Single cell sequencing maps skeletal muscle cellular diversity as disease severity increases in dystrophic mouse models

Duchenne muscular dystrophy (DMD) is caused by out-of-frame mutations in the DMD gene resulting in the absence of a functional dystrophin protein, leading to a devastating and progressive lethal muscle-wasting disease. Little is known about cellular heterogeneity as disease severity increases. Advan...

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Detalles Bibliográficos
Autores principales: Saleh, Kholoud K., Xi, Haibin, Switzler, Corey, Skuratovsky, Emily, Romero, Matthew A., Chien, Peggie, Gibbs, Devin, Gane, Lily, Hicks, Michael R., Spencer, Melissa J., Pyle, April D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646951/
https://www.ncbi.nlm.nih.gov/pubmed/36388984
http://dx.doi.org/10.1016/j.isci.2022.105415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646951/
https://www.ncbi.nlm.nih.gov/pubmed/36388984
http://dx.doi.org/10.1016/j.isci.2022.105415

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