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Abnormal membranerepair as a new concept for muscular dystrophy and search for new disease genes

Research Project

Project/Area Number 23659454
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Neurology
Research InstitutionKobe University

Principal Investigator

KANAGAWA Motoi  神戸大学, 医学研究科, 講師 (00448044)

Co-Investigator(Kenkyū-buntansha) TODA Tatsushi  神戸大学, 医学研究科, 教授 (30262025)
Co-Investigator(Renkei-kenkyūsha) NAGAMORI Shushi  大阪大学, 医学系研究科, 助教 (90467572)
MIYAKE Katsuya  香川大学, 医学部, 准教授 (30219745)
Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords細胞・組織 / 筋ジストロフィー / 膜修復 / ジスフェルリン / 神経分子病態学 / 細胞膜修復
Research Abstract

Anti-dysferlin antibodies and a method to isolate dysferlin-containing vesicle were established, which enables us to analyze components of the dysferlin-containing membranes. Proteins up-regulated correlatively to disease severity of muscular dystrophy were identified. Analyses of double mutant mice of dysferlin and other muscular dystrophy mice showed that dysferlin-deficiency led more severe muscular dystrophic phenotype. These results will contribute to deeper understanding of muscular dystrophy pathogenesis.

Report

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

    (4 results)

All 2011 Other

All Presentation (2 results) Remarks (2 results)

  • [Presentation] The dysferlin-mediated membrane repair system contributes to maintenance of skeletal muscle cell viability in mouse models of muscular dystrophy2011

    • Author(s)
      戸田 達史
    • Organizer
      World Muscle Society
    • Place of Presentation
      アルマンシル、ポルトガル
    • Related Report
      2012 Final Research Report
  • [Presentation] The dysferlin-mediated membrane repair system contributes to maintenance of skeletal muscle cell viability in mouse models of muscular dystrophy2011

    • Author(s)
      戸田 達史
    • Organizer
      世界筋学会
    • Place of Presentation
      アルマンシル、ポルトガル
    • Related Report
      2011 Research-status Report
  • [Remarks]

    • URL

      http://www.med.kobe-u.ac.jp/clgene/

    • Related Report
      2012 Final Research Report
  • [Remarks]

    • URL

      http://www.med.kobe-u.ac.jp/clgene/

    • Related Report
      2011 Research-status Report

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

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