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. 2017 Feb 16;7:42675. doi: 10.1038/srep42675

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Copyright © 2017, The Author(s)

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The 16HBE cells were transfected with Lyn siRNA. (A) Western blot analysis of Lyn, STAT6 and the phosphorylation of STAT6 in Lyn^−/− and untransfected (NT) cells exposed to IL-4. (B) Relative density of STAT6 and phosphorylation of STAT6 in IL-4-treated Lyn knockdown and NT cells. (C) Western blot analysis of Lyn, STAT6 and phosphorylated STAT6 in Lyn^−/− and NT cells exposed to IL-13. (D) Relative density of STAT6 and phosphorylated STAT6 in IL-13-treated Lyn^−/− and NT cells. β-actin was used as the loading control. All data are representative of three experiments, and a statistical analysis was performed.