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1 ypothalamus, insula/superior temporal gyrus, medial prefrontal cortex).
2 DMN regions (posterior cingulate/precuneus, medial prefrontal cortex).
3 g-range FC in posterior cingulate cortex and medial prefrontal cortex.
4 l site for synchronizing the hippocampus and medial prefrontal cortex.
5 lutamatergic synapses in the hippocampus and medial prefrontal cortex.
6 s in the amygdala that are controlled by the medial prefrontal cortex.
7 ated by ketamine in parallel but only in the medial prefrontal cortex.
8 tion, posterior cingulate cortex, and dorsal medial prefrontal cortex.
9 regarding alternative choice options in the medial prefrontal cortex.
10 he rTPJ with ventral and dorsal parts of the medial prefrontal cortex.
11 with cortical thickness in their insula and medial prefrontal cortex.
12 h systems based on confidence/uncertainty in medial prefrontal cortex.
13 ne sex differences in gene expression in the medial prefrontal cortex.
14 emotion-related brain regions, including the medial prefrontal cortex.
15 cuitry, centered on the ventral striatum and medial prefrontal cortex.
16 rneurons on pyramidal layer 5 neurons in the medial prefrontal cortex.
17 viors include the amygdala, hippocampus, and medial prefrontal cortex.
18 ve network including the hippocampus and the medial prefrontal cortex.
19 ducing stable DNA methylation changes in the medial prefrontal cortex.
20 bens shell, the dorsal raphe nucleus and the medial prefrontal cortex.
21 re synchronized between the thalamus and the medial prefrontal cortex.
22 e merit prediction error affects activity in medial-prefrontal cortex.
23 ssing GABAergic cortical interneurons in the medial prefrontal cortex, (2) GABA-mediated synaptic tra
25 refrontal cortex-amygdala-accumbens, ventral medial prefrontal cortex-amygdala, and orbitofrontal cor
26 and functional connections within the dorsal medial prefrontal cortex-amygdala-accumbens circuit, as
27 ntified three segregated communities: dorsal medial prefrontal cortex-amygdala-accumbens, ventral med
28 ow that inputs to the nucleus accumbens from medial prefrontal cortex and amygdala regulate alcohol-s
30 mory involves hippocampal projections to the medial prefrontal cortex and amygdala; however the relat
31 twork seed, and two connections (between the medial prefrontal cortex and both the right superior par
32 l NRG1 infusion into the dorsal hippocampus, medial prefrontal cortex and dorsal striatum measured by
33 ed within striatal projection neurons in the medial prefrontal cortex and in striatal medium spiny ne
34 n volume were detected in the right and left medial prefrontal cortex and in the periventricular area
36 ivity involving the caudate nucleus, insula, medial prefrontal cortex and other domain-specific regio
37 PCC emotion-related deactivation and greater medial prefrontal cortex and PCC emotion-dependent funct
38 ed adolescents with MDD demonstrated reduced medial prefrontal cortex and PCC emotion-related deactiv
39 ctivity of the two primary nodes of the DMN: medial prefrontal cortex and posterior cingulate cortex
40 net weight change.Elevated activation in the medial prefrontal cortex and supplementary motor area, c
41 between unexpected reward processing in the medial prefrontal cortex and the generation of motivatio
42 ative modulation of connectivity between the medial prefrontal cortex and the posterior cingulate cor
43 d this evoked activity to originate from the medial prefrontal cortex and to exhibit a linear corresp
44 s to localize the effects of ketamine to the medial prefrontal cortex and venlafaxine to the amygdala
46 ections from the basolateral amygdala to the medial prefrontal cortex and ventral hippocampus during
47 luding the anterior temporal cortex, rostral medial prefrontal cortex, and anterior midcingulate cort
48 of amphetamine CPP, DeltaFosB in the NAc and medial prefrontal cortex, and decreases in VTA dopamine
49 d lower WM volume bilaterally in orbital and medial prefrontal cortex, and greater GM volume in poste
50 of a hedonic network (comprising the aNAcSh, medial prefrontal cortex, and lateral hypothalamus) recr
51 ortantly clarify the roles of the precuneus, medial prefrontal cortex, and lateral parietal cortex, i
54 n RSFC between midline cortical regions, the medial prefrontal cortex, and MTL regions, and increases
55 la, orbitofrontal cortex, ventral and dorsal medial prefrontal cortex, and nucleus accumbens core and
56 fected sites included the brainstem, ventral medial prefrontal cortex, and superior temporal lobe, mo
57 argets, including the nucleus accumbens, the medial prefrontal cortex, and the basolateral amygdala.
58 ntal cortex and inferior frontal gyrus), the medial prefrontal cortex, and the dorsal anterior cingul
59 on the amygdala and different regions in the medial prefrontal cortex; and dopaminergically modulated
60 uding bilateral ATL, inferior frontal gyrus, medial prefrontal cortex, angular gyrus, posterior MTG,
61 und significant functional activation in the medial prefrontal cortex, anterior cingulate, precuneus
62 cted need to stop on a given trial, in right medial prefrontal cortex/anterior cingulate cortex, caud
63 lternative choice options implemented by the medial prefrontal cortex appears to be one important exp
64 at principal neurons in the circuitry of the medial prefrontal cortex are altered in distinct ways in
65 ng mTOR activity in layer 2/3 neurons of the medial prefrontal cortex are associated with tonic-cloni
68 g a transcranial magnetic stimulation to the medial prefrontal cortex (Brodmann area 10) and the dors
70 tivation of the prelimbic (PL) region of the medial prefrontal cortex by baclofen/muscimol (B/M) duri
71 ward and emotional-regulation brain regions (medial prefrontal cortex, cingulate cortex, and insula)
73 ents, while abnormalities in a temporal pole-medial prefrontal cortex circuit might speak to the soci
75 connectivity between right temporal pole and medial prefrontal cortex, combined with years of educati
76 ety jointly influenced left amygdala to left medial prefrontal cortex connectivity during face emotio
78 functional connectivity between the PCC and medial prefrontal cortex; connectivity increased with ag
79 of evidence suggests that sex differences in medial prefrontal cortex-dependent cognitive functions a
80 s a 3-6 Hz oscillatory signature, with BLA-->medial prefrontal cortex directionality signaling the re
81 effort of multiple brain regions, the dorsal medial prefrontal cortex (DMPFC) is most closely associa
82 ave brought into question whether the dorsal medial prefrontal cortex (DMPFC), a region long associat
83 e behaviors affected by the OF require dorso-medial prefrontal cortex (dmPFC), we searched for synapt
85 tamine into the prelimbic (PL) region of the medial prefrontal cortex duplicated the effects of syste
87 lf-reflection and cognitive processes in the medial prefrontal cortex during evaluation of social fee
89 hat the cortical sources in sensorimotor and medial prefrontal cortex even distinguished between pred
90 ure in rostral and dorsal anterior cingulate/medial prefrontal cortex (fMRI z = 2.113, P < .001; VBM
91 igonucleotide-mediated gene knockdown in the medial prefrontal cortex, followed by behavioral trainin
92 network as in the healthy control group, the medial prefrontal cortex had a "hyperregulatory" effect
93 Although the prelimbic cortex (PL, part of medial prefrontal cortex) has been implicated in social
94 w that, in macaque monkeys, the amygdala and medial prefrontal cortex have a role in establishing an
95 eus of the amygdala (BLA) and prelimbic (PL) medial prefrontal cortex have been implicated in reward-
96 addition, infusing CPP into the infralimbic medial prefrontal cortex (IL-mPFC), a structure implicat
98 bition of the infralimbic subdivision of the medial prefrontal cortex (ilPFC) increases the proportio
100 gdala, paraventricular thalamus, and ventral medial prefrontal cortex in context-induced relapse afte
101 icated the infralimbic (IL) subregion of the medial prefrontal cortex in extinction of auditory fear
102 of this study was to clarify the role of the medial prefrontal cortex in self-appraisal processes in
103 nd, smaller network originates in regions of medial prefrontal cortex, including a major contribution
104 sant effects of GLYX-13 are blocked by intra-medial prefrontal cortex (intra-mPFC) infusion of an ant
105 ther nodal regions of the DMN, including the medial prefrontal cortex, lateral inferior parietal cort
106 t different regions of the orbitofrontal and medial prefrontal cortex make distinct contributions to
107 lternative choice options implemented by the medial prefrontal cortex might contribute to ongoing dru
108 al spine density on pyramidal neurons in the medial prefrontal cortex (mPFC) 2 h later, suggesting th
109 differentially expressed in the amygdala and medial prefrontal cortex (mPFC) a week after immobilizat
110 campal (vCA1) neurons projecting to both the medial prefrontal cortex (mPFC) and amygdala are activat
112 onnectivity converged on the same regions of medial prefrontal cortex (mPFC) and inferior frontal gyr
114 functional and structural alterations in the medial prefrontal cortex (mPFC) and nucleus accumbens (N
115 ring adolescence decreased n-3 PUFAs in both medial prefrontal cortex (mPFC) and nucleus accumbens, i
116 coupling between spindle oscillations in the medial prefrontal cortex (mPFC) and ripple oscillations
118 ductions in patients with MDD--especially in medial prefrontal cortex (mPFC) and the hippocampus--but
119 regardless of motivated response and to the medial prefrontal cortex (MPFC) and the VS in reward con
120 decreases in functional coupling between the medial prefrontal cortex (MPFC) and ventral striatum ove
123 bute to extinction impairments by modulating medial prefrontal cortex (mPFC) circuits involved in fea
124 eal a molecular mechanism that acts on local medial prefrontal cortex (mPFC) circuits to coordinate r
126 We sought to test the hypothesis that the medial prefrontal cortex (mPFC) controls interactions am
127 Using fMRI in humans, we found that the medial prefrontal cortex (mPFC) correlated with the mean
128 Here we show that beta-amyloid burden in medial prefrontal cortex (mPFC) correlates significantly
130 ition center (PMC), locus coeruleus (LC) and medial prefrontal cortex (mPFC) during cystometry in una
132 ontaneous change to an alternative strategy, medial prefrontal cortex (MPFC) encoded information that
134 nstration of m(6)A upregulation in the mouse medial prefrontal cortex (mPFC) following behavioral tra
135 ng world has been linked to the integrity of medial prefrontal cortex (mPFC) function in several spec
136 holine receptor is an important modulator of medial prefrontal cortex (mPFC) functions, such as the w
137 udied the role of DNA methylation regulating medial prefrontal cortex (mPFC) gene expression and alco
138 ted to represent specific episodes while the medial prefrontal cortex (MPFC) generalizes, other accou
139 that chronic stress increases inhibition of medial prefrontal cortex (mPFC) glutamatergic output neu
143 ateral complex of the amygdala (BLA) and the medial prefrontal cortex (mPFC) has emerged as a crucial
144 ns of synaptic structure and function in the medial prefrontal cortex (mPFC) have been implicated in
145 els of gamma-aminobutyric acid (GABA) in the medial prefrontal cortex (mPFC) have been reported in an
146 how that reduced cholinergic transmission in medial prefrontal cortex (mPFC) impaired appetitive trac
147 verely disrupts the columnar organization of medial prefrontal cortex (mPFC) in a transcription- and
148 Recent studies investigating the role of the medial prefrontal cortex (mPFC) in neuropathic pain have
149 prelimbic cortex, two adjacent areas of the medial prefrontal cortex (mPFC) in rodents, provide sele
150 long-range, top-down control exerted by the medial prefrontal cortex (mPFC) in the dorsal raphe nucl
151 gher cognitive functions associated with the medial prefrontal cortex (mPFC) including attention and
152 w gamma coupling between the hippocampus and medial prefrontal cortex (mPFC) is augmented in a geneti
163 et, it is unclear how neural activity in the medial prefrontal cortex (mPFC) is modulated during task
164 sted as an enduring interneuronopathy in the medial prefrontal cortex (mPFC) later in the life of off
165 of parental care and the developing amygdala-medial prefrontal cortex (mPFC) network-that is at the c
166 ced functional GABAergic transmission in the medial prefrontal cortex (mPFC) of adult MIA offspring.
168 ort that the level of m(6)A increases in the medial prefrontal cortex (mPFC) of mice in response to b
169 tutively active or dominant-negative, to the medial prefrontal cortex (mPFC) of rats allowed control
170 rom multiple single-unit recordings from the medial prefrontal cortex (mPFC) of rats while the animal
171 osphorylation of ribosomal protein S6 in the medial prefrontal cortex (mPFC) of stress-compromised ra
173 into either the infralimbic division of the medial prefrontal cortex (mPFC) or the basolateral amygd
174 the role of the ventral hippocampus (vHipp)-medial prefrontal cortex (mPFC) pathway in ketamine's an
175 onic contributions of two direct hippocampal-medial prefrontal cortex (mPFC) pathways, one arising in
176 evidence suggests that both hippocampus and medial prefrontal cortex (mPFC) play a crucial role in m
177 receptor antagonists have revealed that the medial prefrontal cortex (mPFC) plays a central role in
179 s extinction-associated memories: the dorsal medial prefrontal cortex (mPFC) promotes reward seeking,
181 est the hypothesis that anodal tDCS over the medial prefrontal cortex (mPFC) selectively enhances cog
185 that dopaminergic pathway projecting to the medial prefrontal cortex (mPFC) suppresses stress suscep
186 ritical developmental stage during which the medial prefrontal cortex (mPFC) undergoes major changes
187 neuropathic pain.SIGNIFICANCE STATEMENT The medial prefrontal cortex (mPFC) undergoes major reorgani
188 -spiking parvalbumin (FS-PV) interneurons in medial prefrontal cortex (mPFC) uniformly show increased
189 istration or microinfusion directly into the medial prefrontal cortex (mPFC), a node in the corticost
190 s upon a value representation for oneself in medial prefrontal cortex (mPFC), a plasticity also evide
191 ces in brain activation were examined in the medial prefrontal cortex (mPFC), amygdala, and hippocamp
194 le food showed decreased TAAR1 levels in the medial prefrontal cortex (mPFC), and RO5256390 microinfu
195 ed, including expression in the striatum and medial prefrontal cortex (mPFC), and therefore generated
196 ivity were examined in amygdala/hippocampus, medial prefrontal cortex (mPFC), and whole-brain analyse
197 vity with activity in motor cortex (MCx) and medial prefrontal cortex (mPFC), areas involved in motor
198 y in the infralimbic (IL) subdivision of the medial prefrontal cortex (mPFC), associated with comprom
199 eeking behavior and primarily originate from medial prefrontal cortex (mPFC), basolateral amygdala (B
200 ion through its extensive innervation of the medial prefrontal cortex (mPFC), but how the two structu
201 egulated serotonin (5HT) transmission in the medial prefrontal cortex (mPFC), but the cause of this d
202 causally associated with malfunction of the medial prefrontal cortex (mPFC), but underlying molecula
204 nucleus accumbens core (NAc), but not in the medial prefrontal cortex (mPFC), of cocaine-pretreated r
205 d gene expression studies both implicate the medial prefrontal cortex (mPFC), particularly deep-layer
206 infusion also increased spine density in the medial prefrontal cortex (mPFC), suggesting that estroge
207 shape and number in pyramidal neurons in the medial prefrontal cortex (mPFC), this study examines the
208 e NAc receives glutamatergic inputs from the medial prefrontal cortex (mPFC), ventral hippocampus (vH
209 leus accumbens (NAcc), the amygdala, and the medial prefrontal cortex (mPFC), which form an intrinsic
211 include lateral hypothalamus, amygdala, and medial prefrontal cortex (mPFC), yet the neuropharmacolo
213 avior that was accompanied by a reduction in medial prefrontal cortex (mPFC)-DNA methyltransferase 3a
214 ay be mediated by increased influence of the medial prefrontal cortex (mPFC)-STN pathway on decision
215 of the glutamate release probability at the medial prefrontal cortex (mPFC)-to-NAc synapses, but not
240 p x time interaction effect was found in the medial prefrontal cortex (mPFC)/anterior cingulate corte
241 l cerebellum, and hypoactivity in the dorsal medial prefrontal cortex (mPFC); compared with TEC, PTSD
242 lium-originated limbic structures (e.g., the medial prefrontal cortex [mPFC]), and the VLS receives i
243 actions between a core 'self network' (e.g., medial prefrontal cortex; mPFC), a cognitive control net
244 ion procedure to selectively disrupt ventral medial prefrontal cortex neuronal ensembles that were ac
245 tor in multiple brain regions, including the medial prefrontal cortex, nucleus accumbens, central nuc
248 ges and transcriptional abnormalities in the medial prefrontal cortex of immune-challenged and contro
249 vity marker) immunoreactivity in the ventral medial prefrontal cortex of rats that previously receive
251 1.4%, on average, in the anterior cingulate, medial prefrontal cortex, orbital prefrontal cortex, ven
252 were spatially heterogeneous, including the medial prefrontal cortex, orbitofrontal cortex, and diff
253 bic dopamine system (ventral tegmental area, medial prefrontal cortex, orbitofrontal cortex, and nucl
255 euronal atrophy and synaptic deficits in the medial prefrontal cortex (PFC), contributing to developm
256 ion deficits are known to be mediated by the medial prefrontal cortex (PFC), which displays markers o
257 ause dendritic spine plasticity in prelimbic medial prefrontal cortex (PL-mPFC) pyramidal neurons, a
259 , posterior cingulate cortex, precuneus, and medial prefrontal cortex possibly reflecting simulation
260 both groups with several regions, including medial prefrontal cortex, posterior cingulate cortex, hi
261 n positive traits but with activities in the medial prefrontal cortex, posterior cingulate, and occip
262 ity in both the nucleus accumbens (NAcc) and medial prefrontal cortex predicted individual choices to
263 oted aversive learning, while an independent medial prefrontal cortex-projecting ensemble extinguishe
264 he PAG and rostral anterior cingulate cortex/medial prefrontal cortex (rACC/mPFC), key regions in the
265 the second choice point: one in rostrodorsal medial prefrontal cortex (rd-mPFC)/superior frontal gyru
267 th sex differences in gene expression in the medial prefrontal cortex remains unclear and warrants fu
268 that neural patterns in the hippocampus and medial prefrontal cortex represented the featural overla
269 irus-driven expression of progranulin in the medial prefrontal cortex reverses social dominance defic
270 between anterior cingulate cortex and dorso-medial prefrontal cortex (rho = -0.60, P = 0.011), which
271 re interested in determining whether rostral medial prefrontal cortex (rmPFC) neurons participate in
275 h a particular focus on sex differences, the medial prefrontal cortex, social reward, social isolatio
276 ity protein 95, and glutamate receptor 1 and medial prefrontal cortex spine density in the antidepres
279 otheses about the functional organization of medial prefrontal cortex that can be tested explicitly i
280 located in the infralimbic subregion of the medial prefrontal cortex that controls a seeking respons
281 ran et al. (2016) identifies a region of the medial prefrontal cortex that, in concert with the amygd
282 s in the basolateral amygdala project to the medial prefrontal cortex, that these efferents contribut
283 mbic cortex (PrL), and infralimbic cortex of medial prefrontal cortex, the core and shell of NAc, BLA
284 nt schizophrenia risk genes, DISC1, upon the medial prefrontal cortex, the region believed to be most
285 protein 95, and glutamate receptor 1 in the medial prefrontal cortex; these changes were reversed by
286 eal-time activity of associative inputs from medial prefrontal cortex to dorsomedial striatum and sen
287 l bonding, how a functional circuit from the medial prefrontal cortex to nucleus accumbens is dynamic
288 contribution of neural projections from the medial prefrontal cortex to the dorsal periaqueductal gr
289 eraction with the estrous cycle in the adult medial prefrontal cortex transcriptome and report that f
290 luence of the estrous cycle on the adult rat medial prefrontal cortex transcriptome resulting in part
291 of glycine and serine release in the ventral medial prefrontal cortex (vmPFC) contributes to increase
292 anterior cingulate cortex (ACC), and ventral medial prefrontal cortex (vmPFC)) and this stress diathe
293 the role of central amygdala (CeA), ventral medial prefrontal cortex (vmPFC), and orbitofrontal cort
295 rtex, and parahippocampal cortex, as well as medial prefrontal cortex, were recruited during successf
296 marker of self-referential processing (i.e., medial prefrontal cortex) when participants reflected on
298 creased activity in the ventral striatum and medial prefrontal cortex, which significantly predicted
299 as mediated by increased connectivity of the medial prefrontal cortex with the anterior insula and ot
300 s in the paracingulate sulcus, a fold in the medial prefrontal cortex, with a 1 cm reduction in sulca
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