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. 2023 Oct 21;9:387. doi: 10.1038/s41420-023-01688-4

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© The Author(s) 2023

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 — A1/2 Transfection efficiency of hnRNPF plasmid (A1) or hnRNPF siRNAs (A2) evaluated using western blotting in GC cells. B1-4 Migration potential of GC cells transfected with Control + Vector, LINC01189 + Vector, LINC01189 + hnRNPF (Left panel, B1), or NC-siRNA + Scr-siRNA, LINC01189-siRNAp + Scr-siRNA, LINC01189-siRNAp + hnRNPF-siRNAp (right panel, B3) in a wound healing assay. Quantitative results are shown in the center panels (B2 & B4). ****P < 0.001. Migration (C1/2) and invasion (D1/2) transwell assays of GC cells transfected with different treatments. ****P < 0.001.