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Carbon nanoparticles adversely affect CFTR expression and toxicologically relevant pathways

Abstract 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 co...

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Bibliografiske detaljer
Principais autores: Torben Stermann, Thach Nguyen, Burkhard Stahlmecke, Ana Maria Todea, Selina Woeste, Inken Hacheney, Jean Krutmann, Klaus Unfried, Roel P. F. Schins, Andrea Rossi
Format: Artigo
Sprog:Inglês
Udgivet: Nature Portfolio 2022-08-01
Serier:Scientific Reports
Online adgang:https://doi.org/10.1038/s41598-022-18098-8
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