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Pathogenesis of type III hyperlipoproteinemia (dysbetalipoproteinemia): questions, quandaries, and paradoxes

Type III hyperlipoproteinemia (HLP) is a genetic disorder characterized by accumulation of remnant lipoproteins in the plasma and development of premature atherosclerosis. Although receptor binding-defective forms of apolipoprotein (apo) E are the common denominator in this disorder, a number of app...

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Principais autores: Robert W. Mahley, Yadong Huang, Stanley C. Rall, Jr.
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 1999-11-01
Serier:Journal of Lipid Research
Fag:
apolipoprotein E
lipoprotein metabolism
heparan sulfate proteoglycans
LDL receptor
lipolysis
β-VLDL
Online adgang:http://www.sciencedirect.com/science/article/pii/S0022227520324172
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