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Identification of responsible gene(s) for congenital heart defect using the model mice of Down syndrome

Research Project

Project/Area Number 23791194
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pediatrics
Research InstitutionKeio University

Principal Investigator

MIYAMOTO Kenichi  慶應義塾大学, 医学部, 特任助教 (00424185)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2011: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywordsダウン症 / 心奇形 / ノックアウトマウス / Zfp295 / ヒト人工染色体 / 遺伝子量効果
Research Abstract

In this study, we focused on the congenital heart defect that is observed with relatively high frequency in the patients with Down syndrome, and attempted to generate the knockout mice of Zfp295 that is one of the candidate genes for Down syndrome congeni

Report

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

    (2 results)

All 2012

All Presentation (2 results)

  • [Presentation] ヒト人工染色体(HAC)導入マウスを用いたダウン症の原因遺伝子と遺伝子量効果解明への試み2012

    • Author(s)
      宮本 憲一, 鈴木 伸卓, 堺 弘介, 浅川 修一, 岡崎 恒子, 清水 信義, 池野 正史, 工藤 純
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡
    • Related Report
      2012 Final Research Report
  • [Presentation] ヒト人工染色体(HAC)導入マウスを用いたダウン症の原因遺伝子と遺伝子量効果解明の試み2012

    • Author(s)
      宮本憲一
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      マリンメッセ福岡
    • Related Report
      2012 Annual Research Report

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

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