ライフサイエンスコーパス: frontal eye field

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 s and LFP in SEF were compared with those in frontal eye field.

4 rom higher order attention areas such as the frontal eye field.

5 midbrain superior colliculus to the cortical frontal eye field.

6 evoked by electrical microstimulation of the frontal eye field.

7 al cortex, and frontal cortex in or near the frontal eye field.

8 dal superior temporal sulcus area and in the frontal eye field.

9 and spatial attention, such as those of the frontal eye field.

10 l signals in different cell types in macaque frontal eye field.

11 d and this control is exercised by the right frontal eye field.

12 ongside the superior parietal cortex and the frontal eye field.

13 and recorded the activity of neurons in the frontal eye field.

14 rded from visually responsive neurons in the frontal eye field.

15 within the posterior parietal cortex and the frontal eye fields.

16 nse in the smooth eye movement region of the frontal eye fields.

17 tinotopic fMRI activity was localized to the frontal eye fields.

18 um and the smooth eye movement region of the frontal eye fields.

19 ention as well as by microstimulation of the frontal eye fields.

20 or and dorsolateral prefrontal cortices, and frontal eye fields.

21 e time-locked to activation increases in the frontal eye fields.

22 inactivation of the superior colliculus and frontal eye fields.

23 ling from a frontoparietal network including frontal eye fields.

24 eas, the lateral intraparietal area, and the frontal eye fields.

25 ticotectal projections originated within the frontal eye fields.

26 l cortex, bilateral intraparietal sulci, and frontal eye fields.

27 on and studied populations of neurons in the frontal eye fields, a key cortical area containing neuro

28 f particular interest in this process is the frontal eye fields, a region of prefrontal cortex that h

29 Altering either D1- or D2-receptor-mediated frontal eye field activity increased saccadic target sel

30 ng that the population-level organization of frontal eye field activity is important for the transiti

31 ioral performance are affected by changes in frontal eye field activity.

32 Neurons in the frontal eye field, an area involved in converting the ou

33 tial attention task while neurons within the frontal eye field, an oculomotor area within prefrontal

34 wing with electrical microstimulation of the frontal eye field and analysed the resulting, evoked eye

35 n over four frontoparietal cortex locations (frontal eye field and intraparietal sulcus in each hemis

36 ied in several cortical areas, including the frontal eye field and lateral intraparietal area, and on

37 orsal prearcuate cortex in the region of the frontal eye field and neurons in dorsal prefrontal corte

38 mulation of presaccadic areas, including the frontal eye field and superior colliculus (SC).

39 vidence that the lateral intraparietal area, frontal eye field and superior colliculus are involved i

40 ed on neurophysiological observations in the frontal eye field and superior colliculus of behaving mo

41 ort the regulation of eye movements, such as frontal eye field and superior colliculus, are modulated

42 We found a group of neurons in both the frontal eye field and the caudal prefrontal cortex that

43 e cues and the inferred causal structure the frontal eye field and the intraparietal sulcus form a ci

44 The human frontal eye field and two separate regions in the intrap

45 f five optogenetic constructs in the macaque frontal eye field and use electrical microstimulation to

46 etween high-beta oscillatory activity in the Frontal Eye Field and visual detection.

47 ulcus; smaller reductions were also found in frontal eye fields and dorsal parietal cortex.

48 In recent years, recordings in the frontal eye fields and superior colliculus of behaving n

49 ces from the temporoparietal junction on the frontal eye fields and the putamen were modulated by (Ba

50 maintained in the macaque monkey prefrontal (frontal eye fields) and parietal cortex (lateral intrapa

51 over primary motor cortex, premotor cortex, frontal eye field, and dorsolateral prefrontal cortex.

52 Neurons in the lateral intraparietal area, frontal eye field, and superior colliculus exhibit a pat

53 premotor cortex, supplementary motor cortex, frontal eye field, and supplementary eye field can in pr

54 verlaps with the inferior frontal gyrus, the frontal eye field, and the dorsolateral prefrontal corte

55 right dorsolateral prefrontal cortex, right frontal eye-fields, and the posterior cingulate.

56 arrays into areas 8Ad-the putative marmoset frontal eye field-and the lateral intraparietal area of

57 tion regions in visual, fusiform cortex, and frontal eye fields; and in arousal/salience networks inv

58 Before each saccade, neurons in frontal eye field anticipate the impending eye movement

59 as decrements were observed at the bilateral frontal eye field area.

60 th the caudal principal sulcus (area 46) and frontal eye fields (area 8a).

61 racer injections within cortex including the frontal eye fields (areas 46 and 8) labeled areas TPOc,

62 ked by intracortical microstimulation of the frontal eye fields at variable times after presentation

63 raparietal sulcus (IPS), left IPS, and right frontal eye field being the main sources of behavior-enh

64 work that included regions identified as the frontal eye fields, both superior and inferior parietal

65 ow that low-level stimulation of the primate frontal eye fields can induce robust pupil dilation with

66 tion with electrical microstimulation of the frontal eye field, causing an evoked eye movement that i

67 ent functional classes of neurons within the frontal eye field contribute uniquely to these two funct

68 Neural activity in the frontal eye fields controls smooth pursuit eye movements

69 The regions reported to correspond to the "frontal eye fields" did not exhibit any unique visual pr

70 er evidence changes, and many neurons in the frontal eye field displayed a corresponding dip in activ

71 n, so we recorded from single neurons in the frontal eye field, dorsolateral prefrontal cortex, and s

72 We microstimulated the frontal eye fields during redirect behavior and systemat

73 ivity, deficient corollary discharges to the frontal eye fields, dysfunctional pulvinar, claustrum an

74 y antisaccades to be associated with reduced frontal eye field (FEF) activity relative to those prece

75 ultaneously recorded neural responses in the frontal eye field (FEF) and area V4 while monkeys perfor

76 Using paired recordings in the frontal eye field (FEF) and area V4, we found that atten

77 Potential neural substrates include the frontal eye field (FEF) and caudate nucleus, but their d

78 ood oxygen level-dependent time series, that frontal eye field (FEF) and intraparietal sulcus (IPS) a

79 activity than stimulus-driven shifts in the frontal eye field (FEF) and intraparietal sulcus, core r

80 pture by a salient singleton distractor: the frontal eye field (FEF) and the cortex within the intrap

81 By contrast, the frontal eye field (FEF) and the intraparietal sulcus (IP

82 h increased prestimulus BOLD activity in the frontal eye field (FEF) and the posterior inferior front

83 instructions could be decoded both from the frontal eye field (FEF) and the ventrolateral PFC (vlPFC

84 ugh the lateral intraparietal area (LIP) and frontal eye field (FEF) are known to represent the posit

85 While the motor and attentional roles of the frontal eye field (FEF) are well documented, the relatio

86 ntified the volume of a segment of the right frontal eye field (FEF) as positively correlated with an

87 tigated the causal contribution of the human frontal eye field (FEF) by combining repetitive transcra

88 ence has indicated that microstimulating the frontal eye field (FEF) can produce modulations of corti

89 edial-dorsal nucleus of the thalamus (MD) to frontal eye field (FEF) carries such a CD for saccadic e

90 oving dot pattern and that neurons in monkey frontal eye field (FEF) changed their activity when the

91 investigated by recording neurons in monkey frontal eye field (FEF) during an inferred motion task.

92 a (PMV), supplementary motor area (SMA), and frontal eye field (FEF) following intracortical microsti

93 The frontal eye field (FEF) has emerged as a key candidate a

94 We tested the role of the frontal eye field (FEF) in driving presaccadic modulatio

95 of attentional modulation has implicated the frontal eye field (FEF) in driving spatial attention.

96 It is widely held that the frontal eye field (FEF) in prefrontal cortex (PFC) modul

97 The frontal eye field (FEF) in prosimian primates was identi

98 We examine the role of the frontal eye field (FEF) in these processes through the e

99 l PFC and alpha-band power (10-18 Hz) in the frontal eye field (FEF) increased.

100 The frontal eye field (FEF) influences saccade generation vi

101 The frontal eye field (FEF) is a cortical structure involved

102 gnitive functions.SIGNIFICANCE STATEMENT The frontal eye field (FEF) is a critical cortical region fo

103 The frontal eye field (FEF) is a critical region for the dep

104 The frontal eye field (FEF) is a key brain region to study v

105 The frontal eye field (FEF) is a key part of the oculomotor

106 The frontal eye field (FEF) is an area in the primate prefro

107 phase of theta oscillations (3-6 Hz) in the frontal eye field (FEF) is associated with the spatiotem

108 The frontal eye field (FEF) is involved in the transformatio

109 The frontal eye field (FEF) is one of several cortical regio

110 actors by visually responsive neurons in the frontal eye field (FEF) marks the outcome and conclusion

111 ow that visual and pre-saccadic responses of frontal eye field (FEF) neurons are modulated by initial

112 l working memory.SIGNIFICANCE STATEMENT Many frontal eye field (FEF) neurons exhibit spatially tuned

113 e examined changes in spiking variability of frontal eye field (FEF) neurons in a change detection ta

114 Frontal eye field (FEF) neurons show robust, spatially s

115 For elucidating the choice mechanisms, frontal eye field (FEF) neurons were monitored during a

116 xhibit object-selective activity, along with Frontal Eye Field (FEF) neurons, which exhibit spatially

117 We recorded from 231 neurons in the frontal eye field (FEF) of 2 male animals performing a v

118 While recording from neurons in frontal eye field (FEF) of awake monkeys (Macaca mulatta

119 -term memory, the activity of neurons in the frontal eye field (FEF) of macaque monkeys was recorded

120 l of saccade sequences, we recorded from the frontal eye field (FEF) of macaque monkeys while they pe

121 Single neurons were recorded in the frontal eye field (FEF) of monkeys performing a popout s

122 perturbing dopaminergic activity within the frontal eye field (FEF) of monkeys performing a saccadic

123 We monitored activity in the frontal eye field (FEF) of monkeys trained to make a sac

124 We stimulated the frontal eye field (FEF) of passively fixating monkeys an

125 identified two functional subregions in the frontal eye field (FEF) of the Cebus monkey, a smooth ey

126 ng targets by microstimulation in either the frontal eye field (FEF) or the superior colliculus (SC),

127 The frontal eye field (FEF) participates in selecting the lo

128 Recent evidence indicates that the frontal eye field (FEF) participates in the deployment o

129 ospatial information, neural activity in the frontal eye field (FEF) persists and is thought to be an

130 The frontal eye field (FEF) plays a well-established role in

131 tic stimulation (TMS) delivered to the right Frontal Eye Field (FEF) prior to the onset of a laterali

132 nial Magnetic Stimulation (TMS) to the right Frontal Eye Field (FEF) prior to the onset of a laterali

133 Neuronal activity in the frontal eye field (FEF) ranges from purely motor (relate

134 ests that visually responsive neurons in the frontal eye field (FEF) respond to visual targets even w

135 noninvasive neurostimulation over the right frontal eye field (FEF) to isolate the behavioral effect

136 ion of the corticotectal projection from the frontal eye field (FEF) to the superior colliculus (SC).

137 The activity of neurons in the frontal eye field (FEF) was consistently modulated accor

138 This includes the frontal eye field (FEF) where nearly half of the neurons

139 We recorded from neurons in area 46 and the frontal eye field (FEF) while monkeys performed a memory

140 We recorded from neurons in the frontal eye field (FEF), a cortical area that responds t

141 In the frontal eye field (FEF), a key area enabling top-down at

142 In the frontal eye field (FEF), an area assumed to control spat

143 fferent roles in this familiar activity--the frontal eye field (FEF), an area in the prefrontal corte

144 in part via its direct projections from the frontal eye field (FEF), an area involved in selective a

145 ikely source of this attentional bias is the frontal eye field (FEF), an area of the frontal cortex i

146 possible source is the PFC, particularly the frontal eye field (FEF), an area of the PFC implicated i

147 is present at the single-neuron level in the frontal eye field (FEF), an area that receives both visu

148 n control the activity of neurons within the frontal eye field (FEF), an oculomotor area of the prefr

149 SMA), presupplementary motor area (pre-SMA), frontal eye field (FEF), and cingulate motor areas, CMAr

150 ork, namely, the intraparietal sulcus (IPS), frontal eye field (FEF), and supplementary eye field.

151 dorsolateral prefrontal cortex (dlPFC), the frontal eye field (FEF), and the lateral intraparietal a

152 hich lateral intraparietal cortex (LIP), the frontal eye field (FEF), and the mediodorsal pulvinar (m

153 network for volitional ocular motor control-frontal eye field (FEF), dorsal anterior cingulate corte

154 ctivations approximately 300 ms after cue in frontal eye field (FEF), lateral intraparietal area (LIP

155 task in the inferior parietal lobule (IPL), frontal eye field (FEF), middle frontal gyrus (MFG), and

156 scribed topographic areas in frontal cortex [frontal eye field (FEF), PreCC/IFS (precentral cortex/in

157 ions of primary motor cortex (M1c, M1r), the frontal eye field (FEF), the dorsal oculomotor area (OMD

158 elated activity was observed in the SEF, the frontal eye field (FEF), the superior parietal lobule (S

159 (LS), temporal parietal junction (TPJ), and frontal eye field (FEF), was affected by information acc

160 motor transform is partly implemented in the frontal eye field (FEF), where visually responsive neuro

161 rk, including intraparietal sulcus (IPS) and frontal eye field (FEF), whereas cues predicting angry f

162 We investigated this question in the monkey frontal eye field (FEF), which is implicated in voluntar

163 a (PMV), supplementary motor area (SMA), and frontal eye field (FEF).

164 lomotor tasks, and refer to this area as the frontal eye field (FEF).

165 was reduced during local inactivation of the frontal eye field (FEF).

166 l for guiding visual attention - such as the frontal eye field (FEF).

167 refrontal cortex (rVLPFC) and the bi-lateral frontal eye field (FEF).

168 ght power densities (</=100 mW/mm(2)) in the frontal eye field (FEF).

169 drug cue reactivity while men showed higher frontal eye field (FEF)/dorsolateral PFC (dlPFC) drug re

170 utions at a late stage of visual processing [frontal eye field (FEF)] and as a comparison, an early s

171 f the striatum in the basal ganglia) and the frontal eye field (FEF, in prefrontal cortex).

172 We examined these contributions in frontal eye field (FEF; N = 51) and as a comparison, an

173 ated the emergence of neural learning in the frontal eye fields (FEF(SEM)) and the floccular complex

174 t from the smooth eye movement region of the frontal eye fields (FEF(SEM)) could implement gain contr

175 The smooth eye movement region of the frontal eye fields (FEF(SEM)) is a critical node in the

176 ons in the smooth eye movement region of the frontal eye fields (FEF(SEM)).

177 by electrically stimulating sites within the frontal eye fields (FEF) and measuring its effect on the

178 ltaneously recorded neuronal activity in the frontal eye fields (FEF) and primary visual cortex (V1)

179 a role in visually guided eye movements: the frontal eye fields (FEF) and the medial eye fields (MEF)

180 The frontal eye fields (FEF) are thought to mediate response

181 the lateral intraparietal area (LIP) and the frontal eye fields (FEF) exhibit persistent activity tha

182 Here, we present neural evidence in the frontal eye fields (FEF) for serial, covert shifts of at

183 d electrical microstimulation of the macaque frontal eye fields (FEF) modulates the pupillary light r

184 S to examine cortical activations within the frontal eye fields (FEF) while initiating vergence eye m

185 In striate cortex (V1), the frontal eye fields (FEF), and the intraparietal sulcus (

186 the lateral intraparietal cortex (LIP), the frontal eye fields (FEF), and the superior colliculus (S

187 whereas those at higher levels, such as the frontal eye fields (FEF), are thought to modulate sensor

188 ising the intraparietal sulcus (IPS) and the frontal eye fields (FEF), controls the voluntary deploym

189 ing by simultaneously recording from macaque frontal eye fields (FEF), lateral intraparietal area (LI

190 n all sites considered: V4, MT, lateral PFC, frontal eye fields (FEF), lateral intraparietal cortex (

191 rid-like codes, entorhinal cortex, saccades, frontal eye fields (FEF), memory, functional magnetic re

192 saccadic thresholds of the directly adjacent Frontal Eye Fields (FEF), saccades were only rarely evok

193 ies: dorsolateral prefrontal cortex (dlPFC), frontal eye fields (FEF), superior parietal lobule (SPL)

194 ressor), were observed with seeds within the frontal eye fields (FEF), superior parietal lobule (SPL)

195 argets following stimulation of the DMFC and frontal eye fields (FEF).

196 s in the posterior parietal cortex (PPC) and frontal eye fields (FEF).

197 d rostral (M3) cingulate motor cortices; the frontal eye fields (FEF); pre-supplementary motor cortex

198 tal area (LIP), prefrontal cortex (PFC), and frontal eye fields (FEF)] of monkeys reporting the color

199 t that the putative human homolog of macaque frontal eye fields (FEF+) is critical for this improveme

200 to show that stimulation of the right human frontal eye-field (FEF) produced a characteristic topogr

201 odulations in intraparietal sulcus (IPS) and frontal-eye field (FEF), and transient less selective mo

202 One such frontal cortical area, the frontal-eye field (FEF), has been shown to have fast vis

203 aparietal [LIP], posterior parietal area 7A, frontal eye field [FEF], and prefrontal cortex [PFC]) wh

204 Neural activity within the frontal eye fields (FEFs) and intermediate layers of the

205 Single neurons in the frontal eye fields (FEFs) and lateral intraparietal area

206 The frontal eye fields (FEFs) and the anterior cingulate cor

207 ed the hypothesis that alpha oscillations in frontal eye fields (FEFs) are causally involved in the t

208 E STATEMENT The superior colliculus (SC) and frontal eye fields (FEFs) are two of the best-studied ar

209 seudo-population analyses in SC and cortical frontal eye fields (FEFs) corroborated this hypothesis.

210 , we show that single pulses of TMS over the frontal eye fields (FEFs) in awake NHPs evoked rapid (wi

211 The activity of 91 neurons in the frontal eye fields (FEFs) of two macaque monkeys was rec

212 led by top-down signals generated within the Frontal Eye Fields (FEFs) that can change the excitabili

213 ojecting from the superior colliculus to the frontal eye fields (FEFs) via the mediodorsal thalamus (

214 l electrical microstimulation of the primate frontal eye fields (FEFs), a cortical component of the o

215 While the frontal eye fields (FEFs), intraparietal sulcus, and tem

216 ed a network of activation that included the frontal eye fields (FEFs), supplementary eye fields (SMA

217 dorsal frontoparietal regions [including the frontal eye fields (FEFs)] were correlated with RT in al

218 establish attentional control signals in the frontal eye field in a cell type-specific manner.

219 In area 8Ad, the putative frontal eye field in marmosets, rhythmic alpha-band acti

220 e parietal eye fields in PD in contrast with frontal eye fields in controls, in line with the shift m

221 Single-pulse TMS stimulation of the right frontal eye field increased this distractor-related devi

222 d that on antisaccade trials most neurons in frontal eye fields initially select the singleton while

223 cortices, and the dorsal attention circuits (frontal eye fields, intraparietal sulcus).

224 These findings show that the frontal eye field is involved in visual and not just mot

225 ding cortex sometimes considered part of the frontal eye field, is probably homologous to the premoto

226 multaneously recorded activity from multiple frontal eye field neurons and asked whether they interac

227 -dependent cooperation and competition among frontal eye field neurons during visual target selection

228 We recorded from populations of frontal eye field neurons in macaque monkeys engaged in

229 s of the neuronal response of populations of frontal eye field neurons, suggesting that these neurons

230 In the frontal eye field, neurons use corollary discharge to sh

231 On successful trials, neurons in the frontal eye field not only discriminated the target from

232 basis of visual and saccade selection in the frontal eye field of macaque monkeys using a singleton s

233 data from electrical microstimulation of the frontal eye field of male macaques during a value-based

234 and metrics of eye movements evoked from the frontal eye field of monkeys, while holding the mean int

235 altered D1-receptor-mediated activity in the frontal eye field of the prefrontal cortex and measured

236 ades, we recorded from single neurons in the frontal eye field of two male rhesus monkeys shifting ga

237 tent with this idea, microstimulation of the frontal eye fields, one of several areas that control th

238 d from the left postcentral sulcus and right frontal eye field onto the right pIPS and were selective

239 interprets cells in the superior colliculus, frontal eye field, parietal cortex, mesencephalic reticu

240 eye-movement network for saccade generation (frontal eye fields, posterior parietal cortex, and highe

241 ior and dorsal to the arcuate sulcus and the frontal eye fields produce signals that guide the alloca

242 eper layers, the results suggest that MT and frontal eye field projections to the SC were sparse in e

243 immediately anterior to the saccade-related frontal eye field region is involved in vergence and ocu

244 gmenti pontis, which receives input from the frontal eye field region of frontal cortex, and this cor

245 The posterior cingulate cortex and frontal eye field represent choice prediction error and

246 Distinct neurons in the frontal eye field respond to visual stimuli or control t

247 ger analysis, we further show that the right frontal-eye field (rFEF) exerted feedback control of the

248 -down signals by a single TMS pulse over the frontal eye field (right FEF), while manipulating the st

249 rior parietal cortex (left > right), and the frontal eye fields (right > left).

250 ents, and suggest that the definition of the frontal eye fields should be expanded to include this re

251 absolute preference for reaches, whereas the frontal eye field showed little or no effector selectivi

252 egions, such as supplementary eye fields and frontal eye fields, showed increased activation that was

253 cortex (right middle frontal gyrus and left frontal eye field), supplementary motor cortex, anterior

254 ere we identified a subset of neurons in the frontal eye field that preferentially responded to items

255 ple task to reveal neurons in and around the frontal eye fields that encode where an animal should no

256 g., intraparietal sulcus areas IPS1-IPS4 and frontal eye fields) that are commonly associated with sp

257 rior precuneus, medial intraparietal sulcus, frontal eye fields) that showed the most robust activati

258 tial attention: the lateral premotor cortex (frontal eye fields), the posterior parietal cortex and t

259 e cortex, the superior parietal lobules, the frontal eye fields, the supplementary motor area and the

260 res in the posterior parietal cortex and the frontal eye fields; the language network on epicentres i

261 redicted by the delay-period activity of the frontal eye fields; the magnitude of delay-period activi

262 g saccade triggering suppression reaches the frontal eye field through a different pathway, or a diff

263 We argue that connections from the frontal eye fields to ventral parietal sources represent

264 Neuronal activity in the frontal eye field was directionally tuned before both pr

265 ch found that, when neural activation in the frontal eye fields was boosted by magnetic stimulation,

266 rontal sulcus (cSFS), in the vicinity of the frontal eye fields, was associated with shifting the foc

267 ex (MT+), left intraparietal cortex, and the frontal eye field, were activated at the onset of the dy

268 ibres to the caudate body originate from the frontal eye fields, which play an important role in the