Molecular Docking and QSAR Studies as Computational Tools Exploring the Rescue Ability of F508del CFTR Correctors

Cystic fibrosis (CF) is the autosomal recessive disorder most recurrent in Caucasian populations. Different mutations involving the cystic fibrosis transmembrane regulator protein (CFTR) gene, which encodes the CFTR channel, are involved in CF. A number of life-prolonging therapies have been conceiv...

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Detalles Bibliográficos
Autores principales: Righetti, Giada, Casale, Monica, Liessi, Nara, Tasso, Bruno, Salis, Annalisa, Tonelli, Michele, Millo, Enrico, Pedemonte, Nicoletta, Fossa, Paola, Cichero, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663332/
https://www.ncbi.nlm.nih.gov/pubmed/33138251
http://dx.doi.org/10.3390/ijms21218084

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663332/
https://www.ncbi.nlm.nih.gov/pubmed/33138251
http://dx.doi.org/10.3390/ijms21218084

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