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. 2019 Dec 5;19(2):1017–1023. doi: 10.3892/etm.2019.8287

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Copyright: © Zhou 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 4. — RT-qPCR to confirm RNA sequencing results from WNT10B-treated and control dermal papilla cells. A total of 7 genes were selected for the qRT-PCR analysis, including RPL17, RPL39, ROCK2, CYFIP2, FGF14, PPP2R5E and VEGFB. The data are presented as the mean ± SEM of three independent experiments. RT-qPCR, reverse-transcription quantitative PCR; WNT10B, Wnt family member 10B; RPL17, ribosomal protein L17; RPL39, ribosomal protein L39; ROCK2, Rho associated coiled-coil containing protein kinase 2; CYFIP2, cytoplasmic FMR1 interacting protein 2; FGF14, fibroblast growth factor 14; PPP2R5E, protein phosphatase 2 regulatory subunit B′ε; VEGFB, vascular endothelial growth factor B; NC, negative control.