ライフサイエンスコーパス: geniculate nucleus

1 mus (the equivalent to the mammalian lateral geniculate nucleus).

2 in other thalamic nuclei (e.g., the lateral geniculate nucleus).

3 g from ipsilateral auditory thalamus (medial geniculate nucleus).

4 lamic neuroepithelium to the ventral lateral geniculate nucleus.

5 ventral basal nucleus and the dorsal lateral geniculate nucleus.

6 cts to multiple areas, including the lateral geniculate nucleus.

7 nogeniculate axon segregation in the lateral geniculate nucleus.

8 l-type-specific layers in the dorsal lateral geniculate nucleus.

9 6 with identified projections to the lateral geniculate nucleus.

10 ation of retinal axons in the dorsal lateral geniculate nucleus.

11 in interneurons of the mouse dorsal lateral geniculate nucleus.

12 ld centers of neurons in the macaque lateral geniculate nucleus.

13 l RGCs in the ventral portion of the lateral geniculate nucleus.

14 n to the magnocellular layers of the lateral geniculate nucleus.

15 l to the magnocellular layers of the lateral geniculate nucleus.

16 rhodamine dextran injected into the lateral geniculate nucleus.

17 the principal layers of the macaque lateral geniculate nucleus.

18 rior colliculus, the retina, and the lateral geniculate nucleus.

19 elay, from both M and P cells of the lateral geniculate nucleus.

20 s in the mammalian retina and dorsal lateral geniculate nucleus.

21 ns between the retina and the dorsal lateral geniculate nucleus.

22 ections to the margins of the dorsal lateral geniculate nucleus.

23 in the next stage of processing, the lateral geniculate nucleus.

24 metabolism in the caudate/putamen and medial geniculate nucleus.

25 cipal neurons that can project to the medial geniculate nucleus.

26 other forms of selectivity in rodent lateral geniculate nucleus.

27 holera toxin beta from retina to the lateral geniculate nucleus (60% decrease), and to the superior c

28 Within the ventral medial geniculate nucleus, a modular organization, revealed wit

29 cell (RGC) projections to the dorsal lateral geniculate nucleus, a process that involves activity-dep

30 superior colliculus (SC) and dorsal lateral geniculate nucleus and are restricted to a specific lami

31 butions of visual neurons in macaque lateral geniculate nucleus and cortical areas V1, V2 and MT, rev

32 on-columnar mouse V1 from the dorsal lateral geniculate nucleus and feedback projections from multipl

33 fects that alter projections from the medial geniculate nucleus and from the caudal ventrobasal nucle

34 ions, and the tecto-recipient dorsal lateral geniculate nucleus and its projections are detailed.

35 act white-matter pathway between the lateral geniculate nucleus and motion area hMT+.

36 usively contralateral; to the dorsal lateral geniculate nucleus and posterior pretectal nucleus are p

37 ptive visual response changes in the lateral geniculate nucleus and primary visual cortex following n

38 inding, the connectivity between the lateral geniculate nucleus and primary visual cortex measured wi

39 visual information processing in the lateral geniculate nucleus and primary visual cortex.

40 The lateral geniculate nucleus and pulvinar are examples of two diff

41 These pathways enable the lateral geniculate nucleus and pulvinar to regulate the informat

42 Projections from the lateral geniculate nucleus and pulvinar to V1 were present at 4

43 corticothalamic pathways to the dorsolateral geniculate nucleus and pulvinar, as well as the prevalen

44 as the thalamus, including both the lateral geniculate nucleus and pulvinar.

45 Cs project exclusively to the dorsal lateral geniculate nucleus and superior colliculus and in both t

46 targets in the brain, including the lateral geniculate nucleus and superior colliculus.

47 s and 2 other visual structures: the lateral geniculate nucleus and the primary visual cortex.

48 al connectivity pattern originating from the geniculate nucleus and the pulvinar nuclei.

49 y project differently to the ventral lateral geniculate nucleus and the superior colliculus.

50 ore provide visual input to both the lateral geniculate nucleus and the superior colliculus.

51 nigra pars compacta, ventral tegmental area, geniculate nucleus and the superior colliculus.

52 retrograde transport from the dorsal lateral geniculate nucleus and thus likely contribute to the pat

53 The optic nerve, lateral geniculate nucleus and visual cortex provide alternative

54 an ipsilateral pathway between LGN (lateral geniculate nucleus) and human motion area MT+/V5 (bypass

55 and the interlaminar portions of the lateral geniculate nucleus, and efferent projections to the supe

56 ypes, through distinct layers of the lateral geniculate nucleus, and into primary visual cortex (V1),

57 , interneurons moving to the ventral lateral geniculate nucleus, and neocortical cells going to the a

58 e labeling of neurons in the cortex, lateral geniculate nucleus, and superior colliculus, and can be

59 detected even earlier, in the human lateral geniculate nucleus, and that attentional feedback select

60 ise, the superior colliculus, dorsal lateral geniculate nucleus, and the posterior nucleus of the pul

61 s activity in the developing retina, lateral geniculate nucleus, and visual cortex instruct the axona

62 ical stimulation (TBS) of the dorsal lateral geniculate nucleus, are sufficient to account for SRP.

63 the physical inversion of the dorsal lateral geniculate nucleus, as well as the lateral posterior and

64 Neurons in the lateral geniculate nucleus cannot perform the spatial color calc

65 he thalamic reticular nucleus to the lateral geniculate nucleus complete the earliest feedback loop i

66 As in other carnivores, the dorsal lateral geniculate nucleus consisted of three main layers, A, A1

67 ns and thalamic relay neurons of the lateral geniculate nucleus contributed to tonic conductance caus

68 Response magnitude in the lateral geniculate nucleus did not increase with locomotion, dem

69 passes V1, and connects the thalamic lateral geniculate nucleus directly with the extrastriate cortic

70 es of nonretinal input to the dorsal lateral geniculate nucleus (dLGN) and play a major role in modul

71 ed the membrane properties of dorsal lateral geniculate nucleus (dLGN) and pulvinar nucleus relay neu

72 C to two thalamic nuclei: the dorsal lateral geniculate nucleus (dLGN) and the lateral posterior nucl

73 (RGC) axon projections in the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (S

74 d parvocellular layers of the dorsal lateral geniculate nucleus (dLGN) are distinguished by unique re

75 eyes initially overlap in the dorsal-lateral geniculate nucleus (dLGN) but subsequently refine to occ

76 revealed that neurons in mouse dorsolateral geniculate nucleus (dLGN) can undergo rapid ocular domin

77 GNIFICANCE STATEMENT Only the dorsal lateral geniculate nucleus (dLGN) connects to cortex to serve fo

78 Thalamocortical neurons in dorsal lateral geniculate nucleus (dLGN) dynamically convey visual info

79 The local interneurons in the dorsal lateral geniculate nucleus (dLGN) give rise to two distinct syna

80 The dorsal lateral geniculate nucleus (dLGN) in carnivores and primates is

81 The dorsal lateral geniculate nucleus (dLGN) is a model system for understa

82 The dorsal lateral geniculate nucleus (dLGN) is a sensory thalamic relay ar

83 ty between the retina and the dorsal lateral geniculate nucleus (dLGN) is established by gradients of

84 The conventional view of the dorsal lateral geniculate nucleus (dLGN) is that of a simple relay of v

85 The dorsal lateral geniculate nucleus (dLGN) is the primary thalamic relay

86 The dorsal lateral geniculate nucleus (dLGN) not only serves as the obligat

87 ed dextran amine (BDA) in the dorsal lateral geniculate nucleus (dLGN) of anesthetized cats and spiny

88 The dorsal lateral geniculate nucleus (dLGN) of the mouse has emerged as a

89 The dorsal lateral geniculate nucleus (dLGN) of the mouse is a model system

90 med projection neurons in the dorsal lateral geniculate nucleus (dLGN) of the rat was examined by fil

91 In rat, the dorsal lateral geniculate nucleus (dLGN) of the thalamus is the primary

92 Within the dorsal lateral geniculate nucleus (dLGN) of the thalamus, retinal gangl

93 nhibitory interneurons in the dorsal lateral geniculate nucleus (dLGN) process visual information by

94 The dorsal lateral geniculate nucleus (dLGN) receives visual information fr

95 Simultaneous recording in the dorsal lateral geniculate nucleus (dLGN) revealed that these reflect ch

96 The dorsal lateral geniculate nucleus (dLGN) serves as the primary conduit

97 main thalamic drive from the dorsal lateral geniculate nucleus (dLGN) through synaptic contacts term

98 of motion direction in mouse dorsal lateral geniculate nucleus (dLGN) using two-photon calcium imagi

99 thalamic relay neurons of the dorsal lateral geniculate nucleus (dLGN) was studied after ablating tyr

100 In this study of the cat dorsal lateral geniculate nucleus (dLGN) we examined whether labeling f

101 or disfacilitate cells in cat dorsal lateral geniculate nucleus (dLGN) were applied iontophoretically

102 domains in their target, the dorsal lateral geniculate nucleus (dLGN), are crucial for binocular vis

103 superior colliculus (SC) and dorsal lateral geniculate nucleus (dLGN), bridge retinal input and visu

104 its thalamic inputs from the dorsal lateral geniculate nucleus (dLGN), but more rarely in the latera

105 of the suprachiasmatic nucleus, dorsolateral geniculate nucleus (dLGN), intergeniculate leaflet, vent

106 n was observed in the retina, dorsal lateral geniculate nucleus (dLGN), superior colliculus (SC), and

107 developing cells of the mouse dorsal lateral geniculate nucleus (dLGN), synaptic responses evoked by

108 examined whether cells in the dorsal lateral geniculate nucleus (dLGN), the thalamic relay between th

109 ciprocally connected with the dorsal lateral geniculate nucleus (dLGN), the ventral pulvinar nucleus

110 types of DSGCs connect to the dorsal lateral geniculate nucleus (dLGN), the visual thalamic structure

111 contralateral and ipsilateral dorsal lateral geniculate nucleus (dLGN), underpinning disparity-based

112 in their thalamic target, the dorsal lateral geniculate nucleus (dLGN), when crossing at the optic ch

113 rtex but one exception is the dorsal lateral geniculate nucleus (dLGN), which receives layer 6 inputs

114 rding visual responses in the dorsal lateral geniculate nucleus (dLGN).

115 petition for territory in the dorsal lateral geniculate nucleus (dLGN).

116 tical (TC) neurons of the rat dorsal lateral geniculate nucleus (dLGN).

117 relayed to the cortex by the dorsal lateral geniculate nucleus (dLGN).

118 iculate nucleus (PGN) and the dorsal lateral geniculate nucleus (dLGN).

119 t the level of the retina and dorsal lateral geniculate nucleus (dLGN).

120 in deprived layers of the cat dorsal lateral geniculate nucleus (dLGN).

121 or nucleus (LP), as well as the dorsolateral geniculate nucleus (dLGN).

122 rom local interneurons in the dorsal lateral geniculate nucleus (dLGN-INs) provides inhibitory contro

123 evoked responses in the mouse dorsal lateral geniculate nucleus (dLGN; thalamic relay for cortical vi

124 In addition, inputs from the dorsal medial geniculate nucleus (dMGN) increase, whereas those from t

125 e responses of neurons in the dorsal lateral geniculate nucleus during and after the presentation of

126 uency via feedforward input from the lateral geniculate nucleus (e.g., [1]).

127 ) or through microstimulation of the lateral geniculate nucleus (electrically).

128 ves a generalized increase in dorsal lateral geniculate nucleus excitability as dawn progresses that

129 he primary visual cortex to the dorsolateral geniculate nucleus (first-order) and pulvinar (higher-or

130 We explored the murine lateral geniculate nucleus from a comparative physiological pers

131 rlooked koniocellular pathway of the lateral geniculate nucleus has generated interest in how alterna

132 llular layers of the marmoset dorsal lateral geniculate nucleus have binocularly responsive neurons.

133 Using recordings in the lateral geniculate nucleus, here we demonstrate that the relevan

134 ade degeneration of the ipsilesional lateral geniculate nucleus in both experimental groups, suggesti

135 s questions about the role of dorsal lateral geniculate nucleus in early binocular processing.

136 different rhythms that emerge in the lateral geniculate nucleus in the thalamus during different atte

137 hallucinations were connected to the lateral geniculate nucleus in the thalamus while lesions causing

138 ic tectum (superior colliculus), and lateral geniculate nucleus in vertebrates; and retina, lamina, a

139 led important roles for pulvinar and lateral geniculate nucleus in visuospatial perception and attent

140 and pig retina and from mouse dorsal lateral geniculate nucleus in vivo at up to seven ambient light

141 Interneurons in the lateral geniculate nucleus innervate relay cells and each other

142 ast, while clear evidence for dorsal lateral geniculate nucleus input to V1 excitatory neurons was fo

143 nantly contralateral; to the ventral lateral geniculate nucleus, intergeniculate leaflet, and olivary

144 of retinal projections at the dorsal lateral geniculate nucleus is altered in Boc(-/-) mice.

145 about the development of the dorsal lateral geniculate nucleus is limited to circuits involving exci

146 wed that neuron number in the dorsal lateral geniculate nucleus is reduced following early gestationa

147 The lateral geniculate nucleus (LG) is an important subcortical nucl

148 onto neurons within subnuclei of the lateral geniculate nucleus (LGN) [i.e., the dorsal LGN (dLGN), v

149 thalamic terminals in V1 arise from lateral geniculate nucleus (LGN) afferents.

150 activity in two visual centres, the lateral geniculate nucleus (LGN) and cortical area MT, in marmos

151 system, afferents from retina to the lateral geniculate nucleus (LGN) and from LGN to primary visual

152 tinotopically aligned regions in the lateral geniculate nucleus (LGN) and primary visual cortex (V1)

153 which connectivity between the mouse lateral geniculate nucleus (LGN) and primary visual cortex (V1)

154 We used paired recordings, in the lateral geniculate nucleus (LGN) and primary visual cortex (V1),

155 ollowing birth into adulthood in the lateral geniculate nucleus (LGN) and primary visual cortex (V1,

156 , we recorded neural activity in the lateral geniculate nucleus (LGN) and pulvinar of 2 macaque monke

157 in retinotopic map formation in the lateral geniculate nucleus (LGN) and superior colliculus (SC).

158 via the koniocellular layers of the lateral geniculate nucleus (LGN) and the medial portion of the i

159 In mammals, the lateral geniculate nucleus (LGN) and the superior colliculus (SC

160 rtical visual structures such as the lateral geniculate nucleus (LGN) and the superior colliculus (SC

161 s (ventral and dorsal pulvinar), the lateral geniculate nucleus (LGN) and visual cortex (area V4) pri

162 cells and project in parallel to the lateral geniculate nucleus (LGN) and/or the superior colliculus.

163 cal projection neurons in the dorsal lateral geniculate nucleus (LGN) by 7 d after lesion.

164 The lateral geniculate nucleus (LGN) contains a unique and numerous

165 The responses of neurons in lateral geniculate nucleus (LGN) exhibit powerful suppressive ph

166 es impinging on relay neurons in the lateral geniculate nucleus (LGN) generate synaptic potentials, w

167 ere we demonstrate that the thalamic lateral geniculate nucleus (LGN) has a causal role in V1-indepen

168 nes of evidence show that the murine lateral geniculate nucleus (LGN) has unique attributes, compared

169 e-specific visual projections to the lateral geniculate nucleus (LGN) have not previously been identi

170 ugh the magno- and parvocells of the lateral geniculate nucleus (LGN) indirectly to extrastriate visu

171 to feed-forward models that rely on lateral geniculate nucleus (LGN) input alone.

172 ecise connections between retina and lateral geniculate nucleus (LGN) involves the activity-dependent

173 In the visual system, the thalamic lateral geniculate nucleus (LGN) is generally thought to encode

174 to the superior colliculus (SC) and lateral geniculate nucleus (LGN) is guided by molecular cues, an

175 SIGNIFICANCE STATEMENT: The lateral geniculate nucleus (LGN) is the gateway through which re

176 New stereological assessments of lateral geniculate nucleus (LGN) neuron numbers and volumes in f

177 cross simulated cone photoreceptors, lateral geniculate nucleus (LGN) neurons, and perceptual judgeme

178 ctive changes in the firing of mouse lateral geniculate nucleus (LGN) neurons, leading to increased f

179 Neurons in the lateral geniculate nucleus (LGN) not only provide feedforward in

180 rain slice preparation of the dorsal lateral geniculate nucleus (LGN) of macaque monkeys that have ch

181 ive field property of neurons in the lateral geniculate nucleus (LGN) of the dorsal thalamus, influen

182 Within the lateral geniculate nucleus (LGN) of the dorsal thalamus, these c

183 anization of retinotopic maps in the lateral geniculate nucleus (LGN) of the thalamus and early visua

184 way links the visual cortex with the lateral geniculate nucleus (LGN) of the thalamus and is the firs

185 esponse properties of neurons in the lateral geniculate nucleus (LGN) of the thalamus in the alert ma

186 driving input from the eyes via the lateral geniculate nucleus (LGN) of the thalamus.

187 sequences on visual responses in the lateral geniculate nucleus (LGN) of the thalamus.

188 ayers of their target structure, the lateral geniculate nucleus (LGN) of the thalamus.

189 ching cerebral cortex is through the lateral geniculate nucleus (LGN) of the thalamus.

190 n passes from the retina through the lateral geniculate nucleus (LGN) of the thalamus.

191 ensembles of maturing neurons in the lateral geniculate nucleus (LGN) of the thalamus.

192 o functionally map the koniocellular lateral geniculate nucleus (LGN) projection to primary visual co

193 occurs not only in the responses of lateral geniculate nucleus (LGN) relay cells but also in their a

194 stence of orientation selectivity in lateral geniculate nucleus (LGN) relay cells.

195 ions from the two eyes to the dorsal lateral geniculate nucleus (LGN) segregate to form non-overlappi

196 rallel visual pathways in the dorsal lateral geniculate nucleus (LGN) show distinct patterns of inter

197 e neurones make more synapses in the lateral geniculate nucleus (LGN) than retinal ganglion cells, ye

198 cats, thalamocortical neurons in the lateral geniculate nucleus (LGN) that operate in a conventional

199 S mechanism in selective wiring from lateral geniculate nucleus (LGN) to primary visual cortex, OS re

200 of spikes between the retina and the lateral geniculate nucleus (LGN) with the goal of determining wh

201 tral response curves of cells in the lateral geniculate nucleus (LGN) with the reflectance spectra of

202 ses in the superior colliculus (SC), lateral geniculate nucleus (LGN), and two retinotopic pulvinar n

203 n the main thalamic input to V1, the lateral geniculate nucleus (LGN), are considered to be only weak

204 m which they receive afferences: the lateral geniculate nucleus (LGN), due to optic neuritis (ON) and

205 and optic tracts to the level of the lateral geniculate nucleus (LGN), faithfully reproducing the cro

206 ts with that of their afferents from lateral geniculate nucleus (LGN), in response to similar stimuli

207 the primary visual cortex (V1), the lateral geniculate nucleus (LGN), or the optic tract were scanne

208 Ret(+) RGCs project to the lateral geniculate nucleus (LGN), pretectal area (PTA) and super

209 ependence of neural responses in the lateral geniculate nucleus (LGN), primary visual cortex (V1), an

210 patterns of VGLUT1 and VGLUT2 in the lateral geniculate nucleus (LGN), superior colliculus, pulvinar

211 In the lateral geniculate nucleus (LGN), the cells relaying the retinal

212 nd receptive field of neurons in the lateral geniculate nucleus (LGN), there is an extraclassical, no

213 ual system passes through the dorsal lateral geniculate nucleus (LGN), where nerve signals originatin

214 t only in visual cortex, but also in lateral geniculate nucleus (LGN), where protein localization cor

215 smitted to cortex via neurons in the lateral geniculate nucleus (LGN), where they are processed in bu

216 ng (main signature) activity for the lateral geniculate nucleus (LGN), which in turn drives the prima

217 chromatic-specific circuitry in the lateral geniculate nucleus (LGN).

218 monocular maps en route through the lateral geniculate nucleus (LGN).

219 rent classes of relay neurons in the lateral geniculate nucleus (LGN).

220 t or the feedforward inputs from the lateral geniculate nucleus (LGN).

221 principal visual relay nucleus, the lateral geniculate nucleus (LGN).

222 relay between retina and cortex, the lateral geniculate nucleus (LGN).

223 ideal testbed for such models is the lateral geniculate nucleus (LGN).

224 in colocalized regions of the cat's lateral geniculate nucleus (LGN).

225 receptive fields of 118 cells in the lateral geniculate nucleus (LGN).

226 attern of correlated activity in the lateral geniculate nucleus (LGN).

227 ividual principal cells in the mouse lateral geniculate nucleus (LGN).

228 sustained channels in the retina and lateral geniculate nucleus (LGN).

229 s, rhythmic firing of neurons in the lateral geniculate nucleus (LGN).

230 ed following tracer injection in the lateral geniculate nucleus (LGN).

231 n visual cortex and visual thalamus [lateral geniculate nucleus (LGN)].

232 nse to electrical stimulation of the lateral geniculate nucleus (LGN, 3+ spikes at >600 Hz), and simp

233 isual thalamus (especially the right lateral geniculate nucleus [LGN]), right caudate nucleus, and bi

234 ing spiking activity in subcortical (lateral geniculate nucleus, LGN) and cortical (area MT) visual a

235 ty between the left visual thalamus (lateral geniculate nucleus, LGN) and V5/MT, a cerebral cortex re

236 ectivity of single thalamic neurons (lateral geniculate nucleus, LGN) onto putative fast-spike inhibi

237 or of retinotopically aligned dorsal lateral geniculate nucleus (LGNd) neurons, usually recorded simu

238 idual sustained and transient dorsal lateral geniculate nucleus (LGNd) neurons.

239 ntibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat.

240 N, IGL, OPN, ventral division of the lateral geniculate nucleus (LGv), and preoptic area, but the ove

241 The lateral geniculate nucleus, like all thalamic nuclei, has two cl

242 eus (dLGN), intergeniculate leaflet, ventral geniculate nucleus (magnocellular part), lateroposterior

243 o in thalamocortical slices of A1 and medial geniculate nucleus (MGN) in mouse from postnatal day 1 (

244 principal auditory relay nucleus, the medial geniculate nucleus (MGN), and principal visual relay nuc

245 thalamocortical projections from the medial geniculate nucleus (MGN).

246 Repetitive stimulation of the ventral medial geniculate nucleus (MGv) evoked robust short-term depres

247 The ventral division of the medial geniculate nucleus (MGv) receives almost all of its asce

248 e intensity of the stimulation in the medial geniculate nucleus (MGv).

249 that I(h) recorded from IGL, but not ventral geniculate nucleus, neurons in HCN2(+/+) mice and rats a

250 cells in recordings from the dorsal lateral geniculate nucleus of anesthetized cats.

251 al recordings from retina and dorsal lateral geniculate nucleus of cone-deficient and visually intact

252 In the lateral geniculate nucleus of macaque, we recorded from neurons

253 sthesia with checkerboards activated lateral geniculate nucleus of monkey S, while full-field moving

254 e CNIC remain largely separate in the medial geniculate nucleus of the gerbil.

255 easing or decreasing the size of the lateral geniculate nucleus of the mouse thalamus resulted in a c

256 ere neurons in the retina and dorsal lateral geniculate nucleus of the thalamus (dLGN) are morphologi

257 discharges of neurons in the dorsal lateral geniculate nucleus of the thalamus (dLGN).

258 the retina is relayed to the dorsal lateral geniculate nucleus of the thalamus (LGd).

259 Even though the lateral geniculate nucleus of the thalamus (LGN) is associated w

260 ties of the synaptic inputs from the lateral geniculate nucleus of the thalamus (LGN) onto L4 neurons

261 The dorsal lateral geniculate nucleus of the thalamus (LGN) receives the ma

262 mination in the postnatal mouse dorsolateral geniculate nucleus of the thalamus and sensorimotor cort

263 ether microstimulation of the dorsal lateral geniculate nucleus of the thalamus can generate localize

264 niculocortical axons from the dorsal lateral geniculate nucleus of the thalamus innervate layer 4 (L4

265 nhibitory interneurons of the dorsal lateral geniculate nucleus of the thalamus modulate the activity

266 dies have shown that activity in the lateral geniculate nucleus of the thalamus strongly reflects per

267 ctrically stimulating neurons in the lateral geniculate nucleus of the thalamus while simultaneously

268 o accompanied by degeneration of the lateral geniculate nucleus of the thalamus, and 90% of beta reti

269 in cat area 17, originating from the lateral geniculate nucleus of the thalamus.

270 a sends to the visual cortex via the lateral geniculate nucleus of the thalamus.

271 tor of the magnocellular part of the ventral geniculate nucleus, olivary pretectal nucleus, and SC op

272 right anterior thalamic radiation and right geniculate nucleus optic tracts (P < .0001).

273 in discrete laminar zones within the lateral geniculate nucleus or superior colliculus, demonstrating

274 the suprachiasmatic nucleus, ventral lateral geniculate nucleus, pretectal nuclear complex and the Ed

275 ation of eye-specific retinal dorsal lateral geniculate nucleus projections commences.

276 ulus, visual dorsal thalamus (dorsal lateral geniculate nucleus, pulvinar and lateral posterior nucle

277 The dorsal lateral geniculate nucleus receives projections from visuotopica

278 n the retinal ganglion cells and the lateral geniculate nucleus reduces variation in the presynaptic

279 PGN) or thalamocortical cells in the lateral geniculate nucleus resulted in depolarization and increa

280 e the superior colliculus and dorsal lateral geniculate nucleus, retinotopically organized nuclei med

281 f the visual pathway and on into the lateral geniculate nucleus, superior colliculus, and other visua

282 investigate the architecture of the lateral geniculate nucleus, superior colliculus, and primary vis

283 ling, we investigated how rat dorsal lateral geniculate nucleus thalamocortical neurons integrate exc

284 elay, in the these nuclei and in the lateral geniculate nucleus, the superior colliculus, and the lat

285 ions project similarly to the dorsal lateral geniculate nucleus, they project differently to the vent

286 the adaptation of neurons in the cat lateral geniculate nucleus to changes in stimulus contrast and c

287 ses of receptive fields in the cat's lateral geniculate nucleus to describe how inhibition helps to e

288 from the koniocellular layers of the lateral geniculate nucleus to hMT+, we propose that this altered

289 d involvement in multiple sclerosis: lateral geniculate nucleus to primary visual cortex and mediodor

290 encies of 20 ms and a mean estimated lateral geniculate nucleus to primary visual cortex transfer tim

291 lamocortical neurons projecting from lateral geniculate nucleus to visual cortex.

292 logical activity in the mouse dorsal lateral geniculate nucleus under exposure to a simulated dawn.

293 ctivity distribution, with decreased lateral geniculate nucleus V2 density (F, -8.28; P < .05), a sig

294 oject to the pretectum (PT), ventral lateral geniculate nucleus (vLGN) or parabigeminal nucleus (PBG)

295 The lateral geniculate nucleus was only modulated by 3 to 9% luminan

296 ng seed voxels antero-lateral to the lateral geniculate nucleus, we applied this technique to 20 cont

297 jections from M6 cells to the dorsal lateral geniculate nucleus were confirmed by retrograde tracing,

298 t (for example, retinal input to the lateral geniculate nucleus), whereas higher order relays (for ex

299 his measure of contrast in the cat's lateral geniculate nucleus, which relays signals from retina to

300 than time constants observed in the lateral geniculate nucleus, which were on the order of tens of s