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. 2013 Aug 5;8(8):e70371. doi: 10.1371/journal.pone.0070371

Figure 4. Loss of C/ebpβ is insufficient to rescue PHPV like eye phenotype of Tgfβ2 KO mouse.

Figure 4

(A) Representative photomicrographs of hematoxylin- and eosin-stained slides of E15.5 embryos showing the primary vitreous hyperplasia in C/ebpβ+/+, Tgfβ2−/− embryos (a) is NOT corrected by additional loss of expression of C/ebpβ in C/ebpβ −/−, Tgfβ2−/− embryos (b-d). Arrows denote the cellular area of the primary vitreous. (B) Quantitative analyses show that the average cell numbers in the vitreous have little change in C/ebpβ −/−, Tgfβ2−/− embryos at E13.5 as compared with C/ebpβ +/+, Tgfβ2−/− littermates.