MMP-7 is a predictive biomarker of disease progression in patients with idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with poor prognosis, which is characterised by destruction of normal lung architecture and excessive deposition of lung extracellular matrix. The heterogeneity of disease progression in patients with IPF poses significant...

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Detalles Bibliográficos
Autores principales: Bauer, Yasmina, White, Eric S., de Bernard, Simon, Cornelisse, Peter, Leconte, Isabelle, Morganti, Adele, Roux, Sebastien, Nayler, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395293/
https://www.ncbi.nlm.nih.gov/pubmed/28435843
http://dx.doi.org/10.1183/23120541.00074-2016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395293/
https://www.ncbi.nlm.nih.gov/pubmed/28435843
http://dx.doi.org/10.1183/23120541.00074-2016

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