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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...
Autores principales: | Kurche, Jonathan S., Stancil, Ian T., Michalski, Jacob E., Yang, Ivana V., Schwartz, David A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
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 |
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