Lipid Mediators Regulate Pulmonary Fibrosis: Potential Mechanisms and Signaling Pathways

Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease of unknown etiology characterized by distorted distal lung architecture, inflammation, and fibrosis. The molecular mechanisms involved in the pathophysiology of IPF are incompletely defined. Several lung cell types including alveolar...

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Detalles Bibliográficos
Autores principales: Suryadevara, Vidyani, Ramchandran, Ramaswamy, Kamp, David W., Natarajan, Viswanathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352853/
https://www.ncbi.nlm.nih.gov/pubmed/32549377
http://dx.doi.org/10.3390/ijms21124257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352853/
https://www.ncbi.nlm.nih.gov/pubmed/32549377
http://dx.doi.org/10.3390/ijms21124257

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