PCSK9, du gène à la protéine : un nouvel acteur dans l’homéostasie du cholestérol
Author:
Publisher
EDP Sciences
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://www.medecinesciences.org/10.1051/medsci/20062211916/pdf
Reference18 articles.
1. Abifadel M, Varret M, Rabes JP,et al.Mutations inPCSK9cause autosomal dominant hypercholesterolemia.Nat Genet2003; 34 : 154–6.
2. Seidah NG, Benjannet S, Wickham L,et al.The secretory proprotein convertase neural apoptosis-regulated convertase 1 (NARC-1) : liver regeneration and neuronal differentiation.Proc Natl Acad Sci USA2003; 100 : 928–33.
3. Allard D, Amsellem S, Abifadel M,et al.Novel mutations of thePCSK9gene cause variable phenotype of autosomal dominant hypercholesterolemia.Hum Mutat2005; 26 : 497.
4. Timms KM, Wagner S, Samuels ME,et al.A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree.Hum Genet2004; 114 : 349–53.
5. Leren TP. Mutations in thePCSK9gene in Norwegian subjects with autosomal dominant hypercholesterolemia.Clin Genet2004; 65 : 419–22.
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1. The rs7552841 polymorphism of protein convertase subtilisin/kexin type 9 is associated with cardiac tissue damage biomarkers and lipid profile in Tunisian patients with coronary artery disease;Gene Reports;2024-12
2. Living the PCSK9 Adventure: from the Identification of a New Gene in Familial Hypercholesterolemia Towards a Potential New Class of Anticholesterol Drugs;Current Atherosclerosis Reports;2014-07-23
3. Differential effects of PCSK9 loss of function variants on serum lipid and PCSK9 levels in Caucasian and African Canadian populations;Lipids in Health and Disease;2013-05-10
4. Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease;Human Mutation;2009-02-03
5. Après le récepteur des LDL et l'apolipoprotéine B, l'hypercholestérolémie familiale révèle son troisième protagoniste: PCSK9;Annales d'Endocrinologie;2007-06
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