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. 2016 Apr 29;12:1744806916646111. doi: 10.1177/1744806916646111

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© The Author(s) 2016

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 1. — Neuronal markers and gene ontology analysis on RNA samples. The SH-SY5Y, F-11, and ND7/23 cell lines do not fit into existing categories of peripheral neurons, yet gene ontology analysis demonstrates that the cell lines transcriptomes retain similar ratios of enriched biological processes compared to whole DRGs. (a) Expression of markers commonly used to identify specific peripheral neuron sub-populations, microglia, and non-neuronal cells by the SH-SY5Y, F-11, and ND7/23 cell lines. (b) Gene ontology analysis of whole DRGs. (c) Gene ontology analysis of SH-SY5Y cells. (d) Gene ontology analysis of F-11 cells (aligned to the mouse genome). (e) Gene ontology analysis of F-11 cells (aligned to the rat genome). (f) Gene ontology analysis of ND7/23 cells (aligned to the mouse genome). (g) Gene ontology analysis of ND7/23 cells (aligned to the rat genome).