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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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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6387034/ https://ncbi.nlm.nih.gov/pubmed/30704051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20030593 |
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