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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
7
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pubmed:dateCreated |
2002-3-6
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pubmed:abstractText |
Genetic mutations in the uridine diphosphate (UDP)-glucuronosyltransferase 1A (UGT1A) enzyme promoter have been associated with unconjugated hyperbilirubinemia and Gilbert syndrome. The effects of UGT1A promoter polymorphisms on serum bilirubin levels and symptomatic gallstone formation were studied in a cohort of children with sickle cell anemia (SCA).
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1077-4114
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
448-51
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pubmed:dateRevised |
2011-10-6
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pubmed:meshHeading |
pubmed-meshheading:11878580-Adolescent,
pubmed-meshheading:11878580-Adult,
pubmed-meshheading:11878580-Anemia, Sickle Cell,
pubmed-meshheading:11878580-Bilirubin,
pubmed-meshheading:11878580-Child,
pubmed-meshheading:11878580-Child, Preschool,
pubmed-meshheading:11878580-Cholelithiasis,
pubmed-meshheading:11878580-DNA Primers,
pubmed-meshheading:11878580-Genotype,
pubmed-meshheading:11878580-Glucuronosyltransferase,
pubmed-meshheading:11878580-Heterozygote,
pubmed-meshheading:11878580-Homozygote,
pubmed-meshheading:11878580-Humans,
pubmed-meshheading:11878580-Polymerase Chain Reaction,
pubmed-meshheading:11878580-Polymorphism, Genetic,
pubmed-meshheading:11878580-Promoter Regions, Genetic,
pubmed-meshheading:11878580-Retrospective Studies
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pubmed:year |
2001
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pubmed:articleTitle |
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
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pubmed:affiliation |
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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