The Mystery of PCSK9
Author:
Affiliation:
1. From the Department of Biochemistry, University of Wisconsin-Madison, Wisc.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
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1. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
2. Mutations in the PCSK9 gene in Norwegian subjects with autosomal dominant hypercholesterolemia
3. A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree
4. The secretory proprotein convertase neural apoptosis-regulated convertase 1 (NARC-1): Liver regeneration and neuronal differentiation
5. Functional characterization of Narc 1, a novel proteinase related to proteinase K
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2. Effects of Tanshinone IIA on the modulation of miR-33a and the SREBP-2/Pcsk9 signaling pathway in hyperlipidemic rats;Molecular Medicine Reports;2016-04-14
3. Selection and characterization of human PCSK9 antibody from phage displayed antibody library;Biochemical and Biophysical Research Communications;2015-08
4. Correction to “The Potential Role of Anti-PCSK9 Monoclonal Antibodies in the Management of Hypercholesterolemia”;Reviews in Cardiovascular Medicine;2015-03-30
5. The Potential Role of Anti-PCSK9 Monoclonal Antibodies in the Management of Hypercholesterolemia;Reviews in Cardiovascular Medicine;2014-12-30
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