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Regulated recycling of mutant CFTR is partially restored by pharmacological treatment

Efficient trafficking of the cystic fibrosis transmembrane conductance regulator (CFTR) to and from the cell surface is essential for maintaining channel density at the plasma membrane (PM) and ensuring proper physiological activity. The most common mutation, F508del, exhibits reduced surface expres...

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Détails bibliographiques
Auteurs principaux: Holleran, John P., Zeng, Jianxin, Frizzell, Raymond A., Watkins, Simon C.
Format: Artigo
Langue:Inglês
Publié: The Company of Biologists 2013
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3687701/
https://ncbi.nlm.nih.gov/pubmed/23572510
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.120196
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