Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells

Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, with most of the mortality given by the lung disease. Human amniotic mesenchymal stromal (stem) cells (hAMSCs) hold great promise for regenerative medicine in the field of lung disease; however, th...

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Detalles Bibliográficos
Autores principales: Carbone, Annalucia, Castellani, Stefano, Favia, Maria, Diana, Anna, Paracchini, Valentina, Di Gioia, Sante, Seia, Manuela, Casavola, Valeria, Colombo, Carla, Conese, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190909/
https://www.ncbi.nlm.nih.gov/pubmed/24894806
http://dx.doi.org/10.1111/jcmm.12303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190909/
https://www.ncbi.nlm.nih.gov/pubmed/24894806
http://dx.doi.org/10.1111/jcmm.12303

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