ライフサイエンスコーパス: prefrontal

1 drial gene expression are key players in the prefrontal adaptations observed in individuals with high

2 that specialized coordination in the medial prefrontal-amygdala network underlies social-decision pr

3 ted interactions of neuronal activity in the prefrontal-amygdala pathways critically contribute to so

4 pping MRI findings of a smaller structure in prefrontal and anterior cingulate cortex.

5 eta power suppression (13-22 Hz, ~350 ms) in prefrontal and auditory cortex.

6 Regions of the prefrontal and cingulate cortices play important roles i

7 mpaired hippocampal connectivity to multiple prefrontal and default mode network regions, and disrupt

8 indicated a very high level of similarity in prefrontal and hippocampal afferents but some difference

9 value distractors have different impacts on prefrontal and parietal regions, we designed a dual rout

10 sed to study structural connectivity between prefrontal and striatal regions as critical nodes for ac

11 s the existence of robust sex differences in prefrontal and striatal resting state networks that may

12 ble and less temporally precise responses in prefrontal and temporoparietal cortex; these higher-orde

13 paralimbic (cingulo-insular and ventromedial prefrontal), and cognitive control (ventrolateral prefro

14 oice, rather than on dorsolateral and medial prefrontal areas involved in several forms of cognitive

15 DBS lead, placement impacting fibers to left prefrontal areas should be avoided to maximize improveme

16 Dorsolateral and polar prefrontal areas that are associated with complex cognit

17 ontal), and cognitive control (ventrolateral prefrontal) areas, as well as in sensorimotor and visual

18 -0.01), by thickness of the left dorsomedial prefrontal (beta = -0.029; CI: -0.061 to -0.0047) and ar

19 trate the formation and use of a schema in a prefrontal brain region to support a complex cognitive o

20 tural and functional changes in striatal and prefrontal brain regions, among others.

21 stems in modulating working memory coding in prefrontal circuits.SIGNIFICANCE STATEMENT Ongoing delay

22 nd endocannabinoid modulation in hippocampal-prefrontal communication.

23 Smaller right dorsolateral prefrontal cortex (DLPFC) (i.e., middle and superior fro

24 bilateral thalami and the left dorsolateral prefrontal cortex (DLPFC) as our regions of interest, we

25 uR5 signaling in the postmortem dorsolateral prefrontal cortex (DLPFC) derived from 17 patients and a

26 dendritic spines in the primate dorsolateral prefrontal cortex (dlPFC) express the molecular machiner

27 active or sham rTMS to the left dorsolateral prefrontal cortex (dlPFC) for 20 consecutive weekdays.

28 and/or phosphorylation state in dorsolateral prefrontal cortex (DLPFC) from 22 pairs of SZ and matche

29 onal pathways were obtained for dorsolateral prefrontal cortex (DLPFC) gray matter and layer 3 and la

30 the role of the hippocampus and dorsolateral prefrontal cortex (dlPFC) in mediating such retrieval.

31 Dorsolateral prefrontal cortex (dlPFC) is associated with cognition,

32 tissue fractions obtained from dorsolateral prefrontal cortex (dlPFC) of 15 MDD and 15 matched non-p

33 ic overview of glutamate in the dorsolateral prefrontal cortex (DLPFC) of patients with schizophrenia

34 pression levels of these TFs in dorsolateral prefrontal cortex (DLPFC) of SCZ patients.

35 ivity (FC) between amygdala and dorsolateral prefrontal cortex (DLPFC), and had increased negative FC

36 Working memory relies on the dorsolateral prefrontal cortex (dlPFC), where microcircuits of pyrami

37 sion of 10 Hz rTMS to the right dorsolateral prefrontal cortex (dlPFC).

38 (HD-tDCS) to the left or right dorsolateral prefrontal cortex (DLPFC).

39 h channel count recordings in dorsal-lateral prefrontal cortex (dlPFC; 768 electrodes) while monkeys

40 r cingulate cortex (PCC) and the dorsomedial prefrontal cortex (DMPC).

41 ormation is represented in the dorsal medial prefrontal cortex (dmPFC) across excitatory and inhibito

42 ing between the amygdala and the dorsomedial prefrontal cortex (dmPFC) has been implicated in the gen

43 rtex, inferior frontal gyrus and dorsomedial prefrontal cortex (IFG, dmPFC).

44 Previous work has shown that the infralimbic prefrontal cortex (IL-PFC) is important for processing s

45 nsivity, with a prominent role of the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA)

46 involved in emotional regulation, the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA).

47 onal atrophy and synaptic loss in the medial prefrontal cortex (mPFC) and hippocampus.

48 omic and functional relay between the medial prefrontal cortex (mPFC) and the hippocampus (HPC).

49 ularity-based parcellation of the rat medial prefrontal cortex (mPFC) combined with seed-based connec

50 ally, gene expression analysis in the medial prefrontal cortex (mPFC) for a subset of genes previousl

51 rences in learned fear inhibition and medial prefrontal cortex (mPFC) function.

52 amatergic system and its receptors in medial prefrontal cortex (mPFC) has been implicated in major de

53 of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but their d

54 Using targeted medial prefrontal cortex (mPFC) infusions, these effects were l

55 Here, we demonstrated the medial prefrontal cortex (mPFC) is a site of learning-induced p

56 en the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC) is known to be necessary for no

57 ergic axon terminals arising from the medial prefrontal cortex (mPFC) to the dorsal raphe nucleus (DR

58 he orbitofrontal cortex (OFC) and the medial prefrontal cortex (mPFC), as mice learned olfactory asso

59 inhibitory neurons, especially in the medial prefrontal cortex (mPFC), have been found in different p

60 hase coupling between hippocampus and medial prefrontal cortex (mPFC).

61 ot glutamate principle neurons in the medial prefrontal cortex (mPFC).

62 is detrimental to proper functioning of the prefrontal cortex (PFC) and establishment of appropriate

63 OMER1), is significantly reduced in both the prefrontal cortex (PFC) and induced pluripotent stem cel

64 e mesocorticolimbic circuitry, including the prefrontal cortex (PFC) and mesolimbic dopamine (DA) pat

65 examine mitochondrial gene expression in the prefrontal cortex (PFC) and nucleus accumbens (NAc) of m

66 critical for learning and memory such as the prefrontal cortex (PFC) and the hippocampus (HPC).

67 r psychopathologies associated with amygdala-prefrontal cortex (PFC) circuits.

68 timulation (tDCS) to examine the role of the prefrontal cortex (PFC) in neural oscillatory activity a

69 The prefrontal cortex (PFC) integrates incoming information

70 multiple lines of evidence indicate that the prefrontal cortex (PFC) is particularly sensitive to, an

71 Modulation by the prefrontal cortex (PFC) is thought to be key for both pr

72 can jeopardize neuronal function and in the prefrontal cortex (PFC) it may contribute to compulsive

73 led in a single dish and differentiated into prefrontal cortex (PFC) lineages to efficiently test ear

74 mpus (vHipp,) basolateral amygdala (BLA) and prefrontal cortex (PFC) onto identified medium spiny neu

75 (Disc1-KD) in mature mouse astrocytes of the prefrontal cortex (PFC) or the hippocampus would produce

76 Interactions between the thalamus and prefrontal cortex (PFC) play a critical role in cognitiv

77 The prefrontal cortex (PFC) plays a critical role in curbing

78 e how specific transcriptomic types of mouse prefrontal cortex (PFC) projection neurons relate to axo

79 ntly demonstrated that carbachol delivery to prefrontal cortex (PFC) restored wakefulness despite con

80 The prefrontal cortex (PFC)'s functions are thought to inclu

81 ssure is associated with deactivation of the prefrontal cortex (PFC), an area important for executive

82 onal atrophy and synaptic loss in the medial prefrontal cortex (PFC), and this leads to behavioral an

83 ssion and reduced PV expression in the adult prefrontal cortex (PFC), contributing to a behavioral ph

84 Prefrontal cortex (PFC), hippocampus (HPC), and spleen w

85 In the prefrontal cortex (PFC), PV expression appears last and

86 tween the hippocampus and right dorsolateral prefrontal cortex (PFC), which in turn was negatively co

87 ittent alcohol drinking resulted in enhanced prefrontal cortex (PFC)-driven excitation of prodynorphi

88 eract with activity-silent mechanisms in the prefrontal cortex (PFC).

89 ylation and decreased levels of HDAC6 in the prefrontal cortex (PFC).

90 ons exist, we implanted eight Utah arrays in prefrontal cortex (PFC; area 46) of two male macaque mon

91 e mouse basolateral amygdala (BLA)-prelimbic prefrontal cortex (plPFC) circuit is engaged by stress a

92 tor (CB1R)-mediated actions in the prelimbic prefrontal cortex (PrL-PFC).

93 The rostromedial prefrontal cortex (rmPFC) is an important brain region t

94 sporter gene expression in the ventrolateral prefrontal cortex (vlPFC) and most strongly in the amygd

95 specifically within the right ventrolateral prefrontal cortex (vlPFC) and most strongly in the right

96 ders exhibited greater amygdala-ventromedial prefrontal cortex (vmPFC) connectivity when processing t

97 The role of the ventromedial prefrontal cortex (vmPFC) in human pavlovian threat cond

98 terior cingulate cortex (dACC), ventromedial prefrontal cortex (VMPFC), and intraparietal sulcus (IPS

99 itically on the hippocampus and ventromedial prefrontal cortex (vmPFC), but their respective roles ar

100 egions, orbitofrontal (OFC) and ventromedial prefrontal cortex (vmPFC), during two-option choice with

101 ations of belief uncertainty in ventromedial prefrontal cortex (vmPFC).

102 is reflected in a medial-lateral division of prefrontal cortex - with lateral frontal pole (FPl) supp

103 DD consented to receive MST applied over the prefrontal cortex according to an open-label protocol.

104 as increased basal extracellular dopamine in prefrontal cortex and 5-hydroxytryptamine in hippocampus

105 ands designed to drive theta oscillations in prefrontal cortex and alpha oscillations in parietal cor

106 tal gyrus and a dissociation in the anterior prefrontal cortex and anterior insula.

107 s between anterior cingulate cortex, lateral prefrontal cortex and anterior striatum.

108 ed effective connectivity between the medial prefrontal cortex and basal ganglia related to depressio

109 urface area (SA) in dorsolateral/dorsomedial prefrontal cortex and caudal anterior cingulate cortex w

110 tainty is represented in right rostrolateral prefrontal cortex and drives directed exploration, while

111 rtainty is represented in right dorsolateral prefrontal cortex and drives random exploration.

112 eft orbitofrontal cortex, right ventromedial prefrontal cortex and left ventral striatum.

113 ast, boundary-evoked responses in the medial prefrontal cortex and middle temporal gyrus increase acr

114 etween transcriptional alterations in medial prefrontal cortex and nucleus accumbens in human MDD and

115 , we found that activity within ventromedial prefrontal cortex and precuneus was additionally modulat

116 bunits permit rapid cholinergic responses in prefrontal cortex and protect these responses from desen

117 The prefrontal cortex and striatum form a recurrent network

118 showed lower nodal centrality metrics in the prefrontal cortex and subcortical regions, and higher no

119 connectivity between the right dorsolateral prefrontal cortex and the parietal cortex in non-relapse

120 y involved in spatial navigation: the medial prefrontal cortex and the right entorhinal cortex (EHC).

121 oupling of HFO bursts were also found in the prefrontal cortex and ventral striatum which, although o

122 Neural variability modulation through prefrontal cortex appears instrumental for permitting an

123 we put forward the idea that alterations in prefrontal cortex architecture and function, which are i

124 shown that higher-order regions such as the prefrontal cortex are critical to attentional processing

125 e fMRI pattern analysis revealed the lateral prefrontal cortex as the only region that encodes predom

126 We show that fast rhythmic activity in the prefrontal cortex becomes prominent during the second po

127 selective reductions of salience signals in prefrontal cortex but also diminished the influence of s

128 s review uses the example of amygdala-medial prefrontal cortex circuitry development to illustrate a

129 and findings that tDCS administration to the prefrontal cortex during task training may be an effecti

130 prefrontal cortex function makes the primate prefrontal cortex especially vulnerable to off-target ef

131 We find that neurons of the human prefrontal cortex exhibit hemispheric differences in DNA

132 ne cell markers were measured by qPCR in the prefrontal cortex from 37 people with schizophrenia/schi

133 eculate that the unique neuropharmacology of prefrontal cortex function makes the primate prefrontal

134 we investigated the lipidome composition of prefrontal cortex gray matter in 396 cognitively healthy

135 ial secondary motor subregions of the medial prefrontal cortex have heterogeneous responses to stress

136 rformed proteomic sequencing of dorsolateral prefrontal cortex in 438 older individuals and found ass

137 s from auditory cortex in standard trials to prefrontal cortex in deviant trials.

138 A core discovery concerns the role of the prefrontal cortex in exerting top-down control over mnem

139 s have been extensively studied in the adult prefrontal cortex in the context of cognitive (dys)funct

140 ironmental sequences are stored in the human prefrontal cortex in the form of structured event comple

141 f endocannabinoid signaling in the prelimbic prefrontal cortex is a core neurobiological substrate fo

142 The lateral prefrontal cortex is involved in the integration of mult

143 ANCE STATEMENT A developmental disruption of prefrontal cortex maturation has been implicated in the

144 provides a fundamental framework for how the prefrontal cortex may handle the abundance of schemas ne

145 rmore, connectivity between the amygdala and prefrontal cortex mediated the relationship between mate

146 gated in parallel to reveal their effects on prefrontal cortex neurogenesis.

147 try by profiling DNA methylation in isolated prefrontal cortex neurons from control and PD brain hemi

148 monstrate that overexpression of C4 in mouse prefrontal cortex neurons leads to perturbations in dend

149 eaning leads to a failure to activate medial prefrontal cortex neurons projecting to the posterior pa

150 UD by using RNA sequencing of dorsal-lateral prefrontal cortex neurons.

151 und to alter in expression within the medial prefrontal cortex of FKBP5 knockout mice were selected.

152 collecting neural activity in dorsal-lateral prefrontal cortex of macaques using eight microelectrode

153 Indeed, VS decreased ACh release in the prefrontal cortex of male rats.

154 ENT The hippocampal formation and the medial prefrontal cortex of mammals represent the surrounding p

155 rinsically bursting pyramidal neurons in the prefrontal cortex of mice.

156 Here, we show that the lateral prefrontal cortex of non-human primates contains two min

157 sion on a retention test in the ventromedial prefrontal cortex of rats trained in contextual fear con

158 choice-related activity before dorsolateral prefrontal cortex or the amygdala.

159 T interneuron-evoked disinhibition of medial prefrontal cortex output neurons and recruitment of remo

160 ial-affective brain regions, with the medial prefrontal cortex playing a central role in the integrat

161 These results suggest that the lateral prefrontal cortex plays a key role in inferring and maki

162 cortex, temporoparietal junction, and medial prefrontal cortex promotes honesty, particularly in indi

163 nced excitatory glutamatergic input to mouse prefrontal cortex pyramidal cells, leading to antidepres

164 s after stimulation of the left dorsolateral prefrontal cortex resulted in faster task performance in

165 photoactivation of SNAP-mGluR2 in the medial prefrontal cortex reversibly modulates working memory in

166 We acquired dorsolateral/medial prefrontal cortex samples from individuals with Alzheime

167 0 and GHRH agonist MR-409, on isolated mouse prefrontal cortex specimens treated with lipopolysacchar

168 euronal timescales are functionally dynamic: prefrontal cortex timescales expand during working memor

169 Second, event-related directed medial prefrontal cortex to basal ganglia effective connectivit

170 effect of glutamatergic projections from the prefrontal cortex to the nucleus accumbens has been argu

171 et and thus positioned the TMS coil over the prefrontal cortex using scalp measurements.

172 layer II/III pyramidal neurons of the medial prefrontal cortex via CXCR4-dependent stimulation of the

173 structure-function coupling in rostrolateral prefrontal cortex was associated with executive performa

174 Seeds in the amygdala and dorsolateral prefrontal cortex were explored.

175 of others' opinions in the posterior medial prefrontal cortex when opinions are disconfirming.

176 stral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expressed context-depend

177 ion of non-VIP ChAT(+) neurons in the medial prefrontal cortex with a distinct developmental origin t

178 ginal gyrus in IPL links decision regions in prefrontal cortex with premotor regions, where the motor

179 hronization of confidence representations in prefrontal cortex with reward prediction errors in basal

180 ncorporates hierarchical gating to model the prefrontal cortex's ability to flexibly encode and use m

181 at are important for valuation (ventromedial prefrontal cortex) and positive reinforcement-related pr

182 endothelial cells) cells of cortical (medial prefrontal cortex) and subcortical (hippocampus) brain r

183 al regions (somatosensory, visual, motor and prefrontal cortex) to assess the generalizability of the

184 n regions (amygdala, anterior cingulate, and prefrontal cortex).

185 or deficits, elevated synaptic inhibition in prefrontal cortex, abnormal baseline and social interact

186 as (posterior cingulate cortex, ventromedial prefrontal cortex, and anterior cingulate cortex) and de

187 icrodialysis in nucleus accumbens and medial prefrontal cortex, and ex vivo striatal dopamine reuptak

188 ons (anterior cingulate cortex, dorsolateral prefrontal cortex, and primary visual cortex) in human p

189 eted on the posteromedial cortex, the medial prefrontal cortex, and the cingulum.

190 des inferior parietal cortex, dorsal lateral prefrontal cortex, and the dorsal striatum, has minimal

191 dorsal anterior cingulate, the dorsolateral prefrontal cortex, and the lateral orbitofrontal cortex,

192 , that includes the amygdala, ventral medial prefrontal cortex, and ventral striatum, has substantial

193 ncy at which they synchronize across lateral prefrontal cortex, anterior cingulate cortex and anterio

194 ious perception, including some areas in the prefrontal cortex, appear to be primarily predictive of

195 ce in several key regions, namely the medial prefrontal cortex, basolateral amygdala, hippocampus, an

196 o when infused locally into the ventromedial prefrontal cortex, basolateral amygdala, or hippocampal

197 the periphery, and also in the amygdala and prefrontal cortex, brain structures critically involved

198 context cues evolves over time in the medial prefrontal cortex, but not in animals that cannot form n

199 subjective valuation, including ventromedial prefrontal cortex, correlated with both higher social re

200 l-projecting cerebellar lobules and anterior prefrontal cortex, forming circuits that seem to be uniq

201 ation of its human homolog, the ventromedial prefrontal cortex, has been implicated in suppressing av

202 Neural ensembles in prefrontal cortex, hippocampus, and simulated neural net

203 d activity within the major divisions of the prefrontal cortex, including orbitofrontal, ventrolatera

204 uided direction comparisons, area MT and the prefrontal cortex, revealing their likely interactions d

205 ctivity from visual area V4, as well as from prefrontal cortex, slowly drifted together with these be

206 ular redox status, are reduced in the medial prefrontal cortex, striatum, and thalamus in schizophren

207 es were associated with higher volume of the prefrontal cortex, temporal cortex, and medial orbitofro

208 signal, was represented in the ventrolateral prefrontal cortex, temporoparietal junction, and rostral

209 evel-dependent responses in the ventromedial prefrontal cortex, the dorsal anterior cingulate, the do

210 on signals in the insula, temporal lobe, and prefrontal cortex, while DA depletion affected social re

211 atients displayed significantly lower medial prefrontal cortex-posteromedial cortex functional connec

212 The machine learning medial prefrontal cortex-posteromedial cortex multimodal classi

213 o myelinating oligodendrocytes in the medial prefrontal cortex.

214 r-alpha and interleukin-6 gene expression in prefrontal cortex.

215 n responses of the striatum and ventromedial prefrontal cortex.

216 modulation of corticothalamic neurons in the prefrontal cortex.

217 A levels in the nucleus accumbens and medial prefrontal cortex.

218 ession information from the developing human prefrontal cortex.

219 organization of cognitive control within the prefrontal cortex.

220 en the cmA and the precuneus and dorsomedial prefrontal cortex.

221 nderlies remote memory storage in the medial prefrontal cortex.

222 aptic alterations in a microcircuit model of prefrontal cortex.

223 ganglia and other regions such as the medial prefrontal cortex.

224 the amygdala, hypothalamus and dorsolateral prefrontal cortex.

225 loop that links the PVT and the ventromedial prefrontal cortex.

226 connectivity between sgACC and dorsolateral prefrontal cortex.

227 rea 12 [12o]), cingulate cortex, and lateral prefrontal cortex.

228 ocial reward prediction encoding only in the prefrontal cortex.

229 an organizational structure that mirrors the prefrontal cortex.

230 creased calbindin-positive neuron density in prefrontal cortex.

231 participants and each agent recruited medial prefrontal cortex/pregenual anterior cingulate (pgACC).

232 inferior parietal lobule, left dorsolateral prefrontal cortex/superior frontal gyrus, and left media

233 for disorganized schizotypy, also in medial prefrontal cortex; all false discovery rate-corrected ps

234 Exaggerated prefrontal cortical activity likely underpins the inflex

235 n part through an adaptive reorganization of prefrontal cortical activity.

236 sFC) to investigate the relationship between prefrontal cortical and striatal neural interactions, an

237 unctional imaging studies suggest a role for prefrontal cortical dopaminergic abnormalities in impair

238 Whereas higher levels of medial prefrontal cortical glutamate were associated with negat

239 y of midbrain dopamine neurons and of medial prefrontal cortical neurons.

240 ally plausible explanation of how a class of prefrontal cortical pyramidal neurons achieve efficient

241 comparison subjects and covaried with dorsal prefrontal cortical thickness; structure-response associ

242 Following a brief review of prefrontal cortical, anterior cingulate, and striatal co

243 nnectivity in orbitofrontal and ventromedial prefrontal cortical-striatal circuits-pathways criticall

244 ity of >100 neurons in the monkey visual and prefrontal cortices is comparable with or better than th

245 activation in anterior cingulate and lateral prefrontal cortices while they view socially relevant vi

246 correlated with electric fields strengths in prefrontal cortices, and no correlation was found on the

247 atory responses in visual and 'higher-order' prefrontal cortices.

248 N = 207; 57 active smokers) human postmortem prefrontal cortices.

249 transmission onto pyramidal neurons, disrupt prefrontal excitatory-inhibitory balance, and alter proc

250 lign with the relationship between disrupted prefrontal function and cognitive rigidity in AN patient

251 y, the data also suggest that the diminished prefrontal GABAergic function could arise from a deficit

252 aling during adolescence enables the gain of prefrontal GABAergic function, which is required for mai

253 cation at higher resolution, vHPC input onto prefrontal GABAergic interneurons was specifically disru

254 Here, we tested the hypothesis that prefrontal glutamate and GABA levels are reduced by FTLD

255 Critically, we found that prefrontal glutamate could be robustly and exclusively p

256 Our findings suggest that abnormal prefrontal-hippocampal circuit dynamics are candidate ne

257 hibited poor memory abilities and disordered prefrontal-hippocampal functional connectivity.

258 -frequency coupling in the PFC and HPC while prefrontal-hippocampal synchronization was strengthened,

259 eral regions in T2DM patients, including the prefrontal, hippocampus, amygdala, insular, cingulate, c

260 cal areas: somatosensory, visual, motor, and prefrontal (i.e., ventromedial orbitofrontal) cortex.

261 ions support a role for feedforward parietal-prefrontal information processing deficits in delusional

262 dividual variability in feedforward parietal-prefrontal information updating in patients with schizop

263 ntrol by increasing the efficacy of anterior prefrontal inhibition over the sensorimotor cortex.

264 essing, but far less is understood regarding prefrontal laterality differences in attention processin

265 otein levels were also associated with lower prefrontal-limbic TSPO availability and PTSD severity.

266 Ventromedial prefrontal myelin density, indexed by magnetisation tran

267 The delicate balance among primate prefrontal networks is necessary for homeostasis and beh

268 The anterior cingulate is a critical hub in prefrontal networks through connections with functionall

269 ssociated with hyperactivity in the amygdala-prefrontal networks, and normalization of this aberrant

270 The ongoing activity of prefrontal neurons after a stimulus has disappeared is c

271 IFICANCE STATEMENT Ongoing delay activity of prefrontal neurons constitutes a neuronal correlate of w

272 earch suggests that neural activity spanning prefrontal, parietal, temporal, and visual areas support

273 n male volunteers, resting EEG and TEPs from prefrontal (PFC) and parietal (PAR) cortex were measured

274 12, and 18-22 months old APP/PS1 mice in the prefrontal (PFC), somatosensory (SS2), and primary motor

275 Left prefrontal piTBS monotherapy is effective for the treatm

276 ode strength and/or degree values in several prefrontal, premotor and temporal regions, as well as st

277 Tissue samples were removed from prefrontal, primary motor, and primary visual cortices a

278 nsistent discrepancies additionally recruits prefrontal processes.

279 age regions of the striatum and connected to prefrontal-projecting cerebellar lobules and anterior pr

280 tory activities for reward processing in the prefrontal region during REM sleep, and inhibited neural

281 Cingulate and prefrontal regions did not fully replicate.

282 onditions is associated with deactivation of prefrontal regions important for attentional control, wo

283 (ventral value pathway; VVP), interface with prefrontal regions of the primate brain to guide value-b

284 tivation was found in the medial and lateral prefrontal regions, most pronounced during processing of

285 as the medial and lateral dorsal and ventral prefrontal regions.

286 ical volumes in PTSD patients are smaller in prefrontal regulatory regions, as well as in broader emo

287 " network, the ventral striatal/ventromedial prefrontal "reward" network, and the lateral orbitofront

288 DPX) Task), after receiving 20 min of active prefrontal stimulation at 2 mA or sham stimulation.

289 Treatments that target this functional prefrontal-striatal pathology could improve early treatm

290 cantly affected functional disruption of the prefrontal-striatal responses to stress images and to al

291 flected in the updating of brain activity in prefrontal-striatal-limbic circuits.

292 gher-level language processing, such as left prefrontal, superior and middle temporal areas, and ante

293 ronal or glial cytoplasmic inclusions in the prefrontal, temporal and cingulate cortices or the under

294 pleted two tasks known to elicit hippocampal-prefrontal theta coupling: a spatial memory task (during

295 lts causally establish dissociable roles for prefrontal theta oscillations and parietal alpha oscilla

296 n these settings, whereas another mechanism (prefrontal theta-band activity) is involved in exploitin

297 anied by white matter changes in the ventral prefrontal tract, although the integrity of the uncinate

298 endent cohorts of patients who received left prefrontal transcranial magnetic stimulation (TMS) for t

299 In study 2, this specific prefrontal-ventral striatal dysfunction was associated w

300 ning in human participants via plasticity in prefrontal white matter tracts and a colocalized increas