Gene expression evaluated by reverse transcription, quantitative real-time PCR (RT-qPCR) in control and in 100 μM RSV-treated C6 glioma cells.

mRNA samples isolated from cells incubated for 24 h were analyzed by RT-qPCR using specific probes for Atp1b2, Vamp2, Rab2a, and Dnm1. β-actin mRNA was used as control. Data are mean ± SEM of four independent experiments. * p < 0.05 according to Student’s t test.