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中文摘要
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英文摘要
The University of Minnesota Muscular Dystrophy Center (UMN-MDCenter) has grown in scope and breadth since being organized to improve collaboration in basic, clinical and translational investigation of muscle biology and disease. Success of the MDCenter has recently helped recruit several prominent muscle investigators to Minnesota, capitalizing on existing strength to create what is now a unique multifaceted program focused on understanding muscle and treating muscle disease. To maximize interaction, collaboration and productivity of the expanding MDCenter, we are applying for NIAMS Core Center support with the following specific aims: 1) Core B: To strengthen and increase accessibility of a research core that provides clinical specimens to muscle investigators, and uses the CLIA-certified muscle biopsy laboratory to characterize human and animal muscle with comprehensive histological and immunostaining methods. 2) Core C: To strengthen and expand a repository of murine muscular dystrophy models for muscle investigators, which is coupled with the unique ability of our Center to characterize human and animal muscle force generation at molecular, cellular and whole tissue levels. 3) Core A: To provide administrative support for the research cores, and to establish a pilot and feasibility program for new independent investigators, which will strengthen and extend current MDCenter programs for undergraduate, graduate and post-doctoral trainees. 4) To increase institutional, regional and national awareness of UMN-MDCenter and CCMBM to enhance provision of institutional resources commensurate with the potential of this program.
期刊论文(12)
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会议论文
Equine developmental orthopaedic diseases--a genome-wide association study of first phalanx plantar osteochondral fragments in Standardbred trotters.
马发育性骨科疾病——标准种马第一趾骨足底骨软骨碎片的全基因组关联研究。
DOI: 10.1111/age.12064
发表时间: 2013
期刊: Animal genetics
影响因子: 2.4
作者: [Lykkjen,S, Dolvik,NI, McCue,ME, Rendahl,AK, Mickelson,JR, Røed,KH]
通讯作者: Røed,KH
DOI: 10.1152/ajpcell.00279.2011
发表时间: 2012-04-01
期刊: AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
影响因子: 5.5
作者: [Bandschapp, Oliver, Soule, Charles L., Iaizzo, Paul A.]
通讯作者: Iaizzo, Paul A.
Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice.
Flt-1 单倍体不足通过 mdx 小鼠中脉管系统的发育增加改善肌营养不良表型。
DOI: 10.1093/hmg/ddq334
发表时间: 2010
期刊: Human molecular genetics
影响因子: 3.5
作者: [Verma,Mayank, Asakura,Yoko, Hirai,Hiroyuki, Watanabe,Shuichi, Tastad,Christopher, Fong,Guo-Hua, Ema,Masatsugu, Call,JarrodA, Lowe,DawnA, Asakura,Atsushi]
通讯作者: Asakura,Atsushi
DOI: 10.1111/jvim.12133
发表时间: 2013-09
期刊: Journal of veterinary internal medicine
影响因子: 2.6
作者: [Raffaella B Teixeira;Aaron Rendahl;S. Anderson;James R. Mickelson;D. Sigler;B. Buchanan;R. Coleman;Molly E. McCue]
通讯作者: Raffaella B Teixeira;Aaron Rendahl;S. Anderson;James R. Mickelson;D. Sigler;B. Buchanan;R. Coleman;Molly E. McCue
Muscular Dystrophy Center Core Laboratories
  • 批准号:
    8139109
  • 项目类别:
  • 资助金额:
    $60.4万
  • 财政年份:
    2009
  • 负责人:
    JAMES M ERVASTI
  • 依托单位:
Muscular Dystrophy Center Core Laboratories
  • 批准号:
    8323822
  • 项目类别:
  • 资助金额:
    $60.4万
  • 财政年份:
    2009
  • 负责人:
    JAMES M ERVASTI
  • 依托单位:
Costamere Defects in Muscular Dystrophies
  • 批准号:
    8213728
  • 项目类别:
  • 资助金额:
    $34.63万
  • 财政年份:
    2005
  • 负责人:
    JAMES M ERVASTI
  • 依托单位:
Costamere Defects in Muscular Dystrophies
  • 批准号:
    7173799
  • 项目类别:
  • 资助金额:
    $33.32万
  • 财政年份:
    2005
  • 负责人:
    JAMES M ERVASTI
  • 依托单位:
海外基金