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. 2016 Oct 27;6:35811. doi: 10.1038/srep35811

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Copyright © 2016, The Author(s)

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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(a) Hierarchical clustering analysis of human cell surface marker screening panel. Microarrays were used to examine expression profiles of 262 cell surface marker genes and SLC2A1 (GLUT1, IH clinical biomarker) normal and neoplastic SC controls (HUVEC, Bone Marrow SC, Cord Blood SC, Mesenchymal SC, and Glioblastoma CSC). The gene expression intensity data images were generated with Partek Genomics Suite Software. (b–g) Microarray gene significance dot plot. The dot plots compare the expression of significant genes between HemSC ^GLUT1+ and HUVEC (control) to exhibit large gene expression changes (Bone Marrow SC - *BM, Cord Blood SC - *CB, Glioblastoma CSC - *G, HemSC GLUT1^high - *IH^GLUT1+, Hem ^ENG+− IH^CD105+, HUVEC endothelial progenitor (control) - *E, Mesenchymal SC - *M) of sample gene set including SLC2A1 (GLUT1 clinical marker), NT5E (CD73), ILR1, SLC7A5 (CD98), MME (CD10), and CD44.