Chaotic activation of developmental signalling pathways drives idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is characterised by an important remodelling of lung parenchyma. Current evidence indicates that the disease is triggered by alveolar epithelium activation following chronic lung injury, resulting in alveolar epithelial type 2 cell hyperplasia and bronchiolisation...

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Detalles Bibliográficos
Autores principales: Froidure, Antoine, Marchal-Duval, Emmeline, Homps-Legrand, Meline, Ghanem, Mada, Justet, Aurélien, Crestani, Bruno, Mailleux, Arnaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488512/
https://www.ncbi.nlm.nih.gov/pubmed/33208483
http://dx.doi.org/10.1183/16000617.0140-2019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488512/
https://www.ncbi.nlm.nih.gov/pubmed/33208483
http://dx.doi.org/10.1183/16000617.0140-2019

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