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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...
Autores principales: | Rapino, Daniele, Sabirzhanova, Inna, Lopes-Pacheco, Miquéias, Grover, Rahul, Guggino, William B., Cebotaru, Liudmila |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
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 |
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