Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy-Reference-Cited by-同舟云学术

Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy

Published:2018-07 Issue:7 Volume:9 Page:
ISSN:2041-4889
Container-title:Cell Death & Disease
language:en
Short-container-title:Cell Death Dis

Author:

Piñol-Jurado Patricia,Suárez-Calvet Xavier^ORCID,Fernández-Simón Esther,Gallardo Eduard,de la Oliva Natalia,Martínez-Muriana Anna,Gómez-Gálvez Pedro,Escudero Luis M.,Pérez-Peiró María,Wollin Lutz,de Luna Noemi,Navarro Xavier^ORCID,Illa Isabel,Díaz-Manera Jordi

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology

Link

http://www.nature.com/articles/s41419-018-0792-6.pdf

Reference64 articles.

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3. Guiraud, S. & Davies, K. E. Pharmacological advances for treatment in Duchenne muscular dystrophy. Curr. Opin. Pharmacol. 34, 36–48 (2017).

4. Tedesco, F. S., Dellavalle, A., Diaz-Manera, J., Messina, G. & Cossu, G. Repairing skeletal muscle: regenerative potential of skeletal muscle stem cells. J. Clin. Invest. 120, 11–19 (2010).

5. Cossu, G. et al. Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy. EMBO Mol. Med. 7, 1513–1528 (2015).

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