LED therapy modulates M1/M2 macrophage phenotypes and mitigates dystrophic features in treadmill-trained mdx mice
Author:
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s43630-024-00626-2.pdf
Reference38 articles.
1. Emery, A. E. H. (2002). The muscular dystrophies. The Lancet, 359(9307), 687–695. https://doi.org/10.1016/s0140-6736(02)07815-7
2. Shin, J., Tajrishi, M. M., Ogura, Y., & Kumar, A. (2013). Wasting mechanisms in muscular dystrophy. The International Journal of Biochemistry & Cell Biology, 45(10), 2266–2279. https://doi.org/10.1016/j.biocel.2013.05.001
3. Tidball, J. G., Welc, S. S., & Wehling-Henricks, M. (2018). Immunobiology of inherited muscular dystrophies. Comprehensive Physiology, 8(4), 1313–1356. https://doi.org/10.1002/cphy.c170052
4. Verhaart, I. E. C., & Aartsma-Rus, A. (2019). Therapeutic developments for Duchenne muscular dystrophy. Nature Reviews. Neurology, 15(7), 373–386. https://doi.org/10.1038/s41582-019-0203-3
5. Theret, M., Saclier, M., Messina, G., & Rossi, F. M. V. (2022). Macrophages in skeletal muscle dystrophies, an entangled partner. Journal of Neuromuscular Diseases, 9(1), 1–23. https://doi.org/10.3233/jnd-210737
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