NEGISHI YUTAKA 根岸豊

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Yutaka Negishi 根岸豊

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Researcher Number	40798344
Other IDs
Affiliation (Current)	2025: 名古屋市立大学, 医薬学総合研究院(医学), 助教
Affiliation (based on the past Project Information) *help	2022 – 2024: 名古屋市立大学, 医薬学総合研究院(医学), 助教 2019 – 2021: 名古屋市立大学, 医薬学総合研究院(医学), 研究員 2018: 名古屋市立大学, 大学院医学研究科, 研究員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator モデルマウス / Schaaf-Yang症候群 / 脳オルガノイド / 脳形成障害 / リン脂質 / PNPLA8 / 急性脳症 / MAGEL2遺伝子 / CRISPER/Cas9 / Prader-Willi症候群 / CRISPR/Cas9 / MAGEL2

PNPLA関連神経変性疾患の発症メカニズム解明と治療法開発Principal Investigator
- Principal Investigator
  
  根岸豊
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University
Schaaf-Yang症候群に伴う脳症様症状の発症メカニズム解明と治療法開発Principal Investigator
- Principal Investigator
  
  根岸豊
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University
Analyses of the onset mechanism of Schaaf-Yang syndromePrincipal Investigator
- Principal Investigator
  
  Yutaka Negishi
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University

All 2023 2022 2021 2020 2019 2018

All Journal Article Presentation

[Journal Article] A nationwide survey of Schaaf-Yang syndrome in Japan2022
- Author(s)
  Negishi Yutaka、Kurosawa Kenji、Takano Kyoko、Matsubara Keiko、Nishiyama Takeshi、Saitoh Shinji
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 67 Issue: 12 Pages: 735-738
- DOI
  10.1038/s10038-022-01089-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K15885
[Journal Article] SCN8A-related developmental and epileptic encephalopathy with ictal asystole requiring cardiac pacemaker implantation2021
- Author(s)
  Negishi Yutaka、Aoki Yusuke、Itomi Kazuya、Yasuda Kazushi、Taniguchi Hiroaki、Ishida Atsushi、Arakawa Takeshi、Miyamoto Sachiko、Nakashima Mitsuko、Saitsu Hirotomo、Saitoh Shinji
- Journal Title
  
  Brain and Development
  
  Volume: 43 Issue: 7 Pages: 804-808
- DOI
  10.1016/j.braindev.2021.03.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H03641, KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-21K15885
[Journal Article] Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes2020
- Author(s)
  Ieda Daisuke、Negishi Yutaka、Miyamoto Tomomi、Johmura Yoshikazu、Kumamoto Natsuko、Kato Kohji、Miyoshi Ichiro、Nakanishi Makoto、Ugawa Shinya、Oishi Hisashi、Saitoh Shinji
- Journal Title
  
  PLOS ONE
  
  Volume: 15 Issue: 8 Pages: e0237814-e0237814
- DOI
  10.1371/journal.pone.0237814
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K21497, KAKENHI-PROJECT-20K21583, KAKENHI-ORGANIZER-19H05739, KAKENHI-PLANNED-19H05740, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-18K15682
[Journal Article] Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy2019
- Author(s)
  Negishi Yutaka、Ieda Daisuke、Hori Ikumi、Nozaki Yasuyuki、Yamagata Takanori、Komaki Hirofumi、Tohyama Jun、Nagasaki Keisuke、Tada Hiroko、Saitoh Shinji
- Journal Title
  
  Orphanet Journal of Rare Diseases
  
  Volume: 14 Issue: 1 Pages: 277-277
- DOI
  10.1186/s13023-019-1249-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08258, KAKENHI-PROJECT-18K15682, KAKENHI-PROJECT-18K19524
[Presentation] Schaaf-Yang 症候群は小児内分泌科医も知っておくべき疾患である～本邦の全国疫学調査から～2023
- Author(s)
  松原圭子、根岸豊、黒澤健司、高野亨子、西山毅、齋藤伸治
- Organizer
  第56回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-21K15885
[Presentation] Schaaf-Yang症候群の全国疫学調査2022
- Author(s)
  根岸豊, 黒澤健司, 高野亨子, 松原圭子, 西山毅, 齋藤伸治
- Organizer
  第64回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-21K15885
[Presentation] Schaaf-Yang症候群の全国疫学調査（第一報）2021
- Author(s)
  根岸豊、黒澤健司、高野亨子、松原圭子、西山毅、齋藤伸治
- Organizer
  第44回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-21K15885
[Presentation] Generation of a mouse model carrying mutation in Magel22019
- Author(s)
  Daisuke Ieda, Yutaka Negishi, Tomomi Miyamoto, Natsuko Kumamoto, Kohji Kato, Shinya Ugawa, Hisashi Oishi, Shinji Saitoh
- Organizer
  第61回日本小児神経学会学術集会　日本-台湾　新生児・小児神経ワークショップ
- Data Source
  KAKENHI-PROJECT-18K15682
[Presentation] Schaaf-Yang症候群の臨床像検討とトランスジェニックマウスを用いた病態解析2018
- Author(s)
  根岸豊, 家田大輔, 中村勇治, 堀いくみ, 服部文子, 野崎靖之, 小牧宏文, 遠山潤, 長崎啓佑, 多田弘子, 大石久史, 齋藤伸治
- Organizer
  第60回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-18K15682

1. 齋藤伸治 (00281824)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
2. 大石久史 (30375513)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 才津浩智

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
4. 山形崇倫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. 中西真

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

NEGISHI YUTAKA 根岸 豊

Yutaka Negishi 根岸 豊

Research Projects

Research Products

Co-Researchers

PNPLA関連神経変性疾患の発症メカニズム解明と治療法開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Schaaf-Yang症候群に伴う脳症様症状の発症メカニズム解明と治療法開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Analyses of the onset mechanism of Schaaf-Yang syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] A nationwide survey of Schaaf-Yang syndrome in Japan2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] SCN8A-related developmental and epileptic encephalopathy with ictal asystole requiring cardiac pacemaker implantation2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy2019

Author(s)

Journal Title

DOI

Data Source

[Presentation] Schaaf-Yang 症候群は小児内分泌科医も知っておくべき疾患である ～本邦の全国疫学調査から～2023

Author(s)

Organizer

Data Source

[Presentation] Schaaf-Yang症候群の全国疫学調査2022

Author(s)

Organizer

Data Source

[Presentation] Schaaf-Yang症候群の全国疫学調査（第一報）2021

Author(s)

Organizer

Data Source

[Presentation] Generation of a mouse model carrying mutation in Magel22019

Author(s)

Organizer

Data Source

[Presentation] Schaaf-Yang症候群の臨床像検討とトランスジェニックマウスを用いた病態解析2018

Author(s)

Organizer

Data Source

NEGISHI YUTAKA 根岸豊

Yutaka Negishi 根岸豊

[Presentation] Schaaf-Yang 症候群は小児内分泌科医も知っておくべき疾患である～本邦の全国疫学調査から～2023