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Neuronal survival: The activation of these signaling pathways promotes neuronal survival by enhancing cell survival signals and inhibiting cell death signals

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The cellular studies using CHO cells indicated that the pre-treatment of DSePA significantly upregulated the mRNA expressions of seleno-GPxs ( GPx1 , GPx2 , GPx3 , and GPx4 ), increased total GPx activity, and concurrently improved the viability of irradiated cells with a dose modification factor of 1.53 [85]