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. 2020 Jun 23;15(12):1370–1385. doi: 10.1080/15592294.2020.1782655

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© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

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Figure 1. — Cyp2a5 expression in liver of PSE and control in E17.5, D3 mice and adult offspring

Cyp2a5 mRNA expression in whole liver of foetal offspring (E17.5, a and b), neonatal offspring (D3, c and d) and adult offspring (e and f) in PSE (closed symbols) and control groups (open symbols). Data are shown as individual values. If not stated otherwise, the comparison of shown groups was not significant. (Mann–Whitney U-test). *p ≤ 0.05, *** p ≤ 0.001 (Mann–Whitney U-test). Circle (○) symbol(s) = male, square (□) symbol(s) = female.