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Nakade Shota  中出 翔太

Researcher Number 70795509
Other IDs
  • ORCIDhttps://orcid.org/0000-0003-4721-9408
Affiliation (based on the past Project Information) *help 2017 – 2018: 広島大学, 理学研究科, 研究員
Review Section/Research Field
Principal Investigator
Medical genome science
Keywords
Principal Investigator
ノックイン / 癌 / ゲノム / スクリーニング / がん細胞 / CRISPR-Cas9 / ゲノム編集
  • Research Projects

    (1 results)
  • Research Products

    (9 results)
  • Co-Researchers

    (1 People)
  •  Development of intercellular device to record the extracellular stimuli with self-targeting CRISPR-Cas9Principal Investigator

    • Principal Investigator
      Nakade Shota
    • Project Period (FY)
      2017 – 2018
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Medical genome science
    • Research Institution
      Hiroshima University

All 2018 2017

All Journal Article Presentation

  • [Journal Article] Biased genome editing using the local accumulation of DSB repair molecules system.2018

    • Author(s)
      Nakade S, Mochida K, Kunii A, Nakamae K, Aida T, Tanaka K, Sakamoto N, Sakuma T, Yamamoto T
    • Journal Title

      Nature Communications

      Volume: 9(1) Issue: 1 Pages: 3270-3270

    • DOI

      10.1038/s41467-018-05773-6

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K07241, KAKENHI-PROJECT-18K19494, KAKENHI-PROJECT-17H01409, KAKENHI-PROJECT-17H02216, KAKENHI-PROJECT-16K07085, KAKENHI-PROJECT-17K15045
  • [Journal Article] Cancer induction and suppression with transcriptional control and epigenome editing technologies.2017

    • Author(s)
      Nakade S, Yamamoto T, Sakuma T.
    • Journal Title

      Journal of human genetics

      Volume: 1 Issue: 2 Pages: 187-194

    • DOI

      10.1038/s10038-017-0377-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K15045, KAKENHI-PROJECT-16K18478
  • [Presentation] Parallel generation of multiplex knock-in cell collections using CRISPR-Cas9 assisted by locally enhanced MMEJ.2018

    • Author(s)
      Nakade Shota、Mochida Keiji、Kunii Atsushi、Nakamae Kazuki、Aida Tomomi、Tanaka Kohichi、Sakamoto Naoaki、Sakuma Tetsushi、Yamamoto Takashi
    • Organizer
      FASEB Science Research Conference 2018
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] Biased genome editing using the LoAD (local accumulation of DSB repair molecules) system.2018

    • Author(s)
      Sakuma T, Nakade S, Mochida K, Nakamae K, Aida T, Tanaka K, Sakamoto N, and Yamamoto T.
    • Organizer
      Precision Genome Editing with Programmable Nucleases (B1)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] Biased genome editing using the LoAD (local accumulation of DSB repair molecules) system.2018

    • Author(s)
      Nakade Shota、Mochida Keiji、Kunii Atsushi、Nakamae Kazuki、Aida Tomomi、Tanaka Kohichi、Sakamoto Naoaki、Sakuma Tetsushi、Yamamoto Takashi
    • Organizer
      CHSL meeting 2018, Genome Engineering: The CRISPR/Cas Revolution.
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] LoADシステム:ゲノム編集において任意のDSB修復経路を誘導する汎用的手法2018

    • Author(s)
      中出翔太、持田圭次、中前和恭、相田知海、田中光一、坂本尚昭、佐久間哲史、山本卓
    • Organizer
      第三回ゲノム編集学会
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] 短い相同配列を介した遺伝子ノックインにおいて選択される DSB 修復経路の解析2017

    • Author(s)
      中出翔太、中前和恭、佐久間哲史、山本卓
    • Organizer
      ConBio2017
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] PITCh法によるノックインの過程で生じる DSB 修復経路の選択とその正確性2017

    • Author(s)
      中出翔太、中前和恭、佐久間哲史、山本卓
    • Organizer
      第二回ゲノム編集学会
    • Data Source
      KAKENHI-PROJECT-17K15045
  • [Presentation] Selective choice of MMEJ repair pathway and its accuracy profile during the process of PITCh knock-in.2017

    • Author(s)
      Nakade S, Sakuma T, Nakamae K, Yamamoto T
    • Organizer
      CSHL meeting, Genome Engineering: The CRISPR/Cas Revolution
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K15045
  • 1.  坂本 尚昭
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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