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Methods for diagnosing individuals with an increased risk to develop a deficiency based on mdr1 gene polymorphism

机译:基于mdr1基因多态性诊断罹患缺陷风险增加的个体的方法

摘要

The present invention relates to in vitro methods of diagnosing an increased risk to develop a renal, liver or colon deficiency, a deficiency in lymphoid cells or a deficiency at the blood brain barrier. Furthermore, the present invention also relates to the use of a MDR-1 gene single nucleotide polymorphism for the preparation of a diagnostic composition for diagnosing a renal, liver or colon deficiency, a deficiency in lymphoid cells or a deficiency at the blood brain barrier. Preferably, the renal, liver or colon deficiencies, the deficiency in lymphoid cells or the deficiencies at the blood brain barrier are caused by cancer.
机译:本发明涉及诊断肾,肝或结肠缺乏,淋巴样细胞缺乏或血脑屏障缺乏的风险增加的体外方法。此外,本发明还涉及MDR-1基因单核苷酸多态性在制备用于诊断肾,肝或结肠缺乏症,淋巴样细胞缺乏症或血脑屏障缺乏症的诊断组合物中的用途。优选地,肾,肝或结肠的缺陷,淋巴样细胞的缺陷或血脑屏障的缺陷是由癌症引起的。

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