Loss of SP-A in the Lung Exacerbates Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a devastating and common chronic lung disease that is pathologically characterized by the destruction of lung architecture and the accumulation of extracellular matrix in the lung. Previous studies have shown an association between lung surfactant protein (SP)...

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Detalles Bibliográficos
Autores principales: Kim, Kyunghwa, Shin, Dasom, Lee, Gaheon, Bae, Hyunsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141401/
https://www.ncbi.nlm.nih.gov/pubmed/35628104
http://dx.doi.org/10.3390/ijms23105292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141401/
https://www.ncbi.nlm.nih.gov/pubmed/35628104
http://dx.doi.org/10.3390/ijms23105292

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