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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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Библиографические подробности
Опубликовано в: :Int J Mol Sci
Главные авторы: Corasolla Carregari, Victor, Monforte, Mauro, Di Maio, Giuseppe, Pieroni, Luisa, Urbani, Andrea, Ricci, Enzo, Tasca, Giorgio
Формат: Artigo
Язык:Inglês
Опубликовано: MDPI 2020
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7795508/
https://ncbi.nlm.nih.gov/pubmed/33396627
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22010290
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