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Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.

作者信息

Friedlander Y, Dann E J, Leitersdorf E

出版信息

Hum Genet. 1993 Apr;91(3):299-300. doi: 10.1007/BF00218280.

DOI:10.1007/BF00218280
PMID:8478017
Abstract
摘要

相似文献

1
Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.
Hum Genet. 1993 Apr;91(3):299-300. doi: 10.1007/BF00218280.
2
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100.家族性高胆固醇血症和家族性载脂蛋白B-100缺陷的双杂合子的表型表达。
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3
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.
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Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.
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Absence of familial defective apolipoprotein B-100 in Japanese patients with familial hypercholesterolaemia.日本家族性高胆固醇血症患者中不存在家族性缺陷载脂蛋白B-100
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Angiotensin-converting enzyme DD genotype and cardiovascular disease in heterozygous familial hypercholesterolemia.血管紧张素转换酶DD基因型与杂合子家族性高胆固醇血症中的心血管疾病
Circulation. 1998 May 12;97(18):1780-3. doi: 10.1161/01.cir.97.18.1780.
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Hypercholesterolaemia due to familial defective apolipoprotein B-100 in two Australian families.两个澳大利亚家庭中因家族性载脂蛋白B-100缺陷导致的高胆固醇血症。
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[Absence of DNA polymorphisms on the region of the APOV gene coding the proposed low density lipoprotein-binding domain of the ApoB-100 protein].[载脂蛋白B-100蛋白拟低密度脂蛋白结合域编码区域的APOV基因不存在DNA多态性]
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Hypocholesterolemic effects of cholestyramine and colestipol in patients with familial defective apolipoprotein B-100.消胆胺和考来替泊对家族性载脂蛋白B-100缺陷患者的降胆固醇作用。
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Intima-media thickness and atherosclerotic plaques in familial defective apolipoprotein B-100 and familial hypercholesterolemia.家族性载脂蛋白B-100缺陷症和家族性高胆固醇血症患者的内膜中层厚度与动脉粥样硬化斑块
Ann N Y Acad Sci. 2002 Jun;967:528-34. doi: 10.1111/j.1749-6632.2002.tb04312.x.

引用本文的文献

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ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature.黎巴嫩人群中载脂蛋白B-100的R3500Q突变：文献综述及患病率
Mol Biol Rep. 2007 Dec;34(4):267-70. doi: 10.1007/s11033-006-9041-7. Epub 2006 Dec 8.

本文引用的文献

1
Plasma Lp(a), apolipoprotein(a) isoforms and acute myocardial infarction in men and women: a case-control study in the Jerusalem population.血浆脂蛋白(a)、载脂蛋白(a)异构体与男性和女性急性心肌梗死：耶路撒冷人群的病例对照研究
Atherosclerosis. 1993 Jan 25;98(2):139-51. doi: 10.1016/0021-9150(93)90124-d.
2
The role of XbaI polymorphism of the apolipoprotein B gene in determining levels and covariability of lipid and lipoprotein variables in a sample of Israeli offspring with family history of myocardial infarction.
Atherosclerosis. 1993 Jan 25;98(2):165-77. doi: 10.1016/0021-9150(93)90126-f.
3
DNA sequence of the human apolipoprotein B gene.人类载脂蛋白B基因的DNA序列。
DNA. 1987 Aug;6(4):363-72. doi: 10.1089/dna.1987.6.363.
4
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.
5
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.
6
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.
7
Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.
J Lipid Res. 1990 Aug;31(8):1337-49.
8
Allele frequency estimation from data on relatives.基于亲属数据的等位基因频率估计。
Am J Hum Genet. 1991 Jan;48(1):22-5.
9
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.
10
Hypercholesterolaemia due to familial defective apolipoprotein B-100 in two Australian families.两个澳大利亚家庭中因家族性载脂蛋白B-100缺陷导致的高胆固醇血症。
Med J Aust. 1991 Oct 21;155(8):572-3. doi: 10.5694/j.1326-5377.1991.tb93902.x.