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Toll like Receptor signalling by Prevotella histicola activates alternative NF-κB signalling in Cystic Fibrosis bronchial epithelial cells compared to P. aeruginosa

Cystic Fibrosis (CF), caused by mutations affecting the CFTR gene, is characterised by viscid secretions in multiple organ systems. CF airways contain thick mucus, creating a gradient of hypoxia, which promotes the establishment of polymicrobial infection. Such inflammation predisposes to further in...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Bertelsen, Anne, Elborn, Stuart J., Schock, Bettina C.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7544055/
https://ncbi.nlm.nih.gov/pubmed/33031374
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0235803
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