Mucins as a New Frontier in Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pulmonary disease with a median survival of 3–5 years after diagnosis. Recent evidence identifies mucins as key effectors in cell growth and tissue remodeling processes compatible with the processes observed in IPF. Mucin...

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Detalles Bibliográficos
Autores principales: Ballester, Beatriz, Milara, Javier, Cortijo, Julio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780288/
https://www.ncbi.nlm.nih.gov/pubmed/31514468
http://dx.doi.org/10.3390/jcm8091447

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780288/
https://www.ncbi.nlm.nih.gov/pubmed/31514468
http://dx.doi.org/10.3390/jcm8091447

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