首页> 外国专利> POLYMORPHISMS IN THE HUMAN ALPHA4 INTEGRIN SUBUNIT GENE, SUITABLE FOR DIAGNOSIS AND TREATMENT OF INTEGRIN LIGAND MEDIATED DISEASES

POLYMORPHISMS IN THE HUMAN ALPHA4 INTEGRIN SUBUNIT GENE, SUITABLE FOR DIAGNOSIS AND TREATMENT OF INTEGRIN LIGAND MEDIATED DISEASES

机译:人α4整合素亚基基因的多态性,适合诊断和治疗整合素配体介导的疾病

摘要

This invention relates to polymorphisms in the human alpha 4 integrin subunit gene, in particular the invention is based on the discovery of five single nucleotide polymorphisms (SNPs) in the coding region of the human alpha 4 integrin subunit gene and eight in the promoter region. The invention also relates to methods and materials for analysing allelic variation in the alpha 4 integrin subunit gene, and to the use of alpha 4 integrin subunit polymorphism in the diagnosis and treatment of integrin ligand mediated diseases such as multiple sclerosis, rheumatoid arthritis, atherosclerosis and allergic asthma.
机译:本发明涉及人α4整联蛋白亚基基因中的多态性,特别是本发明是基于在人α4整联蛋白亚基基因的编码区中有五种单核苷酸多态性(SNP)和在启动子区域中八种的发现。本发明还涉及用于分析α4整联蛋白亚基基因的等位基因变异的方法和材料,并且涉及α4整联蛋白亚基多态性在整联蛋白配体介导的疾病例如多发性硬化,类风湿性关节炎,动脉粥样硬化和糖尿病的诊断和治疗中的用途。过敏性哮喘。

著录项

  • 公开/公告号EP1112381A1

    专利类型

  • 公开/公告日2001-07-04

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB;

    申请/专利号EP19990946354

  • 发明设计人 MORTEN JOHN EDWARD NORRIS;

    申请日1999-09-15

  • 分类号C12Q1/68;G06F17/30;

  • 国家 EP

  • 入库时间 2022-08-22 01:15:25

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