Rchr
J-GLOBAL ID:201801014127978335   Update date: Oct. 12, 2020

Hayashi Shinichiro

Hayashi Shinichiro
Affiliation and department:
Research field  (1): Developmental biology
Papers (20):
  • Moe Kitazawa, Shinichiro Hayashi, Michihiro Imamura, Shin'ichi Takeda, Yumiko Oishi, Tomoko Kaneko-Ishino, Fumitoshi Ishino. Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes. Development (Cambridge, England). 2020. 147. 21
  • Yoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, Madoka Mori-Yoshimura, Yasushi Oya, Akihiko Ishiyama, Hirofumi Komaki, Seigo Nakamura, Susumu Fujikawa, Takashi Kanda, et al. ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features. Neurology. 2020
  • Michio Inoue, Jantima Tanboon, Shinya Hirakawa, Hirofumi Komaki, Takeshi Fukushima, Hiroyuki Awano, Takashi Tajima, Kenji Yamazaki, Ryutaro Hayashi, Tatsuo Mori, et al. Association of Dermatomyositis Sine Dermatitis and With Anti-Nuclear Matrix Protein 2 Autoantibodies. JAMA neurology. 2020
  • Mariko Okubo, Satoru Noguchi, Shinichiro Hayashi, Harumasa Nakamura, Hirofumi Komaki, Masafumi Matsuo, Ichizo Nishino. Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy. Human genetics. 2020. 139. 2. 247-255
  • 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, et al. 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. 日本筋学会学術集会プログラム・抄録集. 2019. 5回. 67-67
more...
MISC (2):
  • Shinichiro Hayashi, Bernadette Drayton, Frederic Aurade, Frederic Relaix. Conserved functions of PAX3/7 during evolution. DEVELOPMENTAL BIOLOGY. 2011. 356. 1. 247-247
  • Shinichiro Hayashi, Bernadette Drayton, Frederic Aurade, Didier Rocancourt, Margaret Buckingham, Frederic Relaix. Conserved functions of Pax3/7 during evolution. DEVELOPMENTAL BIOLOGY. 2010. 344. 1. 528-529
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