Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese-Reference-Cited by-同舟云学术

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Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

Published:1998-09 Issue:1 Volume:46 Page:21-26
ISSN:1521-6543
Container-title:IUBMB Life
language:en
Short-container-title:TBMB

Author:

Akaba Kazuhiro,Kimura Toshiyuki,Sasaki Ayako,Tanabe Saori,Ikegami Tohru,Hashimoto Motoya,Umeda Hitoshi,Yoshida Hiroshi,Umetsu Kazuo,Chiba Hitoshi,Yuasa Isao,Hayasaka Kiyoshi

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Genetics,Molecular Biology,Biochemistry

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Population-scale variability of the human UDP-glycosyltransferase gene family;Journal of Genetics and Genomics;2024-07

2. Fetal and neonatal bilirubin metabolism;Frontiers in Pediatrics;2023-02-07

3. Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns: A Preliminary Study;International Journal of Environmental Research and Public Health;2022-10-12

4. Safety, Tolerability, Pharmacokinetics, and Acceptability of Oral and Long-Acting Cabotegravir in HIV-Negative Chinese Men;Antimicrobial Agents and Chemotherapy;2022-03-15

5. UGT1A1 rs4148323 A Allele is Associated With Increased 2-Hydroxy Atorvastatin Formation and Higher Death Risk in Chinese Patients With Coronary Artery Disease;Frontiers in Pharmacology;2021-03-08

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