Neonatal Jaundice and Bilirubin UDP-Glucuronosyl Transferase 1A1 Gene Polymorphism in Turkish Patients
Author:
Publisher
Wiley
Subject
Pharmacology,Toxicology,General Medicine
Reference17 articles.
1. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
2. Gilbert syndrome accelerates development of neonatal jaundice
3. Is Breastfeeding Really Favoring Early Neonatal Jaundice?
4. Predictive Ability of a Predischarge Hour-specific Serum Bilirubin for Subsequent Significant Hyperbilirubinemia in Healthy Term and Near-term Newborns
5. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome
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1. The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia;Children;2023-07-06
2. Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey;Turkish Archives of Pediatrics;2022-05-13
3. Deep Insight Into Long Non-coding RNA and mRNA Transcriptome Profiling in HepG2 Cells Expressing Genotype IV Swine Hepatitis E Virus ORF3;Frontiers in Veterinary Science;2021-04-29
4. The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility;BMC Medical Genetics;2020-11-06
5. Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis;Gene;2020-04
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