
Subject
Pharmacology (medical)
Reference47 articles.
1. Gilbert syndrome;Fretzayas;Eur J Pediatr,2012
2. Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome);Strassburg;Best Pract Res Clin Gastroenterol,2010
3. The genetic basis of the reduced expression of bilirubin UDP glucuronosyltransferase 1 in Gilbert's syndrome;Bosma;N Engl J Med,1995
4. Function, genetic polymorphism, and transcriptional regulation of human UDP-glucuronosyltransferase (UGT) 1A1;Sugatani;Drug Metab Pharmacokinet,2013
5. The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence;Mackenzie;Pharmacogenetics,1997
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