- 2023 - 2027 先天性腎尿路生殖器症候群の発症メカニズム解明に向けた基礎的・臨床的アプローチ
- 2021 - 2024 腎尿細管エンドサイトーシスを制御する転写調節システムの解明
- 2021 - 2024 Genetic analysis and elucidation of pathology of focal segmental glomerulosclerosis based on a clinicopathological database
- 2020 - 2023 小児膜性腎症の原因抗原の探索
- 2020 - 2023 腎臓発生におけるCBWD1の分子機構の解明
- 2018 - 2021 Elucidation of molecular mechanism of proteinuria mediated by Cubilin
- 2017 - 2020 Intracellular role of CBWD1, a novel causative gene of congenital anomalies of the kidney and urinary tract
- 2017 - 2020 Clinicopathologic approach to pediatric membranous nephropathy associated with congenital anomaly of kidney and urinary tract and the antigenic target
- 2016 - 2019 Analysis on molecular mechanism of mesangial proliferative glomerulonephritis
- 2016 - 2018 Proteomic analysis of urinary exosome of pediatric kidney diseases
- 2015 - 2017 Identification of a novel gene for congenital anomalies of the kidney and urinary tract - the role of CBWD1 in the kidney development-
- 2013 - 2015 Identify a new gene which is important for the kidney development - Toward the achievement of regenerative medicine of kidney -
- 2012 - 2014 ネフロン前駆細胞自己複製法の開発
- 2010 - 2011 蛋白尿発症におけるTRPC6の役割
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