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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Detalles Bibliográficos
Autores principales: Caparrós-Martín, Jose A., Flynn, Stephanie, Reen, F. Jerry, Woods, David F., Agudelo-Romero, Patricia, Ranganathan, Sarath C., Stick, Stephen M., O’Gara, Fergal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277992/
https://www.ncbi.nlm.nih.gov/pubmed/32384684
http://dx.doi.org/10.3390/diagnostics10050282

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277992/
https://www.ncbi.nlm.nih.gov/pubmed/32384684
http://dx.doi.org/10.3390/diagnostics10050282

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