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. 2018 May 17;18(1):882–892. doi: 10.3892/mmr.2018.9034

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Copyright: © Xu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 2. — (A) Three lncRNAs (Map2k3os, Dnm3os and Abhd11os) identified by RNA-Seq were verified by RT-qPCR. **P<0.01 vs. the sham group. (B) Three mRNAs (Gadd45a, Cldn4 and Tbxa2r) identified by RNA-Seq were verified by RT-qPCR. **P<0.01 vs. the sham group. Abhd11os, abhydrolase domain containing 11, opposite strand; Cldn4, claudin 4; Dnm3os, dynamin 3, opposite strand; Gadd45a, growth arrest and DNA damage-inducible α; lncRNA, long non-coding RNA; Map2k3os, mitogen-activated protein kinase kinase 3, opposite strand; RNA-Seq, RNA-sequencing; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; Tbxa2r, thromboxane A2 receptor.