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. 2016 Aug 24;11(8):e0161205. doi: 10.1371/journal.pone.0161205

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© 2016 Sarmah et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 9 — (A-F) Tg(Tcf/Lef-miniP:dGFP);Tg(myl7:nlsKikGR) double transgenic zebrafish showed two rows of cardiomyocytes (red cells) at the AVC expressing GFP (Wnt active) in control embryos (A-C); ethanol treated embryos showed weak GFP expressing cardiomyocytes that were not restricted at the AVC (D-F) at 52 hpf. (G-L) Tg(Tcf/Lef-miniP:dGFP);Tg(myl7:nlsKikGR) double transgenic zebrafish showed long cardiomyocytes with strong GFP signal at the AVC and faint GFP signal in the ventricular cardiomyocytes in control embryos (G, H); ethanol exposed embryos showed weak GFP labeling at the AVC as compared to control (I-L). Arrows: Long cardiomyocytes with strong GFP signal. (M-O) Optical section of the heart of 75 hpf embryos showed GFP expression in the endocardial cells (arrowheads) at the AVC in the control embryo (M) and in ethanol treated embryos (N, O). A: Atrium, V: ventricle.