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. 2017 Apr 10;7:46304. doi: 10.1038/srep46304

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Copyright © 2017, The Author(s)

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(a) Western blotting assay was used to detect the levels of p-JNK (46 kDa and 55 kDa) and JNK (46 kDa and 55 kDa) after different durations of exposure to 4.8% sevoflurane or control conditions. (b) The expression of p-JNK/JNK in FNSCs on exposure to sevoflurane for different durations. All p-JNK/JNK data are given as mean ± standard deviation from at least three separate experiments. (c) JNK inhibition by the specific inhibitor SP600125 rescued FNSCs from cell damage and enhanced cell viability. Data were analyzed by one-way ANOVA followed by Tukey multiple-comparison tests. *P < 0.05, ***P < 0.001.