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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 |
2007-3-22
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pubmed:abstractText |
The genetic background of familial combined hyperlipidemia (FCHL) has not been fully clarified. Because several nuclear receptors play pivotal roles in lipid metabolism, we tested the hypothesis that genetic variants of nuclear receptors contribute to FCHL.
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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 |
Apr
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pubmed:issn |
1524-4636
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pubmed:author |
pubmed-author:ClaudelThierryT,
pubmed-author:InazuAkihiroA,
pubmed-author:KatsudaShojiS,
pubmed-author:KawashiriMasa-akiMA,
pubmed-author:KobayashiJunjiJ,
pubmed-author:KoizumiJunjiJ,
pubmed-author:KuipersFolkertF,
pubmed-author:MabuchiHiroshiH,
pubmed-author:MiwaKenjiK,
pubmed-author:MizunoMihokoM,
pubmed-author:NoharaAtsushiA,
pubmed-author:TakataMutsukoM,
pubmed-author:TsuchidaMasayukiM,
pubmed-author:YamagishiMasakazuM
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pubmed:issnType |
Electronic
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
923-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17272748-Adult,
pubmed-meshheading:17272748-Aged,
pubmed-meshheading:17272748-Animals,
pubmed-meshheading:17272748-COS Cells,
pubmed-meshheading:17272748-Cercopithecus aethiops,
pubmed-meshheading:17272748-Cholesterol, LDL,
pubmed-meshheading:17272748-Coronary Artery Disease,
pubmed-meshheading:17272748-Dyslipidemias,
pubmed-meshheading:17272748-Female,
pubmed-meshheading:17272748-Gene Frequency,
pubmed-meshheading:17272748-Genetic Variation,
pubmed-meshheading:17272748-Heterozygote,
pubmed-meshheading:17272748-Humans,
pubmed-meshheading:17272748-Hyperlipidemia, Familial Combined,
pubmed-meshheading:17272748-Lipids,
pubmed-meshheading:17272748-Lipoprotein Lipase,
pubmed-meshheading:17272748-Male,
pubmed-meshheading:17272748-Middle Aged,
pubmed-meshheading:17272748-PPAR alpha,
pubmed-meshheading:17272748-Promoter Regions, Genetic,
pubmed-meshheading:17272748-Receptors, Cytoplasmic and Nuclear,
pubmed-meshheading:17272748-Retinoid X Receptor gamma,
pubmed-meshheading:17272748-Transfection
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pubmed:year |
2007
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pubmed:articleTitle |
High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.
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pubmed:affiliation |
Department of Lipidology, Graduate School of Medical Science, Kanazawa University, Takara-machi 13-1, Kanazawa 920-8641, Japan. a-nohara@med.kanazawa-u.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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