Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells

Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) chloride (Cl-) channel regulated by protein kinases, phosphatases, divalent cations and by protein-protein interac...

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Detalles Bibliográficos
Autores principales: Calvez, Marie-Laure, Benz, Nathalie, Huguet, Florentin, Saint-Pierre, Aude, Rouillé, Elise, Coraux, Christelle, Férec, Claude, Kerbiriou, Mathieu, Trouvé, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690610/
https://www.ncbi.nlm.nih.gov/pubmed/29145426
http://dx.doi.org/10.1371/journal.pone.0187774

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690610/
https://www.ncbi.nlm.nih.gov/pubmed/29145426
http://dx.doi.org/10.1371/journal.pone.0187774

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