Serum inflammatory profiles in cystic fibrosis mice with and without Bordetella pseudohinzii infection

Cystic fibrosis (CF) is an autosomal recessive disease caused by dysfunctional cystic fibrosis transmembrane conductance regulator (CFTR) protein, and is marked by an accumulation of mucus in affected airways resulting in persistent infection and chronic inflammation. Quantitative differences in inf...

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Detalles Bibliográficos
Autores principales: Litman, Paul M., Day, Alexander, Kelley, Thomas J., Darrah, Rebecca J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413329/
https://www.ncbi.nlm.nih.gov/pubmed/34475490
http://dx.doi.org/10.1038/s41598-021-97033-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413329/
https://www.ncbi.nlm.nih.gov/pubmed/34475490
http://dx.doi.org/10.1038/s41598-021-97033-9

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