Simple Genetics for a Complex Disease
Author:
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference10 articles.
1. Potential of Proprotein Convertase Subtilisin/Kexin Type 9 Based Therapeutics
2. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
3. PCSK9: a convertase that coordinates LDL catabolism
4. Molecular Characterization of Loss-of-Function Mutations in PCSK9 and Identification of a Compound Heterozygote
5. The C679X mutation in PCSK9 is present and lowers blood cholesterol in a Southern African population
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1. Targeting PCSK9 to tackle cardiovascular disease;Pharmacology & Therapeutics;2023-09
2. Hepatic inactivation of murine Surf4 results in marked reduction in plasma cholesterol;eLife;2022-10-04
3. Targeting ASGR1 to lower cholesterol;Nature Metabolism;2022-08-04
4. A genome-wide case-only test for the detection of digenic inheritance in human exomes;Proceedings of the National Academy of Sciences;2020-07-27
5. A genome-wide case-only test for the detection of digenic inheritance in human exomes;2020-02-07
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