Ontology highlight
ABSTRACT:
SUBMITTER: Stermann T
PROVIDER: S-EPMC9395428 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
Stermann Torben T Nguyen Thach T Stahlmecke Burkhard B Todea Ana Maria AM Woeste Selina S Hacheney Inken I Krutmann Jean J Unfried Klaus K Schins Roel P F RPF Rossi Andrea A
Scientific reports 20220822 1
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 as major contributors to the global health burden of air pollution. However, their effects on the expression of CFTR and associated genes in lung epithelial cells have not yet been investigated. We th ...[more]