An in silico FSHD muscle fiber for modeling DUX4 dynamics and predicting the impact of therapy

Facioscapulohumeral muscular dystrophy (FSHD) is an incurable myopathy linked to the over-expression of the myotoxic transcription factor DUX4. Targeting DUX4 is the leading therapeutic approach, however, it is only detectable in 0.1–3.8% of FSHD myonuclei. How rare DUX4 drives FSHD and the optimal...

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Detalles Bibliográficos
Autores principales: Cowley, Matthew V, Pruller, Johanna, Ganassi, Massimo, Zammit, Peter S, Banerji, Christopher RS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Cell Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287159/
https://www.ncbi.nlm.nih.gov/pubmed/37184373
http://dx.doi.org/10.7554/eLife.88345

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287159/
https://www.ncbi.nlm.nih.gov/pubmed/37184373
http://dx.doi.org/10.7554/eLife.88345

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