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Journal Abstract Search

79 related items for PubMed ID: 8593673

  • 21. Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers.
    Tutdibi O, Brinkmeier H, Rüdel R, Föhr KJ.
    J Physiol; 1999 Mar 15; 515 ( Pt 3)(Pt 3):859-68. PubMed ID: 10066910
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  • 23. Unacylated Ghrelin Enhances Satellite Cell Function and Relieves the Dystrophic Phenotype in Duchenne Muscular Dystrophy mdx Model.
    Reano S, Angelino E, Ferrara M, Malacarne V, Sustova H, Sabry O, Agosti E, Clerici S, Ruozi G, Zentilin L, Prodam F, Geuna S, Giacca M, Graziani A, Filigheddu N.
    Stem Cells; 2017 Jul 15; 35(7):1733-1746. PubMed ID: 28436144
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  • 24. Expression patterns of regulatory RNAs, including lncRNAs and tRNAs, during postnatal growth of normal and dystrophic (mdx) mouse muscles, and their response to taurine treatment.
    Butchart LC, Terrill JR, Rossetti G, White R, Filipovska A, Grounds MD.
    Int J Biochem Cell Biol; 2018 Jun 15; 99():52-63. PubMed ID: 29578051
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  • 25. Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
    Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP.
    Cell; 2002 Sep 06; 110(5):639-48. PubMed ID: 12230980
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  • 28. Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy.
    Pasteuning-Vuhman S, Putker K, Tanganyika-de Winter CL, Boertje-van der Meulen JW, van Vliet L, Overzier M, Plomp JJ, Aartsma-Rus A, van Putten M.
    PLoS One; 2018 Sep 06; 13(5):e0197388. PubMed ID: 29763467
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  • 33. Expression of the murine Duchenne muscular dystrophy gene in muscle and brain.
    Chamberlain JS, Pearlman JA, Muzny DM, Gibbs RA, Ranier JE, Caskey CT, Reeves AA.
    Science; 1988 Mar 18; 239(4846):1416-8. PubMed ID: 3347839
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  • 35. Mechanical Overloading Increases Maximal Force and Reduces Fragility in Hind Limb Skeletal Muscle from Mdx Mouse.
    Ferry A, Parlakian A, Joanne P, Fraysse B, Mgrditchian T, Roy P, Furling D, Butler-Browne G, Agbulut O.
    Am J Pathol; 2015 Jul 18; 185(7):2012-24. PubMed ID: 26009153
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  • 36. Skeletal muscle perfusion and stem cell delivery in muscle disorders using intra-femoral artery canulation in mice.
    Matthias N, Hunt SD, Wu J, Darabi R.
    Exp Cell Res; 2015 Nov 15; 339(1):103-11. PubMed ID: 26341268
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  • 37. Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.
    Araki E, Nakamura K, Nakao K, Kameya S, Kobayashi O, Nonaka I, Kobayashi T, Katsuki M.
    Biochem Biophys Res Commun; 1997 Sep 18; 238(2):492-7. PubMed ID: 9299538
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  • 39. Overexpression of copper/zinc superoxide dismutase: a novel cause of murine muscular dystrophy.
    Rando TA, Crowley RS, Carlson EJ, Epstein CJ, Mohapatra PK.
    Ann Neurol; 1998 Sep 18; 44(3):381-6. PubMed ID: 9749606
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