Jaundice, genes and promoters
- 1 September 2000
- journal article
- Published by Elsevier in Journal of Hepatology
- Vol. 33 (3) , 476-479
- https://doi.org/10.1016/s0168-8278(00)80285-8
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 geneJournal of Hepatology, 2000
- Human UDP-Glucuronosyltransferases: Metabolism, Expression, and DiseaseAnnual Review of Pharmacology and Toxicology, 2000
- Expression of the UDP-glucuronosyltransferase 1A Locus in Human ColonJournal of Biological Chemistry, 1998
- Differential Expression of the UGT1A Locus in Human Liver, Biliary, and Gastric Tissue: Identification ofUGT1A7 and UGT1A10 Transcripts in Extrahepatic TissueMolecular Pharmacology, 1997
- The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's SyndromeNew England Journal of Medicine, 1995
- A phenylalanine codon deletion at the UGT1 gene complex locus of a Crigler-Najjar type I patient generates a pH-sensitive bilirubin UDP-glucuronosyltransferase.Journal of Biological Chemistry, 1993
- A mutation in bilirubin uridine 5′-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type IIGastroenterology, 1993
- Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.Journal of Clinical Investigation, 1992
- Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type IThe FASEB Journal, 1992
- Sequence of Exons and the Flanking Regions of Human Bilirubin–Udp–Glucuronosyltransferase Gene Complex and Identification of A Genetic Mutation in A Patient With Crigler–Najjar Syndrome, Type IHepatology, 1992