ライフサイエンスコーパス: frontal cortex

1 gative correlation, with regions in the left frontal cortex.

2 s for SNAP-25, PSD-95, VAMP, and syntaxin in frontal cortex.

3 fine subtypes of cells present in the mouse frontal cortex.

4 o examine allele-specific DNA methylation in frontal cortex.

5 rect current stimulation applied to the left frontal cortex.

6 entrainment emerged in premotor and superior frontal cortex.

7 explains fMRI responses in posterior-medial frontal cortex.

8 rly in parietal/sensory regions and later in frontal cortex.

9 sitive, ubiquitin-positive aggregates in the frontal cortex.

10 l delta rhythms between 1-4 Hz in the medial frontal cortex.

11 l connectivity between temporal and inferior frontal cortex.

12 ivity for sound classes emerges first in the frontal cortex.

13 s are correlated with activity of the medial frontal cortex.

14 pitotemporal, left premotor, and left middle frontal cortex.

15 and 21 human neuronal subpopulations in the frontal cortex.

16 milar inflammatory profile in CHMP2B patient frontal cortex.

17 (R>L), right subcallosal and right anterior frontal cortex.

18 lobe toward functional connectivity with the frontal cortex.

19 r-order areas, including the hippocampus and frontal cortex.

20 s in a network including the hippocampus and frontal cortex.

21 of cognitive control that is orchestrated by frontal cortex.

22 vity of the vATL to regions of occipital and frontal cortex.

23 ctivity between the hippocampus and superior frontal cortex.

24 k-switching activation in the right inferior frontal cortex.

25 accompanied by changes of neural activity in frontal cortex.

26 mus (PeF), periaqueductal gray, amygdala and frontal cortex.

27 tex, orbitofrontal cortex, and left superior frontal cortex.

28 ustral neurons attenuated SW activity in the frontal cortex.

29 bilateral anterior insula and right inferior frontal cortex.

30 ctivation in S1, with minimal propagation to frontal cortex.

31 spindles in temporoparieto-occipital than in frontal cortex.

32 network that includes specialized patches in frontal cortex.

33 can influence its synaptic expression in the frontal cortex.

34 s, akin to a physics engine, in parietal and frontal cortex.

35 this cognitive impairment, but not increased frontal cortex 5-HT(2A)R density or psychedelic-induced

36 , including Ruminococcaceae, correlated with frontal cortex 5-HT(2A)R density.

37 tuttering participants in the right inferior frontal cortex (-7.3%; P = .02), inferior frontal white

38 ownstream effects on BBB permeability in the frontal cortex (a region previously shown to be the most

39 n to anterior cingulate cortex within medial frontal cortex, a group of subcortical structures includ

40 hypoactivity was found in the right inferior frontal cortex, a region highly implicated in cognitive

41 ocation of NF-kappaB in both mouse and human frontal cortex, a trafficking event triggered via 5-HT2A

42 hypothesize that the close coupling between frontal cortex activity and this natural, active primate

43 that this social context-dependent change in frontal cortex activity is supported by several mechanis

44 Damage primarily to inferior frontal cortex affected the production of syntactically

45 nd surrounding astrocytic processes in mouse frontal cortex after 6-8 h of sleep, spontaneous wake, o

46 tatistics warp neural representations in the frontal cortex, allowing the mapping of sensory inputs t

47 in the cingulate region of the mouse medial frontal cortex, an associative region that matures durin

48 r causality analysis, we identified inferior frontal cortex and anterior temporal regions to receive

49 ross a range of brain regions, including the frontal cortex and basal ganglia.

50 the left hippocampus and the right superior frontal cortex and between the right amygdala and the ri

51 to play a prominent role in ASD, such as the frontal cortex and cerebellum.

52 rting with neural signaling molecules in the frontal cortex and ending in the modulation of developme

53 me comparative studies link this to a larger frontal cortex and even larger frontal white matter in h

54 sections confirmed higher Syn I (S9) in the frontal cortex and greater coexpression of Syn I and PP2

55 The results highlight the role of frontal cortex and Hgamma activity in deviance detection

56 of cortical surface area are low toward the frontal cortex and high toward the caudo-medial (occipit

57 lts with ADHD, confirming involvement of the frontal cortex and highlighting regions deserving furthe

58 h and loss of gray matter, especially in the frontal cortex and hippocampus, some focus in drug devel

59 DNA methylation of Th and Bdnf genes in the frontal cortex and hippocampus.

60 al in areas of early amyloidosis such as the frontal cortex and hippocampus.

61 it has been linked to neural activity in the frontal cortex and in sensory motion areas.

62 ierarchical organization of posterior medial frontal cortex and its interaction with the basal gangli

63 ierarchical organization of posterior medial frontal cortex and its interaction with the BG, where a

64 recorded single neurons in the human medial frontal cortex and medial temporal lobe while subjects h

65 -specific long noncoding RNA RP1-269M15.3 in frontal cortex and nucleus accumbens basal ganglia, resp

66 s of rodents revealed that FXG expression in frontal cortex and olfactory bulb followed consistent pa

67 ors protein levels in the nucleus accumbens, frontal cortex and putamen were determined using western

68 ary nucleus, and between ADGRV1 and EFHC2 in frontal cortex and putamen.

69 cortical thinning in parietal, occipital and frontal cortex and reduced hippocampal volume.

70 with neuroimaging changes in specific medial frontal cortex and subcortical structures, suggesting th

71 odulation pattern that began earliest in the frontal cortex and subsequently flowed downstream to the

72 alpha-synuclein-enriched brain fraction from frontal cortex and substantia nigra pars compacta tissue

73 The frontal cortex and temporal lobes together regulate comp

74 e total volume of distribution (V(T)) in the frontal cortex and the cerebellum derived from a kinetic

75 levels of tau and TDP-43 were inverse in the frontal cortex and the cerebellum.

76 nstrate functional boundaries of the lateral frontal cortex and the corresponding network topologies

77 ncreased activation within the dACC, orbital frontal cortex and the mid-inferior frontal gyri.

78 as involved in locomotion, as well as in the frontal cortex and the olfactory bulb.

79 othesis that the coupling between the dorsal frontal cortex and the right temporoparietal cortex is m

80 the chromatin landscape in the hypothalamus, frontal cortex, and amygdala of socially challenged mice

81 m three cerebral regions (angular gyrus, mid-frontal cortex, and anterior cingulate gyrus).

82 single cells from human adult visual cortex, frontal cortex, and cerebellum.

83 across regions of the amygdala, hippocampus, frontal cortex, and hypothalamus.

84 so had atrophy in the medial temporal lobes, frontal cortex, and other brain regions.

85 sub-regions, including midbrain, cerebellum, frontal cortex, and pons.

86 he supplementary motor area, superior medial frontal cortex, and putamen-brain circuits respectively

87 subgenual anterior cingulate cortex/orbital frontal cortex, and the magnitude of connectivity positi

88 derived from the substantia nigra, putamen, frontal cortex, and white matter, and were all significa

89 the contents of dreaming, yet activation of frontal cortex appears necessary for perception and can

90 owing that more effective TMS targets in the frontal cortex are functionally connected to deep limbic

91 ical states, suggesting subregions of medial frontal cortex are functionally heterogeneous.

92 relative roles of distinct subregions within frontal cortex are poorly understood.

93 ention have identified areas of parietal and frontal cortex as sources of attentional control.

94 dorsal extrastriate, posterior parietal, and frontal cortex as well as the thalamus, including both t

95 We propose that neurons in frontal cortex, as in other cortical regions, form a spa

96 exchange was determined by the state of the frontal cortex at the time a vocalization was heard, and

97 s behavioral inhibition critically relies on frontal cortex - basal ganglia circuits.

98 d that a node within MDC, located in midline frontal cortex, becomes active during the early stage of

99 ated with increased activation in the medial frontal cortex beneath the anode; showing a positive cor

100 loid and global cognitive scores (eg, in the frontal cortex: beta = -0.13; 95% CI: -0.23, -0.02; P =

101 The frontal cortex binding potential (BP(ND)(frontal)) was c

102 ses find the most significant enrichment for frontal cortex brain expressed genes.

103 ly structural and functional changes in left frontal cortex, but also disruption of a wider syntactic

104 ri et al. (2019) show that neurons in medial frontal cortex, but not a nearby premotor area, encode t

105 rease in inhibitory neurotransmission in the frontal cortex, but not the somatosensory cortex, sugges

106 al hormones could regulate maturation of the frontal cortex by this mechanism.

107 ha oscillatory activity in the left inferior frontal cortex, canonical Broca's area, and inversely re

108 ge, n = 12) male C57BL/6 mice, and performed frontal cortex cell type-specific molecular profiling, u

109 ns in the expression of complex I with SZ in frontal cortex, cerebellum and striatum, whereas evidenc

110 mplex I and IV, such as in peripheral blood, frontal cortex, cerebellum, and substantia nigra.

111 for retrospective sensory information, while frontal cortex codes for prospective action.

112 Left frontal cortex coherence in the 2-5 Hz range also predic

113 in BDD, by sparser bottom-up striatum-medial frontal cortex connectivity in MDD, and by sparse connec

114 In addition, we found that increased NAcc-frontal cortex connectivity in typically developing yout

115 sting CBF and regional CBF of right superior frontal cortex correlated positively with creatinine-nor

116 es including being in eQTLs in blood and the frontal cortex, CpG islands and shores, and exons.

117 8; P=8.25 x 10(-21)) and left rostral middle frontal cortex (d=-0.276; P=2.99 x 10(-19)).

118 tilization behavior," where individuals with frontal cortex damage inappropriately grasp affording ob

119 c inhibitory mechanism has ramifications for frontal cortex-dependent behaviors and cortico-cortical

120 ion of tonic inhibition and performance in a frontal-cortex-dependent reversal-learning task.

121 enriched circRNA abundantly expressed in the frontal cortex, derived from Homer protein homolog 1 (HO

122 exonic splicing regulators and those within frontal cortex-derived DNase I hypersensitivity sites ar

123 with beta oscillations in the left inferior frontal cortex diminishes verbal working memory capacity

124 g data from 610 postmortem Dorso-Lateral Pre-Frontal Cortex (DLPFC) samples in the CommondMind Consor

125 oning strategy, we recorded from dorsomedial frontal cortex (DMFC) and anterior cingulate cortex (ACC

126 ss populations of neurons in the dorsomedial frontal cortex (DMFC), DMFC-projecting neurons in the ve

127 net (combined) value signals in dorsomedial frontal cortex (dmFC).

128 nscriptional co-expression (P<0.0001) in the frontal cortex during fetal development and in the tempo

129 taneous beta activity from somatosensory and frontal cortex emerged as noncontinuous beta events typi

130 The medial frontal cortex enables performance monitoring, indexed b

131 into a 'ventrodorsal gradient' model, where frontal cortex engagement along this axis depends on seq

132 its and provides insight into how the medial frontal cortex exerts top-down control of cognitive proc

133 HIV infection associates with reduced brain frontal cortex expression of the antioxidant/anti-inflam

134 ific for promoter regions and cerebellum and frontal cortex expression, suggesting a major impact of

135 igated afferent inputs from all areas in the frontal cortex (FC) to different subregions in the rostr

136 APOE epsilon4, we examined the dorsolateral frontal cortex from deceased participants within a commu

137 rochemiluminescent-based immunoassays in the frontal cortex from foetuses to adults with Down syndrom

138 The frontal cortex from patients with WS similarly showed re

139 ingulate cortex > insula > caudate/putamen > frontal cortex > temporal cortex > thalamus, consistent

140 Functional anatomy in frontal cortex has been elusive and controversial.

141 The frontal cortex has been implicated in a number of cognit

142 The medial frontal cortex has been linked to voluntary action, but

143 Neuronal oscillations in the frontal cortex have been hypothesized to play a role in

144 the broad functional boundaries of marmoset frontal cortex have yet to be established.

145 Brains were dissected into frontal cortex, hippocampus, cerebellum, and brainstem.

146 RNA sequencing (RNAseq) analysis of the frontal cortex identified UPF3B-regulated RNAs, includin

147 in random order 1 week apart: right inferior frontal cortex (IFC) stimulation preceding right presupp

148 o support emotion perception is the inferior frontal cortex (IFC).

149 expression within portions of human inferior frontal cortex implicated in human speech and singing.

150 ecific cortical thickness differences in the frontal cortex in adults, support previous work emphasiz

151 The role of the frontal cortex in consciousness remains a matter of deba

152 haracterize functional network topologies of frontal cortex in healthy, normally functioning marmoset

153 ction, it has remained uncertain whether the frontal cortex in nonhuman primates plays a similar role

154 oreover, selective atrophy within the medial frontal cortex in older adults predicted a temporal disp

155 logopenic variant, within the left inferior frontal cortex in patients with the non-fluent/agrammati

156 y analyzing population recordings from mouse frontal cortex in perceptual decision-making tasks, we s

157 anterior-to-posterior tau load ratio in the frontal cortex in preclinical cases was 12-fold greater

158 Although the relative expansion of the frontal cortex in primate evolution is generally accepte

159 t mediates between the limbic system and the frontal cortex in reward-related processing, we propose

160 s has long indicated the crucial role of the frontal cortex in speech production, it has remained unc

161 in humans and implicate the posterior-medial frontal cortex in this process.

162 ed across cortex revealed a crucial role for frontal cortex in triggering this cortex-wide phenomenon

163 lower baseline glucose metabolism than HC in frontal cortex including anterior cingulate, which was a

164 Subregions of the frontal cortex including the orbitofrontal cortex (OFC)

165 om thalamic neurons projecting to the medial frontal cortex indicated that this phenomenon originates

166 f amygdala, basal-ganglia, thalamus, orbital frontal cortex, inferior frontal gyrus and dorsomedial p

167 The medial frontal cortex is important for goal-directed behaviours

168 mping activity are disrupted when the medial frontal cortex is inactivated.

169 In this review, we argue that a part of the frontal cortex known as the anterior cingulate cortex (A

170 early activation of semantic constraints in frontal cortex (LBA45) as W1 was heard.

171 that C4-dependent circuit dysfunction in the frontal cortex leads to decreased social interactions in

172 rocessing network, comprising left posterior frontal cortex, left posterior temporal cortex, and the

173 The functionality of much of human lateral frontal cortex (LFC) has been characterized as "multiple

174 FC structures.SIGNIFICANCE STATEMENT Lateral frontal cortex (LFC) is known to play a number of critic

175 ly derive boundaries of the marmoset lateral frontal cortex (LFC) using ultra-high field (9.4 T) rest

176 itectonically defined regions of the lateral frontal cortex (LFC) with primates, the fingerprinting m

177 egions at school age, including the superior frontal cortex, lingual gyrus, posterior cingulate, and

178 For all mice, frontal cortex, liver, and small/large intestines were c

179 horylation of Syn I serine 9, site 1, in the frontal cortex lysates and synaptosome preparations of m

180 Together, these findings suggest that medial frontal cortex maintains separate predictive models for

181 The frontal cortex matures late in development, showing dram

182 how critically reconsidering the role of the frontal cortex may further delineate NCCs, (3) advocate

183 The frontal cortex may therefore balance consistency with fl

184 o nucleus accumbens (mesolimbic circuit) and frontal cortex (mesocortical circuit).

185 y minutes of inphase stimulation over medial frontal cortex (MFC) and right lateral prefrontal cortex

186 This process depends on the medial frontal cortex (MFC) and the medial temporal lobe, but i

187 refrontal cortex (dlPFC), followed by medial frontal cortex (mFC) and then by orbitofrontal cortex (O

188 With the medial frontal cortex (MFC) centrally implicated in several maj

189 nuated delta activity (1-4 Hz) in the medial frontal cortex (MFC) during interval timing.

190 Influential theories of Medial Frontal Cortex (MFC) function suggest that the MFC regis

191 mechanisms of reward signaling by the medial frontal cortex (MFC) have not been resolved.

192 work showed that inactivation of the medial frontal cortex (MFC) impairs interval timing and attenua

193 n licking and reward signaling by the medial frontal cortex (MFC), a key cortical region for reward-g

194 s among orbital frontal cortex (OFC), medial frontal cortex (MFC), and amygdala are thought to underl

195 Orbitofrontal cortex (OFC), medial frontal cortex (MFC), and amygdala mediate stimulus-rewa

196 ychotic clozapine led to a decrease in mouse frontal cortex mGlu2 mRNA, an effect that required expre

197 ed the antipsychotic profile of LY379268 and frontal cortex mGlu2/3 receptor density in wild-type mic

198 nd prevented increases in Csf1r and Cd11b in frontal cortex microglia following CUS.

199 Previous studies suggest that volume loss in frontal cortex might be an important contributor, but fi

200 avioral deficits designed to test medial pre-frontal cortex (mPFC) and hippocampal learning and memor

201 cial signaling, we recorded the responses of frontal cortex neurons as freely moving marmosets engage

202 d across a broadly distributed population of frontal cortex neurons when marmosets heard a conspecifi

203 A recent study of marmoset frontal cortex observed modulated neural activities asso

204 that truncated STMN2 RNA was elevated in the frontal cortex of a cohort of patients with FTLD-TDP but

205 naptic expression of uPA is decreased in the frontal cortex of AD brains and 5xFAD mice, and uPA trea

206 ce of uPA, but not uPAR, is decreased in the frontal cortex of AD patients and 5xFAD mice, and in cer

207 e profiling of DNA hydroxymethylation of the frontal cortex of AD patients from China, emphasizing an

208 capacities of these neurons in auditory and frontal cortex of behaving rats.

209 s, etc.) were significantly increased in the frontal cortex of C9orf72 ALS patients.

210 -to-process length ratio was observed in the frontal cortex of children and young adults with Down sy

211 xpression of AQP4 was analyzed in postmortem frontal cortex of cognitively healthy and histopathologi

212 pendent decline in lactate levels within the frontal cortex of control mice, whereas lactate levels r

213 or a novel pattern of neural activity in the frontal cortex of freely moving, naturally behaving, mar

214 ontribute to movement cancellation in medial frontal cortex of macaque monkeys.

215 orded electroencephalogram (EEG) over medial frontal cortex of macaques performing a stop signal (cou

216 Moreover, microglia isolated from the frontal cortex of mice exposed to CUS show elevated CSF1

217 onist LY379268 to activate G-proteins in the frontal cortex of mice.

218 However, it has remained unclear whether the frontal cortex of nonhuman primates is involved in the p

219 uch flexibility, we recorded from the medial frontal cortex of nonhuman primates trained to produce d

220 We recorded in the frontal cortex of patients performing a Stroop task and

221 gs to examine the activity of neurons in the frontal cortex of rats and first observed that the distr

222 phenotype previously observed in postmortem frontal cortex of schizophrenic subjects.

223 ed with the higher S9 phosphorylation in the frontal cortex of SIV-infected macaques.

224 perinuclear aggregates in the somata of the frontal cortex of SIV-infected macaques.

225 ations, which casts doubt on the role of the frontal cortex of the Old World monkeys in vocal communi

226 the GNGT, enhanced response in the inferior frontal cortex of the poly-drug group was found.

227 filtering, pointing to a pivotal role of the frontal cortex of the right hemisphere in limiting inter

228 ording cell activity simultaneously from the frontal cortex of two interacting monkeys, trained to co

229 mitant decrease in lactate levels within the frontal cortex of wild-type mice.

230 tical projections originating in the orbital frontal cortex (OFC) prevents mice from shifting from go

231 ltered functional interactions among orbital frontal cortex (OFC), medial frontal cortex (MFC), and a

232 rticle reviews the effects of lesions to the frontal cortex on the ability to carry out active though

233 as applied to one of two targets in the left frontal cortex, one functionally connected (target 1) an

234 udate nucleus (P = .01), thalamus (P = .04), frontal cortex (P = .01), occipital cortex (P = .004), a

235 in individuals with higher AD-PRS across the frontal cortex (P(FWE) < 0.05).

236 eased binding of (11)C-PIB with aging in the frontal cortex, parietotemporal cortex, hippocampus, and

237 The change in the state of the frontal cortex persisted throughout the conversation and

238 Medial frontal cortex persistent activity, on the other hand, w

239 Human frontal cortex plays a crucial role in speech production

240 nificantly related to patient's outcome were frontal cortex, posterior cingulate cortex, thalamus, pu

241 lucinations (VH) with bilateral dorsolateral-frontal cortex, posterior cingulate, and parietal metabo

242 egions including rostral middle and superior frontal cortex, precentral gyrus, and inferior parietal

243 Opioid receptor density in the frontal cortex predicted social laughter rates.

244 edial prefrontal cortex, and lateral orbital frontal cortex predicted treatment response.

245 Recordings from the frontal cortex provided evidence that the brain updates

246 he amygdala, white matter, cingulum, insula, frontal cortex, putamen, temporal and parietal cortices,

247 ntracellular localization of mGluR2 in mouse frontal cortex pyramidal neurons.

248 6, p = 0.02), caudate (r = -0.66, p < 0.01), frontal cortex (r = -0.52, p = 0.04), hippocampus (r = -

249 Specifically, EEG in the pre-frontal cortex reflects not only cortical activity, but

250 ise, relative to their precision in superior frontal cortex (replicated across studies, combined n =

251 rtex, globus pallidus, insula, striatum, and frontal cortex, respectively, consistent with the known

252 by the basal ganglia, extended amygdala, and frontal cortex, respectively.

253 rientation, and functional connectivity with frontal cortex saccade centers.

254 We analyzed 128 suitable frontal cortex samples, from prion-affected patients (va

255 predictable and unpredictable changes, with frontal cortex sensitive to unpredictable events.

256 us during pregnancy induced up-regulation of frontal cortex serotonin 5-HT(2A) receptor (5-HT(2A)R) d

257 ision-making, which in mammals relies on the frontal cortex, specifically the orbitofrontal cortex (O

258 elatively greater tau burden in the anterior frontal cortex, striatum and subthalamic nucleus suggest

259 d that semantic effects on reading depend on frontal cortex subserving control over concrete semantic

260 together with vibrissal motor cortex, vM1 (a frontal cortex target of vS1), while rats compared the i

261 ons known to accumulate amyloid, such as the frontal cortex, temporal cortex, and posterior cingulate

262 MV in the anterior cingulate cortex, orbital frontal cortex, temporal pole, and insula, which were co

263 al connectivity profiles of the ventromedial frontal cortex, temporoparietal junction, and precuneus.

264 category was more accurately represented in frontal cortex than auditory cortex, via ensembles of no

265 tofrontal cortex (OFC) is a subregion of the frontal cortex that allows organisms to link behaviors a

266 cal morphological organization of the medial frontal cortex that can be traced from Old World monkeys

267 ral areas of parietal, occipitotemporal, and frontal cortex that exhibit action category codes that a

268 phrenia involves abnormalities in the medial frontal cortex that lead to cognitive deficits.

269 e identify a pull-push inhibitory circuit in frontal cortex that originates in vasoactive intestinal

270 se genes are expressed in the human superior frontal cortex, that heritable genetic factors influence

271 totemporal junction, the lateral and orbital frontal cortex, the anterior insula, and mesiotemporal s

272 ons were functionally connected to the right frontal cortex, the region most activated in functional

273 oral responses to conflict trials throughout frontal cortex; this activity was correlated with behavi

274 hibitory GABAergic interneurons in the mouse frontal cortex through ephrin-A5-induced growth cone col

275 en rs31746 and PCDH-beta8 mRNA expression in frontal cortex tissue (P<1 x 10(-5)).

276 combination of cultured cell lines, primate frontal cortex tissue and two human adenocarcinomas, and

277 sion of small GTPase proteins in post-mortem frontal cortex tissues from AD patients with different d

278 -wide profiles of both 5mC and 5hmC in human frontal cortex tissues from late-onset Chinese AD patien

279 contribution of the left versus right dorsal frontal cortex to distraction filtering.

280 te long-range inputs with local circuitry in frontal cortex to implement top-down attentional control

281 kami et al. (2017) relate neural activity in frontal cortex to stochastic and deterministic component

282 tions of neurons in both hippocampal CA1 and frontal cortex under one framework that avoids the pitfa

283 ical states to discrete subregions in medial frontal cortex using relatively unbiased data-driven met

284 ed gene expression in the human dorsolateral frontal cortex using RNA- Seq to populate a whole gene c

285 ecreases in fMRI BOLD activity in the orbito-frontal cortex, ventral cingulate gyrus, dorsal cingulat

286 lcal morphological variability of the medial frontal cortex was assessed in Old World monkeys (macaqu

287 However, activity in the posterior medial frontal cortex was elevated in AN following punishment.

288 ) in the PVN, but not in the hippocampus and frontal cortex, was significantly higher in SHRs than in

289 Although the structural boundaries of frontal cortex were described in marmosets at the start

290 y, and perivascular AQP4 localization in the frontal cortex were evaluated.

291 hoices are preferentially represented in the frontal cortex when required.

292 uences in temporal pole and posterior orbito-frontal cortex, which are constructed backwards from rew

293 However, in frontal cortex, which is involved in cognition, neural r

294 y patterns in a separate language area, left frontal cortex, which predicts the word that participant

295 + GM reductions predominantly located in the frontal cortex while PD- had GM reductions in subcortica

296 activity was strong in temporal and inferior frontal cortex, while during low SNR strong entrainment

297 verity, to functional connectivity of orbito-frontal cortex with caudate nucleus and to structural ch

298 ted by connectivity between the right orbito-frontal cortex with caudate nucleus bilaterally.

299 tional connectivity between the: (1) orbital frontal cortex with hippocampus/parahippocampal gyrus; a

300 nding of increased beta-bursting over medial frontal cortex with movement cancellation in humans is d