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Journal Abstract Search
281 related items for PubMed ID: 23514457
1. At the "junction" of spinal muscular atrophy pathogenesis: the role of neuromuscular junction dysfunction in SMA disease progression. Goulet BB, Kothary R, Parks RJ. Curr Mol Med; 2013 Aug; 13(7):1160-74. PubMed ID: 23514457 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
5. Motor neuronal repletion of the NMJ organizer, Agrin, modulates the severity of the spinal muscular atrophy disease phenotype in model mice. Kim JK, Caine C, Awano T, Herbst R, Monani UR. Hum Mol Genet; 2017 Jul 01; 26(13):2377-2385. PubMed ID: 28379354 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. Reduced survival of motor neuron (SMN) protein in motor neuronal progenitors functions cell autonomously to cause spinal muscular atrophy in model mice expressing the human centromeric (SMN2) gene. Park GH, Maeno-Hikichi Y, Awano T, Landmesser LT, Monani UR. J Neurosci; 2010 Sep 08; 30(36):12005-19. PubMed ID: 20826664 [Abstract] [Full Text] [Related]
9. Defects in neuromuscular junction remodelling in the Smn(2B/-) mouse model of spinal muscular atrophy. Murray LM, Beauvais A, Bhanot K, Kothary R. Neurobiol Dis; 2013 Jan 08; 49():57-67. PubMed ID: 22960106 [Abstract] [Full Text] [Related]
11. 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 08; 55():102750. PubMed ID: 32339936 [Abstract] [Full Text] [Related]
15. Astrocytes influence the severity of spinal muscular atrophy. Rindt H, Feng Z, Mazzasette C, Glascock JJ, Valdivia D, Pyles N, Crawford TO, Swoboda KJ, Patitucci TN, Ebert AD, Sumner CJ, Ko CP, Lorson CL. Hum Mol Genet; 2015 Jul 15; 24(14):4094-102. PubMed ID: 25911676 [Abstract] [Full Text] [Related]
16. iPSC-derived functional human neuromuscular junctions model the pathophysiology of neuromuscular diseases. Lin CY, Yoshida M, Li LT, Ikenaka A, Oshima S, Nakagawa K, Sakurai H, Matsui E, Nakahata T, Saito MK. JCI Insight; 2019 Sep 19; 4(18):. PubMed ID: 31534050 [Abstract] [Full Text] [Related]
19. Pathologic Alterations in the Proteome of Synaptosomes from a Mouse Model of Spinal Muscular Atrophy. Eshraghi M, Gombar R, De Repentigny Y, Vacratsis PO, Kothary R. J Proteome Res; 2019 Aug 02; 18(8):3042-3051. PubMed ID: 31262178 [Abstract] [Full Text] [Related]