Cargando…
Persistent Fibroadipogenic Progenitor Expansion Following Transient DUX4 Expression Provokes a Profibrotic State in a Mouse Model for FSHD
FSHD is caused by loss of silencing of the DUX4 gene, but the DUX4 protein has not yet been directly detected immunohistologically in affected muscle, raising the possibility that DUX4 expression may occur at time points prior to obtaining adult biopsies for analysis, with consequent perturbations o...
Autores principales: | Bosnakovski, Darko, Oyler, David, Mitanoska, Ana, Douglas, Madison, Ener, Elizabeth T., Shams, Ahmed S., Kyba, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880758/ https://www.ncbi.nlm.nih.gov/pubmed/35216102 http://dx.doi.org/10.3390/ijms23041983 |
Ejemplares similares
-
Biphasic Myopathic Phenotype of Mouse DUX, an ORF within Conserved FSHD-Related Repeats
por: Bosnakovski, Darko, et al.
Publicado: (2009) -
Muscle pathology from stochastic low level DUX4 expression in an FSHD mouse model
por: Bosnakovski, Darko, et al.
Publicado: (2017) -
Author Correction: Muscle pathology from stochastic low level DUX4 expression in an FSHD mouse model
por: Bosnakovski, Darko, et al.
Publicado: (2018) -
Transplantation of PSC-derived myogenic progenitors counteracts disease phenotypes in FSHD mice
por: Azzag, Karim, et al.
Publicado: (2022) -
Prospective isolation of human fibroadipogenic progenitors with CD73
por: Goloviznina, Natalya A., et al.
Publicado: (2020)