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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. 4. — The effects of rTMS on the differentiation of NSCs after ICH. (A) Representative photographs of immunofluorescence co-staining of NSCs for DAPI (blue), Nestin (green) and DCX (red) and (B) immunofluorescence co-staining of NSCs for DAPI (blue), Nestin (green) and GFAP (red) in the sham, ICH, and ICH+rTMS groups at 72 h after ICH. (C) Quantitative analyses of DCX-positive and (D) GFAP-positive cells in the sham, ICH, and ICH+rTMS groups at 72 h after ICH. n = 5 for immunofluorescence staining analysis. Scale bar = 10 μm; **p < 0.01 vs. sham; ^#p < 0.05 vs. ICH.