首页> 外国专利> METHOD FOR DIAGNOSING AFFECTION RISK OF PROSTATIC DISEASE USING NEW GENE POLYMORPHISM

METHOD FOR DIAGNOSING AFFECTION RISK OF PROSTATIC DISEASE USING NEW GENE POLYMORPHISM

机译:新基因多态性诊断前列腺疾病患病风险的方法

摘要

PROBLEM TO BE SOLVED: To obtain gene polymorphism useful for diagnosing a prostatic disease such as prostate cancer, prostatomegaly, etc., or its affection risk and to provide a diagnostic method and a diagnostic kit using the same.;SOLUTION: The single nucleotide polymorphism of HPC2/ELAC2 has a specific human-derived base sequence. The polynucleotide is useful for identifying the single nucleotide polymorphism of the HPC2/ELAC2. The method for diagnosing the prostatic disease or its affection risk comprises identifying the single nucleotide polymorphism of HPC2/ELAC2. The kit for diagnosing the prostatic disease or its affection risk contains a reagent for identifying the single nucleotide polymorphism of the HPC2/ELAC2. The gene polymorphism of codon 627 is not found in Caucasian species and has high possibility of gene polymorphism characteristic of the yellow-skinned races, especially of Japanese. Consequently the prostatic disease or its affection risk of the yellow-skinned races, especially Japanese, which is not diagnosed by a method using known codon 541, is diagnosed using the codon 627.;COPYRIGHT: (C)2004,JPO
机译:解决的问题:获得可用于诊断前列腺疾病(例如前列腺癌,前列腺肥大等)或其患病风险的基因多态性,并提供使用它们的诊断方法和诊断试剂盒;解决方案:单核苷酸多态性HPC2 / ELAC2的片段具有特定的人源碱基序列。该多核苷酸可用于鉴定HPC2 / ELAC2的单核苷酸多态性。诊断前列腺疾病或其患病风险的方法包括鉴定HPC2 / ELAC2的单核苷酸多态性。诊断前列腺疾病或其患病风险的试剂盒包含用于鉴定HPC2 / ELAC2单核苷酸多态性的试剂。在高加索物种中未发现密码子627的基因多态性,并且具有黄皮人种特别是日本人的基因多态性特征的可能性很高。因此,使用密码子627诊断未通过已知541密码子方法诊断出的黄皮肤人种(尤其是日本人)的前列腺疾病或其患病风险。; COPYRIGHT:(C)2004,JPO

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