Kato Yoichi 加藤洋一

Researcher Number	10815161
Other IDs
Affiliation (Current)	2023: 名古屋市立大学, 医薬学総合研究院(医学), 教授
Affiliation (based on the past Project Information) *help	2019 – 2022: 名古屋市立大学, 医薬学総合研究院(医学), 教授 2018: 名古屋市立大学, 大学院医学研究科, 教授
Review Section/Research Field	Principal Investigator 0702:Biology at cellular to organismal levels, and related fields / Medium-sized Section 52:General internal medicine and related fields Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
Keywords	Principal Investigator 繊毛 / アフリカツメガエル / TGF-beta / 発生生物学 / TGF-betaシグナル / ジュベール症候群関連疾患 / VUS Except Principal Investigator 巨脳症 / オルガノイド / 脳オルガノイド … More / iPS細胞 / 神経発生 / 尿路結石 / オートファジー / オミクス解析 / ゲノム創薬 Less

生体内免疫応答と修復機構の統合的解析による尿路結石の病態解明と溶解療法への展開
- Principal Investigator
  
  安井孝周
- Project Period (FY)
  2022 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
- Research Institution
  Nagoya City University
ジュベール症候群関連疾患の遺伝子診断のためのVUSの病因性スクリーニング法の開発Principal Investigator
- Principal Investigator
  
  加藤洋一
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Nagoya City University
Uncover pathomechanism of megalencephaly using brain organdies.
- Principal Investigator
  
  齋藤伸治
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University
The molecular mechanism of ciliogenesis controlled by TGF-beta signalingPrincipal Investigator
- Principal Investigator
  
  Kato Yoichi
- Project Period (FY)
  2019
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Review Section
  
  0702:Biology at cellular to organismal levels, and related fields
- Research Institution
  Nagoya City University

All 2022 2021 2020 2019

All Journal Article Presentation

[Journal Article] Four pedigrees with aminoacyl-tRNA synthetase abnormalities2022
- Author(s)
  Okamoto Nobuhiko、Miya Fuyuki、Tsunoda Tatsuhiko、Kanemura Yonehiro、Saitoh Shinji、Kato Mitsuhiro、Yanagi Kumiko、Kaname Tadashi、Kosaki Kenjiro
- Journal Title
  
  Neurol Sci
  
  Volume: 43 Pages: 2765-2774
- DOI
  10.1007/s10072-021-05626-z
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-20K09916
[Journal Article] A novel missense variant in CUL3 shows altered binding ability to BTB-adaptor proteins leading to diverse phenotypes of CUL3-related disorders2021
- Author(s)
  Kato Kohji、Miya Fuyuki、Oka Yasuyoshi、Mizuno Seiji、Saitoh Shinji
- Journal Title
  
  J Hum Genet.
  
  Volume: 66 Pages: 491-498
- DOI
  10.1038/s10038-020-00868-9
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K21583, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-18H03372, KAKENHI-PROJECT-20K16897, KAKENHI-PROJECT-19K23823
[Journal Article] Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability2021
- Author(s)
  Okamoto Nobuhiko、Miya Fuyuki、Kitai Yukihiro、Tsunoda Tatsuhiko、Kato Mitsuhiro、Saitoh Shinji、Kanemura Yonehiro、Kosaki Kenjiro
- Journal Title
  
  Neurol Sci
  
  Volume: - Pages: 2975-2978
- DOI
  10.1007/s10072-021-05152-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K21583, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-20H03646
[Presentation] VPS35L pathogenic variants cause 3C/Ritscher-Scinzel-like syndrome: Description of two novel cases confirming the pathogenicity and clinical diversity.2021
- Author(s)
  Otsuji S, Kato K, Lequesne CH, Mizuno S, Rio M, Miyatake S, Nishio Y, Matsumoto N, Cormier-Daire V, Saitoh
- Organizer
  American Society of Human Genetics Virtual Meeting 2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] ミトコンドリアホスホリパーゼPNPLA8機能喪失は神経系細胞においてミトコンドリアダイナミクス異常を引き起こす.2021
- Author(s)
  中村勇治、嶋田逸誠、加藤洋一、齋藤伸治
- Organizer
  第66回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] MYCN gain-of-function variants induce excess proliferation of neurons and cause a novel megalencephaly syndrome.2021
- Author(s)
  Yosuke Nishio, Kohji Kato, Tran Mau-Them Frederic, Shiomi Otsuji, Chloe Quelin, Hisashi Oishi, Yoshiyuki Takahashi, Shinji Saitoh
- Organizer
  American Society of Human Genetics Virtual Meeting 2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] PNPLA8 deficiency induces microcephaly and reduces neurogenesis in a brain organoid model.2021
- Author(s)
  Nakamura Y, Shimada I, Fujimoto M, Sato E, Ieda D, Hattori A, Miya F, Tsunoda T, Okubo Y, Haginoya K, Koshimizu E, Miyatake S, Matsumoto N, Arioka Y, Ozaki N, Kato Y, Saitoh S
- Organizer
  第63回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] A novel case with biallelic VPS35L variants confirms VPS35L as a causative gene of 3C/Ritscher-Schinzel-like syndrome.2020
- Author(s)
  Shiomi Otsuji, Kohji Kato, Seiji Mizuno, Satoko Miyatake, Naomichi Matsumoto, Shinji Saitoh
- Organizer
  第65回人類遺伝学会
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] TGF-beta シグナルに制御される繊毛形成の機序の解明2019
- Author(s)
  加藤洋一
- Organizer
  繊毛研究会
- Data Source
  KAKENHI-PROJECT-19K21193

1. 二宮裕將 (40514237)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
2. 伊藤雅之 (50243407)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 齋藤伸治 (00281824)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. 嶋田逸誠 (40833265)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. 宮冬樹 (50415311)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
7. 安井孝周 (40326153)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 田口和己 (00595184)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 安藤亮介 (30381867)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 海野怜 (40755683)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. 岡田淳志 (70444966)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 杉野輝明 (70881746)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 濱本周造 (80551267)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 松永民秀 (40209581)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 郡健二郎 (30122047)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 8 results
17. 要匡

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 柳久美子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 岡泰由

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kato Yoichi 加藤 洋一

Research Projects

Research Products

Co-Researchers

生体内免疫応答と修復機構の統合的解析による尿路結石の病態解明と溶解療法への展開

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

ジュベール症候群関連疾患の遺伝子診断のためのVUSの病因性スクリーニング法の開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Uncover pathomechanism of megalencephaly using brain organdies.

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The molecular mechanism of ciliogenesis controlled by TGF-beta signalingPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Four pedigrees with aminoacyl-tRNA synthetase abnormalities2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A novel missense variant in CUL3 shows altered binding ability to BTB-adaptor proteins leading to diverse phenotypes of CUL3-related disorders2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability2021

Author(s)

Journal Title

DOI

Data Source

[Presentation] VPS35L pathogenic variants cause 3C/Ritscher-Scinzel-like syndrome: Description of two novel cases confirming the pathogenicity and clinical diversity.2021

Author(s)

Organizer

Data Source

[Presentation] ミトコンドリアホスホリパーゼPNPLA8機能喪失は神経系細胞においてミトコンドリアダイナミクス異 常を引き起こす.2021

Author(s)

Organizer

Data Source

[Presentation] MYCN gain-of-function variants induce excess proliferation of neurons and cause a novel megalencephaly syndrome.2021

Author(s)

Organizer

Data Source

[Presentation] PNPLA8 deficiency induces microcephaly and reduces neurogenesis in a brain organoid model.2021

Author(s)

Organizer

Data Source

[Presentation] A novel case with biallelic VPS35L variants confirms VPS35L as a causative gene of 3C/Ritscher-Schinzel-like syndrome.2020

Author(s)

Organizer

Data Source

[Presentation] TGF-beta シグナルに制御される繊毛形成の機序の解明2019

Author(s)

Organizer

Data Source

Kato Yoichi 加藤洋一

[Presentation] ミトコンドリアホスホリパーゼPNPLA8機能喪失は神経系細胞においてミトコンドリアダイナミクス異常を引き起こす.2021