A unique haplotype of the apolipoprotein B-100 allele associated with familial defective apolipoprotein B-100 in a Chinese man discovered during a study of the prevalence of this disorder-Reference-Cited by-同舟云学术

A unique haplotype of the apolipoprotein B-100 allele associated with familial defective apolipoprotein B-100 in a Chinese man discovered during a study of the prevalence of this disorder

Published:1993-07 Issue:7 Volume:34 Page:1149-1154
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Bersot TP,Russell SJ,Thatcher SR,Pomernacki NK,Mahley RW,Weisgraber KH,Innerarity TL,Fox CS

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference19 articles.

1. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia;Innerarity;J. Lipid Res.,1990

2. In vivo evidence for reduced binding of low density lipoproteins to receptors as a cause of primary moderate hypercholesterolemia;Vega;J. Clin. Invest.,1986

3. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding;Innerarity;Proc. Natl. Acad. Sci. USA.,1987

4. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100;Soria;Proc. Natl. Acad. Sci. USA.,1989

5. 13C NMR evidence that substitution of glutamine for arginine 3500 in familial defective apolipoprotein B-100 disrupts the conformation of the receptor-binding domain;Lund-Katz;J. Biol. Chem.,1991

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