Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches

Spinal muscular atrophy (SMA) is a primary genetic cause of infant mortality due to mutations in the Survival Motor Neuron (SMN) 1 gene. No cure is available. Antisense oligonucleotides (ASOs) aimed at increasing SMN levels from the paralogous SMN2 gene represent a possible therapeutic strategy. Her...

Descripción completa

Detalles Bibliográficos
Autores principales: Nizzardo, Monica, Simone, Chiara, Dametti, Sara, Salani, Sabrina, Ulzi, Gianna, Pagliarani, Serena, Rizzo, Federica, Frattini, Emanuele, Pagani, Franco, Bresolin, Nereo, Comi, Giacomo, Corti, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485234/
https://www.ncbi.nlm.nih.gov/pubmed/26123042
http://dx.doi.org/10.1038/srep11746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485234/
https://www.ncbi.nlm.nih.gov/pubmed/26123042
http://dx.doi.org/10.1038/srep11746

Ejemplares similares