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. 2021 May 25;12(6):536. doi: 10.1038/s41419-021-03834-1

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© The Author(s) 2021

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. 2 — A, B qRT-PCR analysis of circ_0001367 expression in LN229 and T98G cells after transfection of the expression vector or shRNA. C, D Clone formation assays showed the clone formation ability of LN229 and T98G cells transfected with the expression vector or shRNA. E–H Cell proliferation analysis by EdU assay after LN229 and T98G cells were transfected with the expression vector or shRNA. I, J Cell migration analysis with a Transwell assay after glioma cells were transfected with the expression vector or shRNA. K, L Cell invasion was evaluated via Transwell assay after glioma cells were transfected with the expression vector or shRNA. Each experiment was performed in triplicate. Data are expressed as mean ± SD, **P < 0.01.