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Induction of miR-23b by RIG-I signaling, SeV and RV infection, or IFN-β treatment. HeLa cells stably expressing FK/RIG were treated with AP (A). B–E, HeLa cells were infected with SeV (B), infected with RV16 (C), RV1B (D), or treated with IFN-β (1000 units/ml) (E). The miRNA fraction was extracted at the time points indicated and the amount of miR-23b was determined by real-time PCR.
