Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF) is a devastating disease of unknown etiology. The pathogenic mechanisms are unclear, but evidence indicates that aberrantly activated alveolar epithelial cells secrete a variety of mediators which induce the migration, proliferation and activation of fibroblasts a...
Main Authors: | Buendía-Roldán, Ivette, Ruiz, Víctor, Sierra, Patricia, Montes, Eduardo, Ramírez, Remedios, Vega, Anita, Salgado, Alfonso, Vargas, Mario H., Mejía, Mayra, Pardo, Annie, Selman, Moisés |
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Format: | Online |
Language: | English |
Published: |
Public Library of Science
2016
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158056/ |
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