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Journal Abstract Search

260 related items for PubMed ID: 19074460

  • 1. Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy.
    Rose FF, Mattis VB, Rindt H, Lorson CL.
    Hum Mol Genet; 2009 Mar 15; 18(6):997-1005. PubMed ID: 19074460
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  • 2. Transgenic inactivation of murine myostatin does not decrease the severity of disease in a model of Spinal Muscular Atrophy.
    Rindt H, Buckley DM, Vale SM, Krogman M, Rose FF, Garcia ML, Lorson CL.
    Neuromuscul Disord; 2012 Mar 15; 22(3):277-85. PubMed ID: 22079083
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  • 3. The effect of the DcpS inhibitor D156844 on the protective action of follistatin in mice with spinal muscular atrophy.
    Harris AW, Butchbach ME.
    Neuromuscul Disord; 2015 Sep 15; 25(9):699-705. PubMed ID: 26055638
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  • 4. Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy.
    Bowerman M, Murray LM, Boyer JG, Anderson CL, Kothary R.
    BMC Med; 2012 Mar 07; 10():24. PubMed ID: 22397316
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  • 14. Detection of human survival motor neuron (SMN) protein in mice containing the SMN2 transgene: applicability to preclinical therapy development for spinal muscular atrophy.
    Mattis VB, Butchbach ME, Lorson CL.
    J Neurosci Methods; 2008 Oct 30; 175(1):36-43. PubMed ID: 18771690
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  • 16. ZPR1 prevents R-loop accumulation, upregulates SMN2 expression and rescues spinal muscular atrophy.
    Kannan A, Jiang X, He L, Ahmad S, Gangwani L.
    Brain; 2020 Jan 01; 143(1):69-93. PubMed ID: 31828288
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