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. 2007 Feb 20;104(9):3450–3455. doi: 10.1073/pnas.0611680104

Fig. 1.

Fig. 1.

BMAL1 and CLOCK and NPAS2 differ in severity of BP variation and maintenance according to the severity of the genotype. (A) MAP telemetry recordings averaged each hour from three 24-h periods in WT, Bmal1−/−, Clockmut, and Npas2mut mice. MAP recordings were significantly different (Kruskal–Wallis test) for Bmal1−/− (light phase, P < 0.05; dark phase, P < 0.0001) and Npas2mut mice (both light and dark phase. P < 0.0001). Clockmut mice were significantly different only during the light phase (P < 0.05). MAP recordings taken separately during light and dark phases in Bmal1+/+ vs. Bmal1−/− (B) (n = 8; ∗, P < 0.05; †, P < 0.001), WT vs. Clockmut (C) (n = 4–8) WT vs. Npas2mut mice (D) (n = 8; ∗, P < 0.05), and delayed acrophase (time of peak) of MAP rhythm in Npas2mut vs. WT (D) (n = 8, P < 0.05). White boxes denote lights on, and dark boxes denote lights off.