UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia

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UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia

Table_1_Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing.DOCX

Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in neonatal hyperbilirubinemia (

NIAID Data Ecosystem20

Datasheet1_Developing and evaluating a predictive model for neonatal hyperbilirubinemia based on UGT1A1 gene polymorphism and clinical risk factors.pdf

BackgroundNeonatal hyperbilirubinemia (NHB) is one of the most common diseases in the neonatal period. Without timely diagnosis and treatment, it can lead to long-term complications. In severe cases,

NIAID Data Ecosystem00

DataSheet_1_Combined Effects of UGT1A1 and SLCO1B1 Variants on Chinese Adult Mild Unconjugated Hyperbilirubinemia.docx

The potential for genetic variation to cause adult unconjugated hyperbilirubinemia is increasingly being recognized. However, the cumulative effects of genetic variants have not been fully illuminated

NIAID Data Ecosystem10

Defective UGT1A1 causes hyperbilirubinemia

UDP-glucuronosyltransferases (UGTs) play a major role in the conjugation and therefore elimination of potentially toxic xenobiotics and endogenous compounds. The 1-1 isoform UGT1A1 is able to act upon

reactome.org60

Mouse gene Ugt1a1

Phenotype data for mouse gene Ugt1a1. Includes Ugt1a1's significant phenotypes, expression, images, histopathology and more.