Suzuki Toshimitsu 鈴木俊光

… Alternative Names

鈴木俊光スズキトシミツ

SUZUKI Toshimitsu 鈴木俊光

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Researcher Number	20373318
Other IDs
Affiliation (Current)	2025: 名古屋市立大学, 医薬学総合研究院(医学), 講師
Affiliation (based on the past Project Information) *help	2025: 名古屋市立大学, 医薬学総合研究院(医学), 講師 2020 – 2023: 名古屋市立大学, 医薬学総合研究院(医学), 講師 2019: 名古屋市立大学, 医薬学総合研究院(医学), 助教 2018: 国立研究開発法人理化学研究所, 脳神経科学研究センター, 研究員 2016 – 2017: 国立研究開発法人理化学研究所, 脳科学総合研究センター, 研究員 … More 2013 – 2014: 独立行政法人理化学研究所, 脳科学総合研究センター, 研究員 2009 – 2012: The Institute of Physical and Chemical Research, 神経遺伝研究チーム, 研究員 2008: The Institute of Physical and Chemical Research, 神経遺伝研究チーム, 基礎科学特別研究員 2006: 独立行政法人理化学研究所, 神経遺伝研究チーム, 基礎科学特別研究員 2004 – 2005: 独立行政法人理化学研究所, 神経遺伝研究チーム, リサーチアソシエイト Less
Review Section/Research Field	Principal Investigator Psychiatric science / Basic Section 52030:Psychiatry-related / Neurology
Keywords	Principal Investigator EFHC1 / てんかん / 若年性ミオクロニーてんかん / JME / マウスモデル / 統合失調症 / Nav1.2 / SCN2A / コンディショナルノックアウトマウス / 特発性てんかん … More / 若年性ミオクローヌスてんかん / 発症神経回路 / 自閉スペクトラム症 / 神経回路 / 社会性行動障害 / 神経発達症 / 若年ミオクロニーてんかん / ICK / CILK1 / myoclonin1 / 年性ミオクロニーてんかん / ＥＦＨＣ１ / IP_3レセプター / 小胞体カルシウム / IP3レセプター / 脳室拡大 / 痙攣感受性 / ミオクロニー発作 / 痙攣 / 抗体アレイ / 相互作用 / Cav2.3 / カルシウムチャネル / 6p12 Less

Research Projects
(8 results)
Research Products
(15 results)

SCN2A遺伝子変異による精神・神経疾患発症神経回路の解明Principal Investigator
- Principal Investigator
  
  鈴木俊光
- Project Period (FY)
  2025 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52030:Psychiatry-related
- Research Institution
  Nagoya City University
SCN2A遺伝子変異による社会性行動障害に関わる神経回路の解明Principal Investigator
- Principal Investigator
  
  鈴木俊光
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52030:Psychiatry-related
- Research Institution
  Nagoya City University
Elucidating the pathology of epilepsy caused by EFHC1 and CILK1 variantsPrincipal Investigator
- Principal Investigator
  
  Suzuki Toshimitsu
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52030:Psychiatry-related
- Research Institution
  Nagoya City University
Elucidating the pathology of epilepsy caused by EFHC1 mutationsPrincipal Investigator
- Principal Investigator
  
  Suzuki Toshimitsu
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Psychiatric science
- Research Institution
  Institute of Physical and Chemical Research
Characterization of Ehhc1 conditional knockout mouse and understand the pathology of epilepsyPrincipal Investigator
- Principal Investigator
  
  SUZUKI TOSHIMITSU
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Psychiatric science
- Research Institution
  The Institute of Physical and Chemical Research
Understanding the pathology of epilepsy through the regulation of endoplasmic reticulum calcium homeostasisPrincipal Investigator
- Principal Investigator
  
  SUZUKI Toshimitsu
- Project Period (FY)
  2010 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Psychiatric science
- Research Institution
  The Institute of Physical and Chemical Research
Understanding the pathology of juvenile myoclonic epilepsy (JME) using Ehhc1-deficient mousePrincipal Investigator
- Principal Investigator
  
  SUZUKI Toshimitsu
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Psychiatric science
- Research Institution
  The Institute of Physical and Chemical Research
若年性ミオクローヌスてんかん新規原因遺伝子の機能解析Principal Investigator
- Principal Investigator
  
  鈴木俊光
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  The Institute of Physical and Chemical Research

All 2023 2021 2020 2011 2009 2008 Other

All Journal Article Presentation

[Journal Article] Inversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response2023
- Author(s)
  Suzuki Toshimitsu、Hattori Satoko、Mizukami Hiroaki、Nakajima Ryuichi、Hibi Yurina、Kato Saho、Matsuzaki Mahoro、Ikebe Ryu、Miyakawa Tsuyoshi、Yamakawa Kazuhiro
- Journal Title
  
  Molecular Neurobiology
  
  Volume: 61 Issue: 2 Pages: 622-634
- DOI
  10.1007/s12035-023-03610-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07620, KAKENHI-PROJECT-23K05860, KAKENHI-PROJECT-22H04922, KAKENHI-PROJECT-23K27490
[Journal Article] Epilepsy protein Efhc1/myoclonin1 is expressed in cells with motile cilia but not in neurons or mitotic apparatuses in brain2020
- Author(s)
  Suzuki Toshimitsu、Inoue Ikuyo、Yamakawa Kazuhiro
- Journal Title
  
  Scientific Reports
  
  Volume: 10 Issue: 1
- DOI
  10.1038/s41598-020-79202-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08058
[Journal Article] Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility2009
- Author(s)
  Toshimitsu Suzuki, Hiroyuki Miyamoto, Takashi Nakahari, Ikuyo Inoue, Takahiro Suemoto, Bin Jiang, Yuki Hirota, Shigeyoshi Itohara, Takaomi C. Saido, Tadaharu Tsumoto, Kazunobu Sawamoto, Takao K. Hensch, Antonio V. Delgado-Escueta, Kazuhiro Yamakawa
- Journal Title
  
  Human Molecular Genetics 18
  
  Pages: 1099-1109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790866
[Journal Article] Efhcl deficiency causes spontaneous myoclonus and increased seizure susceptibility
- Author(s)
  Toshimitsu Suzuki
- Journal Title
  
  Human Molecular Genetics (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] 内側前頭前皮質および腹側被蓋野でのナトリウムチャネルNav1.2の欠損は相反する聴覚性驚愕反応のプレパルス抑制効果を示す2023
- Author(s)
  Suzuki T., and Yamakawa K.
- Organizer
  第46回日本神経科学大会
- Data Source
  KAKENHI-PROJECT-22K07620
[Presentation] Juvenile myoclonic epilepsy responsible protein is expressed in cells with motile cilia but not in neurons.2021
- Author(s)
  Suzuki T., Inoue I., and Yamakawa K.
- Organizer
  第54回日本てんかん学会
- Data Source
  KAKENHI-PROJECT-19K08058
[Presentation] Myoclonin1 deficiency in ependymal cells increases seizure susceptibility2020
- Author(s)
  鈴木　俊光
- Organizer
  第43回神経科学会
- Data Source
  KAKENHI-PROJECT-19K08058
[Presentation] Epilepsy protein myoclonin1 dysfunction causes altered intracellular calcium signaling2011
- Author(s)
  鈴木俊光
- Organizer
  Society for Neuroscience, 2011
- Place of Presentation
  Washington Convention Center(Washington, DC,米国)
- Year and Date
  2011-11-13
- Data Source
  KAKENHI-PROJECT-22791154
[Presentation] Epilepsy protein myoclonin1 dysfunction causes altered intracellular Ca^<2+> signaling2011
- Author(s)
  Toshimitsu Suzuki, Kripamoy Aguan, Hideaki Mizuno, Takeshi Nakamura, Ikuyo Inoue, Katsuhiko Mikoshiba, Atsushi Miyawaki and Kazuhiro Yamakawa
- Organizer
  Society for Neuroscience
- Place of Presentation
  Washington, DC, USA
- Year and Date
  2011-11-13
- Data Source
  KAKENHI-PROJECT-22791154
[Presentation] Efhc1変異マウスで頻出する自然誘発ミオクローヌス2009
- Author(s)
  鈴木俊光
- Organizer
  日本てんかん学会
- Place of Presentation
  東京
- Year and Date
  2009-10-18
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] Mice lacking epilepsy gene, Efhc1, cause spontaneous myoclonus2009
- Author(s)
  鈴木俊光
- Organizer
  annual meeting of the Society for Neuroscience
- Place of Presentation
  Washington, DC, USA
- Year and Date
  2009-11-15
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] Efhc1欠損マウスにおける痙攣閾値の低下2009
- Author(s)
  鈴木俊光
- Organizer
  日本神経科学会
- Place of Presentation
  東京
- Year and Date
  2009-07-09
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] Mice lacking epilepsy gene, Efhc1, cause spontaneous myoclonus2008
- Author(s)
  Toshimitsu Suzuki
- Organizer
  annual meeting of the Society for Neuroscience
- Place of Presentation
  Washington, DC
- Year and Date
  2008-11-15
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] Efhc1欠損マウスにおける痙攣閾値の低下2008
- Author(s)
  Toshimitsu Suzuki
- Organizer
  日本神経科学会
- Place of Presentation
  東京
- Year and Date
  2008-07-09
- Data Source
  KAKENHI-PROJECT-20790866
[Presentation] Efhc1変異マウスで頻出する自然誘発ミオクローヌス2008
- Author(s)
  Toshimitsu Suzuki
- Organizer
  日本てんかん学会
- Place of Presentation
  東京
- Year and Date
  2008-10-18
- Data Source
  KAKENHI-PROJECT-20790866

Suzuki Toshimitsu 鈴木 俊光

鈴木 俊光 スズキ トシミツ

SUZUKI Toshimitsu 鈴木 俊光

Research Projects

Research Products

SCN2A遺伝子変異による精神・神経疾患発症神経回路の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

SCN2A遺伝子変異による社会性行動障害に関わる神経回路の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidating the pathology of epilepsy caused by EFHC1 and CILK1 variantsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidating the pathology of epilepsy caused by EFHC1 mutationsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Characterization of Ehhc1 conditional knockout mouse and understand the pathology of epilepsyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Understanding the pathology of epilepsy through the regulation of endoplasmic reticulum calcium homeostasisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Understanding the pathology of juvenile myoclonic epilepsy (JME) using Ehhc1-deficient mousePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

若年性ミオクローヌスてんかん新規原因遺伝子の機能解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Inversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Epilepsy protein Efhc1/myoclonin1 is expressed in cells with motile cilia but not in neurons or mitotic apparatuses in brain2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility2009

Author(s)

Journal Title

Data Source

[Journal Article] Efhcl deficiency causes spontaneous myoclonus and increased seizure susceptibility

Author(s)

Journal Title

Data Source

[Presentation] 内側前頭前皮質および腹側被蓋野でのナトリウムチャネルNav1.2の欠損は相反する聴覚性驚愕反応のプレパルス抑制効果を示す2023

Author(s)

Organizer

Data Source

[Presentation] Juvenile myoclonic epilepsy responsible protein is expressed in cells with motile cilia but not in neurons.2021

Author(s)

Organizer

Data Source

[Presentation] Myoclonin1 deficiency in ependymal cells increases seizure susceptibility2020

Suzuki Toshimitsu 鈴木俊光

鈴木俊光スズキトシミツ

SUZUKI Toshimitsu 鈴木俊光