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AOYAMA Hiroshi  青山 洋史

ORCIDConnect your ORCID iD *help
Researcher Number 40374699
Other IDs
Affiliation *help 2015 – 2018 : 東京薬科大学, 薬学部, 准教授
2013 : 東京大学, 分子細胞生物学研究所, 助教
2012 – 2013 : 東京薬科大学, 薬学部, 准教授
2007 – 2009 : The University of Tokyo, 分子細胞生物学研究所, 助教
Review Section/Research Field
Principal Investigator
Drug development chemistry / Chemical pharmacy
Except Principal Investigator
Drug development chemistry
Keywords
Principal Investigator
C型肝炎 / HCV / 酵素阻害 / ホスホン酸エステル / 有機化学 / 虚血性疾患 / ミトコンドリア / 血液凝固 / 虚血/再灌流障害 / フォールディング … More / アミノ酸 / セリンプロテアーゼ / タンパク質 / ダントロレン / 有機合成 / 虚血・再灌流障害 / 光親和性標識 / 生理活性 / PTP … More
Except Principal Investigator
酵素阻害剤 / 生理活性物質 / 核内受容体リガンド / 変異ロドプシン / 脱炭酸 / ジフェニルペンタン / 核内受容体 / 蛋白質相互作用 / 酵素選択性 / トラフィッキング / テンプレート / 構造活性相関 / トリアゾキノリン類 / サリドマイド / 結合定数 / 化合部物ライブラリー / ミミック / 光学分割 / 抗アンドロゲン / ホスホン酸 / ロドプシン / ホスホプロリン / マルチテンプレート / 医薬分子機能学 / 細胞内局在 / フォールディング異常症 / 抗ウイルス剤 / プロリン / ニーマン・ピック病C型 / ジペプチド / プロテアーゼ阻害剤 / 構造展開 / ホスホニル化反応 / 生物応答調節 / フォールディング / 生物活性 / 網膜色素変性症 / ホスフィン酸 / ケミカルジェネティクス / プロテアーゼ / 阻害形式 / 錯体形成 / ジペプチドイソスター / 蛋白変性症 / バイオイソスター / 生物応答調節剤創製法 / PPAR / 膜タンパク質 / 肝臓X受容体 Less
  • Research Projects

    (6results)
  • Research Products

    (44results)
  • Co-Researchers

    (10People)
  •  Basic pharmaceutical study of relationship between phosphorus atom introduction and non-competition of inhibitorPrincipal Investigator

    • Principal Investigator
      青山 洋史
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Drug development chemistry
    • Research Institution
      Tokyo University of Pharmacy and Life Science
  •  Application of phosphate mimetics to development of biologically active compounds

    • Principal Investigator
      Yokomatsu Tsutomu
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Drug development chemistry
    • Research Institution
      Tokyo University of Pharmacy and Life Science
  •  Basic medicinal chemistry based on behavioral structure-building regulation of proteinPrincipal Investigator

    • Principal Investigator
      AOYAMA hiroshi
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Drug development chemistry
    • Research Institution
      Tokyo University of Pharmacy and Life Science
  •  Chemical control of protein dramatype

    • Principal Investigator
      HASHIMOTO Yuichi
    • Project Period (FY)
      2010 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Drug development chemistry
    • Research Institution
      The University of Tokyo
  •  Biological response modification based on multi-template and dramatype approaches.

    • Principal Investigator
      HASHIMOTO Yuichi
    • Project Period (FY)
      2007 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Drug development chemistry
    • Research Institution
      The University of Tokyo
  •  Basic medicinal chemistry in novel biologically active compounds based on behavioral regulation of proteinPrincipal Investigator

    • Principal Investigator
      AOYAMA Hiroshi
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Chemical pharmacy
    • Research Institution
      The University of Tokyo

All 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 Other

All Journal Article Presentation

  • [Journal Article] A novel and facile route for the synthesis of medetomidine as the α2-adrenoceptor agonist2017

    • Author(s)
      Kaboudin Babak、Haghighat Hamideh、Aieni Samira、Behrouzi Leila、Kazemi Foad、Kato Jun-ya、Aoyama Hiroshi、Yokomatsu Tsutomu
    • Journal Title

      Journal of the Iranian Chemical Society

      Volume : 14 Pages : 1735-1739

    • DOI
      10.1007/s13738-017-1114-0
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K08033
  • [Journal Article] Synthesis of 5-aminobenzoimidazo[1,2-a]quinoline derivatives through one-pot two-step cascade reaction2016

    • Author(s)
      J. Kato, Y. Ito, R. Ijuin, H. Aoyama, and T. Yokomatsu
    • Journal Title

      Heterocycles

      Volume : xx

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25460155
  • [Journal Article] Competitive Tryptase Inhibitor Skeleton: Shift in Molecular Recognition Resulted from Skeletal Conversion of Carboxylate into Phosphonate2015

    • Author(s)
      Hiroshi Aoyama, Ryosuke Ijuin, Jun-ya Kato, Sarasa Urushiyama, Masashi Tetsuhashi, Yuichi Hashimoto, Tsutomu Yokomatsu
    • Journal Title

      Bioorg. Med. Chem. Lett.

      Volume : 25 Pages : 3676-3680

    • DOI
      10.1016/j.bmcl.2015.06.039
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K08033, KAKENHI-PROJECT-25460155
  • [Journal Article] Small- molecular Inhibitors of Ca^2+-induced Mitochondrial Permeability Transition (MPT) Derived from Muscle Relaxant Dantrolene, Bioorg2013

    • Author(s)
      Shinpei Murasawa 他8名
    • Journal Title

      Med. Chem

      Volume : 20 Pages : 6384-6393

    • DOI
      10.1016/j.bmc.2012.08.062
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22249006, KAKENHI-PROJECT-21790107, KAKENHI-PROJECT-24790119
  • [Journal Article] A Novel and Simple Method for the Preparation of (R)- and (S)-Pyrrolidine-2-phosphonic Acids: Phosphonic Acid Analogues of Proline2013

    • Author(s)
      Babak Kaboudin, Jun-ya Kato, Hiroshi Aoyama, and Tsutomu Yokomatsu
    • Journal Title

      Tetrahedron: Asymmetry

      Volume : 24 Pages : 1562-1566

    • DOI
      10.1016/j.tetasy.2013.10.013
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25460155
  • [Journal Article] A Catalyst-free, Three-component Decarboxylative Coupling of Amino Acids with Aldehydes and H-dialkylphosphites for the Synthesis of α-Aminophosphonates2013

    • Author(s)
      Babak Kaboudin, Leila Karami, Jun-ya Kato, Hiroshi Aoyama, and Tsutomu Yokomatsu
    • Journal Title

      Tetrahedron Lett.

      Volume : 54 Pages : 4872-4875

    • DOI
      10.1016/j.tetlet.2013.06.129
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25460155
  • [Journal Article] Novel strategy for synthesis of substituted benzimidazo[1,2-a]quinolones2013

    • Author(s)
      Jun-ya Kato, Yutaro Ito, Ryosuke Ijuin, Hiroshi Aoyama, Tsutomu Yokomatsu
    • Journal Title

      Org. Lett.

      Volume : 15 Pages : 3794-3797

    • DOI
      10.1021/ol4017723
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24790119, KAKENHI-PROJECT-25460147
  • [Journal Article] Design, synthesis, and biological evaluation of novel trans repression-selective liver X receptor (LXR) ligands with 5,11-dihydro-5-methyl-11-methylene-6 H-dibenz[b,e]azepin-6-one skeleton2012

    • Author(s)
      Atsushi Aoyama
    • Journal Title

      J. Med. Chem.

      Volume : 55 Pages : 7360-7377

    • DOI
      10.1021/jm3002394
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21790107, KAKENHI-PROJECT-22249006
  • [Journal Article] Fused heterocyclic amido compounds as anti-hepatitis C virus agents2011

    • Author(s)
      Hiroshi Aoyama, Masahiko Nakamura
    • Journal Title

      Bioorg. Med. Chem.

      Volume : 19 Pages : 2675-2687

    • DOI
      10.1016/j.bmc.2011.03.002
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-11J09835, KAKENHI-PROJECT-22249006
  • [Journal Article] Structural development studies of anti-hepatitis virus C virus agents2010

    • Author(s)
      M.Nakamura, A.Aoyama, M.T.M.Salim, M.Okamoto, M.Baba, M.Baba, H.Miyachi, Y.Hashimoto, H.Aoyama
    • Journal Title

      Bioorg. Med. Chem

      Volume : 18 Pages : 2402-2411

    • DOI
      10.1016/j.bmc.2010.02.057
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22249006
  • [Journal Article] Nitrogen-containing fused-heteroaromatic compounds as a anti-bovine diarrhea virus (BVDV) agents.2010

    • Author(s)
      Aoyama H, Baba M, Hashimoto Y
    • Journal Title

      Curr. Bioactive Comp. 6(2)

      Pages : 118-128

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Polymethylated γ-carbolines with potent anti-bovine viral diarrhea virus(BVDV)activity.2009

    • Author(s)
      Hiroshi Aoyama, 他6名
    • Journal Title

      Heterocycles 77

      Pages : 779-785

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Polymethylated γ-carbolines with potent anti-bovine viral diarrhea virus (BVDV) activity.2009

    • Author(s)
      Hiroshi Aoyama, 他6名
    • Journal Title

      Heterocycles 77(2)

      Pages : 779-785

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Liver X receptor(LXR)modulators with dibenz[b,f][1,4]oxazepin-11-one,(Z)-dibenz[b,f]azocin-6-one, and 11, 12-dihydrodibenz[b,f]azocin-6-one skeleton.2009

    • Author(s)
      Atsushi Aoyama, 他4名
    • Journal Title

      Heterocycles 78

      Pages : 2209-2216

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Degradation-promoters of cellular inhibitor of apoptosis protein 1 based on bestatin and actinonin.2008

    • Author(s)
      Sato S, Tetsuhashi M, Sekine K, Miyachi H, Naito M, Hashimoto Y, Aoyama H
    • Journal Title

      Bioorg. Med. Chem. 16(8)

      Pages : 4685-4698

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Co-existence of alpha-glucosidase-inhibitory activity and liver X receptor-regulatory activities and their separation by structural development.2008

    • Author(s)
      Dodo K, Aoyama H, Noguchi-Yachide T, Makishima M, Miyachi H, Hashimoto Y
    • Journal Title

      Bioorg. Med. Chem. 16(8)

      Pages : 4272-4285

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Demonstration of direct binding of cIAP1 degradationpromoting bestatin analogs to BIR3 domain : synthesis and application of fluorescent bestatin ester analogs2008

    • Author(s)
      S. Sato, H. Aoyama et.al.
    • Journal Title

      Bioorg. Med. Chem. Lett 18

      Pages : 3354-3358

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Demonstration of Direct Binding of cIAP1 Degradation-promoting Bestatin Analogs to BIR3 Domain : Synthesis and Application of Fluorescent Bestatin Ester Analogs2008

    • Author(s)
      Shinichi Sato, Hiroshi Aoyama, Hiroyuki Miyachi, Mikihiko Naito, Yuichi Hashimoto
    • Journal Title

      Bioorg. Med. Chem. Lett 18

      Pages : 3354-3358

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Degradation-promoters of Cellular Inhibitor of Apoptosis Protein 1 Based on Bestatin and Actinonin2008

    • Author(s)
      Shinichi Sato, Masashi Tetsuhashi, Keiko Sekine, Hiroyuki Miyachi, Mikihiko Naito, Yuichi Hashimoto, Hiroshi Aoyama
    • Journal Title

      Bioorg. Med. Chem 16

      Pages : 4685-4698

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Degradationpromoters of Cellular Inhibitor of Apoptosis Protein 1 Based on B estatin and Actinonin2008

    • Author(s)
      S. Sato, H. Aoyama et.al.
    • Journal Title

      Bioorg. Med. Chem 16

      Pages : 4685-4698

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Fusarielin A as an Anti-angiogenic and Anti-proliferative Agent : Basic Biological Characterization2008

    • Author(s)
      Haruka Fujimoto, Hiroshi Aoyama, Tomomi Noguchi-Yachide, Yuichi Hashimoto, Hisayoshi Kobayashi
    • Journal Title

      Chem. Pharm. Bull 56

      Pages : 298-304

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] LXR antagonists with a 5-substituted phenanthridin-6-one skeleton: Synthesis and LXR transrepression activities of conformationally restricted carba-To901317 analogs.2008

    • Author(s)
      Atsushi Aoyama, 他5名
    • Journal Title

      Heterocycles 76(1)

      Pages : 137-142

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Journal Article] Development of Tubulin-Polymerization Inhibitors Based on the Thalidomide Skeleton2007

    • Author(s)
      Hiroshi Aoyama
    • Journal Title

      Chem. Phann. Bull. 55

      Pages : 944-949

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Development of Tubulin-polymerization Inhibitors Based on the Thalidomide Skeleton2007

    • Author(s)
      Hiroshi Aoyama, Tomomi Noguchi, Takashi Misawa, Takanori Nakamura, Hiroyuki Miyachi, Yuichi Hashimoto, Hisayoshi Kobayashi
    • Journal Title

      Chem. Pharm. Bull 55

      Pages : 944-949

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Journal Article] Development of tubulin-polymerization inhibitors based on thalidomide skeleton2007

    • Author(s)
      H. Aoyama, 他6名
    • Journal Title

      Chelnica1 & Pharmaceutical Bullietin 55

      Pages : 944-949

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] Synthesis of a-Aminophosphonates from a;-Amino Acids by Catalyst-free Three-component Decarboxylative Coupling Reactions2014

    • Author(s)
      B. Kaboudin, L. Karami, J. Kato,H.Aoyama, and T. Yokomatsu
    • Organizer
      20th International Conference on Phosphorus Chemistry
    • Place of Presentation
      Doubline, Ireland
    • Data Source
      KAKENHI-PROJECT-25460155
  • [Presentation] 疫調節作用選択的な肝臓X受容体(LXR)リガンドの創製2012

    • Author(s)
      青山惇、梅田(遠藤)香織、岸田健治、大金賢司、谷内出(野口)友美、青山洋史、石川稔、宮地弘幸、槇島誠、橋本祐一
    • Organizer
      日本レチノイド研究会第23回学術集会
    • Place of Presentation
      米子
    • Data Source
      KAKENHI-PROJECT-22249006
  • [Presentation] Liver X Receptor (LXR)リガンドの構造展開によるTransrepression作用選択的リガンドの創製2012

    • Author(s)
      青山惇, 他6名
    • Organizer
      日本薬学会第132年会
    • Place of Presentation
      札幌
    • Year and Date
      2012-03-31
    • Data Source
      KAKENHI-PROJECT-22249006
  • [Presentation] 免疫調節作用選択的な肝臓X受容体(LXR)リガンドの創製2012

    • Author(s)
      青山惇 他9名
    • Organizer
      日本レチノイド研究会第23回学術集会
    • Place of Presentation
      米子(鳥取県)
    • Data Source
      KAKENHI-PROJECT-22249006
  • [Presentation] LXRリガンドの構造展開による選択的IL-6産生抑制剤の創製2011

    • Author(s)
      青山惇, 他4名
    • Organizer
      日本レチノイド研究会第22回学術集会
    • Place of Presentation
      東京
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PROJECT-22249006
  • [Presentation] LXRを介した抗炎症作用を有する選択的リガンドの創製2010

    • Author(s)
      青山惇, 他6名
    • Organizer
      日本薬学会第130年会
    • Place of Presentation
      岡山
    • Year and Date
      2010-03-29
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] フタルイミド骨格を基盤としたトリプターゼ阻害剤の創製2009

    • Author(s)
      鉄橋正士、橋本祐一、青山洋史
    • Organizer
      第28回メディシナルケミストリーシンポジウム
    • Place of Presentation
      東京
    • Year and Date
      2009-11-26
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] 配座固定を基盤とした核内受容体LXRの新規リガンド創製2009

    • Author(s)
      青山惇、他7名
    • Organizer
      日本薬学会第129年会
    • Place of Presentation
      京都
    • Year and Date
      2009-03-26
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] 3,3-diindolylmethane (DIM)誘導体におけるHL-60細胞分化促進活性2009

    • Author(s)
      谷内出友美、鉄橋正士、青山洋史、橋本祐一
    • Organizer
      日本薬学会第129年会
    • Place of Presentation
      京都
    • Year and Date
      2009-03-26
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] 抗BVDV活性を指標とした3環性γ-カルボリン類縁体による抗ウイルス効果2008

    • Author(s)
      青山洋史、他8名
    • Organizer
      第52回日本薬学会関東支部大会
    • Place of Presentation
      東京
    • Year and Date
      2008-10-04
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] 配座固定を基盤とした核内受容体LXRの新規アンタゴニスト創製2008

    • Author(s)
      青山惇、他7名
    • Organizer
      第34回反応と合成の進歩シンポジウム
    • Place of Presentation
      京都
    • Year and Date
      2008-11-04
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] 配座固定を基盤とした核内受容体LXRの新規リガンド創製2008

    • Author(s)
      青山惇、他7名
    • Organizer
      第27回メディシナルケミストリーシンポジウム
    • Place of Presentation
      大阪
    • Year and Date
      2008-11-26
    • Data Source
      KAKENHI-PROJECT-19390028
  • [Presentation] Fusarielin Aの生物活性とその分子基盤2008

    • Author(s)
      藤本悠、青山洋史、谷内出(野口)友美、橋本祐一、小林久芳
    • Organizer
      日本薬学会第128年会
    • Place of Presentation
      横浜
    • Year and Date
      2008-03-26
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Presentation] タンパク質寿命制御に立脚した新規アポトーシス誘導剤創製研究2008

    • Author(s)
      佐藤伸一、青山洋史、鉄橋正士、宮地弘幸、内藤幹彦、橋本祐一
    • Organizer
      日本薬学会第128年会
    • Place of Presentation
      横浜
    • Year and Date
      2008-03-27
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Presentation] cIAP1減少を介した新規アポトーシス誘導剤の合成研究2007

    • Author(s)
      佐藤伸一、青山洋史、内藤幹彦、宮地弘幸、橋本祐一、棚谷綾
    • Organizer
      第33回反応と合成の進歩シンポジウム
    • Place of Presentation
      長崎
    • Year and Date
      2007-11-05
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Presentation] cIAP1減少を介した新規アポトーシス誘導剤創製研究2007

    • Author(s)
      佐藤伸一、青山洋史、棚谷綾、内藤幹彦、宮地弘幸、橋本祐一
    • Organizer
      第26回メディシナルケミストリーシンポジウム
    • Place of Presentation
      相模原
    • Year and Date
      2007-11-28
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Presentation] Fusarielin Aの生物活性とその分子基盤2007

    • Author(s)
      藤本悠、青山洋史、谷内出(野口)友美、橋本祐一、小林久芳
    • Organizer
      第49回天然有機化合物討論会
    • Place of Presentation
      札幌
    • Year and Date
      2007-09-19
    • Data Source
      KAKENHI-PROJECT-19790007
  • [Presentation] 多置換[1,2,4]トリアゾロ[1,5-a]キノリン類の新規合成法の開発

    • Author(s)
      加藤 淳也、成瀬 央、伊集院 良祐、青山 洋史、横松 力
    • Organizer
      第44回複素環討論会
    • Place of Presentation
      札幌市
    • Year and Date
      2014-09-10 – 2014-09-13
    • Data Source
      KAKENHI-PROJECT-25460155
  • [Presentation] Synthesis of a-Aminophosphonates from a-Amino Acids by Catalyst-free Three-component Decarboxylative Coupling Reactions

    • Author(s)
      B. Kaboudin, L. Karami, J. Kato, H. Aoyama, and T. Yokomatsu
    • Organizer
      20th International Conference on Phosphorus Chemistry
    • Place of Presentation
      Dublin, Ireland
    • Year and Date
      2014-06-28 – 2014-07-02
    • Data Source
      KAKENHI-PROJECT-25460155
  • 1.  NOGUCHI Tomomi (20401284)
    # of Collaborated Projects : 2results
    # of Collaborated Products : 4results
  • 2.  HASHIMOTO Yuichi (90164798)
    # of Collaborated Projects : 2results
    # of Collaborated Products : 9results
  • 3.  KOBAYASHI Hisayoshi (80225531)
    # of Collaborated Projects : 2results
    # of Collaborated Products : 0results
  • 4.  ISHIKAWA Minoru (70526839)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 2results
  • 5.  SUGITA Kazuyuki (60542090)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 1results
  • 6.  MATSUMOTO Yotaro (90420041)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 0results
  • 7.  MISAWA Takashi (40709820)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 0results
  • 8.  Yokomatsu Tsutomu (70158369)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 7results
  • 9.  伊集院 良祐 (40442925)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 2results
  • 10.  KABOUDIN Babak
    # of Collaborated Projects : 1results
    # of Collaborated Products : 4results

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