The Detection of Bile Acids in the Lungs of Paediatric Cystic Fibrosis Patients Is Associated with Altered Inflammatory Patterns

Background: Cystic fibrosis (CF) is a hereditary disorder in which persistent unresolved inflammation and recurrent airway infections play major roles in the initiation and progression of the disease. Little is known about triggering factors modulating the transition to chronic microbial infection a...

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Udgivet i:Diagnostics (Basel)
Main Authors: Caparrós-Martín, Jose A., Flynn, Stephanie, Reen, F. Jerry, Woods, David F., Agudelo-Romero, Patricia, Ranganathan, Sarath C., Stick, Stephen M., O’Gara, Fergal
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2020
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7277992/
https://ncbi.nlm.nih.gov/pubmed/32384684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics10050282
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