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. 2022 Dec 29;24(1):136–147. doi: 10.1038/s41590-022-01372-2

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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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Extended Data Fig. 5 — Bone marrow cells from CD45.1/CD45.2 Nir3 sufficient mice (WT) and CD45.2 Nir3^–/– mice (Nir3^–/–) were mixed at a 1:1 ratio and adoptively transferred into CD45.1 hosts for six weeks. (a) DN NKT cells and IEL precursors (IELp) are gated from DN thymocytes. (b) The percentages of WT and Nir3^–/– cells in each subset were quantified. N = 5 mice. Data are shown as the mean ± s.e.m. and are representative of 2 independent experiments. P values were determined using a two-tailed Student’s t-test.

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