首页> 外国专利> METHODS FOR DIAGNOSING INDIVIDUALS WITH AN INCREASED RISK TO DEVELOP A DEFICIENCY BASED ON MDR1 GENE POLYMORPHISM

METHODS FOR DIAGNOSING INDIVIDUALS WITH AN INCREASED RISK TO DEVELOP A DEFICIENCY BASED ON MDR1 GENE POLYMORPHISM

机译:基于MDR1基因多态性的个体诊断风险增加的方法

摘要

The present invention relates to in vitro methods of diagnosing an increasedrisk to develop a renal, liver or colon deficiency, a deficiency in lymphoidcells or a deficiency at the blood brain barrier. Furthermore, the presentinvention also relates to the use of a MDR-1 gene single nucleotidepolymorphism for the preparation of a diagnostic composition for diagnosing arenal, liver or colon deficiency, a deficiency in lymphoid cells or adeficiency at the blood brain barrier. Preferably, the renal, liver or colondeficiencies, the deficiency in lymphoid cells or the deficiencies at theblood brain barrier are caused by cancer.
机译:本发明涉及体外诊断增高的方法。有发展成肾,肝或结肠缺乏症,淋巴缺乏症的风险细胞或血脑屏障不足。而且,现在本发明还涉及MDR-1基因单核苷酸的用途多态性用于制备用于诊断肝癌的诊断组合物肾,肝或结肠缺乏症,淋巴样细胞缺乏症或血脑屏障缺乏症。优选地,肾,肝或结肠缺乏症,淋巴样细胞缺乏症或血脑屏障是由癌症引起的。

著录项

  • 公开/公告号CA2430269A1

    专利类型

  • 公开/公告日2002-06-06

    原文格式PDF

  • 申请/专利权人 EPIDAUROS BIOTECHNOLOGIE AG;

    申请/专利号CA20002430269

  • 发明设计人 BRINKMANN ULRICH;SIEGSMUND MICHAEL;

    申请日2000-11-29

  • 分类号C12Q1/68;A61K38/00;A61P43/00;

  • 国家 CA

  • 入库时间 2022-08-22 00:40:36

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