Article

UGT1A1 Mutation Association with Increased Bilirubin Levels and Severity of Unconjugated Hyperbilirubinemia in ABO Incompatible Newborns of China

2021-01-08

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Neonatal hyperbilirubinemia causing jaundice is common in East Asian population. Uridine diphosphate glucuronosyltransferase isoenzyme (UGT1A1) glucuronidates bilirubin and converts the toxic form of bilirubin to its nontoxic form.<bold>Method:</bold> A retrospective study was conducted to review clinical information of ABO hemolysis neonates (ABO HDN) admitted...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 7b00f034-7a0e-553e-b1b4-910055cd8543
DOI: 10.21203/rs.3.rs-33510/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

UGT1A1 Mutation Association with Increased Bilirubin Levels and Severity of Unconjugated Hyperbilirubinemia in ABO Incompatible Newborns of ChinaDOI 10.21203/rs.3.rs-33510/v1Read

UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.Semantic proximity Read

[Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].Semantic proximity Read

UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns.Semantic proximity Read

Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.Semantic proximity Read

[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].Semantic proximity Read

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern ChinaSemantic proximity Read

UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.Semantic proximity Read

[UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children].Semantic proximity Read

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China.Semantic proximity Read

Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.Semantic proximity Read

Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan.Semantic proximity Read

Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.Semantic proximity Read