Zobrazeno 1 - 4 of 4 pro vyhledávání: '"Hirotomo Shioi"'
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Akademický článek
Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families.
Autor: Hiroko Okuda, Atsuko Noguchi, Hatasu Kobayashi, Daiki Kondo, Kouji H Harada, Shohab Youssefian, Hirotomo Shioi, Risako Kabata, Yuki Domon, Kazufumi Kubota, Yutaka Kitano, Yasunori Takayama, Toshiaki Hitomi, Kousaku Ohno, Yoshiaki Saito, Takeshi Asano, Makoto Tominaga, Tsutomu Takahashi, Akio Koizumi
Publikováno v: PLoS ONE, Vol 11, Iss 5, p e0154827 (2016)
Painful peripheral neuropathy has been correlated with various voltage-gated sodium channel mutations in sensory neurons. Recently Nav1.9, a voltage-gated sodium channel subtype, has been established as a genetic influence for certain peripheral pain
Externí odkaz: https://doaj.org/article/806648927d904f768752537abf236d38
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3
Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families
Autor: Yasunori Takayama, Toshiaki Hitomi, Akio Koizumi, Kousaku Ohno, Tsutomu Takahashi, Yoshiaki Saito, Yutaka Kitano, Takeshi Asano, Kouji H. Harada, Makoto Tominaga, Daiki Kondo, Hatasu Kobayashi, Atsuko Noguchi, Hirotomo Shioi, Hiroko Okuda, Yuki Domon, Shohab Youssefian, Kazufumi Kubota, Risako Kabata
Publikováno v: PLoS ONE, Vol 11, Iss 5, p e0154827 (2016)
PLoS ONE
Painful peripheral neuropathy has been correlated with various voltage-gated sodium channel mutations in sensory neurons. Recently Nav1.9, a voltage-gated sodium channel subtype, has been established as a genetic influence for certain peripheral pain
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eeff78837494d74a4bb44d6e561e07f
http://hdl.handle.net/10295/00006325
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4
Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo
Autor: Toshiaki Hitomi, Daisuke Taura, Masakatsu Sone, Kouji H. Harada, Hirohiko Imai, Hatasu Kobayashi, Akio Koizumi, Toshiyuki Habu, Hiroko Okuda, Susumu Miyamoto, Hirotomo Shioi, Yasushi Takagi, Tetsuya Matsuda, Yoshiko Matsuda
Publikováno v: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background P.R4810K of RNF 213 (mysterin: rs112735431), which is an AAA + ATP ase, is the susceptibility polymorphism for moyamoya disease ( MMD ) in East Asians. However, the role of RNF 213 R4810K in the etiology of MMD is unknown. Methods and Resu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e65ed052e1bbcaa098e1ec31547d87cb
https://doi.org/10.1161/jaha.115.002146
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