Evidence for phosphorylation requirement for human bilirubin UDP-glucuronosyltransferase (UGT1A1) activity
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference19 articles.
1. Hereditary jaundice and disorders of bilirubin metabolism;Roy Chowdhury,1995
2. Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler–Najjar Type I patient;Ritter;J. Clin. Invest.,1992
3. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert’s syndrome;Bosma;New Engl. J. Med.,1995
4. Identification of bilirubin UDP-GTs in the human alimentary tract in accordance with the gut as a putative metabolic organ;McDonnell;Biochem. Pharmacol.,1996
5. UDP-glucuronosyltransferase activity in human liver and colon;Strassburg;Gastroenterology,1999
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