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1 ive patterning paradigm assessing configural association learning.
2 animals were tested in visual object-reward association learning.
3 hat two objects are associated, i.e., visual association learning.
4 atum and highlight a role in stimulus-action association learning.
5 rrel cortex during whisker-dependent sensory association learning.
6 tion protocol can enhance subsequent spatial association learning.
7 to facial expressions is driven by emotional association learning.
8 econds-long neural sequences during temporal association learning and suggest that trace fear conditi
9 the screen-and-select approach based on some association learning and the parsimonious uncertainty qu
10 nformation types available during contextual association learning and used model-based fMRI in conjun
11 ng of a monkey during a single session of an association learning experiment and identified learning
12 nnection was without effect on object-reward association learning for an equivalent delayed reward.
13 nd, Ocean cells are dispensable for temporal association learning, for which Island cells are crucial
15 aboratory test of this capacity--conditional association learning--have revealed that frontal lobe st
17 mine is vital for coordinated motion and for association learning linked to behavioral reinforcement.
19 s of excitatory/inhibitory balance and sound association learning mechanisms in the NCM, a system tha
20 /salience to stimuli, stimulus-reinforcement association learning, motivation, and socio-emotional co
21 ple discrimination paradigm assessing simple association learning or a negative patterning paradigm a
22 oidance response without affecting cue-shock association learning, reactive escape behaviors, or expr
25 ry for the ability to learn new visuospatial associations (learning-to-learn) and to make reward-guid