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DMEM/F12 media supplemented with 10% fetal bovine serum and 1% streptomycin/penicillin (E490-20ML, VWR, Radnor, PA, USA). Cells were subcultured separately into four groups (control, 1-h Dex-treated, 24-h Dex-treated, and 48-h Dex-treated) using six
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Department of Neurosurgery, Technical University Munich (TMU), Munich, Germany
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Medizinische Klinik Und Poliklinik III, University Hospital Carl Gustav Carus, Dresden, Germany
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Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, Birmingham, UK
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( 33 ) and more recently developed MUC-1 ( 34 ), CU-ACC1 and CU-ACC2 cells ( 35 ). NCI-H295R cells were cultured in Dulbecco’s modified eagle medium (DMEM)/F12, HEPES media) (Gibco, 11330032), supplemented with 2.5% Nu-Serum growth media supplement
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Study population Participants were recruited through flyers at Umeå University Hospital and Umeå University grounds as well as through social media. Inclusion criteria were age 18–65 years and total abstinence from liquorice for 4 weeks prior to the