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5. 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 [Abstract] [Full Text] [Related]
6. 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; 5(2):152-63. PubMed ID: 26683872 [Abstract] [Full Text] [Related]
7. 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; 337():113587. PubMed ID: 33382987 [Abstract] [Full Text] [Related]
8. Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein. Anderton RS, Meloni BP, Mastaglia FL, Boulos S. Mol Neurobiol; 2013 Apr; 47(2):821-32. PubMed ID: 23315303 [Abstract] [Full Text] [Related]
9. Recapitulation of spinal motor neuron-specific disease phenotypes in a human cell model of spinal muscular atrophy. Wang ZB, Zhang X, Li XJ. Cell Res; 2013 Mar; 23(3):378-93. PubMed ID: 23208423 [Abstract] [Full Text] [Related]
10. 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]
13. Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Burghes AH, Beattie CE. Nat Rev Neurosci; 2009 Aug 08; 10(8):597-609. PubMed ID: 19584893 [Abstract] [Full Text] [Related]
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15. Pharmacologically induced mouse model of adult spinal muscular atrophy to evaluate effectiveness of therapeutics after disease onset. Feng Z, Ling KK, Zhao X, Zhou C, Karp G, Welch EM, Naryshkin N, Ratni H, Chen KS, Metzger F, Paushkin S, Weetall M, Ko CP. Hum Mol Genet; 2016 Mar 01; 25(5):964-75. PubMed ID: 26758873 [Abstract] [Full Text] [Related]
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18. 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]
19. 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 20; 22(5):1029-36. PubMed ID: 23512182 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]