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. 2021 Jul 28;12:719951. doi: 10.3389/fphar.2021.719951

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Copyright © 2021 Amato, Rossino, Cammalleri, Timperio, Fanelli, Dal Monte, Pucci and Casini.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Baseline and endpoint densitometric analysis of RBPMS-immunostained RGCs in whole mount retinas. Immunofluorescence photomicrographs show representative RBPMS immunostaining in central and peripheral areas of D2b, (A,D), D2e (B,E) and D2+LG (C,F) retinas. Scale bar, 100 µm. (G) analysis of RBPMS positive cell density in D2b (gray boxes), D2e (white boxes), and D2+LG (dashed boxes) retinas. Box plots describe the statistical distribution of n = 4 independent retinas. Data were analyzed using two-way ANOVA with Bonferroni post-hoc test. *p < 0.05 vs D2.