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. 2013 May 6;110(21):E1923–E1932. doi: 10.1073/pnas.1303916110

Fig. 3.

Fig. 3.

Lmnb1CS/CS embryos have smaller brains and exhibit a defect in layering of neurons in the cerebral cortex. (AC) Photographs of wild-type, Lmnb1CS/CS, Lmnb2CS/CS, Lmnb1+/−, and Lmnb1−/− mice at E19– postnatal day (P)1. (Scale bars, 5 mm.) (DF) Mouse brains viewed from the top at E19–P1. (Scale bars, 1 mm.) (GI) H&E staining of coronal and sagittal brain sections at E19–P1. (Scale bars, 1 mm.) (J) Sizes of the cortex and midbrain in wild-type, Lmnb1CS/CS (B1CS), and Lmnb2CS/CS (B2CS) embryos (measured from the top of brains, see E). Lmnb1+/+, n = 6; Lmnb1CS/CS, n = 5; Lmnb2+/+, n = 4; Lmnb2CS/CS, n = 5. The midbrain was 21.5 ± 7.6% smaller in Lmnb1CS/CS mice than in wild-type mice, P < 0.0001; the cortex was 9.1 ± 4.6% smaller in Lmnb1CS/CS mice than in wild-type mice, P = 0.0072. Values represent mean ± SD (K) Immunofluorescence microscopy of the cerebral cortex of E19–P1 wild-type (WT, Lmnb1+/+), Lmnb1CS/CS (B1CS), Lmnb2CS/CS (B2CS), Lmnb1+/−, and Lmnb1−/− embryos with antibodies against Cux1 (red) and Ctip2 (green). The layering of cortical neurons in Lmnb1−/− embryos was abnormal, as reported previously (24). Lmnb1CS/CS mice also exhibited a cortical layering defect, but it was milder than in Lmnb1−/− mice. No abnormalities were detected in Lmnb1+/− mice. (Scale bars, 100 µm.)