Hirotomo Shioi

Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo

D. Taura, M. Sone, S. Miyamoto, 2015, Journal of the American Heart Association.

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

M. Tominaga, H. Okuda, A. Koizumi, 2016, PloS one.