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202 related items for PubMed ID: 31273192

  • 1. 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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  • 2. A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology.
    Bowerman M, Murray LM, Beauvais A, Pinheiro B, Kothary R.
    Neuromuscul Disord; 2012 Mar 04; 22(3):263-76. PubMed ID: 22071333
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  • 3. Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn2B/- mouse model of spinal muscular atrophy.
    Reedich EJ, Kalski M, Armijo N, Cox GA, DiDonato CJ.
    Exp Neurol; 2021 Mar 04; 337():113587. PubMed ID: 33382987
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  • 7. Motor unit recovery following Smn restoration in mouse models of spinal muscular atrophy.
    Comley LH, Kline RA, Thomson AK, Woschitz V, Landeros EV, Osman EY, Lorson CL, Murray LM.
    Hum Mol Genet; 2022 Sep 10; 31(18):3107-3119. PubMed ID: 35551393
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  • 11. Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy.
    Martinez TL, Kong L, Wang X, Osborne MA, Crowder ME, Van Meerbeke JP, Xu X, Davis C, Wooley J, Goldhamer DJ, Lutz CM, Rich MM, Sumner CJ.
    J Neurosci; 2012 Jun 20; 32(25):8703-15. PubMed ID: 22723710
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  • 12. Activation of Muscle-Specific Kinase (MuSK) Reduces Neuromuscular Defects in the Delta7 Mouse Model of Spinal Muscular Atrophy (SMA).
    Feng Z, Lam S, Tenn ES, Ghosh AS, Cantor S, Zhang W, Yen PF, Chen KS, Burden S, Paushkin S, Ayalon G, Ko CP.
    Int J Mol Sci; 2021 Jul 27; 22(15):. PubMed ID: 34360794
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  • 14. Stasimon Contributes to the Loss of Sensory Synapses and Motor Neuron Death in a Mouse Model of Spinal Muscular Atrophy.
    Simon CM, Van Alstyne M, Lotti F, Bianchetti E, Tisdale S, Watterson DM, Mentis GZ, Pellizzoni L.
    Cell Rep; 2019 Dec 17; 29(12):3885-3901.e5. PubMed ID: 31851921
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  • 16. The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy.
    Kariya S, Mauricio R, Dai Y, Monani UR.
    Neurosci Lett; 2009 Jan 16; 449(3):246-51. PubMed ID: 19010394
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  • 19. AAV9-DOK7 gene therapy reduces disease severity in Smn2B/- SMA model mice.
    Kaifer KA, Villalón E, Smith CE, Simon ME, Marquez J, Hopkins AE, Morcos TI, Lorson CL.
    Biochem Biophys Res Commun; 2020 Sep 10; 530(1):107-114. PubMed ID: 32828271
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  • 20. Selective Neuromuscular Denervation in Taiwanese Severe SMA Mouse Can Be Reversed by Morpholino Antisense Oligonucleotides.
    Lin TL, Chen TH, Hsu YY, Cheng YH, Juang BT, Jong YJ.
    PLoS One; 2016 Sep 10; 11(4):e0154723. PubMed ID: 27124114
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