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. 2018 Oct 30;43(3):306–313. doi: 10.5114/ceji.2018.80050

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Copyright: © 2018 Polish Society of Experimental and Clinical Immunology

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.

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Fig. 2 — The morphology of dendritic cells (DCs) expanded from UCB CD34⁺ precursors and stimulated with LPS (100 μg/ml) or IFN-γ (10 ng/ml) in comparison to unstimulated control cells (C). UCB precursors were separated into adhering (giving rise to A-DCs) and non-adhering (giving rise to NA-DCs) fractions and cultured in the same conditions as All-CB precursors (giving rise to All-DCs)