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rdf:type |
|
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lifeskim:mentions |
umls-concept:C0020557,
umls-concept:C0026882,
umls-concept:C0030705,
umls-concept:C0032105,
umls-concept:C0042285,
umls-concept:C0205082,
umls-concept:C0205164,
umls-concept:C0205214,
umls-concept:C0205396,
umls-concept:C0428460,
umls-concept:C1280500,
umls-concept:C1424878
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pubmed:issue |
6
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pubmed:dateCreated |
2008-7-8
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|
pubmed:abstractText |
The importance of the apolipoprotein A5 (APOA5) gene in determining plasma triglyceride (TG) levels has been demonstrated in transgenic and knockout mice and confirmed by human association studies in different ethnic groups.
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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:issn |
1434-6621
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
46
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pubmed:owner |
NLM
|
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pubmed:authorsComplete |
Y
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pubmed:pagination |
773-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18601597-Adult,
pubmed-meshheading:18601597-Aged,
pubmed-meshheading:18601597-Apolipoproteins A,
pubmed-meshheading:18601597-Cholesterol,
pubmed-meshheading:18601597-Czechoslovakia,
pubmed-meshheading:18601597-Female,
pubmed-meshheading:18601597-Gene Frequency,
pubmed-meshheading:18601597-Genetic Predisposition to Disease,
pubmed-meshheading:18601597-Genetic Testing,
pubmed-meshheading:18601597-Genotype,
pubmed-meshheading:18601597-Humans,
pubmed-meshheading:18601597-Hypertriglyceridemia,
pubmed-meshheading:18601597-Male,
pubmed-meshheading:18601597-Middle Aged,
pubmed-meshheading:18601597-Mutation,
pubmed-meshheading:18601597-Triglycerides
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pubmed:year |
2008
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pubmed:articleTitle |
APOA5 Ala315>Val, identified in patients with severe hypertriglyceridemia, is a common mutation with no major effects on plasma lipid levels.
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pubmed:affiliation |
Institute for Clinical and Experimental Medicine, Prague, Czech Republic. jaroslav.hubacek@ikem.cz
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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