Hypercholesterolemias, Familial Defective ApoB (FDB) and LDL Receptor Defects
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Elsevier
Reference14 articles.
1. Identification of the low density lipoprotein receptor-binding site in apolipoprotein B100 and the modulation of its binding activity by the carboxyl terminus in familial defective apo-B100;Boren;J. Clin. Invest.,1998
2. The molecular mechanism for the genetic disorder familial defective apolipoprotein B100;Boren;J. Biol. Chem.,2001
3. Immunoelectron microscopy of low density lipoproteins yields a ribbon and bow model for the conformation of apolipoprotein B on the lipoprotein surface;Chatterton;J. Lipid Res.,1995
4. Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia;Gaffney;Arterioscler. Thromb. Vasc. Biol.,1995
5. Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein;Garcia;Science,2001
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