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1 al (frontal eye fields) and parietal cortex (lateral intraparietal area).
2 neurons was comparable with that seen in the lateral intraparietal area, a cortical area that is a pa
3 atterns of activity were not observed in the lateral intraparietal area, an area linked to the fronto
4 nse modulates the activity of neurons in the lateral intraparietal area, an area of primate cortex th
5 mologs of macaque parietal areas such as the lateral intraparietal area and parietal reach region.
6 l areas, including the frontal eye field and lateral intraparietal area, and one of their direct, sub
7 x, motion-selective dorsal stream areas, the lateral intraparietal area, and the frontal eye fields.
8          For both tasks, firing rates in the lateral intraparietal area appeared to reflect the accum
9                 Much evidence implicates the lateral intraparietal area as a candidate priority map i
10 ation and electrical microstimulation in the lateral intraparietal area during a visuospatial discrim
11                   Neurons in area 7a and the lateral intraparietal area fire before and during visual
12                                          The lateral intraparietal area, for example, responds prefer
13           It will describe evidence that the lateral intraparietal area, frontal eye field and superi
14                               Neurons in the lateral intraparietal area, frontal eye field, and super
15            This region may correspond to the lateral intraparietal area in macaque monkeys.
16             Injections into a portion of the lateral intraparietal area labeled second-order neurons
17                                 Although the lateral intraparietal area (LIP) and frontal eye field (
18 us of the superior temporal sulcus (FST) and lateral intraparietal area (LIP) and the animals correct
19 cent hypothesis suggests that neurons in the lateral intraparietal area (LIP) and the parietal reach
20 t 150 ms after a saccade, gain fields in the lateral intraparietal area (LIP) are unreliable.
21 was shown that single neurons in the macaque lateral intraparietal area (LIP) can predict the amount
22 g, recent evidence shows that neurons in the lateral intraparietal area (LIP) carry both spatial and
23 In contrast, the selectivity of cells in the lateral intraparietal area (LIP) did not directly depend
24                  For example, neurons in the lateral intraparietal area (LIP) encode both the locatio
25                               Neurons in the lateral intraparietal area (LIP) encoded these attention
26  studies have shown that some neurons in the lateral intraparietal area (LIP) exhibit anticipatory re
27 e found that single neurons in the macaque's lateral intraparietal area (LIP) exhibit gradual firing
28 eaches than saccades, whereas signals in the lateral intraparietal area (LIP) gave better predictions
29                                          The lateral intraparietal area (LIP) has been implicated as
30                                  The macaque lateral intraparietal area (LIP) has been implicated in
31 nt years a distributed network including the lateral intraparietal area (LIP) has been implicated in
32 ort to elucidate these circuits, the primate lateral intraparietal area (LIP) has been interpreted as
33 decades, neurophysiological responses in the lateral intraparietal area (LIP) have received extensive
34 rsolateral prefrontal cortex (dlPFC) and the lateral intraparietal area (LIP) in monkeys using a memo
35                                          The lateral intraparietal area (LIP) in the macaque contains
36 ovelty affects visual salience in the monkey lateral intraparietal area (LIP) in ways that are indepe
37            We tested the hypothesis that the lateral intraparietal area (LIP) integrates disparate ta
38                                          The lateral intraparietal area (LIP) is a subdivision of the
39                                          The lateral intraparietal area (LIP) is essential for this p
40      We previously found that neurons in the lateral intraparietal area (LIP) of Macaca mulatta refle
41 neurons in the frontal eye fields (FEFs) and lateral intraparietal area (LIP) of macaques are prefere
42               It has been suggested that the lateral intraparietal area (LIP) of macaques plays a fun
43 corded the activity of single neurons in the lateral intraparietal area (LIP) of rhesus macaques to d
44 lected in the firing rates of neurons in the lateral intraparietal area (LIP) of rhesus monkeys perfo
45  an initial study of neural responses in the lateral intraparietal area (LIP) of the cerebral cortex
46 rk has suggested that neural activity in the lateral intraparietal area (LIP) of the monkey brain ref
47               The activity of neurons in the lateral intraparietal area (LIP) of the monkey predicts
48 neurons in the middle temporal area (MT) and lateral intraparietal area (LIP) of two macaque monkeys.
49 dies suggest that neural activity in macaque lateral intraparietal area (LIP) provides a useful windo
50                  For example, neurons in the lateral intraparietal area (LIP) reflect learned associa
51               Firing rates of neurons in the lateral intraparietal area (LIP) reflected the accumulat
52 ommunicated by eye movements, neurons in the lateral intraparietal area (LIP) represent the accumulat
53 studies indicate that neural activity in the lateral intraparietal area (LIP) represents the gradual
54                          Many neurons in the lateral intraparietal area (LIP) responded more strongly
55                            Recordings in the lateral intraparietal area (LIP) reveal that parietal co
56 ulation appears substantially earlier in the lateral intraparietal area (LIP) than in an anatomically
57 nstrate that the responses of neurons in the lateral intraparietal area (LIP) to a task-irrelevant di
58      We investigated neural responses in the lateral intraparietal area (LIP) to transient, distracti
59 ts to define retinotopic maps in the macaque lateral intraparietal area (LIP) using histological, ele
60 ffects of electrical microstimulation in the lateral intraparietal area (LIP) while monkeys performed
61 nd correlated the activity of neurons in the lateral intraparietal area (LIP) with the monkey's atten
62    Here, we show that neurons in the primate lateral intraparietal area (LIP), a cortical area previo
63 ctivity from populations of neurons from the lateral intraparietal area (LIP), a cortical node in the
64              To answer this, we focus on the lateral intraparietal area (LIP), an area that has been
65 300 ms after cue in frontal eye field (FEF), lateral intraparietal area (LIP), and cuneus support ear
66 any parietal neurons, such as in the macaque lateral intraparietal area (LIP), are strongly influence
67 e analyzed single-neuron recordings from the lateral intraparietal area (LIP), during a perceptual de
68      Neurons in one of its subdivisions, the lateral intraparietal area (LIP), have visual responses
69 ea four (V4), inferior temporal cortex (IT), lateral intraparietal area (LIP), prefrontal cortex (PFC
70 sion, we recorded from single neurons in the lateral intraparietal area (LIP), which has been implica
71 e movements may be guided by activity in the lateral intraparietal area (LIP), which is thought to re
72 versible pharmacological inactivation of the lateral intraparietal area (LIP), which plays a role in
73 ormation that is used to solve the task, and lateral intraparietal area (LIP), which represents the t
74  about the internal circuitry of the primate lateral intraparietal area (LIP).
75  direct neural correlate of decisions in the lateral intraparietal area (LIP).
76 ust neuronal category representations in the lateral intraparietal area (LIP).
77 he lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)] specifically biased ch
78 vity in the posterior parietal cortex [human lateral intraparietal area (LIP)], the anterior cingulat
79 jections centered in the neighboring ventral lateral intraparietal area (LIPv) revealed inputs mainly
80         We demonstrate that decision-related lateral intraparietal area neurons typically undergo gra
81 , we recorded from individual neurons in the lateral intraparietal area of monkeys performing a task
82             Neuronal responses in the monkey lateral intraparietal area revealed that bound changes a
83 icity for effector choice, with cells in the lateral intraparietal area selective for saccades and ce
84                               Neurons in the lateral intraparietal area showed anticipatory activity
85 provided a better statistical description of lateral intraparietal area spike trains than diffusion-t
86 al visual areas of behaving rhesus macaques (lateral intraparietal area, ventral intraparietal area,
87 We studied the activity of neurons in monkey lateral intraparietal area while monkeys performed a vis
88   We recorded the activity of neurons in the lateral intraparietal area while monkeys performed an in

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