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Targeting the PI3K/Akt/mTOR signalling pathway in Cystic Fibrosis

Deletion of phenylalanine 508 of the cystic fibrosis transmembrane conductance regulator (ΔF508 CFTR) is a major cause of cystic fibrosis (CF), one of the most common inherited childhood diseases. ΔF508 CFTR is a trafficking mutant that is retained in the endoplasmic reticulum (ER) and unable to rea...

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Dades bibliogràfiques
Publicat a:Sci Rep
Autors principals: Reilly, R., Mroz, M. S., Dempsey, E., Wynne, K., Keely, S. J., McKone, E. F., Hiebel, C., Behl, C., Coppinger, J. A.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5550428/
https://ncbi.nlm.nih.gov/pubmed/28794469
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-06588-z
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