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. 2019 Jun 7;10:2529. doi: 10.1038/s41467-019-10404-9

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — JNK inhibition decreases proliferation of human glioma-derived H3.3K27M cells. a, b Transmitted light pictures (a) and cell viability plots (b) of human glioma-derived cells with wild type (SF9421, black; SF9402, gray) or K27M mutant (SF8628, red) H3.3, treated with different concentrations of JNK inhibitor SP600125. N = 4 for all conditions. Significance was tested for using one-way ANOVA