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. 2014 Jan 19;33(1):10. doi: 10.1186/1756-9966-33-10

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Copyright © 2014 Zhang et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Effect of miR-302b on cell proliferation and apoptosis. (A-B) After pcDNA™6.2-GW/EmGFP-miR-302b (miR-302b) or Anti-miR-302b inhibitor (anti-miR-302b) transduction, the growth of TE-1 cells (A) and Ec9706 cells (B) was analyzed at different time points and compared to anti-miR-Inhibitors-Negative Control (control)/pcDNA™6.2-GW/EmGFP-miR (mock) cells using the MTT assay. (C) Flow cytometric analysis of the effect of miR-302b on apoptosis of TE-1 cells. (D-E) Flow cytometric analysis of the effect of miR-302b on the apoptosis of TE-1 cells (D) and Ec9706 cells (E). *P < 0.05 compared with the respective control.