Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Shio Mitsuzawa"'
Autor:
Temma Soga, Naoki Suzuki, Kengo Kato, Ai Kawamoto-Hirano, Yuko Kawauchi, Rumiko Izumi, Masaya Toyoshima, Shio Mitsuzawa, Tomomi Shijo, Kensuke Ikeda, Hitoshi Warita, Yukio Katori, Masashi Aoki, Masaaki Kato
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects motor neurons selectively. In particular, weakness in respiratory and swallowing muscles occasionally causes aspiration pneumonia and chok
Externí odkaz:
https://doaj.org/article/4c463839e80b4dfd84ba536642627e43
Autor:
Tetsuya Akiyama, Naoki Suzuki, Mitsuru Ishikawa, Koki Fujimori, Takefumi Sone, Jiro Kawada, Ryo Funayama, Fumiyoshi Fujishima, Shio Mitsuzawa, Kensuke Ikeda, Hiroya Ono, Tomomi Shijo, Shion Osana, Matsuyuki Shirota, Tadashi Nakagawa, Yasuo Kitajima, Ayumi Nishiyama, Rumiko Izumi, Satoru Morimoto, Yohei Okada, Takayuki Kamei, Mayumi Nishida, Masahiro Nogami, Shohei Kaneda, Yoshiho Ikeuchi, Hiroaki Mitsuhashi, Keiko Nakayama, Teruo Fujii, Hitoshi Warita, Hideyuki Okano, Masashi Aoki
Publikováno v:
EBioMedicine, Vol 45, Iss , Pp 362-378 (2019)
Background: The characteristic structure of motor neurons (MNs), particularly of the long axons, becomes damaged in the early stages of amyotrophic lateral sclerosis (ALS). However, the molecular pathophysiology of axonal degeneration remains to be f
Externí odkaz:
https://doaj.org/article/09b1c2d9afee403f938bc1b807d2caa6
Autor:
Nicolas Leventoux, Satoru Morimoto, Kenju Hara, Shiho Nakamura, Fumiko Ozawa, Shio Mitsuzawa, Tetsuya Akiyama, Ayumi Nishiyama, Naoki Suzuki, Hitoshi Warita, Masashi Aoki, Hideyuki Okano
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101896- (2020)
Amyotrophic Lateral Sclerosis is the most common motor neuron degenerative disease in adults, and TARDBP gene mutations have been reported to be involved in the pathogenesis. We present here how we generated the human induced pluripotent stem cell (h
Externí odkaz:
https://doaj.org/article/0fef719d79ce4b98ac14b36800e2a90c
Autor:
Tomomi Shijo, Ryoukichi Ikeda, Naoki Suzuki, Jun Ohta, Jun Suzuki, Ai Hirano-Kawamoto, Kengo Kato, Kensuke Ikeda, Rumiko Izumi, Shio Mitsuzawa, Hitoshi Warita, Masaaki Kato, Masashi Aoki, Yukio Katori
Publikováno v:
The Tohoku Journal of Experimental Medicine. 259:293-300
Autor:
Tomomi Shijo, Naoki Suzuki, Hitoshi Warita, Yuko Kawauchi, Shio Mitsuzawa, Kensuke Ikeda, Rumiko Izumi, Risako Ono, Akiyuki Ohno, Masaya Toyoshima, Ryuhei Harada, Hiroshi Kuroda, Masaaki Kato, Masashi Aoki
Publikováno v:
Neurology and Clinical Neuroscience. 10:239-244
Autor:
Masaya Toyoshima, Naoki Suzuki, Shio Mitsuzawa, Temma Soga, Rumiko Izumi, Kazuhiro Mitsui, Shigehito Miyagi, Masashi Aoki, Masaaki Kato
Publikováno v:
Internal Medicine.
Autor:
Masaya Toyoshima, Naoki Suzuki, Shio Mitsuzawa, Temma Soga, Rumiko Izumi, Kazuhiro Mitsui, Shigehito Miyagi, Masashi Aoki, Masaaki Kato
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 2, p305-307, 3p
Autor:
Shio Mitsuzawa, Risako Ono, Mitsuru Ishikawa, Hiroya Ono, Rumiko Izumi, Masashi Aoki, Kensuke Ikeda, Ryo Funayama, Takefumi Sone, Matsuyuki Shirota, Shohei Kaneda, Hiroaki Mitsuhashi, Jiro Kawada, Akiyuki Ohno, Teruo Fujii, Hideyuki Okano, Satoru Morimoto, Ayumi Nishiyama, Keiko Nakayama, Shion Osana, Naoko Nakamura, Tomomi Shijo, Tetsuya Akiyama, Hitoshi Warita, Yoshiho Ikeuchi, Naoki Suzuki, Tadashi Nakagawa
Publikováno v:
Stem Cell Reports
Summary Amyotrophic lateral sclerosis (ALS) is an adult-onset incurable motor neuron (MN) disease. The reasons for selective MN vulnerability in ALS are unknown. Axonal pathology is among the earliest signs of ALS. We searched for novel modulatory ge
Autor:
Temma Soga, Naoki Suzuki, Kengo Kato, Ai Kawamoto-Hirano, Yuko Kawauchi, Rumiko Izumi, Masaya Toyoshima, Shio Mitsuzawa, Tomomi Shijo, Kensuke Ikeda, Hitoshi Warita, Yukio Katori, Masashi Aoki, Masaaki Kato
Publikováno v:
BMC neurology. 22(1)
Background Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects motor neurons selectively. In particular, weakness in respiratory and swallowing muscles occasionally causes aspiration pneumonia and choking, whic
Autor:
Fumiyoshi Fujishima, Jiro Kawada, Mitsuru Ishikawa, Hiroaki Mitsuhashi, Hideyuki Okano, Keiko Nakayama, Kensuke Ikeda, Mayumi Nishida, Shio Mitsuzawa, Rumiko Izumi, Matsuyuki Shirota, Ryo Funayama, Tomomi Shijo, Tetsuya Akiyama, Yasuo Kitajima, Shohei Kaneda, Masahiro Nogami, Hiroya Ono, Shion Osana, Yohei Okada, Naoki Suzuki, Takefumi Sone, Takayuki Kamei, Teruo Fujii, Satoru Morimoto, Ayumi Nishiyama, Masashi Aoki, Hitoshi Warita, Tadashi Nakagawa, Koki Fujimori, Yoshiho Ikeuchi
Publikováno v:
EBioMedicine
Background The characteristic structure of motor neurons (MNs), particularly of the long axons, becomes damaged in the early stages of amyotrophic lateral sclerosis (ALS). However, the molecular pathophysiology of axonal degeneration remains to be fu