The J. D. mutation in familial hypercholesterolemia: Amino acid substitution in cytoplasmic domain impedes internalization of LDL receptors-Reference-Cited by-同舟云学术

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The J. D. mutation in familial hypercholesterolemia: Amino acid substitution in cytoplasmic domain impedes internalization of LDL receptors

Published:1986-04 Issue:1 Volume:45 Page:15-24
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Davis C.Geoffrey,Lehrman Mark A.,Russell David W.,Anderson Richard G.W.,Brown Michael S.,Goldstein Joseph L.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference33 articles.

1. A mutation that impairs the ability of lipoprotein receptors to localise in coated pits on the cell surface of human fibroblasts;Anderson;Nature,1977

2. Visualization of acidic organelles in intact cells by electron microscopy;Anderson,1984

3. Immunologic cross-reactivity of the LDL receptor from bovine adrenal cortex, human fibroblasts, canine liver and adrenal gland, and rat liver;Beisiegel;J. Biol. Chem.,1981

4. Monoclonal antibodies to the low density lipoprotein receptor as probes for study of receptor-mediated endocytosis and the genetics of familial hypercholesterolemia;Beisiegel;J. Biol. Chem.,1981

5. Immunoblot analysis of low density lipoprotein receptors in fibroblasts from subjects with familial hypercholesterolemia;Beisiegel;J. Biol. Chem.,1982

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