Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome-Reference-Cited by-同舟云学术

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Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome

Published:2015-02-06 Issue:8 Volume:35 Page:2050-2056
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver Int

Author:

Shiu Tzu-Yue¹,Huang Hsin-Hung¹,Lin Hsuan-Hwai¹,Shih Yu-Lueng¹,Chu Heng-Cheng¹,Chang Wei-Kuo¹,Hsieh Tsai-Yuan¹

Affiliation:

1. Division of Gastroenterology; Department of Internal Medicine; Tri-Service General Hospital; National Defense Medical Center; Taipei Taiwan

Funder

Foundation for Medical Research of the Tri-Service General Hospital

National Defense Medical Center

Publisher

Wiley

Subject

Hepatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/liv.12785/fullpdf

Reference35 articles.

1. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene;Raijmakers;J Hepatol,2000

2. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome;Bosma;N Engl J Med,1995

3. Population studies on Gilbert's syndrome;Owens;J Med Genet,1975

4. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome;Monaghan;Lancet,1996

5. Human UDP-glucuronosyltransferases: metabolism, expression, and disease;Tukey;Annu Rev Pharmacol Toxicol,2000

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