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. 2024 Sep 30;10:84. doi: 10.1038/s41523-024-00692-w

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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. 1 — Formation of major ribociclib metabolites over time was correlated with CYP3A5 genotype status. Human liver microsomes from a CYP3A5 NM (CYP3A5 *1/*1) had the greatest ribociclib metabolite formation followed by IM (CYP3A5 *1/*3) and PM (CYP3A5 *3/*3). Graphs represent three technical replicates per datapoint, error bars show standard deviation.