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Idiopathic Pulmonary Fibrosis: Epithelial-mesenchymal interactions and emerging therapeutic targets

Idiopathic pulmonary fibrosis (IPF) is a chronic fibrotic disease of the lung that is marked by progressive decline in pulmonary function and ultimately respiratory failure. Genetic and environmental risk factors have been identified that indicate injury to, and dysfunction of the lung epithelium is...

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Detalhes bibliográficos
Publicado no:Matrix Biol
Main Authors: Hewlett, Justin C., Kropski, Jonathan A., Blackwell, Timothy S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6146058/
https://ncbi.nlm.nih.gov/pubmed/29625182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.matbio.2018.03.021
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