Cystic Fibrosis Defective Response to Infection Involves Autophagy and Lipid Metabolism

Cystic fibrosis (CF) is a hereditary disease, with 70% of patients developing a proteinopathy related to the deletion of phenylalanine 508. CF is associated with multiple organ dysfunction, chronic inflammation, and recurrent lung infections. CF is characterized by defective autophagy, lipid metabol...

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Veröffentlicht in:Cells
Hauptverfasser: Mingione, Alessandra, Ottaviano, Emerenziana, Barcella, Matteo, Merelli, Ivan, Rosso, Lorenzo, Armeni, Tatiana, Cirilli, Natalia, Ghidoni, Riccardo, Borghi, Elisa, Signorelli, Paola
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2020
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7463682/
https://ncbi.nlm.nih.gov/pubmed/32781626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9081845
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