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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
18
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pubmed:dateCreated |
1995-11-2
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pubmed:abstractText |
People with Gilbert's syndrome have mild, chronic unconjugated hyperbilirubinemia in the absence of liver disease or overt hemolysis. Hepatic glucuronidating activity, essential for efficient biliary excretion of bilirubin, is reduced to about 30 percent of normal.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0028-4793
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
333
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
1171-5
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pubmed:dateRevised |
2010-3-24
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pubmed:meshHeading |
pubmed-meshheading:7565971-Adolescent,
pubmed-meshheading:7565971-Adult,
pubmed-meshheading:7565971-Base Sequence,
pubmed-meshheading:7565971-Case-Control Studies,
pubmed-meshheading:7565971-Crigler-Najjar Syndrome,
pubmed-meshheading:7565971-Female,
pubmed-meshheading:7565971-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:7565971-Gilbert Disease,
pubmed-meshheading:7565971-Glucuronosyltransferase,
pubmed-meshheading:7565971-Homozygote,
pubmed-meshheading:7565971-Humans,
pubmed-meshheading:7565971-Male,
pubmed-meshheading:7565971-Middle Aged,
pubmed-meshheading:7565971-Molecular Sequence Data,
pubmed-meshheading:7565971-Mutation,
pubmed-meshheading:7565971-TATA Box
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pubmed:year |
1995
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pubmed:articleTitle |
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
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pubmed:affiliation |
Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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