Identification of a Defect in the UGT1A1 Gene Promoter and Its Association with Hyperbilirubinemia
- 1 March 2002
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 292 (2) , 492-497
- https://doi.org/10.1006/bbrc.2002.6683
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Prolonged Unconjugated Hyperbilirubinemia Associated With Breast Milk and Mutations of the Bilirubin Uridine Diphosphate- Glucuronosyltransferase GenePediatrics, 2000
- Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 geneJournal of Hepatology, 2000
- Association of Neonatal Hyperbilirubinemia With Bilirubin UDP-Glucuronosyltransferase PolymorphismPediatrics, 1999
- Gilbert’s syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newbornThe Journal of Pediatrics, 1999
- Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type IIBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1998
- The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergencePharmacogenetics, 1997
- Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndromeThe Lancet, 1996
- The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's SyndromeNew England Journal of Medicine, 1995
- Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndromeThe Lancet, 1995
- Isolation and properties of conjugated bilirubin from bileBiochemical Journal, 1970