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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...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2013
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| Schlagworte: | |
| Online Zugang: | 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 |
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