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1 n regions (amygdala, anterior cingulate, and prefrontal cortex).
2 A levels in the nucleus accumbens and medial prefrontal cortex.
3 ession information from the developing human prefrontal cortex.
4 organization of cognitive control within the prefrontal cortex.
5 en the cmA and the precuneus and dorsomedial prefrontal cortex.
6 nderlies remote memory storage in the medial prefrontal cortex.
7 aptic alterations in a microcircuit model of prefrontal cortex.
8 ganglia and other regions such as the medial prefrontal cortex.
9 the amygdala, hypothalamus and dorsolateral prefrontal cortex.
10 d cortical thickness in the bilateral medial prefrontal cortex.
11 teins crucial for synaptic plasticity in the prefrontal cortex.
12 loop that links the PVT and the ventromedial prefrontal cortex.
13 ving the hippocampus, nucleus accumbens, and prefrontal cortex.
14 connectivity between sgACC and dorsolateral prefrontal cortex.
15 iptomic cell types and subtypes of the human prefrontal cortex.
16 tterns within the amygdala, hippocampus, and prefrontal cortex.
17 rea 12 [12o]), cingulate cortex, and lateral prefrontal cortex.
18 deficits in monkeys expressing hM4Di in the prefrontal cortex.
19 ocial reward prediction encoding only in the prefrontal cortex.
20 an organizational structure that mirrors the prefrontal cortex.
21 creased calbindin-positive neuron density in prefrontal cortex.
22 o myelinating oligodendrocytes in the medial prefrontal cortex.
23 r-alpha and interleukin-6 gene expression in prefrontal cortex.
24 n responses of the striatum and ventromedial prefrontal cortex.
25 modulation of corticothalamic neurons in the prefrontal cortex.
27 or deficits, elevated synaptic inhibition in prefrontal cortex, abnormal baseline and social interact
28 DD consented to receive MST applied over the prefrontal cortex according to an open-label protocol.
29 for disorganized schizotypy, also in medial prefrontal cortex; all false discovery rate-corrected ps
30 as increased basal extracellular dopamine in prefrontal cortex and 5-hydroxytryptamine in hippocampus
31 ands designed to drive theta oscillations in prefrontal cortex and alpha oscillations in parietal cor
35 ed effective connectivity between the medial prefrontal cortex and basal ganglia related to depressio
36 the thalamus is strongly connected with the prefrontal cortex and basal ganglia, areas which have be
37 urface area (SA) in dorsolateral/dorsomedial prefrontal cortex and caudal anterior cingulate cortex w
38 A) and gene expression changes in the medial prefrontal cortex and CeA from the same animals used for
39 tainty is represented in right rostrolateral prefrontal cortex and drives directed exploration, while
41 s to be necessary to the stability of medial prefrontal cortex and hippocampal cell assembly formatio
42 es aberrant circuit wiring in the developing prefrontal cortex and leads to deficits in juvenile and
44 ity in two networks involving 1) the lateral prefrontal cortex and medial caudate nucleus and 2) the
45 ast, boundary-evoked responses in the medial prefrontal cortex and middle temporal gyrus increase acr
46 etween transcriptional alterations in medial prefrontal cortex and nucleus accumbens in human MDD and
47 rain regions implicated in depression-medial prefrontal cortex and nucleus accumbens-of humans with M
48 , we found that activity within ventromedial prefrontal cortex and precuneus was additionally modulat
49 bunits permit rapid cholinergic responses in prefrontal cortex and protect these responses from desen
51 showed lower nodal centrality metrics in the prefrontal cortex and subcortical regions, and higher no
52 eta frequency neural oscillations in lateral prefrontal cortex and suppressing irrelevant information
54 hered information activated the dorsolateral prefrontal cortex and the midbrain, whereas arbitrating
55 connectivity between the right dorsolateral prefrontal cortex and the parietal cortex in non-relapse
56 y involved in spatial navigation: the medial prefrontal cortex and the right entorhinal cortex (EHC).
57 oupling of HFO bursts were also found in the prefrontal cortex and ventral striatum which, although o
58 at are important for valuation (ventromedial prefrontal cortex) and positive reinforcement-related pr
59 endothelial cells) cells of cortical (medial prefrontal cortex) and subcortical (hippocampus) brain r
60 as (posterior cingulate cortex, ventromedial prefrontal cortex, and anterior cingulate cortex) and de
61 icrodialysis in nucleus accumbens and medial prefrontal cortex, and ex vivo striatal dopamine reuptak
62 ons (anterior cingulate cortex, dorsolateral prefrontal cortex, and primary visual cortex) in human p
63 Activity in the orbitofrontal cortex, medial prefrontal cortex, and putamen represented the relative
65 des inferior parietal cortex, dorsal lateral prefrontal cortex, and the dorsal striatum, has minimal
66 dorsal anterior cingulate, the dorsolateral prefrontal cortex, and the lateral orbitofrontal cortex,
67 , that includes the amygdala, ventral medial prefrontal cortex, and ventral striatum, has substantial
68 ncy at which they synchronize across lateral prefrontal cortex, anterior cingulate cortex and anterio
69 ious perception, including some areas in the prefrontal cortex, appear to be primarily predictive of
71 we put forward the idea that alterations in prefrontal cortex architecture and function, which are i
72 shown that higher-order regions such as the prefrontal cortex are critical to attentional processing
73 e fMRI pattern analysis revealed the lateral prefrontal cortex as the only region that encodes predom
74 etic ablation of GABA(B) receptors in medial prefrontal cortex astrocytes altered low-gamma oscillati
75 ce in several key regions, namely the medial prefrontal cortex, basolateral amygdala, hippocampus, an
76 o when infused locally into the ventromedial prefrontal cortex, basolateral amygdala, or hippocampal
77 We show that fast rhythmic activity in the prefrontal cortex becomes prominent during the second po
78 er played a causal role: inactivating medial prefrontal cortex before outcome strengthened learning f
79 the periphery, and also in the amygdala and prefrontal cortex, brain structures critically involved
80 selective reductions of salience signals in prefrontal cortex but also diminished the influence of s
81 context cues evolves over time in the medial prefrontal cortex, but not in animals that cannot form n
82 ular glutamate and synaptic formation in the prefrontal cortex, but the initial cellular trigger that
84 s review uses the example of amygdala-medial prefrontal cortex circuitry development to illustrate a
85 resulting imbalance of medial temporal lobe-prefrontal cortex connectivity partially mediated the as
87 subjective valuation, including ventromedial prefrontal cortex, correlated with both higher social re
89 age of onset of SCZ in both the dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex (OFC)
90 bilateral thalami and the left dorsolateral prefrontal cortex (DLPFC) as our regions of interest, we
91 uR5 signaling in the postmortem dorsolateral prefrontal cortex (DLPFC) derived from 17 patients and a
92 dendritic spines in the primate dorsolateral prefrontal cortex (dlPFC) express the molecular machiner
93 active or sham rTMS to the left dorsolateral prefrontal cortex (dlPFC) for 20 consecutive weekdays.
94 and/or phosphorylation state in dorsolateral prefrontal cortex (DLPFC) from 22 pairs of SZ and matche
95 onal pathways were obtained for dorsolateral prefrontal cortex (DLPFC) gray matter and layer 3 and la
96 the role of the hippocampus and dorsolateral prefrontal cortex (dlPFC) in mediating such retrieval.
98 tissue fractions obtained from dorsolateral prefrontal cortex (dlPFC) of 15 MDD and 15 matched non-p
99 ic overview of glutamate in the dorsolateral prefrontal cortex (DLPFC) of patients with schizophrenia
102 patial gene expression in human dorsolateral prefrontal cortex (DLPFC) using spectral imaging and dot
103 ivity (FC) between amygdala and dorsolateral prefrontal cortex (DLPFC), and had increased negative FC
104 n primary auditory cortex (AC), dorsolateral prefrontal cortex (dlPFC), and the basolateral amygdala
105 e tested the involvement of the dorsolateral prefrontal cortex (dlPFC), in anxiety expression using 1
106 Working memory relies on the dorsolateral prefrontal cortex (dlPFC), where microcircuits of pyrami
109 h channel count recordings in dorsal-lateral prefrontal cortex (dlPFC; 768 electrodes) while monkeys
111 ormation is represented in the dorsal medial prefrontal cortex (dmPFC) across excitatory and inhibito
112 al prefrontal cortex (vmPFC) and dorsomedial prefrontal cortex (dmPFC) are positioned to exert top-do
113 ing between the amygdala and the dorsomedial prefrontal cortex (dmPFC) has been implicated in the gen
114 polarization was observed in the dorsomedial prefrontal cortex (DMPFC), a brain region associated wit
115 cal role in guiding growing axons toward the prefrontal cortex during adolescence and in the maturati
116 and findings that tDCS administration to the prefrontal cortex during task training may be an effecti
118 prefrontal cortex function makes the primate prefrontal cortex especially vulnerable to off-target ef
120 ied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with both bulk RNA
121 l-projecting cerebellar lobules and anterior prefrontal cortex, forming circuits that seem to be uniq
122 ne cell markers were measured by qPCR in the prefrontal cortex from 37 people with schizophrenia/schi
123 eculate that the unique neuropharmacology of prefrontal cortex function makes the primate prefrontal
124 we investigated the lipidome composition of prefrontal cortex gray matter in 396 cognitively healthy
127 ation of its human homolog, the ventromedial prefrontal cortex, has been implicated in suppressing av
128 ial secondary motor subregions of the medial prefrontal cortex have heterogeneous responses to stress
130 urbation on emergent network activity in the prefrontal cortex, identifying a window for possible int
132 Previous work has shown that the infralimbic prefrontal cortex (IL-PFC) is important for processing s
133 rformed proteomic sequencing of dorsolateral prefrontal cortex in 438 older individuals and found ass
134 with the anode placed over left-dorsolateral prefrontal cortex in a prospective open-label study.
136 A core discovery concerns the role of the prefrontal cortex in exerting top-down control over mnem
137 s have been extensively studied in the adult prefrontal cortex in the context of cognitive (dys)funct
138 ironmental sequences are stored in the human prefrontal cortex in the form of structured event comple
139 s in monkeys suggests a pivotal role for the prefrontal cortex in the representation of abstract rule
140 d activity within the major divisions of the prefrontal cortex, including orbitofrontal, ventrolatera
141 f endocannabinoid signaling in the prelimbic prefrontal cortex is a core neurobiological substrate fo
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 tional activation of the MD thalamus and the prefrontal cortex (Minzenberg et al., 2009), which are r
147 nsivity, with a prominent role of the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA)
148 involved in emotional regulation, the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA).
151 omic and functional relay between the medial prefrontal cortex (mPFC) and the hippocampus (HPC).
152 temporal parietal junction (TPJ), and medial prefrontal cortex (MPFC) are frequently identified as ke
153 ularity-based parcellation of the rat medial prefrontal cortex (mPFC) combined with seed-based connec
154 ally, gene expression analysis in the medial prefrontal cortex (mPFC) for a subset of genes previousl
156 amatergic system and its receptors in medial prefrontal cortex (mPFC) has been implicated in major de
157 ) and infralimbic (IL) regions of the medial prefrontal cortex (mPFC) have been implicated in differe
158 tivity between the cerebellum and the medial prefrontal cortex (mPFC) in mice; showed that the mPFC m
159 of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but their d
163 en the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC) is known to be necessary for no
164 y modulate activity in neurons of the medial prefrontal cortex (mPFC) projecting to the nucleus accum
166 ergic axon terminals arising from the medial prefrontal cortex (mPFC) to the dorsal raphe nucleus (DR
167 he core empathy network including the medial prefrontal cortex (mPFC) was more engaged for events hap
168 on principal glutamatergic neurons in medial prefrontal cortex (mPFC) without any effect on glutamate
169 he orbitofrontal cortex (OFC) and the medial prefrontal cortex (mPFC), as mice learned olfactory asso
170 ) brain oscillatory activities in the medial prefrontal cortex (mPFC), basolateral amygdala (BLA), do
171 mine (DA) neurons that project to the medial prefrontal cortex (mPFC), but not to nucleus accumbens (
172 inhibitory neurons, especially in the medial prefrontal cortex (mPFC), have been found in different p
173 of synaptic glutamatergic proteins in medial prefrontal cortex (mPFC), suggesting that G-CSF influenc
177 lel evidence, however, shows that the medial prefrontal cortex (mPFC; a critical node of the neocorti
178 y in the nucleus accumbens [NAcc] and medial prefrontal cortex [MPFC] as well as decreased activity i
180 try by profiling DNA methylation in isolated prefrontal cortex neurons from control and PD brain hemi
181 monstrate that overexpression of C4 in mouse prefrontal cortex neurons leads to perturbations in dend
182 eaning leads to a failure to activate medial prefrontal cortex neurons projecting to the posterior pa
184 ith increased FOLH1 mRNA in the dorsolateral prefrontal cortex of brains from unaffected subjects and
185 und to alter in expression within the medial prefrontal cortex of FKBP5 knockout mice were selected.
186 collecting neural activity in dorsal-lateral prefrontal cortex of macaques using eight microelectrode
187 examine ~80,000 nuclei from the dorsolateral prefrontal cortex of male individuals with MDD (n = 17)
189 ENT The hippocampal formation and the medial prefrontal cortex of mammals represent the surrounding p
192 sion on a retention test in the ventromedial prefrontal cortex of rats trained in contextual fear con
193 l hippocampus, nucleus accumbens, and medial prefrontal cortex) of susceptible, resilient, and unstre
194 ion increased the impact of the ventromedial prefrontal cortex on the amygdala, and decreased the imp
196 both targets showed that connectivity to the prefrontal cortex, orbitofrontal cortex, and cingulate c
197 T interneuron-evoked disinhibition of medial prefrontal cortex output neurons and recruitment of remo
198 d expression at 89 genes in the dorsolateral prefrontal cortex (P <= 9.43 x 10-6), including 20 novel
199 is detrimental to proper functioning of the prefrontal cortex (PFC) and establishment of appropriate
200 OMER1), is significantly reduced in both the prefrontal cortex (PFC) and induced pluripotent stem cel
201 e mesocorticolimbic circuitry, including the prefrontal cortex (PFC) and mesolimbic dopamine (DA) pat
202 examine mitochondrial gene expression in the prefrontal cortex (PFC) and nucleus accumbens (NAc) of m
205 pid antidepressant-like effects by enhancing prefrontal cortex (PFC) glutamate transmission; however,
206 timulation (tDCS) to examine the role of the prefrontal cortex (PFC) in neural oscillatory activity a
207 mpus (vHipp), basolateral amygdala (BLA) and prefrontal cortex (PFC) inputs revealed a hierarchy of s
209 of development when limbic connection of the prefrontal cortex (PFC) involved in emotional processing
210 multiple lines of evidence indicate that the prefrontal cortex (PFC) is particularly sensitive to, an
212 can jeopardize neuronal function and in the prefrontal cortex (PFC) it may contribute to compulsive
213 led in a single dish and differentiated into prefrontal cortex (PFC) lineages to efficiently test ear
216 mpus (vHipp,) basolateral amygdala (BLA) and prefrontal cortex (PFC) onto identified medium spiny neu
217 (Disc1-KD) in mature mouse astrocytes of the prefrontal cortex (PFC) or the hippocampus would produce
220 e how specific transcriptomic types of mouse prefrontal cortex (PFC) projection neurons relate to axo
221 ntly demonstrated that carbachol delivery to prefrontal cortex (PFC) restored wakefulness despite con
222 MEG recordings showed that hippocampus and prefrontal cortex (PFC) were involved in the task and fu
224 eostasis during postnatal development of the prefrontal cortex (PFC), allowing for optimal DA-mediate
225 ssure is associated with deactivation of the prefrontal cortex (PFC), an area important for executive
226 onal atrophy and synaptic loss in the medial prefrontal cortex (PFC), and this leads to behavioral an
227 ssion and reduced PV expression in the adult prefrontal cortex (PFC), contributing to a behavioral ph
232 tween the hippocampus and right dorsolateral prefrontal cortex (PFC), which in turn was negatively co
233 ittent alcohol drinking resulted in enhanced prefrontal cortex (PFC)-driven excitation of prodynorphi
238 , nucleus accumbens (NAcc), and ventromedial prefrontal cortex (PFC)] predicted cognitive-behavioral
239 ons exist, we implanted eight Utah arrays in prefrontal cortex (PFC; area 46) of two male macaque mon
240 rietal area 7A, frontal eye field [FEF], and prefrontal cortex [PFC]) while monkeys performed a task
242 ial-affective brain regions, with the medial prefrontal cortex playing a central role in the integrat
244 e mouse basolateral amygdala (BLA)-prelimbic prefrontal cortex (plPFC) circuit is engaged by stress a
245 atients displayed significantly lower medial prefrontal cortex-posteromedial cortex functional connec
247 participants and each agent recruited medial prefrontal cortex/pregenual anterior cingulate (pgACC).
249 cortex, temporoparietal junction, and medial prefrontal cortex promotes honesty, particularly in indi
250 nced excitatory glutamatergic input to mouse prefrontal cortex pyramidal cells, leading to antidepres
251 s after stimulation of the left dorsolateral prefrontal cortex resulted in faster task performance in
252 uided direction comparisons, area MT and the prefrontal cortex, revealing their likely interactions d
253 photoactivation of SNAP-mGluR2 in the medial prefrontal cortex reversibly modulates working memory in
255 ncorporates hierarchical gating to model the prefrontal cortex's ability to flexibly encode and use m
257 ctivity from visual area V4, as well as from prefrontal cortex, slowly drifted together with these be
258 0 and GHRH agonist MR-409, on isolated mouse prefrontal cortex specimens treated with lipopolysacchar
259 ular redox status, are reduced in the medial prefrontal cortex, striatum, and thalamus in schizophren
260 inferior parietal lobule, left dorsolateral prefrontal cortex/superior frontal gyrus, and left media
262 es were associated with higher volume of the prefrontal cortex, temporal cortex, and medial orbitofro
263 signal, was represented in the ventrolateral prefrontal cortex, temporoparietal junction, and rostral
264 evel evidence of genomic networks within the prefrontal cortex that contribute to the pathophysiology
265 evel-dependent responses in the ventromedial prefrontal cortex, the dorsal anterior cingulate, the do
267 produce endogenous theta stimulation in the prefrontal cortex, thereby enhancing inhibitory control
268 euronal timescales are functionally dynamic: prefrontal cortex timescales expand during working memor
269 significantly associated with methylation in prefrontal cortex tissue at multiple CpG sites, includin
271 effect of glutamatergic projections from the prefrontal cortex to the nucleus accumbens has been argu
272 al regions (somatosensory, visual, motor and prefrontal cortex) to assess the generalizability of the
274 layer II/III pyramidal neurons of the medial prefrontal cortex via CXCR4-dependent stimulation of the
275 sporter gene expression in the ventrolateral prefrontal cortex (vlPFC) and most strongly in the amygd
276 specifically within the right ventrolateral prefrontal cortex (vlPFC) and most strongly in the right
280 ders exhibited greater amygdala-ventromedial prefrontal cortex (vmPFC) connectivity when processing t
282 Importantly, the role of the ventromedial prefrontal cortex (vmPFC) in the acquisition of pavlovia
283 RI, we show that entorhinal and ventromedial prefrontal cortex (vmPFC) representations perform a much
284 terior cingulate cortex (dACC), ventromedial prefrontal cortex (VMPFC), and intraparietal sulcus (IPS
285 itically on the hippocampus and ventromedial prefrontal cortex (vmPFC), but their respective roles ar
286 egions, orbitofrontal (OFC) and ventromedial prefrontal cortex (vmPFC), during two-option choice with
288 and impulse regulation including the ventral prefrontal cortex (VPFC) and dorsal PFC (DPFC), insula a
289 structure-function coupling in rostrolateral prefrontal cortex was associated with executive performa
292 stral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expressed context-depend
293 on signals in the insula, temporal lobe, and prefrontal cortex, while DA depletion affected social re
294 for cognitive control is tightly tied to the prefrontal cortex, whose expansion in humans relative to
295 ion of non-VIP ChAT(+) neurons in the medial prefrontal cortex with a distinct developmental origin t
296 ginal gyrus in IPL links decision regions in prefrontal cortex with premotor regions, where the motor
297 hronization of confidence representations in prefrontal cortex with reward prediction errors in basal
298 is reflected in a medial-lateral division of prefrontal cortex - with lateral frontal pole (FPl) supp
299 ctional network involving ventral and dorsal prefrontal cortex, with the dorsal system preferentially
300 dicted that HD-tDCS of the left versus right prefrontal cortex would differentially modulate performa