A role for the terminal C5-C9 complement pathway in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease characterized by damage to the alveolar epithelium, leading to fibrosis and excessive accumulation of extracellular matrix in the interstitium of the lung. In the present study we performed high-resolution proteom...

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Detalles Bibliográficos
Autores principales: Sikkeland, Liv I. B., Ueland, Thor, Lund, May B., Durheim, Michael Thomas, Mollnes, Tom Eirik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444977/
https://www.ncbi.nlm.nih.gov/pubmed/37621463
http://dx.doi.org/10.3389/fmed.2023.1236495

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444977/
https://www.ncbi.nlm.nih.gov/pubmed/37621463
http://dx.doi.org/10.3389/fmed.2023.1236495

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