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Additionally, the lack of efficient companies impairs their translation into the center. Here, we contrast the kinetics of miRNA-133a task after transfection of U87MG glioblastoma cells with either a home-made lipopolyplexes (LPRi) or using the RNAiMax transfection reagent. For this specific purpose, we combined miRNA intracellular trafficking tests by confocal microscopy with our formerly explained RILES miRNA-ON reporter system subcloned here in a lentivirus expression vector (LentiRILES) for longi

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