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. 2019 Dec 6;20(3):328–338. doi: 10.1007/s12012-019-09557-2

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© The Author(s) 2019

Open AccessThis 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 https://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — Relative mRNA expression levels of a tyrosine hydroxylase (Th), b β-myosin heavy chain (Mhc-β) in the hearts in saline- and doxorubicin (DOX) -treated wild-type (WT) and NPY-OE^DβH (NPY-OE) mice (n = 6–8/group). Values are presented as means ± SEM, p = 0.065 DOX vs. saline, two-way ANOVA treatment effect; # p < 0.05, NPY-OE vs. WT, two-way ANOVA genotype effect