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Methods for the predicting and detecting silent brain infarction ischemic stroke patients using hyperhomocysteinemia by the polymorphism of thymidylate synthase enhancer region gene

机译:通过胸苷酸合酶增强子区域基因多态性预测和检测高同型半胱氨酸血症导致的脑梗死缺血性卒中的方法

摘要

The present invention is a high homocysteine serum factor gene polymorphisms with Timmy Delay bit synthase enhancer region (TSER) asymptomatic cerebral infarction and cerebral infarction onset by a method for prediction or diagnosis. ; The invention asymptomatic cerebral infarction and cerebral infarction onset by serum containing a gene polymorphism and homocysteine Timmy Delay bit synthase enhancer region to the gene to predict or diagnose, measure the delay tree thymidine synthase enhancer region (Thymidylate synthase enhancer resion) genotype from DNA extracted from the blood specimen, and analyze the polymorphism from the measured genotype and asymptomatic cerebral infarction and hypercholesterolemia by homocysteine provides a method for the prediction or diagnosis infarction. ; The invention asymptomatic cerebral infarction and cerebral infarction onset by simply high homocysteine serum to determine the presence of an allele containing a mutation represented by the TSER 2R and was able to provide a way to predict or diagnose.
机译:本发明是一种高同型半胱氨酸血清因子基因多态性,其通过预测或诊断的方法具有蒂米延迟位合酶增强子区域(TSER)无症状的脑梗塞和脑梗塞发作。 ;本发明的无症状性脑梗塞和脑梗死是由含有基因多态性的基因和高半胱氨酸蒂米延迟位合酶增强子区域的基因来预测或诊断,测量延迟树胸苷合酶增强子区域(胸苷酸合酶增强子)基因型的。血样,并根据测得的基因型和无症状性脑梗死和高半胱氨酸血症引起的高胆固醇血症分析其多态性,为预测或诊断梗塞提供了一种方法。 ;本发明无症状性脑梗塞和仅通过高半胱氨酸血清高发来确定包含由TSER 2R代表的突变的等位基因的存在,并且能够提供一种预测或诊断的方法。

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