Sentence examples for behavioral effects that are from inspiring English sources

Exact(6)

Central injections of serotonin (5-HT) produce hyperdipsic and hypnogenic behavioral effects that are correlated to decreased Fos-immunorreactivity of 5-HT neurons in free-feeding pigeons.

Furthermore, dynorphins may produce robust cellular and behavioral effects that are not mediated through opioid receptors.

We hypothesize that simultaneous differential training of the SMA and the PHC will cause behavioral effects that are linked to the functional role of each trained ROI.

Thus, slowed or hampered neurodevelopmental maturation in SHR/NCrl may interact with (time of) PCB exposure and produce behavioral effects that are different or more severe in SHR/NCrl than in WKY/NHsd controls.

Mothers of NICU babies also experience the effects of separation; thus, our intervention is also designed to increase maternal exposure to her infant through the Calming Cycle interactions, with the goal of promoting biological and behavioral effects that are contingent upon normal co-regulatory interactions.

Some studies have additionally shown that self-regulation leads to behavioral effects that are specific to the functional role of the targeted cortical area (Bray, Shimojo, & O'Doherty, 2007 ; Caria et al., 2007; deCharms et al., 2005; Rota et al., 2009; Scharnowski, Hutton, Josephs, Weiskopf, & Rees, 2012; Shibata, Watanabe, Sasaki, & Kawato, 2011 ; Weiskopf et al., 2003, 2004).

Similar(54)

Selective optogenetic inhibition of the CRFCeA-BNST pathway but not CRFCeA-SI, CRFCeA-LH/pSTN, or CRFCeA-PBN pathway recapitulated the behavioral effects that were observed when CeA CRF neurons were inhibited.

Pretreatment with the CRF1 receptor antagonist R121919 mimicked the effect of optogenetic inhibition by reducing action potential firing and occluded the effect of optogenetic inhibition, strongly suggesting that the behavioral effects that were observed after the optogenetic inhibition of CRF CeA neurons and CRFCeA-BNST terminals is mediated by the CRF-CRF1 system.

The fact that there were no differential changes in maternal depression for the two groups indicates that it was not changes in the mothers' emotional state which moderated the mentalization and behavioral effects that were found.

Control of these two regions caused characteristic behavioral effects that were related to the specific function of the brain region, i.e. reaction time changes were related to regulating activity in the SMA, and changes in memory performance were related to regulating activity in the PHC.

Our findings emphasize the need to continue examining the biomechanical and behavioral effects that may be associated with injury incidence and reporting across all ages.

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