Modeling the ACVR1(R206H) mutation in human skeletal muscle stem cells

Abnormalities in skeletal muscle repair can lead to poor function and complications such as scarring or heterotopic ossification (HO). Here, we use fibrodysplasia ossificans progressiva (FOP), a disease of progressive HO caused by ACVR1(R206H) (Activin receptor type-1 receptor) mutation, to elucidat...

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Detalles Bibliográficos
Autores principales: Barruet, Emilie, Garcia, Steven M, Wu, Jake, Morales, Blanca M, Tamaki, Stanley, Moody, Tania, Pomerantz, Jason H, Hsiao, Edward C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Cell Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8691832/
https://www.ncbi.nlm.nih.gov/pubmed/34755602
http://dx.doi.org/10.7554/eLife.66107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8691832/
https://www.ncbi.nlm.nih.gov/pubmed/34755602
http://dx.doi.org/10.7554/eLife.66107

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