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. 2009 Jul 29;29(30):9614–9624. doi: 10.1523/JNEUROSCI.2284-09.2009

Figure 4.

Figure 4.

Cdk-inhibitor p27 and cD-Cdk effector retinoblastoma (pRb) in the cortex of cD2−/− and cD1−/− mice and WT littermates. A–L, The labeling intensity of p27 is increased in cD2−/− mice (B, F, J) compared with cD2+/+ (A, E, I) at early and later ages in the neurogenic period. Nuclei immunostained for pRb were diminished in abventricular cortical regions in cD2−/− (D, H, L) relative to cD2+/+ (C, G, K) across the neurogenic period. M–T, Immunolabeling for p27 was paler in the ventricular zone of cD1−/− (N, R) compared with WT (M, Q) at all ages examined. Labeling for pRb was unchanged in cD1−/− (P, T) compared with WT (O, S). Labeling was examined in three to five cases per genotype.