Serum Lipoprotein Lipase Concentration and Risk for Future Coronary Artery Disease-Reference-Cited by-同舟云学术

Serum Lipoprotein Lipase Concentration and Risk for Future Coronary Artery Disease

Published:2006-03 Issue:3 Volume:26 Page:637-642
ISSN:1079-5642
Container-title:Arteriosclerosis, Thrombosis, and Vascular Biology
language:en
Short-container-title:ATVB

Author:

Rip Jaap¹,Nierman Melchior C.¹,Wareham Nicholas J.¹,Luben Robert¹,Bingham Sheila A.¹,Day Nicholas E.¹,van Miert Joram N.I.¹,Hutten Barbara A.¹,Kastelein John J.P.¹,Kuivenhoven Jan Albert¹,Khaw Kay-Tee¹,Boekholdt S. Matthijs¹

Affiliation:

1. From the Departments of Vascular Medicine (J.R., M.C.N., J.N.I.M., J.J.P.K., J.A.K.), Cardiology (S.M.B.), and Clinical Epidemiology and Biostatistics (B.A.H.), Academic Medical Center, Amsterdam, The Netherlands; Medical Research Council Epidemiology Unit (N.J.W.), Cambridge, United Kingdom; Medical Research Council Dunn Nutrition Unit (S.A.B.), Cambridge, United Kingdom; and the Department of Public Health and Primary Care (R.L., N.E.D., K.T.K.), Institute of Public Health, University of Cambridge...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference41 articles.

1. Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein.

2. Brunzell J. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: Sriver C Baudet A Sly W Valle D eds. The Metabolic and Molecular Basis of Inherited Disease 7th ed. New York: McGraw-Hill; 1995: 1913–1932.

3. Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

4. No evidence of accelerated atherosclerosis in a 66-yr-old chylomicronemia patient homozygous for the nonsense mutation (Tyr61→Stop) in the lipoprotein lipase gene

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