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KOHNO Michiaki  河野 通明

ORCIDConnect your ORCID iD *help
Researcher Number 00027335
Other IDs
Affiliation (based on the past Project Information) *help 2012: 京都大学, 薬学研究科(研究院), 研究員
2011 – 2012: 京都大学, 薬学研究科, 研究員
2007 – 2010: Nagasaki University, 大学院・医歯薬学総合研究科, 教授
2005 – 2006: 長崎大学, 大学院医歯薬学総合研究科, 教授
2002 – 2005: 長崎大学, 大学院・医歯薬学総合研究科, 教授 … More
2004: Nagasaki University, Graduate School of Biomedical Sciences, Professor, 医歯薬学総合研究科, 教授
1997 – 2001: Nagasaki University, Pharmaceutical Sciences, Professor, 薬学部, 教授
1993 – 1996: 岐阜薬科大学, 薬学部, 助教授
1994: Gifu Pharmaceutical University Pharmacy, Associate Professor, 薬学部, 助手
1992: 岐阜薬科大学, 助教授
1990 – 1991: 岐阜薬科大学, 薬学部, 助教授
1986 – 1990: 岐阜薬科大学, 助教授 Less
Review Section/Research Field
Principal Investigator
Biological pharmacy / Biological Sciences / Functional biochemistry / Biological pharmacy / 医薬分子機能学 / 代謝生物化学 / Clinical oncology
Except Principal Investigator
Dermatology / Neurology / 植物生理学
Keywords
Principal Investigator
細胞がん化 / MAPキナーゼ / ERK-MAPキナーゼ / MEK阻害剤 / がん化学療法 / アポトーシス / p38MAPキナーゼ / 骨形成因子 / 神経成長因子 / 細胞周期 … More / MAPキナーゼ・キナーゼ / GEF-H1 / ERK-MAP kinase / 細胞運動 / p38 MAP kinase / c-Jun N-terminal Kinase / JNK / チューブリン / 併用療法 / チオフラボン誘導体 / MAPキナーゼカスケード / シグナル伝達 / 細胞増殖因子 / 中間径フィラメント / 細胞質分裂 / RhoA / Matrix metalloproteinase / Sprouty / Cell Motility / 細胞機能制御 / NF-M / p27^<Kip1> / 細胞分化 / 細胞増殖 / Cell Differentiation / 核移行 / TGF-βスーパーファミリー / 肝細胞増殖因子 / Bone Morphogenetic Protein / Nerve Growth Factor / 動物個体系 / HDAC阻害剤 / HDAC 阻害剤 / 微小管重合阻害剤 / ERK-MAPキナーゼ経路 / チューブリン重合阻害剤 / 併用効果 / 細胞質微小管 / MMP-9 / ポリフェノール / Xenograft / ERK-MAPキナーゼ系 / 多機能因子 / 制がん剤 / 細胞周期動態 / シグナル分子 / フラボン / 阻害剤 / ヒトがん細胞 / 受容体 / インターロイキン-1 / 繊維芽細胞 / 創傷修復 / 腫瘍壊死因子 / Spindle Checkpoint / Cell Cycle / Intermediate Filaments / Intracellular Localization / ERK-MAP Kinase / ケラチン8 / 細胞内局在性 / p90^<RSK> / スピンドルチェックポイント / スピンドルチェックポイト / 細胞周期制御 / c-Jun N-Terminal Kinase / 細胞内局在 / Cell cycle / GEH-H1 / Cytoskeletone / Regulation of cell function / MMP / 細胞質分裂制御 / GTP交換因子 / GDP / Negative Feedback Inhibitor / 中間系フィラメント / 細胞骨格系 / p38 MAPキナーゼ / Polyphenol / Molecular Target / Anti-inflammatory agent / Anti-tumor agent / Specific inhibitor / c-Jun N-terminal kinase / MAP kinase pathway / MAPキナーゼキナーゼ / 特異的阻害剤 / 分子標的 / 抗炎症剤 / 抗がん剤 / Matrix mettaloproteinase-9 / Neurofilament Proteins / p27^<Klp1> / Cell Proliferation / ERK / 神経細胞分化 / 細胞分散運動 / マトリックスメタロプロテアーゼ / ニューロフィラメント / TGF-beta Superfamily / Hepatocyte Growth Factor / ERK MAP kinases / Cell Growth Control / 細胞骨格 / 転写因子 / 分化因子 / 増殖因子 / 血小板由来増殖因子 / ERK MAPキナーゼ / 細胞増殖・分化 / Nerve regeneration / Receptor / Interleukin-1 / Fibroblasts / Wound healing / Tumor Necrosis factor-alpha / 末梢神経再生 / GTPase-activating protein / PI3-kinase / Phospolipase C / Receptor tyrosine kinase / Protein kinase C / Pertussis toxin-sensitive GTP-binding protein / Peptide growth factor / p21^<ras>ーGTPア-ゼ活性化蛋白質 / ホスホリパ-ゼC / GTP結合蛋白質 / G蛋白質活性化因子 / PI3キナ-ゼ / ホスフォリパ-ゼC / 受容体チロシンキナ-ゼ / Cキナ-ゼ / 百日咳毒素感受性G蛋白質 / チロシンリン酸化反応 / pp60^<src> / 発がん遺伝子 / ペプチド増殖因子 / 微小管阻害剤 / Bcl-2 ファミリー蛋白質 / MEK 阻害剤 / ERK-MAP キナーゼ経路 / Akt系 / PI3キナーゼ / 活性酸素種 / ERK-MAPキナーゼ路 / TRAIL / TNFα / 紡錘体微小管 / 転移 / チューブリン阻害剤 / CDK阻害タンパク質 / GABA作動性神経細胞 / PC12細胞 / 神経栄養因子 / TGFβスーパーファミリー / Cdk阻害タンパク質 / MAPキナーゼ・キナーゼ(MEK) / pp125^<FAK> / 増殖阻害 / Ras / 転写調節領域 / チロシンリン酸化 / ヒトがん細胞株 / 分子細胞生物学 / 蛋白質リン酸化反応 / 細胞増殖・分化制御 / 増階シグナル伝達 / 細胞骨格蛋白質 / MAPキナ-ゼ / 微小管結合蛋白質 / セリン・スレオニンキナ-ゼ / チロシンキナ-ゼ / チロシンリン酸化蛋白質 … More
Except Principal Investigator
増殖因子 / EGF / FGF / シグナル伝達 / TGFβ / Cキナーゼ / トランスフォーメーション / TGF / bFGF / リポソーム / HGF / 癌と間質との相互作用 / サイトカイン / MAPキナーゼ / c-met / チロシンキナ-ゼ / チロシン燐酸化 / TNF / nerve regeneration / TNF-alpha / wound healing / skin ulser / 線維芽細胞 / 神経成長因子 / 腫瘍壊死因子 / 神経再生 / TNF-α / 創傷治癒 / 創傷 / periphral tissue / cerebrospinal fluid / serum / neurotrophic factor (NTF) / nerve growth factor (NGF) / diagnosis / enzyme immunoassay (EIA) / neurotrophin-3 (NT-3) / 特異性 / 再現性 / 最少検出量 / 酵素免疫側定法(EIA) / 抗体 / NGF / NT-3 / GFGF / 神経栄養因子 / 早期診断法 / 酵素免疫測定法 / 老人痴呆症 / signal transduction / Phosphorylation / Phytochrome / Glandular trichomes / Monoterpenoid / Thymus vulgaris L. / Labiatae / モノテルペン / タイム / リン酸化反応 / 光情報伝達 / フィトクロム / 腺毛 / 腺鱗 / モノテルペノイド / タチジャコウソウ / シソ科 / 増殖促進シグナル / V型コラーゲン / インスリン受容体キナーゼ / DNA合成促進因子 / PI代謝回転 / チロシンリン酸化 / src / ras / myc / 受容体 / IGFーI / インスリン / ヘパリン / 細胞接着因子 / ビトロネクチン / フィブロネクチン / レセプター / IGF / Hrs / アポトーシス / インターフェロン / p115 / 増殖因子レセプター / 癌抑制遺伝子 / ERMファミリー / 細胞接着分子 / チロシンキナーゼ受容体 / FGFレセプター / K-sam / インスリンレセプター / カルホスチンC / 肝細胞増殖因子 / インスリン受容体 / PDーECGF / cripto / cーmet / 転写因子 / GCF / 癌遺伝子 / 増殖因子系遺伝子の転写因子 / TGFα / EGFレセプタ- / レセプタ-系 / オートクリン制御 Less
  • Research Projects

    (36 results)
  • Research Products

    (73 results)
  • Co-Researchers

    (38 People)
  •  Targeting the ERK-MAP kinase pathway in cancer therapyPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Clinical oncology
    • Research Institution
      Kyoto University
      Nagasaki University
  •  Targeting the ERK-MAP kinase pathway in cancer therapyPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      2005 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  Role of MAP kinase cascades in the regulation of diverse cellular functionsPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  チューブリン重合阻害剤の抗腫瘍効果発現機構に対する再検討Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  Role of MAP Kinase Cascade in the Regulation of Diverse Cellular FunctionsPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      2002 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  MAPキナーゼカスケードを構成するシグナル分子を標的とした細胞増殖阻害物質の探索Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      2001 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  チューブリン重合阻害剤の抗腫瘍効果発現機構に対する再検討Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      2001
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  MAPキナーゼカスケードを構成するシグナル分子を標的とした細胞増殖阻害物質の探索Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      2000
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Nagasaki University
  •  MAPキナーゼカスケードを構成するシグナル分_2を標的とした細胞増殖阻害物質の検索Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1999
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Nagasaki University
  •  骨形成因子が神経栄養因子活性を持つことの生物学的意義の解明Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1999
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  Development of specific inhibitors against MAP kinase pathwaysPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      1999 – 2001
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  MAPキナーゼカスケードを構成するシグナル分子を標的とした細胞増殖阻害物質の探索Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1998
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Nagasaki University
  •  Role of MAP Kinase Cascade in the Regulation of Diverse Cellular Fuctions.Principal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      1998 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
  •  ヒトがん細胞におけるMAPキナーゼカスケードの異常-細胞がん化との相関Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1997
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Nagasaki University
  •  MAPキナーゼカスケードを構成するシグナル分子を標的とした細胞増殖阻害物質の検索Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Gifu Pharmaceutical University
  •  Role of the ERK MAP Kinase Cascade in the Regulation of Cell Proliferation and Differentiation.Principal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Biological pharmacy
    • Research Institution
      Nagasaki University
      Gifu Pharmaceutical University
  •  細胞増殖因子からみた癌細胞と間質細胞との相互作用-その分子機構-

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Hiroshima University
  •  MAPキナーゼの恒常的活性化がヒトがん発生の直接的な原因となる可能性の検討Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Gifu Pharmaceutical University
  •  創傷修復過程における末梢神経再生の分子機構-腫瘍壊死因子によるNGF遺伝子の発現制御Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Functional biochemistry
    • Research Institution
      Gifu Pharmaceutical University
  •  Development of anti-skin ulcer drug based on the new concept -Application of the stimulatory effect of TNF-alpha on the production of NGF in fibroblastsPrincipal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      医薬分子機能学
    • Research Institution
      Gifu Pharmaceutical University
  •  細胞増殖因子からみた癌細胞と間質細胞との相互作用 -その分子機構-

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Hiroshima University
  •  Development of anti-skin ulcer drug based on the new concept-application of the effect of TNF-alpha on regeneration of peripheral nerve.

    • Principal Investigator
      TAKIGAWA Masahiro
    • Project Period (FY)
      1994 – 1995
    • Research Category
      Grant-in-Aid for Developmental Scientific Research (B)
    • Research Field
      Dermatology
    • Research Institution
      Hamamatsu University School of Medicine
  •  細胞増殖因子からみた癌細胞と間質細胞との相互作用 -その分子機構-

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Hiroshima University
  •  細胞増殖因子作用における41-kDa、43-kDa・MAPキナーゼ活性化の役割Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Functional biochemistry
    • Research Institution
      Gifu Pharmaceutical University
  •  Development of the Enzyme Immunoassay System for the Substances Related to the Pathogenesis of Alzheimer's Disease

    • Principal Investigator
      HAYASHI Kyozo
    • Project Period (FY)
      1993 – 1994
    • Research Category
      Grant-in-Aid for Developmental Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      Gifu Pharmaceutical University
  •  癌の増殖における増殖因子の相互作用とその分子機構

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1992
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Hiroshima University
  •  癌の増殖における増殖因子の相互作用とその分子機構

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1991
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Hiroshima University
  •  細胞増殖因子作用における41K,43K蛋白質チロシンリン酸化反応促進の役割ー41K,43K蛋白質のcDNAクロ-ニングPrincipal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1991
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Gifu Pharmaceutical University
  •  癌の増殖における増殖因子の相互作用とその分子機構

    • Principal Investigator
      田原 榮一
    • Project Period (FY)
      1990
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Hiroshima University
  •  Phytochrome-mediated formation of terpenoids and glandular trichomes, and rapid tyrosine phosphorylation of a 25-kDa protein in thyme seedlings

    • Principal Investigator
      TANAKA Shigeo
    • Project Period (FY)
      1990 – 1991
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      植物生理学
    • Research Institution
      Kyoto University
  •  Regulation of mitogenic signaling pathways which involve the function of GTP-binding protein-Possible involvement of protein tyrosine phosphorylation.Principal Investigator

    • Principal Investigator
      KOHNO Michiaki
    • Project Period (FY)
      1990 – 1991
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      代謝生物化学
    • Research Institution
      Gifu Pharmaceutical University
  •  細胞増殖因子作用の分子機構とトランスフォーメーション

    • Principal Investigator
      清水 信義
    • Project Period (FY)
      1989
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Keio University
  •  細胞増殖因子作用の分子機構とトランスフォーメーション

    • Principal Investigator
      清水 信義
    • Project Period (FY)
      1988
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Keio University
  •  誘発型発癌遺伝子および増殖因子による細胞のGo/Gi期からS期への移行機構の比較解析Principal Investigator

    • Principal Investigator
      河野 通明
    • Project Period (FY)
      1988
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Gifu Pharmaceutical University
  •  細胞増殖因子作用の分子機構とトランスフォーメーション

    • Principal Investigator
      清水 信義
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Keio University
  •  細胞増殖因子の作用機構とトランスフォーメーションの研究

    • Principal Investigator
      清水 信義
    • Project Period (FY)
      1986
    • Research Category
      Grant-in-Aid for Cancer Research
    • Research Institution
      Keio University

All 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 Other

All Journal Article Presentation Book

  • [Book] 細胞死実験プロトコール(編集:刀祢重信、小路武彦)(分担執筆)2011

    • Author(s)
      坂元利影、河野通明
    • Total Pages
      224
    • Publisher
      羊土社
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Book] 細胞死実験プロトコール2011

    • Author(s)
      坂元利彰、河野通明
    • Total Pages
      224
    • Publisher
      羊土社
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Book] 細胞内シグナル伝達経路の選択的遮断を基盤としたがん治療戦略2008

    • Author(s)
      尾崎恵一、谷村進、河野通明
    • Publisher
      ファルマシア
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Book] シグナル伝達- 1. MAPキナーゼ経路, がんの分子標的治療(鶴雄隆編)2008

    • Author(s)
      河野通明
    • Publisher
      南山堂
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Book] がんの分子標的治療(鶴尾隆編集)2008

    • Author(s)
      河野通明(分担執筆)
    • Publisher
      南山堂
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Book] シグナル伝達系, 新臨床腫瘍学(日本臨床腫瘍学会編)2006

    • Author(s)
      河野通明
    • Publisher
      南江堂
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Blockade of the ERK pathway enhances the therapeutic efficacy of the histone deacetylase inhibitor MS-275 in human tumor xenograft models2013

    • Author(s)
      Sakamoto, T., Ozaki, K., Fujio, K., Kajikawa, S., Uesato, S., Watanabe, K., Tanimura, S., Koji, T. & Kohno, M
    • Journal Title

      Biochem. Biophys. Res. Commun

      Volume: 433 Pages: 456-462

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Inhibition of the p38 MAPK pathway ameliorates renal fibrosis in an NPHP2 mouse model2012

    • Author(s)
      Sugiyama, N., Kohno, M. & Yokoyama, T.
    • Journal Title

      Nephrol. Dial. Transplant

      Volume: 27 Pages: 1351-1358

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Up-regulation of pro-apoptotic protein Bim and down-regulation of anti-apoptotic protein Mcl-1 cooperatively mediate enhanced tumor cell death induced by the combination of ERK kinase (MEK) inhibitor and microtubule inhibitor.2012

    • Author(s)
      Kawabata, T. Tanimura, S., Asai, K., Kawasaki, R., Matsumaru, Y. & Kohno, M.
    • Journal Title

      J. Biol. Chem.

      Volume: 287 Pages: 10289-10300

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Up-regulation of pro-apoptotic protein Bim and down-regulation of anti-apoptotic protein Mcl-1 cooperatively mediate enhanced tumor cell death induced by the combination of ERK kinase (MEK) inhibitor and microtubule inhibitor2012

    • Author(s)
      Kawabata, T., Kohno, M., et al
    • Journal Title

      J.Biol.Chem.

      Volume: 287 Issue: 13 Pages: 10289-10300

    • DOI

      10.1074/jbc.m111.319426

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340, KAKENHI-PROJECT-23790090
  • [Journal Article] Targeting the extracellular signal-regulated kinase pathway in cancer therapy.2011

    • Author(s)
      Kohno, M., Tanimura, S. & Ozaki, K.
    • Journal Title

      Biol. Pharm. Bull.

      Volume: 34 Pages: 1781-1784

    • NAID

      130001872595

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] SH3P2 is a negative regulator of cell motility whose function is inhibited by RSK-mediated phosphorylation.2011

    • Author(s)
      Tanimura, S., Hashizume, J., Kurosaki, Y., Sei,K., Gotoh, A., Ohtake, R., Kawano, M., Watanabe, K. & Kohno. M.
    • Journal Title

      Genes Cells

      Volume: 16 Pages: 514-526

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] SH3P2 is a negative regulator of cell motility whose function is inhibited by RSK-mediated phosphorylation2011

    • Author(s)
      Tanimura, S., Kohno, M., et al
    • Journal Title

      Genes Cells

      Volume: 16 Issue: 5 Pages: 514-526

    • DOI

      10.1111/j.1365-2443.2011.01503.x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Targeting the Extracellular Signal-Regulated Kinase Pathway in Cancer Therapy2011

    • Author(s)
      Kohno M., Tanimura S., Ozaki K.
    • Journal Title

      Biological and Pharmaceutical Bulletin

      Volume: 34 Issue: 12 Pages: 1781-1784

    • DOI

      10.1248/bpb.34.1781

    • NAID

      130001872595

    • ISSN
      0918-6158, 1347-5215
    • Language
      English
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21590166, KAKENHI-PROJECT-22300340
  • [Journal Article] Peumusolide A, unprecedented NES non- antagonistic inhibitor for nuclear export of MEK.2010

    • Author(s)
      Tamura, S., Hattori, Y., Kaneko, M., Shimizu, N., Tanimura, S., Kohno, M. & Murakami, N.
    • Journal Title

      Tetrahedron Lett.

      Volume: 51 Pages: 1678-1681

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Blockade of the extracellularsignal-regulated kinase pathway enhances the therapeutic efficacy of microtubule destabilizing agents in human tumor xenograft models.2010

    • Author(s)
      Watanabe, K., Tanimura, S., Uchiyama, A., Sakamoto, T., Kawabata, T., Ozaki, K. & Kohno, M.
    • Journal Title

      Clin. Cancer Res

      Volume: 16 Pages: 1170-1178

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Journal Article] Blockade of the ERK or PI3K-Akt signaling pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib.2010

    • Author(s)
      Ozaki, K., Kosugi, M., Baba, N., Fujio, K., Sakamoto, T., Kimura, S., Tanimura, S., Kohno, M.
    • Journal Title

      Biochem. Biophys. Res. Commun. 391

      Pages: 1610-1615

    • NAID

      120006983583

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Blockade of the extracellular signal-regulated kinase pathway enhances the therapeutic efficacy of microtubuledestabilizing agents in human tumor xenograft models.2010

    • Author(s)
      Watanabe, K., Tanimura, S., Uchiyama, A., Sakamoto, T., Kawabata, T., Ozaki, K., Kohno, M.
    • Journal Title

      Clin. Cancer Res. 16

      Pages: 1170-1178

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] unprecedented NES non-antagonistic inhibitor for nuclear export of MEK.2010

    • Author(s)
      Tamura, S., Hattori, Y., Kaneko, M., Shimizu, N., Tanimura, S., Kohno, M., Murakami, N. Peumusolide A
    • Journal Title

      Tetrahedron Lett. 51

      Pages: 1678-1681

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Blockade of constitutively activated ERK signaling enhances cytotoxicity of microtubule-destabilizing agents in tumor cells.2009

    • Author(s)
      Tanimura, S., Uchiyama, A., Watanabe, K., Yasunaga, M., Inada, Y., Kawabata, T., Iwashita, K., Noda, S., Ozaki, K., Kohno, M.
    • Journal Title

      Biochem. Biophys. Res. Commun. 378

      Pages: 650-655

    • NAID

      120006983970

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] GEF-H1 mediates tumor necrosis factor-α-induced Rho activation and myosin phosphorylation: Role in the regulation of tubular paracellular permeability.2009

    • Author(s)
      Kakiashvili, E., Speight, P., Waheed, F., Seth, R., Lodyga, M., Tanimura, S., Kohno, M., Rotstein, O.D., Kapus, A., Szaszi, K.
    • Journal Title

      J. Biol. Chem. 284

      Pages: 11454-11466

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Histone deacetylase inhibitors enhance the chemosensitivity of tumor cells with cross-resistance to a wide range of DNA-damaging drugs.2008

    • Author(s)
      Ozaki, K., Kishikawa, F., Tanaka, M., Sakamoto, T., Tanimura, S, Kohno, M.
    • Journal Title

      Cancer Sci. 99

      Pages: 376-384

    • NAID

      10024002722

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] ERK1/2 phosphorylate GEF-H1 to enhance its guanine nucleotide exchange activity toward RhoA.2008

    • Author(s)
      Fujishiro, S., Tanimura, S., Mure, S., Kashimoto, Y., Watanabe, K, Kohno, M.
    • Journal Title

      Biochem. Biophys. Res. Commun. 368

      Pages: 162-167

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Blockade of the phosphatidylinositol 3-kinase-Akt signaling pathway enhances induction of apoptosis by microtubule-destabilizing agents in tumor cells in which the pathway is constitutively activated.2007

    • Author(s)
      Fujiwara, Y., Hosokawa, Y., Watanabe, K., Tanimura, S., Ozaki, K., Kohno, M.
    • Journal Title

      Mol.Cancer Ther. 6

      Pages: 1133-1142

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Enantioselective total synthesis of (+)- Ottelione A, (-)-Ottelione B, (+)-3-epi- Otterlione A and preliminary evaluation of antitumor activity.2007

    • Author(s)
      Araki, H., Inoue, M., Suzuki, T., Yamori, T., Kohno, M., Watanabe, K., Abe, H., Katoh, T.
    • Journal Title

      Chem. Eur. J. 13

      Pages: 9866-9881

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Requirement of ERK MAP kinase in mouse preimplantation development.2007

    • Author(s)
      Maekawa, M., Yamamoto, T., Kohno, M., Takeichi, M., Nishida, E.
    • Journal Title

      Development 134

      Pages: 2751-2759

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Blockade of the phosphatidylinositol 3-kinase-Akt signaling pathway enhances induction of apoptosis by microtubuledestabilizing agents in tumor cells in which the pathway is constitutively activated.2007

    • Author(s)
      Fujiwara, Y., Hosokawa, Y., Watanabe, K., Tanimura, S., Ozaki, K, Kohno, M.
    • Journal Title

      Mol. Cancer Ther. 6

      Pages: 1133-1142

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Anticancer drugs up-regulate HspBP1 and thereby antagonize the prosurvival function of Hsp70 in tumor cells.2007

    • Author(s)
      Tanimura, S., Hirano, A., Hashizume, J., Yasunaga, M., Kawabata, T., Ozaki, K, Kohno, M.
    • Journal Title

      J. Biol. Chem. 282

      Pages: 35430-35439

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Targeting the ERK signaling pathway in Cancer Therapy2006

    • Author(s)
      Kohno, M.
    • Journal Title

      Ann. Medicine 38巻

      Pages: 200-211

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Targeting the ERK signaling pathway in Cancer Therapy2006

    • Author(s)
      Kohno, M.
    • Journal Title

      Ann.Medicine 38巻

      Pages: 200-211

    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Targeting the ERK signaling pathway in Cancer Therapy (Invited Review).2006

    • Author(s)
      Kohno, M., Pouyssegur, J.
    • Journal Title

      Ann.Medicine 38

      Pages: 200-211

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Targeting the ERK signaling pathway in Cancer Therapy. Ann.2006

    • Author(s)
      Kohno, M., Pouyssegur, J.
    • Journal Title

      Medicine 38

      Pages: 200-211

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] ERK inhibition slows disease progression in mice with polycystic kidney disease.2006

    • Author(s)
      Omori, S., Hida, M., Fujita, H., Takahashi, H., Tanimura, S., Kohno, M., Awazu, M.
    • Journal Title

      J.Am.Soc.Nephrol. 17

      Pages: 1604-1614

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Targeting the ERK signaling pathway in Cancer Therapy2006

    • Author(s)
      Kohno, M.
    • Journal Title

      Ann. Medicine 38巻

      Pages: 200-211

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Inhibition of the PI3 kinase/Akt pathway enhances doxorubicin-induced apoptotic cell death in tumor cells in a p53-dependent manner.2006

    • Author(s)
      Fujiwara, Y., Kawada, K., Takano, D., Tanimura, S., Ozaki, K., Kohno, M.
    • Journal Title

      Biochem.Biophys.Res.Commun. 340

      Pages: 560-566

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Blockade of the ERK pathway markedly sensitizes tumor cells to HDAC inhibitor-induced cell death.2006

    • Author(s)
      Ozaki, K., Minoda, A., Kishikawa, F., Kohno, M.
    • Journal Title

      Biochem.Biophys.Res.Commun. 339

      Pages: 1171-1177

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Blockade of the ERK pathway markedly sensitizes tumor cells to HDAC inhibitor-induced cell death.2006

    • Author(s)
      Ozaki, K., Minoda, A., Kishikawa, F, Kohno, M.
    • Journal Title

      Biochem. Biophys. Res. Commun. 339

      Pages: 1171-1177

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Suppression of tumor cell invasiveness by hydrolysable tannins (plant polyphenols) via the inhibition of matrix metalloproteinase-2/-9 activity.2005

    • Author(s)
      Tanimura, S., Kadomoto, R., Tanaka, T., Zhang, Y., Kouno, I., Kohno, M.
    • Journal Title

      Biochem.Biophys.Res.Commun. 330

      Pages: 1306-1313

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Efficient Suppression of Fibroblast Growth Factor-2-induced ERK Activation by the Cooperative Interaction among Mammalian Sprouty Isoforms.2005

    • Author(s)
      Ozaki, K., Miyazaki, S., Tanimura, S, Kohno, M.
    • Journal Title

      J. Cell Sci. 118

      Pages: 5861-5871

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Constitutive activation of the 41- and 43-kDa mitogen-activated protein (MAP) kinases in the progression of prostate cancer to an androgen-independent state.2005

    • Author(s)
      Oka, H., Chatani, Y., Kohno, M., Kawakita, M., Ogawa, O.
    • Journal Title

      Int.J.Urol. 12

      Pages: 899-905

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] ERK-MAP kinase inhibitors in cancer therapy.2005

    • Author(s)
      Kohno, M., Pouyssegur, J.
    • Journal Title

      Annals Medicine (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Hetero-oligomerization of mammalian Sprouty1 and Sprouty4 efficiently suppresses fibroblast growth factor-2-induced ERK activation by preventing the association of Grb2-Sos1 complex with FRS2.2005

    • Author(s)
      Ozaki, K., Miyazaki, S., Tanimura, S., Kohno, M.
    • Journal Title

      Oncogene (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Suppression of tumor cell invasiveness by hydrolysable tannins (plant polyphenols) via the inhibition of matrix metalloproteinase-2/ -9 activity.2005

    • Author(s)
      Tanimura, S., Kadomoto, R., Tanaka, T., Zhang, Y., Kouno, I, Kohno, M.
    • Journal Title

      Biochem. Biophys. Res. Commun. 330

      Pages: 1306-1313

    • Data Source
      KAKENHI-PROJECT-17016056
  • [Journal Article] Suppression of tumor cell invasiveness by hydrolysable tannins (plant polyphenols) via the inhibition of matrix metalloproteinase-2/-9 activity.2005

    • Author(s)
      Tanimura, S., Kadomoto, R., Tanaka, T., Zhang, Y., Kouno, I., Kohno, M.
    • Journal Title

      Biochem.Biophys.Res.Commun. 330

      Pages: 1306-1313

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Efficient Suppression of Fibroblast Growth Factor-2-induced ERK Activation by the Cooperative Interaction among Mammalian Sprouty Isoforms.2005

    • Author(s)
      Ozaki, K., Miyazaki, S., Tanimura, S., Kohno, M.
    • Journal Title

      J.Cell Sci. 118

      Pages: 5861-5871

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Journal Article] Synthesis and structure-activity relationships of thioflavone derivatives as specific inhibitors of the ERK-MAP kinase signaling pathway.2004

    • Author(s)
      Kataoka, T., Watanabe, S., Mori, E., Kadomoto, R., Tanimura, S., Kohno, M.
    • Journal Title

      Bioorg.Med.Chem. 12

      Pages: 2397-2407

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] チューブリン阻害活性の検定2004

    • Author(s)
      河野通明
    • Journal Title

      癌と化学療法 31巻

      Pages: 501-506

    • Data Source
      KAKENHI-PROJECT-13218101
  • [Journal Article] ERK-MAPキナーゼカスケードを標的とした癌治療2004

    • Author(s)
      河野通明
    • Journal Title

      現代医療 36巻

      Pages: 1401-1410

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] ERK-MAPキナーゼカスケードを標的とした癌治療2004

    • Author(s)
      河野通明
    • Journal Title

      現代医療 36巻

      Pages: 1401-1410

    • Data Source
      KAKENHI-PROJECT-13218101
  • [Journal Article] チューブリン阻害活性の検定2004

    • Author(s)
      河野通明
    • Journal Title

      癌と化学療法 31巻

      Pages: 501-506

    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Pharmacological inhibitors of the ERK signaling pathway : Application as anticancer drugs.2003

    • Author(s)
      Kohno, M., Pouyssegur, J.
    • Journal Title

      Prog.Cell Cycle Res. 5

      Pages: 219-224

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Specific blockade of the ERK pathway inhibits the invasiveness of tumor cells : down-regulation of matrix metalloproteinase-3/-9/-14 and CD44.2003

    • Author(s)
      Tanimura, S., Asato, K., Fujishiro, S., Kohno, M.
    • Journal Title

      Biochem.Biophys.Res.Commun. 304

      Pages: 801-806

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Pharmacological inhibitors of the ERK signaling pathway : Application as anticancer drugs.2003

    • Author(s)
      Kohno, M.
    • Journal Title

      Prog.Cell Cycle Res. 5巻

      Pages: 219-244

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Prolonged Nuclear Retention of Activated Extracellular Signal-Regulated Kinase1/2 is Required for Hepatocyte Growth Factor-induced Cell Motility.2002

    • Author(s)
      Tanimura, S., Nomura, K., Ozaki, K., Tsujimoto, M., Kondo, T., Kohno, M.
    • Journal Title

      J.Biol.Chem. 277

      Pages: 28256-28264

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14370747
  • [Journal Article] Anticancer drugs up-regulate HspBP1 and thereby antagonize the prosurvival function of Hsp70 in tumor cells.

    • Author(s)
      Tanimura, S., Hirano, A., Hashizume, J., Tasunaga, M., Kawabata, T., Ozaki, K., Kohno, M.
    • Journal Title

      J.Biol.Chem. (under review)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390020
  • [Presentation] UNC45 によるMyosin1E の細胞内局在制御2012

    • Author(s)
      平田弦也、 谷村 進、木原康孝、 尾崎惠一、武田弘資、 河野通明
    • Organizer
      第29回日本薬学会九州支部大会
    • Place of Presentation
      熊本県
    • Year and Date
      2012-12-09
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin1E によるカベオラ形成制御と細胞運動2012

    • Author(s)
      中原康子、 谷村 進、浜松絢子、尾崎惠一、武田弘資、河野通明
    • Organizer
      第29回日本薬学会九州支部大会
    • Place of Presentation
      熊本県
    • Year and Date
      2012-12-09
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin1E の細胞運動亢進作用はUNC45-Hsp90 複合体による細胞内局在制御によって調節される2012

    • Author(s)
      谷村 進、 平田弦也、大山 要、中原康子、松丸由美、尾崎惠一、武田弘資、河野通明
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡県
    • Year and Date
      2012-12-15
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] MEK and microtubule inhibitors together kill tumor cells through up-regulation of Bim and down-regulation of Mcl-12012

    • Author(s)
      谷村 進、河野通明
    • Organizer
      第71回日本癌学会学術大会
    • Place of Presentation
      北海道
    • Year and Date
      2012-09-20
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin1Eは糸状仮足の形成制御を介して細胞運動を促進する2011

    • Author(s)
      谷村進、河野通明, 他
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Year and Date
      2011-10-05
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] HC-toxinとPD184352の併用はBimの発現上昇を介してROSの蓄積と細胞死を相乗的に誘導する2011

    • Author(s)
      尾崎恵一、河野通明, 他
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Year and Date
      2011-10-03
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin 1E による細胞運動制御の分子メカニズム2011

    • Author(s)
      森田和幹、平田弦也、中原康子、 谷村 進、河野通明
    • Organizer
      第28回日本薬学会九州支部大会
    • Place of Presentation
      福岡県
    • Year and Date
      2011-12-10
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin 1E enhances cell motility via the induction of filopodia formation: essential role of phosphorylation on Ser7362011

    • Author(s)
      谷村 進、橋詰淳哉、渡邉一石、 河野通明
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      愛知県
    • Year and Date
      2011-10-05
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] MEK 阻害剤と微小管重合阻害剤の併用による細胞死誘導増強作用の分子機構2010

    • Author(s)
      浅井廣平、川畑拓誠、内山 綾、 谷村 進、河野通明
    • Organizer
      第27回日本薬学会九州支部大会
    • Place of Presentation
      長崎県
    • Year and Date
      2010-12-11
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] MEK阻害剤とHDAC阻害剤の併用による抗腫瘍効果増強-Xenograftでの検討-2010

    • Author(s)
      坂元利彰、藤尾康祐、梶川修平、上里新一、渡邉一石、 谷村 進、 尾崎恵一、河野通明
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪府
    • Year and Date
      2010-09-23
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] 新規細胞運動制御因子 SH3P2 は Myosin 1E と結合する2010

    • Author(s)
      河野通宏、橋詰淳哉、森田和幹、金丸雄祐、谷村 進、河野通明
    • Organizer
      第27回日本薬学会九州支部大会
    • Place of Presentation
      長崎県
    • Year and Date
      2010-12-11
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] 新規タンパク質 SH3P2 による細胞運動制御の分子機構2010

    • Author(s)
      谷村 進、大竹里佳、河野通宏、橋詰淳哉、後藤愛依子、黒崎由希子、瀬井香奈子、河野通明
    • Organizer
      第83回日本生化学会大会
    • Place of Presentation
      兵庫県
    • Year and Date
      2010-12-08
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin 1E は invadopodia の形成を介してがん細胞の浸潤を調節する2010

    • Author(s)
      谷村 進、橋詰淳哉、後藤愛依子、河野通宏、大竹里佳、渡邉一石、河野通明
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪府
    • Year and Date
      2010-09-23
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Myosin 1E による細胞運動制御の分子機構2010

    • Author(s)
      大竹里佳、橋詰淳哉、中原康子、 谷村 進、河野通明
    • Organizer
      第27回日本薬学会九州支部大会
    • Place of Presentation
      長崎県
    • Year and Date
      2010-12-11
    • Data Source
      KAKENHI-PROJECT-22300340
  • [Presentation] Blockade of the ERK pathway enhances the antitumor activity of microtubule-destabilizing agents in vitro and in vivo.2008

    • Author(s)
      Watanabe, K., Tanimura, S., Yasunaga, M. Uchiyama, A, Kohno, M.
    • Organizer
      AACR Annual Meeting 2008
    • Place of Presentation
      San Diego
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Presentation] ERK-MAPキナーゼ経路の選択的遮断を基盤としたがん化学療法の開発2007

    • Author(s)
      河野通明
    • Organizer
      第66回日本がん学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2007-10-04
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Presentation] Targeting the ERK signaling pathway in cancer therapy2007

    • Author(s)
      河野通明、谷村進、尾崎惠一、渡邊一石
    • Organizer
      第65回日本癌学会総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-17016056
  • [Presentation] Blockade of the PI3-kinase-Akt signaling pathway enhances induction of apoptosis by microtubule- destabilizing agents in tumor cells in which the pathway is constitutively activated.2007

    • Author(s)
      Watanabe, K., Fujiwara, Y., Tanimura, S., Ozaki, K, Kohno, M.
    • Organizer
      AACR Annual Meeting 2007
    • Place of Presentation
      Los Angeles
    • Data Source
      KAKENHI-PROJECT-17016056
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