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Levels and subcellular localization of VRK2 may modulate different responses where the assembly of JIP1 complexes is required, since in its presence the level of activation will be lower the higher the level of VRK2 protein is.
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One important issue about eye movements is that the duration of stimulus observation in MTS tasks can be modulated by different response topographies, as suggested by Kato et al. (2008).
Sphingosine-1-phosphate (S1P) can regulate endothelial barrier function, but the sources of the S1P that provide this activity in vivo and its importance in modulating different inflammatory responses are unknown.
Ca2+ efflux from intracellular stores, in particular endoplasmic reticulum (ER), has a fundamental role in modulating different cellular responses.
The PUFA capacity to modulate different signaling pathways involved in inflammation response has been extensively studied in both physiological and pathological conditions [ 14, 16].
Although incongruence induced a bias toward different responses, this bias was not modulated by priming.
Thus glucose may differentially modulate different receptors involved in auxin signaling controlling different physiological responses via different mechanisms of action.
These responses may occur because the heterodimers formed between the two ER subtypes may identify and modulate different genes than either receptor alone [ 2, 11].
The liver enzymatic antioxidant defense is modulated in response to the redox status changes initiated by Si/SiO2 QDs. Figure 5 shows the different responses of SOD and CAT to silicon-based QDs accumulation in the liver of C. gibelio.
Different relationships dictate different responses.
The portraits evoke different responses.
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