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Mining the genome for lipid genes

Published:2014-10 Issue:10 Volume:1842 Page:1993-2009
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Kuivenhoven Jan Albert,Hegele Robert A.^ORCID

Funder

Fondation Leducq

Netherlands CardioVascular Research Initiative

European Union

Canadian Institutes of Health Research

Heart and Stroke Foundation of Ontario

Edith Schulich Vinet Canada Research Chair (Tier 1) in Human Genetics

Jacob J. Wolfe Distinguished Medical Research Chair (RRTD)

Martha Blackburn Chair in Cardiovascular Research

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference218 articles.

1. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia;Abifadel;Nat. Genet.,2003

2. Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease;Abifadel;Hum Mutat.,2009

3. Expression cloning of SR-BI, a CD36-related class B scavenger receptor;Acton;J. Biol. Chem.,1994

4. AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34;Agarwal;Nat. Genet.,2002

5. Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia;Agarwal;Hum. Mol. Genet.,2003

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