首页> 外国专利> GENETIC DIAGNOSIS OF HYPERTENSION OR HYPOTENSION UTILIZING POLYMORPHISM IN MATRIX METALLOPROTEINASE 9 GENE AND NUCLEIC ACID MOLECULE USED THEREFOR

GENETIC DIAGNOSIS OF HYPERTENSION OR HYPOTENSION UTILIZING POLYMORPHISM IN MATRIX METALLOPROTEINASE 9 GENE AND NUCLEIC ACID MOLECULE USED THEREFOR

机译:利用基质金属蛋白酶9基因中的多态性对高血压或低血压的遗传诊断

摘要

PROBLEM TO BE SOLVED: To provide a method for genetic diagnosis of hypertension or hypotension in females.;SOLUTION: A codon encoding alanine in Ala20Val polymorphism in a matrix metalloproteinase 9 gene is used as a risk factor for the hypertension in the females. Furthermore, a T allele in C(-1562) T polymorphism and a codon encoding glutamine in Arg668Gln polymorphism are used as the risk factor for the hypotension in the females.;COPYRIGHT: (C)2005,JPO&NCIPI
机译:解决的问题:提供一种遗传诊断女性高血压或低血压的方法。;解决方案:基质金属蛋白酶9基因Ala20Val多态性编码丙氨酸的密码子被用作女性高血压的危险因素。此外,C(-1562)T多态性的T等位基因和Arg668Gln多态性的编码谷氨酰胺的密码子被用作女性低血压的危险因素。;版权:(C)2005,JPO&NCIPI

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