Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man.
Open Access
- 1 July 1994
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 269 (27) , 17960-17964
- https://doi.org/10.1016/s0021-9258(17)32403-1
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Identification of an A-to-G Missense Mutation in Exon 2 of the UGT1 Gene Complex That Causes Crigler-Najjar Syndrome Type 2Genomics, 1993
- The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locusPharmacogenetics, 1992
- Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.Journal of Clinical Investigation, 1990
- Orthotopic liver transplantation for type I Crigler-Najjar syndromeHepatology, 1986
- An unusual case of Crigler-Najjar disease in the adultJournal of Hepatology, 1985
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Unconjugated Bilirubin and an Increased Proportion of Bilirubin Monoconjugates in the Bile of Patients with Gilbert's Syndrome and Crigler-Najjar DiseaseJournal of Clinical Investigation, 1977
- Bilirubin conjugates in bile of man and rat in the normal state and in liver diseaseJournal of Clinical Investigation, 1972
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- CHRONIC UNCONJUGATED HYPERBILIRUBINEMIA WITHOUT OVERT SIGNS OF HEMOLYSIS IN ADOLESCENTS AND ADULTS*Journal of Clinical Investigation, 1962