Response to the Letter by Ebara et al-Reference-Cited by-同舟云学术

Response to the Letter by Ebara et al

Published:2008-06-06 Issue:11 Volume:102 Page:
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circulation Research

Author:

Liu George¹,Hayden Michael R.²

Affiliation:

1. Institute of Cardiovascular Sciences, Peking University, Beijing, China

2. Department of Medical Genetics, University of British Columbia, Centre for Molecular Medicine and Therapeutics, Vancouver, Canada,

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference7 articles.

1. Brunzell JD. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: Scriver CR Beaudet AL Sly WS Valle D eds. The Metabolic Basis of Inherited Disease. Vol 2 . New York: McGraw-Hill; 1995: 1913–1932.

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

3. Novel LPL mutation (L303F) found in a patient associated with coronary artery disease and severe systemic atherosclerosis

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

5. Spontaneous Atherosclerosis in Aged Lipoprotein Lipase–Deficient Mice With Severe Hypertriglyceridemia on a Normal Chow Diet

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1. Enhanced atherothrombotic formation after oxidative injury by FeCl3 to the common carotid artery in severe combined hyperlipidemic mice;Biochemical and Biophysical Research Communications;2009-08