ライフサイエンスコーパス: frontal cortex

1 ortex in the superior frontal gyrus (midline frontal cortex).

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

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

4 rect current stimulation applied to the left frontal cortex.

5 of cognitive control that is orchestrated by frontal cortex.

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

7 ctivity between the hippocampus and superior frontal cortex.

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

9 accompanied by changes of neural activity in frontal cortex.

10 ein-binding than controls, especially in the frontal cortex.

11 m impaired connectivity between auditory and frontal cortex.

12 active and senescent microglial cells in the frontal cortex.

13 sensorimotor areas in the basal ganglia and frontal cortex.

14 cortex and both the hippocampus and inferior frontal cortex.

15 etal regions and only limited atrophy in the frontal cortex.

16 ocalizes with auditory processing in lateral frontal cortex.

17 the precuneus, inferior parietal, and medial frontal cortex.

18 of which have a strong functional impact on frontal cortex.

19 e left intraparietal sulcus with the orbital frontal cortex.

20 entrainment emerged in premotor and superior frontal cortex.

21 ve dc electrical stimulation over the medial-frontal cortex.

22 t levels, which were not affected in control frontal cortex.

23 oral lobe network shows strong activation of frontal cortex.

24 of noninvasive brain stimulation over medial-frontal cortex.

25 pamine-rich midbrain regions and the lateral frontal cortex.

26 processes widely held to be supported by the frontal cortex.

27 regions of the brain have a strong impact on frontal cortex.

28 functional connectivity at the medial-dorsal frontal cortex.

29 t for cognition, such as the hippocampus and frontal cortex.

30 ntation of task-relevant stimuli observed in frontal cortex.

31 explains fMRI responses in posterior-medial frontal cortex.

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

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

34 l connectivity between temporal and inferior frontal cortex.

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

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

37 and 21 human neuronal subpopulations in the frontal cortex.

38 milar inflammatory profile in CHMP2B patient frontal cortex.

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

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

41 lobe toward functional connectivity with the frontal cortex.

42 1; hypothalamus, -20%, p < .01) or achieved (frontal cortex, -14%, p < .01).

43 ure responses and 5-HT2AR binding density in frontal cortex ([(3)H]-ketanserin radioligand binding).

44 y qPCR in the hippocampus, hypothalamus, and frontal cortex, 4 or 24h post-treatment.

45 n recent ex-smokers, most prominently in the frontal cortex (42%) and thalamus (57%).

46 p < .01), hypothalamus (-16%, p = .03), and frontal cortex (-7%, p = .08).

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

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

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

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

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

52 e GABAergic interaction between amygdala and frontal cortex adds a new dimension to the complex regul

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

54 e, calpain-2, showed a rapid increase in the frontal cortex after blast exposure and it was significa

55 spectrin, showed significant increase in the frontal cortex after blast exposure at all the time poin

56 Mutant mice displayed a narrowing of the frontal cortex, although cortical layers were normally o

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

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

59 The frontal cortex and basal ganglia form a set of parallel

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

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

62 ated with smaller fALFF in the left superior frontal cortex and bilateral temporoparietal junction in

63 ysis showed significant levels of DAI at the frontal cortex and cerebellum at multiple time points af

64 lved in the degradation were analyzed in the frontal cortex and cerebellum using Western blotting wit

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

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

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

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

69 en-eleven-translocation hydroxylase 1 in the frontal cortex and hippocampus but not in cerebellum; no

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

71 lein mice displayed neurodegeneration in the frontal cortex and hippocampus, the alpha-synuclein wild

72 ne methyltransferases and demethylase in the frontal cortex and hippocampus.

73 athological changes, particularly in the pre-frontal cortex and hippocampus.

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

75 cortex, auditory association cortex, orbital frontal cortex and inferior parietal lobe) for 28 subjec

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

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

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

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

80 amplitude of low fluctuation in the orbital frontal cortex and posterior cingulate cortex, and exhib

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

82 prk1, Oprm1, and PDYN mRNA expression in the frontal cortex and striatum.

83 projections from the basal forebrain to the frontal cortex and supported by visual semantic loops wi

84 vation in key inhibitory regions of inferior frontal cortex and thalamus, but increased activation of

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

86 bic prefrontal cortex and other areas of the frontal cortex and the insular cortex with hypothalamic,

87 ve less cortical thinning of the left medial frontal cortex and the right middle temporal cortex.

88 cell types (neuronal and glial inclusions in frontal cortex and white matter, respectively).

89 lateral prefrontal cortex and right inferior frontal cortex) and memory control (hippocampus) are ass

90 isual cortex), category-selective (posterior frontal cortex), and control demand-selective (insula, c

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

92 ed with the rat sensory-motor cortex, medial frontal cortex, and amygdalar regions.

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

94 d small heterodimer partner increased in the frontal cortex, and blocking FXR signaling delayed AOM-i

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

96 ctivity in auditory cortex, hippocampus, and frontal cortex, and functional connectivity among them.

97 d in a subset of mice across the cerebellum, frontal cortex, and hippocampus, as well as at different

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

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

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

101 Long-range projections from the frontal cortex are known to modulate sensory processing

102 s; however, functional subdivisions of human frontal cortex are only coarsely mapped.

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

104 chitectural subdivisions of the caudolateral frontal cortex, areas 6Va and 8C, in marmoset monkeys.

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

106 tory cortices at 6 and 12 months and also at frontal cortex at 6 months.

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

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

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

110 antagonist ketanserin) and the 5HT2A in the frontal cortex (blocked by both ketanserin and SB742457)

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

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

113 m superior colliculus through MD thalamus to frontal cortex, but there is little evidence that this c

114 reliably observed when we stimulated medial-frontal cortex, but when we stimulated posterior parieta

115 The N100 and LICI in the frontal cortex-but not in the motor cortex-were indicato

116 ctive potentiation of GABAA receptors in the frontal cortex by systemic zolpidem administration also

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

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

119 xetimide binding was strongly reduced in the frontal cortex compared with wild-type mice.

120 elin expression in the cortical plate of the frontal cortex, concomitant with an inversion of cortica

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

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

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

124 8; P=8.25 x 10(-21)) and left rostral middle frontal cortex (d=-0.276; P=2.99 x 10(-19)).

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

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

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

128 we investigated how neurons in dorso-lateral frontal cortex (dl-FC) of freely-moving ferrets encode t

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

130 this suggests that premotor activity in the frontal cortex does not have a role in the accumulation

131 us --> dorsal striatum --> insula --> medial frontal cortex, dorsolateral prefrontal cortex, anterior

132 ry cortical processing can strongly activate frontal cortex, downstream auditory regions, such as voi

133 tients failed to activate the right inferior frontal cortex during both conditions, and connectivity

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

135 elopment in autism spectrum disorder and the frontal cortex during fetal development in schizophrenia

136 ndicators of the mean neural activity in the frontal cortex during locomotion; thus, the results from

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

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

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

140 Although the medial frontal cortex exhibits a sensitivity to reaction time o

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

142 Whether such mechanisms occur in frontal cortex (FC) and affect behavioral outcome is not

143 ults identify the necessary subregion of the frontal cortex for WM and specify how this influential a

144 linical studies suggesting that induction of frontal cortex gamma oscillations during tasks that enga

145 .005 and vs 0.465 [0.32] for AD; P = .02; in frontal cortex gray matter: 0.006 [0.004] for R47H_AD vs

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

147 Although recent research has shown that the frontal cortex has a critical role in perceptual decisio

148 Damage to left inferior frontal cortex has been associated with syntactic defici

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

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

151 ty that, in healthy-functioning individuals, frontal cortex helps ensure that irrelevant affordance p

152 mygdala, anterior cingulate cortex, caudate, frontal cortex, hypothalamus, pallidum, putamen, thalamu

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

154 ChIP-seq, provide evidence that PBX promotes frontal cortex identity by repressing genes that promote

155 ect in the backward connection from inferior frontal cortex (IFC) to occipitotemporal cortex over tim

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

157 y suggests pathological hypoperfusion of the frontal cortex in Alzheimer's disease.

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

159 Activation of medial frontal cortex in fMRI studies is associated with a wide

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

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

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

163 rophysiological deficits associated with the frontal cortex in Pick1 knockout mice, which show D-seri

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

165 entially phosphorylated (>15% change) in the frontal cortex in schizophrenia.

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

167 an organizational principle for the role of frontal cortex in the control of perceptual decision mak

168 ated using noninvasive stimulation of medial-frontal cortex in the human brain.

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

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

171 under the control of striatum that activates frontal cortex in vivo.

172 in addition to OTC, regions in parietal and frontal cortex in which neural similarity was related to

173 x (in whole-brain analysis) and left orbital frontal cortex (in region-of-interest analysis).

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

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

176 error processing regions of the dorsomedial frontal cortex, including the left and right presuppleme

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

178 We conclude that rule learning sculpts frontal cortex interconnectivity and adjusts a thermosta

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

180 r, the effective connectivity of pathways to frontal cortex is poorly understood.

181 -pulse electrical stimulation of ipsilateral frontal cortex led to robust short-latency (<20 ms) inte

182 ciculus) and cortical gray matter (in medial frontal cortex, left insula, Heschl's gyrus, and cerebel

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

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

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

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

187 The frontal cortex matures late in development, showing dram

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

189 The frontal cortex may therefore balance consistency with fl

190 ssociation with cortical lesion count in the frontal cortex (mean [SD] thalamus volume, 8.89 [1.1] cm

191 The frontal cortex mediates cognitive control and motivation

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

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

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

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

196 The functional organization of human medial frontal cortex (MFC) is a subject of intense study.

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

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

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

200 sponsive regions to other brain areas (e.g., frontal cortex) might be altered, and (3) cortical regio

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

202 atal exposure to maternal immune activation, frontal cortex mRNA levels were also markedly elevated f

203 ated in multichannel recordings from primary frontal cortex networks, where the overall activity chan

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

205 udy quantified the changes in how rat medial frontal cortex neurons respond to the same actions when

206 In the present study, ensembles of medial frontal cortex neurons were recorded from rats trained t

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

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

209 Here we show that rTMS applied over the frontal cortex of awaken mice induces dopamine D2 recept

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

211 In frontal cortex of cases with hippocampal sclerosis of ag

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

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

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

215 ral activity in the somatosensory cortex and frontal cortex of head-fixed mice during locomotion.

216 on was also increased by 44% (p<0.02) in the frontal cortex of KLF11 wild-type mice (Klf11(+/+)) vs K

217 pregulation of mitochondria-related genes in frontal cortex of lithium-treated, IMPA1 and Slc5a3 KO m

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

219 e sites in the superior temporal and ventral frontal cortex of monkeys and use functional magnetic re

220 onal networks formed by primary cells of the frontal cortex of NMRI mice.

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

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

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

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

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

226 PET and amyloid histology was highest in the frontal cortex of transgenic mice (11C-PIB BPND: 0.93+/-

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

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

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

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

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

232 slated exon in hippocampus (P 1.3 x 10(-8)), frontal cortex (P 1.3 x 10(-9)) and temporal cortex (P1.

233 scription of alternatively spliced exon 3 in frontal cortex (P=9.2 x 10(-6)) and temporal cortex (P=2

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

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

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

237 Frontal cortex plays a central role in the control of vo

238 Human frontal cortex plays a crucial role in speech production

239 The posterior medial frontal cortex (pMFC), a key area for monitoring errors,

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

241 that the cingulate (Cg) region of the mouse frontal cortex powerfully influences sensory processing

242 ion conflict and activity in the dorsomedial frontal cortex (pre-SMA BOLD and mediofrontal theta in E

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 enhances content-specific representations in frontal cortex, presumably by a dopamine-mediated increa

246 hen distraction is likely, a region in right frontal cortex proactively implements attentional contro

247 hat a peri-choice signal generated in medial frontal cortex provides a source of input to this post-d

248 oral lobe and white matter connectivity with frontal cortex, respectively.

249 Spectral analyses of TMS-evoked responses in frontal cortex revealed non-linear changes in gamma band

250 The right inferior frontal cortex (rIFC) is specifically associated with at

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

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

253 idespread activation of forebrain, including frontal cortex, sensorimotor cortex, and striatum, and t

254 frontal, and parietal lobes and right medial-frontal cortex) showed lesser growth in diabetes, as did

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

256 t visual-biased attention regions in lateral frontal cortex, superior precentral sulcus (sPCS) and in

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

258 lation associations were also significant in frontal cortex, temporal cortex and pons: P ranging from

259 al cortex, medial prefrontal cortex, orbital frontal cortex, temporal cortex, and medial temporal lob

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

261 cingulate cortex, insula, caudate, putamen, frontal cortex, temporal cortex, and thalamus.

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

263 lt mode network and the second comprises the frontal cortex, thalamus, and caudate regions that are c

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

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

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

267 dense connections with areas of parietal and frontal cortex that were more widespread.

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

269 In frontal cortex the MAG:PLP1 ratio was significantly redu

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

271 nd-B retention was first noted in the medial frontal cortex, then the precuneus, lateral frontal and

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

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

274 We suggest that a pathway from the frontal cortex through the SCi operates in parallel with

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 f VT ranged from 0.82 mL cm(-3) in the right frontal cortex to 0.46 mL cm(-3) in the corpus callosum,

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

279 or the view that oscillatory activity in the frontal cortex underlies adaptive adjustments in cogniti

280 imultaneously across all layers of agranular frontal cortex using linear electrode arrays.

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

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

283 and laminar organization: hypoplasia of the frontal cortex, ventral expansion of the dorsomedial cor

284 s from their activation volumes to 1) medial frontal cortex via forceps minor and uncinate fasciculus

285 of connections to the bilateral ventromedial frontal cortex (via forceps minor and left uncinate fasc

286 ell of interest recently in the ventromedial frontal cortex (VMF), a brain region critical to associa

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

288 Furthermore, the left inferior frontal cortex was functionally connected with the intac

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

290 passing direct current through human medial-frontal cortex, we could enhance the event-related poten

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

292 tivity of auditory cortex to hippocampus and frontal cortex, which may be responsible for keeping suc

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

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

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

296 frontal control" hypothesis by "loading" the frontal cortex with an effortful working memory (WM) tas

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

298 ncy bands over lateral temporal and inferior frontal cortex, with an earlier latency for Hgamma than

299 egions of the human fetal brain, such as the frontal cortex, with marked enrichment for genes where c

300 or cingulate cortex/precuneus and the medial frontal cortex yielded optimal group separation and show