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294 related items for PubMed ID: 10066910

  • 1. 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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  • 2. Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of beta-dystroglycan.
    Dowling P, Lohan J, Ohlendieck K.
    Eur J Cell Biol; 2003 May 15; 82(5):222-30. PubMed ID: 12800977
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  • 3. Long-term study of Ca(2+) homeostasis and of survival in collagenase-isolated muscle fibres from normal and mdx mice.
    De Backer F, Vandebrouck C, Gailly P, Gillis JM.
    J Physiol; 2002 Aug 01; 542(Pt 3):855-65. PubMed ID: 12154184
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  • 4. Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy.
    Dowling P, Doran P, Ohlendieck K.
    Biochem J; 2004 Apr 15; 379(Pt 2):479-88. PubMed ID: 14678011
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  • 5. Mutual interference of myotonia and muscular dystrophy in the mouse: a study on ADR-MDX double mutants.
    Heimann P, Augustin M, Wieneke S, Heising S, Jockusch H.
    Neuromuscul Disord; 1998 Dec 15; 8(8):551-60. PubMed ID: 10093061
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  • 7. Branched fibres in old dystrophic mdx muscle are associated with mechanical weakening of the sarcolemma, abnormal Ca2+ transients and a breakdown of Ca2+ homeostasis during fatigue.
    Head SI.
    Exp Physiol; 2010 May 15; 95(5):641-56. PubMed ID: 20139167
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  • 9. Elevated subsarcolemmal Ca2+ in mdx mouse skeletal muscle fibers detected with Ca2+-activated K+ channels.
    Mallouk N, Jacquemond V, Allard B.
    Proc Natl Acad Sci U S A; 2000 Apr 25; 97(9):4950-5. PubMed ID: 10781103
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  • 10. L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle.
    Friedrich O, von Wegner F, Chamberlain JS, Fink RH, Rohrbach P.
    PLoS One; 2008 Mar 12; 3(3):e1762. PubMed ID: 18516256
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  • 11. Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice.
    Head SI.
    J Physiol; 1993 Sep 12; 469():11-9. PubMed ID: 8271194
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  • 12. Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress.
    Leijendekker WJ, Passaquin AC, Metzinger L, Rüegg UT.
    Br J Pharmacol; 1996 Jun 12; 118(3):611-6. PubMed ID: 8762085
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  • 14. Mini-dystrophin restores L-type calcium currents in skeletal muscle of transgenic mdx mice.
    Friedrich O, Both M, Gillis JM, Chamberlain JS, Fink RH.
    J Physiol; 2004 Feb 15; 555(Pt 1):251-65. PubMed ID: 14594987
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  • 16. Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice.
    Collet C, Allard B, Tourneur Y, Jacquemond V.
    J Physiol; 1999 Oct 15; 520 Pt 2(Pt 2):417-29. PubMed ID: 10523411
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  • 17. Depolarization-induced contraction and SR function in mechanically skinned muscle fibers from dystrophic mdx mice.
    Plant DR, Lynch GS.
    Am J Physiol Cell Physiol; 2003 Sep 15; 285(3):C522-8. PubMed ID: 12724137
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  • 18. Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers.
    Vandebrouck C, Martin D, Colson-Van Schoor M, Debaix H, Gailly P.
    J Cell Biol; 2002 Sep 16; 158(6):1089-96. PubMed ID: 12235126
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  • 20. Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse.
    Yeung EW, Whitehead NP, Suchyna TM, Gottlieb PA, Sachs F, Allen DG.
    J Physiol; 2005 Jan 15; 562(Pt 2):367-80. PubMed ID: 15528244
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