Rchr
J-GLOBAL ID：201801014127978335
Update date: Nov. 26, 2025
Hayashi Shinichiro
Hayashi Shinichiro
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Research field (1)：
Developmental biology
Research theme for competitive and other funds (5)：
2025 - 2028 世界最大級筋レポジトリを活用した先進的オミクス解析による自己免疫性筋炎の病態解明
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 (47)：
Seung-Ah Lee, Megumu Ogawa, Yoshihiko Saito, Rui Shimazaki, Tomonari Awaya, Motoyasu Hosokawa, Ryo Kurosawa, Hiroaki Ohara, Akihide Takeuchi, Shinichiro Hayashi, et al. Substitutions of nucleotides at the 3' ends of COL6A1/2/3 exons induce exon skipping associated with collagen VI-related muscular dystrophies and therapeutic strategies. Genetics in Medicine. 2025. 101431-101431
Yukako Nishimori, Jantima Tanboon, Munenori Oyama, Haruhiko Motegi, Yui Tomo, Mari Oba, Ai Yamanaka, Kazuma Sugie, Shigeaki Suzuki, Shinichiro Hayashi, et al. Anti-mitochondrial M2 antibody-positive myositis may be an independent subtype of autoimmune myositis. Journal of neurology. 2025. 272. 3. 206-206
Shunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, Jantima Tanboon, Francia Victoria De Los Reyes, Kyuto Sonehara, Yu-ichi Goto, Yukinori Okada, Shinichiro Hayashi, Ichizo Nishino. Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosis. Nature Communications. 2025. 16. 1
Rui Shimazaki, Yoshihiko Saito, Tomonari Awaya, Narihiro Minami, Ryo Kurosawa, Motoyasu Hosokawa, Hiroaki Ohara, Shinichiro Hayashi, Akihide Takeuchi, Masatoshi Hagiwara, et al. Profiling of pathogenic variants in Japanese patients with sarcoglycanopathy. Orphanet Journal of Rare Diseases. 2025. 20. 1
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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MISC (12)：
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
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
北澤萌恵, 林晋一郎, 今村道博, 武田伸一, 大石由美子, 金児(石野)知子, 石野史敏. マウスにおけるPeg11/Rtl1の欠損と過剰発現はTemple症候群とKagami-Ogata症候群に関連した異なる筋肉異常を引き起こす. 日本分子生物学会年会プログラム・要旨集(Web). 2020. 43rd
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
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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