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Endocytic Trafficking of CFTR in Health and Disease
The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl-selective anion channel expressed in epithelial tissues. Mutations in CFTR lead to the debilitating genetic disease cystic fibrosis (CF). Within each epithelial cell, CFTR interacts with a large number of transient macromolecular...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1964799/ https://ncbi.nlm.nih.gov/pubmed/17098482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcf.2006.09.002 |
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