ライフサイエンスコーパス: medial prefrontal cortex

1 exclusively based on activation patterns in medial prefrontal cortex.

2 or temporal lobe and later engagement of the medial prefrontal cortex.

3 uced activity in cue-encoding neurons in the medial prefrontal cortex.

4 ent produces rapid synaptic responses in the medial prefrontal cortex.

5 ate into myelinating oligodendrocytes in the medial prefrontal cortex.

6 eased GluR1 and synaptic connectivity in the medial prefrontal cortex.

7 ustering responses, and decreased amyloid in medial prefrontal cortex.

8 opamine inputs to nucleus accumbens, but not medial prefrontal cortex.

9 he rTPJ with ventral and dorsal parts of the medial prefrontal cortex.

10 rneurons on pyramidal layer 5 neurons in the medial prefrontal cortex.

11 viors include the amygdala, hippocampus, and medial prefrontal cortex.

12 ve network including the hippocampus and the medial prefrontal cortex.

13 ducing stable DNA methylation changes in the medial prefrontal cortex.

14 bens shell, the dorsal raphe nucleus and the medial prefrontal cortex.

15 re synchronized between the thalamus and the medial prefrontal cortex.

16 nit mRNA levels in the nucleus accumbens and medial prefrontal cortex.

17 that underlies remote memory storage in the medial prefrontal cortex.

18 basal ganglia and other regions such as the medial prefrontal cortex.

19 ncreased cortical thickness in the bilateral medial prefrontal cortex.

20 inputs to the hippocampal formation and the medial prefrontal cortex.

21 e merit prediction error affects activity in medial-prefrontal cortex.

22 k=1,305, respectively) and cingulate cortex/medial prefrontal cortex (-12, -8, 68; k=2,217).

23 the glutamatergic neurons of the infralimbic medial prefrontal cortex, a brain region critical for fe

24 Patients who relapsed displayed reduced medial prefrontal cortex activation during model-based d

25 c impact of sleep loss is linked to impaired medial prefrontal cortex activity and associated connect

26 us (and for disorganized schizotypy, also in medial prefrontal cortex; all false discovery rate-corre

27 ns throughout the fear circuit including the medial prefrontal cortex, amygdala, and hippocampus.

28 By contrast, medial prefrontal cortex and a hippocampal-amygdala bord

29 ow that inputs to the nucleus accumbens from medial prefrontal cortex and amygdala regulate alcohol-s

30 s associated with greater recruitment of the medial prefrontal cortex and anterior cingulate cortex i

31 High-frequency dTMS over the medial prefrontal cortex and anterior cingulate cortex s

32 The functional anatomy of the medial prefrontal cortex and basal ganglia has been exte

33 rd-linked effective connectivity between the medial prefrontal cortex and basal ganglia related to de

34 twork seed, and two connections (between the medial prefrontal cortex and both the right superior par

35 ala (CeA) and gene expression changes in the medial prefrontal cortex and CeA from the same animals u

36 (gamma-aminobutyric acidergic) genes in the medial prefrontal cortex and CeA.

37 l NRG1 infusion into the dorsal hippocampus, medial prefrontal cortex and dorsal striatum measured by

38 appears to be necessary to the stability of medial prefrontal cortex and hippocampal cell assembly f

39 n contrast, boundary-evoked responses in the medial prefrontal cortex and middle temporal gyrus incre

40 erlap between transcriptional alterations in medial prefrontal cortex and nucleus accumbens in human

41 n two brain regions implicated in depression-medial prefrontal cortex and nucleus accumbens-of humans

42 ivity involving the caudate nucleus, insula, medial prefrontal cortex and other domain-specific regio

43 sociated with advanced connectivity with the medial prefrontal cortex and superior temporal gyrus, wh

44 net weight change.Elevated activation in the medial prefrontal cortex and supplementary motor area, c

45 al magnetic stimulation (dTMS) targeting the medial prefrontal cortex and the anterior cingulate cort

46 Using fMRI, we show that the medial prefrontal cortex and the entorhinal portion of t

47 and corticothalamic pathways connecting the medial prefrontal cortex and the mediodorsal thalamus (M

48 ards and heightened activity in the anterior medial prefrontal cortex and the posterior cingulate cor

49 ative modulation of connectivity between the medial prefrontal cortex and the posterior cingulate cor

50 ypically involved in spatial navigation: the medial prefrontal cortex and the right entorhinal cortex

51 Amyloid plaques were accumulated more in the medial prefrontal cortex and the septal nuclei, both of

52 ections from the basolateral amygdala to the medial prefrontal cortex and ventral hippocampus during

53 value of the delayed reward and activity of medial prefrontal cortex and ventral striatum.

54 scular endothelial cells) cells of cortical (medial prefrontal cortex) and subcortical (hippocampus)

55 amate microdialysis in nucleus accumbens and medial prefrontal cortex, and ex vivo striatal dopamine

56 d lower WM volume bilaterally in orbital and medial prefrontal cortex, and greater GM volume in poste

57 ortantly clarify the roles of the precuneus, medial prefrontal cortex, and lateral parietal cortex, i

58 This network comprises the hippocampus, medial prefrontal cortex, and left angular gyrus, among

59 f neural regions, including the hippocampus, medial prefrontal cortex, and left angular gyrus.

60 la, orbitofrontal cortex, ventral and dorsal medial prefrontal cortex, and nucleus accumbens core and

61 ed regions, including the nucleus accumbens, medial prefrontal cortex, and orbitofrontal cortex, duri

62 ork state involving insula, dorsolateral and medial prefrontal cortex, and posterior regions of defau

63 Activity in the orbitofrontal cortex, medial prefrontal cortex, and putamen represented the re

64 fected sites included the brainstem, ventral medial prefrontal cortex, and superior temporal lobe, mo

65 as targeted on the posteromedial cortex, the medial prefrontal cortex, and the cingulum.

66 ntal cortex and inferior frontal gyrus), the medial prefrontal cortex, and the dorsal anterior cingul

67 cation was observed in specific areas of the medial prefrontal cortex, and these areas exhibited a di

68 circuit, that includes the amygdala, ventral medial prefrontal cortex, and ventral striatum, has subs

69 uding bilateral ATL, inferior frontal gyrus, medial prefrontal cortex, angular gyrus, posterior MTG,

70 lternative choice options implemented by the medial prefrontal cortex appears to be one important exp

71 at principal neurons in the circuitry of the medial prefrontal cortex are altered in distinct ways in

72 butyric acidergic neurons in the infralimbic medial prefrontal cortex are involved in the suppression

73 stria terminalis, basolateral amygdala, and medial prefrontal cortex as principal sources of CRH(+)

74 hat genetic ablation of GABA(B) receptors in medial prefrontal cortex astrocytes altered low-gamma os

75 imbalance in several key regions, namely the medial prefrontal cortex, basolateral amygdala, hippocam

76 he latter played a causal role: inactivating medial prefrontal cortex before outcome strengthened lea

77 tioned context cues evolves over time in the medial prefrontal cortex, but not in animals that cannot

78 Hdac1 overexpression in neurons of the medial prefrontal cortex, but not in the dorsal or ventr

79 tivation of the prelimbic (PL) region of the medial prefrontal cortex by baclofen/muscimol (B/M) duri

80 ward and emotional-regulation brain regions (medial prefrontal cortex, cingulate cortex, and insula)

81 The involvement of the temporal pole-medial prefrontal cortex circuit in a model highly predi

82 ents, while abnormalities in a temporal pole-medial prefrontal cortex circuit might speak to the soci

83 This review uses the example of amygdala-medial prefrontal cortex circuitry development to illust

84 connectivity between right temporal pole and medial prefrontal cortex, combined with years of educati

85 ety jointly influenced left amygdala to left medial prefrontal cortex connectivity during face emotio

86 Decreased amygdala-medial prefrontal cortex connectivity may mediate emotio

87 However, neural responses in the medial prefrontal cortex differed, such that patients wi

88 s a 3-6 Hz oscillatory signature, with BLA-->medial prefrontal cortex directionality signaling the re

89 sex information is represented in the dorsal medial prefrontal cortex (dmPFC) across excitatory and i

90 e behaviors affected by the OF require dorso-medial prefrontal cortex (dmPFC), we searched for synapt

91 hat the cortical sources in sensorimotor and medial prefrontal cortex even distinguished between pred

92 Our study identifies a pair of specific medial prefrontal cortex excitatory and inhibitory neuro

93 ork region (i) had greater connectivity with medial prefrontal cortex, falling within the same networ

94 network as in the healthy control group, the medial prefrontal cortex had a "hyperregulatory" effect

95 Although the prelimbic cortex (PL, part of medial prefrontal cortex) has been implicated in social

96 eus of the amygdala (BLA) and prelimbic (PL) medial prefrontal cortex have been implicated in reward-

97 us (HC) and prelimbic (PrL) subregion of the medial prefrontal cortex have been linked with context f

98 and medial secondary motor subregions of the medial prefrontal cortex have heterogeneous responses to

99 addition, infusing CPP into the infralimbic medial prefrontal cortex (IL-mPFC), a structure implicat

100 bition of the infralimbic subdivision of the medial prefrontal cortex (ilPFC) increases the proportio

101 ructural connectivity of the amygdala to the medial prefrontal cortex in CES rats.

102 (2020) show that the medial prefrontal cortex in mice computes a confidence-d

103 e ventral hippocampus and 36.5% lower in the medial prefrontal cortex in Neto2(-/-) compared to the N

104 ivity across the social brain network and in medial prefrontal cortex in particular.

105 of this study was to clarify the role of the medial prefrontal cortex in self-appraisal processes in

106 We demonstrate a prominent role for the medial prefrontal cortex in the exertion of control over

107 RI) studies have reported involvement of the medial prefrontal cortex including the anterior cingulat

108 Neurons in the medial prefrontal cortex, including projections to the d

109 sant effects of GLYX-13 are blocked by intra-medial prefrontal cortex (intra-mPFC) infusion of an ant

110 differentially expressed in the amygdala and medial prefrontal cortex (mPFC) a week after immobilizat

111 ity deficits observed suggests dysfunctional medial prefrontal cortex (mPFC) activity.

112 leus (MD) is reciprocally connected with the medial prefrontal cortex (mPFC) and also receives inputs

113 campal (vCA1) neurons projecting to both the medial prefrontal cortex (mPFC) and amygdala are activat

114 A brain network comprising the medial prefrontal cortex (mPFC) and amygdala plays impor

115 nflammation on the structure and function of medial prefrontal cortex (mPFC) and amygdala, which are

116 ctures involved in emotional regulation, the medial prefrontal cortex (mPFC) and basolateral amygdala

117 s responsivity, with a prominent role of the medial prefrontal cortex (mPFC) and basolateral amygdala

118 PRF preferentially activated medial prefrontal cortex (mPFC) and bed nucleus of the s

119 as neuronal atrophy and synaptic loss in the medial prefrontal cortex (mPFC) and hippocampus.

120 on of new with old memories supported by the medial prefrontal cortex (mPFC) and medial temporal lobe

121 ring adolescence decreased n-3 PUFAs in both medial prefrontal cortex (mPFC) and nucleus accumbens, i

122 coupling between spindle oscillations in the medial prefrontal cortex (mPFC) and ripple oscillations

123 nt anatomic and functional relay between the medial prefrontal cortex (mPFC) and the hippocampus (HPC

124 Neural oscillations in hippocampus and medial prefrontal cortex (mPFC) are a hallmark of rodent

125 Volumetric reductions in the hippocampus and medial prefrontal cortex (mPFC) are among the most well-

126 (PCC), temporal parietal junction (TPJ), and medial prefrontal cortex (MPFC) are frequently identifie

127 s from the ventral hippocampus (vHIP) to the medial prefrontal cortex (mPFC) are implicated in severa

128 Computations in the medial prefrontal cortex (mPFC) are thought to be centra

129 The hippocampus and the medial prefrontal cortex (mPFC) are traditionally associ

130 ven modularity-based parcellation of the rat medial prefrontal cortex (mPFC) combined with seed-based

131 , and hypo-connectivity between the rTPJ and medial prefrontal cortex (mPFC) compared to healthy cont

132 Impaired function in the medial prefrontal cortex (mPFC) contributes to depressio

133 Pyramidal neurons from layers II-III of the medial prefrontal cortex (mPFC) displayed profound synap

134 The medial prefrontal cortex (mPFC) drives behavioral flexib

135 ition center (PMC), locus coeruleus (LC) and medial prefrontal cortex (mPFC) during cystometry in una

136 Brain activity in medial prefrontal cortex (MPFC) during exposure to persu

137 DAR and AMPAR expression and function in the medial prefrontal cortex (mPFC) during juvenile and adol

138 rom ventral/intermediate hippocampus (HC) to medial prefrontal cortex (mPFC) during SWS in male mice

139 naling in the ventral hippocampus (vHip) and medial prefrontal cortex (mPFC) during the formation of

140 BDNF mRNA expression increased in the medial prefrontal cortex (mPFC) following nicotine withd

141 Finally, gene expression analysis in the medial prefrontal cortex (mPFC) for a subset of genes pr

142 x differences in learned fear inhibition and medial prefrontal cortex (mPFC) function.

143 holine receptor is an important modulator of medial prefrontal cortex (mPFC) functions, such as the w

144 he glutamatergic system and its receptors in medial prefrontal cortex (mPFC) has been implicated in m

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

146 Dysfunction of the medial prefrontal cortex (mPFC) has been linked to the c

147 ns of synaptic structure and function in the medial prefrontal cortex (mPFC) have been implicated in

148 bic (PL) and infralimbic (IL) regions of the medial prefrontal cortex (mPFC) have been implicated in

149 els of gamma-aminobutyric acid (GABA) in the medial prefrontal cortex (mPFC) have been reported in an

150 how that reduced cholinergic transmission in medial prefrontal cortex (mPFC) impaired appetitive trac

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

152 connectivity between the cerebellum and the medial prefrontal cortex (mPFC) in mice; showed that the

153 ons from ventral/intermediate hippocampus to medial prefrontal cortex (mPFC) in sleep-dependent memor

154 e role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but

155 Using targeted medial prefrontal cortex (mPFC) infusions, these effects

156 Low miR-218 expression in the medial prefrontal cortex (mPFC) is a consistent trait of

157 The medial prefrontal cortex (mPFC) is a critical component

158 The medial prefrontal cortex (mPFC) is a key brain region su

159 The medial prefrontal cortex (mPFC) is a major neural direct

160 Here, we demonstrated the medial prefrontal cortex (mPFC) is a site of learning-in

161 ly reported that dopamine D1 receptor in the medial prefrontal cortex (mPFC) is activated by subthres

162 w gamma coupling between the hippocampus and medial prefrontal cortex (mPFC) is augmented in a geneti

163 In chronic pain, the medial prefrontal cortex (mPFC) is deactivated and mPFC-

164 The rodent medial prefrontal cortex (mPFC) is generally regarded as

165 The medial prefrontal cortex (mPFC) is involved in regulatin

166 n between the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC) is known to be necessary

167 et, it is unclear how neural activity in the medial prefrontal cortex (mPFC) is modulated during task

168 As a key hub in corticolimbic inhibition, medial prefrontal cortex (mPFC) may be involved in distu

169 AAV-Cre-mediated SIRT1 knockdown in the medial prefrontal cortex (mPFC) of adult male mice induc

170 ced functional GABAergic transmission in the medial prefrontal cortex (mPFC) of adult MIA offspring.

171 Specifically, pyramidal neurons in the medial prefrontal cortex (mPFC) of GluN2C knockout mice

172 gosine-1-phosphate receptor 3 (S1PR3) in the medial prefrontal cortex (mPFC) of rats regulates resili

173 osphorylation of ribosomal protein S6 in the medial prefrontal cortex (mPFC) of stress-compromised ra

174 internodal length were detected only in the medial prefrontal cortex (mPFC) of susceptible mice, wit

175 into either the infralimbic division of the medial prefrontal cortex (mPFC) or the basolateral amygd

176 the role of the ventral hippocampus (vHipp)-medial prefrontal cortex (mPFC) pathway in ketamine's an

177 onic contributions of two direct hippocampal-medial prefrontal cortex (mPFC) pathways, one arising in

178 The medial prefrontal cortex (mPFC) plays a key role in top-

179 The medial prefrontal cortex (mPFC) plays an essential role

180 ectively modulate activity in neurons of the medial prefrontal cortex (mPFC) projecting to the nucleu

181 The medial prefrontal cortex (mPFC) provides instructions fo

182 The medial prefrontal cortex (mPFC) receives information reg

183 Different medial prefrontal cortex (mPFC) regions have been implic

184 est the hypothesis that anodal tDCS over the medial prefrontal cortex (mPFC) selectively enhances cog

185 Neuroimaging studies of the medial prefrontal cortex (mPFC) suggest that the dorsal

186 that dopaminergic pathway projecting to the medial prefrontal cortex (mPFC) suppresses stress suscep

187 ciated with an increased contribution of the medial prefrontal cortex (mPFC) to the DMN spatial mode.

188 lutamatergic axon terminals arising from the medial prefrontal cortex (mPFC) to the dorsal raphe nucl

189 neuropathic pain.SIGNIFICANCE STATEMENT The medial prefrontal cortex (mPFC) undergoes major reorgani

190 that the core empathy network including the medial prefrontal cortex (mPFC) was more engaged for eve

191 landscape in the nucleus accumbens (NAc) and medial prefrontal cortex (mPFC) were performed via data-

192 tivity on principal glutamatergic neurons in medial prefrontal cortex (mPFC) without any effect on gl

193 rdinated neural activity in the hippocampus, medial prefrontal cortex (mPFC), and amygdala.

194 to threat, overall reduced activation of the medial prefrontal cortex (mPFC), and increased threat-in

195 le food showed decreased TAAR1 levels in the medial prefrontal cortex (mPFC), and RO5256390 microinfu

196 ed, including expression in the striatum and medial prefrontal cortex (mPFC), and therefore generated

197 reas, the orbitofrontal cortex (OFC) and the medial prefrontal cortex (mPFC), as mice learned olfacto

198 stimulation of the 5-HT(1A) receptor in the medial prefrontal cortex (mPFC), as opposed to the somat

199 0-80 Hz) brain oscillatory activities in the 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 ing neurons in the infralimbic region of the medial prefrontal cortex (mPFC), but not in the hippocam

202 A) dopamine (DA) neurons that project to the medial prefrontal cortex (mPFC), but not to nucleus accu

203 egulated serotonin (5HT) transmission in the medial prefrontal cortex (mPFC), but the cause of this d

204 these inhibitory neurons, especially in the medial prefrontal cortex (mPFC), have been found in diff

205 ajor projection regions, the hippocampus and medial prefrontal cortex (mPFC), in male but not female

206 As a subdivision of the medial prefrontal cortex (mPFC), M2 can be defined by a

207 d gene expression studies both implicate the medial prefrontal cortex (mPFC), particularly deep-layer

208 ional connectivity among three core regions: medial prefrontal cortex (mPFC), posterior parietal cort

209 lation of synaptic glutamatergic proteins in medial prefrontal cortex (mPFC), suggesting that G-CSF i

210 systemically and via microinjection into the medial prefrontal cortex (mPFC), up to 7 days before IES

211 istent with stress-induced activation of the medial prefrontal cortex (mPFC), we found that the preli

212 leus accumbens (NAcc), the amygdala, and the medial prefrontal cortex (mPFC), which form an intrinsic

213 However, the role of NPY signaling in the medial prefrontal cortex (mPFC), which provides top-down

214 including the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC), while immediate 'reacti

215 We also tested performance in a medial prefrontal cortex (mPFC)-dependent rule-shifting

216 avior that was accompanied by a reduction in medial prefrontal cortex (mPFC)-DNA methyltransferase 3a

217 ay be mediated by increased influence of the medial prefrontal cortex (mPFC)-STN pathway on decision

218 by brain structures such as the amygdala and medial prefrontal cortex (mPFC).

219 y between the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC).

220 mbrane recruitment of RGS7 via GPR158 in the medial prefrontal cortex (mPFC).

221 ransmission of acetylcholine (ACh) in rodent medial prefrontal cortex (mPFC).

222 mTORC1 signaling and synaptic changes in the medial prefrontal cortex (mPFC).

223 ain intrinsic functional connectivity in the medial prefrontal cortex (mPFC).

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

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

226 enual anterior cingulate cortex (sgACC), and medial prefrontal cortex (mPFC).

227 V1 but also in the primary auditory (A1) and medial prefrontal cortex (mPFC).

228 connected with the hippocampus (Hip) and the medial prefrontal cortex (mPFC).

229 amate transmission and synaptogenesis in the medial prefrontal cortex (mPFC).

230 (pCREB) to CREB ratio in the hippocampus and medial prefrontal cortex (mPFC).

231 s DA and GABAergic transmission in the adult medial prefrontal cortex (mPFC).

232 amygdala (BLA), nucleus accumbens (NAc), and medial prefrontal cortex (mPFC).

233 ated extracellular glycine levels within the medial prefrontal cortex (mPFC).

234 theta phase coupling between hippocampus and medial prefrontal cortex (mPFC).

235 , but not glutamate principle neurons in the medial prefrontal cortex (mPFC).

236 states in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC).

237 trin-1 guidance cue receptor gene Dcc in the medial prefrontal cortex (mPFC).

238 p x time interaction effect was found in the medial prefrontal cortex (mPFC)/anterior cingulate corte

239 l cerebellum, and hypoactivity in the dorsal medial prefrontal cortex (mPFC); compared with TEC, PTSD

240 Parallel evidence, however, shows that the medial prefrontal cortex (mPFC; a critical node of the n

241 activity in the nucleus accumbens [NAcc] and medial prefrontal cortex [MPFC] as well as decreased act

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 owing weaning leads to a failure to activate medial prefrontal cortex neurons projecting to the poste

245 RNAs found to alter in expression within the medial prefrontal cortex of FKBP5 knockout mice were sel

246 ges and transcriptional abnormalities in the medial prefrontal cortex of immune-challenged and contro

247 STATEMENT The hippocampal formation and the medial prefrontal cortex of mammals represent the surrou

248 vity marker) immunoreactivity in the ventral medial prefrontal cortex of rats that previously receive

249 sses the activity of SST interneurons in the medial prefrontal cortex of the awake mouse.

250 Single-nucleus RNA sequencing of the medial prefrontal cortex of the brain revealed significa

251 (ventral hippocampus, nucleus accumbens, and medial prefrontal cortex) of susceptible, resilient, and

252 The exaggerated influence of the medial prefrontal cortex on the posterior cingulate cort

253 were spatially heterogeneous, including the medial prefrontal cortex, orbitofrontal cortex, and diff

254 for SST interneuron-evoked disinhibition of medial prefrontal cortex output neurons and recruitment

255 bcortical reward circuitry, and parts of the medial prefrontal cortex overlapping with the default-mo

256 duced synaptic plasticity in the hippocampal-medial prefrontal cortex pathway.

257 es neuronal atrophy and synaptic loss in the medial prefrontal cortex (PFC), and this leads to behavi

258 euronal atrophy and synaptic deficits in the medial prefrontal cortex (PFC), contributing to developm

259 ause dendritic spine plasticity in prelimbic medial prefrontal cortex (PL-mPFC) pyramidal neurons, a

260 of social-affective brain regions, with the medial prefrontal cortex playing a central role in the i

261 The medial prefrontal cortex plays a key role in higher orde

262 n positive traits but with activities in the medial prefrontal cortex, posterior cingulate, and occip

263 Coma patients displayed significantly lower medial prefrontal cortex-posteromedial cortex functional

264 The machine learning medial prefrontal cortex-posteromedial cortex multimodal

265 ity in both the nucleus accumbens (NAcc) and medial prefrontal cortex predicted individual choices to

266 etween participants and each agent recruited medial prefrontal cortex/pregenual anterior cingulate (p

267 oted aversive learning, while an independent medial prefrontal cortex-projecting ensemble extinguishe

268 gulate cortex, temporoparietal junction, and medial prefrontal cortex promotes honesty, particularly

269 the second choice point: one in rostrodorsal medial prefrontal cortex (rd-mPFC)/superior frontal gyru

270 Greater caudate and medial prefrontal cortex reactivity to gain outcomes and

271 ated from the rostral insula and portions of medial prefrontal cortex, regions that are associated wi

272 that neural patterns in the hippocampus and medial prefrontal cortex represented the featural overla

273 irus-driven expression of progranulin in the medial prefrontal cortex reverses social dominance defic

274 where photoactivation of SNAP-mGluR2 in the medial prefrontal cortex reversibly modulates working me

275 We acquired dorsolateral/medial prefrontal cortex samples from individuals with A

276 Reduced model-based medial prefrontal cortex signatures in those who relapse

277 h a particular focus on sex differences, the medial prefrontal cortex, social reward, social isolatio

278 ic transmission and cue-specific activity of medial prefrontal cortex somatostatin (SST) interneurons

279 Medial prefrontal cortex spine density was also examined

280 of cellular redox status, are reduced in the medial prefrontal cortex, striatum, and thalamus in schi

281 The involvement of medial prefrontal cortex suggests that when these oscill

282 mbic cortex (PrL), and infralimbic cortex of medial prefrontal cortex, the core and shell of NAc, BLA

283 The medial prefrontal cortex, the hippocampus, and the thala

284 nt schizophrenia risk genes, DISC1, upon the medial prefrontal cortex, the region believed to be most

285 Second, event-related directed medial prefrontal cortex to basal ganglia effective conn

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 ward-related effective connectivity from the medial prefrontal cortex to striatum was associated with

289 contribution of neural projections from the medial prefrontal cortex to the dorsal periaqueductal gr

290 (MD) with extrahippocampal regions and with medial prefrontal cortex underlies its role in execution

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

292 anterior cingulate cortex (dACC), the ventro-medial prefrontal cortex (vmPFC) and the anterior insula

293 of glycine and serine release in the ventral medial prefrontal cortex (vmPFC) contributes to increase

294 Recent studies suggest that the ventral medial prefrontal cortex (vmPFC) encodes both operant dr

295 trength of others' opinions in the posterior medial prefrontal cortex when opinions are disconfirming

296 uditory stimuli increased activations in the medial prefrontal cortex when presented at expected loca

297 marker of self-referential processing (i.e., medial prefrontal cortex) when participants reflected on

298 The medial prefrontal cortex, which has a central role in se

299 the rostral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expressed context

300 population of non-VIP ChAT(+) neurons in the medial prefrontal cortex with a distinct developmental o