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. 2018 Mar 28;8:5295. doi: 10.1038/s41598-018-23630-w

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© The Author(s) 2018

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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Reduced calcium transient amplitude and slowed calcium re-uptake in sorafenib (10 µM) treated murine ventricular cardiomyocytes. Representative calcium transients (above) and original 2D calcium wave line-scan (below) (a) and summary data for calcium transient amplitude (b), time to 50 and 90% (RT10) decay of calcium transient signal (c,d), and relaxation constant Tau (e). n = 17 cells/10 hearts, *p < 0.001 for treatment/time interaction and p < 0.05 vs. control by 2-way mixed ANOVA with Welch’s post hoc t-test.