Specific Mutations in ABCA1 Have Discrete Effects on ABCA1 Function and Lipid Phenotypes Both In Vivo and In Vitro-Reference-Cited by-同舟云学术

Specific Mutations in ABCA1 Have Discrete Effects on ABCA1 Function and Lipid Phenotypes Both In Vivo and In Vitro

Published:2006-08-18 Issue:4 Volume:99 Page:389-397
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circulation Research

Author:

Singaraja Roshni R.¹,Visscher Henk¹,James Erick R.¹,Chroni Angeliki¹,Coutinho Jonathan M.¹,Brunham Liam R.¹,Kang Martin H.¹,Zannis Vassilis I.¹,Chimini Giovanna¹,Hayden Michael R.¹

Affiliation:

1. From the Center for Molecular Medicine and Therapeutics (R.R.S., H.V., E.R.J., J.M.C., L.R.B., M.H.K., M.R.H.), University of British Columbia and Child and Family Research Institute, Vancouver, British Columbia, Canada; the Whitaker Cardiovascular Institute (A.C., V.I.Z.), Boston University School of Medicine, Boston, Mass; and Institut Nationale de la Santé et de la Recherche Médicale/Centre Nationale de Recherche Scientifique et Universite de La Mediterranee (G.C.), Marseille, France.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference28 articles.

1. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

2. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

3. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

4. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes

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