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METHOD OF DETECTING ETHIOLOGIC FACTOR OF BRONCHIAL ASTHMA
METHOD OF DETECTING ETHIOLOGIC FACTOR OF BRONCHIAL ASTHMA
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机译:检测支气管哮喘的病因的方法
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摘要
A means of detecting an ethiologic factor of human bronchial asthma, in particular, infant bronchial asthma. This means is characterized by detecting a specific polymorphism in human Iλβassociated protein gene, for example, a polymorphism associated with at least one amino acid mutation selected from the group consisting of, in the amino acid sequence of the human Iλβ-associated protein represented by SEQ ID NO:1, mutation of Ile at the 816-position into Leu, mutation of Ile at the 830-position into Met, mutation of Cys at the 1072-position into Ser and mutation of Pro at the 1158-position into Leu, or a polymorphism associated with at least one nucleic acid mutation selected from the group consisting of, in the code region of the human Iλβassociated protein gene represented by SEQ ID NO:2, mutation of T at the 819-position into C, mutation of G at the 2295-position into A, mutation of A at the 2446-position into C, mutation of A at the 2490-position into G, mutation of T at the 3214-position into A and mutation of C at the 3473-position into T, and a haplotype having such a mutation.
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机译:一种检测人支气管哮喘,特别是婴儿支气管哮喘的ethioologic因子的方法。该手段的特征在于检测人Iλβ相关蛋白基因中的特异性多态性,例如,与选自SEQ ID NO:1的人Iλβ相关蛋白的氨基酸序列中的至少一种氨基酸突变相关的多态性。 ID NO:1,Ile在816位突变为Leu,Ile在830位突变为Met,Cys在1072位的突变为Ser,而Pro在1158位的突变为Leu,或一种与至少一种选自由SEQ ID NO:2表示的人Iλβ相关蛋白基因的编码区中的核苷酸区域中的突变相关的多态性,该突变是由819位的T突变为C,将2295位变成A,将2446位的A突变为C,将2490位的A突变为G,将3214位的T突变为A,将3473位的C突变为T和具有这种突变的单倍型。
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