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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: van Meegen, Marit Arianne, Terheggen-Lagro, Suzanne Willemina Julia, Koymans, Kirsten Judith, van der Ent, Cornelis Korstiaan, Beekman, Jeffrey Matthijn
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2013
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3590182/
https://ncbi.nlm.nih.gov/pubmed/23483918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0057617
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak