- 2022 - 2025 非症候性原発性萌出不全における遺伝的要因の探索と新規治療法の確立
- 2020 - 2023 原因遺伝子同定とそれに基づくプレシジョン・デンティストリーの構築を目指す基盤研究
- 2019 - 2022 Suggestion for an approach to metabolic bone disease by applying the culture system for inducing differentiation into osteocyte
- 2017 - 2020 Identification of the unknown mechanism of the congenital maxillofacial abnormalities using advanced genome sequence and analysis
- 2016 - 2019 The role of Shh gradient for secondary palate development
- 2015 - 2019 Elucidation of the pathogenesis of cleft palate and tooth devevelopment problmes using new molecular technology.
- 2015 - 2017 Research for developmental mechanism of congenital craniofacial anomalies with Runx/Cbfb signaling
- 2014 - 2016 In vivo live-imaging of the growing root tip to understand the molecular and cellular mechanism of the root development
- 2013 - 2015 Research for molecular diagnosis and treatment of cleft palate with Runx signaling
- 2012 - 2015 Novel functions of Runx genes as causal genes for ectodermal dysplasia
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