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Journal Abstract Search


202 related items for PubMed ID: 31273192

  • 41. Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy.
    Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M.
    Hum Mol Genet; 2006 Feb 01; 15(3):511-8. PubMed ID: 16396995
    [Abstract] [Full Text] [Related]

  • 42. Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages.
    Laird AS, Mackovski N, Rinkwitz S, Becker TS, Giacomotto J.
    Hum Mol Genet; 2016 May 01; 25(9):1728-38. PubMed ID: 26908606
    [Abstract] [Full Text] [Related]

  • 43. Muscle-specific SMN reduction reveals motor neuron-independent disease in spinal muscular atrophy models.
    Kim JK, Jha NN, Feng Z, Faleiro MR, Chiriboga CA, Wei-Lapierre L, Dirksen RT, Ko CP, Monani UR.
    J Clin Invest; 2020 Mar 02; 130(3):1271-1287. PubMed ID: 32039917
    [Abstract] [Full Text] [Related]

  • 44. Established Stem Cell Model of Spinal Muscular Atrophy Is Applicable in the Evaluation of the Efficacy of Thyrotropin-Releasing Hormone Analog.
    Ohuchi K, Funato M, Kato Z, Seki J, Kawase C, Tamai Y, Ono Y, Nagahara Y, Noda Y, Kameyama T, Ando S, Tsuruma K, Shimazawa M, Hara H, Kaneko H.
    Stem Cells Transl Med; 2016 Feb 02; 5(2):152-63. PubMed ID: 26683872
    [Abstract] [Full Text] [Related]

  • 45. 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]

  • 46. Muscle-restricted nuclear receptor interaction protein knockout causes motor neuron degeneration through down-regulation of myogenin at the neuromuscular junction.
    Chen HH, Tsai LK, Liao KY, Wu TC, Huang YH, Huang YC, Chang SW, Wang PY, Tsao YP, Chen SL.
    J Cachexia Sarcopenia Muscle; 2018 Aug 01; 9(4):771-785. PubMed ID: 29608040
    [Abstract] [Full Text] [Related]

  • 47. Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn2B/- mouse model of SMA.
    Carlini MJ, Triplett MK, Pellizzoni L.
    PLoS One; 2022 Aug 01; 17(8):e0267990. PubMed ID: 35913953
    [Abstract] [Full Text] [Related]

  • 48. 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 01; 122(3):331-41. PubMed ID: 21681521
    [Abstract] [Full Text] [Related]

  • 49. Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy.
    Ling KK, Gibbs RM, Feng Z, Ko CP.
    Hum Mol Genet; 2012 Jan 01; 21(1):185-95. PubMed ID: 21968514
    [Abstract] [Full Text] [Related]

  • 50. 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 01; 20(11):744-52. PubMed ID: 20832308
    [Abstract] [Full Text] [Related]

  • 51. Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy.
    Zhang Z, Pinto AM, Wan L, Wang W, Berg MG, Oliva I, Singh LN, Dengler C, Wei Z, Dreyfuss G.
    Proc Natl Acad Sci U S A; 2013 Nov 26; 110(48):19348-53. PubMed ID: 24191055
    [Abstract] [Full Text] [Related]

  • 52. 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
    [Abstract] [Full Text] [Related]

  • 53. Fast motor axon loss in SMARD1 does not correspond to morphological and functional alterations of the NMJ.
    Krieger F, Elflein N, Ruiz R, Guerra J, Serrano AL, Asan E, Tabares L, Jablonka S.
    Neurobiol Dis; 2013 Jun 21; 54():169-82. PubMed ID: 23295857
    [Abstract] [Full Text] [Related]

  • 54. SMN controls neuromuscular junction integrity through U7 snRNP.
    Tisdale S, Van Alstyne M, Simon CM, Mentis GZ, Pellizzoni L.
    Cell Rep; 2022 Sep 20; 40(12):111393. PubMed ID: 36130491
    [Abstract] [Full Text] [Related]

  • 55. 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
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  • 56. A large animal model of spinal muscular atrophy and correction of phenotype.
    Duque SI, Arnold WD, Odermatt P, Li X, Porensky PN, Schmelzer L, Meyer K, Kolb SJ, Schümperli D, Kaspar BK, Burghes AH.
    Ann Neurol; 2015 Mar 19; 77(3):399-414. PubMed ID: 25516063
    [Abstract] [Full Text] [Related]

  • 57. Opposite Synaptic Alterations at the Neuromuscular Junction in an ALS Mouse Model: When Motor Units Matter.
    Tremblay E, Martineau É, Robitaille R.
    J Neurosci; 2017 Sep 13; 37(37):8901-8918. PubMed ID: 28821658
    [Abstract] [Full Text] [Related]

  • 58. Notch Signaling Mediates Astrocyte Abnormality in Spinal Muscular Atrophy Model Systems.
    Ohuchi K, Funato M, Yoshino Y, Ando S, Inagaki S, Sato A, Kawase C, Seki J, Saito T, Nishio H, Nakamura S, Shimazawa M, Kaneko H, Hara H.
    Sci Rep; 2019 Mar 06; 9(1):3701. PubMed ID: 30842449
    [Abstract] [Full Text] [Related]

  • 59. Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophy.
    Van Alstyne M, Simon CM, Sardi SP, Shihabuddin LS, Mentis GZ, Pellizzoni L.
    Genes Dev; 2018 Aug 01; 32(15-16):1045-1059. PubMed ID: 30012555
    [Abstract] [Full Text] [Related]

  • 60. SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.
    See K, Yadav P, Giegerich M, Cheong PS, Graf M, Vyas H, Lee SG, Mathavan S, Fischer U, Sendtner M, Winkler C.
    Hum Mol Genet; 2014 Apr 01; 23(7):1754-70. PubMed ID: 24218366
    [Abstract] [Full Text] [Related]


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