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1 impulsive action) and delayed gratification (impulsive choice).
2 mediate over large, delayed rewards (greater impulsive choice).
3 dopamine signaling are associated with high-impulsive choice.
4 dopamine signaling are associated with high-impulsive choice.
5 s caused increased impulsive action, but not impulsive choice.
6 were sufficient to bidirectionally influence impulsive choice.
7 oaches, we dissociated impulsive action from impulsive choice.
8 he role of serotonin in impulsive action and impulsive choice.
9 whereas 8-OH-DPAT infused into OFC decreased impulsive choice.
10 e the systemic effect of ADHD medications on impulsive choice.
11 ng state VLF oscillations during waiting and impulsive choice.
12 ally assess attention, impulsive action, and impulsive choice.
13 ase reversed this relationship, resulting in impulsive choice.
14 enhance learning from rewarding outcomes and impulsive choice.
15 ay discounting task commonly used to measure impulsive choice.
16 ay-discounting task commonly used to measure impulsive choice.
17 gic signaling would benefit and exhibit less impulsive choice.
18 ecific neural mechanisms linking NAc D2Rs to impulsive choice.
19 counting, which measures a different form of impulsive choice.
20 ecision caution characteristic of unsafe and impulsive choices.
21 ceipt, is an established behavioral model of impulsive choice, a key component of a broader impulsivi
25 ggression are correlated with differences in impulsive choice and decreased serotonin (5-HT) innervat
26 est that cognitive reappraisal helps control impulsive choice and the process is mediated by the vent
27 ered cocaine can cause lasting elevations in impulsive choice, and that the high levels of impulsive
28 ort the conclusion that impulsive action and impulsive choice are distinct behavioral phenotypes with
31 egulation in CINs of the mouse NAc increases impulsive choice as measured in a delay discounting task
32 that serotonin is involved in the control of impulsive choice, as characterized by high preference fo
33 echol-O-methyltransferase gene predicts both impulsive choice behavior and activity levels in the dPF
35 ine exposure can cause enduring increases in impulsive choice behavior, consistent with observations
37 Animals were screened for aggressive and impulsive choice behaviors and categorized into Low-Aggr
38 our hypothesis, L-DOPA had no main effect on impulsive choice, but reduced risk-seeking for gains in
39 raising cortical dopamine levels attenuates impulsive choice by changing corticostriatal function.
47 self-administered cocaine displayed greater impulsive choice (enhanced preference for the small imme
51 NAc projection elicited a robust increase in impulsive choice in rats with lower vs. higher baseline
55 eward delivery, indicating that the enhanced impulsive choice in these rats may be related to deficit
56 ipt of the small, immediate reward increased impulsive choice in young rats but had no effect in aged
57 ms, with the hot system proposed to generate impulsive choices in the presence of a proximate reward.
58 osure reduced impulsive action but increased impulsive choice, indicating that chronic stress hormone
60 evated impulsive choice, or whether elevated impulsive choice is solely a predisposing factor for coc
61 mpulsive choice, and that the high levels of impulsive choice observed in human cocaine users may be
64 ot clear whether cocaine use causes elevated impulsive choice, or whether elevated impulsive choice i
65 f the two systems may underlie apathetic and impulsive choice patterns in neurological and psychiatri
66 ocaine use is associated with high levels of impulsive choice (preference for immediate over delayed
68 est the hypothesis that impulsive action and impulsive choice represent statistically independent beh
69 These data show that male rats exhibit less impulsive choice than females and that this difference i
75 al effects between groups, as aggression and impulsive choice were both inhibited in H-Agg animals, w
76 and eticlopride infused into mPFC increased impulsive choice, whereas 8-OH-DPAT infused into OFC dec