A Polymorphic Mutation, c.-3279T>G, in the UGT1A1 Promoter Is a Risk Factor for Neonatal Jaundice in the Malay Population-Reference-Cited by-同舟云学术

A Polymorphic Mutation, c.-3279T>G, in the UGT1A1 Promoter Is a Risk Factor for Neonatal Jaundice in the Malay Population

Published:2010-04 Issue:4 Volume:67 Page:401-406
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Yusoff Surini,Takeuchi Atsuko,Ashi Chitose,Tsukada Masako,Ma'Amor Nur H,Zilfalil Bin A,Yusoff Narazah M,Nakamura Tsutomu,Hirai Midori,Harahap Indra S K,Lee Myeong J,Nishimura Noriyuki,Takaoka Yutaka,Morikawa Satoru,Morioka Ichiro,Yokoyama Naoki,Matsuo Masafumi,Nishio Hisahide,Van Rostenberghe Hans

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference37 articles.

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

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

3. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

4. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome

5. Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease

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1. Association of gallstone and polymorphisms of UGT1A1*27 and UGT1A1*28 in patients with hepatitis B virus-related liver failure;Open Medicine;2022-01-01

2. Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbilirubinemia in an Iranian Population;IRAN J NEONATOL;2021

3. Pharmacogenetics/Pharmacogenomics of Drug-Metabolizing Enzymes and Transporters;Reference Module in Biomedical Sciences;2021

4. The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility;BMC Medical Genetics;2020-11-06

5. Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy;Journal of Tropical Pediatrics;2020-06-24