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Autor:
Kostas A. Papavassiliou, Amalia A. Sofianidi, Fotios G. Spiliopoulos, Vassiliki A. Gogou, Antonios N. Gargalionis, Athanasios G. Papavassiliou
Publikováno v:
Cells, Vol 13, Iss 18, p 1519 (2024)
Pulmonary fibrosis (PF) is a severe, irreversible lung disease characterized by progressive scarring, with idiopathic pulmonary fibrosis (IPF) being the most prevalent form. IPF’s pathogenesis involves repetitive lung epithelial injury leading to f
Externí odkaz:
https://doaj.org/article/50c91672bdee468a85f02797fb6709c8
