Kato Yoichi 加藤洋一

Researcher Number	10815161
Other IDs
Affiliation (Current)	2025: 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 – 2025: 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 Medium-sized Section 52:General internal medicine and related fields / 0702:Biology at cellular to organismal levels, and related fields Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Basic Section 52040:Radiological sciences-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
Keywords	Principal Investigator アフリカツメガエル / 繊毛 / VUS / ジュベール症候群関連疾患 / TGF-betaシグナル / 発生生物学 / TGF-beta Except Principal Investigator 巨脳症 / 難治性脳腫瘍 / 陽子線 … More / 超高線量率照射 / FLASH / ゲノム創薬 / オミクス解析 / オートファジー / 尿路結石 / iPS細胞 / オルガノイド / 神経幹細胞 / 外側放射状グリア / 神経発生 / 脳オルガノイド Less

陽子線 FLASH 照射による難治性脳腫瘍根絶へ向けた開発
- Principal Investigator
  
  岩田宏満
- Project Period (FY)
  2024 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52040:Radiological sciences-related
- Research Institution
  Nagoya City University
Integrative approach for mechanism of megalencephaly
- Principal Investigator
  
  齋藤伸治
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University
Elucidation of the pathophysiology of urolithiasis and development to dissolution therapy by integrative analysis of immune response and repair mechanisms in vivo
- 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 – 2024
- 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
  
  Saitoh Shinji
- 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)
  2018 – 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 2024 2023 2022 2021 2020 2019

All Journal Article Presentation

[Journal Article] Phagocytosis model of calcium oxalate monohydrate crystals generated using human induced pluripotent stem cell-derived macrophages2024
- Author(s)
  Okada Tomoki、Okada Atsushi、Aoki Hiromasa、Onozato Daichi、Kato Taiki、Takase Hiroshi、Ohshima Shigeru、Sugino Teruaki、Unno Rei、Taguchi Kazumi、Hamamoto Shuzo、Ando Ryosuke、Shimada Issei S.、Hashita Tadahiro、Iwao Takahiro、Matsunaga Tamihide、Yasui Takahiro
- Journal Title
  
  Urolithiasis
  
  Volume: 52 Issue: 1 Pages: 51-51
- DOI
  10.1007/s00240-024-01553-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K09562, KAKENHI-PROJECT-20K18149, KAKENHI-PROJECT-22H00486, KAKENHI-PROJECT-23K27730
[Journal Article] Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome2023
- Author(s)
  Nishio Yosuke、Kato Kohji、Tran Mau-Them Frederic、Futagawa Hiroshi、Quelin Chloe、Masuda Saori、Vitobello Antonio、Otsuji Shiomi、Shawki Hossam H.、Oishi Hisashi、Thauvin-Robinet Christel、Takenouchi Toshiki、Kosaki Kenjiro、Takahashi Yoshiyuki、Saitoh Shinji
- Journal Title
  
  Human Genetics and Genomics Advances
  
  Volume: 4 Issue: 4 Pages: 100238-100238
- DOI
  10.1016/j.xhgg.2023.100238
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K14945, KAKENHI-PROJECT-23KJ1817, KAKENHI-PROJECT-23K05601, KAKENHI-PROJECT-20H03646
[Journal Article] Utility of tissue-specific gene expression scores for gene prioritization in Mendelian diseases2022
- Author(s)
  Kato Daiki、Mitsuhashi Satomi、Miya Fuyuki、Saitoh Shinji、Okamoto Nobuhiko、Tsunoda Tatsuhiko、Kochi Yuta
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 67 Issue: 12 Pages: 739-742
- DOI
  10.1038/s10038-022-01071-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-21K19501
[Journal Article] Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome2022
- Author(s)
  Otsuji Shiomi、Nishio Yosuke、Tsujita Maki、Rio Marlene、Huber Celine、Anton-Plagaro Carlos、Mizuno Seiji、Kawano Yoshihiko、Miyatake Satoko、Simon Marleen、van Binsbergen Ellen、van Jaarsveld Richard H、Matsumoto Naomichi、Cormier-Daire Valerie、J.Cullen Peter、Saitoh Shinji、Kato Kohji
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 60 Issue: 4 Pages: 359-367
- DOI
  10.1136/jmg-2022-108602
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08631, KAKENHI-PROJECT-19K23823, KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-20K16897, KAKENHI-PROJECT-23K14945, KAKENHI-PROJECT-23KJ1817, KAKENHI-PROJECT-23K27520
[Journal Article] Four pedigrees with aminoacyl-tRNA synthetase abnormalities2021
- Author(s)
  Okamoto Nobuhiko、Miya Fuyuki、Tsunoda Tatsuhiko、Kanemura Yonehiro、Saitoh Shinji、Kato Mitsuhiro、Yanagi Kumiko、Kaname Tadashi、Kosaki Kenjiro
- Journal Title
  
  Neurological Sciences
  
  Volume: 43 Issue: 4 Pages: 2765-2774
- DOI
  10.1007/s10072-021-05626-z
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H03646, KAKENHI-PROJECT-20K09916
[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
  
  Neurological Sciences
  
  Volume: - Issue: 7 Pages: 2975-2978
- DOI
  10.1007/s10072-021-05152-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K21583, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-20H03646
[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
  
  Journal of Human Genetics
  
  Volume: 66 Issue: 5 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
[Presentation] Gain-of-function MYCN causes a megalencephaly- polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.2023
- Author(s)
  Nishio Y, Kato K, Mau-Them Frederic T, Futagawa H, Quelin C, Masuda S, Vitobello A, Otsuji S, Shawki HH, Oishi H, Thauvin-Robinet C, Takenouchi T, Kosaki K, Takahashi Y, Saitoh S.
- Organizer
  American Society of Human Genetics 2023 meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] Gain-of-function MYCN causes a megalencephaly- polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.2023
- Author(s)
  Nishio Y, Kato K, Mau-Them Frederic T, Futagawa H, Quelin C, Masuda S, Vitobello A, Otsuji S, Shawki HH, Oishi H, Thauvin-Robinet C, Takenouchi T, Kosaki K, Takahashi Y, Saitoh S.
- Organizer
  Asian Society of Pediatric Research 2023 meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] The complex of LARP6 and DNAAF6 in membrane-loss compartments controls the expression of α-tubulin protein in differentiation of multi-ciliated cells2023
- Author(s)
  加藤洋一
- Organizer
  CPH Cilia and Centrosome
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K21584
[Presentation] Discovery of drugs that promote the phagocytic ability of macrophages to calcium oxalate crystals using the FDA-approved Drug Library2022
- Author(s)
  Okada　Atsushi, Takase Hiroshi, Isogai Masahiko, Okada Tomoki, Hattori Tatsuya, Chaya Ryosuke, Kawase Kengo, Tanaka Yutaro, Kato Taiki, Sugino Teruaki, Unno Rei, Taguchi Kazumi, Hamamoto Shuzo, Ando Ryosuke, Hashita Tadahiro, Tozawa Keiichi, Matsunaga Tamihide, Kohri Kenjiro, Yasui Takahiro
- Organizer
  American Urological Association Annual Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22H00486
[Presentation] The complex of LARP6 and DNAAF6 in membrane-loss compartments controls the expression of α-tubulin protein in differentiation of multi-ciliated cells2022
- Author(s)
  加藤洋一
- Organizer
  Cold Spring Harbor Asia Cilia and Centrosome Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K21584
[Presentation] 繊毛形成におけるRNA結合タンパクLARP6の役割2022
- Author(s)
  加藤洋一
- Organizer
  日本分子生物学会
- Data Source
  KAKENHI-PROJECT-20K21584
[Presentation] Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome.2022
- Author(s)
  Otsuji S, Nishio Y, Tsujita M, Rio M, Huber C, Anton-Plagaro C, Mizuno S, Kawano Y, Miyatake S, Simon M, van Binsbergen E, van Jaarsveld RH, Matsumoto N, Cormier-Daire V, J Cullen P, Saitoh S, Kato K
- Organizer
  American Society of Human Genetics Annual Meeting 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20H03646
[Presentation] Biallelic variants in PNPLA8 disrupt cortical gyrification through aberrant mitochondrial dynamics.2022
- Author(s)
  Nakamura Y, Shimada IS, 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64回日本小児神経学会学術集会
- 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] 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] 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] 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. 嶋田逸誠 (40833265)

# of Collaborated Projects: 3 results

# of Collaborated Products: 3 results
2. Saitoh Shinji (00281824)

# of Collaborated Projects: 2 results

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

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
4. 二宮裕將 (40514237)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 宮冬樹 (50415311)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
8. 田口和己 (00595184)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. 郡健二郎 (30122047)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. 安藤亮介 (30381867)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
11. 松永民秀 (40209581)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
12. 海野怜 (40755683)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
13. 岡田淳志 (70444966)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
14. 杉野輝明 (70881746)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
15. 濱本周造 (80551267)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
16. 岩田宏満 (40611588)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 柴田泰宏 (10534745)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 鵜川眞也 (20326135)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 粂和彦 (30251218)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 歳藤利行 (30377965)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 冨田淳 (40432231)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. 荻野浩幸 (60315885)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. 平山亮一 (90435701)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. 有岡祐子 (10709497)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. 永田浩一 (50252143)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 13 results
27. 加藤耕治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 辻田麻紀

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kato Yoichi 加藤 洋一

Research Projects

Research Products

Co-Researchers

陽子線 FLASH 照射による難治性脳腫瘍根絶へ向けた開発

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Integrative approach for mechanism of megalencephaly

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of the pathophysiology of urolithiasis and development to dissolution therapy by integrative analysis of immune response and repair mechanisms in vivo

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] Phagocytosis model of calcium oxalate monohydrate crystals generated using human induced pluripotent stem cell-derived macrophages2024

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Utility of tissue-specific gene expression scores for gene prioritization in Mendelian diseases2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Four pedigrees with aminoacyl-tRNA synthetase abnormalities2021

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

[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

[Presentation] Gain-of-function MYCN causes a megalencephaly- polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.2023

Author(s)

Organizer

Data Source

[Presentation] Gain-of-function MYCN causes a megalencephaly- polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.2023

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