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1 us specificity that can be characteristic of repetition priming.
2 g event-related potentials (ERPs) and masked repetition priming.
3 erence with a repeated name can affect basic repetition priming.
4 luence the neuronal plasticity necessary for repetition priming.
5 age processing and their modification during repetition priming.
6 y, and during implicit memory as measured by repetition priming.
7 or the involvement of feedback mechanisms in repetition priming.
8 based on the same mechanism responsible for repetition priming.
10 we address the pharmacological modulation of repetition priming, a basic form of learning, using even
12 resent study was to determine whether masked repetition priming affects ERPs differently depending on
14 tient E.P. has demonstrated normal levels of repetition priming and at-chance recognition performance
16 study was to further probe the link between repetition priming and repetition suppression/enhancemen
18 s with prior exposure to the pictures (i.e., repetition priming) and with presentation of valid word
19 ve skill learning; perceptual and conceptual repetition priming; and several forms of conditioning.
20 Non-conscious mnemonic influences, such as repetition priming, are thought to have a negligible eff
22 riming, L1-L2 translation priming, and L1-L1 repetition priming, but not for L2-L1 translation primin
23 course model during comprehension can affect repetition priming, but the nature of this effect may de
25 associated with facilitation processes from repetition priming dependent on sex and independent of a
26 nges in human brain activity associated with repetition priming during word generation were character
27 , even though we observed the expected sound repetition priming effect for positive and neutral words
28 that these reductions may underlie an amodal repetition-priming effect existing at processing stages
29 The other rotation conditions only showed repetition priming effects on the early perceptual compo
30 y the 30 degrees rotation condition produced repetition priming effects on the N/P190, N300 and N400.
32 ing-related changes also exhibited increased repetition priming effects, suggesting common neural sub
40 brain activity related to skill learning and repetition priming in a mirror-reading task were examine
42 vely, during memory retrieval as assessed by repetition priming in an event-related potential (ERP) s
43 these effects can be explained by short-term repetition priming in the context of serial scanning mod
46 are related to implicit memory--measured by repetition priming--in a test that emphasized conceptual
47 ay be modulated in a top-down fashion during repetition priming, independent of (or in parallel with)
49 driven by concurrent excitation-inhibition, repetition priming is indirect as it is preferentially i
50 nts may be made on the basis of familiarity, repetition priming is not the source of this feeling of
51 nents were significantly modulated for L2-L2 repetition priming, L1-L2 translation priming, and L1-L1
52 nlike in previous behavioral studies, masked repetition priming led to a reduction in positive recogn
53 direct versus indirect, i.e., CPG-dependent, repetition priming may be related to the type of input t
54 skills, and suggest that skill learning and repetition priming may have common substrates within a p
55 2 (cerebral peptide 2), we hypothesized that repetition priming may involve persistent peptidergic ne
57 related with less response facilitation from repetition priming of global targets in men, but with gr
61 nance imaging (fMRI) studies have shown that repetition priming of visual objects is typically accomp
63 rain functional MRI (fMRI) was used during a repetition priming paradigm to study 34 young adults, 33
66 extensive item-specific practice (long-term repetition priming) resulted in a virtual elimination of
68 nges are not related to implicit memory in a repetition priming test that emphasized perceptual (or s
70 state is maintained through MCC-independent repetition priming that is embedded in the properties of
71 tivations in the same region associated with repetition priming, that activation in this region refle
74 d event-related potentials (ERPs) and masked repetition priming to examine the time-course of picture
75 eding system of Aplysia californica displays repetition priming via an increase in the activity of th
79 urse of cross-script translation priming and repetition priming was examined in two different scripts
80 etal, and occipitotemporal regions; however, repetition priming was not predicted by pattern similari
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