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1 gic (LC-NE) neurons induces anxiety-like and aversive behavior.
2 ons is alone sufficient for anxiety-like and aversive behavior.
3 eurons are necessary to mediate KOR-mediated aversive behavior.
4 eward or shock, elicits either appetitive or aversive behavior.
5 n suppressing feeding as <0.1% DEET elicited aversive behavior.
6 oth have a restrictive effect on fearful and aversive behavior.
7 ease also showed the largest increases in an aversive behavior.
8 l through the gut-neural axis to control the aversive behavior.
9 same visual stimulus can drive appetitive or aversive behavior.
10  the formation and retrieval of this learned aversive behavior.
11 ted regions implicated in reward-seeking and aversive behaviors.
12 ironmental variables to ultimately fine tune aversive behaviors.
13 cocaine-evoked modifications and drug-driven aversive behaviors.
14 al firing in the NAc is sufficient to induce aversive behaviors.
15  tuned taste neurons in the brain to trigger aversive behaviors.
16 onergic neurons may be sufficient to mediate aversive behaviors.
17 , the CS controls conflicting appetitive and aversive behaviors.
18 s, including its involvement in a variety of aversive behaviors.
19 e stimuli, whereas silencing them attenuates aversive behaviors.
20 de evidence showing that VPMpc also mediates aversive behaviors.
21 einforcing properties of rewards and induces aversive behaviors.
22 cholinergic neurons, which mediate different aversive behaviors.
23 functional role of LDTg in the regulation of aversive behaviors, and further characterizing LHb as a
24 roles in motor coordination, appetitive, and aversive behavior, as well as neuropsychiatric disorders
25 female mice, its impact on the rewarding and aversive behaviors associated with morphine exposure, an
26  months but not at 7 months and a deficit in aversive behavior at 20 months of age.
27 ys important roles in learned appetitive and aversive behaviors, but whether it plays a role in media
28 dala, providing a general mechanism for fear/aversive behavior driven by auditory stimuli.
29 alamus, in the arbitration of appetitive and aversive behavior during motivational conflict.
30 strated that the velvet ant's sting produced aversive behavior in a predatory praying mantis.
31 mine, and neuropeptides in the inhibition of aversive behavior in Caenorhabditis elegans.
32 scue of the KOR-mediated NAc DA response and aversive behavior in DATCre-KOR KO animals.
33  outside the CNS, we used CGRP-induced light-aversive behavior in mice as a measure of migraine-assoc
34  previous error outcomes, predictive of risk-aversive behavior in that trial, and underactive in adol
35 itoneal) injection of CGRP resulted in light-aversive behavior in wild-type CD1 mice similar to avers
36 shows that the encoding of certain avoidance/aversive behaviors in cortical neuron activity differed
37 genous NOP agonist nociceptin attenuates the aversive behaviors in Post-EtOH rats without causing any
38 sensory receptors in the oral cavity trigger aversive behaviors in response to acid stimuli.
39  appetitive motivated behaviors, its role in aversive behavior is controversial.
40 that the neuronal mechanisms of KOR-mediated aversive behavior may include both dopaminergic and sero
41 ion of monoamines and peptides on C. elegans aversive behavior mediated by a pair of polymodal, nocic
42  abolishes the serotonergic sensitization of aversive behavior mediated by the two nociceptive ASH se
43  NLXM-mediated OIRD reversal did not produce aversive behaviors observed after NLX.
44    Activating these neurons does not trigger aversive behavior on its own but rather amplifies respon
45 Tg has been shown to play a critical role in aversive behaviors, particularly those involving behavio
46 ransgenic mice (nestin/hRAMP1) display light-aversive behavior that is greatly enhanced by intracereb
47 swim and inescapable footshock both produced aversive behaviors that were blocked by a kappa-opioid r
48 hways may control a variety of other passive aversive behaviors, their elucidation may help understan
49 ous receptor sites were sufficient for light-aversive behavior, then wild-type mice should also show
50 ed by nlp-3 appear to stimulate ASH-mediated aversive behavior through the neuropeptide receptor-17 (
51 o the mouth and skin and did not demonstrate aversive behavior toward capsaicin.
52 l aversive taste memory, resulting in strong aversive behavior upon retrieval.
53 ell elicits robust conditioned and real-time aversive behavior via KOR activation, and in contrast, p
54  disrupts arbitration between appetitive and aversive behaviors when they are in conflict but has no