Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis
J Wang, J Yin, M Xue, J Lyu, Y Wan - Gene, 2020 - Elsevier
Objective To identify the association between UGT1A1 Gly71Arg and TATA promoter
polymorphisms and neonatal hyperbilirubinemia. Methods The studies related to the …
polymorphisms and neonatal hyperbilirubinemia. Methods The studies related to the …
UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia
Genetic factors are implicated in pathogenesis of neonatal hyperbilirubinemia. In this nested
case-control study, we determined 1) frequency of thymine-adenine (TA) n promoter …
case-control study, we determined 1) frequency of thymine-adenine (TA) n promoter …
Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism
L Travan, S Lega, S Crovella, M Montico… - The Journal of …, 2014 - Elsevier
Objective To assess whether UGT1A1 promoter polymorphisms associated with Gilbert
Syndrome (GS) occur with a greater frequency in neonates with severe hyperbilirubinemia …
Syndrome (GS) occur with a greater frequency in neonates with severe hyperbilirubinemia …
The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1) promoter gene polymorphism in …
A Riskin, Y Bravdo, C Habib, I Maor, J Mousa… - Children, 2023 - mdpi.com
Glucose-6-phosphate dehydrogenase (G6PD) deficiency and polymorphism in uridine
diphosphate glucuronosyl transferase 1A1 (UGT1A1) were associated with significant …
diphosphate glucuronosyl transferase 1A1 (UGT1A1) were associated with significant …
[HTML][HTML] Association of neonatal hyperbilirubinemia with UGT1A1 gene polymorphisms: A meta-analysis
Z Yu, K Zhu, L Wang, Y Liu, J Sun - Medical science monitor …, 2015 - ncbi.nlm.nih.gov
Background The results of studies on association between the polymorphisms in the coding
region and the promoter of uridine diphosphateglucuronosyl transferase 1A1 (UGT1A1) and …
region and the promoter of uridine diphosphateglucuronosyl transferase 1A1 (UGT1A1) and …
Association of neonatal hyperbilirubinemia with uridine diphosphate‐glucuronosyltransferase 1A1 gene polymorphisms: Meta‐analysis
J Long, S Zhang, X Fang, Y Luo, J Liu - Pediatrics International, 2011 - Wiley Online Library
Background: Recent reports have suggested that genetic factors, including mutations in the
coding region or promoter of uridine diphosphate‐glucuronosyltransferase 1A1 (UGT1A1) …
coding region or promoter of uridine diphosphate‐glucuronosyltransferase 1A1 (UGT1A1) …
UGT1A1 基因多态性与新生儿黄疸遗传关联性的Meta 分析
杨琳， 丁俊杰， 周文浩 - 中国循证儿科杂志, 2010 - cjebp.net
目的评价不同人群UGT1A1 基因GLY71ARG 多态性, TATA 重复多态性与新生儿黄疸的遗传
关联性. 方法制定原始文献的纳入标准, 排除标准及检索策略, 检索PubMed, EMBASE, Web of …
关联性. 方法制定原始文献的纳入标准, 排除标准及检索策略, 检索PubMed, EMBASE, Web of …
Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations
R Lin, X Wang, Y Wang, F Zhang, Y Wang… - Human …, 2009 - Wiley Online Library
Numerous studies have shown that the (TA) n repeat polymorphism in the uridine
diphosphate glycosyltransferase 1 (UGT1A1) gene promoter is associated with …
diphosphate glycosyltransferase 1 (UGT1A1) gene promoter is associated with …
[HTML][HTML] Review of the contribution of genetic factors to hyperbilirubinemia and kernicterus risk in neonates: a targeted update
JF Watchko - Pediatric Medicine, 2021 - pm.amegroups.org
The genesis of neonatal hyperbilirubinemia is characterized by etiologic heterogeneity,
environmental modulation, and the interaction of multiple gene loci. In addition to inherited …
environmental modulation, and the interaction of multiple gene loci. In addition to inherited …