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. 2019 Dec 11;19(2):1370–1378. doi: 10.3892/etm.2019.8317

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Copyright: © Wang et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 2. — Treatment with 6965 decreases plaque stability. Representative images of (A) macrophages, (B) smooth muscle cells and (C) apoptosis from the control and 6965-treated groups (magnification, ×40). Macrophage and SMC contents were analyzed through immunohistochemistry. TUNEL staining was used to detect apoptotic cells. Data are presented as the percentage of stained plaque areas in the entirety of the lesions. Data are shown as the mean ± standard deviation. *P<0.05 and **P<0.01 vs. the control. TUNEL, Terminal deoxynucleotidyl transferase-mediated dUTP nick end labelling; SMC, smooth muscle cell.