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In both experiments, we observed more alpha power while participants viewed High- rather than Low-Competition novel silhouettes.
In both experiments we observed the inclusion of labeled B10L cells into the trophectoderm layer (Figure 3A, B; Figure S2).
In both experiments, we observed two-step separation of sizes resulting in four distinct populations, with sequential Boolean and single bivariate gating producing similar results (Figure 4C and Figures S1 and S2).
In both experiments, we observed no additive or synergistic effects between different miRNAs (Fig. 3B).
In both experiments we observed more severe phenotypes than that caused by hINSC96Y alone.
Finally, in both experiments, we observed similar letter identification performance in static and moving hand conditions.
Similar(53)
In both experiments, we observe a correlative diminution of the pyrrhotite signature at 35 K with increasing temperature.
When comparing the performance results of both experiments, we observe that, in general, the overall performance of our approach does not significantly differ using a different set of inputs.
For both sets of additional experiments we observed results that are qualitatively similar to those in 3 (Supplementary Figures 9 and 10).
In both in vitro and in vivo experiments we observed that the process of apoptosis was induced by the activation of death ligand TRAIL (Fig. S2, Fig. S3 and Fig. 6).
In our experiments, we observed that both p53 and ERK get activated as early as 1 h after Triphala treatment.
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