✦ LIBER ✦

Family 1 uridine-5′-diphosphate glucuronosyltransferases (UGT1A): from Gilbert’s syndrome to genetic organization and variability

✍ Scribed by Christian P. Strassburg; Tim O. Lankisch; Michael P. Manns; Ursula Ehmer

Book ID: 105870666
Publisher: Springer-Verlag
Year: 2008
Tongue: English
Weight: 930 KB
Volume: 82
Category: Article
ISSN: 0340-5761
DOI: 10.1007/s00204-008-0314-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Genetic lesions of bilirubin uridine-dip

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: Correlation of genotype to phenotype

✍ Ajit Kadakol; Siddhartha S. Ghosh; Baljit S. Sappal; Girish Sharma; Jayanta Roy 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 314 KB

Uridine-diphosphoglucuronate glucuronosyltransferases (UGTs) are a family of enzymes that conjugate various endogenous and exogenous compounds with glucuronic acid and facilitate their excretion in the bile. Bilirubin-UGT(1) (UGT1A1) is the only isoform that significantly contributes to the conjugat

Genetic linkage to the collagen α1 (V) g

Genetic linkage to the collagen α1 (V) gene (COL5A1) in two British Ehlers–Danlos syndrome families with variable type I and II phenotypes

✍ N.P. BURROWS; A.C. NICHOLLS; J.R.W. YATES; A.J. RICHARDS; F.M. POPE 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 234 KB