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Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.Experimental Neurology|May 1, 2007
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expressionStefania Corti, Monica Nizzardo, Martina Nardini, et al.Brain : a Journal of Neurology|April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis modelStefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)Stefania Corti, Monica Nizzardo, Martina Nardini, et al.Human Molecular Genetics|August 11, 2016
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neuronsFederica Rizzo, Dario Ronchi, Sabrina Salani, et al.Scientific Reports|April 7, 2017
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavinFederica Rizzo, Agnese Ramirez, Claudia Compagnucci, et al.Brain : a Journal of Neurology|December 25, 2009
Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in miceStefania Corti, Monica Nizzardo, Martina Nardini, et al.Experimental Neurology|February 8, 2011
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanismsMonica Nizzardo, Martina Nardini, Dario Ronchi, et al.Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.Journal of Medical Genetics|December 18, 2012
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutationsMarianna Ciccolella, Stefania Corti, Michela Catteruccia, et al.Pageof 7