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1 d place-preference protocol so as to mediate Pavlovian conditioning.
2 raining infusions dose-dependently disrupted Pavlovian conditioning.
3 rather than substantially different forms of Pavlovian conditioning.
4 heir estrous cycle stage on the first day of Pavlovian conditioning.
5 tially support model-based mechanisms during Pavlovian conditioning.
6 ing but not of associative learning, such as Pavlovian conditioning.
7 itioned reinforcing value through appetitive Pavlovian conditioning.
8 t a profoundly larger reward response during Pavlovian conditioning.
9 hensively capturing learning and behavior in Pavlovian conditioning.
10 ould support model-based computations during Pavlovian conditioning.
11 and computes a negative prediction error in Pavlovian conditioning.
12 ning and a similar dichotomy in the realm of Pavlovian conditioning.
13 c effects are typically demonstrated through Pavlovian conditioning.
14 a classical Model-Free system, necessary for Pavlovian conditioning.
15 NMDARs in the dopamine system to appetitive Pavlovian conditioning.
16 lic voltammetry was combined with appetitive Pavlovian conditioning.
17 dopamine receptor in aversive and appetitive pavlovian conditioning.
18 aged when potentiated feeding is produced by pavlovian conditioning.
19 h intrinsic enhanced excitability underlying pavlovian conditioning.
20 ar whether similar mechanisms operate during Pavlovian conditioning.
21 rate a reward prediction error signal during Pavlovian conditioning.
22 neurons of a CS and US used for associative Pavlovian conditioning.
23 neuronal excitability are two mechanisms for Pavlovian conditioning.
25 ew results are captured by a recent model of Pavlovian conditioning,(12)(,)(13) HeiDI, and both are c
27 ral reinforcement learning contexts, such as Pavlovian conditioning and decisions guided by reward hi
28 med from the LAT of anesthetized rats during pavlovian conditioning and during the presentation of st
30 In this study, human participants underwent Pavlovian conditioning and extinction before we manipula
32 l over behavior by enhancing both appetitive Pavlovian conditioning and instrumental pursuit of CS.SI
33 ans, we conducted four experiments combining Pavlovian conditioning and outcome devaluation procedure
34 of membrane DOR expression in CINs and both pavlovian conditioning and pavlovian-instrumental transf
35 cations for the mechanistic understanding of Pavlovian conditioning and provide a more nuanced unders
36 e projections from the VTA are necessary for Pavlovian conditioning and specifically implicate the PF
37 ygdala (LA) during consolidation of aversive pavlovian conditioning and that this memory requires cap
38 The administration of the antagonists during Pavlovian conditioning and/or testing abolished the enha
39 events provides the possibility to predict (Pavlovian conditioning) and control (operant conditionin
40 timulus (CS) and unconditioned stimulus (US; pavlovian conditioning), and from verbal instructions ab
41 d memory (e.g., semantic associative memory, Pavlovian conditioning, and instrumental learning), with
42 degradation of the instrumental contingency, Pavlovian conditioning, and Pavlovian-instrumental trans
43 n encodes model-based representations during Pavlovian conditioning, and that these representations a
45 ining infusions of muscimol had no effect on Pavlovian conditioning but produced a dose-dependent eff
46 g the CS did not suppress the acquisition of Pavlovian conditioning but was required for the subseque
52 asted learning from direct experience (i.e., Pavlovian conditioning) (experiment 1) against two commo
54 Because predictability is fundamental to Pavlovian conditioning, failure to predict panic attacks
55 rogress in understanding the neural basis of Pavlovian conditioning has stimulated a new wave of rese
56 ing in dopamine neurons was not required for Pavlovian conditioning; however, NMDARs in D(1) dopamine
58 uation insensitive and devaluation sensitive Pavlovian conditioning in humans, we conducted four expe
60 exhume the experiments of Beatrice Gelber on Pavlovian conditioning in the ciliate Paramecium aurelia
61 ity and the response to clicks changed after Pavlovian conditioning in which blink responses were eli
62 ce learning has been proposed as a model for Pavlovian conditioning, in which an animal learns to pre
63 hat the interaction between instrumental and Pavlovian conditioning induces powerful motivational bia
68 nt an impetus for a fundamental shift in how Pavlovian conditioning is interpreted: animals learn abo
81 re lesions did not have any marked effect on Pavlovian conditioning or on Pavlovian-instrumental tran
83 ed male and female adult C57BL/6 J mice to a Pavlovian conditioning paradigm that paired footshock wi
84 ot reliably evoke behavior in an optogenetic pavlovian conditioning paradigm, and activation of SC->V
90 aversive-only and mixed-valence cue-outcome Pavlovian conditioning paradigms in male and female mice
92 quail (Coturnix japonica) were compared in a Pavlovian conditioning procedure in which presentation o
94 nted, male DBA/2J mice underwent an unbiased Pavlovian-conditioning procedure for ethanol-induced CPP
99 ty and synaptic drive that contribute to the pavlovian conditioning process, here we used in vivo int
104 esent the first clear evidence that, through Pavlovian conditioning, rats can develop preferences for
105 ss tasks that examine food-specific satiety, Pavlovian conditioning, reinforcer devaluation, and simu
112 o encode cue-reward prediction errors during Pavlovian conditioning, signaling discrepancies between
113 omotes a negative reward prediction error in Pavlovian conditioning.SIGNIFICANCE STATEMENT Stimuli th
115 nction in the water maze, like extinction in Pavlovian conditioning, suppresses the original associat
116 the timing of optogenetic manipulations in a Pavlovian conditioning task and examining the influence
117 We trained head-fixed mice on an olfactory Pavlovian conditioning task and measured the coding prop
119 tients of both sexes performed an appetitive Pavlovian conditioning task probing both stimulus-value
123 s is directly necessary for performance on a Pavlovian conditioning task, without affecting locomotor
127 N=25, aged 19-52 years) completed a passive (Pavlovian) conditioning task with appetitive (monetary g
128 he involvement of D1/D5 receptors in various pavlovian conditioning tasks in mammals; however, these
130 any test of instrumental conditioning or in Pavlovian conditioning, they failed to show any positive
133 tensin receptor blocker losartan on aversive Pavlovian conditioning using a probabilistic learning pa
136 st-scan cyclic voltammetry as rats underwent pavlovian conditioning, we demonstrate that a single str
137 examine the cellular and molecular basis of Pavlovian conditioning, we previously identified a pair
138 ear whether a similar distinction applies in Pavlovian conditioning, where responses have been found
140 ic temperature by combining thermoregulatory Pavlovian conditioning with engram-labelling technology,
142 gnals did not emerge in the DLS, even during Pavlovian conditioning with SNc dopamine neuron activati
143 y limbic area involved in fear responses and pavlovian conditioning with the potential to directly re