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Polymorphisms in the human alpha4 integrin subunit gene, suitable for diagnosis and treatment of integrin ligand mediated diseases

机译:人类alpha4整合素亚基基因中的多态性,适用于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AU5876899A

    专利类型

  • 公开/公告日2000-04-10

    原文格式PDF

  • 申请/专利权人 ZENECA LIMITED;

    申请/专利号AU19990058768

  • 发明设计人 JOHN EDWARD NORRIS MORTEN;

    申请日1999-09-15

  • 分类号C12Q1/68;G06F17/30;

  • 国家 AU

  • 入库时间 2022-08-22 01:51:30

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