Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase.

Samankaltaisia teoksia

• Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.
  Tekijä: van Es, H H, et al.
  Julkaistu: (1990)
• Bilirubin glucuronidation by intact Gunn rat fibroblasts expressing bilirubin UDP-glucuronosyltransferase.
  Tekijä: Seppen, J, et al.
  Julkaistu: (1996)
• Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene
  Tekijä: IOLASCON, A., et al.
  Julkaistu: (2000)
• Hepatic Conversion of Bilirubin Monoglucuronide to Diglucuronide in Uridine Diphosphate-Glucuronyl Transferase-Deficient Man and Rat by Bilirubin Glucuronoside Glucuronosyltransferase
  Tekijä: Chowdhury, J. Roy, et al.
  Julkaistu: (1978)
• Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis
  Tekijä: Zheng, Bixia, et al.
  Julkaistu: (2014)