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. 2022 Apr 27;29(11):1600–1615. doi: 10.1038/s41417-022-00466-1

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© The Author(s) 2022

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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Fig. 4 — Serum samples were analyzed by MBFCM. Differences in marker expressions on serum-derived EVs from AML (n = 3), ALL (n = 3), CLL (n = 2) and Healthy samples (n = 4) are shown in mean values. For statistical comparison of more than two groups one-way analysis of variance (ANOVA) with Benjamini-Hochberg adjustments for multiple comparisons was applied. Differences were considered as ‘borderline significant’ (^#) with p-values between 0.05 and 0.1 and as ‘significant’ (*) with p-values between 0.01 and 0.05.