Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan

The rate limiting step of bilirubin excretion is the glucuronidation of bilirubin in the liver, a process that is catalyzed by an enzyme, Uridine glucuronyl transferase. This enzyme is encoded by the UGT1A1 gene. In several populations, mutations in this gene have been shown to cause neonatal jaundi...

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Main Author: Ma'amor, Nur Hasnah
Format: Thesis
Language:English
Published: 2012
Subjects:
Online Access:http://eprints.usm.my/42246/
http://eprints.usm.my/42246/1/NUR_HASNAH_MA%27AMOR.pdf
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author Ma'amor, Nur Hasnah
author_facet Ma'amor, Nur Hasnah
author_sort Ma'amor, Nur Hasnah
building USM Institutional Repository
collection Online Access
description The rate limiting step of bilirubin excretion is the glucuronidation of bilirubin in the liver, a process that is catalyzed by an enzyme, Uridine glucuronyl transferase. This enzyme is encoded by the UGT1A1 gene. In several populations, mutations in this gene have been shown to cause neonatal jaundice. However data on the Malaysian Malay population are scanty at best. The objectives of this study included: to determine the frequency of variants in the exons of the UGT1A1 gene in a population of term Malay neonates with jaundice and without jaundice, and to correlate the genotype finding with some phenotypic data.
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institution Universiti Sains Malaysia
institution_category Local University
language English
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publishDate 2012
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spelling usm-422462019-04-12T05:26:22Z http://eprints.usm.my/42246/ Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan Ma'amor, Nur Hasnah R5-920 Medicine (General) The rate limiting step of bilirubin excretion is the glucuronidation of bilirubin in the liver, a process that is catalyzed by an enzyme, Uridine glucuronyl transferase. This enzyme is encoded by the UGT1A1 gene. In several populations, mutations in this gene have been shown to cause neonatal jaundice. However data on the Malaysian Malay population are scanty at best. The objectives of this study included: to determine the frequency of variants in the exons of the UGT1A1 gene in a population of term Malay neonates with jaundice and without jaundice, and to correlate the genotype finding with some phenotypic data. 2012-04 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/42246/1/NUR_HASNAH_MA%27AMOR.pdf Ma'amor, Nur Hasnah (2012) Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan. Masters thesis, Universiti Sains Malaysia.
spellingShingle R5-920 Medicine (General)
Ma'amor, Nur Hasnah
Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title_full Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title_fullStr Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title_full_unstemmed Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title_short Screening Of UGT1A1 Gene And Genotype-Phenotype Correlationship In Neonatal Jaundice From A Sample Of Newborns In Kelantan
title_sort screening of ugt1a1 gene and genotype-phenotype correlationship in neonatal jaundice from a sample of newborns in kelantan
topic R5-920 Medicine (General)
url http://eprints.usm.my/42246/
http://eprints.usm.my/42246/1/NUR_HASNAH_MA%27AMOR.pdf