PAX7, a Key for Myogenesis Modulation in Muscular Dystrophies through Multiple Signaling Pathways: A Systematic Review

Muscular dystrophy is a heterogenous group of hereditary muscle disorders caused by mutations in the genes responsible for muscle development, and is generally defined by a disastrous progression of muscle wasting and massive loss in muscle regeneration. Pax7 is closely associated with myogenesis, w...

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Detalles Bibliográficos
Autores principales: Rahman, Nor Idayu A., Lam, Chung Liang, Sulaiman, Nadiah, Abdullah, Nur Atiqah Haizum, Nordin, Fazlina, Ariffin, Shahrul Hisham Zainal, Yazid, Muhammad Dain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487808/
https://www.ncbi.nlm.nih.gov/pubmed/37685856
http://dx.doi.org/10.3390/ijms241713051

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487808/
https://www.ncbi.nlm.nih.gov/pubmed/37685856
http://dx.doi.org/10.3390/ijms241713051

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