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. 2022 Mar 14;28(4):743–751. doi: 10.1038/s41591-022-01720-7

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

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Extended Data Fig. 3 — Left: Histograms showing surface antigen expression in a representative primary KMT2A-rearranged infant B-ALL sample relative to negative control. Right: Scatterplot showing percentage of cells in each sample expressing ELP-characteristic antigens > negative control (n = 2 xenograft, n = 4 primary KMT2A-rearranged infant B-ALL). Line= mean; 82% CD7⁺, 93% CD127⁺ and 82% FLT3⁺).