Anisomycin Activates Utrophin Upregulation Through a p38 Signaling Pathway

Duchenne muscular dystrophy is a recessive X‐linked disease characterized by progressive muscle wasting; cardiac or respiratory failure causes death in most patients by the third decade.  The disease is caused by mutations in the dystrophin gene that lead to a loss of functional dystrophin protein....

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Detalles Bibliográficos
Autores principales: Hadwen, Jeremiah, Farooq, Faraz, Witherspoon, Luke, Schock, Sarah, Mongeon, Kevin, MacKenzie, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132359/
https://www.ncbi.nlm.nih.gov/pubmed/29877606
http://dx.doi.org/10.1111/cts.12562

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132359/
https://www.ncbi.nlm.nih.gov/pubmed/29877606
http://dx.doi.org/10.1111/cts.12562

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