Rchr
J-GLOBAL ID:200901098901869403   Update date: Sep. 20, 2024

Oyamada Hideto

オヤマダ ヒデト | Oyamada Hideto
Affiliation and department:
Research field  (1): Pharmacology
Research theme for competitive and other funds  (9):
  • 2019 - 2024 悪性高熱症の遺伝子診断を目指した1型リアノジン受容体遺伝子変異体の作製と発現
  • 2016 - 2019 A trial for establishment of the cell banks as the models of malignant hyperthemia
  • 2003 - 2006 SCREENING FOR THE FUNCTIONAL DOMAINS IN THE RYANODINE RECEPTOR
  • 2002 - 2003 DEVELOPMENT OF THE VISUALIZED DOMINANT NEGATIVE METHOD FOR THE CALCIUM RELEASE CHANNEL
  • 2000 - 2002 SPATIO-TEMPORAL ANALYSIS OF CA^<2+> RELEASE CHANNEL RELATED TO THE VARIOUS TYPE OF THE INTRACELLULAR CA^<2+> SIGNALS
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Papers (65):
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MISC (78):
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Lectures and oral presentations  (42):
  • Construction and integration of the All-in-One type single double-conditional shRNA expression vectors for spatio-temporal gene and/or cell targeting
    (The 42nd Annual Meeting of the Japan Neuroscience Society 2019)
  • ヒト乳がん細胞株MDA-MB-231のCD44陽性細胞においてmicroRNA-17、-93はp21発現を抑制する
    (日本癌学会総会記事 2017)
  • ヒト角膜上皮細胞における紫外線誘発細胞毒性に対する緑茶カテキンの抑制効果についての検討(学位甲)
    (昭和学士会雑誌 2016)
  • MDA-MB-231 CD44陽性細胞はTublin阻害剤曝露後miR-93増加によりp21発現を抑制する
    (日本癌学会総会記事 2016)
  • TNBCのBasal likeではEribulinとROS阻害剤の併用添加で酸化ストレス増加を抑制する
    (日本乳癌学会総会プログラム抄録集 2015)
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Professional career (1):
  • 博士(医学) (東京大学医学系研究科)
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