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Journal Abstract Search

108 related items for PubMed ID: 15907291

  • 1. A 1.3 kb promoter fragment confers spatial and temporal expression of utrophin A mRNA in mouse skeletal muscle fibers.
    Stocksley MA, Chakkalakal JV, Bradford A, Miura P, De Repentigny Y, Kothary R, Jasmin BJ.
    Neuromuscul Disord; 2005 Jun; 15(6):437-49. PubMed ID: 15907291
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  • 4. Increased expression of utrophin in a slow vs. a fast muscle involves posttranscriptional events.
    Gramolini AO, Bélanger G, Thompson JM, Chakkalakal JV, Jasmin BJ.
    Am J Physiol Cell Physiol; 2001 Oct; 281(4):C1300-9. PubMed ID: 11546668
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  • 5. Targeted inhibition of Ca2+ /calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle.
    Chakkalakal JV, Michel SA, Chin ER, Michel RN, Jasmin BJ.
    Hum Mol Genet; 2006 May 01; 15(9):1423-35. PubMed ID: 16551657
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  • 10. Changes in acetylcholine receptor function induce shifts in muscle fiber type composition.
    Jin TE, Wernig A, Witzemann V.
    FEBS J; 2008 May 01; 275(9):2042-54. PubMed ID: 18384381
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  • 11. Duchenne muscular dystrophy and the neuromuscular junction: the utrophin link.
    Gramolini AO, Jasmin BJ.
    Bioessays; 1997 Sep 01; 19(9):747-50. PubMed ID: 9297964
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  • 12. Utrophin upregulation for treating Duchenne or Becker muscular dystrophy: how close are we?
    Miura P, Jasmin BJ.
    Trends Mol Med; 2006 Mar 01; 12(3):122-9. PubMed ID: 16443393
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  • 19. The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies.
    Banks GB, Chamberlain JS.
    Curr Top Dev Biol; 2008 Mar 01; 84():431-53. PubMed ID: 19186250
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