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Yatsuka Hiroyuki  八塚 洋之

ORCIDConnect your ORCID iD *help
Researcher Number 00812299
Other IDs
Affiliation (Current) 2026: 大分大学, 医学部, 客員研究員
Affiliation (based on the past Project Information) *help 2024: 大分大学, 医学部, 客員研究員
2021 – 2023: 大分大学, 医学部, 助教
2020: 大分大学, 医学部, 医員
Review Section/Research Field
Principal Investigator
Basic Section 56060:Ophthalmology-related
Keywords
Principal Investigator
RNAエキソソーム / 神経変性疾患 / ゼブラフィッシュ / 遺伝子改変 / 網膜色素変性症 / 遺伝性網膜変性症 / 疾患動物モデル / ラパマイシン / 網膜電図 / 背地適応 / 網膜
  • Research Projects

    (2 results)
  • Research Products

    (6 results)
  • Co-Researchers

    (1 People)
  •  RNA代謝異常による遺伝性網膜変性症の疾患モデル作製と網膜機能解析Principal Investigator

    • Principal Investigator
      八塚 洋之
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      Oita University
  •  Development of a disease model of hereditary retinal degeneration caused by abnormal RNA metabolism and elucidation of the pathogenic mechanismPrincipal Investigator

    • Principal Investigator
      Yatsuka Hiroyuki
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      Oita University

All 2025 2024 2022 2020

All Journal Article Presentation

  • [Journal Article] Exosc2 deficiency leads to developmental disorders by causing a nucleotide pool imbalance in zebrafish2020

    • Author(s)
      Yatsuka Hiroyuki、Hada Kazumasa、Shiraishi Hiroshi、Umeda Ryohei、Morisaki Ikuko、Urushibata Hirotaro、Shimizu Nobuyuki、Sebastian Wulan Apridita、Hikida Takatoshi、Ishitani Tohru、Hanada Reiko、Shimada Tatsuo、Kimoto Kenichi、Kubota Toshiaki、Hanada Toshikatsu
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 533 Issue: 4 Pages: 1470-1476

    • DOI

      10.1016/j.bbrc.2020.10.044

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K21502, KAKENHI-PROJECT-20K18348, KAKENHI-PLANNED-16H06568, KAKENHI-PROJECT-19H03412, KAKENHI-PROJECT-20H03644, KAKENHI-PROJECT-18K06963, KAKENHI-PROJECT-18K08522, KAKENHI-PUBLICLY-20H05365, KAKENHI-PROJECT-18H02542
  • [Presentation] Functional Analysis of a Novel SLC45A2 Mutation (c.208T>C) in Oculocutaneous Albinism Type 42025

    • Author(s)
      漆畑 博太郎, 清水 誠之, 八塚 洋之, 井上 真紀, 白石 裕士, 井原 健二, 花田 俊勝 (大分大学)
    • Organizer
      第130回日本解剖学会・第102回日本生理学会・第98回日本薬理学会 合同大会
    • Data Source
      KAKENHI-PROJECT-23K15910
  • [Presentation] SLC45A2の新規遺伝子変異(c.208T>c)は優性遺伝型の眼皮膚白皮症4型の原因となる2024

    • Author(s)
      漆畑博太郎, 清水誠之, 八塚洋之, 井上真紀, 白石裕士,井原健二, 花田俊勝
    • Organizer
      第47回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-23K15910
  • [Presentation] RNAエキソソーム関連神経変性疾患における網膜変性の病態メカニズムの解明2022

    • Author(s)
      八塚 洋之
    • Organizer
      第61回日本網膜硝子体学会総会
    • Data Source
      KAKENHI-PROJECT-20K18348
  • [Presentation] Molecular mechanism of RNA exosome related diseases of zebrafish disease model2020

    • Author(s)
      八塚 洋之
    • Organizer
      第93回日本生化学会大会
    • Data Source
      KAKENHI-PROJECT-20K18348
  • [Presentation] RNA代謝異常による神経変性疾患モデル作製と発症機序の解明2020

    • Author(s)
      八塚 洋之
    • Organizer
      第97回日本生理学会大会
    • Data Source
      KAKENHI-PROJECT-20K18348
  • 1.  石谷 太
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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