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 …
[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 …
Nursing diagnosis of neonatal jaundice: study of clinical indicators
AVVC Dantas, LJR Farias, SJ de Paula… - Journal of pediatric …, 2018 - Elsevier
Purpose This study aimed to identify the defining characteristics of, and examine their
association with, the nursing diagnosis (ND) of Neonatal Jaundice (00194) in sample of …
association with, the nursing diagnosis (ND) of Neonatal Jaundice (00194) in sample of …
Genetic variations in bilirubin metabolism genes and their association with unconjugated hyperbilirubinemia in adults
AS Chiddarwar, SZ D'Silva, RB Colah… - Annals of Human …, 2017 - Wiley Online Library
Objective: The present study was undertaken to investigate the genotype and allele
frequencies of the variants in the four bilirubin metabolism genes (UGT1A1, OATP2 …
frequencies of the variants in the four bilirubin metabolism genes (UGT1A1, OATP2 …
Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR …
R Amandito, R Rohsiswatmo, E Carolina… - Frontiers in …, 2019 - frontiersin.org
Background: Single nucleotide polymorphism (SNP) variants of the uridine diphosphate
glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in …
glucuronosyltransferase 1A1 (UGT1A1) gene have been studied as an important factor in …
UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns
Objective: To study the contribution of UGT1A1 gene variants and clinical risk factors in
modulating hyperbilirubinemia risk in newborns. Study design: Seven UGT1A1 gene …
modulating hyperbilirubinemia risk in newborns. Study design: Seven UGT1A1 gene …
Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects
C Rodrigues, E Vieira, R Santos, J de Carvalho… - Blood Cells, Molecules …, 2012 - Elsevier
The Gilbert syndrome is a benign form of unconjugated hyperbilirubinemia, mainly
associated with alterations in UGT1A1 gene. This work investigated the effect of UGT1A1 …
associated with alterations in UGT1A1 gene. This work investigated the effect of UGT1A1 …
Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates
S D'Silva, RB Colah, K Ghosh, MB Mukherjee - Gene, 2014 - Elsevier
Genetic association studies have linked a number of single nucleotide polymorphisms
(SNPs) with unconjugated hyperbilirubinemia. The present study was undertaken to validate …
(SNPs) with unconjugated hyperbilirubinemia. The present study was undertaken to validate …
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 …