First International Workshop on Familial Defective apo B-100, Munich, November 1991.

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作者信息

Schuster H, Humphries S, Rauh G, Keller C

机构信息

Medizinische Poliklinik, Universität München.

出版信息

Clin Investig. 1992 Oct;70(10):961-4. doi: 10.1007/BF00180448.

DOI:10.1007/BF00180448

PMID:1360285

Abstract

摘要

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First International Workshop on Familial Defective apo B-100, Munich, November 1991.

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本文引用的文献

In vivo evidence for reduced binding of low density lipoproteins to receptors as a cause of primary moderate hypercholesterolemia.低密度脂蛋白与受体结合减少作为原发性中度高胆固醇血症病因的体内证据。

J Clin Invest. 1986 Nov;78(5):1410-4. doi: 10.1172/JCI112729.

Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.家族性载脂蛋白B-100缺陷：单克隆抗体MB47与异常低密度脂蛋白的结合增强。

Proc Natl Acad Sci U S A. 1988 Dec;85(24):9758-62. doi: 10.1073/pnas.85.24.9758.

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.一种特定载脂蛋白B突变与家族性缺陷载脂蛋白B-100之间的关联。

Proc Natl Acad Sci U S A. 1989 Jan;86(2):587-91. doi: 10.1073/pnas.86.2.587.

Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol.

Atherosclerosis. 1990 Jun;82(3):177-83. doi: 10.1016/0021-9150(90)90038-k.

Low density lipoprotein-induced growth of U937 cells: a novel method to determine the receptor binding of low density lipoprotein.低密度脂蛋白诱导U937细胞生长：一种测定低密度脂蛋白受体结合的新方法。

J Lipid Res. 1990 Jan;31(1):37-44.

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases.

Atherosclerosis. 1990 Jan;80(3):235-42. doi: 10.1016/0021-9150(90)90031-d.

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.

J Lipid Res. 1990 Aug;31(8):1337-49.

Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich.

Arteriosclerosis. 1990 Jul-Aug;10(4):577-81. doi: 10.1161/01.atv.10.4.577.

Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100.

Klin Wochenschr. 1991 May 3;69(7):320-4. doi: 10.1007/BF01644767.

Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100.与家族性载脂蛋白B100缺陷相关的人类载脂蛋白B突变的单倍型分析。

Am J Hum Genet. 1990 Oct;47(4):712-20.

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