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Ohsawa Ryosuke  大澤 亮介

ORCIDConnect your ORCID iD *help
Researcher Number 20719356
Other IDs
Affiliation (based on the past Project Information) *help 2021: 広島大学, 原爆放射線医科学研究所, 助教
2014 – 2017: 広島大学, 原爆放射線医科学研究所, 助教
Review Section/Research Field
Principal Investigator
Basic Section 52020:Neurology-related / Nerve anatomy/Neuropathology
Except Principal Investigator
Basic / Social brain science
Keywords
Principal Investigator
ALS / 筋萎縮性側索硬化症 / ミクログリア / OPTN / OPTN(Optineurin) / 自然免疫 / オートファジー / Optineurin / 神経変性疾患
Except Principal Investigator
遺伝性脊髄小脳変性症 … More / 神経科学 / 遺伝子 / 脳神経疾患 / Ca チャンネル / 脊髄小脳変性症 Less
  • Research Projects

    (3 results)
  • Research Products

    (2 results)
  • Co-Researchers

    (8 People)
  •  筋萎縮性側索硬化症原因遺伝子OPTNによる自然免疫系における役割Principal Investigator

    • Principal Investigator
      大澤 亮介
    • Project Period (FY)
      2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52020:Neurology-related
    • Research Institution
      Hiroshima University
  •  Study of cerebellum disturbance by genetic approaches

    • Principal Investigator
      Kawakami Hideshi
    • Project Period (FY)
      2014 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Basic / Social brain science
    • Research Institution
      Hiroshima University
  •  Identification of molecular mechanism underlying ALS pathogenesis by Optineurin mutationPrincipal Investigator

    • Principal Investigator
      Ohsawa Ryosuke
    • Project Period (FY)
      2014 – 2015
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Nerve anatomy/Neuropathology
    • Research Institution
      Hiroshima University

All 2015 2014

All Journal Article

  • [Journal Article] A mutation in the low voltage -gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia.2015

    • Author(s)
      Morino H., Matsuda Y., Muguruma K., Miyamoto R., Ohsawa R., Ohtake T., Otobe R., Watanabe M., Maruyama H., Hashimoto K., Kawakami H.
    • Journal Title

      Molecular Brain

      Volume: 8 Issue: 1 Pages: 1-9

    • DOI

      10.1186/s13041-015-0180-4

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K07089, KAKENHI-PROJECT-15K15083, KAKENHI-PLANNED-23111008, KAKENHI-PLANNED-25117006, KAKENHI-PROJECT-24220007, KAKENHI-PROJECT-26293211, KAKENHI-PROJECT-26242085
  • [Journal Article] Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features.2014

    • Author(s)
      Morino H
    • Journal Title

      Neurology

      Volume: 83 Issue: 22 Pages: 2054-2061

    • DOI

      10.1212/wnl.0000000000001036

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PLANNED-23111008, KAKENHI-PROJECT-26242085, KAKENHI-PROJECT-26293211
  • 1.  Kawakami Hideshi (70253060)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 2.  森野 豊之 (10397953)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 3.  福士 雅也 (50313515)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 4.  山本 卓 (90244102)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 5.  丸山 博文 (90304443)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  外丸 祐介 (90309352)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  平木 啓子 (10455397)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 8.  六車 恵子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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