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Sato Shigeru  佐藤 茂

ORCIDConnect your ORCID iD *help
Researcher Number 70738525
Other IDs
Affiliation (Current) 2025: 大阪大学, 大学院 医学系研究科, 准教授
Affiliation (based on the past Project Information) *help 2025: 大阪大学, 大学院 医学系研究科, 准教授
2021 – 2024: 大阪大学, 大学院医学系研究科, 准教授
2019 – 2022: 大阪大学, 医学系研究科, 准教授
Review Section/Research Field
Principal Investigator
Basic Section 56060:Ophthalmology-related
Except Principal Investigator
Basic Section 56060:Ophthalmology-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
Keywords
Principal Investigator
網膜色素変性症 / 黄斑ジストロフィー / 全エクソーム解析 / 遺伝性網膜変性症 / 新規原因遺伝子 / 網羅的遺伝子解析 / 遺伝的異質性 / ゼブラフィッシュ / 網膜色素変性 / 全エクソームシーケンス … More
Except Principal Investigator
… More ヒトiPS細胞 / 眼分化 / iPS細胞 / オルガノイド / ゼブラフィッシュ / 疾患感受性変異 / 再生医療 / ゲノム / 加齢黄斑変性 / 眼科学 / 器官発生 Less
  • Research Projects

    (5 results)
  • Research Products

    (20 results)
  • Co-Researchers

    (6 People)
  •  遺伝性網膜変性症の新規遺伝子の同定―遺伝子ノックアウト動物を利用して―Principal Investigator

    • Principal Investigator
      佐藤 茂
    • Project Period (FY)
      2025 – 2027
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      The University of Osaka
  •  遺伝性網膜変性症の新規原因遺伝子の同定とその網膜変性の分子機序の解明Principal Investigator

    • Principal Investigator
      佐藤 茂
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      Osaka University
  •  ヒトオルガノイドを用いた器官発生の網羅的検討

    • Principal Investigator
      辻川 元一
    • Project Period (FY)
      2021 – 2024
    • Research Category
      Grant-in-Aid for Challenging Research (Exploratory)
    • Review Section
      Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
    • Research Institution
      Osaka University
  •  Polygenic Factors in AMD

    • Principal Investigator
      辻川 元一
    • Project Period (FY)
      2021 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      Osaka University
  •  Identification of novel causative genes for retinitis pigmentosa - Utilizing data from whole exome analysis of affected patientsPrincipal Investigator

    • Principal Investigator
      Sato Shigeru
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 56060:Ophthalmology-related
    • Research Institution
      Osaka University

All 2024 2023 2022 2021 2020 2019

All Journal Article Presentation

  • [Journal Article] Two Japanese Families with Pigmented Paravenous Retinochoroidal Atrophy and HK1 Mutation: A Case Report2024

    • Author(s)
      Sato Shigeru、Morimoto Takeshi、Fujikado Takashi、Tanaka Sayaka、Sai Sou、Tsujikawa Motokazu、Nishida Kohji
    • Journal Title

      Case Reports in Ophthalmology

      Volume: 15 Issue: 1 Pages: 8-14

    • DOI

      10.1159/000534237

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Journal Article] Extensive Macular Atrophy with Pseudodrusen in a Japanese Patient Evaluated by Wide-Field OCTA2022

    • Author(s)
      Sato Shigeru、Morimoto Takeshi、Fujikado Takashi、Tanaka Sayaka、Tsujikawa Motokazu、Nishida Kohji
    • Journal Title

      Case Reports in Ophthalmology

      Volume: 13 Issue: 3 Pages: 847-854

    • DOI

      10.1159/000526970

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K19616, KAKENHI-PROJECT-23K21480, KAKENHI-PROJECT-21K19570
  • [Journal Article] A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa.2021

    • Author(s)
      Nishiguchi KM, Miya F, Mori Y, Fujita K, Akiyama M, Kamatani T, Koyanagi Y, Sato K, Takigawa T, Ueno S, Tsugita M, Kunikata H, Cisarova K, Nishino J, Murakami A, Abe T, Momozawa Y, Terasaki H, Wada Y, Sonoda KH, Rivolta C, Tsunoda T, Tsujikawa M, Ikeda Y, Nakazawa T.
    • Journal Title

      Commun Biol

      Volume: 4 Issue: 1 Pages: 140-140

    • DOI

      10.1038/s42003-021-01662-9

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K09989, KAKENHI-PROJECT-17K11448, KAKENHI-PROJECT-20K09765, KAKENHI-PROJECT-21K19570
  • [Journal Article] Novel mutation identified in Leber congenital amaurosis - a case report2020

    • Author(s)
      Sato Shigeru、Morimoto Takeshi、Tanaka Sayaka、Hotta Kikuko、Fujikado Takashi、Tsujikawa Motokazu、Nishida Kohji
    • Journal Title

      BMC Ophthalmology

      Volume: 20 Issue: 1 Pages: 313-313

    • DOI

      10.1186/s12886-020-01577-9

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08979, KAKENHI-PROJECT-19K09992, KAKENHI-PROJECT-18K19616, KAKENHI-PROJECT-18H04116, KAKENHI-PROJECT-19H01063, KAKENHI-PROJECT-17K11448
  • [Journal Article] Eleven-year follow-up of a Japanese retinitis pigmentosa patient with an HK1 gene mutation.2019

    • Author(s)
      Sato S, Morimoto T, Hotta K, Fujikado T, Nishida K
    • Journal Title

      Ophthalmic Genet.

      Volume: 40 Issue: 5 Pages: 466-469

    • DOI

      10.1080/13816810.2019.1678179

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19K08979, KAKENHI-PROJECT-19K09992, KAKENHI-PROJECT-18K19616, KAKENHI-PROJECT-16H05487, KAKENHI-PROJECT-19H01063
  • [Presentation] Genetic diagnosis and identification of new candidate causative genes of retinitis pigmentosa by whole exsome sequencing2024

    • Author(s)
      佐藤茂、森本壮、不二門尚、田中さやか、辻川元一、西田幸二
    • Organizer
      ARVO
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 遺伝性網膜変性症の新規原因遺伝子の同定-Meowth1の検討2023

    • Author(s)
      上中知帆、佐藤茂、新井悠之介、立野琢巳、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] Two Japanese families of pigmented paravenous chorioretinal atrophy due to HK1 gene mutation2023

    • Author(s)
      佐藤茂、森本壮、不二門尚、田中さやか、辻川元一、西田幸二
    • Organizer
      ARVO
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜色素変性症79の発症機序解明を目指した疾患モデル動物の作製2023

    • Author(s)
      立野琢巳、佐藤茂、 新井悠之、上中知帆、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム2023年度成果発表会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] Connecting ciliaに局在する”Gelionの網膜における機能解析2023

    • Author(s)
      立野琢巳、佐藤茂、新井悠之、上中知帆、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] Evanは遺伝性網膜ジストロフィの新規原因遺伝子候補である2023

    • Author(s)
      新井悠之介、佐藤茂、上中知帆、立野琢巳、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] Meowth1 遺伝子の役割 遺伝性網膜変性症の新規原因遺伝子の可能性2023

    • Author(s)
      上中知帆、佐藤茂、新井悠之介、立野琢巳、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム2023年度成果発表会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜色素変性症の新規原因候補遺伝子としてのGelion遺伝子の機能解析2023

    • Author(s)
      立野琢己、佐藤茂、新井悠之介、上中知帆、辻川元一
    • Organizer
      遺伝子改変動物作成支援成果発表会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜におけるMeowth1遺伝子の解析2023

    • Author(s)
      上中知帆、佐藤茂、新井悠之介、立野琢己、辻川元一
    • Organizer
      遺伝子改変動物作成支援成果発表会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜色素変性症の新規原因遺伝子の 同定に向けたGelion遺伝子の解析2022

    • Author(s)
      立野琢己、佐藤茂、新井悠之介、上中知帆、、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム2022年度若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜におけるMeowth1遺伝子の解析2022

    • Author(s)
      上中知帆、佐藤茂、新井悠之介、立野琢己、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム2022年度若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 網膜における遺伝子Evan の解析2022

    • Author(s)
      新井悠之介、佐藤茂、上中知帆、立野琢己 、辻川元一
    • Organizer
      先端モデル動物作成支援プラットフォーム2022年度若手支援技術講習会
    • Data Source
      KAKENHI-PROJECT-22K09833
  • [Presentation] 27-year follow-up of Japanese siblings with juvenile cone rod dystrophy 13 due to a novel RPGRIP1 gene mutation2020

    • Author(s)
      Shigeru Sato, Takeshi Morimoto, Kikuko Hotta, Motokazu Tsujikawa, Takashi Fujikado, Kohji Nishida
    • Organizer
      ARVO(米国)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K09992
  • [Presentation] Novel OPA1 gene mutations in Japanese patients with optic atrophy2019

    • Author(s)
      Shigeru Sato, Noriyasu Hashida, Takeshi Morimoto, Kikuko Hotta, Takashi Fujikado , Kohji Nishida
    • Organizer
      ARVO(米国)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K09992
  • [Presentation] TTC8遺伝子に新規コンパウンドヘテロ変異を認めた 日本人Bardet-Biedl症候群の1例2019

    • Author(s)
      佐藤茂、森本壮、堀田紀久子、不二門尚、西田幸二
    • Organizer
      第64回日本人類遺伝学学会
    • Data Source
      KAKENHI-PROJECT-19K09992
  • 1.  辻川 元一 (70419472)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 13 results
  • 2.  不二門 尚 (50243233)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 7 results
  • 3.  秋山 雅人 (10757686)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 4.  UENO Shinji
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 5.  HOTTA Kikuko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 6.  寺崎 浩子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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