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Journal Abstract Search

159 related items for PubMed ID: 21681521

  • 1. The spinal muscular atrophy mouse model, SMAΔ7, displays altered axonal transport without global neurofilament alterations.
    Dale JM, Shen H, Barry DM, Garcia VB, Rose FF, Lorson CL, Garcia ML.
    Acta Neuropathol; 2011 Sep; 122(3):331-41. PubMed ID: 21681521
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  • 3. Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice.
    Kong L, Wang X, Choe DW, Polley M, Burnett BG, Bosch-Marcé M, Griffin JW, Rich MM, Sumner CJ.
    J Neurosci; 2009 Jan 21; 29(3):842-51. PubMed ID: 19158308
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  • 15. Motor transmission defects with sex differences in a new mouse model of mild spinal muscular atrophy.
    Deguise MO, De Repentigny Y, Tierney A, Beauvais A, Michaud J, Chehade L, Thabet M, Paul B, Reilly A, Gagnon S, Renaud JM, Kothary R.
    EBioMedicine; 2020 May 21; 55():102750. PubMed ID: 32339936
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  • 16. Ultrastructural changes in diaphragm neuromuscular junctions in a severe mouse model for Spinal Muscular Atrophy and their prevention by bifunctional U7 snRNA correcting SMN2 splicing.
    Voigt T, Meyer K, Baum O, Schümperli D.
    Neuromuscul Disord; 2010 Nov 21; 20(11):744-52. PubMed ID: 20832308
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  • 17. Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy.
    Courtney NL, Mole AJ, Thomson AK, Murray LM.
    Cell Death Dis; 2019 Jul 04; 10(7):515. PubMed ID: 31273192
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  • 19. The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophy.
    Ahmad S, Wang Y, Shaik GM, Burghes AH, Gangwani L.
    Hum Mol Genet; 2012 Jun 15; 21(12):2745-58. PubMed ID: 22422766
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  • 20. Defective neuromuscular junction organization and postnatal myogenesis in mice with severe spinal muscular atrophy.
    Dachs E, Hereu M, Piedrafita L, Casanovas A, Calderó J, Esquerda JE.
    J Neuropathol Exp Neurol; 2011 Jun 15; 70(6):444-61. PubMed ID: 21572339
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