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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
Publicado en:Respir Res
Main Authors: Pardo, Annie, Cabrera, Sandra, Maldonado, Mariel, Selman, Moisés
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2016
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4779202/
https://ncbi.nlm.nih.gov/pubmed/26944412
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-016-0343-6
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