ライフサイエンスコーパス: prefrontal

1 Intensity of prefrontal activation (HbO2 concentration) was not clear

2 disorder-specific reduced left dorsolateral-prefrontal activation and reduced posterior cingulate de

3 During transient inhibition, MPH increased prefrontal activation for both groups and increased stri

4 globin and deoxygenated hemoglobin inferring prefrontal activation were recorded using Optical Topogr

5 oute to the goal, bilateral inferior lateral prefrontal activity scales with the planning demands of

6 m the claustrum-insular region to the medial prefrontal and anterior cingulate cortex of the common m

7 part of general executive control, engaging prefrontal and anterior cingulate cortices similarly to

8 ng reciprocal and bilateral connections with prefrontal and cingulate areas as well as strong recipro

9 ons and the errors thereof within the medial prefrontal and fusiform cortices.

10 erties of ketamine, structural remodeling of prefrontal and hippocampal neurons has been proposed as

11 ely associated with caudal left dorsolateral prefrontal and lateral temporo-parietal cortices.

12 in patients with ESLD compared to HC in the prefrontal and left temporal regions.

13 mative sentences, negated ones led to medial prefrontal and more widespread motor source activation,

14 g brain regions, especially between inferior prefrontal and occipital/parietal lobes.

15 ns of activity in nucleus accumbens, lateral prefrontal and parahippocampal cortices, and other regio

16 participants attend to two adjacent stimuli, prefrontal and parietal cortex shows a selective enhance

17 g and correlated with grey matter density in prefrontal and parietal cortex, as well as the hippocamp

18 to that stimulus is selectively enhanced in prefrontal and parietal cortex.

19 t of the responses is modulated similarly to prefrontal and parietal cortex.

20 ity depends on communication between lateral prefrontal and parietal cortices.

21 The data also identified unique prefrontal and striatal circuitry as a putative marker o

22 iety influenced amygdala connectivity to the prefrontal and temporal cortex.

23 tive relationships seen in sulcal regions in prefrontal and temporal cortices, and negative relations

24 major portions of CPC streamlines leave the prefrontal and temporal cortices.

25 The medial prefrontal - anterior cingulate cortex appears most tigh

26 The medial prefrontal areas 32, 24, 14, and 25 (mPFC) form part of

27 etwork of occipital, parietal, premotor, and prefrontal areas maximally activated by tactile stimulat

28 ple the superior colliculus (SC), as well as prefrontal areas responsible for top-down control.

29 Value furthermore modulated coupling between prefrontal areas, brainstem, and spinal cord, which migh

30 ance in deep pyramidal cells in temporal and prefrontal association neocortex.

31 rs regulate the excitability of a unique, IT prefrontal cell population, thereby defining novel circu

32 The prefrontal cingulate area (Cg), visual, oculomotor, and

33 l strategy that would allow normalization of prefrontal circuitry in addiction.

34 sia contextual treatment information engages prefrontal conceptual processes, which can suppress pred

35 Medial prefrontal connections were restricted mainly to a ventr

36 by multiple direct and indirect hippocampal-prefrontal connections.

37 release and inhibits IM neurons, compromises prefrontal control of the amygdala, and sets off a gener

38 under external constraints heavily recruited prefrontal control regions, whereas natural, voluntary s

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

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

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

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

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

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

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

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

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

48 3 (L3) and layer 5 (L5) of the dorsolateral prefrontal cortex (DLPFC), we sought to determine if tra

49 9 residue (H3K9me1), in the rat dorsomedial prefrontal cortex (dmPFC).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 The prefrontal cortex (PFC) underlies higher cognitive proce

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 Lateral prefrontal cortex encoded profit gained from harming oth

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

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

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

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

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

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

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

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

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

156 The prefrontal cortex is responsible for higher order cognit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 Human prefrontal cortex supports goal-directed behavior by rep

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

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

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

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

176 Prefrontal cortex tissue sections from 20 matched pairs

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 =2.2 x 10(-8)) with epigenetic ageing of the prefrontal cortex, independent of the proportion of neur

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 d nucleotide metabolic processes in the male prefrontal cortex.

216 low in the ventral striatum and ventromedial prefrontal cortex.

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

218 GABAergic and glutamatergic signaling in the prefrontal cortex.

219 rol signal originating from the dorsolateral prefrontal cortex.

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

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

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

223 ue of infralimbic cortex in the ventromedial prefrontal cortex.

224 and inhibitory neurotransmission within the prefrontal cortex.

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

226 ns are distributed across subnetworks within prefrontal cortex.

227 in an overlapping region of the ventromedial prefrontal cortex.

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

229 ian hormones increase inhibitory tone in the prefrontal cortex.

230 ated by cortical thinning in the dorsomedial prefrontal cortex.

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

232 ed using frozen tissue from the dorsolateral prefrontal cortex.

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

234 in cortical volume in bilateral dorsomedial prefrontal cortex.

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

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

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

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

239 solimbic (ventral striatal and midbrain) and prefrontal cortical (dorsolateral prefrontal cortex) reg

240 It has been argued that normalization of prefrontal cortical activity drives remission from ADHD,

241 re) and requires spillover of glutamate from prefrontal cortical afferents.

242 Upstream, medial prefrontal cortical projections provide gamma-rhythmic i

243 nning in schizophrenia prodromes and reduced prefrontal cortical thickness in chronic schizophrenia p

244 n the lateral orbitofrontal and dorsolateral prefrontal cortices compared with healthy men and female

245 Dopamine in prefrontal cortices is implicated in cognitive and emoti

246 her cortical areas, such as the parietal and prefrontal cortices, mnemonically encode the remembered

247 lities in the basal ganglia, cerebellum, and prefrontal cortices.

248 ogical and genetic manipulations that affect prefrontal D3 receptors alter anxiety, social interactio

249 Prefrontal-dependent deficits in the spatiotemporal coor

250 emotional functions, and the dysfunction of prefrontal dopamine has been associated with cognitive a

251 e for higher order cognitive processing, and prefrontal dysfunction is believed to underlie many of t

252 O) activity (2-8 Hz), coupled to activity at prefrontal electrode Fz, and STN beta activity (13-30 Hz

253 functioning of a recently described cingular-prefrontal emotion and motor regulation network.

254 After their generation, the prefrontal engram cells, with support from hippocampal m

255 ifficult to ascertain whether this extent of prefrontal enlargement follows general allometric growth

256 ilitate associative synaptic potentiation in prefrontal excitatory circuits.

257 These receptors are important for prefrontal executive function because pharmacological an

258 ay downstream of D2Rs that may contribute to prefrontal function under normal and pathological condit

259 c subthalamic nucleus and right dorsolateral prefrontal functional connectivity in healthy controls,

260 Among attempters, reductions in amygdala-prefrontal functional connectivity may be associated wit

261 tent with current theories of rodent/primate prefrontal functional similarity, and provide insight in

262 her BOLD activation to SS in the precentral, prefrontal, fusiform, and posterior cingulate cortices b

263 Higher hippocampal, but not prefrontal GABA, predicted stronger fronto-hippocampal c

264 as found to be associated with cingulate and prefrontal grey matter volumes.

265 Our data show that prefrontal infusions of KYNA attenuated the inhibitory c

266 networks, especially information concerning prefrontal lateralization of function.

267 lating the development and plasticity of the prefrontal-limbic network, which therefore may increase

268 areas provide strong input to the SCm, while prefrontal motor area 2 (M2), and somatosensory areas pr

269 aling the temporally orchestrated changes in prefrontal network synchrony modulated by acetylcholine

270 heir results have broad implications for how prefrontal networks integrate the two learning mechanism

271 ue detection and neural activity dynamics in prefrontal networks remains unclear.

272 sociation between adult symptom severity and prefrontal neuronal activity was confined to the time wi

273 in the task-related spike activity of medial prefrontal neurons correspond with increased activity of

274 petitive behaviours, how projection-specific prefrontal neurons encode reward-relevant information to

275 aging to monitor the activity of dorsomedial prefrontal neurons in mice during an appetitive Pavlovia

276 naptic input can enhance the excitability of prefrontal neurons over timescales on the order of secon

277 aviors emerge from the coordinated firing of prefrontal neurons.

278 o delineate the cholinergic contributions to prefrontal oscillations during cue detection in rats.

279 metacognition and suggest a crucial role for prefrontal oscillations in metacognitive performance.

280 recordings from posterior parietal (PPC) and prefrontal (PFC) cortices in two male monkeys that perfo

281 exhibited convergent changes in ventromedial prefrontal physiology, including increased task-induced

282 t- and long-term Mef2c upregulation in mouse prefrontal projection neurons consistently resulted in e

283 In addition to intra-cortical connectivity, prefrontal projection neurons innervate subcortical stru

284 rrestin, we find that the effects of D2Rs on prefrontal pyramidal neurons are actually mediated by pa

285 es in posterior recruitment and increases in prefrontal recruitment.

286 ons coupled with an increased recruitment of prefrontal regions across multiple cognitive tasks.

287 iated with differential recruitment of right prefrontal regions implicated in selective attention and

288 lts help shape models of how hippocampal and prefrontal regions support navigation, planning and futu

289 e VIIb, which is functionally connected with prefrontal regions supporting cognitive control.

290 s identified a network of regions, including prefrontal regions, to code stimulus-specific informatio

291 Examining targeted prefrontal regions, we found that pairs of voxels with s

292 1 components, with the latter originating in prefrontal regions.

293 tion showed the expected activation in right prefrontal regions.

294 s question, we recorded neural activity in a prefrontal sensorimotor area while monkeys naturally swi

295 loration is related to sudden disruptions in prefrontal sensorimotor control and rapid, reward-depend

296 ons in insula, cingulate, medial and lateral prefrontal, superior temporal, and superior parietal cor

297 al connectivity between the amygdala and the prefrontal systems may contribute to the emergence of an

298 on Paper: Should a Few Null Findings Falsify Prefrontal Theories of Conscious Perception?, by Brian O

299 nce specifically is orchestrated by means of prefrontal theta oscillations.

300 performance is associated specifically with prefrontal theta-band activity.