Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic donors and apo A-I-deficient patients but not of Tangier disease patients

Author:

von Eckardstein Arnold,Huang Yadong,Kastelein John J.P,Geisel Jürgen,Real José T,Kuivenhoven Jan-Albert,Miccoli Roberto,Noseda Giorgio,Assmann Gerd

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference45 articles.

1. Tangier disease—combined clinical staff conference at the National Institutes of Health;Fredrickson;Ann Intern Med,1961

2. Assmann G, von Eckardstein A, Brewer HB Jr. Familial HDL deficiency. Tangier disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The Metabolic and Molecular Basis of Inherited Disease, 7th ed. New York: McGraw-Hill, 1995:2053–72.

3. Reverse cholesterol transport in plasmas of patients with different forms of familial high density lipoprotein deficiency;Von Eckardstein;Arterioscler Thromb Vasc Biol,1995

4. Molecular physiology of reverse cholesterol transport;Fielding;J Lipid Res,1995

5. Physiological role and clinical relevance of high-density lipoprotein subclasses;Von Eckardstein;Curr Opin Lipidol,1994

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