ライフサイエンスコーパス: ventrolateral

1 Responses in ventrolateral and anterior thalamic nuclei tracked learn

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

3 al anterior cingulate cortex (dACC), and the ventrolateral and dorsolateral prefrontal cortex (VLPFC,

4 relations between family income at age 9 and ventrolateral and dorsolateral prefrontal cortex activit

5 wer family income at age 9 exhibited reduced ventrolateral and dorsolateral prefrontal cortex activit

6 under ketamine in the habenula, insula, and ventrolateral and dorsolateral prefrontal cortices of th

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

8 These results also confirm a role for ventrolateral and dorsomedial PFC in the execution of re

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

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

11 althy volunteers demonstrates involvement of ventrolateral and, notably, anterior thalamus in biasing

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

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

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

15 Most ventrolateral ARC TH cells did not contain dopamine and

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

17 However, GHSR-positive neurons in ventrolateral areas did not express markers for cardiova

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

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

20 subgenus completely lacked CRY in the large ventrolateral clock neurons (lLN(v) s) and showed reduce

21 owed reduced PDF immunostaining in the small ventrolateral clock neurons (sLN(v) s).

22 ressing the activity of wake-promoting large ventrolateral clock neurons, and suppression of neuronal

23 expressing neurons, which includes the small ventrolateral clock neurons, is sleep promoting.

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

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

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

27 tive tissue to abaxial musculature and forms ventrolateral dermis of the interlimb body wall.

28 The PV1-nucleus is located within the ventrolateral division of the medial forebrain bundle.

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

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

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

32 cond, rule representations maintained in the ventrolateral frontal and parietal cortex are independen

33 Human ventrolateral frontal cortex (vlFC) is identified with c

34 dition, one distinctively human component in ventrolateral frontal pole.

35 tanding the connectivity of the areas in the ventrolateral frontal region that are involved in langua

36 The superficial thoracic ventrolateral funiculus (VLF) contains both ascending an

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

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

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

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

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

42 perifornical lateral hypothalamus (LH), and ventrolateral, medial, and median preoptic areas (VLPO,

43 -ir neurons), area postrema (AP, 8%), caudal ventrolateral medulla (17%), midline raphe (40%), ventro

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

45 e C1 catecholamine cell group of the rostral ventrolateral medulla (RVLM) and the nucleus of the soli

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

47 The rostral ventrolateral medulla (RVLM) contains neurons critical f

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

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

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

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

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

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

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

55 ulated presympathetic neurons in the rostral ventrolateral medulla (RVLM), but the underlining electr

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

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

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

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

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

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

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

63 The C1 neurons, located in the rostral ventrolateral medulla (VLM), are activated by pain, hypo

64 ured orexin-A mRNA expression in the rostral ventrolateral medulla and antagonized both orexin recept

65 laminergic biosynthetic enzymes revealed the ventrolateral medulla as the source of catecholaminergic

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

67 injection of angiotensin II into the rostral ventrolateral medulla is dependent upon expression of th

68 Photostimulation of ventrolateral medulla neurons expressing the PRSx8-ChR2-

69 ATP released in the ventrolateral medulla oblongata during hypoxia attenuate

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

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

72 ased orexin-A mRNA expression in the rostral ventrolateral medulla, and blocking orexin receptors mar

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

74 antocellular nucleus, the rostral and caudal ventrolateral medulla, the (pre)-Botzinger complex, and

75 sympathetic premotor neurons of the rostral ventrolateral medulla, the C1 neurons.

76 projections to supraspinal sites such as the ventrolateral medulla, the dorsal vagal complex, the dor

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

78 including catecholaminergic neurons, in the ventrolateral medulla.

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

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

81 4) neurons of as yet unknown function in the ventrolateral medulla.

82 ites within the brain, including the rostral ventrolateral medulla.

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

84 nucleus of the hypothalamus and the rostral ventrolateral medulla.

85 Here we test whether these rostral ventrolateral medullary catecholaminergic (RVLM-CA) neur

86 Activation of rostral ventrolateral medullary catecholaminergic (RVLM-CA) neur

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

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

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

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

91 nhibiting transcription factors expressed in ventrolateral midbrain such as Helt, Tle4, Otx1, Sox1 an

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

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

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

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

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

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

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

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

100 ), relaxin-3 fibers were concentrated in the ventrolateral nucleus of rostral LS and the ventral nucl

101 the four rostral segments, a complete set of ventrolateral (O fate) and dorsolateral (P fate) ectoder

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

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

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

105 %, P=0.032) across prefrontal (dorsolateral, ventrolateral, orbital), anterior cingulate and parietal

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

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

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

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

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

111 ral PAG generating fight and flight, and the ventrolateral PAG generating freezing and immobility.

112 re-I cell firing, whereas stimulation in the ventrolateral PAG inhibited not only pre-I cells but als

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

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

115 It has recently been shown that the ventrolateral part of the periaqueductal gray (VLPAG) an

116 the hypothalamic attack area (comprising the ventrolateral part of the ventromedial hypothalamic nucl

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

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

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

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

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

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

123 The ventrolateral periaqueductal gray (vlPAG) is an integral

124 e pathway between central amygdala (CeA) and ventrolateral periaqueductal gray (vlPAG) is implicated

125 The midbrain ventrolateral periaqueductal gray (vlPAG) is known to be

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

127 ar nociceptive responses, from the brainstem ventrolateral periaqueductal gray (vlPAG).

128 olateral medulla (17%), midline raphe (40%), ventrolateral periaqueductal gray (VLPAG, 15%), lateral

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

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

131 The PVH and ventrolateral periaqueductal gray were recipients of GAB

132 tain waking muscle tone such as those in the ventrolateral periaqueductal gray, lateral pontine tegme

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

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

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

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

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

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

139 parately over either dorsolateral (DLPFC) or ventrolateral PFC (VLPFC) in humans before performance o

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

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

142 gions (ventral anterior cingulate cortex and ventrolateral PFC) when processing angry vs. neutral and

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

144 Activity in left ventrolateral PFC, left inferior frontal gyrus, and left

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

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

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

148 of pMN-like ependymoradial glial cells in a ventrolateral position at the central canal.

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

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

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

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

153 Both orbitofrontal and ventrolateral prefrontal areas contribute to updating th

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

155 ibition accompanied by hypoactivation in the ventrolateral prefrontal cortex (PFC).

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

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

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

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

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

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

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

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

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

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

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

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

168 showed TD deficits and reduced activation of ventrolateral prefrontal cortex (VLPFC)/insula, inferior

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

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

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

172 Reduced left ventrolateral prefrontal cortex activity to win may refl

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

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

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

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

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

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

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

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

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

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

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

184 In the dorsolateral and ventrolateral prefrontal cortex during fetal development

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

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

187 Although the amygdala and ventrolateral prefrontal cortex have been implicated in

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

189 Specifically, activity in right ventrolateral prefrontal cortex increased preferentially

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

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

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

193 ivity in the hypothalamus, ventromedial, and ventrolateral prefrontal cortex were significantly reduc

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

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

196 nto a verbal label or word that involves the ventrolateral prefrontal cortex, and one sensitive to th

197 nsion in the temporal parietal junction, the ventrolateral prefrontal cortex, and the dorsal anterior

198 ccuracy) as well as reduced activity in left ventrolateral prefrontal cortex, anterior insula, and or

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

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

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

202 ificant LPP-BOLD correlation was observed in ventrolateral prefrontal cortex, insula, and posterior c

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

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

205 as, including significantly more activity in ventrolateral prefrontal cortex, whereas human activatio

206 connectivity between the caudate nucleus and ventrolateral prefrontal cortex, which anticorrelated wi

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

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

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

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

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

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

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

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

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

216 ity of the hippocampus with dorsolateral and ventrolateral prefrontal cortices and the basal ganglia

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

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

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

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

221 amygdala (emotional brain) modulation by the ventrolateral prefrontal-subcortical circuit, which inte

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

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

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

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

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

227 orsomedial hypothalamus (DMH), and thence to ventrolateral preoptic nuclei (VLPO) and lateral hypotha

228 wn that the wake-active TMN and sleep-active ventrolateral preoptic nucleus (VLPO) are reciprocally c

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

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

231 promoting component of this circuitry is the ventrolateral preoptic nucleus (VLPO), a hypothalamic re

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

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

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

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

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

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

238 trolateral proisocortical motor area (ProM), ventrolateral primary somatosensory cortex (S1), rostral

239 om the dorsolateral premotor cortex (LPMCd), ventrolateral proisocortical motor area (ProM), ventrola

240 ons (PNs) interconnecting the AMMC, inferior ventrolateral protocerebrum (IVLP), and ventrolateral pr

241 rior ventrolateral protocerebrum (IVLP), and ventrolateral protocerebrum (VLP) regions of the central

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

243 In caudal PAG, activity was localized to the ventrolateral region.

244 otzinger complex, and the rostral and caudal ventrolateral respiratory group.

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

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

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

248 the anterior commissure; stimulation of more ventrolateral sites in VS impaired extinction.

249 bodies located in the ventral portion of the ventrolateral somata group and projections along the inn

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

251 The ventrolateral striatum showed long-term potentiation usi

252 ould only be seen close to the graft, in the ventrolateral striatum where the graft-derived reinnerva

253 al to the transplant (i.e., dorsolateral and ventrolateral striatum) and compared the effects of dopa

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

255 The ventrolateral subdivision of the murine ventromedial hyp

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

257 inter-male aggression are located within the ventrolateral subdivision of the ventromedial hypothalam

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

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

260 In the caudal NTS, the ventrolateral subdivision received notable innervation f

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

262 in that the effect of ATP was higher in the ventrolateral subdivision, which is densely innervated f

263 r complex, nucleus ambiguus, commissural and ventrolateral subnuclei of solitary tract nucleus, and r

264 , nucleus ambiguus, hypoglossal nucleus, and ventrolateral subnucleus of solitary tract nucleus), and

265 Activity in lateral and ventrolateral subregions also grouped with distinct emot

266 minent in the dorsomedial, dorsolateral, and ventrolateral subsectors.

267 known direct pathways between the AL and the ventrolateral, superior medial, and posterior lateral pr

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

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

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

271 ing VA/VL (ventral anterior thalamic nucleus/ventrolateral thalamic nucleus), targeted neurons in L2/

272 However, only ventrolateral thalamic stimulation in essential tremor m

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

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

275 The ventrolateral thalamocortical loop appears to amplify al

276 , which includes the subthalamic nucleus and ventrolateral thalamus and has broad frequency-amplitude

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

278 Ventrolateral thalamus contains subdivisions devoted to

279 destruction or deep brain stimulation of the ventrolateral thalamus has been efficacious in all tremo

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

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

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

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

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

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

286 of terminal fields (PV1-CTF) was identified ventrolateral to the aqueduct on the edge of the PAG.

287 tributed to this small, circumscribed column ventrolateral to the aqueduct, the prime target of the P

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

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

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

291 f VGluT1 boutons increased along three axes: ventrolateral-to-dorsomedial, ventral-to-dorsal, and lat

292 (the PV1-nucleus) has been identified in the ventrolateral tuberal hypothalamus in various species.

293 jor fiber bundle connecting dorsolateral and ventrolateral visual cortex.

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

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

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

297 ght-dissociated circadian oscillators in the ventrolateral (vl-) and dorsomedial (dm-) SCN, respectiv

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

299 es revealed that SF1-positive neurons in the ventrolateral VMH (VMH(vl)) persist in Z/EG(Sf1:Cre) emb

300 cal inactivation of either dorsomedial VS or ventrolateral VS, suggesting an extrastriatal mechanism.