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Journal Abstract Search

237 related items for PubMed ID: 28504671

  • 21. Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration.
    Arnold WD, Duque S, Iyer CC, Zaworski P, McGovern VL, Taylor SJ, von Herrmann KM, Kobayashi DT, Chen KS, Kolb SJ, Paushkin SV, Burghes AH.
    PLoS One; 2016; 11(12):e0167077. PubMed ID: 27907033
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  • 23. 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
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  • 24. Altered electrical properties in Drosophila neurons developing without synaptic transmission.
    Baines RA, Uhler JP, Thompson A, Sweeney ST, Bate M.
    J Neurosci; 2001 Mar 01; 21(5):1523-31. PubMed ID: 11222642
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  • 25. Central and peripheral defects in motor units of the diaphragm of spinal muscular atrophy mice.
    Neve A, Trüb J, Saxena S, Schümperli D.
    Mol Cell Neurosci; 2016 Jan 01; 70():30-41. PubMed ID: 26621405
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  • 26. Characterization of a murine model of SMA.
    Donnelly EM, Quach ET, Hillery TM, Heeke BL, Snyder BR, Handy CR, O'Connor DM, Boulis NM, Federici T.
    Neurobiol Dis; 2012 Mar 01; 45(3):992-8. PubMed ID: 22198571
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  • 29. The Antisense Transcript SMN-AS1 Regulates SMN Expression and Is a Novel Therapeutic Target for Spinal Muscular Atrophy.
    d'Ydewalle C, Ramos DM, Pyles NJ, Ng SY, Gorz M, Pilato CM, Ling K, Kong L, Ward AJ, Rubin LL, Rigo F, Bennett CF, Sumner CJ.
    Neuron; 2017 Jan 04; 93(1):66-79. PubMed ID: 28017471
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  • 30. The Classical Complement Pathway Mediates Microglia-Dependent Remodeling of Spinal Motor Circuits during Development and in SMA.
    Vukojicic A, Delestrée N, Fletcher EV, Pagiazitis JG, Sankaranarayanan S, Yednock TA, Barres BA, Mentis GZ.
    Cell Rep; 2019 Dec 03; 29(10):3087-3100.e7. PubMed ID: 31801075
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  • 31. Glial Activation and Central Synapse Loss, but Not Motoneuron Degeneration, Are Prevented by the Sigma-1 Receptor Agonist PRE-084 in the Smn2B/- Mouse Model of Spinal Muscular Atrophy.
    Cerveró C, Blasco A, Tarabal O, Casanovas A, Piedrafita L, Navarro X, Esquerda JE, Calderó J.
    J Neuropathol Exp Neurol; 2018 Jul 01; 77(7):577-597. PubMed ID: 29767748
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  • 32. Mechanisms involved in spinal cord central synapse loss in a mouse model of spinal muscular atrophy.
    Tarabal O, Caraballo-Miralles V, Cardona-Rossinyol A, Correa FJ, Olmos G, Lladó J, Esquerda JE, Calderó J.
    J Neuropathol Exp Neurol; 2014 Jun 01; 73(6):519-35. PubMed ID: 24806302
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  • 35. 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 01; 49():57-67. PubMed ID: 22960106
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  • 38. Distinct frequency-dependent regulation of nerve terminal excitability and synaptic transmission by IA and IK potassium channels revealed by Drosophila Shaker and Shab mutations.
    Ueda A, Wu CF.
    J Neurosci; 2006 Jun 07; 26(23):6238-48. PubMed ID: 16763031
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