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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1999-8-26
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pubmed:databankReference |
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pubmed:abstractText |
Genes have a major role in the control of high-density lipoprotein (HDL) cholesterol (HDL-C) levels. Here we have identified two Tangier disease (TD) families, confirmed 9q31 linkage and refined the disease locus to a limited genomic region containing the gene encoding the ATP-binding cassette transporter (ABC1). Familial HDL deficiency (FHA) is a more frequent cause of low HDL levels. On the basis of independent linkage and meiotic recombinants, we localized the FHA locus to the same genomic region as the TD locus. Mutations in ABC1 were detected in both TD and FHA, indicating that TD and FHA are allelic. This indicates that the protein encoded by ABC1 is a key gatekeeper influencing intracellular cholesterol transport, hence we have named it cholesterol efflux regulatory protein (CERP).
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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 |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1061-4036
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pubmed:author |
pubmed-author:Ashbourne-ExcoffonK JKJ,
pubmed-author:BrewerCC,
pubmed-author:Brooks-WilsonAA,
pubmed-author:CollinsJ AJA,
pubmed-author:CookE DEDJr,
pubmed-author:DenisMM,
pubmed-author:FichtelAA,
pubmed-author:FrohlichJJ,
pubmed-author:GenestJJJr,
pubmed-author:HaydenM RMR,
pubmed-author:KasteleinJ JJJ,
pubmed-author:KoopBB,
pubmed-author:LoubserOO,
pubmed-author:MarcilMM,
pubmed-author:MartindaleDD,
pubmed-author:MolhuizenH OHO,
pubmed-author:MorganKK,
pubmed-author:MottSS,
pubmed-author:OueletteB FBF,
pubmed-author:PimstoneSS,
pubmed-author:RoomeTT,
pubmed-author:SchererSS,
pubmed-author:SensenC WCW,
pubmed-author:YuLL,
pubmed-author:ZhangL HLH,
pubmed-author:van DamMM
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pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
336-45
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10431236-ATP-Binding Cassette Transporters,
pubmed-meshheading:10431236-Adult,
pubmed-meshheading:10431236-Amino Acid Sequence,
pubmed-meshheading:10431236-Base Sequence,
pubmed-meshheading:10431236-Cholesterol, HDL,
pubmed-meshheading:10431236-Chromosomes, Human, Pair 9,
pubmed-meshheading:10431236-Female,
pubmed-meshheading:10431236-Genetic Linkage,
pubmed-meshheading:10431236-Genetic Markers,
pubmed-meshheading:10431236-Glycoproteins,
pubmed-meshheading:10431236-Humans,
pubmed-meshheading:10431236-Male,
pubmed-meshheading:10431236-Models, Genetic,
pubmed-meshheading:10431236-Molecular Sequence Data,
pubmed-meshheading:10431236-Mutation,
pubmed-meshheading:10431236-Pedigree,
pubmed-meshheading:10431236-Physical Chromosome Mapping,
pubmed-meshheading:10431236-Sequence Homology, Amino Acid,
pubmed-meshheading:10431236-Tangier Disease
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pubmed:year |
1999
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pubmed:articleTitle |
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.
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pubmed:affiliation |
Xenon Bioresearch Inc., NRC Innovation Centre, Vancouver, British Columbia, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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