Bilirubin metabolism and UDP ‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response
Author:
Affiliation:
1. Department of Clinical Pathology Cathay General Hospital Taipei Taiwan
2. Department of Medical Laboratory Science and Biotechnology Central Taiwan University of Science and Technology Taichung Taiwan
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/kjm2.12579
Reference99 articles.
1. Effect of UDP‐glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome
2. Uridine diphosphate glucuronosyltransferase 1A1
3. Variations in the UDP-glucuronosyltransferase 1A1 gene for the development of unconjugated hyperbilirubinemia in Taiwanese
4. Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome
5. Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II
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1. Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia;Pediatrics & Neonatology;2024-09
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