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Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures
CFTR is a highly regulated apical chloride channel of epithelial cells that is mutated in cystic fibrosis (CF). In this study, we characterized the apical stability and intracellular trafficking of wild-type and mutant CFTR in its native environment, i.e., highly differentiated primary human airway...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Physiological Society
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2838667/ https://ncbi.nlm.nih.gov/pubmed/20008117 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00016.2009 |
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