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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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Bibliografski detalji
Izdano u:Respir Res
Glavni autori: Pardo, Annie, Cabrera, Sandra, Maldonado, Mariel, Selman, Moisés
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Online pristup: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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