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Journal Abstract Search

112 related items for PubMed ID: 15483645

  • 1. Duchenne muscular dystrophy: stalled at the junction?
    Ségalat L, Anderson JE.
    Eur J Hum Genet; 2005 Jan; 13(1):4-5. PubMed ID: 15483645
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  • 2. SNF-6 is an acetylcholine transporter interacting with the dystrophin complex in Caenorhabditis elegans.
    Kim H, Rogers MJ, Richmond JE, McIntire SL.
    Nature; 2004 Aug 19; 430(7002):891-6. PubMed ID: 15318222
    [Abstract] [Full Text] [Related]

  • 3. Acetylcholine receptor organization at the dystrophic extraocular muscle neuromuscular junction.
    Marques MJ, Pertille A, Carvalho CL, Santo Neto H.
    Anat Rec (Hoboken); 2007 Jul 19; 290(7):846-54. PubMed ID: 17492672
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  • 4. Alterations of neuromuscular junctions in Duchenne muscular dystrophy.
    Lovering RM, Iyer SR, Edwards B, Davies KE.
    Neurosci Lett; 2020 Oct 15; 737():135304. PubMed ID: 32818587
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  • 5. C Histomorphology of neuromuscular junction in Duchenne muscular dystrophy.
    Theroux MC, Olivant A, Akins RE.
    Paediatr Anaesth; 2008 Mar 15; 18(3):256-9. PubMed ID: 18230070
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  • 7. The SLO-1 BK channel of Caenorhabditis elegans is critical for muscle function and is involved in dystrophin-dependent muscle dystrophy.
    Carre-Pierrat M, Grisoni K, Gieseler K, Mariol MC, Martin E, Jospin M, Allard B, Ségalat L.
    J Mol Biol; 2006 Apr 28; 358(2):387-95. PubMed ID: 16527307
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  • 9. Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy.
    Gardner KL, Kearney JA, Edwards JD, Rafael-Fortney JA.
    Gene Ther; 2006 May 28; 13(9):744-51. PubMed ID: 16307000
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  • 10. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin.
    Rooney JE, Welser JV, Dechert MA, Flintoff-Dye NL, Kaufman SJ, Burkin DJ.
    J Cell Sci; 2006 Jun 01; 119(Pt 11):2185-95. PubMed ID: 16684813
    [Abstract] [Full Text] [Related]

  • 11. [Clinical pathologic studies and genetic analysis of a female Duchenne muscular dystrophy family].
    Feng HY, Zhang C, Li Z, Yao XL, Zeng Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 01; 22(1):65-7. PubMed ID: 15696483
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  • 12. Prednisone reduces muscle degeneration in dystrophin-deficient Caenorhabditis elegans.
    Gaud A, Simon JM, Witzel T, Carre-Pierrat M, Wermuth CG, Ségalat L.
    Neuromuscul Disord; 2004 Jun 01; 14(6):365-70. PubMed ID: 15145337
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  • 15. Caenorhabditis elegans as a Model System for Duchenne Muscular Dystrophy.
    Ellwood RA, Piasecki M, Szewczyk NJ.
    Int J Mol Sci; 2021 May 05; 22(9):. PubMed ID: 34063069
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  • 16. Dissecting the signaling and mechanical functions of the dystrophin-glycoprotein complex.
    Judge LM, Haraguchiln M, Chamberlain JS.
    J Cell Sci; 2006 Apr 15; 119(Pt 8):1537-46. PubMed ID: 16569668
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  • 17. Hyperproliferation of synapses on spinal motor neurons of Duchenne muscular dystrophy and myotonic dystrophy patients.
    Nagao M, Kato S, Hayashi H, Misawa H.
    Acta Neuropathol; 2003 Dec 15; 106(6):557-60. PubMed ID: 12920538
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  • 19. The involvement of oxidative stress in determining the severity and progress of pathological processes in dystrophin-deficient muscles.
    Niebrój-Dobosz I, Hausmanowa-Petrusewicz I.
    Acta Biochim Pol; 2005 Dec 15; 52(2):449-52. PubMed ID: 15990924
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