Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive and devastating lung disorder of unknown origin, with very poor prognosis and no effective treatment. The disease is characterized by abnormal activation of alveolar epithelial cells, which secrete numerous mediators involved in the expansion of t...

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Detalles Bibliográficos
Autores principales: Pardo, Annie, Cabrera, Sandra, Maldonado, Mariel, Selman, Moisés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779202/
https://www.ncbi.nlm.nih.gov/pubmed/26944412
http://dx.doi.org/10.1186/s12931-016-0343-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779202/
https://www.ncbi.nlm.nih.gov/pubmed/26944412
http://dx.doi.org/10.1186/s12931-016-0343-6

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