Glycosylation structure and enzyme activity of lecithin:cholesterol acyltransferase from human plasma, HepG2 cells, and baculoviral and Chinese hamster ovary cell expression systems

Author:

Miller K R,Wang J,Sorci-Thomas M,Anderson R A,Parks J S

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference26 articles.

1. Familial lecithinxholesterol acyltransferase deficiency, including fish eye disease. In The Metabolic Basis of Inherited Disease;Norum,1989

2. Microheterogeneity and physical properties of human lecithin-cholesterol acyltransferase;Doi;J. Biol. Chem.,1983

3. Lecithinxholesterol acyltransferase. In Advances in Cholesterol Research;Fielding,1990

4. Lecithinxholesterol acyltransferase: role of N-linked glycosylation in enzyme function;Karmin;Biochem.J.,1993

5. Effects of inhibitors of N-linked oligosaccharide processing on the secretion, stability and activity of lecithinxholesterol acyltransferase;Collet;Biochemistry.,1991

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