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. 2019 Mar 4;28(5):568–584. doi: 10.1177/0963689719834870

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© The Author(s) 2019

This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Fig. 6. — The effects of rTMS on the differentiation of NSCs in vitro. (A) Representative photographs of light microscopy in the control and rTMS groups. Scale bar = 100 μm; (B) Representative photographs of immunofluorescence co-staining of NSCs for DAPI (blue), GFAP (green), and DCX (red) in the control and rTMS groups. Quantitative analyses of (C) DCX-positive cells and (D) GFAP-positive cells in neurospheres in the control and rTMS groups. n = 5 for immunofluorescence staining analysis. Scale bar = 20 μm; *p < 0.05 vs. control. **p < 0.01 vs. control.