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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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| Vydáno v: | Matrix Biol |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
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| Témata: | |
| On-line přístup: | 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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