Idiopathic Pulmonary Fibrosis and Lung Cancer: Mechanisms and Molecular Targets

Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pulmonary disease with a median survival of 2–4 years after diagnosis. A significant number of IPF patients have risk factors, such as a history of smoking or concomitant emphysema, both of which can predispose the patien...

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Detalles Bibliográficos
Autores principales: Ballester, Beatriz, Milara, Javier, Cortijo, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387034/
https://www.ncbi.nlm.nih.gov/pubmed/30704051
http://dx.doi.org/10.3390/ijms20030593

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387034/
https://www.ncbi.nlm.nih.gov/pubmed/30704051
http://dx.doi.org/10.3390/ijms20030593

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