ライフサイエンスコーパス: prefrontal cortex

1 d nucleotide metabolic processes in the male prefrontal cortex.

2 GABAergic and glutamatergic signaling in the prefrontal cortex.

3 low in the ventral striatum and ventromedial prefrontal cortex.

4 s on pyramidal layer 5 neurons in the medial prefrontal cortex.

5 rol signal originating from the dorsolateral prefrontal cortex.

6 or processing in the ventral striatum by the prefrontal cortex.

7 e dorsal midbrain, and the left ventromedial prefrontal cortex.

8 and a higher gene expression level in human prefrontal cortex.

9 ue of infralimbic cortex in the ventromedial prefrontal cortex.

10 ian hormones increase inhibitory tone in the prefrontal cortex.

11 and inhibitory neurotransmission within the prefrontal cortex.

12 es observed in CA3, or the Fr2 region of the prefrontal cortex.

13 ns are distributed across subnetworks within prefrontal cortex.

14 in an overlapping region of the ventromedial prefrontal cortex.

15 , a process dependent on the hippocampus and prefrontal cortex.

16 ated by cortical thinning in the dorsomedial prefrontal cortex.

17 N parallels that between the hippocampus and prefrontal cortex.

18 companied by distinct modulation patterns in prefrontal cortex.

19 nclude the amygdala, hippocampus, and medial prefrontal cortex.

20 ork including the hippocampus and the medial prefrontal cortex.

21 sensory input or recurrent processing in the prefrontal cortex.

22 nfluence the development and function of the prefrontal cortex.

23 late, medial frontal gyrus, and dorsolateral prefrontal cortex.

24 nd restoration, in electrodes over the right prefrontal cortex.

25 ith attenuated acetylcholine (ACh) levels in prefrontal cortex.

26 imulation (tDCS) over the right dorsolateral prefrontal cortex.

27 ed using frozen tissue from the dorsolateral prefrontal cortex.

28 tivity to the left ventral and right rostral prefrontal cortex.

29 in cortical volume in bilateral dorsomedial prefrontal cortex.

30 r is higher in layers 2/superficial 3 of the prefrontal cortex.

31 A noradrenergic receptor (a2A-NAR) acting in prefrontal cortex.

32 with ventral and dorsal parts of the medial prefrontal cortex.

33 n areas, including the inferior temporal and prefrontal cortex [1-8].

34 This is especially relevant for the prefrontal cortex, abnormal connectivity of which is cen

35 Fos(-) non-ensembles.SIGNIFICANCE STATEMENT Prefrontal cortex activity plays a critical role in oper

36 In order to test whether the ventromedial prefrontal cortex activity related to choice values is i

37 rait anger positively modulated dorsolateral prefrontal cortex-amygdala coupling.

38 implicating dysregulated triangular sensory-prefrontal-cortex-amygdala circuitry: intrinsic sensory

39 ice-encoding pattern signals in parietal and prefrontal cortex and (ii) predicted by phasic, pupil-li

40 ects of trait anger on amygdala-dorsolateral prefrontal cortex and amygdala-lateral orbitofrontal cor

41 ions including the striatum, insula, lateral prefrontal cortex and anterior cingulate in response to

42 eed, and two connections (between the medial prefrontal cortex and both the right superior parietal l

43 Here, we stimulated cholinergic receptors in prefrontal cortex and examined its effects on neurons th

44 tion on DNA from 161 single neurons from the prefrontal cortex and hippocampus of 15 normal individua

45 l activation is elevated in the dorsolateral prefrontal cortex and hippocampus of untreated patients

46 the lateral prefrontal cortex (dorsolateral prefrontal cortex and inferior frontal gyrus), the media

47 lative to controls in the right dorsolateral prefrontal cortex and left hippocampus, along with cereb

48 network connectivity, including between the prefrontal cortex and limbic structures.

49 nvolving the caudate nucleus, insula, medial prefrontal cortex and other domain-specific regions was

50 ed with cortical thinning of the dorsomedial prefrontal cortex and posterior temporal cortex.

51 ns, with effort PEs expressed in dorsomedial prefrontal cortex and reward PEs in ventral striatum.

52 (decreased grey matter in right dorsolateral prefrontal cortex and right inferior temporal gyrus; inc

53 erative cues (primes), novices disengage the prefrontal cortex and seem to accept the observed operat

54 cantly increased DeltaFosB expression in the prefrontal cortex and striatum.

55 vant brain regions, such as the dorsolateral prefrontal cortex and the angular and cingulate gyri.

56 odulation of connectivity between the medial prefrontal cortex and the posterior cingulate cortex tha

57 ated functional connectivity between lateral prefrontal cortex and the profit-sensitive region of dor

58 connection (between the right ventrolateral prefrontal cortex and the right temporal-parietal juncti

59 efrontal cortex including dorsal and ventral prefrontal cortex and utilized a series of task paradigm

60 al hippocampus, dorsolateral and dorsomedial prefrontal cortex, and caudate nucleus.

61 er-responses to SS in the precentral cortex, prefrontal cortex, and default mode network and these br

62 WM volume bilaterally in orbital and medial prefrontal cortex, and greater GM volume in posterior th

63 the default mode network, left dorsolateral prefrontal cortex, and insula, and reduced connectivity

64 is network comprises the hippocampus, medial prefrontal cortex, and left angular gyrus, among other r

65 l regions, including the hippocampus, medial prefrontal cortex, and left angular gyrus.

66 s are mediated by the amygdala, ventromedial prefrontal cortex, and striatum.

67 sites included the brainstem, ventral medial prefrontal cortex, and superior temporal lobe, mostly on

68 rtex and inferior frontal gyrus), the medial prefrontal cortex, and the dorsal anterior cingulate cor

69 single TMS pulses to the right dorsolateral prefrontal cortex; and 4) greater ventromedial prefronta

70 ementary motor area, premotor, and the right prefrontal cortex are involved in vibrotactile WM coding

71 ssion of CYP11B2 and MR (NR3C2) genes in the prefrontal cortex area (PFC) and central nucleus of the

72 ing-state and choice-related activity of the prefrontal cortex as part of the general performance-mon

73 sed volume and thickness of the left lateral prefrontal cortex as well as increased thickness of the

74 abnormal activation was evident in the left prefrontal cortex as well as the anterior insula, the ri

75 cytoplasm of neurons and glial cells of the prefrontal cortex at 4 and 24 hours post-delivery, with

76 Increased ventromedial prefrontal cortex-bilateral inferior lateral parietal co

77 on-suicides (MDD, N=9) in the dorsal lateral prefrontal cortex (Brodmann Area 9) of sudden death medi

78 ne a specific neural projection by which the prefrontal cortex can control and adapt social behavior.

79 Removal of acetylcholine from prefrontal cortex can disrupt short-term memory performa

80 y-dependent synaptic plasticity in the mouse prefrontal cortex, characterized by a broader temporal w

81 d emotional-regulation brain regions (medial prefrontal cortex, cingulate cortex, and insula) and low

82 The involvement of the temporal pole-medial prefrontal cortex circuit in a model highly predictive o

83 hile abnormalities in a temporal pole-medial prefrontal cortex circuit might speak to the social-emot

84 results support the hypothesis that a mature prefrontal cortex competes with implicit learning of wor

85 s did more positive amygdala-to-ventromedial prefrontal cortex connectivity.

86 d that neuronal activity in the dorsolateral prefrontal cortex conveyed the necessary information for

87 tion of gray matter density in ventrolateral prefrontal cortex correlates tightly with irrational beh

88 tion of gray matter density in ventrolateral prefrontal cortex correlates with economic irrationality

89 e anterior cingulate cortex and ventromedial prefrontal cortex could provide more targeted therapies

90 ting emotional behaviors, and dysfunction of prefrontal cortex-dependent networks has been broadly im

91 buted to deficient inhibitory control by the prefrontal cortex, difficulty in controlling intrusive t

92 Hz oscillatory signature, with BLA-->medial prefrontal cortex directionality signaling the recurrenc

93 KEY POINTS: Layer 2/3 neurons of the prefrontal cortex display higher gain of somatic excitab

94 genes and 20 immune pathways in dorsolateral prefrontal cortex (DLPFC) (144 schizophrenia and 196 con

95 neural circuitry including the dorsolateral prefrontal cortex (DLPFC) and appear to arise during the

96 layer 3 pyramidal cells in the dorsolateral prefrontal cortex (DLPFC) appears to contribute to cogni

97 el-dependent (BOLD) signal, and dorsolateral prefrontal cortex (DLPFC) glutamate+glutamine (Glx) were

98 vo, in brain-expressed genes of dorsolateral prefrontal cortex (DLPFC) neurons.

99 nt for credit assignment in the dorsolateral prefrontal cortex (dlPFC) of two male rhesus macaques pe

100 The primate dorsolateral prefrontal cortex (dlPFC) subserves top-down regulation

101 neural circuitry in the primate dorsolateral prefrontal cortex (DLPFC) supports a range of cognitive

102 ain factors (amygdala, pACC and dorsolateral prefrontal cortex (DLPFC)) to test the effects of forest

103 rior parietal lobule, bilateral dorsolateral prefrontal cortex (DLPFC), and bilateral middle temporal

104 ally involve dysfunction of the dorsolateral prefrontal cortex (dlPFC), but there are few treatments

105 3 (L3) and layer 5 (L5) of the dorsolateral prefrontal cortex (DLPFC), we sought to determine if tra

106 lity is mainly subserved by the dorsolateral prefrontal cortex (DLPFC).

107 with the expression of GAD25 in dorsolateral prefrontal cortex (DLPFC).

108 ociated with dysfunction of the dorsolateral prefrontal cortex (DLPFC).

109 9 residue (H3K9me1), in the rat dorsomedial prefrontal cortex (dmPFC).

110 elevant information)], that span the lateral prefrontal cortex (dorsolateral prefrontal cortex and in

111 oes not alter synaptic strength in the mouse prefrontal cortex during an early period of withdrawal,

112 t correlation with activation in dorsomedial prefrontal cortex during goal-directed acquisition of st

113 fferences localized to the left dorsolateral prefrontal cortex during response selection and the post

114 ly, [oxy-Hb] change in the left dorsolateral prefrontal cortex during SAT showed a positive correlati

115 analysis revealed that anterior dorsomedial prefrontal cortex encoded inferences about action-values

116 Lateral prefrontal cortex encoded profit gained from harming oth

117 These results suggest that the prefrontal cortex encodes individually unique components

118 cortical sources in sensorimotor and medial prefrontal cortex even distinguished between predicted f

119 d primates and find that great ape and human prefrontal cortex expansion are non-allometrically deriv

120 n and activity, as well as AP levels, in the prefrontal cortex; furthermore, finasteride (10-100 mg/k

121 A recent study suggests that the prefrontal cortex gradually becomes critical as a storag

122 as in the healthy control group, the medial prefrontal cortex had a "hyperregulatory" effect on the

123 ugh the prelimbic cortex (PL, part of medial prefrontal cortex) has been implicated in social behavio

124 of the adolescent mouse forebrain (striatum, prefrontal cortex, hippocampus, amygdala, and bed nucleu

125 cingulate cortex [sgACC], left dorsolateral prefrontal cortex, hippocampus, and basolateral amygdala

126 on, infusing CPP into the infralimbic medial prefrontal cortex (IL-mPFC), a structure implicated in e

127 vation of mGlu5 receptors in the infralimbic prefrontal cortex (IL-PFC) facilitates learning during e

128 spective roles of the left and right lateral prefrontal cortex in active thought.

129 ght of the well-known functional role of the prefrontal cortex in cognition and memory?

130 al cortex (often referred to as ventromedial prefrontal cortex in humans; vmPFC/mOFC) is involved in

131 icular, numerous studies have implicated the prefrontal cortex in the control of social behavior, but

132 provide support for the role of the lateral prefrontal cortex in understanding others' emotions, by

133 ral and EEG study, we focused on the lateral prefrontal cortex including dorsal and ventral prefronta

134 and structure in the rostral and dorsomedial prefrontal cortex including the anterior cingulate.

135 =2.2 x 10(-8)) with epigenetic ageing of the prefrontal cortex, independent of the proportion of neur

136 ation tests: the left anterior ventrolateral prefrontal cortex/insula, the dorsal midbrain, and the l

137 g animal training.SIGNIFICANCE STATEMENT The prefrontal cortex is a brain region believed to support

138 The prefrontal cortex is a critical neuroanatomical hub for

139 Thus, dorsomedial prefrontal cortex is a crucial component of the short-te

140 epresentation of task-related information in prefrontal cortex is individually unique and preserved a

141 The prefrontal cortex is responsible for higher order cognit

142 CANCE STATEMENT A core function of the human prefrontal cortex is to control the signal flow in senso

143 measured by 1H MRS in the left dorsolateral prefrontal cortex (l-DLPFC) and bilateral hippocampal re

144 f a greater density of CB+ ChC cartridges in prefrontal cortex layer 2 from schizophrenia subjects su

145 ively in LC neurons with spinal (LC(:SC)) or prefrontal cortex (LC(:PFC)) projections.

146 d that patterns of activation in the lateral prefrontal cortex (LPFC) as well as in face-selective ar

147 The lateral prefrontal cortex (LPFC) is essential for higher-level c

148 The lateral prefrontal cortex (lPFC) of primates is hypothesized to

149 The lateral prefrontal cortex (LPFC) plays a central role in the pri

150 edial frontal cortex (MFC) and right lateral prefrontal cortex (lPFC) synchronized theta ( approximat

151 nclude the nucleus accumbens (NAcc), lateral prefrontal cortex (LPFC), insula, subgenual anterior cin

152 New findings also indicate that the prefrontal cortex may play an equally important role in

153 In particular, activity in the prefrontal cortex mediated the effect of value on nocebo

154 In addition to the hippocampus and prefrontal cortex, mice subjected to ELS exhibit increas

155 the female-specific hub gene Dusp6 in mouse prefrontal cortex mimicked stress susceptibility in fema

156 Prefrontal cortex modulates sensory signals in extrastri

157 A brain network comprising the medial prefrontal cortex (mPFC) and amygdala plays important ro

158 olescence decreased n-3 PUFAs in both medial prefrontal cortex (mPFC) and nucleus accumbens, increase

159 enter (PMC), locus coeruleus (LC) and medial prefrontal cortex (mPFC) during cystometry in unanesthet

160 Brain activity in medial prefrontal cortex (MPFC) during exposure to persuasive m

161 receptor is an important modulator of medial prefrontal cortex (mPFC) functions, such as the working

162 In humans and rodents, the medial prefrontal cortex (mPFC) has been implicated in suppress

163 Dysfunction of the medial prefrontal cortex (mPFC) has been linked to the cognitiv

164 gamma-aminobutyric acid (GABA) in the medial prefrontal cortex (mPFC) have been reported in antipsych

165 t reduced cholinergic transmission in medial prefrontal cortex (mPFC) impaired appetitive trace condi

166 disrupts the columnar organization of medial prefrontal cortex (mPFC) in a transcription- and activit

167 coupling between the hippocampus and medial prefrontal cortex (mPFC) is augmented in a genetic mouse

168 ither the infralimbic division of the medial prefrontal cortex (mPFC) or the basolateral amygdala (BL

169 ntributions of two direct hippocampal-medial prefrontal cortex (mPFC) pathways, one arising in the do

170 opaminergic pathway projecting to the medial prefrontal cortex (mPFC) suppresses stress susceptibilit

171 athic pain.SIGNIFICANCE STATEMENT The medial prefrontal cortex (mPFC) undergoes major reorganization

172 d neural activity in the hippocampus, medial prefrontal cortex (mPFC), and amygdala.

173 showed decreased TAAR1 levels in the medial prefrontal cortex (mPFC), and RO5256390 microinfused int

174 expression studies both implicate the medial prefrontal cortex (mPFC), particularly deep-layer projec

175 cumbens (NAcc), the amygdala, and the medial prefrontal cortex (mPFC), which form an intrinsic networ

176 in decreased 5HTergic innervation of medial prefrontal cortex (mPFC).

177 rinsic functional connectivity in the medial prefrontal cortex (mPFC).

178 nterior cingulate cortex (sgACC), and medial prefrontal cortex (mPFC).

179 telencephalic structures such as the medial prefrontal cortex (mPFC).

180 e interaction effect was found in the medial prefrontal cortex (mPFC)/anterior cingulate cortex (ACC)

181 iginated limbic structures (e.g., the medial prefrontal cortex [mPFC]), and the VLS receives inputs f

182 between a core 'self network' (e.g., medial prefrontal cortex; mPFC), a cognitive control network [e

183 We find that ensembles of dorsomedial prefrontal cortex neurons differentiate between expected

184 ing, we found that L2/3 pyramidal neurons in prefrontal cortex of fmr1(-/y) mouse fired more action p

185 rrent stimulation over the left dorsolateral prefrontal cortex of human participants [n = 70, 45 fema

186 similar Npas4 downregulation occurred in the prefrontal cortex of human patients with schizophrenia.

187 ry has been the nature of differences in the prefrontal cortex of humans versus other animals [1].

188 transcriptional abnormalities in the medial prefrontal cortex of immune-challenged and control offsp

189 d that differentially expressed genes in the prefrontal cortex of individuals with Alzheimer disease

190 both GMV and NAA/Cr in the left dorsolateral prefrontal cortex of patients with CFS.

191 egulation of serotonin signalling within the prefrontal cortex of Phf8 deficient mice and identify th

192 y suggests that the influence of the FEF and prefrontal cortex on attentional modulation of cortical

193 The exaggerated influence of the medial prefrontal cortex on the posterior cingulate cortex in d

194 cipal pyramidal neurons of the orbitofrontal prefrontal cortex (oPFC) were also imaged and enumerated

195 tion, voluntary switching did not engage the prefrontal cortex or elicit behavioral switch costs.

196 ine affecting neural processing in striatum, prefrontal cortex, or both.

197 ith smaller nonsignificant elevations in the prefrontal cortex (p = .342, Cohen's d = 0.38) and insul

198 ynaptic plasticity in the hippocampal-medial prefrontal cortex pathway.

199 rking memory have focused on the key role of prefrontal cortex (PFC) [1-8].

200 omic and metabonomic profiling approaches on prefrontal cortex (PFC) and hippocampal (HPC) tissue fro

201 Acetylcholine is released in the prefrontal cortex (PFC) and is a key modulator of cognit

202 The amygdala and prefrontal cortex (PFC) appear to have critical roles in

203 ncentrations of kynurenic acid (KYNA) in the prefrontal cortex (PFC) are thought to contribute to the

204 TATEMENT Dopamine D2 receptors (D2Rs) in the prefrontal cortex (PFC) are thought to play important ro

205 verexpressed the NMDAR GluN2D subunit in the prefrontal cortex (PFC) as compared to ANAs while the tw

206 MDD group showed reduced GBCr in the prefrontal cortex (PFC) but increased GBCr in the poster

207 ific, with the 5-HT4 receptor upregulated in prefrontal cortex (PFC) but not striatum or hippocampus

208 Is activity in prefrontal cortex (PFC) critical for conscious perceptio

209 usceptibility to psychopathologies involving prefrontal cortex (PFC) dysfunction.

210 n making by recording intraoperative STN and prefrontal cortex (PFC) electrophysiology as participant

211 n of 5-HT to Rac1) are observed in the mouse prefrontal cortex (PFC) following chronic exposure to st

212 Dopaminergic input to the prefrontal cortex (PFC) increases throughout adolescence

213 The prefrontal cortex (PFC) is crucial for accurate memory p

214 The prefrontal cortex (PFC) is thought to flexibly regulate

215 Here, we report that microstimulation in the prefrontal cortex (PFC) modulates the gain of the PLR, c

216 l glutamatergic (NMDA and AMPA) responses in prefrontal cortex (PFC) neurons and used pharmacological

217 or-mediated deletion of cacna1c in the adult prefrontal cortex (PFC) of mice recapitulates the antide

218 ral intraparietal area (VIP) and the lateral prefrontal cortex (PFC) of rhesus monkeys.

219 ently unknown whether dopaminergic inputs to prefrontal cortex (PFC) play similar or distinct roles.

220 dependent (BOLD) signals in the ventromedial prefrontal cortex (PFC) tracked the latent growth of cum

221 The prefrontal cortex (PFC) underlies higher cognitive proce

222 (MD) shares reciprocal connectivity with the prefrontal cortex (PFC), and decreased MD-PFC connectivi

223 rapidly activates the mTORC1 pathway in the prefrontal cortex (PFC), and that infusion of the select

224 tidepressant response and nonresponse in the prefrontal cortex (PFC), nucleus accumbens, hippocampus,

225 In the prefrontal cortex (PFC), PV(+) neuron activity is involv

226 entropy under isoflurane in area V1 and the prefrontal cortex (PFC)-as predicted by our alternative

227 ressed throughout limbic circuits, including prefrontal cortex (PFC).

228 n of prediction error processing through the prefrontal cortex (PFC).

229 ollowing, are thought to be supported by the prefrontal cortex (PFC).

230 is restricted to the brain, particularly the prefrontal cortex (PFC).

231 ted in neuropsychiatric disorders, including prefrontal cortex (PFC).

232 regulating glutamatergic function within the prefrontal cortex (PFC).

233 The prefrontal cortex plays a critical role in regulating em

234 The medial prefrontal cortex plays a key role in higher order cogni

235 reatment) acts directly within the prelimbic prefrontal cortex (PrL-PFC) to potentiate reinstatement.

236 ersive learning, while an independent medial prefrontal cortex-projecting ensemble extinguished avers

237 about the dialog between the hippocampus and prefrontal cortex provide new insights into the operatio

238 the amplitude of NMDA EPSCs in mouse layer 5 prefrontal cortex pyramidal neurons without affecting AM

239 Greater caudate and medial prefrontal cortex reactivity to gain outcomes and increa

240 lesions that included the same ventromedial prefrontal cortex region disrupted normal subjective eva

241 ontal gyrus, or via damage to dorsal lateral prefrontal cortex regions, resulting in deteriorated per

242 brain) and prefrontal cortical (dorsolateral prefrontal cortex) regions during reward anticipation at

243 hosphorylation of key phosphoproteins in the prefrontal cortex related to synaptic plasticity.

244 disrupts inhibition of striatal circuits by prefrontal cortex, rendering animals insensitive to pote

245 eural patterns in the hippocampus and medial prefrontal cortex represented the featural overlap acros

246 iven expression of progranulin in the medial prefrontal cortex reverses social dominance deficits in

247 at 5-weeks, as was decreased parahippocampal-prefrontal cortex RSFC.

248 dissociation between the right ventrolateral prefrontal cortex (rVLPFC) and the bi-lateral frontal ey

249 provide experimental evidence that the human prefrontal cortex's activity is consistent with a Bayesi

250 (CLP), and serum and brain (hippocampus and prefrontal cortex) samples were obtained at days 1, 15,

251 Here we investigate prefrontal cortex scaling across anthropoid primates and

252 alized streamlines in the right dorsolateral prefrontal cortex-sensorimotor striatum negatively corre

253 ticular focus on sex differences, the medial prefrontal cortex, social reward, social isolation, and

254 icits are associated with dysfunction in the prefrontal cortex, striatum, and amygdala.

255 representing tissue from four brain regions (prefrontal cortex, striatum, hippocampus and cerebellum)

256 to reveal relationships between ventromedial prefrontal cortex structure and multi-informant measures

257 d neural activity in the rat hippocampus and prefrontal cortex, structures critical for memory proces

258 Human prefrontal cortex supports goal-directed behavior by rep

259 transient increases in synaptic strength at prefrontal cortex synapses in the nucleus accumbens.

260 diction is characterized by abnormalities in prefrontal cortex that are thought to allow drug-associa

261 ork centered in the medial and ventrolateral prefrontal cortex that is exclusively engaged in social

262 nhanced the firing of neurons in the primate prefrontal cortex that subserve top-down attentional con

263 etics to map a functional gradient in rodent prefrontal cortex that supports inhibitory control.

264 OTR-expressing VTA neurons project to NAc, prefrontal cortex, the extended amygdala, and other fore

265 d 3 to 7 years; volume of a subregion of the prefrontal cortex, the inferior frontal gyrus, in childr

266 , including the dorsomedial and dorsolateral prefrontal cortex, the intraparietal sulcus, and the ant

267 the anterior insula, the right ventrolateral prefrontal cortex, the right intraparietal sulcus, and t

268 ted by connectivity between the striatum and prefrontal cortex; this connectivity selectively increas

269 Prefrontal cortex tissue sections from 20 matched pairs

270 e activity of associative inputs from medial prefrontal cortex to dorsomedial striatum and sensorimot

271 ng, how a functional circuit from the medial prefrontal cortex to nucleus accumbens is dynamically mo

272 bution of neural projections from the medial prefrontal cortex to the dorsal periaqueductal gray, a b

273 ificant interaction effect indicating higher prefrontal cortex uptake in apolipoprotein E (APOE) epsi

274 n dendrites in Brodmann area 46 dorsolateral prefrontal cortex using the Golgi-Cox technique in 12 ag

275 ween PE and activity within the ventromedial prefrontal cortex, ventral striatum, and other structure

276 rts downstream influence on the ventromedial prefrontal cortex/ventral striatum.

277 s, which exhibit enhanced PAC, interact with prefrontal cortex via enhanced low-frequency phase synch

278 emonstrate that neurons in the ventrolateral prefrontal cortex (vlPFC) of monkeys performing a shape

279 bitofrontal cortex (antOFC) or ventrolateral prefrontal cortex (vlPFC).

280 tivity between hippocampus and ventrolateral prefrontal cortex (vlPFC).

281 oup had lower activation of the ventromedial prefrontal cortex (vmPFC) during extinction recall (etap

282 region and general value coding ventromedial prefrontal cortex (vmPFC) predicted choice behavior.

283 OFC and general value coding in ventromedial prefrontal cortex (vmPFC) predicted individual differenc

284 have provided evidence that the ventromedial prefrontal cortex (vmPFC) signals the satisfaction we ex

285 t anticipatory value signals in ventromedial prefrontal cortex (vmPFC) were attenuated in older adult

286 d with activity patterns in the ventromedial prefrontal cortex (vmPFC), a key node in the brain's val

287 n within areas 25 and 32 of the ventromedial prefrontal cortex (vmPFC), but a causal relationship bet

288 The ventromedial prefrontal cortex (vmPFC), insula, amygdala, hypothalamu

289 gulation of emotions, including ventromedial prefrontal cortex (vmPFC), posteromedial cortex (PMC), h

290 rors co-varied with activity in ventromedial prefrontal cortex (vmPFC).

291 l connectivity between NAcc and ventromedial prefrontal cortex (vmPFC).

292 ural correlates of value within ventromedial prefrontal cortex (vmPFC).

293 pathways connecting the amygdala and ventral prefrontal cortex (vPFC) are linked with trait anxiety,

294 isual cortex and highest in the dorsolateral prefrontal cortex, whereas the GABA measure showed the o

295 d significant activation of the dorsolateral prefrontal cortex, whereas this activation pattern was n

296 The medial prefrontal cortex, which has a central role in self-appr

297 ding food PS may be processed in the lateral prefrontal cortex, which is a region that is implicated

298 This phenomenon is largely confined to prefrontal cortex, which is arguably less specialized an

299 cular changes that reduce myelination of the prefrontal cortex, which may be an underlying basis for

300 low slow-wave sleep intensity over the right prefrontal cortex-which has been shown to be linked to r