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Use of gene alterations in the human gene chk1 which, for the check point kinase 1 codes

机译:基因改变在人类基因chk1中的应用,该基因用于检查点激酶1

摘要

The present invention relates to the use of gene alterations in the human gene chk1 (chek1) which, for the check point kinase 1, for predicting the course of cancer diseases and for predicting the response to pharmacological or not - pharmacological therapeutic measures for the treatment of cancerous diseases and for predicting undesirable side effects. Furthermore, the invention relates to the provision of individual gene variants, with the aid of which further for the above-mentioned purposes, gene alterations which can be used, can be detected, and can be validated. Such gene alterations can reside in that, in the promoter of chk1 at position - 1143 a degree of substitution vn guanine to thymine is present, at position - 1400 cytosine to thymine, at position - 1453 to a substitution of thymine, cytosine is present or at position - 1454 an insertion of a cytosine is present. The gene alterations can be individually or collectively in arbitrary combinations by means of the person skilled in the art is familiar to the method can be detected.
机译:本发明涉及在人类基因chk1(chek1)中的基因改变在检查点激酶1中的用途,其用于预测癌症疾病的进程以及用于预测对药理学或非药理学的反应-用于治疗的药理学治疗措施癌性疾病并预测不良副作用。此外,本发明涉及单个基因变体的提供,借助所述基因变体进一步用于上述目的,可以使用,可以检测并可以验证基因改变。这样的基因改变可以在于,在位置1143处chk1的启动子中,存在鸟嘌呤对鸟嘌呤的vn鸟嘌呤取代度,在位置1453处被胸腺嘧啶的胞嘧啶,在位置1453处对胸腺嘧啶的取代存在胞嘧啶或在位置-1454,存在胞嘧啶的插入。可以通过本领域技术人员熟悉的方法可以单独地或共同地以任意组合的方式进行基因改变。

著录项

  • 公开/公告号DE102006054292A1

    专利类型

  • 公开/公告日2009-01-08

    原文格式PDF

  • 申请/专利权人

    申请/专利号DE20061054292

  • 发明设计人

    申请日2006-11-17

  • 分类号C12Q1/68;

  • 国家 DE

  • 入库时间 2022-08-21 19:09:52

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