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Our results further imply that many families of genes not previously implicated in glial cell biology are modulated by REST and CoREST in a developmental stage- and cell type specific manner, which suggests that they may have selective roles in promoting aspects of glial cell identity, function, and connectivity and/or repressing characteristics of alternate lineages.
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There, we observed that learning was modulated by sleep stages.
Although a few studies found that the connectivity patterns in resting brains were remarkably consistent across sessions acquired at different time (from minutes apart to months apart) [51], [52], our results by direct comparison indicate that the activity within the DMN was not only modulated by different resting conditions but also by the order of the same type of resting condition (i.e., EC).
Almost eleven years of coastal altimetry data (2002 2012) from X-TRACK, 20–40 km from the coast, reveal a persistent seasonal poleward flow from July to October and equatorward flow, modulated by mesoscale processes the rest of the year.
For example, in social insects, during the nest-moving or the foraging, it can be the number of both recruiting and aggregated insects that is important [12], [50] while a study of sheep by Gautrais et al [24] showed that in transitions from activity to inactivity, decisions are modulated by both active and resting conspecifics.
The properties and kinetics of voltage-dependent conductances or the electrogenic properties of the neuron due to changes in anatomy may be modulated by S6K1 to alter resting excitability.
Inspired by prior work, which demonstrated that fractal scaling of BOLD signal is increased at rest and modulated by task performance5,6,7, we hypothesize that fractal scaling decreases globally as a function of cognitive effort.
These results suggest that the TAS1R3-R757C acido acid substitution may affect general functions of TAS1R1/TAS1R3 such as cell surface expression, dimerization of TAS1R1 and TAS1R3 or the dynamic equilibrium between the active and resting conformations modulated by the presence/absence of ligand as shown in mGluR1 [27], [27].
Repeated paired TMS led to an increase in PMv-M1 BOLD functional connectivity while participants performed the task (paired t-test: t(13) = -2.59, p = 0.023; Figure 2C), while PMv-M1 BOLD coupling at rest was not modulated by the intervention (t(14) = -0.07, p = 0.94; Figure 2F).
The data are modulated by 16QAM modulation.
DOI: http://dx.doi.org/10.7554/eLife.06195.010 We further characterized the nature of the resting K+ conductance modulated by Bk.
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