Genetic polymorphisms of UDP-glucuronosyltransferase in Asians:UGT1A1* 28 is a common allele in Indians

This publication has 10 references indexed in Scilit:

• Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese
  Pharmacogenetics, 2000
• UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians
  Pharmacogenetics, 1999
• The UGT1A1*28 allele is relatively rare in a Japanese population
  Pharmacogenetics, 1998
• Racial variability in the UDP-glucuronosyltransferase 1 ( UGT1A1 ) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
  Proceedings of the National Academy of Sciences, 1998
• UGT1*1 genotyping in a Canadian Inuit population
  Pharmacogenetics, 1997
• Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
  The Lancet, 1996
• Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II
  Biochemical and Biophysical Research Communications, 1993
• Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I
  The FASEB Journal, 1992
• Population studies on Gilbert's syndrome.
  Journal of Medical Genetics, 1975
• Ethnic differences in neonatal jaundice: Comparison of Japanese and Caucasian newborn infants
  American Journal of Obstetrics and Gynecology, 1975