Skeletal Muscle MicroRNA and Messenger RNA Profiling in Cofilin-2 Deficient Mice Reveals Cell Cycle Dysregulation Hindering Muscle Regeneration

Congenital myopathies are rare skeletal muscle diseases presenting in early age with hypotonia and weakness often linked to a genetic defect. Mutations in the gene for cofilin-2 (CFL2) have been identified in several families as a cause of congenital myopathy with nemaline bodies and cores. Here we...

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Detalles Bibliográficos
Autores principales: Morton, Sarah U., Joshi, Mugdha, Savic, Talia, Beggs, Alan H., Agrawal, Pankaj B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395318/
https://www.ncbi.nlm.nih.gov/pubmed/25874796
http://dx.doi.org/10.1371/journal.pone.0123829

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395318/
https://www.ncbi.nlm.nih.gov/pubmed/25874796
http://dx.doi.org/10.1371/journal.pone.0123829

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