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Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis

Cystic Fibrosis (CF) is the most common autosomal recessive lethal disorder among Caucasian populations. CF results from mutations and resulting dysfunction of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). CFTR is a cyclic AMP-dependent chloride channel that is localized to the api...

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Detalhes bibliográficos
Main Authors: Chanoux, Rebecca A., Rubenstein, Ronald C.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Research Foundation 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3398409/
https://ncbi.nlm.nih.gov/pubmed/22822398
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2012.00137
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