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MUTATIONS AND POLYMORPHISMS OF FMS-RELATED TYROSINE KINASE 1

机译:FMS相关酪氨酸激酶1的突变和多态性

摘要

This invention relates generally to the analytical testing of tissue samples in vitro, and more particularly to aspects of genetic polymorphisms and mutations of the FLTl gene. The invention provides new FLTl mutations and SNPs, useful in the diagnosis and treatment of subjects in need thereof. Accordingly, the various aspects of the present invention relate to polynucleotides encoding the FLTl mutations of the invention, expression vectors encoding the FLTl mutant polypeptides of the invention and organisms that express the FLTl mutant and polymorphic polynucleotides and/or FLTl mutant/polymorphic polypeptides of the invention. The various aspects of the present invention further relate to.diagnostic/theranostic methods and kits that use the FLTl mutations and polymorphisms of the invention to identify individuals predisposed to disease or to classify individuals with regard to drug responsiveness, side effects, or optimal drug dose.
机译:本发明总体上涉及体外组织样品的分析测试,并且更具体地涉及FLT1基因的遗传多态性和突变的方面。本发明提供了新的FLT1突变和SNP,可用于诊断和治疗需要其的受试者。因此,本发明的各个方面涉及编码本发明的FLT1突变的多核苷酸,编码本发明的FLT1突变体多肽的表达载体和表达所述FLT1突变体的多态性多核苷酸和/或FLT1突变体/多态性多肽的生物。发明。本发明的各个方面还涉及使用本发明的FLT1突变和多态性的诊断/热诊断方法和试剂盒,以鉴定易患疾病的个体或就药物反应性,副作用或最佳药物剂量对个体进行分类。 。

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