Carbon nanoparticles adversely affect CFTR expression and toxicologically relevant pathways

Cystic fibrosis is an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) that can lead to terminal respiratory failure. Ultrafine carbonaceous particles, which are ubiquitous in ambient urban and indoor air, are increasingly considered...

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Detalles Bibliográficos
Autores principales: Stermann, Torben, Nguyen, Thach, Stahlmecke, Burkhard, Todea, Ana Maria, Woeste, Selina, Hacheney, Inken, Krutmann, Jean, Unfried, Klaus, Schins, Roel P. F., Rossi, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395428/
https://www.ncbi.nlm.nih.gov/pubmed/35995803
http://dx.doi.org/10.1038/s41598-022-18098-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395428/
https://www.ncbi.nlm.nih.gov/pubmed/35995803
http://dx.doi.org/10.1038/s41598-022-18098-8

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