Dysregulated Cell–Cell Communication Characterizes Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a progressive disease of older adults characterized by fibrotic replacement of functional gas exchange units in the lung. The strongest risk factor for IPF is a genetic variantin the promoter region of the gel-forming mucin, MUC5B. To better understand how the...

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Detalles Bibliográficos
Autores principales: Kurche, Jonathan S., Stancil, Ian T., Michalski, Jacob E., Yang, Ivana V., Schwartz, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600037/
https://www.ncbi.nlm.nih.gov/pubmed/36291184
http://dx.doi.org/10.3390/cells11203319

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600037/
https://www.ncbi.nlm.nih.gov/pubmed/36291184
http://dx.doi.org/10.3390/cells11203319

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