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. 2021 Oct 21;12:548. doi: 10.1186/s13287-021-02614-0

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 1 — Isolation and characterization of human hair follicle-derived mesenchymal stem cells (HF-MSCs). A Cells that migrated from hair follicles and proliferated onto the culture plate exhibited fibroblast-like characteristics (bar = 200 μm). B Flow cytometry was used to measure the cell surface expression of MSC biomarkers. The cells expressed CD29, CD44, CD73, CD90, CD105 but not CD31, CD34, CD45, HLA-DR. C Immunofluorescence analysis was used to measure the surface markers of HF-MSCs. The cells expressed CD44, CD73, CD90, CD105 but not CD31, CD34, CD45 (bar = 100 μm)