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GENETIC POLYMORPHISM ASSOCIATED WITH CORONARY HEART DISEASE, METHOD OF DETECTION AND USE THEREOF

机译:与冠心病相关的遗传多态性,检测方法及其用途

摘要

PROBLEM TO BE SOLVED: To provide genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof.SOLUTION: The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular stenosis and MI and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection. The present invention relates to the identification of new SNPs, unique combinations of such SNPs, and haplotypes of SNPs that are associated with CHD, and in particular stenosis and MI.
机译:解决的问题:提供与冠心病有关的遗传多态性,其检测方法和用途。解决方案:本发明基于与冠心病特别是狭窄和MI以及反应有关的遗传多态性的发现去药物治疗。特别地,本发明涉及包含多态性的核酸分子,由该核酸分子编码的变异蛋白,用于检测多态性核酸分子和蛋白质的试剂,使用该核酸和蛋白质的方法以及使用该核酸的方法。用于检测的试剂。本发明涉及新的SNP的鉴定,这种SNP的独特组合以及与CHD,特别是狭窄和MI相关的SNP的单倍型。

著录项

  • 公开/公告号JP2013078314A

    专利类型

  • 公开/公告日2013-05-02

    原文格式PDF

  • 申请/专利权人 CELERA CORP;

    申请/专利号JP20120238755

  • 申请日2012-10-30

  • 分类号C12N15/09;C12Q1/04;C12Q1/68;C07K14/47;C07K16/18;C12N15/02;G01N33/68;C12P21/08;

  • 国家 JP

  • 入库时间 2022-08-21 16:58:22

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