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Fig. 1 Fluorescence (A, C) and bright‐field (B, D) images of live zebrafish embryos upon exposure to rhodamine B at 1 µm for 2 h. For imaging, the embryos were automatically positioned in lateral orientation in glass capillaries using the VAST system. (A, B) Solvent control (0.1% DMSO); (C, D) cyclosporin A (40 µm) treatment.
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Full text @ FEBS Lett.