Exploring the genetic architecture of neonatal hyperbilirubinemia.
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Hyperbilirubinemia in Neonates: Types, Causes, Clinical Examinations, Preventive Measures and Treatments: A Narrative Review ArticleAssociation of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.Perinatal gene transfer to the liver.Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.Pregnane-x-receptor controls hepatic glucuronidation during pregnancy and neonatal development in humanized UGT1 mice.Polymorphic variants of SLCO1B1 in neonatal hyperbilirubinemia in China.Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.Glucose-6-phosphate dehydrogenase--beyond the realm of red cell biology.Current strategies to generate mature human induced pluripotent stem cells derived cholangiocytes and future applications.Association between the Specific UGT1A1 Promoter Sequence Variant (c-3279T>G) and Unconjugated Neonatal Hyperbilirubinemia.A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin EncephalopathyRisk factors associated with unconjugated neonatal hyperbilirubinemia in Malaysian neonates.Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.Effect of genetic variants of bilirubin metabolism on the degree of hyperbilirubinemia in African-American newborns.Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.Modulation of bilirubin neurotoxicity by the Abcb1 transporter in the Ugt1-/- lethal mouse model of neonatal hyperbilirubinemia.The African-American neonate at risk for extreme hyperbilirubinemia: a better management strategy is needed.UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal period.Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study
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P2860
Exploring the genetic architecture of neonatal hyperbilirubinemia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 21 December 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@en
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@nl
type
label
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@en
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@nl
prefLabel
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@en
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@nl
P1476
Exploring the genetic architecture of neonatal hyperbilirubinemia.
@en
P2093
Jon F Watchko
P304
P356
10.1016/J.SINY.2009.11.003
P577
2009-12-21T00:00:00Z