Hayashi Shinichiro 林晋一郎

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Shinichiro Hayashi 林晋一郎

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Researcher Number	10732381
Other IDs
Affiliation (Current)	2025: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所疾病研究第一部, 室長
Affiliation (based on the past Project Information) *help	2017 – 2023: 国立研究開発法人国立精神・神経医療研究センター, 神経研究所疾病研究第一部, 室長 2014 – 2016: 東京医科歯科大学, 難治疾患研究所, 助教
Review Section/Research Field	Principal Investigator Basic Section 49030:Experimental pathology-related / Applied health science
Keywords	Principal Investigator 筋衛星細胞 / 骨格筋 / 筋分化 / 筋幹細胞 / 骨格筋幹細胞 / single核RNA-seq / Pax7 / 幹細胞 / 未分化 / 分化 … More / 筋ジストロフィー / 細胞周期 / Klf5 / 細胞老化 / サルコペニア / 転写制御 / 転写因子 Less

Global analysis of functional maintenance mechanisms in muscle satellite cells.Principal Investigator
- Principal Investigator
  
  Hayashi Shinichiro
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 49030:Experimental pathology-related
- Research Institution
  National Center of Neurology and Psychiatry
Analysis of molecular mechanisms regulating stemness in muscle stem cellsPrincipal Investigator
- Principal Investigator
  
  Hayashi Shinichiro
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 49030:Experimental pathology-related
- Research Institution
  National Center of Neurology and Psychiatry
Identification of the novel mechanism of satellite cell number reduction in sarcopeniaPrincipal Investigator
- Principal Investigator
  
  Hayashi Shinichiro
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Applied health science
- Research Institution
  National Center of Neurology and Psychiatry
  Tokyo Medical and Dental University
Identification of a novel regulatory mechanism in satellite cell homeostasisPrincipal Investigator
- Principal Investigator
  
  Shinichiro Hayashi
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Research Field
  
  Applied health science
- Research Institution
  Tokyo Medical and Dental University

All 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 Other

All Journal Article Presentation Book Patent Other

[Book] 別冊・医学のあゆみ. 遺伝性神経・筋疾患．RNA-seq技術を用いた遺伝性筋疾患診断．2023
- Author(s)
  大久保真理子，林晋一郎
- Total Pages
  6
- Publisher
  医歯薬出版
- Data Source
  KAKENHI-PROJECT-21K06961
[Book] 医学のあゆみ. 283(10). RNA-seq技術を用いた遺伝性筋疾患診断．2022
- Author(s)
  大久保真理子，林晋一郎
- Total Pages
  6
- Publisher
  医歯薬出版
- Data Source
  KAKENHI-PROJECT-21K06961
[Book] 超高齢社会に挑む骨格筋のメディカルサイエンス2018
- Author(s)
  武田伸一、林晋一郎、青木吉嗣、秋本崇之、吾郷由希夫、東浩太郎、池田和博、井上聡、今井祐記、上住聡芳、上住円、内田信一、江口貴大、大川恭行、大澤裕、小川純人、小川渉、小野悠介、鍵田明宏、梶村真吾、金川基、上村大輔　他
- Total Pages
  230
- Publisher
  羊土社
- ISBN
  9784758103701
- Data Source
  KAKENHI-PROJECT-16K16597
[Book] 超高齢社会に挑む骨格筋のメディカルサイエンス2018
- Author(s)
  武田　伸一, 林晋一郎, 他
- Total Pages
  230
- Publisher
  羊土社
- ISBN
  9784758103701
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy2023
- Author(s)
  Eura Nobuyuki、Noguchi Satoru、Ogasawara Masashi、Kumutpongpanich Theerawat、Hayashi Shinichiro、Nishino Ichizo、Mukaino Takahiko、Madoka Mori-Yoshimura、Nagai Makiko、Ochi Masayuki、Shibata Makoto、Shiomi Kazutaka、Yamashita Satoshi、Yamashita Toru、the OPDM/OPMD Image Study Group
- Journal Title
  
  Journal of Neurology
  
  Volume: 270 Issue: 12 Pages: 5988-5998
- DOI
  10.1007/s00415-023-11906-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Inhibitory SMAD6 interferes with BMP dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles2023
- Author(s)
  Asfour Hasan、Hirsinger Estelle、Rouco Raquel、Zarrouki Faouzi、Hayashi Shinichiro、Swist Sandra、Braun Thomas、Patel Ketan、Relaix Frederic、Andrey Guillaume、Stricker Sigmar、Duprez Delphine、Stantzou Amalia、Amthor Helge
- Journal Title
  
  Development
  
  Volume: 150
- DOI
  10.1242/dev.201504
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Muscle pathology of antisynthetase syndrome according to antibody subtypes2023
- Author(s)
  Tanboon Jantima、Inoue Michio、Hirakawa Shinya、Tachimori Hisateru、Hayashi Shinichiro、Noguchi Satoru、Okiyama Naoko、Fujimoto Manabu、Suzuki Shigeaki、Nishino Ichizo
- Journal Title
  
  Brain Pathology
  
  Volume: 33 Issue: 4
- DOI
  10.1111/bpa.13155
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-23K21438
[Journal Article] RILPL1-related OPDM is absent in a Japanese cohort2022
- Author(s)
  Eura Nobuyuki、Iida Aritoshi、Ogasawara Masashi、Hayashi Shinichiro、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 109 Issue: 11 Pages: 2088-2089
- DOI
  10.1016/j.ajhg.2022.10.005
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] RNA-seq analysis, targeted long-read sequencing and in silico prediction to unravel pathogenic intronic events and complicated splicing abnormalities in dystrophinopathy2022
- Author(s)
  Okubo M, Noguchi S, Awaya T, Hosokawa M, Tsukui N, Ogawa M, Hayashi S, Komaki H, Mori-Yoshimura M, Oya Y, Takahashi Y, Fukuyama T, Funato M, Hosokawa Y, Kinoshita S, Matsumura T, Nakamura S, Oshiro A, Terashima H, Nagasawa T, Sato T, Shimada Y, Tokita Y, Hagiwara M, Ogata K, Nishino I
- Journal Title
  
  Human Genetics
  
  Volume: 142 Issue: 1 Pages: 59-71
- DOI
  10.1007/s00439-022-02485-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-20K17509
[Journal Article] Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy2022
- Author(s)
  Ogasawara Masashi、Eura Nobuyuki、Iida Aritoshi、Kumutpongpanich Theerawat、Minami Narihiro、Nonaka Ikuya、Hayashi Shinichiro、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Acta Neuropathologica Communications
  
  Volume: 10 Issue: 1 Pages: 176-176
- DOI
  10.1186/s40478-022-01482-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy2022
- Author(s)
  Yoshioka Wakako、Iida Aritoshi、Sonehara Kyuto、Yamamoto Kazuki、Oya Yasushi、Mori-Yoshimura Madoka、Kurashige Takashi、Okubo Mariko、Ogawa Megumu、Matsuda Fumihiko、Higasa Koichiro、Hayashi Shinichiro、Nakamura Harumasa、Sekijima Masakazu、Okada Yukinori、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Scientific Reports
  
  Volume: 12 Issue: 1 Pages: 21806-21806
- DOI
  10.1038/s41598-022-26419-0
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-20H00620, KAKENHI-PROJECT-23K21722
[Journal Article] Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB42022
- Author(s)
  Inoue Michio、Noguchi Satoru、Inoue Yukiko U.、Iida Aritoshi、Ogawa Megumu、Bengoechea Rocio、Pittman Sara K.、Hayashi Shinichiro、Watanabe Kazuki、Hosoi Yasushi、Sano Terunori、Takao Masaki、Oya Yasushi、Takahashi Yuji、Miyajima Hiroaki、Weihl Conrad C.、Inoue Takayoshi、Nishino Ichizo
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 145 Issue: 2 Pages: 235-255
- DOI
  10.1007/s00401-022-02530-4
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-20K06467
[Journal Article] Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathy2022
- Author(s)
  Ogasawara Masashi,Eura Nobuyuki,Nagaoka Utako,Sato Tatsuro,Arahata Hajime,Hayashi Tomohiro,Okamoto Tomoko,Takahashi Yuji,Mori‐Yoshimura Madoka,Oya Yasushi,Nakamura Akinori,Shimazaki Rui,Sano Terunori,Kumutpongpanich Theerawat,Minami Narihiro,Hayashi Shinichiro,Noguchi Satoru,Iida Aritoshi,Takao Masaki,Nishino Ichizo
- Journal Title
  
  Neuropathology and Applied Neurobiology
  
  Volume: 48 Issue: 3
- DOI
  10.1111/nan.12787
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Simultaneous measurement of the size and methylation of chromosome 4qA-D4Z4 repeats in facioscapulohumeral muscular dystrophy by long-read sequencing2022
- Author(s)
  Hiramuki Yosuke、Kure Yuriko、Saito Yoshihiko、Ogawa Megumu、Ishikawa Keiko、Mori-Yoshimura Madoka、Oya Yasushi、Takahashi Yuji、Kim Dae-Seong、Arai Noriko、Mori Chiaki、Matsumura Tsuyoshi、Hamano Tadanori、Nakamura Kenichiro、Ikezoe Koji、Hayashi Shinichiro、Goto Yuichi、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Journal of Translational Medicine
  
  Volume: 20 Issue: 1 Pages: 517-517
- DOI
  10.1186/s12967-022-03743-7
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-22K07392
[Journal Article] Dermatomyositis2021
- Author(s)
  Tanboon Jantima、Inoue Michio、Saito Yoshihiko、Tachimori Hisateru、Hayashi Shinichiro、Noguchi Satoru、Okiyama Naoko、Fujimoto Manabu、Nishino Ichizo
- Journal Title
  
  Neurology
  
  Volume: 98 Issue: 7
- DOI
  10.1212/wnl.0000000000013176
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-23K21438
[Journal Article] Deep convolutional neural network-based algorithm for muscle biopsy diagnosis2021
- Author(s)
  Kabeya Yoshinori,Okubo Mariko,Yonezawa Sho,Nakano Hiroki,Inoue Michio,Ogasawara Masashi,Saito Yoshihiko,Tanboon Jantima,Indrawati Luh Ari,Kumutpongpanich Theerawat,Chen Yen-Lin,Yoshioka Wakako,Hayashi Shinichiro,Iwamori Toshiya,Takeuchi Yusuke,Tokumasu Reitaro,Takano Atsushi,Matsuda Fumihiko,Nishino Ichizo
- Journal Title
  
  Laboratory Investigation
  
  Volume: 102 Issue: 3 Pages: 220-226
- DOI
  10.1038/s41374-021-00647-w
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.2021
- Author(s)
  Kumutpongpanich T, Ogasawara M, Ozaki A, et al., Hamano T, Sugie K, et al.,
- Journal Title
  
  JAMA Neurol.
  
  Volume: 78(7) Issue: 7 Pages: 853-853
- DOI
  10.1001/jamaneurol.2021.1509
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07909, KAKENHI-PROJECT-20H03588, KAKENHI-PROJECT-19K07967, KAKENHI-PROJECT-20K07890, KAKENHI-PROJECT-21K06961
[Journal Article] Identification of a KLF5-dependent program and drug development for skeletal muscle atrophy2021
- Author(s)
  Liu L, Koike H, Ono T, Hayashi S, Kudo F, Kaneda A, Kagechika H, Manabe I, Nakashima T, Oishi, Y.
- Journal Title
  
  Proc Natl Acad Sci U S A.
  
  Volume: 118 Issue: 35
- DOI
  10.1073/pnas.2102895118
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H03679, KAKENHI-ORGANIZER-17H06391, KAKENHI-PUBLICLY-20H04938, KAKENHI-PUBLICLY-20H04956, KAKENHI-PROJECT-20H00551, KAKENHI-PROJECT-19H03648, KAKENHI-PROJECT-21H03331, KAKENHI-PROJECT-21K06961, KAKENHI-PROJECT-21K19554, KAKENHI-PROJECT-21K17154
[Journal Article] A recurrent homozygous ACTN2 variant associated with core myopathy2021
- Author(s)
  Inoue Michio、Noguchi Satoru、Sonehara Kyuto、Nakamura-Shindo Keiko、Taniguchi Akira、Kajikawa Hiroyuki、Nakamura Hisayoshi、Ishikawa Keiko、Ogawa Megumu、Hayashi Shinichiro、Okada Yukinori、Kuru Satoshi、Iida Aritoshi、Nishino Ichizo
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 142 Issue: 4 Pages: 785-788
- DOI
  10.1007/s00401-021-02363-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K06961
[Journal Article] Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to the Temple and Kagami-Ogata syndromes.2020
- Author(s)
  Kitazawa M, Hayashi S, Imamura H, Takeda S, Oishi Y, Kaneko-Ishino T, Ishino F
- Journal Title
  
  Development
  
  Volume: 147 Issue: 21 Pages: 147-147
- DOI
  10.1242/dev.185918
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K20584, KAKENHI-PROJECT-19KK0182, KAKENHI-PUBLICLY-20H04956, KAKENHI-PROJECT-19H00978, KAKENHI-PROJECT-17K07498, KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-19K23744
[Journal Article] ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features2020
- Author(s)
  Saito Yoshihiko、Nishikawa Atsuko、Iida Aritoshi、Mori-Yoshimura Madoka、Oya Yasushi、Ishiyama Akihiko、Komaki Hirofumi、Nakamura Seigo、Fujikawa Susumu、Kanda Takashi、Yamadera Misaki、Sakiyama Hiroshi、Hayashi Shinichiro、Nonaka Ikuya、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Neurology
  
  Volume: 95 Issue: 11
- DOI
  10.1212/wnl.0000000000010237
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K16589, KAKENHI-PROJECT-18K07082
[Journal Article] Two Japanese LGMDR25 patients with a biallelic recurrent nonsense variant of BVES2020
- Author(s)
  Indrawati Luh Ari、Iida Aritoshi、Tanaka Yuzo、Honma Yutaka、Mizoguchi Koichi、Yamaguchi Tomohisa、Ikawa Masamichi、Hayashi Shinichiro、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Neuromuscular Disorders
  
  Volume: 30 Issue: 8 Pages: 674-679
- DOI
  10.1016/j.nmd.2020.06.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Association of Dermatomyositis Sine Dermatitis With Anti-Nuclear Matrix Protein 2 Autoantibodies2020
- Author(s)
  Michio Inoue, Kazumoto Shibuya (11th) et al.
- Journal Title
  
  JAMA Neurology
  
  Volume: 77 Issue: 7 Pages: 872-872
- DOI
  10.1001/jamaneurol.2020.0673
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07754, KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-18K08263
[Journal Article] CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations2020
- Author(s)
  Ogasawara M, Iida A, Kumutpongpanich T, Ozaki A, Oya Y, Konishi H, Nakamura A, Abe R, Takai H, Hanajima R, Doi H, Tanaka F, Nakamura H, Nonaka I, Wang Z, Hayashi S, Noguchi S, Nishino I.
- Journal Title
  
  Acta Neuropathol Commun
  
  Volume: 8 Issue: 1 Pages: 204-204
- DOI
  10.1186/s40478-020-01084-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07866, KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-18K07503
[Journal Article] Pathologic Features of Anti-Mi-2 Dermatomyositis2020
- Author(s)
  Tanboon Jantima、Inoue Michio、Hirakawa Shinya、Tachimori Hisateru、Hayashi Shinichiro、Noguchi Satoru、Suzuki Shigeaki、Okiyama Naoko、Fujimoto Manabu、Nishino Ichizo
- Journal Title
  
  Neurology
  
  Volume: 96 Issue: 3
- DOI
  10.1212/wnl.0000000000011269
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-18K08263
[Journal Article] Evaluation of the Core Formation Process in Congenital Neuromuscular Disease With Uniform Type 1 Fiber and Central Core Disease2020
- Author(s)
  Ogasawara Masashi、Ogawa Megumu、Nonaka Ikuya、Hayashi Shinichiro、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Journal of Neuropathology & Experimental Neurology
  
  Volume: 79 Issue: 12 Pages: 1370-1375
- DOI
  10.1093/jnen/nlaa104
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-20K16612
[Journal Article] Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy2020
- Author(s)
  Okubo Mariko、Noguchi Satoru、Hayashi Shinichiro、Nakamura Harumasa、Komaki Hirofumi、Matsuo Masafumi、Nishino Ichizo
- Journal Title
  
  Human Genetics
  
  Volume: 139 Issue: 2 Pages: 247-255
- DOI
  10.1007/s00439-019-02107-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress2019
- Author(s)
  Der Vartanian Audrey、Qu?tin Marie、Michineau St?phanie、Aurad? Fr?d?ric、Hayashi Shinichiro、Dubois Christelle、Rocancourt Didier、Drayton-Libotte Bernadette、Szegedi Anik?、Buckingham Margaret、Conway Simon J.、Gervais Marianne、Relaix Fr?d?ric
- Journal Title
  
  Cell Stem Cell
  
  Volume: 24 Issue: 6 Pages: 958-973.e9
- DOI
  10.1016/j.stem.2019.03.019
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Three novel MTM1 pathogenic variants identified in Japanese patients with X‐linked myotubular myopathy2019
- Author(s)
  Nishikawa Atsuko、Iida Aritoshi、Hayashi Shinichiro、Okubo Mariko、Oya Yasushi、Yamanaka Gaku、Takahashi Ikuko、Nonaka Ikuya、Noguchi Satoru、Nishino Ichizo
- Journal Title
  
  Molecular Genetics & Genomic Medicine
  
  Volume: 7 Issue: 5
- DOI
  10.1002/mgg3.621
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10000, KAKENHI-PROJECT-18K07082
[Journal Article] Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy2018
- Author(s)
  Inoue Michio, Iida Aritoshi, Hayashi Shinichiro, Mori-Yoshimura Madoka, Nagaoka Atsushi, Yoshimura Shunsuke, Shiraishi Hirokazu, Tsujino Akira, Takahashi Yuji, Nonaka Ikuya, Hayashi K Yukiko, Noguchi Satoru, Nishino Ichizo
- Journal Title
  
  Human Genome Variation
  
  Volume: 印刷中
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K16597
[Journal Article] A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy.2018
- Author(s)
  Ishiyama A, Iida A, Hayashi S, Komaki H, Sasaki M, Nonaka I, Noguchi S, Nishino I.
- Journal Title
  
  Human Genome Variation
  
  Volume: 5 Issue: 1 Pages: 19-19
- DOI
  10.1038/s41439-018-0018-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Three novel recessive DYSF mutations identified in three patients with muscular dystrophy, limb-girdle, type 2B.2018
- Author(s)
  Okubo M, Iida A, Hayashi S, Mori-Yoshimura M, Oya Y, Watanabe A, Arahata H, El Sherif R, Noguchi S, Nishino I.
- Journal Title
  
  Journal of the Neurological Sciences
  
  Volume: 395 Pages: 169-171
- DOI
  10.1016/j.jns.2018.10.015
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy.2018
- Author(s)
  Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, Nonaka I, Hayashi YK, Noguchi S, Nishino I.
- Journal Title
  
  Human Genome Variation
  
  Volume: 5 Issue: 1 Pages: 9-9
- DOI
  10.1038/s41439-018-0009-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07082
[Journal Article] Bmal1 regulates inflammatory responses in macrophages by modulating enhancer RNA transcription.2017
- Author(s)
  Oishi Y, Hayashi S, Isagawa T, Oshima M, Iwama A, Shimba S, Okamura H and Manabe I.
- Journal Title
  
  Sci Rep
  
  Volume: 7 Issue: 1 Pages: 7086-7086
- DOI
  10.1038/s41598-017-07100-3
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09589, KAKENHI-PROJECT-17K09592, KAKENHI-PUBLICLY-17H05632, KAKENHI-PUBLICLY-17H05636, KAKENHI-PROJECT-15H01843, KAKENHI-PROJECT-16H05295, KAKENHI-PROJECT-16K16597
[Journal Article] LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription.2017
- Author(s)
  Scionti I, Hayashi S, Mouradian S, Girard E, Esteves de Lima J, Morel V, Simonet T, Wurmser M, Maire P, Ancelin K, Metzger E, Schule R, Goillot E, Relaix F, Schaeffer L.
- Journal Title
  
  Cell Reports
  
  Volume: 18 Issue: 8 Pages: 1996-2006
- DOI
  10.1016/j.celrep.2017.01.078
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K16597
[Journal Article] Klf5 regulates muscle differentiation by directly targeting muscle-specific genes in cooperation with MyoD in mice.2016
- Author(s)
  Hayashi S, Manabe I, Suzuki Y, Relaix F, Oishi Y
- Journal Title
  
  eLife
  
  Volume: -
- DOI
  10.7554/elife.17462
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PUBLICLY-15H01506, KAKENHI-PROJECT-26461142, KAKENHI-PROJECT-16K16597
[Patent] 筋サテライト細胞の培養方法2017
- Inventor(s)
  大石由美子、林晋一郎
- Industrial Property Rights Holder
  大石由美子、林晋一郎
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2017-121787
- Filing Date
  2017
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] フランスでの研究生活と研究者コミュニティの形成について2024
- Author(s)
  林晋一郎
- Organizer
  第8回若手による骨格筋細胞研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Application of the Nanopore long-read sequencer to the genetic diagnosis of facioscapulohumeral muscular dystrophy2023
- Author(s)
  Saito Y, Hiramuki Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  第65回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Clinicopathological features of anti-mitochondrial M2 antibody-positive myositis based on a cohort of 201 patients from Japan2023
- Author(s)
  Nishimori Y, Tanboon J, Oyama M, Motegi H, Tomo Y, Oba M, Sugie K, Suzuki S, Hayashi S, Noguchi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] A comparative single nuclei transcriptomics approach to evaluating the terminally differentiated lymphocytes in autoimmune Myositis2023
- Author(s)
  De Los Reyes F, Hayashi S, Noguchi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] A Comparative Transcriptomics Approach to Understanding Autoimmune Myopathies2023
- Author(s)
  DE LOS REYES Francia Victoria、林晋一郎、宇根隼人、TANBOON Jantima、野口悟，西野一三
- Organizer
  第64回日本神経病理学会総会学術研究会．第66回日本神経化学会大会合同大会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Myotendinous junction abnormalities on skeletal muscle imaging common to COL6-related myopathies, ADSS1 myopathy and JAG2 myopathy2023
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] 中心核ミオパチーは先天性筋無力症候群か？2023
- Author(s)
  斎藤良彦，野口悟，林晋一郎，西野一三
- Organizer
  6NCリトリートポスターセッション
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] A large cohort study of muscle imaging in GNE myopathy: Progression profile and diagnostic tips to distinguish from other distal myopathies2023
- Author(s)
  Yoshioka W, Mori-Yoshimura M, Eura N, Saito Y, Oya Y, Hayashi S, Kimura Y, Sato N, Noguchi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Single nuclei transcriptomics in muscle disease2023
- Author(s)
  Hayashi S
- Organizer
  1st Symposium on "Skeletal muscle cells in Growth and Disease"
- Invited
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Decoding Duchenne muscular dystrophy: insights from single nuclei RNA-seq analysis2023
- Author(s)
  Hayashi S, De Los Reyes F, Noguchi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Uncovering DMD transcriptional networks using single nuclei RNA-seq2023
- Author(s)
  Hayashi S
- Organizer
  INSERM-JSPS WORKSHOP
- Invited
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] 多層的トランスクリプトーム解析による筋疾患病態解明2023
- Author(s)
  林晋一郎
- Organizer
  第9回日本筋学会学術集会・第10回筋ジストロフィー医療研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] 抗ミトコンドリアM2抗体陽性筋炎の筋病理学的特徴－世界最大コホートでの解析2023
- Author(s)
  西森裕佳子，タンブーンジャンティマ，大山宗徳，茂木晴彦，塘由惟，大庭真梨，杉江和馬，鈴木重明，林晋一郎，野口悟，西野一三
- Organizer
  第64回日本神経病理学会総会学術研究会．第66回日本神経化学会大会合同大会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] サルコグリカノパチーの遺伝子プロファイル2023
- Author(s)
  島崎塁，斎藤良彦，林晋一郎，野口悟，西野一三
- Organizer
  6NCリトリートポスターセッション
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Single-nucleus RNA sequencing reveals characteristic gene expression in pathologically-specific myofibers in oculopharyngodistal myopathy2023
- Author(s)
  Eura N, Noguchi S, Hayashi S, Nishino I
- Organizer
  28th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Genotype-phenotype correlations in NEB-related myopathies.2022
- Author(s)
  Ogasawara M, Nishimori Y, Eura N, Hashizume L, Miyazaki N, Sugie K, Hayashi S, Noguchi S, Iida A, Nishino I
- Organizer
  MYOLOGY 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] 本邦における骨格筋切片を用いたPompe病スクリーニング2022
- Author(s)
  斎藤良彦，中村公俊，福田冬季子，杉江秀夫，林晋一郎，野口悟，西野一三
- Organizer
  第40回日本神経治療学会学術集会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Inflammatory features on muscle pathology in laminopathy.2022
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  第63回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] CRISPR/Cas9-targeted single molecule long-read sequencing reveals allelic microheterogeneity of triplet repeat expansion in oculopharyngodistal myopathy.2022
- Author(s)
  Eura N, Noguchi S, Ogasawara M, Iida A, Hayashi S, Nishino I
- Organizer
  27th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Intra-myonuclear inclusions differentiate oculopharyngeal muscular dystrophy from oculopharyngodistal myopathy.2022
- Author(s)
  Eura N, Ogasawara M, Hayashi S, Noguchi S, Nishino I
- Organizer
  MYOLOGY 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Neuromuscular junction abnormalities in patients with centronuclear myopathy.2022
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  第64回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Frequent intra-myonuclear inclusions is a distinctive finding of oculopharyngeal muscular dystrophy.2022
- Author(s)
  Eura N, Ogasawara M, Hayashi S, Noguchi S, Nishino I
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Innervation defect: new pathomechanism of centronuclear myopathy?2022
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  MYOLOGY 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Clinicopathological findings of anti-mitochondrial antibody associated myositis.2022
- Author(s)
  Nishimori Y, Oyama M, Motegi H, Hayashi S, Noguchi S, Suzuki S, Nishino I
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Innervation defect: new pathomechanism of centronuclear myopathy?2022
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  27th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Multi-dimensional analyses of the pathomechanism of GNE myopathy with non-catalytic site variant, GNE: c.620A>T.2022
- Author(s)
  Yoshioka W, Iida A, Sonehara K, Yamamoto K, Oya Y, Mori-Yoshimura M, Kurashige T, Okubo M, Ogawa M, Matsuda F, Higasa K, Hayashi S, Nakamura H, Sekijima M, Okada Y, Nishino I, Noguchi S
- Organizer
  MYOLOGY 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Dermatomyositis-specific autoantibodies and muscle MRI findings.2022
- Author(s)
  Une H, Hayashi S, Noguchi S, Nishino I
- Organizer
  MYOLOGY 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Dermatomyositis-specific autoantibodies and muscle MRI findings.2022
- Author(s)
  Une H, Hayashi S, Noguchi S, Nishino I
- Organizer
  27th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Intra-nuclear inclusions can differentiate between oculopharyngeal muscular dystrophy and oculopharyngodistal myopathy.2022
- Author(s)
  Eura N, Ogasawara M, Hayashi S, Noguchi S, Nishino I
- Organizer
  第63回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Screening of small molecules for activation of GNE protein carrying non-catalytic site mutation based on molecular docking simulation.2022
- Author(s)
  Yoshioka W, Yamamoto K, Hayashi S, Sekijima M, Nishino I, Noguchi S
- Organizer
  27th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Clinicopathological findings of anti-mitochondrial antibody associated myositis.2021
- Author(s)
  Nishimori Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Mutation profiling and immunohistochemical characterization of Japanese patients with sarcoglycanopathy.2021
- Author(s)
  Saito Y, Hayashi S, Noguchi S, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] RNA-seq analysis for Dystrophinopathy.2021
- Author(s)
  Okubo M, Noguchi S, Hayashi S, Komaki H, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] GNE pathogenic variant p.D207V rarely leads to myopathy in homozygotes; GNE might not be the only pathogenic determinant of GNE myopathy.2021
- Author(s)
  Yoshioka W, Sonehara K, Iida A, Oya Y, Kurashige T, Okubo M, Ogawa M, Matsuda F, Higasa K, Mori-Yoshimura M, Nakamura H, Hayashi S, Okada Y, Noguchi S, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Clinicopathologic features of oculopharyngodistal myopathy with LRP12 CGG repeat expansions.2021
- Author(s)
  Ogasawara M, Kumutpongpanich T, Ishiura H, Tsuji S, Minami N, Hayashi S, Noguchi S, Iida A, Nishino I
- Organizer
  日本人類遺伝学会第66回大会
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Dermatomyositis: muscle pathology according to antibody subtypes.2021
- Author(s)
  Tanboon J, Inoue M, Saito Y, Hayashi S, Noguchi S, Okiyama N, Fujimoto M, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] Generation and characterization of a Pax7-HA knock-in mouse line.2021
- Author(s)
  Hayashi S, Inoue Y, Kosako H, Inoue T, Noguchi S, Nishino I
- Organizer
  26th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06961
[Presentation] RYR1遺伝子異常によるCongenital neuromuscular disease with uniform type1 fiberは事実上のコアミオパチーである2020
- Author(s)
  小笠原真志，小川　恵，埜中征哉，林晋一郎，野口　悟，西野一三
- Organizer
  第6回日本筋学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] RNA-seqを用いたジストロフィン遺伝子解析2020
- Author(s)
  大久保真理子，野口　悟，林晋一郎，小牧宏文，齋藤伸治，西野一三
- Organizer
  第6回日本筋学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Generation and characterization of Pax7-HA knock-in mice.2020
- Author(s)
  Hayashi S, Inoue Y, Kosako H, Inoue T, Noguchi S, Nishino I
- Organizer
  25th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Screening for Pompe disease using muscle section in Japan.2020
- Author(s)
  Saito Y, Nakamura K, Fukuda T, Sugie H, Hayashi S, Noguchi S, Nishino I
- Organizer
  25th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Congenital neuromuscular disease with uniform type 1 fiber due to RYR1 mutation is a de facto core myopathy.2020
- Author(s)
  Ogasawara M, Ogawa M, Nonaka I, Hayashi S, Noguchi S, Nishino I
- Organizer
  25th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 本邦における骨格筋切片を用いたポンペ病スクリーニング2020
- Author(s)
  斎藤良彦，中村公俊，福田冬季子，杉江秀夫，林晋一郎，野口　悟，西野一三
- Organizer
  第6回日本筋学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Recessive variant of POPDC3 causes a nuclear envelopathy.2020
- Author(s)
  Indrawati LA, Mitsuhashi H, Iida A, Mori-Yoshimmura M, Hayashi S, Noguchi S, Nishino I
- Organizer
  第6回日本筋学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] A dominant variant in DNAJB4 causes a myofibrillar myopathy.2020
- Author(s)
  Inoue M, Iida A, Watanabe K, Hosoi Y, Miyajima H, Hayashi S, Inoue Y, Inoue T, Noguchi S, Nishino I
- Organizer
  25th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Pathogenesis of congenital neuromuscular disease with uniform type 1 fiber and central core disease.2020
- Author(s)
  Ogasawara M, Ogawa M, Hayashi S, Nonaka I, Noguchi S, Nishino I
- Organizer
  第62回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Myopathy in scleroderma/systemic sclerosis patients: From a histopathological point of view.2020
- Author(s)
  Chen Y, Inoue M, Ogasawara M, Saito Y, Indrawati L, Tanboon J, Kumutpongpanich T, Okubo M, Yoshioka W, Hayashi S, Noguchi S, Nishino I
- Organizer
  25th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 筋発生・再生過程における骨格筋細胞の分化制御機構2019
- Author(s)
  林　晋一郎
- Organizer
  第74回日本体力医学会大会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] GNEミオパチーp.D207V変異は軽症型変異であり、ホモ接合体では極めて稀にしか発症しない2019
- Author(s)
  吉岡和香子，飯田有俊，岡田随象，大矢　寧，大久保真理子，小川　恵，松田文彦，日笠幸一郎，森　まどか，中村治雅，林　晋一郎，野口　悟，西野一三
- Organizer
  日本筋学会第5回学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] COX6A2変異は横紋筋特異的なチトクロームc酸化酵素欠損症を引き起こす2019
- Author(s)
  井上道雄，内野俊平，飯田有俊，野口　悟，林　晋一郎，高橋　努，藤井克則，小牧宏文，竹下絵里，埜中征哉，岡田随象，吉澤拓也，Van Lommel L, Schuit F, 後藤雄一，三牧正和，西野一三
- Organizer
  日本筋学会第5回学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Infantile-onset lipid storage myopathy.2019
- Author(s)
  Indrawati LA, Noguchi S, Tanboon J, Ogasawara M, Saito Y, Kumutpongpanich T, Inoue M, Okubo M, Fukuda T, Sugie H, Goto Y, Iida A, Hayashi S, Nishino I
- Organizer
  24th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 次世代シークエンサーを用いたデュシェンヌ/ベッカー型筋ジストロフィーの遺伝学的解析（続報）2019
- Author(s)
  大久保真理子，野口　悟，飯田有俊，林　晋一郎，西野一三
- Organizer
  第64回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] ADSSL1 myopathy is a fatigability disease presenting both nemaline bodies and lipid droplets in skeletal muscles-a study of 57 Japanese cases2019
- Author(s)
  Saito Y, Noguchi S, Nishikawa A, Hayashi S, Iida A, Nishino I
- Organizer
  24th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] ETS1 regulates muscle stem cell proliferation and stemness perpetuation2019
- Author(s)
  Kumutpongpanich T, Hayashi S, Noguchi S, Nishino I
- Organizer
  日本筋学会第5回学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] ETS1 facilitates muscle satellite cell proliferation and stemness perpetuation2019
- Author(s)
  Kumutpongpanich T, Hayashi S, Noguchi S, Nishino I
- Organizer
  24th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 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2019
- Author(s)
  林　晋一郎
- Organizer
  第92回日本生化学会大会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Genetic diagnosis in large Japanese cohort using targeted re-sequencing system2019
- Author(s)
  Okubo M, Iida A, Inoue M, Saito Y, Ogasawara M, Hayashi S, Noguchi S, Nishino I
- Organizer
  24th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Mutation-specific therapy for X-linked myotubular myopathy2019
- Author(s)
  Hayashi S, Noguchi S, Kumutpongpanich T, Iida A, Okubo M, Matsuo M, Nishino I
- Organizer
  24th International Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Frequency of c.620A>T homozygotes is extremely low in Japanese GNE myopathy patients: What is determining the pathogenicity?2018
- Author(s)
  Yoshioka W, Okubo M, Ogawa M, Matsuda F, Higasa K, Mori-Yoshimura M, Oya Y, Kimura E, Nakamura H, Hayashi S, Iida A, Noguchi S, Nishino I
- Organizer
  11th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 骨格筋幹細胞の新規分化制御機構と筋疾患治療への応用2018
- Author(s)
  林晋一郎
- Organizer
  第５４回お茶の水疾患研究会
- Invited
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Novel deep intronic mutations in MTM1 in X-linked myotubular myopathy.2018
- Author(s)
  Kumutpongpanich T, Hayashi S, Iida A, Okubo M, Matsuo M, Noguchi S, Nishino I
- Organizer
  23rd INTERNATIONAL CONGRESS OF THE WORLD MUSCLE SOCIETY
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Establishment of a long-term culture system for Muscle stem cells.2018
- Author(s)
  Hayashi S.
- Organizer
  5th Tissue Engineering and Regenerative Medicine International Society World Congress
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Klf5による骨格筋発生の制御機構2018
- Author(s)
  林晋一郎，大石由美子，真鍋一郎，西野一三
- Organizer
  日本筋学会第4回学術集会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Klf5 has essential roles in myoblast differentiation and survival during fetal muscle development.2018
- Author(s)
  Hayashi S, Oishi Y, Manabe I, Nishino I.
- Organizer
  23rd INTERNATIONAL CONGRESS OF THE WORLD MUSCLE SOCIETY
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Comprehensive analysis in Japan: Nonsense mutation induced exon skipping in Becker muscular dystrophy.2018
- Author(s)
  Okubo M, Noguchi S, Hayashi S, Nishino I.
- Organizer
  11th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Regulation of muscle stem cell function during murine fetal development.2018
- Author(s)
  Hayashi S, Manabe I, Oishi Y, Nishino I.
- Organizer
  11th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Nonsense mutation induced exon skipping in Becker muscular dystrophy.2018
- Author(s)
  Okubo M, Noguchi S, Hayashi S, Matsuo M, Nishino I.
- Organizer
  23rd INTERNATIONAL CONGRESS OF THE WORLD MUSCLE SOCIETY
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] Klf5 regulates myoblast differentiation and apoptosis during fetal muscle development.2018
- Author(s)
  Hayashi S.
- Organizer
  第6回若手による骨格筋細胞研究会
- Data Source
  KAKENHI-PROJECT-18K07082
[Presentation] 骨格筋細胞の新規老化メカニズム解析2017
- Author(s)
  林晋一郎、真鍋一郎、西野一三、大石由美子
- Organizer
  2017年度生命科学系学会合同年次大会(ConBio2017)
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 筋衛星細胞の分化および筋再生におけるKlf5の役割2017
- Author(s)
  林晋一郎, 大塚千聖, 林, 鈴木裕美, 大石由美子
- Organizer
  第5回骨格筋生物学研究会
- Place of Presentation
  東京大学, 東京
- Year and Date
  2017-03-03
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Klf5 is involved in the pathogenesis of muscle atrophy2017
- Author(s)
  Liu Lin, Shinichiro Hayashi, Yumiko Oishi
- Organizer
  2017年度生命科学系学会合同年次大会(ConBio2017)
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 筋衛星細胞の未分化性維持機構の解明と細胞移植治療への応用2017
- Author(s)
  林晋一郎
- Organizer
  「筋ジストロフィー関連疾患の分子病態解明とそれに基づく診断法・治療法開発」(29-4) 西野班班会議
- Invited
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 骨格筋の再生・発生における新規分化制御機構2017
- Author(s)
  林晋一郎
- Organizer
  第３回日本筋学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Klf5は筋芽細胞の増殖を負に制御し、細胞老化を誘導する2017
- Author(s)
  林晋一郎
- Organizer
  第５回若手による骨格筋細胞研究会
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 骨格筋発生過程におけるKlf5の機能解析2017
- Author(s)
  大塚千聖, 林晋一郎, 鈴木裕美, 大石由美子
- Organizer
  第5回骨格筋生物学研究会
- Place of Presentation
  東京大学, 東京
- Year and Date
  2017-03-03
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Klf5 regulates skeletal muscle differentiation by directly targeting muscle-specific genes2016
- Author(s)
  Shinichiro Hayashi, Ichiro Manabe, Yumi Suzuki and Yumiko Oishi
- Organizer
  FASEB Science Research Conferences, KLF and Sp Transcription Factors in Disease and Regenerative Medicine
- Place of Presentation
  Snowmass, Co, USA
- Year and Date
  2016-08-07
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 骨格筋発生におけるKlf5の機能解析2016
- Author(s)
  大塚千聖, 林晋一郎, 鈴木裕美, 大石由美子
- Organizer
  第二回日本筋学会学術集会
- Place of Presentation
  国立精神・神経医療研究センター, 東京
- Year and Date
  2016-08-05
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 骨格筋の分化、再生、発生におけるKlf5の役割2016
- Author(s)
  林晋一郎
- Organizer
  第四回　若手による骨格筋細胞研究会
- Place of Presentation
  ウインクあいち, 名古屋
- Year and Date
  2016-11-14
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 骨格筋発生におけるKlf5の機能解析2016
- Author(s)
  林晋一郎、大塚千聖、鈴木裕美、真鍋一郎、大石由美子
- Organizer
  Molecular Cardiovascular Conference II (2016)
- Place of Presentation
  東京ドームホテル, 東京
- Year and Date
  2016-09-02
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] 筋衛星細胞における新規筋分化制御機構の解明2016
- Author(s)
  林晋一郎、大塚千聖、鈴木裕美、真鍋一郎、大石由美子
- Organizer
  第二回日本筋学会学術集会
- Place of Presentation
  国立精神・神経医療研究センター, 東京
- Year and Date
  2016-08-05
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Klf5 regulates Muscle Differentiation and Development2016
- Author(s)
  林晋一郎
- Organizer
  第4回骨格筋生物学研究会
- Place of Presentation
  松本大学 5号館、6号館（長野県松本市）
- Year and Date
  2016-03-04
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] 骨格筋発生におけるKlf5の機能解析2016
- Author(s)
  林晋一郎、大塚千聖、鈴木裕美、真鍋一郎、大石由美子
- Organizer
  第39回　分子生物学会年会
- Place of Presentation
  パシフィコ横浜, 横浜
- Year and Date
  2016-11-30
- Data Source
  KAKENHI-PROJECT-16K16597
[Presentation] Analysis of conserved and divergent functions of Pax genes during muscle evolution2015
- Author(s)
  林晋一郎
- Organizer
  第三回若手による骨格筋細胞研究会
- Place of Presentation
  九州大学病院キャンパスコラボステーションI・II（福岡県福岡市）
- Year and Date
  2015-11-24
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] Identification of a novel regulatory mechanism during satellite cell differentiation2015
- Author(s)
  林晋一郎
- Organizer
  第38回日本分子生物学学会年会
- Place of Presentation
  神戸ポートアイランド（兵庫県神戸市）
- Year and Date
  2015-12-01
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] 筋衛星細胞における新規筋分化制御機構の解析2015
- Author(s)
  林晋一郎
- Organizer
  第6回 Molecular Cardiovascular Conference II
- Place of Presentation
  ヒルトン福岡シーホーク（福岡県福岡市）
- Year and Date
  2015-09-04
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] Klf5による骨格筋分化制御機構の解析2015
- Author(s)
  林晋一郎
- Organizer
  第1回日本筋学会学術集会
- Place of Presentation
  国立研究開発法人国立精神・神経医療研究センター教育研修棟ユニバーサルホール（東京都小平市）
- Year and Date
  2015-08-08
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] Klf5 regulates skeletal muscle differentiation by controlling Myogenin expression2015
- Author(s)
  Shinichiro Hayashi（林晋一郎）
- Organizer
  Gordon Research Conference, Myogenesis
- Place of Presentation
  Renaissance Tuscany II Ciocco, Lucca, Italy
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26882020
[Presentation] 骨格筋細胞における Klf5 の機能解析
- Author(s)
  林　晋一郎
- Organizer
  第二回若手による骨格筋細胞研究会
- Place of Presentation
  コープイン京都
- Year and Date
  2014-11-04 – 2014-11-05
- Data Source
  KAKENHI-PROJECT-26882020
[]

1. HANAJIMA Ritsuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
2. 石野史敏

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
3. 石野知子(金児知子)

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
4. 斎藤良彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. 山中岳

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 眞鍋一郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. 浜野忠則

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 澁谷和幹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
9. 大石由美子

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Hayashi Shinichiro 林 晋一郎

Shinichiro Hayashi 林 晋一郎

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Global analysis of functional maintenance mechanisms in muscle satellite cells.Principal Investigator

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Analysis of molecular mechanisms regulating stemness in muscle stem cellsPrincipal Investigator

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Identification of the novel mechanism of satellite cell number reduction in sarcopeniaPrincipal Investigator

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Identification of a novel regulatory mechanism in satellite cell homeostasisPrincipal Investigator

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[Book] 別冊・医学のあゆみ. 遺伝性神経・筋疾患．RNA-seq技術を用いた遺伝性筋疾患診断．2023

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[Book] 医学のあゆみ. 283(10). RNA-seq技術を用いた遺伝性筋疾患診断．2022

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[Book] 超高齢社会に挑む骨格筋のメディカルサイエンス2018

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[Book] 超高齢社会に挑む骨格筋のメディカルサイエンス2018

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[Journal Article] Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy2023

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[Journal Article] Inhibitory SMAD6 interferes with BMP dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles2023

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[Journal Article] Muscle pathology of antisynthetase syndrome according to antibody subtypes2023

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[Journal Article] RILPL1-related OPDM is absent in a Japanese cohort2022

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[Journal Article] RNA-seq analysis, targeted long-read sequencing and in silico prediction to unravel pathogenic intronic events and complicated splicing abnormalities in dystrophinopathy2022

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[Journal Article] Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy2022

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Hayashi Shinichiro 林晋一郎

Shinichiro Hayashi 林晋一郎

[Journal Article] Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy2022