Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
about
Hyperbilirubinemia in Neonates: Types, Causes, Clinical Examinations, Preventive Measures and Treatments: A Narrative Review ArticleInherited disorders of bilirubin clearanceNew insights in bilirubin metabolism and their clinical implicationsRisk factors for severe hyperbilirubinemia in neonatesUGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approachBilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.Possible roles of bilirubin and breast milk in protection against retinopathy of prematurity.Prevalence of Gilbert syndrome in parents of neonates with pathologic indirect hyperbilirubinemiaRole of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome.The molecular basis of jaundice: An old symptom revisited.Association between UGT1A1*28*28 genotype and lung cancer in the Japanese population.Inhibitory effect of 5β-pregnane-3α,20β-diol on transcriptional activity and enzyme activity of human bilirubin UDP-glucuronosyltransferase.Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.Defective UGT1A1 causes hyperbilirubinemiaDefective UGT1A4 causes hyperbilirubinemiaCorrelation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.Polymorphisms of the uridine-diphosphoglucuronosyltransferase 1A1 gene and coronary artery disease.UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia.Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.
P2860
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P2860
Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
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2000年學術文章
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2000年學術文章
@zh-hant
name
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@en
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@nl
type
label
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@en
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@nl
prefLabel
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@en
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@nl
P2093
P356
P1433
P1476
Prolonged unconjugated hyperbi ...... glucuronosyltransferase gene.
@en
P2093
P356
10.1542/PEDS.106.5.E59
P407
P577
2000-11-01T00:00:00Z