Pharmacological Correctors of Mutant CFTR Mistrafficking

The lack of phenylalanine 508 (ΔF508 mutation) in the cystic fibrosis (CF) transmembrane conductance regulator (CFTR) Cl(−) channel represents the most frequent cause of CF, a genetic disease affecting multiple organs such as lung, pancreas, and liver. ΔF508 causes instability and misfolding of CFTR...

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Detalles Bibliográficos
Autores principales: Pedemonte, Nicoletta, Galietta, Luis J. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464431/
https://www.ncbi.nlm.nih.gov/pubmed/23060795
http://dx.doi.org/10.3389/fphar.2012.00175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464431/
https://www.ncbi.nlm.nih.gov/pubmed/23060795
http://dx.doi.org/10.3389/fphar.2012.00175

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