The involvement of upstream stimulatory factor 1 in Dutch patients with familial combined hyperlipidemias⃞
Recently, the upstream stimulatory factor 1 gene (USF1) was proposed as a candidate gene for familial combined hyperlipidemia (FCH). In this study, we examined the previously identified risk haplotype of USF1 with respect to FCH and its related phenotypes in 36 Dutch FCH families. The diagnosis of FCH was based on both the traditional diagnostic criteria and a nomogram. The two polymorphisms, USF1s1 and USF1s2, were in complete linkage disequilibrium. No association was found for the individual single nucleotide polymorphisms (SNPs) with FCH defined by the nomogram (USF1s1, P = 0.53; USF1s2, P... Mehr ...
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Dokumenttyp: | Artikel |
Erscheinungsdatum: | 2007 |
Reihe/Periodikum: | Journal of Lipid Research, Vol 48, Iss 1, Pp 193-200 (2007) |
Verlag/Hrsg.: |
Elsevier
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Schlagwörter: | single nucleotide polymorphisms / mRNA expression / total cholesterol / apolipoprotein B / small dense low density lipoprotein / Biochemistry / QD415-436 |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-26630644 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | https://doi.org/10.1194/jlr.M600184-JLR200 |