Isolation of allele-specific, receptor-binding-defective low density lipoproteins from familial defective apolipoprotein B-100 subjects.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference26 articles.
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2. Mapping apolipoprotein B on the low density lipoprotein surface by immunoelectron microscopy;Chatterton;J. Biol. Chem.,1991
3. Plasma lipoproteins. In Encyclopedia of Human Biology , Vol. 6;Innerarity,1990
4. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia;Innerarity;J. Lipid Res.,1990
5. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding;Innerarity;Proc. Natl. Acad. Sci. USA.,1987
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1. Familial Hypercholesterolemia;Genetic Causes of Cardiac Disease;2019
2. Plasma lipoprotein(a) levels in familial defective ApoB;Clinical Lipidology;2014-06-01
3. Mechanisms of Disease: genetic causes of familial hypercholesterolemia;Nature Clinical Practice Cardiovascular Medicine;2007-04
4. Intima-Media Thickness and Atherosclerotic Plaques in Familial Defective Apolipoprotein B-100 and Familial Hypercholesterolemia;Annals of the New York Academy of Sciences;2006-01-24
5. Flow Cytometric Assessment of LDL Ligand Function for Detection of Heterozygous Familial Defective Apolipoprotein B-100;Clinical Chemistry;2000-02-01
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