B. Vidal

uPA deficiency exacerbates muscular dystrophy in MDX mice

A. Luttun, P. Carmeliet, M. Dierssen, 2007, The Journal of cell biology.

Cellular and molecular mechanisms regulating fibrosis in skeletal muscle repair and disease.

C. Mann, P. Muñoz-Cánoves, A. Serrano, 2011, Current topics in developmental biology.

Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor.

P. Muñoz-Cánoves, Vanessa Ruiz-Bonilla, A. Serrano, 2012, Human molecular genetics.

PAI-1–regulated miR-21 defines a novel age-associated fibrogenic pathway in muscular dystrophy

P. Muñoz-Cánoves, Susana Gutarra, A. Serrano, 2012, The Journal of cell biology.

The alkylating carcinogen N-methyl-N’-nitro-N-nitrosoguanidine activates the plasminogen activator inhibitor-1 gene through sequential phosphorylation of p53 by ATM and ATR kinases

E. Appella, P. Muñoz-Cánoves, M. Jardí, 2005, Thrombosis and Haemostasis.

uPA deficiency exacerbates muscular dystrophy in MDX mice

A. Luttun, P. Carmeliet, M. Dierssen, 2007, The Journal of Cell Biology.

The plasminogen activation system in skeletal muscle regeneration: antagonistic roles of urokinase-type plasminogen activator (uPA) and its inhibitor (PAI-1).

P. Muñoz-Cánoves, Á. Díaz-Ramos, R. López-Alemany, 2005, Frontiers in bioscience : a journal and virtual library.

Fibrinogen drives dystrophic muscle fibrosis via a TGFbeta/alternative macrophage activation pathway.

P. Carmeliet, M. Dierssen, P. Muñoz-Cánoves, 2008, Genes & development.

Alpha-enolase plasminogen receptor in myogenesis.

P. Muñoz-Cánoves, Á. Díaz-Ramos, R. López-Alemany, 2005, Frontiers in bioscience : a journal and virtual library.

uPA deficiency exacerbates muscular dystrophy in MDX mice

A. Luttun, P. Carmeliet, M. Dierssen, 2007, The Journal of Cell Biology.