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The analysis of molecular mechanism of Caudal Regression Syndrome (CRS)

Research Project

Project/Area Number 20790163
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field General anatomy (including Histology/Embryology)
Research InstitutionKumamoto University

Principal Investigator

SUZUKI Kentaro  Kumamoto University, 発生医学研究所 (20404345)

Project Period (FY) 2008 – 2009
Project Status Completed (Fiscal Year 2009)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2008: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Keywords先天異常学 / 奇形学 / 尾部退行症候群(人魚病) / 増殖因子 / 尾部退行症候群 / 泌尿生殖器
Research Abstract

Caudal regression syndrome (CRS) comprises developmental anomalies of the caudal vertebrae, urogenital organs and hind limbs. The mermaid like phenotypes has been often described in many literatures including old legends. However, the pathogenetic mechanisms are not understood. This study suggested that Bmp4, one of the Bmp ligands, may be essential molecule to make the caudal body with regulating the expression of patterning genes.

Report

(3 results)
  • 2009 Annual Research Report   Final Research Report ( PDF )
  • 2008 Annual Research Report
  • Research Products

    (2 results)

All 2009

All Presentation (2 results)

  • [Presentation] Wnt/beta-cateninシグナルによる外生殖器原器隆起点の決定メカニズム2009

    • Author(s)
      鈴木堅太郎
    • Organizer
      日本分子生物学会
    • Place of Presentation
      パシフィコ横浜(神奈川)
    • Year and Date
      2009-12-11
    • Related Report
      2009 Annual Research Report
  • [Presentation] Wnt/beta-cateninシグナルによる外生殖器原器隆起点の決定メカニズム2009

    • Author(s)
      鈴木堅太郎、中田翔子、中潟直己、Westphal Heiner、山田源
    • Organizer
      第32回日本分子生物学会
    • Place of Presentation
      パシフィコ横浜、神奈川
    • Related Report
      2009 Final Research Report

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Published: 2008-04-01   Modified: 2016-04-21  

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