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See Latest ArticlesPCSK9 Dominant Negative Mutant Results in Increased LDL Catabolic Rate and Familial Hypobetalipoproteinemia
Arteriosclerosis, Thrombosis, and Vascular Biology, 09/21/09
Cariou B et al. – The results show that heterozygous PCSK9 missense mutations may associate with profound hypobetalipoproteinemia and constitute the first direct evidence in human that decrease of plasma LDLC concentrations associated to PCSK9 LOF mutations are attributable to an increased clearance rate of LDL.
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Reduced fecal sterol excretion in subjects with familial hypoalphalipoproteinemia
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Phospholipase A2-modified LDL particles retain the generated hydrolytic products and are more atherogenic at acidic pH
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