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To quantify fluorescence signal in Tg(NFkB:GFP), Tg(Stat3:EGFP) and cyp11c1 ;Tg(GRE:EGFP) larvae, z-stack images were converted to maximum intensity z-projections, and mean fluorescence was measured in the same region of interest (ROI) using Fiji-ImageJ software

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[22] Lung cancer cells stimulated using glucocorticoids were induced into a reversible dormancy state which was dependent on the IGF-1R and its accompanying survival signaling pathways