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. 2017 Apr 10;37:8. doi: 10.1186/s41232-017-0039-4

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© The Author(s) 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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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Fig. 1 — a Traditional isolation of dental pulp stem/progenitor cells (DPSCs) by adherent culture on dishes. b Prospective isolation of DPSCs by flow cytometric identification of cell surface markers. c Representative fluorescence-activated cell sorting profiles of dental pulp cells. d A representative phase-contrast micrograph of plastic-adherent colony-forming LNGFR^Low+THY-1^High+ cells with fibroblast morphologies. Scale bars = 100 μm