Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yoshihisa Sakagami"'
Autor:
Takahiro Mukai, Masato Kinboshi, Yuki Nagao, Saki Shimizu, Asuka Ono, Yoshihisa Sakagami, Aoi Okuda, Megumi Fujimoto, Hidefumi Ito, Akio Ikeda, Yukihiro Ohno
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Inwardly rectifying potassium (Kir) channel subunits Kir4.1 are specifically expressed in astrocytes and regulate neuronal excitability by mediating spatial potassium buffering. In addition, it is now known that astrocytic Kir4.1 channels are closely
Externí odkaz:
https://doaj.org/article/f2c96035e14f441ea50318f5d64d545c
Autor:
Masato Kinboshi, Asuka Ono, Yukihiro Ohno, Hidefumi Ito, Megumi Fujimoto, Yuki Nagao, Takahiro Mukai, Yoshihisa Sakagami, Aoi Okuda, Saki Shimizu, Akio Ikeda
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Frontiers in Pharmacology
Frontiers in Pharmacology
Inwardly rectifying potassium (Kir) channel subunits Kir4.1 are specifically expressed in astrocytes and regulate neuronal excitability by mediating spatial potassium buffering. In addition, it is now known that astrocytic Kir4.1 channels are closely
Autor:
Kentaro Tokudome, Madoka Hara, Yoshihisa Sakagami, Asuka Ono, Tetsuya Hayashi, Yuki Nagao, Satoshi Nishioka, Takahiro Mukai, Sho Watanabe, Yukihiro Ohno, Ryuji Kato, Yasuo Matsumura, Saki Shimizu, Yoko Ueda
Publikováno v:
Neuroscience Research. 77:202-207
Sleep apnea (SA) causes not only sleep disturbances, but also neurocognitive impairments and/or psychoemotional disorders. Here, we studied the effects of intermittent hypoxia (IH) on forebrain Fos expression using obese diabetic db/db mice to explor
Autor:
Yoshihisa Sakagami, Megumi Fujimoto, Takahiro Mukai, Yuya Harada, Yukihiro Ohno, Yuki Nagao, Asuka Ono, Aoi Okuda, Saki Shimizu
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 7 (2013)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
The inwardly rectifying potassium (Kir) channel Kir4.1 in brain astrocytes mediates spatial K(+) buffering and regulates neural activities. Recent studies have shown that loss-of-function mutations in the human gene KCNJ10 encoding Kir4.1 cause epile
Autor:
Yuki Nagao, Yuya Harada, Takahiro Mukai, Saki Shimizu, Aoi Okuda, Megumi Fujimoto, Asuka Ono, Yoshihisa Sakagami, Yukihiro Ohno
Publikováno v:
Frontiers in Cellular Neuroscience; Jul2013, Vol. 7, p1-10, 10p