Nanomedicine Approaches for the Pulmonary Treatment of Cystic Fibrosis

Cystic fibrosis (CF) is a genetic disease affecting today nearly 70,000 patients worldwide and characterized by a hypersecretion of thick mucus difficult to clear arising from the defective CFTR protein. The over-production of the mucus secreted in the lungs, along with its altered composition and c...

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Detalles Bibliográficos
Autores principales: Velino, Cecilia, Carella, Francesca, Adamiano, Alessio, Sanguinetti, Maurizio, Vitali, Alberto, Catalucci, Daniele, Bugli, Francesca, Iafisco, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Bioengineering and Biotechnology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927921/
https://www.ncbi.nlm.nih.gov/pubmed/31921811
http://dx.doi.org/10.3389/fbioe.2019.00406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927921/
https://www.ncbi.nlm.nih.gov/pubmed/31921811
http://dx.doi.org/10.3389/fbioe.2019.00406

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