Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis

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...

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Bibliographic Details
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
Format: Online
Language:English
Published: Public Library of Science 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158056/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158056/

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