ライフサイエンスコーパス: geniculate nucleus

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

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

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

4 6 with identified projections to the lateral geniculate nucleus.

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

6 in interneurons of the mouse dorsal lateral geniculate nucleus.

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

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

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

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

11 rhodamine dextran injected into the lateral geniculate nucleus.

12 the principal layers of the macaque lateral geniculate nucleus.

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

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

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

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

17 ographically precise inputs from the lateral geniculate nucleus.

18 slice preparation of the rat dorsal lateral geniculate nucleus.

19 area of the monkey and from the cat lateral geniculate nucleus.

20 acellular neural activity in the cat lateral geniculate nucleus.

21 in the separate layers of the Galago lateral geniculate nucleus.

22 other forms of selectivity in rodent lateral geniculate nucleus.

23 lamic neuroepithelium to the ventral lateral geniculate nucleus.

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

25 ventral basal nucleus and the dorsal lateral geniculate nucleus.

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

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

28 The lateral geniculate nucleus, a reciprocal region, had retrogradel

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

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

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

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

33 ling in the thalamus, chiefly in the lateral geniculate nucleus and lateral posterior-pulvinar comple

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

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

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

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

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

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

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

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

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

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

44 tory thalamus [medial division of the medial geniculate nucleus and the adjacent posterior intralamin

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

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

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

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

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

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

51 cleus, and the ventral portion of the medial geniculate nucleus) and higher-order (pulvinar and the m

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

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

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

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

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

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

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

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

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

61 nd that the cell response spectra of lateral geniculate nucleus cells, as well as the reflectance spe

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

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

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

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

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

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

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

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

70 ocortical (TC) neurons of the dorsal lateral geniculate nucleus (dLGN) and ventrobasal complex exhibi

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

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

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

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

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

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

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

78 fic axonal projections to the dorsal lateral geniculate nucleus (dLGN) is a well established model sy

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

80 tex to principal cells in the dorsal lateral geniculate nucleus (dLGN) is markedly enhanced with firi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

112 link within the thalamus, the dorsal lateral geniculate nucleus (dLGN).

113 of eye-specific layers in the dorsal lateral geniculate nucleus (dLGN).

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

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

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

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

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

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

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

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

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

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

124 onnections, minimum amplitude ventral medial geniculate nucleus-evoked EPSCs were recorded.

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

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

127 very small number reaches the dorsal lateral geniculate nucleus from the caudal ganglionic eminence,

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

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

130 ivity based solely on input from the lateral geniculate nucleus, however, propose that the nonlinear

131 of the LMI input as sculpted by the lateral geniculate nucleus, (ii) a priming effect of the long-ra

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

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

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

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

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

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

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

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

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

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

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

143 rincipal thalamic target, the dorsal lateral geniculate nucleus (LGd), in a pattern likely dictated b

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

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

146 sforms information received from the lateral geniculate nucleus (LGN) and distributes it to separate

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

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

149 pecifically examine responses in the lateral geniculate nucleus (LGN) and primary visual cortex (V1)

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

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

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

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

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

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

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

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

158 nship on a fine spatial scale in the lateral geniculate nucleus (LGN) and visual cortex of the cat us

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

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

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

162 visual information converging in the lateral geniculate nucleus (LGN) en route to the visual cortex i

163 that signals recorded from the human lateral geniculate nucleus (LGN) exhibit eye-specific suppressio

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

165 profiles of which differentiated the lateral geniculate nucleus (LGN) from the associated perigenicul

166 koniocellular neurons of the primate lateral geniculate nucleus (LGN) from the primary parvo- and mag

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

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

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

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

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

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

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

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

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

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

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

178 hich include non-DS simple cells and lateral geniculate nucleus (LGN) neurons, by examination of spat

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

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

181 rties of 348 neurons recorded in the lateral geniculate nucleus (LGN) of macaque monkeys aged 1 week

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

183 ntrast sensitivity of neurons in the lateral geniculate nucleus (LGN) of macaque.

184 lue/yellow inputs are relayed by the lateral geniculate nucleus (LGN) of thalamus to primary visual c

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

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

187 re central structures, including the lateral geniculate nucleus (LGN) of the thalamus and (via the LG

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

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

190 The role of the lateral geniculate nucleus (LGN) of the thalamus in visual encod

191 Neurons in the lateral geniculate nucleus (LGN) of the thalamus produce spikes

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

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

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

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

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

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

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

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

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

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

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

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

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

205 ction in the macaque monkey from the lateral geniculate nucleus (LGN) to the motion-selective middle

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

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

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

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

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

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

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

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

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

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

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

217 ffects of the adaptive mechanisms in lateral geniculate nucleus (LGN), the direct recipient of retina

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

219 In the lateral geniculate nucleus (LGN), V1, and V2 of anesthetized mac

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

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

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

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

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

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

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

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

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

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

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

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

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

233 e visual cortex areas V1 and V2, and lateral geniculate nucleus (LGN).

234 in the superior colliculus (SC) and lateral geniculate nucleus (LGN).

235 etinotopic organization of the human lateral geniculate nucleus (LGN).

236 a (PTA), and the IGL division of the lateral geniculate nucleus (LGN).

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

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

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

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

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

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

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

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

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

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

247 Here we show that, in slices of the lateral geniculate nucleus maintained in vitro, activation of th

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

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

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

251 nduces retinal axons to innervate the medial geniculate nucleus (MGN).

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

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

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

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

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

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

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

259 acid (GABA)ergic cells in the dorsal lateral geniculate nucleus of mice, no Dlx genes, which promote

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

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

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

263 superior colliculus (SC), the dorsal lateral geniculate nucleus of the thalamus (dLGN), and the later

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

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

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

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

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

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

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

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

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

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

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

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

276 er of c-Fos-ir neurons in the dorsal lateral geniculate nucleus or suprachiasmatic nucleus (SCN) foll

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

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 ency, the giant cells project to the lateral geniculate nucleus, the thalamic relay to primary visual

286 g rhesus monkeys in first-order (the lateral geniculate nucleus, the ventral posterior nucleus, and t

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

288 the responses of single cells in cat lateral geniculate nucleus to a vertical bar stimulus that was s

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

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

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

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

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

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

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

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

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

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

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

300 thalamus (reticular nucleus, ventral lateral geniculate nucleus, zona incerta, and nucleus of the fie