ライフサイエンスコーパス: ventromedial

1 parenchymal cells by P28, composed mostly of ventromedial and dorsomedial neurons and some glial cell

2 O expression is abundant in brain, including ventromedial and lateral hypothalamic nuclei regulating

3 ypothalamus is comprised of the dorsomedial, ventromedial, and arcuate nuclei, as well as parts of th

4 shift in the recruitment of cells toward the ventromedial, and away from the ventrolateral, spinal co

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

6 fidence was represented with specificity for ventromedial area 10.

7 unctionally segregated across a dorsolateral/ventromedial axis.

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 MRI analysis showed that ventromedial compromise was related to overconfidence, w

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

12 dients of intrinsic dynamics, one spanning a ventromedial-dorsolateral axis and dominated by measures

13 eptor subunits from the dorsolateral pole to ventromedial extremities.

14 from functional connectivity profiles of the ventromedial frontal cortex, temporoparietal junction, a

15 However, some evidence from patients with ventromedial frontal lobe (VMF) damage argues against a

16 TEMENT Neuroeconomic models propose that the ventromedial frontal lobe (VMF) supports multiattribute

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

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

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

20 GHR inactivation in SF1 cells, which include ventromedial hypothalamic neurons, also attenuated the C

21 ne enhances the recovery of hypoglycemia via ventromedial hypothalamic neurons.

22 rons in the ventrolateral subdivision of the ventromedial hypothalamic nucleus (vlVMH) can sense gluc

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 the diversely functioning cell types in the ventromedial hypothalamic nucleus (VMN), we studied the

27 as a notable lack of Pdyn projections to the ventromedial hypothalamic nucleus.

28 on priming via synaptic connections with the ventromedial hypothalamus (VmH) and bed nucleus of the s

29 project to multiple brain regions, including ventromedial hypothalamus (VMH) and lateral parabrachial

30 The ventromedial hypothalamus (VMH) and the brain melanocort

31 The ventromedial hypothalamus (VMH) and the central melanoco

32 rone-receptor (PR)-expressing neurons in the ventromedial hypothalamus (VMH) are active and required

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

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

35 Activation of efferent projections to the ventromedial hypothalamus (VMH) or lateral periaqueducta

36 The ventromedial hypothalamus (VMH) plays chief roles regula

37 It is well recognized that ventromedial hypothalamus (VMH) serves as a satiety cent

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

39 In the rat ventromedial hypothalamus (VMH), leptin-induced action p

40 ator fear in the dorsomedial division of the ventromedial hypothalamus (VMHdm) and the dPAG.

41 dorsomedial and central subdivisions of the ventromedial hypothalamus (VMHdm/c) that express the nuc

42 rons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl(Esr1)) play a causal ro

43 nucleus (MPN) and ventrolateral part of the ventromedial hypothalamus (VMHvl) are essential regions

44 The ventrolateral subdivision of the ventromedial hypothalamus (VMHvl) contains ~4,000 neuron

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

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

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

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

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

50 rons in the ventrolateral subdivision of the ventromedial hypothalamus (VMHvl).

51 Apv-D1R neurons differentially innervate the ventromedial hypothalamus and bed nucleus of the stria t

52 la and its downstream synaptic partners, the ventromedial hypothalamus and bed nucleus of the stria t

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

54 ible inhibition experiments suggest that the ventromedial hypothalamus and periaqueductal gray play d

55 Here, we show that neurons in the mouse ventromedial hypothalamus are activated both by the pres

56 The ventromedial hypothalamus controls both social aggressio

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

58 Analyses of gene expression in the ventromedial hypothalamus indicated that subordinate fem

59 The ventromedial hypothalamus is a central node of the mamma

60 The major efferent target of the ventromedial hypothalamus is the dorsal periaqueductal g

61 Although the ventromedial hypothalamus ventrolateral area (VMHvl) is

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

63 g the birth of early-born neurons within the ventromedial hypothalamus, acting independently of Ascl1

64 the medial amygdala, ventral lateral septum, ventromedial hypothalamus, and hypothalamic paraventricu

65 Nuclei within the ventromedial hypothalamus, extended amygdala and limbic

66 ither the medial preoptic area (MPOA) or the ventromedial hypothalamus, ventrolateral subdivision (VM

67 origins of major neuronal populations of the ventromedial hypothalamus.

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

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

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

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

72 , "ON-cells" and "OFF-cells," in the rostral ventromedial medulla (RVM).

73 nd its descending projections to the rostral ventromedial medulla and spinal cord, as an essential de

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

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

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

77 nding serotonergic circuits from the rostral ventromedial medulla facilitate activation of second-ord

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

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

80 ing of TRPV1-expressing afferents or rostral ventromedial medulla neurons attenuates hyperalgesia dur

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

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

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

84 y mediated by their projection to the caudal ventromedial medulla, where they excite GABAergic neuron

85 ing pain-facilitating neurons of the rostral ventromedial medulla.

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

87 on after noxious stimulation) of the rostral ventromedial medulla.

88 urons also project caudally to the posterior ventromedial medulla.

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

90 , motor thalamic nuclei such as anterior and ventromedial, midline, reticular, and posterior thalamic

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

92 cuate and rapidly expands to dorsomedial and ventromedial neurons by E10.5, peaking throughout the re

93 4 receptor (MC4R) in the paraventricular and ventromedial neurons of the hypothalamus and activates a

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

95 ntral tegmental area (VTA) and ventrolateral-ventromedial nuclei of the thalamus (VL-VM).

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

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

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

99 The ventromedial nucleus of the hypothalamus (VMN) has an im

100 The ventromedial nucleus of the hypothalamus (VMN) is involv

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

102 send processes into the arcuate nucleus, the ventromedial nucleus, and the dorsomedial nucleus of the

103 e in dorsolateral (Caudato-Putamen, DLS) and ventromedial (Nucleus Accumbens Shell, VS) striatal subr

104 ensory, visual, motor, and prefrontal (i.e., ventromedial orbitofrontal) cortex.

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

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

107 Some accounts of ventromedial PFC (vmPFC) suggest that it has a narrow ro

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

109 rected dimensionality reduction within human ventromedial PFC during learning.

110 s associated with stronger engagement of the ventromedial PFC during valuation.

111 modelling and neuroimaging, we show that the ventromedial PFC encodes both reward expectations and pr

112 Moreover, the ventromedial PFC exhibited higher connectivity with the

113 e found no evidence for baseline amygdala or ventromedial PFC volume serving as treatment predictors

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

115 found that activity in the rostrolateral and ventromedial PFC, regions associated with abstract cogni

116 leaves neural signatures in the brain region ventromedial PFC.

117 mechanism of learning through compression in ventromedial PFC.

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

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

120 the "salience" network, the ventral striatal/ventromedial prefrontal "reward" network, and the latera

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

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

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

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

125 observed general semantic representations in ventromedial prefrontal cortex (PFC).

126 eral amygdala, nucleus accumbens (NAcc), and ventromedial prefrontal cortex (PFC)] predicted cognitiv

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

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

129 at THC administration increased amygdala and ventromedial prefrontal cortex (vmPFC) activation during

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

131 The ventromedial prefrontal cortex (vmPFC) and dorsomedial p

132 rrors (US omissions) in regions of interest (ventromedial prefrontal cortex (vmPFC) and nucleus accum

133 of key 'limbic' regions (including amygdala, ventromedial prefrontal cortex (vmPFC) and nucleus accum

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

135 mediately after extinction training into the ventromedial prefrontal cortex (vmPFC) but unlike regula

136 anxiety disorders exhibited greater amygdala-ventromedial prefrontal cortex (vmPFC) connectivity when

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

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

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

140 Across two experimental tasks, the ventromedial prefrontal cortex (VMPFC) encoded an explic

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

142 onnectivity between anterior hippocampus and ventromedial prefrontal cortex (vmPFC) for object-word p

143 The ventromedial prefrontal cortex (vmPFC) has been implicat

144 The role of the ventromedial prefrontal cortex (vmPFC) in human pavlovia

145 UD showed significant hyperreactivity in the ventromedial prefrontal cortex (vmPFC) in response to ne

146 Importantly, the role of the ventromedial prefrontal cortex (vmPFC) in the acquisitio

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

148 The ventromedial prefrontal cortex (vmPFC) is a key brain st

149 The ventromedial prefrontal cortex (vmPFC) is closely associ

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

151 The ventromedial prefrontal cortex (vmPFC) is consistently i

152 roimaging studies.SIGNIFICANCE STATEMENT The ventromedial prefrontal cortex (vmPFC) is one of the mai

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

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

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

156 The ventromedial prefrontal cortex (vmPFC) projection to the

157 ere, using fMRI, we show that entorhinal and ventromedial prefrontal cortex (vmPFC) representations p

158 level of imbalance among goals, whereas the ventromedial prefrontal cortex (vmPFC) signaled the leve

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

160 Disrupted ventromedial prefrontal cortex (vmPFC) value signals may

161 he dorsomedial prefrontal cortex (dmPFC) and ventromedial prefrontal cortex (vmPFC) was consistently

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

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

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

165 seeking and this was mediated by activity in ventromedial prefrontal cortex (vmPFC), a region involve

166 the dorsal anterior cingulate cortex (dACC), ventromedial prefrontal cortex (VMPFC), and intraparieta

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

168 ve structural and functional deficits in the ventromedial prefrontal cortex (vmPFC), but the underlyi

169 st depends critically on the hippocampus and ventromedial prefrontal cortex (vmPFC), but their respec

170 core reward regions, orbitofrontal (OFC) and ventromedial prefrontal cortex (vmPFC), during two-optio

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

172 s in the fronto-limbic system, including the ventromedial prefrontal cortex (vmPFC), nucleus accumben

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

174 The ventromedial prefrontal cortex (vmPFC), which comprises

175 ized neural activity between hippocampus and ventromedial prefrontal cortex (vmPFC), with additional

176 based on a neural network that includes the ventromedial prefrontal cortex (vmPFC).

177 cterized by a dialog between hippocampus and ventromedial prefrontal cortex (vmPFC).

178 the representations of belief uncertainty in ventromedial prefrontal cortex (vmPFC).

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

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

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

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

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

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

185 ippocampus (HC), entorhinal cortex (EC), and ventromedial prefrontal cortex (vmPFC)/medial orbitofron

186 from nine patients with focal lesions to the ventromedial prefrontal cortex / medial orbitofrontal co

187 Ventromedial prefrontal cortex activated more to neutral

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

189 In both cases ventromedial prefrontal cortex activity reflected subjec

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

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

192 aligned with previous studies: prototypes in ventromedial prefrontal cortex and anterior hippocampus

193 h right and left orbitofrontal cortex, right ventromedial prefrontal cortex and left ventral striatum

194 ith subjective value-related activity in the ventromedial prefrontal cortex and midbrain but not with

195 , but that this relationship was mediated by ventromedial prefrontal cortex and moderated by expressi

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

197 al confidence, we found that activity within ventromedial prefrontal cortex and precuneus was additio

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

199 g in favor of social information engaged the ventromedial prefrontal cortex and the amygdala.

200 o types of evaluations, including regions of ventromedial prefrontal cortex and the posterior midline

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

202 the valuation network, with core foci in the ventromedial prefrontal cortex and ventral striatum, als

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

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

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

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

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

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

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

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

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

212 fMRI and Public-good-games, we find that the ventromedial prefrontal cortex encodes immediate expecte

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

214 -level-dependent downregulation and amygdala-ventromedial prefrontal cortex functional connectivity f

215 Ventromedial prefrontal cortex has been linked to choice

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

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

218 c-Fos expression on a retention test in the ventromedial prefrontal cortex of rats trained in contex

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

220 rain stimulation increased the impact of the ventromedial prefrontal cortex on the amygdala, and decr

221 al connectivity-but not hippocampal-anterior ventromedial prefrontal cortex or hippocampal-basolatera

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

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

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

225 Ventromedial prefrontal cortex responsiveness and ventro

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

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

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

229 ion, fMRI responses in entorhinal cortex and ventromedial prefrontal cortex take the form of grid-lik

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

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

232 In doing so, they linked the size of the ventromedial prefrontal cortex with foraging complexity

233 rain areas that are important for valuation (ventromedial prefrontal cortex) and positive reinforceme

234 (e.g. putamen, perigenual anterior cingulate/ventromedial prefrontal cortex) could distinguish the tw

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

236 agents-is based on nonlinear value-coding in ventromedial prefrontal cortex, a key component of the b

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

238 s in some areas (posterior cingulate cortex, ventromedial prefrontal cortex, and anterior cingulate c

239 Analysis focused on amygdala, ventromedial prefrontal cortex, and anterior insula, reg

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

241 xtinction also when infused locally into the ventromedial prefrontal cortex, basolateral amygdala, or

242 imaging studies implicate dysfunction within ventromedial prefrontal cortex, but the causal roles of

243 gnition, and subjective valuation, including ventromedial prefrontal cortex, correlated with both hig

244 nts and activation of its human homolog, the ventromedial prefrontal cortex, has been implicated in s

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

246 Activation of the ventromedial prefrontal cortex, posterior cingulate cort

247 lood-oxygen-level-dependent responses in the ventromedial prefrontal cortex, the dorsal anterior cing

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

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

250 Increased ventromedial prefrontal cortex-bilateral inferior latera

251 was correlated with activity in striatum and ventromedial prefrontal cortex.

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

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

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

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

256 variability in responses of the striatum and ventromedial prefrontal cortex.

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

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

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

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

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

262 ticothalamic loop that links the PVT and the ventromedial prefrontal cortex.

263 nections between the subthalamic nucleus and ventromedial prefrontal cortex.

264 ibre tracts between the ventral striatum and ventromedial prefrontal cortex.

265 tion is likely facilitated by input from the ventromedial prefrontal cortex.

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

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

268 ficant hypoconnectivity in orbitofrontal and ventromedial prefrontal cortical-striatal circuits-pathw

269 em cortical tissue regions: dorsolateral and ventromedial prefrontal cortices and motor cortex.

270 Ventromedial prefrontal GMV reduction was shared in both

271 Ventromedial prefrontal myelin density, indexed by magne

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

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

274 ippocampal), paralimbic (cingulo-insular and ventromedial prefrontal), and cognitive control (ventrol

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

276 ional connectivity changes in orbitofrontal, ventromedial prefrontal, inferotemporal, entorhinal, ret

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

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

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

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

281 eurons (OSNs) located in the dorsomedial and ventromedial regions of the olfactory epithelium (OE) ar

282 and primarily targeted the dorsolateral and ventromedial sectors of contralateral lamina VII.

283 itofrontal, ventrolateral, dorsolateral, and ventromedial sectors, along with the anterior cingulate

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

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

286 ll fate specification and differentiation of ventromedial -specific neurons.

287 The ventromedial striatum, including the nucleus accumbens (

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

289 is associated with cognition, while the most ventromedial subgenual cingulate area 25 (A25) is associ

290 A ventromedial subsystem includes the medial forebrain bun

291 ifferential involvement of fibres connecting ventromedial subthalamic nucleus and orbitofrontal corte

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 ior vermis through the cerebellar nuclei and ventromedial thalamus and culminating in the mPFC.

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

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

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

298 and 2-photon Ca(2+) imaging to determine how ventromedial (VM) and mediodorsal (MD) thalamus target s

299 araventricular (PVN), dorsomedial (DMH), and ventromedial (VMH) hypothalamic nuclei.

300 uronal activation was found in the preoptic, ventromedial (VMH), paraventricular hypothalamic nuclei,