The ΔF508-CFTR mutation inhibits wild-type CFTR processing and function when co-expressed in human airway epithelia and in mouse nasal mucosa

BACKGROUND: Rescue or correction of CFTR function in native epithelia is the ultimate goal of CF therapeutics development. Wild-type (WT) CFTR introduction and replacement is also of particular interest. Such therapies may be complicated by possible CFTR self-assembly into an oligomer or multimer. R...

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Autori principali: Tucker, Torry A, Fortenberry, James A, Zsembery, Akos, Schwiebert, Lisa M, Schwiebert, Erik M
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2012
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3507716/
https://ncbi.nlm.nih.gov/pubmed/22999299
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6793-12-12
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