Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis

Duchenne muscular dystrophy (DMD) is a fatal muscle-wasting disorder caused by mutations in the Dystrophin gene and for which there is currently no cure. To bridge the gap between preclinical and therapeutic evaluation studies, we have generated a rat model for DMD that carries an exon 52 deletion (...

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Detalles Bibliográficos
Autores principales: Taglietti, Valentina, Kefi, Kaouthar, Bronisz-Budzyńska, Iwona, Mirciloglu, Busra, Rodrigues, Mathilde, Cardone, Nastasia, Coulpier, Fanny, Periou, Baptiste, Gentil, Christel, Goddard, Melissa, Authier, François-Jérôme, Pietri-Rouxel, France, Malfatti, Edoardo, Lafuste, Peggy, Tiret, Laurent, Relaix, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036715/
https://www.ncbi.nlm.nih.gov/pubmed/35468843
http://dx.doi.org/10.1186/s40478-022-01355-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036715/
https://www.ncbi.nlm.nih.gov/pubmed/35468843
http://dx.doi.org/10.1186/s40478-022-01355-2

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