Proteomics of Muscle Microdialysates Identifies Potential Circulating Biomarkers in Facioscapulohumeral Muscular Dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is caused by a complex epigenetic mechanism finally leading to the misexpression of DUX4 in skeletal muscle. Detecting DUX4 and quantifying disease progression in FSHD is extremely challenging, thus increasing the need for surrogate biomarkers. We applie...

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Detalles Bibliográficos
Autores principales: Corasolla Carregari, Victor, Monforte, Mauro, Di Maio, Giuseppe, Pieroni, Luisa, Urbani, Andrea, Ricci, Enzo, Tasca, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795508/
https://www.ncbi.nlm.nih.gov/pubmed/33396627
http://dx.doi.org/10.3390/ijms22010290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795508/
https://www.ncbi.nlm.nih.gov/pubmed/33396627
http://dx.doi.org/10.3390/ijms22010290

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