Rchr
J-GLOBAL ID：201801014127978335
Update date: Jan. 31, 2024
Hayashi Shinichiro
Hayashi Shinichiro
Affiliation and department：
Research field (1)：
Developmental biology
Research theme for competitive and other funds (4)：
- 2021 - 2024 筋衛星細胞における機能維持メカニズムのグローバル解析
- 2018 - 2021 Analysis of molecular mechanisms regulating stemness in muscle stem cells
- 2016 - 2018 Identification of the novel mechanism of satellite cell number reduction in sarcopenia
- 2014 - 2016 Identification of a novel regulatory mechanism in satellite cell homeostasis
Papers (43)：
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Nobuyuki Eura, Satoru Noguchi, Masashi Ogasawara, Theerawat Kumutpongpanich, Shinichiro Hayashi, Ichizo Nishino, Takahiko Mukaino, Mori-Yoshimura Madoka, Makiko Nagai, Masayuki Ochi, et al. Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy. Journal of Neurology. 2023. 270. 12. 5988-5998
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Jantima Tanboon, Michio Inoue, Shinya Hirakawa, Hisateru Tachimori, Shinichiro Hayashi, Satoru Noguchi, Naoko Okiyama, Manabu Fujimoto, Shigeaki Suzuki, Ichizo Nishino. Muscle pathology of antisynthetase syndrome according to antibody subtypes. Brain Pathology. 2023. 33. 4. e13155
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Wakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, Kazuki Yamamoto, Yasushi Oya, Madoka Mori-Yoshimura, Takashi Kurashige, Mariko Okubo, Megumu Ogawa, Fumihiko Matsuda, et al. Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy. Scientific Reports. 2022. 12. 1
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Michio Inoue, Satoru Noguchi, Yukiko U. Inoue, Aritoshi Iida, Megumu Ogawa, Rocio Bengoechea, Sara K. Pittman, Shinichiro Hayashi, Kazuki Watanabe, Yasushi Hosoi, et al. Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4. Acta Neuropathologica. 2022
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Masashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, Theerawat Kumutpongpanich, Narihiro Minami, Ikuya Nonaka, Shinichiro Hayashi, Satoru Noguchi, Ichizo Nishino. Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy. Acta neuropathologica communications. 2022. 10. 1. 176-176
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MISC (9)：
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小笠原真志, 小笠原真志, 飯田有俊, THEERAWAT Kumutpongpanich, 尾崎文美, 林晋一郎, 林晋一郎, 野口悟, 野口悟, 西野一三, et al. 遺伝学的診断が確定した眼咽頭遠位型ミオパチーの臨床病理学的特徴. 日本神経学会学術大会プログラム・抄録集. 2021. 62nd
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江浦信之, 小笠原真志, 林晋一郎, 野口悟, 西野一三. 核内封入体によって眼咽頭型筋ジストロフィーと眼咽頭遠位型ミオパチーは鑑別しうる. 日本筋学会学術集会プログラム・抄録集. 2021. 7th
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INDRAWATI Luh Ari, MITSUHASHI Hiroaki, IIDA Aritoshi, MORI-YOSHIMURA Madoka, HAYASHI Shinichiro, NOGUCHI Satoru, NISHINO Ichizo. Recessive variant of POPDC3 causes a nuclear envelopathy. 日本筋学会学術集会プログラム・抄録集. 2020. 6th
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林 晋一郎, 真鍋 一郎, 西野 一三, 大石 由美子. 代謝による炎症・再生コンティニアムの制御と破綻 骨格筋の再生・発生過程における筋細胞の分化制御メカニズム. 日本生化学会大会プログラム・講演要旨集. 2019. 92回. [1S02a-05]
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劉琳, 劉琳, 小池博之, 林晋一郎, 大石由美子, 淺原弘嗣. Zinc-finger transcription factor KLF5 is involved in the pathogenesis of muscle atrophy. 日本筋学会学術集会プログラム・抄録集. 2019. 5th
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