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Analysis of the function of KLF5 in blood cells and elucidation of its underlying molecular mechanism which leads to clinical application

Research Project

Project/Area Number 23791072
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Hematology
Research InstitutionThe University of Tokyo

Principal Investigator

MATSUMURA Takayoshi  東京大学, 医学部附属病院, 助教 (80436485)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords血球細胞 / 巨核球 / 血小板 / 血管新生 / 転写因子 / 血液内科学 / KLF5
Research Abstract

With a broad analysis of the function of KLF5 in blood cells, I found that KLF5 is critical especially to normal functions of platelets. Platelet lineage-specific Klf5-knockout mice showed impaired in vivo thrombus formation and angiogenesis activity, and I investigated the underlying molecular mechanisms. Our results can lead to future therapeutic interventions for various cardiovascular and cancer diseases

Report

(3 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Research-status Report
  • Research Products

    (2 results)

All 2013 Other

All Presentation (2 results)

  • [Presentation] Platelet surface molecules regulated by KLF5 are critical to in vivo thrombus formation and angiogenesis2013

    • Author(s)
      松村 貴由、他
    • Organizer
      第77回日本循環器学会
    • Place of Presentation
      横浜
    • Year and Date
      2013-03-17
    • Related Report
      2012 Final Research Report
  • [Presentation] Platelet surface molecules regulated by KLF5 are critical to in vivo thrombus formation and angiogenesis

    • Author(s)
      松村 貴由
    • Organizer
      第77回日本循環器学会
    • Place of Presentation
      横浜
    • Related Report
      2012 Annual Research Report

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Published: 2011-08-05   Modified: 2019-07-29  

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