Article

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China

2024-07-17

Abstract excerpt

<title>Abstract</title> <p>We explore the allele and genotype distribution of UGT1A1 and BLVRA variants in individuals affected by neonatal hyperbilirubinemia in southern China. Blood specimens were collected from 240 neonates: 126 cases of hyperbilirubinemia and 114 healthy controls. Serum levels of total protein, albumin, bilirubin (total and direct), urea nitrogen, creatinine, and other biochemical parameters...

Topics

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

Identifiers and source

Literature Corpus work: 8b3d8d78-d911-5244-a20e-047af89ddb77
DOI: 10.21203/rs.3.rs-4523536/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern ChinaDOI 10.21203/rs.3.rs-4523536/v1Read

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

Associations between G6PD, OATP1B1 and BLVRA variants and susceptibility to neonatal hyperbilirubinaemia in a Chinese Han populationSemantic proximity Read

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

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

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

Gene Mutation in Neonatal Jaundice - Mutations in UGT1A1 and OATP2 Genes.Semantic proximity Read

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

Investigation of the Association Between G6PD, UGT1A1, and SLCO1B1 Gene Polymorphisms and Neonatal Hyperbilirubinemia Using MALDI-TOF MS TechnologySemantic proximity Read

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

Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai populationSemantic proximity Read

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

[UGT1A1 gene mutations in Chinese Dong neonates in Sanjiang, Guangxi].Semantic proximity Read