Apical CFTR Expression in Human Nasal Epithelium Correlates with Lung Disease in Cystic Fibrosis

INTRODUCTION: Although most individuals with cystic fibrosis (CF) develop progressive obstructive lung disease, disease severity is highly variable, even for individuals with similar CFTR mutations. Measurements of chloride transport as expression of CFTR function in nasal epithelial cells correlate...

Descripción completa

Detalles Bibliográficos
Autores principales: van Meegen, Marit Arianne, Terheggen-Lagro, Suzanne Willemina Julia, Koymans, Kirsten Judith, van der Ent, Cornelis Korstiaan, Beekman, Jeffrey Matthijn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590182/
https://www.ncbi.nlm.nih.gov/pubmed/23483918
http://dx.doi.org/10.1371/journal.pone.0057617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590182/
https://www.ncbi.nlm.nih.gov/pubmed/23483918
http://dx.doi.org/10.1371/journal.pone.0057617

Ejemplares similares