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. 2018 May;59(6):2445–2458. doi: 10.1167/iovs.18-24086

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(A) Photomicrographs of rhodopsin (A1), RIP3 (A2), and DAPI staining in the MCMV-injected eye of an IS Rip3^+/+ mouse at day 7 p.i. As shown in the merged image (A3), rhodopsin+ photoreceptors were rarely colocalized with RIP3 staining. (B) Photomicrographs of glycine (B1), RIP3 (B2), and DAPI staining in the MCMV-injected eye of an IS Rip3^+/+ mouse at day 7 p.i. As shown in the merged image (B3), glycine-stained amacrine cells were rarely colocalized with RIP3 staining. (C) Photomicrographs of TUNEL (C1), RIP3 (C2), and rhodopsin staining in the MCMV-injected eye of an IS Rip3^+/+ mouse at day 7 p.i. As shown in the merged image (C3), TUNEL-stained cells in the outer nuclear layer were not colocalized with RIP3 staining.