ライフサイエンスコーパス: ventrolateral

1 RGC density, extending from dorsotemporal to ventrolateral across the retina and overlapping with the

2 Responses in ventrolateral and anterior thalamic nuclei tracked learn

3 This connectivity profile suggests that ventrolateral and anterior thalamus may represent a nexu

4 g treatment of patients, including the right ventrolateral and dorsolateral prefrontal cortices.

5 his includes prelimbic, infralimbic, medial, ventrolateral and lateral orbital, ventral retrosplenial

6 Critically, the function of ventrolateral and medial OFC->BLA projections is doubly

7 an "overactive" left-sided ventral striatal-ventrolateral and orbitofrontal cortical reward-processi

8 f median neuronal density in the dorsomedial/ventrolateral and pulvinar nuclei compared with the 14 s

9 with various protocerebral targets including ventrolateral and superior neuropils via projections pri

10 We recorded from the orbital, ventrolateral, and dorsolateral prefrontal cortices (OFC

11 ctions to CWA are from the ventral anterior, ventrolateral, and posterior nuclei.

12 c nuclei (globus pallidus-internus [GPi] and ventrolateral anterior nucleus [VLa]) in monkeys perform

13 Here, we show that these ventrolateral anterior temporal subregions form part of

14 Most ventrolateral ARC TH cells did not contain dopamine and

15 Although the ventromedial hypothalamus ventrolateral area (VMHvl) is now well established as a

16 The ventromedial hypothalamus, ventrolateral area (VMHvl) was identified recently as a

17 Ventrolateral area 44 (a key component of the Broca's la

18 r in the OB; tongue-shaped, dorsomedial, and ventrolateral areas, and that not all projection neurons

19 d area, followed by the dorsomedial and then ventrolateral areas.

20 ctivate c-Fos expression within the anterior ventrolateral bed nucleus of the stria terminalis (vlBST

21 Fish, the basal vertebrates, separate ventrolateral body wall musculature of the trunk into tw

22 s expression of dnSNARE in astrocytes of the ventrolateral brainstem had no effect.

23 ient zone of MLd predominantly projects to a ventrolateral cluster of the Ov proper.

24 he lateral column of the rostral PAG and the ventrolateral column of the caudal PAG.

25 intermediate PAG and howls and hisses in the ventrolateral column of the intermediate PAG.

26 orsomedial OE, which is spatially inverse to ventrolateral constitutive expression of the retinoic ac

27 llium of birds then is the homologue of this ventrolateral dorsal pallial part, not of the classic la

28 prefrontal cortex, including orbitofrontal, ventrolateral, dorsolateral, and ventromedial sectors, a

29 ese four quadrants of the SPZ (dorsolateral, ventrolateral, dorsomedial, and ventromedial) by a combi

30 In the ventrolateral endoderm, the Elabela / Aplnr pathway limi

31 gs in macaques and humans: small saccades in ventrolateral FEF and large saccades combined with contr

32 In the primate brain, a set of areas in the ventrolateral frontal (VLF) cortex and the dorsomedial f

33 ral parieto-occipital cortex, precuneus, and ventrolateral-frontal metabolism.

34 6B1 expression, repeated injury, or old age, ventrolateral HBCs diminish in number and generate a nov

35 l and ventral hindgut domains, and show that ventrolateral hindgut cells populate the majority of the

36 longated structure that is lodged within the ventrolateral hypothalamus and lies along the optic trac

37 t adenoviral constructs were targeted to the ventrolateral hypothalamus of Foxb1/Cre mice to label sp

38 lateral in the dorsal horn to dorsomedial to ventrolateral in nTTD, whereas in PrV there is considera

39 We show that ventrolateral lesions impair the influence of WM represe

40 om the orofacial region of the primary (M1), ventrolateral (LPMCv), supplementary (M2), rostral cingu

41 RNA level of preproenkephalin in the rostral ventrolateral medulla (rVLM) 72 hr after EA was increase

42 studies suggest that neurons in the rostral ventrolateral medulla (RVLM) are more responsive to exci

43 Spinally-projecting neurons of the rostral ventrolateral medulla (RVLM) determine sympathetic outfl

44 t microinjection of ethanol into the rostral ventrolateral medulla (RVLM) elicits modest increases in

45 of the SST-2 receptor (sst2 ) in the rostral ventrolateral medulla (RVLM) lower sympathetic nerve act

46 The catecholaminergic neurons in the rostral ventrolateral medulla (RVLM) maintain sympathetic vasomo

47 evealed that glycine released in the rostral ventrolateral medulla (RVLM) plays a critical role in ma

48 Neurons in the rostral ventrolateral medulla (RVLM) regulate blood pressure thr

49 spinal axon collateralization of rat rostral ventrolateral medulla (RVLM) sympathetic premotor neuron

50 ed cardiovascular control within the rostral ventrolateral medulla (RVLM) using selective receptor an

51 he paraventricular nucleus (PVN) and rostral ventrolateral medulla (RVLM) were microdissected for gen

52 ction of [Pyr(1) ]apelin-13 into the rostral ventrolateral medulla (RVLM), a major source of sympatho

53 The C1 cells, located in the rostral ventrolateral medulla (RVLM), are activated by pain, hyp

54 in b neuronal tract tracing from the rostral ventrolateral medulla (RVLM), express NPY Y1 receptor im

55 rnical hypothalamus (PeH) and in the rostral ventrolateral medulla (RVLM), which results in the relea

56 ect to a key presympathetic hub, the rostral ventrolateral medulla (RVLM).

57 oked by activation of neurons in the rostral ventrolateral medulla (RVLM).

58 tatory cardiovascular regions of the rostral ventrolateral medulla (rVLM).

59 central chemosensitive area, and the rostral ventrolateral medulla (RVLM).

60 put of presympathetic neurons in the rostral ventrolateral medulla (RVLM).

61 nucleus tractus solitarius (NTS) and rostral ventrolateral medulla (RVLM)] cytokine surges were blunt

62 However, while catecholamine neurons of the ventrolateral medulla (VLM(CA)) are thought to orchestra

63 y, and amplitude when microinjected into the ventrolateral medulla (VLM) of the anesthetized rat, sug

64 of acid-sensing ion channels (ASICs) in the ventrolateral medulla (VLM) remains uncertain.

65 Moreover, by identifying the ventrolateral medulla as a direct source of metabolic in

66 n the nucleus tractus solitarius and rostral ventrolateral medulla as well as in the adrenal medulla

67 Rostral ventrolateral medulla catecholaminergic neurones (RVLM-C

68 he contribution of catecholaminergic rostral ventrolateral medulla catecholaminergic neurones (RVLM-C

69 and membrane potential were performed in the ventrolateral medulla containing the pre-BotC region.

70 Seizure-related SDs in the ventrolateral medulla correlated with respiratory suppre

71 ctivation of CA neuron subpopulations in the ventrolateral medulla during normoglycemia elicits these

72 total neurons were reduced within the MR and ventrolateral medulla following 30 d of increased InCO(2

73 ATP released in the ventrolateral medulla oblongata during hypoxia attenuate

74 originates from the hypothalamic Arc and the ventrolateral medulla of the brainstem in normal-weight

75 by designer drug) injected into the rostral ventrolateral medulla or treatment with a beta2AR antago

76 tein levels of mGluR5 in the PVN and rostral ventrolateral medulla were significantly higher in SHRs

77 h rate, neurovascular contact at the rostral-ventrolateral medulla, altered baroreflex blood pressure

78 ty throughout the rostrocaudal extent of the ventrolateral medulla, in Sprague Dawley rats treated wi

79 enerated by the pre-Botzinger complex of the ventrolateral medulla, where it is thought that excitati

80 including catecholaminergic neurons, in the ventrolateral medulla.

81 l blood flow (CBF) by activating the rostral ventrolateral medulla.

82 rapezoid nucleus (RTN) reside in the rostral ventrolateral medulla.

83 nucleus of the hypothalamus and the rostral ventrolateral medulla.

84 rons, the majority of which originate in the ventrolateral medulla.

85 s with blood pressure control centers in the ventrolateral medulla.

86 ation (SD) reaches respiratory nuclei in the ventrolateral medulla.

87 ns that project to the rostral aspect of the ventrolateral medulla.

88 B and NPY was observed in the Arc and in the ventrolateral medulla.

89 r activity, including the rostral and caudal ventrolateral medullary regions (RVLM and CVLM, respecti

90 ox32 restricts Pou5f3-Nanog complexes to the ventrolateral mesendoderm by binding Pou5f3 or Nanog in

91 gin and formation of the zebrafish kidney, a ventrolateral mesoderm derivative, and show that AP patt

92 Cells in the ventroinferior (MHbVI) and ventrolateral MHb (MHbVL) subregions expressed functiona

93 ons, stimulation of the ventral anterior and ventrolateral motor part of the thalamus seems to be a v

94 gh-frequency DBS of the ventral anterior and ventrolateral motor part of the thalamus.

95 usculature as an extension of the four-layer ventrolateral muscular patterning of the thorax and abdo

96 nd FLX decreased DA tissue levels in the rat ventrolateral neostriatum compared with TBZ alone, and c

97 osed for the lateral prefrontal cortex: 1) a ventrolateral network (VLPFC) in and ventral to the prin

98 at the protein is localized to the embryonic ventrolateral neural tube where motor neurons arise.

99 lation and arborization rhythms in the small ventrolateral neuron (sLNv) dorsal projection.

100 f arousal-promoting clock neurons, the large ventrolateral neurons (l-LNvs), impairs sleep onset.

101 vinar, mediodorsal, and, to a lesser extent, ventrolateral nuclei volumes compared with the healthy c

102 In ventrolateral OE, HBCs express low p63 levels and prefer

103 located in the most dorsomedial part of the ventrolateral OE, the V-zone:DM.

104 bregion of this heterogeneous structure, the ventrolateral OFC (VLO).

105 Bilateral Bdnf knockdown within the ventrolateral OFC and unilateral Bdnf knockdown accompan

106 Ventrolateral OFC-selective Fmr1 knockdown recapitulated

107 ion of mature, mushroom-shaped spines in the ventrolateral OFC.

108 e medial orbital area, ventral orbital area, ventrolateral orbital area, lateral orbital area, dorsol

109 to the submedius thalamic nucleus (SubM) and ventrolateral orbital cortex (VLO), regions known to reg

110 %, P=0.032) across prefrontal (dorsolateral, ventrolateral, orbital), anterior cingulate and parietal

111 a greater proportion of mature spines in the ventrolateral orbitofrontal cortex (OFC).

112 tomical and behavioral data suggest that the ventrolateral orbitofrontal cortex (VLO), which exhibits

113 prelimbic, medial/ventral orbitofrontal, and ventrolateral orbitofrontal cortex, mediodorsal thalamus

114 forelimbs, as well as a row of flat, keeled ventrolateral osteoderms associated with the gastralia.

115 trate in vivo in rats that activation of the ventrolateral PAG (vlPAG) affects motor systems at multi

116 Activation was observed in ventrolateral PAG (vlPAG) and lateral PAG (lPAG), where

117 We showed activity in the ventrolateral PAG (vlPAG) during anticipation of resisti

118 NTS)-expressing glutamatergic neurons in the ventrolateral PAG (vlPAG) powerfully promote non-rapid e

119 rmediate and rostral portions of lateral and ventrolateral PAG columns in humans is modulated by cogn

120 Moreover, the ventrolateral PAG of KO rats displayed elevated overall

121 nhibition of projections from the PFC to the ventrolateral PAG region and its downstream targets.

122 al gray (PAG), the Su3 and PV2 nuclei of the ventrolateral PAG, the cuneiform nucleus, the mesencepha

123 s based on activity increases in lateral and ventrolateral PAG.

124 fined spade-shaped prostomium with elongated ventrolateral palps.

125 teral hypothalamus-projecting neurons in the ventrolateral part of BNST to regulate feeding, receive

126 um and should therefore be considered a most ventrolateral part of the dorsal pallium (its ventrolate

127 ants, a lateral subpopulation of DR neurons (ventrolateral part of the DR) was lost, whereas the numb

128 striate visual areas received input from the ventrolateral part of the laterodorsal nucleus of the th

129 Recent studies suggest that cells in the ventrolateral part of the ventromedial hypothalamus (VMH

130 bited rapid task learning, we found that the ventrolateral part of the ventromedial hypothalamus (VMH

131 e of LS input on the cells in and around the ventrolateral part of the ventromedial hypothalamus (VMH

132 The medial preoptic nucleus (MPN) and ventrolateral part of the ventromedial hypothalamus (VMH

133 minal fields were densest in the lateral and ventrolateral periaqueductal gray (PAG), lateral parabra

134 nhibition of presynaptic GABA release in the ventrolateral periaqueductal gray (vlPAG) activates the

135 nstem pain-modulatory regions, including the ventrolateral periaqueductal gray (vlPAG) and locus ceru

136 The ventrolateral periaqueductal gray (vlPAG) and neighborin

137 The ventrolateral periaqueductal gray (vlPAG) is a key struc

138 e-prostaglandin (PG) E2 signaling within the ventrolateral periaqueductal gray (vlPAG) is pronocicept

139 The ventrolateral periaqueductal gray (vlPAG) is proposed to

140 eat probability estimates are relayed to the ventrolateral periaqueductal gray (vlPAG) to organize fe

141 tional excitatory synapses on neurons in the ventrolateral periaqueductal gray (vlPAG), and photostim

142 anges, send glutamatergic projections to the ventrolateral periaqueductal gray (vlPAG), which contain

143 parabrachial nucleus, Kolliker-Fuse nucleus, ventrolateral periaqueductal gray area, central nucleus

144 rate that GABA signaling is modulated in the ventrolateral periaqueductal gray by persistent inflamma

145 ion-but not inhibition-of avBST input to the ventrolateral periaqueductal gray impaired consolidation

146 The PVH and ventrolateral periaqueductal gray were recipients of GAB

147 with the exception of the projection to the ventrolateral periaqueductal gray, where the GABAergic c

148 control systems originating in the brainstem ventrolateral periaqueductal grey (VL-PAG), which contro

149 The ventrolateral periaqueductal grey (vlPAG) has a well-est

150 y that produces freezing by disinhibition of ventrolateral periaqueductal grey excitatory outputs to

151 m the central nucleus of the amygdala to the ventrolateral periaqueductal grey that produces freezing

152 of REM-suppressing GABAergic neurons in the ventrolateral periaqueductal grey.

153 ere observed during self-paced suturing, and ventrolateral PFC (VLPFC) deactivations were identified

154 Neurons in the ventrolateral PFC (VLPFC) have been shown to separately

155 manifesting as an unanticipated increase in ventrolateral PFC activation in nonrisk-associated C all

156 lated to functional connectivity between the ventrolateral PFC and ventral striatum in healthy contro

157 t longitudinal declines in activation of the ventrolateral PFC are linked to declines in adolescent r

158 e also show dissociable coding signatures in ventrolateral PFC, a region previously implicated in int

159 Less activation of the right ventrolateral PFC/inferior frontal gyrus during pre-trea

160 The rostral ventrolateral portion of the medulla (RVLM) is composed

161 econd, smaller patch of cells in the caudal, ventrolateral portion.

162 age) sector bends away from V2d, as does the ventrolateral posterior area (VLP) in marmosets and the

163 om the face/head region of the primary (M1), ventrolateral pre- (LPMCv), supplementary (M2), rostral

164 haracterized by increased grey matter in the ventrolateral prefrontal and dorsal premotor cortices.

165 nostic groups, with the notable exception of ventrolateral prefrontal and parietal association cortex

166 stic groups, increased cortical thickness in ventrolateral prefrontal and parietal cortical regions w

167 Both orbitofrontal and ventrolateral prefrontal areas contribute to updating th

168 nual anterior cingulate cortex (P < .05) and ventrolateral prefrontal cortex (P < .05) and hypoactiva

169 orsal anterior cingulate cortex (rdACC), and ventrolateral prefrontal cortex (rVLPFC) and (ii) dorsal

170 tional double dissociation between the right ventrolateral prefrontal cortex (rVLPFC) and the bi-late

171 imaging, we found that a region in the right ventrolateral prefrontal cortex (rVLPFC) was more engage

172 imaging in human adolescents, we found that ventrolateral prefrontal cortex (VLPFC) activation decre

173 er expression, specifically within the right ventrolateral prefrontal cortex (vlPFC) and most strongl

174 serotonin transporter gene expression in the ventrolateral prefrontal cortex (vlPFC) and most strongl

175 an primates has shown that single neurons in ventrolateral prefrontal cortex (VLPFC) exhibit multisen

176 Distributed activity patterns within the ventrolateral prefrontal cortex (VLPFC) indicated the pr

177 To test whether the ventrolateral prefrontal cortex (vlPFC) is a critical re

178 We demonstrated that macaque ventrolateral prefrontal cortex (VLPFC) neurons show rem

179 Here, we demonstrate that neurons in the ventrolateral prefrontal cortex (vlPFC) of monkeys perfo

180 dies demonstrated that single neurons in the ventrolateral prefrontal cortex (VLPFC) of the rhesus mo

181 Before inhibitory demands, posterior ventrolateral prefrontal cortex (VLPFC), an area involve

182 followed by later reduced activation in the ventrolateral prefrontal cortex (VLPFC), dorsal anterior

183 he right inferior frontal junction (IFJ) and ventrolateral prefrontal cortex (VLPFC), respectively.

184 One potential region is the left ventrolateral prefrontal cortex (vlPFC), which shows abn

185 he anterior orbitofrontal cortex (antOFC) or ventrolateral prefrontal cortex (vlPFC).

186 ctional connectivity between hippocampus and ventrolateral prefrontal cortex (vlPFC).

187 e recorded 403 task-related neurons from the ventrolateral prefrontal cortex (VLPFC): unimodal sensor

188 c underactivation predominantly in the right ventrolateral prefrontal cortex (z = 1.229, P < .001).

189 or disorders were associated with lower left ventrolateral prefrontal cortex activity to win (t = 2.6

190 Reduced left ventrolateral prefrontal cortex activity to win may refl

191 the associative cortex was parcellated into ventrolateral prefrontal cortex and dorsolateral prefron

192 olunteers, we found evidence implicating the ventrolateral prefrontal cortex and hippocampus in this

193 greater functional connectivity in the left ventrolateral prefrontal cortex and reduced working memo

194 memory and decision making network involving ventrolateral prefrontal cortex and second somatosensory

195 functional connectivity strength between the ventrolateral prefrontal cortex and the anterior cingula

196 anxiety with cortical thickness in the right ventrolateral prefrontal cortex and the right superior p

197 One connection (between the right ventrolateral prefrontal cortex and the right temporal-p

198 ortex (DLPFC), relatively intact function of ventrolateral prefrontal cortex and variable results in

199 Instead, reduction of gray matter density in ventrolateral prefrontal cortex correlates tightly with

200 und that reduction of gray matter density in ventrolateral prefrontal cortex correlates with economic

201 Instead, older adults recruited bilateral ventrolateral prefrontal cortex differentially for succe

202 on of the dorsolateral prefrontal cortex and ventrolateral prefrontal cortex during affective process

203 nificantly more positive right amygdala-left ventrolateral prefrontal cortex functional connectivity

204 together with findings of increased amygdala-ventrolateral prefrontal cortex functional connectivity,

205 However, whereas the effects of ventrolateral prefrontal cortex inactivation on punishme

206 covered a network centered in the medial and ventrolateral prefrontal cortex that is exclusively enga

207 al parietal cortical thickness, greater left ventrolateral prefrontal cortex thickness, lower right t

208 t learning was predicted to occur, while the ventrolateral prefrontal cortex was found to encode unce

209 nal connectivity between the caudate and the ventrolateral prefrontal cortex was selectively associat

210 etween the pregenual cingulate and the right ventrolateral prefrontal cortex while anticipating rewar

211 tory activity in a network that includes the ventrolateral prefrontal cortex while memory content is

212 tions between these sensorimotor regions and ventrolateral prefrontal cortex, a structure associated

213 including dorsolateral prefrontal cortex and ventrolateral prefrontal cortex, as well as precentral/p

214 responsiveness of the external-task-positive ventrolateral prefrontal cortex, but not of DMN regions,

215 d activation in cognitive control circuitry (ventrolateral prefrontal cortex, insula) during decision

216 s arbitration signal, was represented in the ventrolateral prefrontal cortex, temporoparietal junctio

217 ex as well as the anterior insula, the right ventrolateral prefrontal cortex, the right intraparietal

218 ntation by the anterior cingulate cortex and ventrolateral prefrontal cortex, versus proactive cognit

219 uitment and integration) in dorsolateral and ventrolateral prefrontal cortex, which returned to basel

220 d dissociable connectivity patterns with the ventrolateral prefrontal cortex, with increasing connect

221 ed reduced fractional anisotropy in the left ventrolateral prefrontal cortex-associative striatum and

222 ral prefrontal cortex-sensorimotor striatum, ventrolateral prefrontal cortex-associative striatum, an

223 frontal cortex-associative striatum and left ventrolateral prefrontal cortex-sensorimotor striatum an

224 sorimotor striatum and in the left and right ventrolateral prefrontal cortex-sensorimotor striatum in

225 prefrontal cortex-associative striatum, and ventrolateral prefrontal cortex-sensorimotor striatum).

226 oding of no-go cues into memory, notably the ventrolateral prefrontal cortex.

227 bsample permutation tests: the left anterior ventrolateral prefrontal cortex/insula, the dorsal midbr

228 sfunction in prefrontal cortical (especially ventrolateral prefrontal cortical)-hippocampal-amygdala

229 Dysregulation of the orbitofrontal and ventrolateral prefrontal cortices is implicated in anxie

230 l network (anterior cingulate and dorsal and ventrolateral prefrontal cortices) during cognitive modu

231 ork of regions, including bilateral insulae, ventrolateral prefrontal gyri, superior temporal gyri, a

232 s from frontal motor, inferior parietal, and ventrolateral prefrontal hand-related areas and thus are

233 romedial prefrontal), and cognitive control (ventrolateral prefrontal) areas, as well as in sensorimo

234 ltreatment are in relatively late-developing ventrolateral prefrontal-limbic-temporal regions that ar

235 ith ADHD showed smaller and underfunctioning ventrolateral prefrontal/insular-striatal regions wherea

236 ations implicated in sleep-wake control, the ventrolateral preoptic (VLPO) nucleus has emerged as a k

237 By contrast, c-Fos was absent from the ventrolateral preoptic area (active during sleep).

238 argest synaptic input to the sleep-promoting ventrolateral preoptic area (VLPO) [1] arises from the l

239 n in the SCN compared to the sleep-promoting ventrolateral preoptic area (VLPO), whereas green light

240 rons in the preoptic area, especially in the ventrolateral preoptic area and median preoptic nucleus.

241 l rats and in rats where the sleep-promoting ventrolateral preoptic nucleus (VLPO) is lesioned (male

242 ithin the median preoptic nucleus (MnPO) and ventrolateral preoptic nucleus (VLPO) of the hypothalamu

243 Sleep-active neurons located in the ventrolateral preoptic nucleus (VLPO) play a crucial rol

244 The sleep-promoting ventrolateral preoptic nucleus (VLPO) shares reciprocal

245 citability of sleep-promoting neurons in the ventrolateral preoptic nucleus (VLPO).

246 In rodents, lesions of the hypothalamic ventrolateral preoptic nucleus cause fragmented sleep.

247 e hrGFP-positive fibers were observed in the ventrolateral preoptic nucleus, a known sleep-related st

248 transmitter profile, is the homologue of the ventrolateral preoptic nucleus, but physiological data i

249 ortex, but decreased c-Fos expression in the ventrolateral preoptic nucleus.

250 ate nucleus being the human homologue of the ventrolateral preoptic nucleus.

251 ) (T6I), the ventral complex (T6II), and the ventrolateral protocerebrum (T6III).

252 athway for courtship hearing via third-order ventrolateral protocerebrum Projection Neuron 1 (vPN1) n

253 in the mature OB, was first detected in the ventrolateral region during development.

254 wed significantly increased NM-MRI signal in ventrolateral regions of the substantia nigra (area unde

255 the olfactory bulb (OB) into dorsomedial and ventrolateral regions.

256 reas the lateral SPZ receives input from the ventrolateral SCN and the retinohypothalamic tract (Leak

257 ng focal projections to ventral hippocampus, ventrolateral septum, and LHb originated from the dorsoc

258 tebral arteries (VTAs) that extend along the ventrolateral sides of the spinal cord.

259 s toward the ventromedial, and away from the ventrolateral, spinal cord as the frequency of fictive l

260 find that loss-of-function of D2-MSNs within ventrolateral striatum (VLS) is sufficient to reduce goa

261 (direct) and A2A+ (indirect) neurons in the ventrolateral striatum in head-fixed mice on a fixed tim

262 In contrast, we found that ventrolateral STS is driven preferentially during versio

263 rea (MPOA) or the ventromedial hypothalamus, ventrolateral subdivision (VMHvl) revealed distinct patt

264 The ventrolateral subdivision of the murine ventromedial hyp

265 males through chemogenetic activation of the ventrolateral subdivision of the ventromedial hypothalam

266 ceptor 1-expressing (Esr1(+)) neurons in the ventrolateral subdivision of the ventromedial hypothalam

267 ceptor 1-expressing (Esr1(+)) neurons in the ventrolateral subdivision of the ventromedial hypothalam

268 or-alpha (ERalpha)-expressing neurons in the ventrolateral subdivision of the ventromedial hypothalam

269 estrogen receptor-expressing neurons in the ventrolateral subdivision of the ventromedial hypothalam

270 The ventrolateral subdivision of the ventromedial hypothalam

271 ntral subiculum, the arcuate nucleus and the ventrolateral subdivision of the ventromedial nucleus of

272 entrolateral part of the dorsal pallium (its ventrolateral subdivision).

273 The ventrolateral subfield of the striatum (VLS) is the orof

274 transient but strong regional expression in ventrolateral surface ectoderm at E10.5, much earlier th

275 left inferior frontal gyrus, as well as the ventrolateral temporal cortex, and (3) motor/language ac

276 set of bilateral frontal, Intraparietal, and ventrolateral temporal regions.

277 However, only ventrolateral thalamic stimulation in essential tremor m

278 timulation in Parkinson's disease, P=0.0312; ventrolateral thalamic stimulation in essential tremor,

279 ntrained tremor in all three patient groups (ventrolateral thalamic stimulation in Parkinson's diseas

280 temporal, and superior parietal cortices and ventrolateral thalamic, and medial amygdalo-hippocampal

281 tantly, dorsal caudate connectivity with the ventrolateral thalamus and subthalamic nucleus showed in

282 Ventrolateral thalamus contains subdivisions devoted to

283 ortex (DMFC), DMFC-projecting neurons in the ventrolateral thalamus, and putative target of DMFC in t

284 is achieved by delivering stimulation to the ventrolateral thalamus, timed according to the patient's

285 distal target of the cerebellar nuclei, the ventrolateral thalamus, we observed retrogradely labeled

286 in the cerebellar nuclei and boutons in the ventrolateral thalamus.

287 with increased auditory-sensorimotor network-ventrolateral-thalamus iFC.

288 cts of photo-evoked histamine release in the ventrolateral TMN and VLPO.

289 decreased inhibitory GABAergic inputs to the ventrolateral TMN neurons but produced a membrane hyperp

290 tribution revealed a gradient that runs from ventrolateral to dorsomedial along the axis of the lamin

291 te-stage hem-ablated embryos, whereas cortex ventrolateral to the neocortex expanded dorsally.

292 f the deep mesencephalic nucleus (DpMe) just ventrolateral to the periaquiductal gray, termed the dor

293 m(3) , p < 0.0001) midbrain that was located ventrolateral to the red nucleus and corresponded to the

294 ries have been identified in parietal cortex ventrolateral to visuotopic IPS.

295 nigra (SN), ventral tegmental area (VTA) and ventrolateral-ventromedial nuclei of the thalamus (VL-VM

296 jor fiber bundle connecting dorsolateral and ventrolateral visual cortex.

297 sory neurons (OSNs) forms a dorsomedial (DM)-ventrolateral (VL) gradient in the mouse olfactory epith

298 T neurons and thalamocortical neurons in the ventrolateral (VL) nucleus were remarkably unconnected i

299 medial (dm)PFC, amygdala-dmPFC, and amygdala-ventrolateral (vl)PFC.

300 ions from the medial (MO), ventral (VO), and ventrolateral (VLO) orbitofrontal areas and the caudal p