Rescue of NBD2 Mutants N1303K and S1235R of CFTR by Small-Molecule Correctors and Transcomplementation

Although, the most common Cystic Fibrosis mutation, ΔF508, in the cystic fibrosis transmembrane regulator. (CFTR), is located in nucleotide binding domain (NBD1), disease-causing mutations also occur in NBD2. To provide information on potential therapeutic strategies for mutations in NBD2, we studie...

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Detalles Bibliográficos
Autores principales: Rapino, Daniele, Sabirzhanova, Inna, Lopes-Pacheco, Miquéias, Grover, Rahul, Guggino, William B., Cebotaru, Liudmila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370480/
https://www.ncbi.nlm.nih.gov/pubmed/25799511
http://dx.doi.org/10.1371/journal.pone.0119796

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370480/
https://www.ncbi.nlm.nih.gov/pubmed/25799511
http://dx.doi.org/10.1371/journal.pone.0119796

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