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. 2024 Feb 2;29(5):1440–1449. doi: 10.1038/s41380-024-02422-x

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© The Author(s) 2024

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

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Fig. 2 — The patient-derived iN cells derived from control (panel a) and SZ (panel b) tissue biopsies were subjected to immunofluorescent imaging with MAP2 (FITC-label, green fluorescence) and beta-III tubulin (TRITC-label, red fluorescence) neuron-specific markers [24–26]. Cell nuclei are indicated by DAPI staining (blue fluorescence). MAP2 and beta-III tubulin are shown separately and as merged images.