Sato Shigeru 佐藤茂

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

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

Sato Shigeru 佐藤 茂

Research Projects

Research Products

Co-Researchers

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

Project Period (FY)

Research Category

Review Section

Research Institution

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

Project Period (FY)

Research Category

Review Section

Research Institution

ヒトオルガノイドを用いた器官発生の網羅的検討

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Polygenic Factors in AMD

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Identification of novel causative genes for retinitis pigmentosa - Utilizing data from whole exome analysis of affected patientsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

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

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Extensive Macular Atrophy with Pseudodrusen in a Japanese Patient Evaluated by Wide-Field OCTA2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa.2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel mutation identified in Leber congenital amaurosis - a case report2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Eleven-year follow-up of a Japanese retinitis pigmentosa patient with an HK1 gene mutation.2019

Author(s)

Journal Title

DOI

Data Source

[Presentation] Genetic diagnosis and identification of new candidate causative genes of retinitis pigmentosa by whole exsome sequencing2024

Author(s)

Organizer

Data Source

[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)

Organizer

Data Source

[Presentation] Two Japanese families of pigmented paravenous chorioretinal atrophy due to HK1 gene mutation2023

Author(s)

Organizer

Data Source

[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)

Organizer

Data Source

[Presentation] Connecting ciliaに局在する”Gelionの網膜における機能解析2023

Author(s)

Organizer

Data Source

[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

Sato Shigeru 佐藤茂

[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

[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

[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