首页> 外国专利> DISEASE DIAGNOSIS USING GENETIC MUTATION IN PROMOTER REGION OF -GLUTAMYLCYSTEINE SYNTHETASE LIGHT CHAIN GENE

DISEASE DIAGNOSIS USING GENETIC MUTATION IN PROMOTER REGION OF -GLUTAMYLCYSTEINE SYNTHETASE LIGHT CHAIN GENE

机译:遗传突变在-谷氨酰半胱氨酸合成酶轻链基因启动子区域的疾病诊断

摘要

PROBLEM TO BE SOLVED: To provide a -glutamylcysteine light chain promoter DNA mutant having a mutation at the genetic polymorphism site of the -glutamylcysteine light chain promoter DNA, and to provide a method for evaluating the morbid risk of a coronary artery disease on the basis of the genetic polymorphism.;SOLUTION: This method comprises determining both or one of bases at the -588C/T genetic polymorphism site and the -23G/T genetic polymorphism site in the -glutamylcysteine synthetase light chain promoter gene sequence of a test specimen and then evaluating the morbid risk of the coronary artery disease of the test specimen. And, a DNA is a DNA partial sequence comprising a specific continuous sequence containing both or one of the No.1340 t and the No.1905 t.;COPYRIGHT: (C)2003,JPO
机译:解决的问题:提供在-谷氨酰半胱氨酸轻链启动子DNA的遗传多态性位点处具有突变的-谷氨酰半胱氨酸轻链启动子DNA突变体,并提供基于该方法评估冠状动脉疾病的病态风险的方法。解决方案:该方法包括确定测试样品的-谷氨酰半胱氨酸合成酶轻链启动子基因序列中-588C / T遗传多态性位点和-23G / T遗传多态性位点中的一个或两个碱基,以及然后评估测试样本的冠状动脉疾病的发病风险。并且,DNA是包含特定的连续序列的DNA部分序列,该特定的连续序列包含No.1340t和No.1905t两者或之一。COPYRIGHT:(C)2003,JPO

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