Nishikawa Masashi

ニシカワマサシ | Nishikawa Masashi

Affiliation and department：
Job title： Assistant professor
Homepage URL (2)： https://www.bio.nagoya-u.ac.jp/laboratory/cr.html , https://www.bio.nagoya-u.ac.jp/english/laboratory/cr.html

Research field (5)： Developmental biology , Neuroanatomy and physiology , Neuroscience - general , Cell biology , Molecular biology

Research keywords (7)： Molecular biology , In utero electroporation , G protein , Neurodevelopmental disorders , cytoskeleton , Neurodevelopment , cell signaling pathway

Research theme for competitive and other funds (7)：

2022 - 2027 大脳発達における知的障害責任分子 Rac1の生理機能と分子病態機構の解明
2023 - 2025 Cdc42異常に基づく小頭症・脳皮質形成異常症を伴う知的障害の病態メカニズム解析
2023 - 2025 知的障害責任分子RhoGの神経発達障害メカニズムの解明
2022 - 2023 J-RDMMモデル生物プロジェクト
2021 - 2023 知的障害責任分子Rac3の大脳発達における生理機能と分子病態機構の解明

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Papers (23)：

Masashi Nishikawa, Koh-ichi Nagata, Hidenori Tabata. Live Imaging of Migrating Neurons and Glial Progenitors Visualized by in Utero Electroporation. Methods in Molecular Biology. 2024. 201-209
西川将司. Rac シグナルの破綻による神経発達障害発症機構の解明. 神経化学. 2023
Yumi Tsuneura, Taeko Kawai, Keitaro Yamada, Shintaro Aoki, Mitsuko Nakashima, Shima Eda, Tohru Matsuki, Masashi Nishikawa, Koh-ichi Nagata, Yasushi Enokido, et al. A Novel Constitutively Active c:98G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization. Human Mutation. 2023. 2023. 1-12
Masashi Nishikawa, Tohru Matsuki, Nanako Hamada, Atsuo Nakayama, Hidenori Ito, Koh-ichi Nagata. Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development. Medical Molecular Morphology. 2023
Rie Seyama, Masashi Nishikawa, Yuri Uchiyama, Keisuke Hamada, Yuka Yamamoto, Masahiro Takeda, Takanori Ochi, Monami Kishi, Toshifumi Suzuki, Kohei Hamanaka, et al. A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association. Scientific Reports. 2023. 13. 1

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MISC (1)：

小林知世, 西川将司, 中野駿, 石川奈津子, 大脇千智, 杉山剛志, 山川央, 長瀬隆弘, 上田浩. FYNによるRho活性化因子PLEKHG1の活性制御機構. 生命科学系学会合同年次大会. 2017. 2017年度. [3P-0428]

Lectures and oral presentations (25)：

Rac-グアニンヌクレオチド交換因子 Prex1 の神経発達における生理機能
(第64回日本神経病理学会総会学術研究会/ 第66回日本神経化学会大会合同大会 2023)
低分子量G蛋白質RAC3の病的バリアントによる発達障害の病態形成機構
(第65回日本小児神経学会学術集会 2023)
PLEKHG2ミスセンス変異による神経発達障害の発症メカニズム
(第65回日本小児神経学会学術集会 2023)
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes
(2023)
Expression distribution of the Rac regulatory molecule Rich2 changes with neurodevelopment
(The 46th Annual Meeting of the Molecular Biology Society of Japan (MBSJ2023) 2022)

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Education (3)：

2016 - 2019 Gifu University
2014 - 2016 Nagoya University Graduare School of Pharmaceutical Sciences
2010 - 2014 Gifu University Faculty of Engineering

Professional career (1)：

Engineering (Gifu University)

Work history (3)：

2022/06 - 現在 Nagoya University Division of Biological Sciences, Nagoya University Graduate School of Science, Nagoya Assistant professor
2020/04 - 2022/05 Institute for Developmental Research, Aichi Developmental Disability Center Department of Molecular Neurobiology Research resident
2018/04 - 2020/03 Japan Society for the Promotion of Science

Committee career (2)：

2023/04 - 2026/03 日本臨床分子形態学会評議員
2021/10 - 2021/10 日本臨床分子形態学会第53回日本臨床分子形態学会総会・学術集会実行委員

Awards (3)：

2023 - The Japanese Society for Neurochemistry The Award for Young Investigator of Japanese Society for Neurochemistry Pathophysiological mechanisms underlying neurodevelopmental disorders caused by Rac GTPases dysregulation
2022/05 - 日本生化学会中部支部奨励賞
2021/10 - The Japanese Society for Neurochemistry Best Presentation Award of The Japanese Society for Neurochemistry Pathophysiological significance of RAC3 variants in neurodevelopmental disorders

Association Membership(s) (4)：

日本臨床分子形態学会 , 日本神経化学会 , 日本生化学会 , 日本分子生物学会

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