ライフサイエンスコーパス: premotor cortex

1 ted frontoparietal areas (i.e., parietal and premotor cortex).

2 e mediated by interactions between motor and premotor cortex.

3 not recover after bilateral silencing of the premotor cortex.

4 y-inhibitory balance in perilesional ventral premotor cortex.

5 of neuron packing density include motor and premotor cortex.

6 cial cues modulate MNs in the monkey ventral premotor cortex.

7 tamen in the external capsule, and below the premotor cortex.

8 ferior temporal cortex as well as in ventral premotor cortex.

9 of Wernicke's area, Broca's area, and dorsal premotor cortex.

10 , occipitotemporal, parietal, cingulate, and premotor cortex.

11 d received dense projections from the medial premotor cortex.

12 eech and show focal degeneration of superior premotor cortex.

13 submovements, and a distinct oscillation in premotor cortex.

14 ent had abnormally high activity in the left premotor cortex.

15 h the putamen increased connectivity through premotor cortex.

16 neurons in medial frontal cortex, likely in premotor cortex.

17 st-training gray matter volume in the dorsal premotor cortex.

18 rty first shown for mirror neurons in monkey premotor cortex.

19 g the superior temporal sulcus, parietal and premotor cortex.

20 esponses more frequently than stimulation in premotor cortex.

21 including the posterior parietal cortex and premotor cortex.

22 on that is no longer performed by the dorsal premotor cortex.

23 y cortex SII, posterior parietal cortex, and premotor cortex.

24 ervation conditions within the right ventral premotor cortex.

25 oded in the dorsal striatum and in the right premotor cortex.

26 appropriate activations of frontal motor and premotor cortex.

27 RI activity in posterior parietal and dorsal premotor cortex.

28 orsal, and is eventually centered around the premotor cortex.

29 used to define the motor goal in the PPC and premotor cortex.

30 ects following the application of TMS to the premotor cortex.

31 parietal regions, including bilateral dorsal premotor cortex.

32 ginated in the lateral instead of the medial premotor cortex.

33 tissue loss in the right dorsal ACC and left premotor cortex.

34 multisensory areas, most notably the ventral premotor cortex.

35 gyrus (BA6): the latter region is considered premotor cortex.

36 n of decision-related firing rates in dorsal premotor cortex.

37 right middle temporal gyrus (MTG), and right premotor cortex.

38 ns to the caudal and rostral areas of dorsal premotor cortex (6DC and 6DR, also known as F2 and F7) w

39 anding by recruitment of left dorsal lateral premotor cortex, a region normally devoted to higher-lev

40 Caudal dorsal premotor cortex activity was associated with both psycho

41 ipsilesional motor cortex and contralesional premotor cortex after the intervention.

42 ity patterns with parahippocampal cortex and premotor cortex again suggested fundamental corresponden

43 -a premotor area homologous to the mammalian premotor cortex-alters the statistics of the syllable se

44 e deficits correlated with lesions in dorsal premotor cortex, an area not previously associated with

45 nding motor pathway, where recordings from a premotor cortex analog nucleus reflected changes to temp

46 d in a bilateral network involving the motor/premotor cortex and anterior cingulate gyrus.

47 ith extension of loss involving the inferior premotor cortex and body of the corpus callosum.

48 xel patterns of activity in the left ventral premotor cortex and Broca's area exhibited effective pho

49 and perceptual accuracy in the left ventral premotor cortex and Broca's area.

50 , as well as reductions in motor and lateral premotor cortex and in the basal ganglia.

51 er connectivity in the alpha band with right premotor cortex and left insular-temporal cortex a netwo

52 represent separate cerebellar inputs to the premotor cortex and M1.

53 tex may reveal cerebellar inputs to both the premotor cortex and M1.

54 visuo-motor mirror neurons located in monkey premotor cortex and parietal cortices as well as homolog

55 ng this EEG potential arises from the dorsal premotor cortex and serves an executive-attentional func

56 eling to compare population dynamics between premotor cortex and striatum in mice performing a two-in

57 es myelination within the deep layers of the premotor cortex and subcortical white matter.

58 led focal hypometabolism of superior lateral premotor cortex and supplementary motor area, although t

59 r revealed focal atrophy of superior lateral premotor cortex and supplementary motor area.

60 an attenuated reduction in beta power in the premotor cortex and supplementary motor area.

61 an attenuated reduction in beta power in the premotor cortex and supplementary motor area.

62 integration of the two components in dorsal premotor cortex and supplementary motor areas, two regio

63 asting with the relative code seen in dorsal premotor cortex and the mostly gaze-centered reference f

64 , while many neurons in the dorsal aspect of premotor cortex and the primary motor cortex were simult

65 m the caudally adjacent ventral parts of the premotor cortex and the primary motor cortical region th

66 cal (motor cortex, supplementary motor area, premotor cortex) and subcortical network (subthalamic nu

67 (primary sensory cortex, dorsal and ventral premotor cortex) and the supplementary motor area was co

68 tterns in right superior parietal lobule and premotor cortex, and also left frontopolar cortex, signi

69 rected), intraparietal sulcus, caudal dorsal premotor cortex, and cerebellar lobule VI (t >/= 4.18, w

70 nucleus, thalamus, supplementary motor area, premotor cortex, and dorsolateral prefrontal cortex duri

71 al visual cortex, posterior parietal cortex, premotor cortex, and hippocampus) and with activation of

72 al areas, relative to the shoulder in dorsal premotor cortex, and in muscle- or joint-based coordinat

73 (IPL), bilateral precuneus (PCN), bilateral premotor cortex, and left inferior frontal gyrus.

74 d activity in the lateral cerebellum, dorsal premotor cortex, and parahippocampal gyrus, with covaryi

75 essening of activation in prefrontal cortex, premotor cortex, and posterior parietal cortex, areas th

76 xternally driven) in parietal cortex, dorsal premotor cortex, and primary motor cortex contralateral

77 ce data on premovement activity in motor and premotor cortex, and suggest that synaptic plasticity ma

78 production including inferior frontal gyrus, premotor cortex, and superior temporal gyrus during a pi

79 on at the single neuron level in the ventral premotor cortex, and support the hypothesis of a functio

80 aparietal area, the hand area of the ventral premotor cortex, and the primary motor cortex is necessa

81 of core motor regions comprising M1, lateral premotor cortex, and the supplementary motor area (SMA)

82 he primary motor cortex, the ventral lateral premotor cortex, and the supplementary motor area are es

83 the lateral premotor loop comprising lateral premotor cortex; and (iii) cortico-subcortical interacti

84 posterior inferior temporal cortex and right premotor cortex are consistent with neurophysiologically

85 m the dorsocaudal and medial subdivisions of premotor cortex (areas 6DC and 6M), from somatosensory a

86 erged earliest in down-regulating neurons of premotor cortex, arguing for an initiation of selection

87 xperiment 2, inhibitory stimulation of right premotor cortex as a key node of the dorsal stream decre

88 r area, and the caudal subdivision of dorsal premotor cortex, as well as afferents from cingulate are

89 in the left intraparietal sulcus and dorsal premotor cortex, as well as in the basal ganglia and ant

90 rophy over time were observed throughout the premotor cortex, as well as prefrontal cortex, motor cor

91 inferior frontal gyrus and adjacent ventral premotor cortex, as well as the rostral inferior parieta

92 licated in the mirror neuron system, such as premotor cortex (BA 6) and inferior parietal lobule (BA

93 signed to test the idea that firing rates in premotor cortex become optimized during motor preparatio

94 vate widespread regions of frontal motor and premotor cortex but instead, produces focal, somatotopic

95 ompensatory relationship between putamen and premotor cortex by showing, in the control subjects, tha

96 courtship songs by acting on a region of the premotor cortex called HVC.

97 left dorsal inferior frontal gyrus and left premotor cortex, children who stutter exhibited deactiva

98 code actions at abstract levels whereas the premotor cortex codes actions at the concrete level only

99 d speech representations in sensorimotor and premotor cortex, combined with diffuse reactivation of h

100 ch to a visual target, neurons in the dorsal premotor cortex compare the location of the target, the

101 ased activity in precuneus, frontopolar, and premotor cortex, compared to those of controls.

102 indicate that area F5 in the macaque ventral premotor cortex consists of three different sectors.

103 literature, we suggest that the left dorsal premotor cortex contributes to trajectory control, while

104 Our data suggest premotor cortex could be tested as a target region for n

105 Contralesional dorsal premotor cortex (cPMd) may support residual motor functi

106 re prevalent in superficial layers of dorsal premotor cortex; deeper layers contained more "decreased

107 applied over either the motor hotspot or the premotor cortex demonstrated high inter-individual varia

108 ion for decision-related responses in dorsal premotor cortex.Dorsal premotor cortex (PMd) is thought

109 (PPC), dorsal premotor cortex (PMd), ventral premotor cortex, dorsolateral prefrontal cortex, presupp

110 iven movement plans in contralateral ventral premotor cortex, dorsolateral prefrontal cortex, suprama

111 actile stimulus patterns, the primate dorsal premotor cortex (DPC) neurons exhibit a complex repertoi

112 supplementary motor area (SMA), left dorsal premotor cortex (dPM), and left anterior cingulate corte

113 nt forms of motor simulation: (1) the dorsal premotor cortex (dPMC), associated with automatic motor

114 profiles of individual neurons in the dorsal premotor cortex during comparison of tactile temporal pa

115 ues and examined single neuron activities in premotor cortex during natural vocal exchanges in the co

116 ation (TMS) over the PPC, but not the dorsal premotor cortex, enhances this effect without affecting

117 Mirror neurons in premotor cortex exhibit visuomotor properties that allow

118 eurons (PTNs) within macaque rostral ventral premotor cortex (F5) and (M1) provide direct input to sp

119 iated responses to fearful faces in her left premotor cortex face area and bilaterally in the inferio

120 The premotor cortex face area and inferior parietal lobule a

121 nnectivity between M1 and ipsilateral dorsal premotor cortex further increased dose-dependently after

122 These findings suggest that premotor cortex generates different dynamics depending o

123 sterior-anterior gradient in the left dorsal premotor cortex gradually transitioned from selectivity

124 Supplementary motor area and premotor cortex had spectral power increases within ~200

125 f "mirror neurons" in area F5 of the ventral premotor cortex has prompted many theories as to their p

126 e action representation system including the premotor cortex, has hitherto not been provided.

127 Mirror neurons in area F5 of the monkey premotor cortex have been suggested to play a crucial ro

128 vance of BBA and its laminar organization in premotor cortex have not been completely elucidated.

129 Corpus callosum bisections demonstrated that premotor cortex hemispheres can maintain preparatory act

130 For example, classic studies of vocal-premotor cortex (HVC, acronym is name) in male zebra fin

131 se results show that the disruption of human premotor cortex impairs speech perception, thus demonstr

132 ibited the extrastriate body area and dorsal premotor cortex in 11 PD patients and 12 healthy subject

133 work, we use optogenetic stimulation of the premotor cortex in awake, behaving mice to demonstrate t

134 revealing more about the role of the dorsal premotor cortex in decision making.

135 20) provide evidence of a novel role for the premotor cortex in maintaining the context-dependent inf

136 e of a homologous organization of the dorsal premotor cortex in New and Old World monkeys.

137 of the mouse cortex (a possible homologue of premotor cortex in primates) contains equal proportions

138 distinct from neighboring regions of ventral premotor cortex, in line with recent anatomical connecti

139 th left inferior parietal lobule and ventral premotor cortex, indicating that each LATL subregion exh

140 ing significantly more activation in ventral premotor cortex, inferior parietal cortex, and inferotem

141 mirror neuron system activity within ventral premotor cortex/inferior frontal gyrus.

142 h signals related to motor cortical state in premotor cortex influence effort value computations, ins

143 temporal parietal occipital junction, dorsal premotor cortex, insula, and posterior cingulate cortex

144 show that, 200 ms after stimulus onset, the premotor cortex integrated gaze, gesture, and emotion di

145 n suggests that supplementary motor area and premotor cortex interrupted the gait cycle, while poster

146 n and motor preparation localized to lateral premotor cortex, intraparietal sulcus, and posterior sup

147 increased learning-related activation of the premotor cortex is compatible with the view of DYT1 dyst

148 lcium imaging reveal that neural activity in premotor cortex is correlated with a length scale of 100

149 Dorsal premotor cortex is implicated in somatomotor decisions.

150 area (AIP) and hand area (F5) of the ventral premotor cortex is implicated strongly in the generation

151 uggest that peri-hand space remapping in the premotor cortex is most tightly linked to the subjective

152 The functional impact of premotor cortex is weak, possibly due to inhibitory syst

153 ively coupled modules, as we observed in the premotor cortex, is a hallmark of robust control systems

154 that this mechanism also operates in dorsal premotor cortex, largely accounting for how preparatory

155 However, HD-tDCS over the premotor cortex led to a higher number of responders and

156 ne set of regions (e.g., within left lateral premotor cortex; left precuneus; right posterior cerebel

157 al (v) and dorsal (d) regions of the lateral premotor cortex (LPMC) to spinal levels C5-T1.

158 projections were found from the dorsolateral premotor cortex (LPMCd), ventrolateral proisocortical mo

159 with a dose-dependent enhancement of dorsal premotor cortex-M1 connectivity.

160 ty emerged during learning, originating from premotor cortex (M2), and M2 became predictive of the ac

161 n show that neural populations in the medial premotor cortex (MPC) contain an accurate trial-by-trial

162 asked how oscillatory dynamics in the medial premotor cortex (MPC) contribute to supramodal perceptua

163 vioral data, ensemble recordings from medial premotor cortex (MPC) in macaque monkeys, and computatio

164 We found that neurons in the medial premotor cortex (MPC) of behaving monkeys are tuned to t

165 g accuracy of cell populations in the medial premotor cortex (MPC) of Rhesus monkeys to represent in

166 ural recording technique, we observed in the premotor cortex neural activation and suppression both b

167 study is the discovery of a subpopulation of premotor cortex neurons that was activated by vocal prod

168 However, speech arrest localized to ventral premotor cortex, not the classical Broca's area.

169 terior intraparietal sulcus and left ventral premotor cortex; now, however, we also find activity for

170 orded using laminar electrodes in the dorsal premotor cortex of 2 male rhesus macaques performing a v

171 thickness (VBCT) increases in the bilateral premotor cortex of hemiparetic patients relative to cont

172 e dataset recorded in the striatum and motor-premotor cortex of macaque monkeys performing reaching t

173 Mirror neurons, located in the premotor cortex of macaque monkeys, are activated both b

174 ordings from multiple cortical layers of the premotor cortex of monkeys performing a decision-making

175 We recorded neurons from dorsal premotor cortex of monkeys performing a visual discrimin

176 taneous microelectrode array recordings from premotor cortex of monkeys performing delayed-reach move

177 ost of the activity seen in the parietal and premotor cortex of the human brain is independent of mir

178 ruited areas in the visual dorsal stream and premotor cortex of the intact hemisphere to compensate f

179 al variability of neural responses in dorsal premotor cortex of three monkeys performing a delayed-re

180 electrode arrays implanted in monkey dorsal premotor cortex, of a manyfold higher performance BCI th

181 tivity between prefrontal cortex and lateral premotor cortex OFF medication, compatible with a contex

182 he dorsolateral prefrontal cortex and dorsal premotor cortex onto the contralateral primary motor cor

183 motor-centric and cognitive accounts whether premotor cortex or brain regions in closer relation to p

184 when TMS was delivered over adjacent dorsal premotor cortex or when motor behaviors in late adaptati

185 nts who had damage to the left putamen, left premotor cortex, or both.

186 posterior superior temporal sulcus, and left premotor cortex, OT increased activity during social jud

187 n the left anterior cingulate and the dorsal premotor cortex (P < 0.001).

188 ht midbrain, and decreased rCBF in the right premotor cortex (P < 0.05, corrected).

189 The premotor cortex-particularly the dorsal premotor cortex

190 provide evidence indicating that the dorsal premotor cortex plays a causal role in accurate turn-tak

191 The premotor cortex (PM) is known to be a site of visuo-soma

192 The premotor cortex (PM) receives inputs from parietal corti

193 ietal areas, from primary motor cortex (M1), premotor cortex (PM), the supplementary motor area (SMA)

194 tex (M1) and the secondary motor cortex: the premotor cortex (PMA) and the accessory motor area (SMA)

195 a regular grid of 8 spots covering the left premotor cortex (PMC) and 2 Sham stimulations.

196 ections with functionally matched domains in premotor cortex (PMC) and motor cortex (M1).

197 reignited by a burst of reports implicating premotor cortex (PMC) in speech perception.

198 and the supplementary motor area (SMA), the premotor cortex (PMC), and auditory cortex.

199 agnetic stimulation spots covering the whole premotor cortex (PMC), to identify with accurate spatial

200 ing motor threshold, RMT) to the left dorsal premotor cortex (PMd) (CS2) suppresses the amplitude of

201 Here, we evaluated the role of dorsal premotor cortex (PMd) and lateral prefrontal cortex (LPF

202 Activity in the lateral dorsal premotor cortex (PMd) and the pre-supplementary motor co

203 reaching tasks with multiple targets, dorsal premotor cortex (PMd) appears to represent all possible

204 We applied single-pulse TMS to M1 or dorsal premotor cortex (PMd) during adaptation of rapid arm mov

205 amined population-level responses in macaque premotor cortex (PMd) during the preparatory stage of an

206 ENT For reach-to-grasp movements, the dorsal premotor cortex (PMd) has been implicated in the control

207 As part of these networks, the dorsal premotor cortex (PMd) has been implicated in the control

208 The dorsal premotor cortex (PMd) has long been thought to be a crit

209 indicate a prominent role of the left dorsal premotor cortex (PMd) in action selection based on learn

210 After unilateral stroke, the dorsal premotor cortex (PMd) in the intact hemisphere is often

211 The dorsal premotor cortex (PMd) is part of the cortical network fo

212 d responses in dorsal premotor cortex.Dorsal premotor cortex (PMd) is thought to be involved in makin

213 nsorimotor hand area (SM1) and caudal dorsal premotor cortex (PMd) of the nondominant left hemisphere

214 ing cell activity simultaneously from dorsal premotor cortex (PMd) of two male interacting monkeys tr

215 and high multiunit activity of monkey dorsal premotor cortex (PMd) predicting forthcoming actions on

216 appeared in both tasks, responses of dorsal premotor cortex (PMd) units covaried with action choices

217 The dorsal premotor cortex (PMd) uses prior sensory information for

218 ion profiles in the precuneus and the dorsal premotor cortex (PMd) were indicative of an updating pro

219 Activity in anterior insular cortex (AIC), premotor cortex (PMd), and inferior parietal lobule (IPL

220 (M1), supplementary motor area (SMA), dorsal premotor cortex (PMd), basal ganglia (BG), cerebellum (C

221 the posterior parietal cortex (PPC), dorsal premotor cortex (PMd), ventral premotor cortex, dorsolat

222 In dorsal premotor cortex (PMd), we found that sequence-specific a

223 Neurons in the dorsal premotor cortex (PMd), which is critical for the guidanc

224 The premotor cortex-particularly the dorsal premotor cortex (PMd)-may be a promising alternative tar

225 e parietal reach region (PRR) and the dorsal premotor cortex (PMd).

226 s on the functional integrity of left dorsal premotor cortex (PMd).

227 R), cingulate motor areas (CMAs), and dorsal premotor cortex (PMd).

228 es of the parieto-frontal system: the dorsal premotor cortex (PMd, area 6), primary motor cortex (MI,

229 Inferior frontal gyrus (IFG), ventral premotor cortex (PMv) and inferior parietal lobule (IPL)

230 ctivity of mirror neurons in macaque ventral premotor cortex (PMv) and primary motor cortex (M1) is m

231 nial magnetic stimulation (TMS) near ventral premotor cortex (PMv) and primary motor cortex (M1) with

232 in the inferior parietal lobule and ventral premotor cortex (PMv) can code the intentions of other i

233 interhemispheric connections of the ventral premotor cortex (PMv) distal forelimb representation (DF

234 ng movements of the arm, whereas the ventral premotor cortex (PMv) has been associated with the contr

235 ng movements of the arm, whereas the ventral premotor cortex (PMv) has been associated with the contr

236 Neural activity in ventral premotor cortex (PMv) has been associated with the proce

237 rior intraparietal sulcus (aIPS) and ventral premotor cortex (PMv) in visually mediated state estimat

238 Ventral premotor cortex (PMv) is widely accepted to exert an imp

239 posterior parietal cortex (PPC) and ventral premotor cortex (PMv) represent the position of the uppe

240 By contrast, the ventral premotor cortex (PMv) was associated with shifting betwe

241 es the pattern of connections of the ventral premotor cortex (PMv) with various cortical regions of t

242 Other connections were with ventral premotor cortex (PMV), the caudal half of posterior pari

243 intraparietal sulcus (DIPS) and the ventral premotor cortex (PMv).

244 nterior intraparietal area (AIP) and ventral premotor cortex (PMv).

245 an agent engaged the dorsal pathway and the premotor cortex, possibly to facilitate the preparation

246 am, the critical voxels were concentrated in premotor cortex, pre- and postcentral gyri and supramarg

247 ed in motor representation, including dorsal premotor cortex, pre-supplementary motor area, cerebellu

248 nts are represented in the hand knob area of premotor cortex (precentral gyrus) in people with tetrap

249 y integrated core circuit, spanning parts of premotor cortex, prefrontal cortex, temporal lobe, parie

250 act, including the supplementary motor area, premotor cortex, primary motor cortex, and midcingulate

251 in bilateral secondary somatosensory cortex, premotor cortex, primary motor cortex, insula and poster

252 The preparatory activity of dorsal premotor cortex/primary motor cortex neurons in monkey e

253 rus, visual primary cortex, and motor areas (premotor cortex, putamen, anterior cerebellum).

254 In contrast, inhibition of the left dorsal premotor cortex reduced the posture congruency effect in

255 vity of groups of neurons in primate ventral premotor cortex reflects information related to visually

256 First, bilateral premotor cortex reoriented visuospatial attention specif

257 t postcentral gyrus (rPoG) and right lateral premotor cortex (rPM) is involved in nonverbal auditory

258 ral premotor cortex (rPMv), the right dorsal premotor cortex (rPMd) or the supplementary motor area (

259 d over the right M1 (rM1), the right ventral premotor cortex (rPMv), the right dorsal premotor cortex

260 These findings provide clear evidence of the premotor cortex's involvement in self-initiated vocal pr

261 e observations provide clear evidence of the premotor cortex's involvement in vocal production in a N

262 ity in the dorsomedial prefrontal cortex and premotor cortex scaled with the cost of hierarchical pla

263 estimated white matter tract strength in the premotor cortex seeded from the posterior putamen (as we

264 abstract movement trajectories within dorsal premotor cortex.SIGNIFICANCE STATEMENT The ability to im

265 The major connections of M1 were with premotor cortex, SMA, cingulate motor cortex, somatosens

266 Premotor cortex stimulation revealed that cortico-subtha

267 bjects, the brain's mirror system-comprising premotor cortex, superior temporal sulcus and parietal c

268 e imaging (fMRI), we show that in the medial premotor cortex (supplementary motor area [SMA]) of the

269 motor activity and sound processing (dorsal premotor cortex, supplementary and pre-supplementary mot

270 activity in the sensorimotor cortex, dorsal premotor cortex, supplementary motor area and cerebellum

271 localized to the sensorimotor cortex, dorsal premotor cortex, supplementary motor area and the inferi

272 rior primary motor cortex (BA 4a), bilateral premotor cortex, supplementary motor area, intraparietal

273 t that the organization of the motor cortex, premotor cortex, supplementary motor cortex, frontal eye

274 ce between heterosexual men and women in the premotor cortex/supplementary motor cortex and left medi

275 bpopulations of neurons in the rhesus monkey premotor cortex that allow two planned targets of a sequ

276 neurons' are cells in area F5 of the ventral premotor cortex that are active during both observation

277 discriminated action potentials (spikes) in premotor cortex that triggered electrical stimulation in

278 ified a subpopulation of neurons in marmoset premotor cortex that was activated or suppressed by voca

279 he primary motor cortex, the ventral lateral premotor cortex, the supplementary motor area on the med

280 e left substantia nigra and the left lateral premotor cortex to be significantly more activated in th

281 ive transcranial magnetic stimulation to the premotor cortex to disrupt subjects' ability to perform

282 cted by variability of BOLD responses in the premotor cortex to far stimuli approaching our body.

283 y and optogenetic perturbations in the mouse premotor cortex to probe the robustness of persistent ne

284 quency (77-82 Hz) in a ventral region of the premotor cortex to produce a third rhythm at the sum of

285 r the hypothesised contribution of motor and premotor cortex to the representation of action concepts

286 ssing (amygdala), and motor planning (dorsal premotor cortex) to assess overlap of labeled projection

287 For example, trial-by-trial variability in premotor cortex tracks motor preparation with increasing

288 rimary somatosensory cortex (S1) and ventral premotor cortex (vPM) in nonhuman primates presented wit

289 acellular filling in acute slices of ventral premotor cortex (vPMC) from rhesus monkeys (Macaca mulat

290 Secondly, an area in left premotor cortex was activated in C to a greater extent t

291 underlying the underactive areas in ventral premotor cortex was reduced in people who stutter.

292 Only activity in left premotor cortex was specifically associated with symboli

293 um, the supplementary eye fields, and dorsal premotor cortex, was found to be involved in generating

294 In motor cortex and dorsal premotor cortex, we find that the neural activity that s

295 Selectively in the premotor cortex, we found that ITV, rather than trial-av

296 In sensorimotor and premotor cortex, we observed reliable and temporally pre

297 re is common neural activity in parietal and premotor cortex when executing and observing goal-direct

298 and in the population code of monkey dorsal premotor cortex when obstacles impeded direct reach path

299 of intraparietal sulcus and from the ventral premotor cortex, whereas medial PE forms denser connecti

300 ter the limb disturbance, and then in dorsal premotor cortex, with no effect in parietal regions unti