Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jaciara F. G. Gama"'
Autor:
Jaciara F. G. Gama, Rayza D. Romualdo, Mayara L. de Assis, Luana M. de Oliveira, Thereza Quírico-Santos, Luiz A. Alves, Jussara Lagrota-Candido
Publikováno v:
Biomolecules, Vol 12, Iss 6, p 817 (2022)
Muscle injuries are frequent in individuals with genetic myopathies and in athletes. Skeletal muscle regeneration depends on the activation and differentiation of satellite cells present in the basal lamina of muscle fibers. The skeletal muscle envir
Externí odkaz:
https://doaj.org/article/4db85933bd9e4d27b56b861322f40c56
Autor:
Rafael Ferreira da Silva, Douglas Florindo Pinheiro, Thereza Quirico-Santos, Jaciara F. G. Gama, Jussara Lagrota-Candido
Publikováno v:
Cell and tissue research. 382(3)
Although the primary cause of Duchenne muscular dystrophy (DMD) is a genetic mutation, the inflammatory response contributes directly to severity and exacerbation of the diaphragm muscle pathology. The omentum is a lymphoid organ with unique structur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e6e3731c6c703ac4a9c8cf4ddca8a37
https://pubmed.ncbi.nlm.nih.gov/32661578
https://pubmed.ncbi.nlm.nih.gov/32661578
Autor:
Jussara Lagrota-Candido, Thiago Morais Barbosa, Douglas Florindo Pinheiro, Aline C. Gomes, Jaciara F. G. Gama, Rafael Ferreira da Silva, Thereza Quirico-Santos
Publikováno v:
Cell and tissue research. 377(2)
Duchenne muscular dystrophy is a lethal X-linked muscle wasting disease due to mutations of the dystrophin gene leading to distinct susceptibility to degeneration and fibrosis among skeletal muscles. This study aims at verifying whether intense mdx d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8485427f645d431d964d7f491e8c4b61
https://pubmed.ncbi.nlm.nih.gov/30953145
https://pubmed.ncbi.nlm.nih.gov/30953145