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4 dHip) and parietal cortex (PC) in processing allocentric and egocentric space during acquisition and
5 utable to the failure to distinguish between allocentric and egocentric spatial representations in ex
6 formation of a memory representation that is allocentric and thus independent of our starting point w
7 signal of egocentric boundary distance into allocentric boundary vector cell firing, suggesting that
10 gation in situations that require a flexible allocentric cognitive mapping strategy, but not for situ
12 lls that exhibit the predicted egocentric-by-allocentric conjunctive characteristics and anticipate o
17 mpus in processing egocentric-procedural and allocentric-declarative sequential information, respecti
18 resent an ideal candidate to investigate the allocentric determinants of the brain's cognitive map.
19 to estimate self-motion and the distance and allocentric direction of walls, and to detect drop-offs.
21 us and the inferior occipital gyrus, whereas allocentric directional selectivity (target relative to
25 s impaired working-memory representation for allocentric distance, whereas parietal cortex lesions re
29 t the brain transforms these signals into an allocentric, gravity-centered representation of the worl
30 unction of egocentric cue light location and allocentric head direction in rats running a random sequ
32 on to show a very similar pattern of chronic allocentric learning and accelerated forgetting in a sta
34 ce learning and suggest that deficiencies in allocentric mapping may contribute to these deficits.
35 lts indicate that lesions of the dHip impair allocentric maze acquisition, whereas lesions of the PC
36 m that geometry controls behavior through an allocentric mechanism potentially tied to the hippocampu
37 Rats that had been pretrained on 2 tests of allocentric memory (water maze and T maze) received bila
38 rmore, hippocampal volume reduction impaired allocentric navigation beyond what can be predicted by m
39 TTX groups showed significant impairments in allocentric navigation, but not visually cued navigation
40 on, manifested by poor hippocampus-dependent allocentric navigation, may occur well before the clinic
41 e right hippocampus plays a critical role in allocentric navigation, particularly when cognitive impa
42 n falling on the individual's left side) and allocentric neglect (neglect of the left side of each ob
43 gocentric neglect in one task (tracing), and allocentric neglect in another task (copying), suggestin
48 to study encoding and retrieval of one-trial allocentric place memory in rats; memory relied on visuo
49 ocampal NMDA and AMPA receptors to one-trial allocentric place memory may be central to episodic memo
51 at encoding, but not retrieval, of one-trial allocentric place memory requires the NMDA receptor-depe
52 uccessful performance required the use of an allocentric place strategy, which was increasingly obser
54 h previous research, age-related deficits in allocentric processing result in shifts in preferred nav
55 c reach (remember absolute target location), allocentric reach (remember target location relative to
58 essary transformation between egocentric and allocentric reference frames by placing visual cues at i
61 IP may play a key role in creating a stable, allocentric representation of the environment defined re
62 tively well described, but the corresponding allocentric representations are essentially unknown.
64 l evidence that the MTL computes location in allocentric space and more recent evidence that the MTL
65 ed also relative to the body, or in absolute allocentric space, to allow orientation toward the sound
68 entric cues to solve the procedural task and allocentric spatial cues to solve the declarative task.
69 arietal cortex and hippocampus to memory for allocentric spatial cues, the authors trained rats on a
70 or the acquisition and on-line processing of allocentric spatial information but not for the maintena
74 of this task while sparing performance of an allocentric spatial memory task performed in a radial ar
75 he hippocampus is specifically important for allocentric spatial memory, e.g., the hippocampus is esp
79 fluence of intrahippocampal ANI infusions on allocentric spatial navigation using the Morris water ma
81 show that boundary-based and landmark-based allocentric spatial recall are similarly impaired in pat
83 tion requires coordination of egocentric and allocentric spatial reference frames and may involve vec
85 es not rely exclusively on the processing of allocentric spatial relationships in the maze environmen
86 is critical for the establishment or use of allocentric spatial representations and that selective d
87 Here we review the emerging literature on allocentric spatial representations in 3-D and discuss t
88 strated impairments in the acquisition of an allocentric spatial task, in patients with unilateral hi
89 textual retrieval task was not influenced by allocentric spatial trajectory, but rather by the animal
90 locations, so that monkeys had to rely on an allocentric (spatial relational) representation of the e
91 bian association of sensory information with allocentric state representations in the hippocampus, an
92 the majority of North-Americans preferred an allocentric strategy, while Latin-Americans preferred an
93 There was also greater activation for the allocentric task in right posterior hippocampus and left
94 location was specified), the egocentric and allocentric tasks elicited widely overlapping regions of
96 ntation could be modified from egocentric to allocentric through manipulating the task demands whilst
97 creased with distance for egocentric but not allocentric units, whereas, for both populations, modula
98 ulating the transform with information about allocentric velocity, the equations code for position of
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