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Amplitude modulation effects are discovered of which the mechanism is explained and the period of modulating signal is carried out by phase analysis and averaging method.
Furthermore, if emotional modulation effects are temporally coincident with N170 responses to faces, the topography of this emotional effect can be investigated to examine whether this effect might be characterized as a modulation of the N170, in which the fear minus neutral face N170 would produce a topography that itself resembles a face N170 topography.
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A positive modulation effect was observed in the midcingulate and the dorsomedial prefrontal cortex (P < 0.05).
A negative modulation effect was observed in perigenual cingulate cortex, insula, and medial thalamus (P < 0.05).
We also demonstrate that the mixing of two wave modes is possible whereby a modulation effect is observed.
Forh/d≥0·1 this modulation effect is comparable to that for an infinite rigid wall, while forh/d≤0·01 it resembles the effect for a free surface.
Third, the size and duration of the rate modulation effect were clearly influenced by background texture.
Furthermore, the significant interaction shows that an attentional modulation effect was clearly larger for target displacements than for cursor displacement if the latter was present at all.
Furthermore, lifespan modulation effects have been also reported in worm [ 17, 18, 19], fly [ 20, 21] and mice [ 22, 23] upon downregulation of the conserved insulin/Igf-like pathway.
In z-scan measurements with high repetition rate lasers, which rely on sensing changes in spatial mode, it is challenging to separate the desired n2 Kerr lensing from thermal lensing [ 25]; in the XPMSS method, because thermal diffusion timescales are orders of magnitude longer than the < 1 picosecond timescale of the temporal phase <span class="lh">modulation, thermal effects are readily separable.
Therefore, we are confident that the HuR modulation and consequent RNA effects are integrin-induced.
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