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. 2018 Aug 29;9(9):872. doi: 10.1038/s41419-018-0853-x

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© The Author(s) 2018

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. 3 — Cells derived from three GBM biopsy specimens (GC1, GC2 and GC3) were transfected with an α6-integrin siRNA (si-α6) or a scramble control (si-Scr). Forty-eight hours post-irradiation (6 Gy), propidium iodide staining was performed as described in “Materials and methods section” and the DNA content was analyzed by flow cytometry. Percentage of cells in sub-G1, G1/S and G2/M phases were quantified by the BD Accuri C6 software. Quantifications of three experiments are presented as means ± SD. ***p < 0.001; **0.001 < p < 0.01; *0.01 < p < 0.05.