UDP‐glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia

This publication has 14 references indexed in Scilit:

• Frequencies of UDP‐glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil
  American Journal of Medical Genetics, 2002
• Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia
  The Lancet, 2001
• Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
  Journal of Human Genetics, 1999
• Gilbert syndrome accelerates development of neonatal jaundice
  The Journal of Pediatrics, 1998
• Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
  British Journal of Haematology, 1997
• Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
  Proceedings of the National Academy of Sciences, 1997
• Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1997
• Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
  The Lancet, 1996
• The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome
  New England Journal of Medicine, 1995
• Sickle Cell Disease in a Brazilian Population from Sao Paulo: A Study of the βs Haplotypes
  Human Heredity, 1994