发明名称 染色体優性多発性嚢胞腎の判定方法及び予防・治療薬のスクリーニング方法
摘要 <p><P>PROBLEM TO BE SOLVED: To provide a determination method of autosomal dominant polycystic kidney disease using an autosomal dominant polycystic kidney marker substance, and to provide a method for screening a drug that can be used for drastic therapy and prevention. <P>SOLUTION: Autosomal dominant polycystic kidney disease is determined by detecting or quantitatively determining a marker substance of autosomal dominant polycystic kidney disease (5-methyl-2-deoxycytidine, glucosamine, ectoine, 2-deoxycytidine, allantoate, o-hydroxybenzoic acid, phenaceturic acid, 3-phenylpropionic acid, decanoic acid, hydroxydecanoic acid, and the like), and comparing the obtained results with detection results or quantitative determination results of the marker substance of autosomal dominant polycystic kidney disease in a normal control blood sample. <P>COPYRIGHT: (C)2012,JPO&INPIT</p>
申请公布号 JP5717128(B2) 申请公布日期 2015.05.13
申请号 JP20100261665 申请日期 2010.11.24
申请人 发明人
分类号 G01N33/53;G01N33/15;G01N33/50 主分类号 G01N33/53
代理机构 代理人
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