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. 2016 Dec 29;3(6):ENEURO.0295-16.2016. doi: 10.1523/ENEURO.0295-16.2016

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Copyright © 2016 Surel et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Figure 8. — Microtubule network remodeling in IHCs of diap3-overexpressing mice. A–C″, Fluorescence intensity distribution of microtubules (green) and F-actin (red) at the cuticular plate section through x and y sections in WT (A–A″), Tg 771 (B–B″) and Tg 924 (C–C″) lines at P21 (A, B, C), 1 month (A′, B′, C′), and 2 months (A″, B″, C″). Actin filaments are labeled using phalloidin-rhodamine (red), and microtubules are stained using an antibody against the β2-tubulin subunit (green). Pictures show a high magnification of the cuticular plate section over a single IHC. Thick and thin lines represent the average and individual fluorescence intensities (n = 9 IHCs in each condition), respectively. Right, histograms show the fluorescence average from an area of 4 µm² located at the image center for the different genotypes and age. AU, arbitrary unit. **p < 0.01 (Student’s t-test).