The Smn-Independent Beneficial Effects of Trichostatin A on an Intermediate Mouse Model of Spinal Muscular Atrophy

Spinal muscular atrophy is an autosomal recessive neuromuscular disease characterized by the progressive loss of alpha motor neurons in the spinal cord. Trichostatin A (TSA) is a histone deacetylase inhibitor with beneficial effects in spinal muscular atrophy mouse models that carry the human SMN2 t...

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Detalles Bibliográficos
Autores principales: Liu, Hong, Yazdani, Armin, Murray, Lyndsay M., Beauvais, Ariane, Kothary, Rashmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077776/
https://www.ncbi.nlm.nih.gov/pubmed/24984019
http://dx.doi.org/10.1371/journal.pone.0101225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077776/
https://www.ncbi.nlm.nih.gov/pubmed/24984019
http://dx.doi.org/10.1371/journal.pone.0101225

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