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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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Pubblicato in:Respir Res
Autori principali: Pardo, Annie, Cabrera, Sandra, Maldonado, Mariel, Selman, Moisés
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2016
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Accesso online: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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