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. 2024 Oct 10;11:1111. doi: 10.1038/s41597-024-03965-y

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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. 4 — Overview of the phosphoproteomics data. (A) Principal component analysis of all samples (n = 216). (B) Overlapping upregulated differently expressed phosphosites (DEPs) (adjusted p-value < 0.05; absolute fold change > 1.5 from unstimulated cells) across cell lines at each time point of ligand stimulation. (C) Number of differently expressed phosphosites in each cell line at each time point of ligand stimulation. (D–F) Confirmation of LogFC of Akt and ERK1/2 phosphosites in each cell line compared to unstimulated control cells.