Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference26 articles.
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3. Function, genetic polymorphism, and transcriptional regulation of human UDP-glucuronosyltransferase (UGT) 1A1;Sugatani;Drug Metab Pharmacokinet,2013
4. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome;Bosma;N Engl J Med,1995
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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
2. Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia;Neonatology;2023
3. Bilirubin metabolism and UDP ‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response;The Kaohsiung Journal of Medical Sciences;2022-08
4. Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports;World Journal of Clinical Cases;2022-07-16
5. Rapid detection of the irinotecan‐related UGT1A1 *28 polymorphism by asymmetric PCR melting curve analysis using one fluorescent probe;Journal of Clinical Laboratory Analysis;2022-06-29
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