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...
Saved in:
Main Author: | Ma'amor, Nur Hasnah |
---|---|
Format: | Thesis |
Language: | English |
Published: |
2012
|
Subjects: | |
Online Access: | http://eprints.usm.my/42246/1/NUR_HASNAH_MA%27AMOR.pdf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Identification of the uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) gene mutations in babies with early onset of neonatal jaundice /
by: Norlelawati binti A. Talib
Published: (2004) -
Analysis of nucleotide variants in the promoter region of the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene among neonatal jaundice Malay infants without variations in the exonic regions
by: Ismail, Rosliza
Published: (2015) -
The relationship of 211G to A mutation of uridine diphosphoglucuronosyl tranferase 1A1 gene and severe neonatal jaundice in Malaysian Chinese newborn infants /
by: Wang, May Kay
Published: (2006) -
Study of UDP-glucurunosyl transferase 1A1 gene mutation in severe neonatal jaundice in malay neonates /
by: Azlin Ithnin
Published: (2008) -
Newborn Hearing Screening In The Special Care
Nursery Of Hospital Universiti Sains Malaysia
Kota Bharu
by: Al-khamesy, Khaled Saad
Published: (2002)