Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients

Duchenne muscular dystrophy (DMD) is a rare genetic disease due to dystrophin gene mutations which cause progressive weakness and muscle wasting. Circadian rhythm coordinates biological processes with the 24-h cycle and it plays a key role in maintaining muscle functions, both in animal models and i...

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Dettagli Bibliografici
Pubblicato in:Front Physiol
Autori principali: Rossi, Rachele, Falzarano, Maria Sofia, Osman, Hana, Armaroli, Annarita, Scotton, Chiara, Mantuano, Paola, Boccanegra, Brigida, Cappellari, Ornella, Schwartz, Elena, Yuryev, Anton, Mercuri, Eugenio, Bertini, Enrico, D’Amico, Adele, Mora, Marina, Johansson, Camilla, Al-Khalili Szigyarto, Cristina, De Luca, Annamaria, Ferlini, Alessandra
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2021
Soggetti:
Physiology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8300012/
https://ncbi.nlm.nih.gov/pubmed/34305639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2021.678974
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