Cholesteryl ester synthesis in macrophages: stimulation by beta-very low density lipoproteins from cholesterol-fed animals of several species (Q71481484)

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scientific article published on 01 November 1980

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English	Cholesteryl ester synthesis in macrophages: stimulation by beta-very low density lipoproteins from cholesterol-fed animals of several species	scientific article published on 01 November 1980

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18 October 2019

Cholesteryl ester synthesis in macrophages: stimulation by beta-very low density lipoproteins from cholesterol-fed animals of several species (English)

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18 October 2019

Joseph L. Goldstein

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J L Goldstein

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18 October 2019

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R W Mahley

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18 October 2019

T L Innerarity

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18 October 2019

M S Brown

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18 October 2019

Y K Ho

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18 October 2019

J L Goldstein

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1 November 1980

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18 October 2019

November 1980

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Journal of Lipid Research

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18 October 2019

21

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18 October 2019

8

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18 October 2019

970-980

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18 October 2019

A proposal linking atherogenesis to the interaction of endothelial lipoprotein lipase with triglyceride-rich lipoproteins

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Binding, internalization, and degradation of low density lipoprotein by normal human fibroblasts and by fibroblasts from a case of homozygous familial hypercholesterolemia

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Canine lipoproteins and atherosclerosis. II. Characterization of the plasma lipoproteins associated with atherogenic and nonatherogenic hyperlipidemia

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Protein measurement with the Folin phenol reagent

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Altered Metabolism (In Vivo and In Vitro) of Plasma Lipoproteins after Selective Chemical Modification of Lysine Residues of the Apoproteins

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Release of low density lipoprotein from its cell surface receptor by sulfated glycosaminoglycans

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Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity

1 reference

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Binding site on macrophages that mediates uptake and degradation of acetylated low density lipoprotein, producing massive cholesterol deposition

1 reference

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10.1016/S0022-2275(20)34757-X

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18 October 2019

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