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. 2018 Jun 18;9(7):720. doi: 10.1038/s41419-018-0760-1

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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. 2 — a Sketches of the construction of wild-type or mutant IGF-1 3′-UTR reporter plasmid for miR-129. b The relative luciferase activity was analyzed after the wild-type or mutant IGF-1 3′-UTR reporter plasmid co-transfected into HEK 293T cells with miR-129 mimic (miR-129) or mimic control (NC). **p < 0.01 versus control. Expression of miR-129 in DRGs (c) and proximal nerve stumps (d) following sciatic nerve transection. * p < 0.05 and ** p < 0.01 versus control (0 h post nerve injury). U6 served as internal reference