Rchr
J-GLOBAL ID：201801012915189055   Update date: Oct. 07, 2024

Sugie Atsushi

スギエ アツシ | Sugie Atsushi
Affiliation and department：
新潟大学 脳研究所

About 新潟大学 脳研究所


Job title： 准教授
Homepage URL  (2)： https://www.bri.niigata-u.ac.jp/~neuroscience_disease_sugie/lab/ ,  https://www.bri.niigata-u.ac.jp/~neuroscience_disease_sugie/lab/en/?noredirect=en_US
Research field  (3)： Genomics ,  Neuropathology ,  Molecular biology
Research keywords  (5)： 希少疾患 ,  neurodegeneration ,  Drosophila ,  synapse ,  neuroscience
Research theme for competitive and other funds  (16)：
  • 2024 - 2028 未診断疾患イニシアチブ(Initiative on Rare and Undiagnosed Diseases(IRUD)): 希少・未診断疾患に対する診断プログラム基盤の 開発と患者還元を推進する研究
  • 2024 - 2028 アミロイドの新たな側面:神経細胞の生存メカニズムへの寄与
  • 2023 - 2028 神経炎症の起点を制御する分子機構の解明
  • 2024 - 2027 ヒト緑内障GWASからの個別化創薬プラットフォーム構築研究
  • 2023 - 2024 J-RDMMによる小型モデル生物を用いた希少・未診断疾患のin vivo解析
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Papers (30)：
  • Yohei Nitta, Jiro Osaka, Ryuto Maki, Satoko Hakeda-Suzuki, Emiko Suzuki, Satoshi Ueki, Takashi Suzuki, Atsushi Sugie. Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy. eLife. 2024. 12
  • Samuel D. Chauvin, Shoichiro Ando, Joe A. Holley, Atsushi Sugie, Fang R. Zhao, Subhajit Poddar, Rei Kato, Cathrine A. Miner, Yohei Nitta, Siddharth R. Krishnamurthy, et al. Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans. Nature Communications. 2024. 15. 1
  • Takaya Iida, Arisa Igarashi, Kae Fukunaga, Taiga Aoki, Tomomi Hidai, Kumiko Yanagi, Masahiko Yamamori, Kazuhito Satou, Hayato Go, Tomoki Kosho, et al. Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype. 2024
  • Jiro Osaka, Arisa Ishii, Xu Wang, Riku Iwanaga, Hinata Kawamura, Shogo Akino, Atsushi Sugie, Satoko Hakeda-Suzuki, Takashi Suzuki. Complex formation of immunoglobulin superfamily molecules Side-IV and Beat-IIb regulates synaptic specificity. Cell reports. 2024. 43. 2. 113798-113798
  • Annalisa Vetro, Cristiana Pelorosso, Simona Balestrini, Alessio Masi, Sophie Hambleton, Emanuela Argilli, Valerio Conti, Simone Giubbolini, Rebekah Barrick, Gaber Bergant, et al. Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration. American journal of human genetics. 2023
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MISC (6)：
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Lectures and oral presentations  (27)：
  • Utilizing Drosophila Models and MeDUsA for Deciphering Variants of Uncertain Significance.
    (International Congress of Entomology 2024)
  • ショウジョウバエモデルの視神経疾患治療への応用.
    (東日本神経眼科勉強会 第39回真鶴セミナー 2024)
  • Establishment of Methods for Evaluating Neuroaxonal Degeneration and Research on Molecular Mechanisms for Neuronal Maintenance.
    (UCL IHA Virtual Symposium: Neurodegeneration in Flies 2024)
  • Advancing the Understanding of Variants of Uncertain Significance through Drosophila Model.
    (The 47th Annual Meeting of the Japan Neuroscience Society 2024)
  • Utilizing fly to understand genetic aspects of neurodegenerative diseases
    (NIG International Symposium 2023 2023)
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Education (3)：
  • 2007 - 2010 東京大学大学院 理学系研究科 生物化学専攻
  • 2003 - 2005 Kobe University Graduate School of Science and Technology
  • 1999 - 2003 Kobe University Faculty of Agriculture Department of Biological and Environmental Science
Professional career (1)：
  • 博士(理学)
Work history (5)：
  • 2020/04 - 現在 Niigata University Brain Research Institute Associate Professor
  • 2016/02 - 2020/03 Niigata University Center for Transdisciplinary Research Assistant Professor
  • 2011/12 - 2016/02 ドイツ神経変性疾患研究所 Tavosanis研究室
  • 2010/10 - 2011/12 ドイツ マックスプランク研究所 神経生物学 鈴木研究室
  • 2005/04 - 2007/03 株式会社DHC 研究開発部 分析化学研究室 主任
Association Membership(s) (2)：
The Japanese Society for Neurochemistry ,  THE JAPAN NEUROSCIENCE SOCIETY
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

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