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1 d the area described by others as the cat's "frontal eye fields".
2 to contain the human homolog of the macaque frontal eye fields).
3 d and this control is exercised by the right frontal eye field.
4 midbrain superior colliculus to the cortical frontal eye field.
5 evoked by electrical microstimulation of the frontal eye field.
6 al cortex, and frontal cortex in or near the frontal eye field.
7 dal superior temporal sulcus area and in the frontal eye field.
8 ongside the superior parietal cortex and the frontal eye field.
9 and recorded the activity of neurons in the frontal eye field.
10 rded from visually responsive neurons in the frontal eye field.
11 s and LFP in SEF were compared with those in frontal eye field.
12 rom higher order attention areas such as the frontal eye field.
13 ention as well as by microstimulation of the frontal eye fields.
14 ling from a frontoparietal network including frontal eye fields.
15 or and dorsolateral prefrontal cortices, and frontal eye fields.
16 eas, the lateral intraparietal area, and the frontal eye fields.
17 ticotectal projections originated within the frontal eye fields.
18 l cortex, bilateral intraparietal sulci, and frontal eye fields.
19 within the posterior parietal cortex and the frontal eye fields.
20 nse in the smooth eye movement region of the frontal eye fields.
21 tinotopic fMRI activity was localized to the frontal eye fields.
22 um and the smooth eye movement region of the frontal eye fields.
23 Altering either D1- or D2-receptor-mediated frontal eye field activity increased saccadic target sel
26 tial attention task while neurons within the frontal eye field, an oculomotor area within prefrontal
27 wing with electrical microstimulation of the frontal eye field and analysed the resulting, evoked eye
28 ied in several cortical areas, including the frontal eye field and lateral intraparietal area, and on
29 orsal prearcuate cortex in the region of the frontal eye field and neurons in dorsal prefrontal corte
31 vidence that the lateral intraparietal area, frontal eye field and superior colliculus are involved i
32 ed on neurophysiological observations in the frontal eye field and superior colliculus of behaving mo
35 f five optogenetic constructs in the macaque frontal eye field and use electrical microstimulation to
37 ces from the temporoparietal junction on the frontal eye fields and the putamen were modulated by (Ba
38 maintained in the macaque monkey prefrontal (frontal eye fields) and parietal cortex (lateral intrapa
39 Neurons in the lateral intraparietal area, frontal eye field, and superior colliculus exhibit a pat
40 premotor cortex, supplementary motor cortex, frontal eye field, and supplementary eye field can in pr
45 racer injections within cortex including the frontal eye fields (areas 46 and 8) labeled areas TPOc,
46 ked by intracortical microstimulation of the frontal eye fields at variable times after presentation
47 raparietal sulcus (IPS), left IPS, and right frontal eye field being the main sources of behavior-enh
48 work that included regions identified as the frontal eye fields, both superior and inferior parietal
49 ow that low-level stimulation of the primate frontal eye fields can induce robust pupil dilation with
50 tion with electrical microstimulation of the frontal eye field, causing an evoked eye movement that i
51 ent functional classes of neurons within the frontal eye field contribute uniquely to these two funct
53 The regions reported to correspond to the "frontal eye fields" did not exhibit any unique visual pr
54 n, so we recorded from single neurons in the frontal eye field, dorsolateral prefrontal cortex, and s
56 ivity, deficient corollary discharges to the frontal eye fields, dysfunctional pulvinar, claustrum an
57 y antisaccades to be associated with reduced frontal eye field (FEF) activity relative to those prece
58 ultaneously recorded neural responses in the frontal eye field (FEF) and area V4 while monkeys perfor
60 ood oxygen level-dependent time series, that frontal eye field (FEF) and intraparietal sulcus (IPS) a
61 activity than stimulus-driven shifts in the frontal eye field (FEF) and intraparietal sulcus, core r
62 h increased prestimulus BOLD activity in the frontal eye field (FEF) and the posterior inferior front
63 ugh the lateral intraparietal area (LIP) and frontal eye field (FEF) are known to represent the posit
64 While the motor and attentional roles of the frontal eye field (FEF) are well documented, the relatio
65 ntified the volume of a segment of the right frontal eye field (FEF) as positively correlated with an
66 tigated the causal contribution of the human frontal eye field (FEF) by combining repetitive transcra
67 ence has indicated that microstimulating the frontal eye field (FEF) can produce modulations of corti
68 oving dot pattern and that neurons in monkey frontal eye field (FEF) changed their activity when the
69 investigated by recording neurons in monkey frontal eye field (FEF) during an inferred motion task.
70 a (PMV), supplementary motor area (SMA), and frontal eye field (FEF) following intracortical microsti
72 of attentional modulation has implicated the frontal eye field (FEF) in driving spatial attention.
83 actors by visually responsive neurons in the frontal eye field (FEF) marks the outcome and conclusion
84 ow that visual and pre-saccadic responses of frontal eye field (FEF) neurons are modulated by initial
85 e examined changes in spiking variability of frontal eye field (FEF) neurons in a change detection ta
89 -term memory, the activity of neurons in the frontal eye field (FEF) of macaque monkeys was recorded
91 perturbing dopaminergic activity within the frontal eye field (FEF) of monkeys performing a saccadic
94 identified two functional subregions in the frontal eye field (FEF) of the Cebus monkey, a smooth ey
95 ng targets by microstimulation in either the frontal eye field (FEF) or the superior colliculus (SC),
98 ospatial information, neural activity in the frontal eye field (FEF) persists and is thought to be an
100 ests that visually responsive neurons in the frontal eye field (FEF) respond to visual targets even w
101 noninvasive neurostimulation over the right frontal eye field (FEF) to isolate the behavioral effect
103 We recorded from neurons in area 46 and the frontal eye field (FEF) while monkeys performed a memory
107 fferent roles in this familiar activity--the frontal eye field (FEF), an area in the prefrontal corte
108 in part via its direct projections from the frontal eye field (FEF), an area involved in selective a
109 ikely source of this attentional bias is the frontal eye field (FEF), an area of the frontal cortex i
110 possible source is the PFC, particularly the frontal eye field (FEF), an area of the PFC implicated i
111 is present at the single-neuron level in the frontal eye field (FEF), an area that receives both visu
112 n control the activity of neurons within the frontal eye field (FEF), an oculomotor area of the prefr
113 SMA), presupplementary motor area (pre-SMA), frontal eye field (FEF), and cingulate motor areas, CMAr
114 ork, namely, the intraparietal sulcus (IPS), frontal eye field (FEF), and supplementary eye field.
115 network for volitional ocular motor control-frontal eye field (FEF), dorsal anterior cingulate corte
116 ctivations approximately 300 ms after cue in frontal eye field (FEF), lateral intraparietal area (LIP
117 task in the inferior parietal lobule (IPL), frontal eye field (FEF), middle frontal gyrus (MFG), and
118 scribed topographic areas in frontal cortex [frontal eye field (FEF), PreCC/IFS (precentral cortex/in
119 ions of primary motor cortex (M1c, M1r), the frontal eye field (FEF), the dorsal oculomotor area (OMD
120 elated activity was observed in the SEF, the frontal eye field (FEF), the superior parietal lobule (S
121 (LS), temporal parietal junction (TPJ), and frontal eye field (FEF), was affected by information acc
122 rk, including intraparietal sulcus (IPS) and frontal eye field (FEF), whereas cues predicting angry f
127 utions at a late stage of visual processing [frontal eye field (FEF)] and as a comparison, an early s
129 ated the emergence of neural learning in the frontal eye fields (FEF(SEM)) and the floccular complex
130 t from the smooth eye movement region of the frontal eye fields (FEF(SEM)) could implement gain contr
132 by electrically stimulating sites within the frontal eye fields (FEF) and measuring its effect on the
133 ltaneously recorded neuronal activity in the frontal eye fields (FEF) and primary visual cortex (V1)
134 a role in visually guided eye movements: the frontal eye fields (FEF) and the medial eye fields (MEF)
136 Here, we present neural evidence in the frontal eye fields (FEF) for serial, covert shifts of at
137 d electrical microstimulation of the macaque frontal eye fields (FEF) modulates the pupillary light r
139 whereas those at higher levels, such as the frontal eye fields (FEF), are thought to modulate sensor
140 ising the intraparietal sulcus (IPS) and the frontal eye fields (FEF), controls the voluntary deploym
141 saccadic thresholds of the directly adjacent Frontal Eye Fields (FEF), saccades were only rarely evok
142 ies: dorsolateral prefrontal cortex (dlPFC), frontal eye fields (FEF), superior parietal lobule (SPL)
143 ressor), were observed with seeds within the frontal eye fields (FEF), superior parietal lobule (SPL)
145 d rostral (M3) cingulate motor cortices; the frontal eye fields (FEF); pre-supplementary motor cortex
146 tal area (LIP), prefrontal cortex (PFC), and frontal eye fields (FEF)] of monkeys reporting the color
147 to show that stimulation of the right human frontal eye-field (FEF) produced a characteristic topogr
148 odulations in intraparietal sulcus (IPS) and frontal-eye field (FEF), and transient less selective mo
153 E STATEMENT The superior colliculus (SC) and frontal eye fields (FEFs) are two of the best-studied ar
154 , we show that single pulses of TMS over the frontal eye fields (FEFs) in awake NHPs evoked rapid (wi
156 l electrical microstimulation of the primate frontal eye fields (FEFs), a cortical component of the o
158 ed a network of activation that included the frontal eye fields (FEFs), supplementary eye fields (SMA
159 dorsal frontoparietal regions [including the frontal eye fields (FEFs)] were correlated with RT in al
160 Single-pulse TMS stimulation of the right frontal eye field increased this distractor-related devi
161 d that on antisaccade trials most neurons in frontal eye fields initially select the singleton while
164 ding cortex sometimes considered part of the frontal eye field, is probably homologous to the premoto
165 multaneously recorded activity from multiple frontal eye field neurons and asked whether they interac
166 -dependent cooperation and competition among frontal eye field neurons during visual target selection
169 basis of visual and saccade selection in the frontal eye field of macaque monkeys using a singleton s
170 and metrics of eye movements evoked from the frontal eye field of monkeys, while holding the mean int
171 altered D1-receptor-mediated activity in the frontal eye field of the prefrontal cortex and measured
172 tent with this idea, microstimulation of the frontal eye fields, one of several areas that control th
173 d from the left postcentral sulcus and right frontal eye field onto the right pIPS and were selective
174 interprets cells in the superior colliculus, frontal eye field, parietal cortex, mesencephalic reticu
175 eper layers, the results suggest that MT and frontal eye field projections to the SC were sparse in e
176 immediately anterior to the saccade-related frontal eye field region is involved in vergence and ocu
177 gmenti pontis, which receives input from the frontal eye field region of frontal cortex, and this cor
180 ger analysis, we further show that the right frontal-eye field (rFEF) exerted feedback control of the
182 ents, and suggest that the definition of the frontal eye fields should be expanded to include this re
183 absolute preference for reaches, whereas the frontal eye field showed little or no effector selectivi
184 egions, such as supplementary eye fields and frontal eye fields, showed increased activation that was
185 cortex (right middle frontal gyrus and left frontal eye field), supplementary motor cortex, anterior
186 ple task to reveal neurons in and around the frontal eye fields that encode where an animal should no
187 g., intraparietal sulcus areas IPS1-IPS4 and frontal eye fields) that are commonly associated with sp
188 rior precuneus, medial intraparietal sulcus, frontal eye fields) that showed the most robust activati
189 tial attention: the lateral premotor cortex (frontal eye fields), the posterior parietal cortex and t
190 e cortex, the superior parietal lobules, the frontal eye fields, the supplementary motor area and the
191 res in the posterior parietal cortex and the frontal eye fields; the language network on epicentres i
192 redicted by the delay-period activity of the frontal eye fields; the magnitude of delay-period activi
193 g saccade triggering suppression reaches the frontal eye field through a different pathway, or a diff
195 ch found that, when neural activation in the frontal eye fields was boosted by magnetic stimulation,
196 rontal sulcus (cSFS), in the vicinity of the frontal eye fields, was associated with shifting the foc
197 ex (MT+), left intraparietal cortex, and the frontal eye field, were activated at the onset of the dy
198 ibres to the caudate body originate from the frontal eye fields, which play an important role in the
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