发明名称 多発性嚢胞腎の検査方法および治療剤のスクリーニング方法
摘要 The present invention provides a method of examining polycystic kidney disease or a complication of polycystic kidney disease using a gene(s) selected from the group consisting of NTNG1, POSTN, TNC, KAL1, BST1, ACAT2, INSIG1, SCD, HSD3B1, KRT7, USP40, SULT1E1, BMP6, CD274, CTGF, E2F7, EDN1, FAM43A, FRMD3, MMP10, MYEOV, NR2F1, NRCAM, PDCK1, PLXNA2, SLC30A3, SNAI1, SPOCD1, MMP1, TFPI2, HMGA2, KRTAP4-7, KRTAP4-8, KRTAP4-9, MYPN, RPPH1, and SIAE, and a method of screening for a therapeutic agent or a preventive agent therefore, and further vascular endothelial cells or vascular mural cells obtained via differentiation induction from iPS cells formed from a somatic cell of a subject suffered from polycystic kidney disease and having cerebral aneurysm as a complication.
申请公布号 JP6021021(B2) 申请公布日期 2016.11.02
申请号 JP20130537286 申请日期 2011.11.07
申请人 国立大学法人京都大学 发明人 長船 健二;豊田 太郎;塩田 文彦;中尾 一和;曽根 正勝;田浦 大輔
分类号 C12Q1/68;G01N33/15;G01N33/50;G01N33/68 主分类号 C12Q1/68
代理机构 代理人
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