The models showed that the emergence of synchronisation is very robust, with synchrony coefficient values near unity in most cases.
We show robust oscillatory synchrony between M1 and S1/area 5 cells, agreeing with a role for oscillations in sensorimotor integration.
Using bootstrapped Pearson correlation for transcript levels for the same genes across distinct brain areas, we report robust gene transcript synchrony between the amygdala and cingulate cortex in the human postmortem brain of normal control subjects (n = 14; Control/Permutated data, p<0.000001).
In the primary visual cortex of cats, robust changes in synchrony were observed from one perceptual condition to another, imposed by interocular rivalry (Fries et al. 1997).
When stimulating a large population of cells with soluble chemicals, it is crucial to ensure synchrony and robust control of temporal signal delivery.
Designing specific interbrain statistical analyses, we were able to show that the alpha-mu rhythm was the most robust interbrain oscillatory activity discriminating behavioral synchrony vs. non synchrony in the centroparietal regions of the two interacting partners.
Second, the fact that inter-hemispheric modulation of cortical synchrony was more robust with the IS than with the DS gratings is consistent with the proposal that callosal axons, as intra-areal axons [24] preferentially interconnect neurons with the same selectivity for stimulus orientation [5], [11] [13], [17].
The functional forms of the relations of density compensation with spatial synchrony and persistence are robust to increases in dispersal mortality, landscape dynamics, or density dependence of dispersal.
Robust shifts in amygdala-cingulate gene synchrony were observed in subjects with major depressive disorder (MDD, denoted here "depression") (n = 14; MDD/Permutated data, p<0.000001), significantly affecting between 100 and 250 individual genes (10 30% false discovery rate).
