ライフサイエンスコーパス: ventromedial

1 ns involved in goal-directed action, such as ventromedial and dorsolateral prefrontal cortex and dors

2 Using a causal manipulation of ventromedial and lateral prefrontal function, these resu

3 isolated RNA from single 5-HT neurons in the ventromedial and lateral wings of the DR and performed s

4 led cells were found in the paraventricular, ventromedial, and dorsomedial nuclei as well as in the l

5 fidence was represented with specificity for ventromedial area 10.

6 orsolateral, ventrolateral, dorsomedial, and ventromedial) by a combination of anterograde and retrog

7 r, significant expansion, most marked in the ventromedial caudate bilaterally, the right pulvinar tha

8 ease, and serotonergic degeneration in human ventromedial caudate nucleus from individuals with an AP

9 Immunocytochemistry further revealed that a ventromedial cluster of the Ov proper (Ovvm) contains un

10 of core default mode network regions in the ventromedial cortex and hippocampus.

11 receptor, is expressed in a dorsolateral-to-ventromedial (DL > VM) gradient by the PN dendrites.

12 eptor subunits from the dorsolateral pole to ventromedial extremities.

13 impairment mostly to alterations in amygdala-ventromedial frontal circuits.

14 ad a pattern of connections to the bilateral ventromedial frontal cortex (via forceps minor and left

15 has been a swell of interest recently in the ventromedial frontal cortex (VMF), a brain region critic

16 The ventromedial frontal lobe (VMF) has been implicated in l

17 Damage to the ventromedial frontal lobe also impaired learning about t

18 dimension to associate with reward, and the ventromedial frontal lobe required to learn the reward a

19 appropriate feedback attribution, while the ventromedial frontal lobe was necessary for learning the

20 A common tonotopy with a dorsolateral to ventromedial gradient of low to high frequencies spanned

21 Thus, LS projection to the ventromedial hypothalamic area represents an effective p

22 a, as well as in micropunches of arcuate and ventromedial hypothalamic nuclei (VMN).

23 th the medial preoptic nucleus (POM) and the ventromedial hypothalamic nucleus (VMH) mediating contro

24 Estrogens act in the ventromedial hypothalamic nucleus (VMH) to regulate body

25 role in glucose signaling in neurons of the ventromedial hypothalamic nucleus (VMN), a brain nucleus

26 BN LepRb(CCK) neurons), which project to the ventromedial hypothalamic nucleus.

27 ng the perifornical hypothalamus (PFH; 30%), ventromedial hypothalamus (34%), paraventricular hypotha

28 Metabolic sensing neurons in the ventromedial hypothalamus (VMH) alter their activity whe

29 The ventromedial hypothalamus (VMH) and the brain melanocort

30 The ventromedial hypothalamus (VMH) and the central melanoco

31 ic failure (HAAF) and impaired activation of ventromedial hypothalamus (VMH) glucose-inhibited (GI) n

32 le of glutamatergic neurotransmission in the ventromedial hypothalamus (VMH) in response to hypoglyce

33 -expressing (SF-1-expressing) neurons in the ventromedial hypothalamus (VMH) play an important role i

34 the sodium-glucose transporter SGLT1 in the ventromedial hypothalamus (VMH) plays a role in glucose

35 rone receptor (PR)-expressing neurons in the ventromedial hypothalamus (VMH) that are critical for ma

36 The ventromedial hypothalamus (VMH) was thought to be essent

37 1 cell-surface expression in the BDNF mutant ventromedial hypothalamus (VMH), an energy balance-regul

38 ver longer periods of time, possibly via the ventromedial hypothalamus (VMH), to increase leptin sign

39 The ventrolateral subdivision of the murine ventromedial hypothalamus (VMHvl) contains neurons whose

40 rons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl) control mating and fig

41 that cells in the ventrolateral part of the ventromedial hypothalamus (VMHvl) that express estrogen

42 we found that the ventrolateral part of the ventromedial hypothalamus (VMHvl), an area with a known

43 in and around the ventrolateral part of the ventromedial hypothalamus (VMHvl)-a region required for

44 tion of the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl).

45 rease in the mRNA level of Rfrp in the dorso/ventromedial hypothalamus and Kiss1, Pomc, and Somatosta

46 ergic neurons that project to the medial and ventromedial hypothalamus are required for sympathoadren

47 e targeted to glucose-sensing neurons in the ventromedial hypothalamus in glucokinase-Cre mice, which

48 nsing of glucose-inhibitory neurons from the ventromedial hypothalamus was impaired in BG4KO mice.

49 CRF2 binding in the ventromedial hypothalamus was the same in juveniles, but

50 Nuclei within the ventromedial hypothalamus, extended amygdala and limbic

51 he same subnuclei of the medial amygdala and ventromedial hypothalamus, regions implicated in fear, a

52 affect spine density in the dentate gyrus or ventromedial hypothalamus, suggesting specific effects o

53 Wnt5 forms a dorsolateral-high to ventromedial-low pattern in the antennal lobe neuropil.

54 al brainstem structures, such as the rostral ventromedial medulla (RVM) and locus coeruleus (LC).

55 functional connectivity between the rostral ventromedial medulla (RVM) and other brainstem pain-modu

56 Neurons of the rostral ventromedial medulla (RVM) are thought to critically con

57 Electrical stimulation of the rostral ventromedial medulla (RVM) facilitates pain behaviours i

58 The rostral ventromedial medulla (RVM) is a relay in the descending

59 Neurons in the rostral ventromedial medulla (RVM) play critical and complex rol

60 assumes a pronociceptive role in the rostral ventromedial medulla (RVM) under conditions of periphera

61 C) to the periaqueductal gray to the rostral ventromedial medulla (RVM).

62 receptor-deficient mice suggest the rostral ventromedial medulla as an important site of the cannabi

63 Discrete regions of the rostral ventromedial medulla bidirectionally influence pain perc

64 eptor antagonist rimonabant into the rostral ventromedial medulla blocked acetaminophen-induced antih

65 nduced antihyperalgesia, while local rostral ventromedial medulla injection of AM 404 reduced hyperal

66 ng to CB1 and CB2 receptors in adult rostral ventromedial medulla is altered in persistent inflammati

67 otonin and NMDA mechanisms acting in rostral ventromedial medulla promote analgesia associated with e

68 ence of CB2 receptor function in the rostral ventromedial medulla provides additional rationale for t

69 pre-motor neurons in the spinal cord and/or ventromedial medulla to inhibit motor neurons.

70 gic/GABAergic neurons in the spinal cord and ventromedial medulla.

71 r types of nearby neurons located within the ventromedial medulla.

72 relevant CB1 receptors reside in the rostral ventromedial medulla.SIGNIFICANCE STATEMENT Acetaminophe

73 ronmental sensory-motor interactions and the ventromedial module deals preferentially with visceral c

74 4 receptor (MC4R) in the paraventricular and ventromedial neurons of the hypothalamus and activates a

75 r central sensory center located deep in the ventromedial neuropil of the tritocerebrum and mandibula

76 amus, DEPTOR was expressed in neurons of the ventromedial nucleus (VMH) and colocalized with proopiom

77 Thus, we targeted the hypothalamic ventromedial nucleus (VMH) to selectively overexpress (L

78 these actions is located in the hypothalamic ventromedial nucleus (VMH), and the activation of AMPK i

79 lamic PREP is predominantly expressed in the ventromedial nucleus (VMH), where it regulates glucose-i

80 Previous studies implicate the hypothalamic ventromedial nucleus (VMN) in glycemic control.

81 In the ventromedial nucleus (VMN), a part of the mediobasal hyp

82 that the hypothalamic arcuate nucleus (ARC), ventromedial nucleus (VMN), and lateral hypothalamic are

83 The ventromedial nucleus of the hypothalamus (VMH) plays a c

84 overexpression of GRP78 specifically in the ventromedial nucleus of the hypothalamus was sufficient

85 eus and the ventrolateral subdivision of the ventromedial nucleus of the hypothalamus.

86 or hypothalamus (AH), septal area (SEP), and ventromedial nucleus of the posterior division of the do

87 ated deeper in the parenchyma such as in the ventromedial nucleus were fusiform and showed a bipolar

88 the cohort of immature neurons entering the ventromedial nucleus, some appeared to undergo maturatio

89 uths showed diminished CMA connectivity with ventromedial/orbitofrontal regions.

90 youths exhibited thicker cortex in the left ventromedial PFC (vmPFC) and left precentral gyrus.

91 gyrus (IFG), orbitofrontal cortex (OFC), and ventromedial PFC (vmPFC) have been linked to the regulat

92 tromedial nucleus of the amygdala (CeMA) and ventromedial PFC (vmPFC) have critical roles for emotion

93 However, the CeMA and ventromedial PFC (vmPFC) interaction in reward regulatio

94 ulate and cerebellum and negative weights in ventromedial PFC and local pattern similarity analyses w

95 dicted the microstructure in pathways to the ventromedial PFC and OFC, indexing weaker connections in

96 ivity between, the hippocampus, amygdala and ventromedial PFC during conditioning.

97 ger connectivity between the hippocampus and ventromedial PFC predicted significant improvements in f

98 a and the dorsolateral PFC, dorsomedial PFC, ventromedial PFC, and orbitofrontal cortex (OFC) were de

99 brain, including significant differences in ventromedial PFC, insula, lateral PFC, pre-SMA, and dmPF

100 y between the hippocampus, amygdala, and the ventromedial PFC.

101 lation of immature neurons is present in the ventromedial portion of the adult primate amygdala, a re

102 STN in reactive control is restricted to its ventromedial portion, further implicating this STN subdi

103 ving negative outcomes, ventral striatum and ventromedial prefrontal (VMPFC) activity was decreased i

104 ed in piriform (PC), orbitofrontal (OFC) and ventromedial prefrontal (vmPFC) cortices, respectively.

105 In control subjects, however, ventromedial prefrontal activation was positively associ

106 Amygdala and ventromedial prefrontal activity was related to the way

107 despread network of brain regions, including ventromedial prefrontal and anterior cingulate cortex.

108 deo interaction in anterior cingulate cortex/ventromedial prefrontal cortex (mPFC), activating predom

109 oxygen level dependent (BOLD) signals in the ventromedial prefrontal cortex (PFC) tracked the latent

110 ion of the rostral anterior cingulate cortex/ventromedial prefrontal cortex (rACC/vmPFC) is the most

111 ed connectivity between ventral striatum and ventromedial prefrontal cortex (vmPFC) (corrected P<0.05

112 nin transporter (5-HTT) were measured in the ventromedial prefrontal cortex (vmPFC) and dorsal raphe

113 (GMV) in fear regulatory areas including the ventromedial prefrontal cortex (vmPFC) and hippocampus.

114 The ventral striatum and ventromedial prefrontal cortex (vmPFC) are two central n

115 compared responses of VS neurons to those of ventromedial prefrontal cortex (vmPFC) Area 14 neurons,

116 Growing evidence has identified the ventromedial prefrontal cortex (VMPFC) as a key node of

117 measurements of value difference signals in ventromedial prefrontal cortex (vmPFC) bore out this pre

118 glycine and serine neurotransmitters in the ventromedial prefrontal cortex (vmPFC) cortex in rats fo

119 nin (5-HT) systems are engaged indirectly by ventromedial prefrontal cortex (vmPFC) DBS.

120 ls demonstrated stronger deactivation of the ventromedial prefrontal cortex (vmPFC) during correct an

121 he anxiety group had lower activation of the ventromedial prefrontal cortex (vmPFC) during extinction

122 g during real food choices, we find that the ventromedial prefrontal cortex (vmPFC) encodes children'

123 The ventromedial prefrontal cortex (vmPFC) has been implicat

124 The ventromedial prefrontal cortex (vmPFC) has been shown to

125 f dorsolateral prefrontal cortex (dlPFC) and ventromedial prefrontal cortex (vmPFC) implicated in sel

126 moral decision making is associated with the ventromedial prefrontal cortex (vmPFC) in humans, and da

127 animal studies have recently implicated the ventromedial prefrontal cortex (vmPFC) in memory schema,

128 Previous studies show that the ventromedial prefrontal cortex (vmPFC) inversely and ven

129 Dysfunction in the ventromedial prefrontal cortex (vmPFC) is believed to pl

130 The ventromedial prefrontal cortex (vmPFC) is closely associ

131 Connectivity between the amygdala and ventromedial prefrontal cortex (vmPFC) is compromised in

132 During value-based decision making, ventromedial prefrontal cortex (vmPFC) is thought to sup

133 The ventromedial prefrontal cortex (vmPFC) plays a critical

134 between this region and general value coding ventromedial prefrontal cortex (vmPFC) predicted choice

135 between the OFC and general value coding in ventromedial prefrontal cortex (vmPFC) predicted individ

136 The ventromedial prefrontal cortex (vmPFC) projection to the

137 Here we show that damage to the human ventromedial prefrontal cortex (vmPFC) reduced the influ

138 her levels of perceptual vividness, with the ventromedial prefrontal cortex (VMPFC) showing greater m

139 of research have provided evidence that the ventromedial prefrontal cortex (vmPFC) signals the satis

140 functional imaging (fMRI), we found that the ventromedial prefrontal cortex (vmPFC) supports compensa

141 lood oxygen level-dependent responses in the ventromedial prefrontal cortex (vmPFC) to food aromas co

142 bes (MTL) to episode-specific memory and the ventromedial prefrontal cortex (vmPFC) to generalized, s

143 respective contributions of the amygdala and ventromedial prefrontal cortex (vmPFC) to moral judgment

144 oral contribution of dorsomedial (dmPFC) and ventromedial prefrontal cortex (vmPFC) to simultaneously

145 lood oxygen level dependent (BOLD) signal in ventromedial prefrontal cortex (vmPFC) was parametricall

146 We found that anticipatory value signals in ventromedial prefrontal cortex (vmPFC) were attenuated i

147 late cortex (ACC) was dynamically coupled to ventromedial prefrontal cortex (vmPFC) when adaptive swi

148 a priori defined region of interest (ROI) in ventromedial prefrontal cortex (VMPFC), a brain region s

149 was associated with activity patterns in the ventromedial prefrontal cortex (vmPFC), a key node in th

150 th dysfunction within areas 25 and 32 of the ventromedial prefrontal cortex (vmPFC), but a causal rel

151 The ventromedial prefrontal cortex (vmPFC), insula, amygdala

152 ing patients with focal brain lesions to the ventromedial prefrontal cortex (vmPFC), insula, or amygd

153 dynamic stress-specific mobilization of the ventromedial prefrontal cortex (VmPFC), marked by initia

154 BOLD response to both stimulus types in the ventromedial prefrontal cortex (vmPFC), orbitofrontal co

155 decreases in multiple regions, including the ventromedial prefrontal cortex (vmPFC), posterior cingul

156 essing and regulation of emotions, including ventromedial prefrontal cortex (vmPFC), posteromedial co

157 assical brain valuation regions, such as the ventromedial Prefrontal Cortex (vmPFC), reflected the st

158 lar/dysgranular insular cortex (AIC) and the ventromedial prefrontal cortex (vmPFC).

159 ted activation in the hippocampus and in the ventromedial prefrontal cortex (vmPFC).

160 cortex (OFC) and identity-general reward in ventromedial prefrontal cortex (vmPFC).

161 from these errors co-varied with activity in ventromedial prefrontal cortex (vmPFC).

162 cts competition between value signals in the ventromedial prefrontal cortex (vmPFC).

163 sic functional connectivity between NAcc and ventromedial prefrontal cortex (vmPFC).

164 making and neural correlates of value within ventromedial prefrontal cortex (vmPFC).

165 key brain region for this evaluation is the ventromedial prefrontal cortex (vmPFC).

166 eward circuit," the ventral striatum and the ventromedial prefrontal cortex (vmPFC).

167 The ventromedial prefrontal cortex achieves such integration

168 CC activations but decreased hippocampal and ventromedial prefrontal cortex activations during extinc

169 C group test-retest results showed decreased ventromedial prefrontal cortex activity during winning o

170 In both cases ventromedial prefrontal cortex activity reflected subjec

171 In order to test whether the ventromedial prefrontal cortex activity related to choic

172 which was paralleled by an activation of the ventromedial prefrontal cortex and amygdala.

173 hand, have dysfunctions associated with the ventromedial prefrontal cortex and limbic system, togeth

174 lower gray matter volume in dorsolateral and ventromedial prefrontal cortex and orbitofrontal cortex

175 ced in regions with prominent connections to ventromedial prefrontal cortex and other limbic structur

176 Value signals in the ventromedial prefrontal cortex and prediction errors in

177 so exhibits task-dependent coupling with the ventromedial prefrontal cortex and the striatum, brain a

178 egions central to the valuation process: the ventromedial prefrontal cortex and the ventral striatum.

179 during high incidental anxiety, activity in ventromedial prefrontal cortex and ventral striatum show

180 nimal data suggest that the amygdala and the ventromedial prefrontal cortex are key regions in promot

181 Extinction retention testing points to the ventromedial prefrontal cortex as an essential region in

182 s is found in human cingulate cortex and not ventromedial prefrontal cortex as typically reported for

183 which showed enhanced connectivity with the ventromedial prefrontal cortex between switches.

184 all youths with DBD showed reduced amygdala-ventromedial prefrontal cortex connectivity during high

185 mprovement, as did more positive amygdala-to-ventromedial prefrontal cortex connectivity.

186 rate signals in supplementary motor area and ventromedial prefrontal cortex correlated with participa

187 surface of the anterior cingulate cortex and ventromedial prefrontal cortex could provide more target

188 onally, activity in the teacher's insula and ventromedial prefrontal cortex covaried with the predict

189 e of lesion patients, we show that bilateral ventromedial prefrontal cortex damage impairs visual att

190 tively correlated with responsiveness of the ventromedial prefrontal cortex during extinction learnin

191 ers and dysfunctional down-regulation of the ventromedial prefrontal cortex during retaliation.

192 Furthermore, activity in enhanced ventromedial prefrontal cortex during reward imagination

193 al. (2014) studied how neurons in the monkey ventromedial prefrontal cortex encode value-based decisi

194 self-dimension, whereas HER amplitude in the ventromedial prefrontal cortex encoded the "Me" self-dim

195 spatially targeted deep brain stimulation of ventromedial prefrontal cortex enhanced memory functions

196 pendently and passed this information to the ventromedial prefrontal cortex for integration into an o

197 male risk carriers had an increased amygdala-ventromedial prefrontal cortex functional connectivity a

198 Ventromedial prefrontal cortex has been linked to choice

199 Overall, these findings suggest that chronic ventromedial prefrontal cortex high-frequency stimulatio

200 Our results also demonstrated that chronic ventromedial prefrontal cortex high-frequency stimulatio

201 dies have largely focused on the role of the ventromedial prefrontal cortex in higher-order deliberat

202 l orbitofrontal cortex (often referred to as ventromedial prefrontal cortex in humans; vmPFC/mOFC) is

203 of stimulus meaning, which then informs the ventromedial prefrontal cortex in inhibiting the amygdal

204 and dysfunctional regulatory activity in the ventromedial prefrontal cortex in youths with DBD irresp

205 hood yields new evidence suggesting that the ventromedial prefrontal cortex is a critical neural subs

206 The ventromedial prefrontal cortex is known to play a crucia

207 This novel contrast of patients with ventromedial prefrontal cortex lesions acquired during d

208 ffers from that of patients with adult-onset ventromedial prefrontal cortex lesions--the latter group

209 on and decision-making, here we test whether ventromedial prefrontal cortex may also be critical for

210 of the wild-type valine68BDNF allele in the ventromedial prefrontal cortex of the Met68BDNF mice or

211 d a greater increase in the thickness of the ventromedial prefrontal cortex over the three assessment

212 The ventromedial prefrontal cortex plays a key role in the d

213 n experiment; lesions that included the same ventromedial prefrontal cortex region disrupted normal s

214 We found that enhanced ventromedial prefrontal cortex response during imagined

215 Ventromedial prefrontal cortex responsiveness and ventro

216 otor areas of putamen and the reward-related ventromedial prefrontal cortex strengthened in relation

217 first study to reveal relationships between ventromedial prefrontal cortex structure and multi-infor

218 Our results indicate that ventromedial prefrontal cortex structure is a biomarker

219 MRI, we demonstrate a mechanism by which the ventromedial prefrontal cortex supports such episodic si

220 This effect was observed in a region of ventromedial prefrontal cortex that is sensitive to subj

221 modulating basic neural value signals in the ventromedial prefrontal cortex to incorporate social-dis

222 effect is driven by top-down influences from ventromedial prefrontal cortex to medial striatum.

223 ndividuals with stronger afferences from the ventromedial prefrontal cortex to the medial striatum ar

224 al integrity of white-matter tracts from the ventromedial prefrontal cortex to the medial striatum.

225 In line with previous findings, the ventromedial prefrontal cortex was found to positively r

226 pendently and in parallel, and passed to the ventromedial prefrontal cortex where they are integrated

227 l prefrontal cortex, inferior frontal gyrus, ventromedial prefrontal cortex) equivalently as inhibito

228 ogical patients that focal lesions involving ventromedial prefrontal cortex, acquired during developm

229 under a food-restriction condition, whereas ventromedial prefrontal cortex, and AMPA signaling there

230 connectivity between the hippocampus and the ventromedial prefrontal cortex, and between these region

231 these effects are mediated by the amygdala, ventromedial prefrontal cortex, and striatum.

232 , frontal operculum-anterior insular cortex, ventromedial prefrontal cortex, and the nucleus accumben

233 his 'other-conferred utility' was encoded in ventromedial prefrontal cortex, and these neural signals

234 abnormally lateralized connectivity through ventromedial prefrontal cortex, and unresponsive to dors

235 ons of the DN, the ventral precuneus and the ventromedial prefrontal cortex, covaried, respectively,

236 nd prefrontal cortical regions, specifically ventromedial prefrontal cortex, dorsolateral prefrontal

237 disorders in clusters in the dorsomedial and ventromedial prefrontal cortex, including the anterior c

238 itofrontal cortex (mOFC), a subregion of the ventromedial prefrontal cortex, is uniquely positioned t

239 Activation of the ventromedial prefrontal cortex, posterior cingulate cort

240 parately encoded in distinct brain areas-the ventromedial prefrontal cortex, posterior superior tempo

241 ormance of a subsequent working memory task (ventromedial prefrontal cortex, r = -0.66, P = .003; pos

242 re emotional brain regions, the amygdala and ventromedial prefrontal cortex, show little structural a

243 tum, and the signal of expected value in the ventromedial prefrontal cortex, showing a novel confirma

244 rain systems supporting affective valuation (ventromedial prefrontal cortex, ventral striatum, amygda

245 rrelation between PE and activity within the ventromedial prefrontal cortex, ventral striatum, and ot

246 has reduced functional connectivity with the ventromedial prefrontal cortex, which is implicated in e

247 the amygdala, the nucleus accumbens, and the ventromedial prefrontal cortex, which represent suprapon

248 These data also suggest that ventromedial prefrontal cortex-amygdala connectivity is

249 omedial prefrontal cortex responsiveness and ventromedial prefrontal cortex-amygdala connectivity wer

250 Increased ventromedial prefrontal cortex-bilateral inferior latera

251 es a heretofore unrecognized function of the ventromedial prefrontal cortex-the basic attentional pro

252 icipated economic and sensory rewards in the ventromedial prefrontal cortex.

253 he same way as that of monetary gain, in the ventromedial prefrontal cortex.

254 basis of explicit aggression centered on the ventromedial prefrontal cortex.

255 to top-down model-based information from the ventromedial prefrontal cortex.

256 ed connectivity between the amygdala and the ventromedial prefrontal cortex.

257 e ventral striatum and choice signals in the ventromedial prefrontal cortex.

258 f the ventral striatum/nucleus accumbens and ventromedial prefrontal cortex.

259 re represented in an anterior portion of the ventromedial prefrontal cortex.

260 gyrus, posterior cingulate cortex (PCC), and ventromedial prefrontal cortex.

261 onnections between the nucleus accumbens and ventromedial prefrontal cortex.

262 tral striatum, temporoparietal junction, and ventromedial prefrontal cortex.

263 ebral blood flow in the ventral striatum and ventromedial prefrontal cortex.

264 e, ventral striatum, anterior cingulate, and ventromedial prefrontal cortex.

265 of amplified preference-related activity in ventromedial prefrontal cortex.

266 al tegmental area, striatum, and a region in ventromedial prefrontal cortex.

267 human homologue of infralimbic cortex in the ventromedial prefrontal cortex.

268 atter volume in an overlapping region of the ventromedial prefrontal cortex.

269 ex/insula, the dorsal midbrain, and the left ventromedial prefrontal cortex.

270 ediction errors was driven by input from the ventromedial prefrontal cortex.

271 fective connectivity analysis identified the ventromedial prefrontal cortex/orbitofrontal cortex as t

272 ar cortex exerts downstream influence on the ventromedial prefrontal cortex/ventral striatum.

273 ar cortex activity and connectivity with the ventromedial prefrontal cortex/ventral striatum.

274 Ventromedial prefrontal GMV reduction was shared in both

275 methylfolate exhibited convergent changes in ventromedial prefrontal physiology, including increased

276 consumed beverage (r = -0.46) and decreased ventromedial prefrontal response during logo-elicited an

277 t (ROIs) relevant to MDD (anterior temporal, ventromedial prefrontal, dorsomedial prefrontal cortices

278 rder with psychopathic traits showed reduced ventromedial prefrontal-hypothalamic-limbic activation,

279 rsolateral prefrontal cortex; and 4) greater ventromedial prefrontal/ventral striatal activation duri

280 these neurons were strictly segregated to a ventromedial region of STN.

281 medial and dorsolateral regions to this same ventromedial region.

282 Given that frontopolar connectivity with ventromedial regions during emotion regulation is enhanc

283 opolar cortex exerts downstream influence on ventromedial regions in healthy individuals, these findi

284 Focusing on the local projection within the ventromedial SCN, we found that VIP+ afferents provided

285 ons entering via the labial nerve define the ventromedial sensory center (VMSC) in the maxilla and la

286 BAergic neurons in the pontine central gray; ventromedial, small GABAergic neurons that express FoxP2

287 The ventromedial striatum (VMS) is a node in circuits underp

288 Dopamine neurotransmission in the ventromedial striatum (VMS) mediates acute reinforcing e

289 In particular, dopamine signaling in the ventromedial striatum is thought to encode food reward a

290 I was negatively associated with D2BP in the ventromedial striatum.

291 ntal connections were restricted mainly to a ventromedial strip located in the rostral half of the cl

292 bilateral ventral striatum to right anterior ventromedial subthalamic nucleus consistent with previou

293 the orbitofrontal cortex and the medial and ventromedial superior frontal gyri.

294 ss of Drl in the PNs results in the aberrant ventromedial targeting of the dendrites, a defect that i

295 out the brain, with strong expression in the ventromedial telencephalon, periventricular regions of t

296 f these two protocadherins is similar in the ventromedial telencephalon, thalamus, hypothalamus, faci

297 concurrent inferential tracks: (i) one from ventromedial to dorsomedial PFC regions that makes proba

298 and of aromatase-positive (AR+) neurons, and ventromedial to this, an ovoid, aromatase-negative (AR-)

299 C), occupying a superficial layer within the ventromedial tritocerebrum.

300 o demarcate seven columnar neuropil domains (ventromedial, ventro-lateral, centromedial, central, cen