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199 related items for PubMed ID: 23489475
1. Neurotransmitter release in motor nerve terminals of a mouse model of mild spinal muscular atrophy. Ruiz R, Tabares L. J Anat; 2014 Jan; 224(1):74-84. PubMed ID: 23489475 [Abstract] [Full Text] [Related]
2. 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; 55():102750. PubMed ID: 32339936 [Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy. Kariya S, Park GH, Maeno-Hikichi Y, Leykekhman O, Lutz C, Arkovitz MS, Landmesser LT, Monani UR. Hum Mol Genet; 2008 Aug 15; 17(16):2552-69. PubMed ID: 18492800 [Abstract] [Full Text] [Related]
6. 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]
7. 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 20; 22(3):263-76. PubMed ID: 22071333 [Abstract] [Full Text] [Related]
8. Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy. Lee AJ, Awano T, Park GH, Monani UR. PLoS One; 2012 Mar 20; 7(9):e46353. PubMed ID: 23029491 [Abstract] [Full Text] [Related]
9. 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]
10. Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model. Hua Y, Sahashi K, Rigo F, Hung G, Horev G, Bennett CF, Krainer AR. Nature; 2011 Oct 05; 478(7367):123-6. PubMed ID: 21979052 [Abstract] [Full Text] [Related]
11. Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy. Hunter G, Powis RA, Jones RA, Groen EJ, Shorrock HK, Lane FM, Zheng Y, Sherman DL, Brophy PJ, Gillingwater TH. Hum Mol Genet; 2016 Jul 01; 25(13):2853-2861. PubMed ID: 27170316 [Abstract] [Full Text] [Related]
12. Hypothermia improves disease manifestations in SMA mice via SMN augmentation. Tsai LK, Chen CL, Tsai YC, Ting CH, Chien YH, Lee NC, Hwu WL. Hum Mol Genet; 2016 Feb 15; 25(4):631-41. PubMed ID: 26647309 [Abstract] [Full Text] [Related]
13. Nifedipine Ameliorates Cellular Differentiation Defects of Smn-Deficient Motor Neurons and Enhances Neuromuscular Transmission in SMA Mice. Tejero R, Alsakkal M, Hennlein L, Lopez-Cabello AM, Jablonka S, Tabares L. Int J Mol Sci; 2023 Apr 21; 24(8):. PubMed ID: 37108811 [Abstract] [Full Text] [Related]
14. Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice. Ruiz R, Casañas JJ, Torres-Benito L, Cano R, Tabares L. J Neurosci; 2010 Jan 20; 30(3):849-57. PubMed ID: 20089893 [Abstract] [Full Text] [Related]
15. Calpain Inhibition Increases SMN Protein in Spinal Cord Motoneurons and Ameliorates the Spinal Muscular Atrophy Phenotype in Mice. de la Fuente S, Sansa A, Periyakaruppiah A, Garcera A, Soler RM. Mol Neurobiol; 2019 Jun 20; 56(6):4414-4427. PubMed ID: 30327977 [Abstract] [Full Text] [Related]
16. Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality. Ackermann B, Kröber S, Torres-Benito L, Borgmann A, Peters M, Hosseini Barkooie SM, Tejero R, Jakubik M, Schreml J, Milbradt J, Wunderlich TF, Riessland M, Tabares L, Wirth B. Hum Mol Genet; 2013 Apr 01; 22(7):1328-47. PubMed ID: 23263861 [Abstract] [Full Text] [Related]
17. Restoration of SMN to Emx-1 expressing cortical neurons is not sufficient to provide benefit to a severe mouse model of Spinal Muscular Atrophy. Taylor AS, Glascock JJ, Rose FF, Lutz C, Lorson CL. Transgenic Res; 2013 Oct 01; 22(5):1029-36. PubMed ID: 23512182 [Abstract] [Full Text] [Related]
18. Synaptic withdrawal following nerve injury is influenced by postnatal maturity, muscle-specific properties, and the presence of underlying pathology in mice. Mole AJ, Bell S, Thomson AK, Dissanayake KN, Ribchester RR, Murray LM. J Anat; 2020 Aug 01; 237(2):263-274. PubMed ID: 32311115 [Abstract] [Full Text] [Related]
19. Proteomic assessment of a cell model of spinal muscular atrophy. Wu CY, Whye D, Glazewski L, Choe L, Kerr D, Lee KH, Mason RW, Wang W. BMC Neurosci; 2011 Mar 08; 12():25. PubMed ID: 21385431 [Abstract] [Full Text] [Related]
20. A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy. Monani UR, Pastore MT, Gavrilina TO, Jablonka S, Le TT, Andreassi C, DiCocco JM, Lorson C, Androphy EJ, Sendtner M, Podell M, Burghes AH. J Cell Biol; 2003 Jan 06; 160(1):41-52. PubMed ID: 12515823 [Abstract] [Full Text] [Related] Page: [Next] [New Search]