ライフサイエンスコーパス: lateral geniculate nucleus

1 al thalamus (the equivalent to the mammalian lateral geniculate nucleus).

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

3 in retinogeniculate axon segregation in the lateral geniculate nucleus.

4 rom the ventral basal nucleus and the dorsal lateral geniculate nucleus.

5 nd projects to multiple areas, including the lateral geniculate nucleus.

6 and cell-type-specific layers in the dorsal lateral geniculate nucleus.

7 ventional RGCs in the ventral portion of the lateral geniculate nucleus.

8 l layer 6 with identified projections to the lateral geniculate nucleus.

9 c segregation of retinal axons in the dorsal lateral geniculate nucleus.

10 tentials in interneurons of the mouse dorsal lateral geniculate nucleus.

11 tive field centers of neurons in the macaque lateral geniculate nucleus.

12 rojection to the magnocellular layers of the lateral geniculate nucleus.

13 the superior colliculus, the retina, and the lateral geniculate nucleus.

14 nt signal to the magnocellular layers of the lateral geniculate nucleus.

15 sport of rhodamine dextran injected into the lateral geniculate nucleus.

16 ordering the principal layers of the macaque lateral geniculate nucleus.

17 single relay, from both M and P cells of the lateral geniculate nucleus.

18 finements in the mammalian retina and dorsal lateral geniculate nucleus.

19 onnections between the retina and the dorsal lateral geniculate nucleus.

20 eak projections to the margins of the dorsal lateral geniculate nucleus.

21 d by topographically precise inputs from the lateral geniculate nucleus.

22 lls in a slice preparation of the rat dorsal lateral geniculate nucleus.

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

24 sharpen other forms of selectivity in rodent lateral geniculate nucleus.

25 e prethalamic neuroepithelium to the ventral lateral geniculate nucleus.

26 abeled cholera toxin beta from retina to the lateral geniculate nucleus (60% decrease), and to the su

27 anglion cell (RGC) projections to the dorsal lateral geniculate nucleus, a process that involves acti

28 y to the superior colliculus (SC) and dorsal lateral geniculate nucleus and are restricted to a speci

29 e distributions of visual neurons in macaque lateral geniculate nucleus and cortical areas V1, V2 and

30 to the non-columnar mouse V1 from the dorsal lateral geniculate nucleus and feedback projections from

31 projections, and the tecto-recipient dorsal lateral geniculate nucleus and its projections are detai

32 y an intact white-matter pathway between the lateral geniculate nucleus and motion area hMT+.

33 or exclusively contralateral; to the dorsal lateral geniculate nucleus and posterior pretectal nucle

34 ting adaptive visual response changes in the lateral geniculate nucleus and primary visual cortex fol

35 latter finding, the connectivity between the lateral geniculate nucleus and primary visual cortex mea

36 isms of visual information processing in the lateral geniculate nucleus and primary visual cortex.

37 The lateral geniculate nucleus and pulvinar are examples of

38 These pathways enable the lateral geniculate nucleus and pulvinar to regulate the

39 Projections from the lateral geniculate nucleus and pulvinar to V1 were prese

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

41 Off pDSGCs project exclusively to the dorsal lateral geniculate nucleus and superior colliculus and i

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

43 olliculus and 2 other visual structures: the lateral geniculate nucleus and the primary visual cortex

44 eus, they project differently to the ventral lateral geniculate nucleus and the superior colliculus.

45 y therefore provide visual input to both the lateral geniculate nucleus and the superior colliculus.

46 eled by retrograde transport from the dorsal lateral geniculate nucleus and thus likely contribute to

47 The optic nerve, lateral geniculate nucleus and visual cortex provide alt

48 ed, show an ipsilateral pathway between LGN (lateral geniculate nucleus) and human motion area MT+/V5

49 ustrum, and the interlaminar portions of the lateral geniculate nucleus, and efferent projections to

50 n cell types, through distinct layers of the lateral geniculate nucleus, and into primary visual cort

51 us cells, interneurons moving to the ventral lateral geniculate nucleus, and neocortical cells going

52 to sparse labeling of neurons in the cortex, lateral geniculate nucleus, and superior colliculus, and

53 could be detected even earlier, in the human lateral geniculate nucleus, and that attentional feedbac

54 Likewise, the superior colliculus, dorsal lateral geniculate nucleus, and the posterior nucleus of

55 ontaneous activity in the developing retina, lateral geniculate nucleus, and visual cortex instruct t

56 t electrical stimulation (TBS) of the dorsal lateral geniculate nucleus, are sufficient to account fo

57 ied was the physical inversion of the dorsal lateral geniculate nucleus, as well as the lateral poste

58 Neurons in the lateral geniculate nucleus cannot perform the spatial co

59 We find that the cell response spectra of lateral geniculate nucleus cells, as well as the reflect

60 tor of the thalamic reticular nucleus to the lateral geniculate nucleus complete the earliest feedbac

61 As in other carnivores, the dorsal lateral geniculate nucleus consisted of three main layer

62 le neurons and thalamic relay neurons of the lateral geniculate nucleus contributed to tonic conducta

63 Response magnitude in the lateral geniculate nucleus did not increase with locomot

64 that bypasses V1, and connects the thalamic lateral geniculate nucleus directly with the extrastriat

65 st sources of nonretinal input to the dorsal lateral geniculate nucleus (dLGN) and play a major role

66 e compared the membrane properties of dorsal lateral geniculate nucleus (dLGN) and pulvinar nucleus r

67 om the SC to two thalamic nuclei: the dorsal lateral geniculate nucleus (dLGN) and the lateral poster

68 on cell (RGC) axon projections in the dorsal lateral geniculate nucleus (dLGN) and the superior colli

69 r thalamocortical (TC) neurons of the dorsal lateral geniculate nucleus (dLGN) and ventrobasal comple

70 lular and parvocellular layers of the dorsal lateral geniculate nucleus (dLGN) are distinguished by u

71 the two eyes initially overlap in the dorsal-lateral geniculate nucleus (dLGN) but subsequently refin

72 ssion.SIGNIFICANCE STATEMENT Only the dorsal lateral geniculate nucleus (dLGN) connects to cortex to

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

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

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

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

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

78 ye-specific axonal projections to the dorsal lateral geniculate nucleus (dLGN) is a well established

79 nnectivity between the retina and the dorsal lateral geniculate nucleus (dLGN) is established by grad

80 atement: The conventional view of the dorsal lateral geniculate nucleus (dLGN) is that of a simple re

81 The dorsal lateral geniculate nucleus (dLGN) is the primary thalami

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

83 otinylated dextran amine (BDA) in the dorsal lateral geniculate nucleus (dLGN) of anesthetized cats a

84 The dorsal lateral geniculate nucleus (dLGN) of the mouse has emerg

85 The dorsal lateral geniculate nucleus (dLGN) of the mouse is a mode

86 f confirmed projection neurons in the dorsal lateral geniculate nucleus (dLGN) of the rat was examine

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

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

89 Inhibitory interneurons in the dorsal lateral geniculate nucleus (dLGN) process visual informa

90 The dorsal lateral geniculate nucleus (dLGN) receives visual inform

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

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

93 ives its main thalamic drive from the dorsal lateral geniculate nucleus (dLGN) through synaptic conta

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

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

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

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

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

99 ets, the superior colliculus (SC) and dorsal lateral geniculate nucleus (dLGN), bridge retinal input

100 (V1) and its thalamic inputs from the dorsal lateral geniculate nucleus (dLGN), but more rarely in th

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

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

103 Here we examined whether cells in the dorsal lateral geniculate nucleus (dLGN), the thalamic relay be

104 ex is reciprocally connected with the dorsal lateral geniculate nucleus (dLGN), the ventral pulvinar

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

106 in the contralateral and ipsilateral dorsal lateral geniculate nucleus (dLGN), underpinning disparit

107 rminate in their thalamic target, the dorsal lateral geniculate nucleus (dLGN), when crossing at the

108 isual cortex but one exception is the dorsal lateral geniculate nucleus (dLGN), which receives layer

109 dent competition for territory in the dorsal lateral geniculate nucleus (dLGN).

110 alamocortical (TC) neurons of the rat dorsal lateral geniculate nucleus (dLGN).

111 ivity is relayed to the cortex by the dorsal lateral geniculate nucleus (dLGN).

112 perigeniculate nucleus (PGN) and the dorsal lateral geniculate nucleus (dLGN).

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

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

115 ce and at the level of the retina and dorsal lateral geniculate nucleus (dLGN).

116 ata within deprived layers of the cat dorsal lateral geniculate nucleus (dLGN).

117 ile recording visual responses in the dorsal lateral geniculate nucleus (dLGN).

118 f GABA from local interneurons in the dorsal lateral geniculate nucleus (dLGN-INs) provides inhibitor

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

120 udied the responses of neurons in the dorsal lateral geniculate nucleus during and after the presenta

121 ial frequency via feedforward input from the lateral geniculate nucleus (e.g., [1]).

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

123 psin drives a generalized increase in dorsal lateral geniculate nucleus excitability as dawn progress

124 We explored the murine lateral geniculate nucleus from a comparative physiologi

125 once overlooked koniocellular pathway of the lateral geniculate nucleus has generated interest in how

126 koniocellular layers of the marmoset dorsal lateral geniculate nucleus have binocularly responsive n

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

128 n selectivity based solely on input from the lateral geniculate nucleus, however, propose that the no

129 tructure of the LMI input as sculpted by the lateral geniculate nucleus, (ii) a priming effect of the

130 retrograde degeneration of the ipsilesional lateral geniculate nucleus in both experimental groups,

131 nd raises questions about the role of dorsal lateral geniculate nucleus in early binocular processing

132 predict different rhythms that emerge in the lateral geniculate nucleus in the thalamus during differ

133 visual hallucinations were connected to the lateral geniculate nucleus in the thalamus while lesions

134 ina, optic tectum (superior colliculus), and lateral geniculate nucleus in vertebrates; and retina, l

135 ve revealed important roles for pulvinar and lateral geniculate nucleus in visuospatial perception an

136 d mouse and pig retina and from mouse dorsal lateral geniculate nucleus in vivo at up to seven ambien

137 Interneurons in the lateral geniculate nucleus innervate relay cells and eac

138 In contrast, while clear evidence for dorsal lateral geniculate nucleus input to V1 excitatory neuron

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

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

141 standing about the development of the dorsal lateral geniculate nucleus is limited to circuits involv

142 tudy showed that neuron number in the dorsal lateral geniculate nucleus is reduced following early ge

143 The lateral geniculate nucleus (LG) is an important subcorti

144 their principal thalamic target, the dorsal lateral geniculate nucleus (LGd), in a pattern likely di

145 ynapses onto neurons within subnuclei of the lateral geniculate nucleus (LGN) [i.e., the dorsal LGN (

146 ority of thalamic terminals in V1 arise from lateral geniculate nucleus (LGN) afferents.

147 spiking activity in two visual centres, the lateral geniculate nucleus (LGN) and cortical area MT, i

148 V1 transforms information received from the lateral geniculate nucleus (LGN) and distributes it to s

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

150 from retinotopically aligned regions in the lateral geniculate nucleus (LGN) and primary visual cort

151 tinued following birth into adulthood in the lateral geniculate nucleus (LGN) and primary visual cort

152 tion in which connectivity between the mouse lateral geniculate nucleus (LGN) and primary visual cort

153 MRI to specifically examine responses in the lateral geniculate nucleus (LGN) and primary visual cort

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

155 rception, we recorded neural activity in the lateral geniculate nucleus (LGN) and pulvinar of 2 macaq

156 r, EphB, in retinotopic map formation in the lateral geniculate nucleus (LGN) and superior colliculus

157 ways are via the koniocellular layers of the lateral geniculate nucleus (LGN) and the medial portion

158 In mammals, the lateral geniculate nucleus (LGN) and the superior collic

159 of subcortical visual structures such as the lateral geniculate nucleus (LGN) and the superior collic

160 thalamus (ventral and dorsal pulvinar), the lateral geniculate nucleus (LGN) and visual cortex (area

161 relationship on a fine spatial scale in the lateral geniculate nucleus (LGN) and visual cortex of th

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

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

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

165 elay of visual information converging in the lateral geniculate nucleus (LGN) en route to the visual

166 to show that signals recorded from the human lateral geniculate nucleus (LGN) exhibit eye-specific su

167 The responses of neurons in lateral geniculate nucleus (LGN) exhibit powerful suppre

168 nal spikes impinging on relay neurons in the lateral geniculate nucleus (LGN) generate synaptic poten

169 Here we demonstrate that the thalamic lateral geniculate nucleus (LGN) has a causal role in V1

170 Many lines of evidence show that the murine lateral geniculate nucleus (LGN) has unique attributes,

171 nt of eye-specific visual projections to the lateral geniculate nucleus (LGN) have not previously bee

172 yed through the magno- and parvocells of the lateral geniculate nucleus (LGN) indirectly to extrastri

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

174 on of precise connections between retina and lateral geniculate nucleus (LGN) involves the activity-d

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

176 jections to the superior colliculus (SC) and lateral geniculate nucleus (LGN) is guided by molecular

177 SIGNIFICANCE STATEMENT: The lateral geniculate nucleus (LGN) is the gateway through

178 New stereological assessments of lateral geniculate nucleus (LGN) neuron numbers and volu

179 mpared across simulated cone photoreceptors, lateral geniculate nucleus (LGN) neurons, and perceptual

180 , instructive changes in the firing of mouse lateral geniculate nucleus (LGN) neurons, leading to inc

181 Neurons in the lateral geniculate nucleus (LGN) not only provide feedfo

182 se properties of 348 neurons recorded in the lateral geniculate nucleus (LGN) of macaque monkeys aged

183 vitro brain slice preparation of the dorsal lateral geniculate nucleus (LGN) of macaque monkeys that

184 t receptive field property of neurons in the lateral geniculate nucleus (LGN) of the dorsal thalamus,

185 Within the lateral geniculate nucleus (LGN) of the dorsal thalamus,

186 ts to more central structures, including the lateral geniculate nucleus (LGN) of the thalamus and (vi

187 he reorganization of retinotopic maps in the lateral geniculate nucleus (LGN) of the thalamus and ear

188 CG) pathway links the visual cortex with the lateral geniculate nucleus (LGN) of the thalamus and is

189 ne the response properties of neurons in the lateral geniculate nucleus (LGN) of the thalamus in the

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

191 ives its driving input from the eyes via the lateral geniculate nucleus (LGN) of the thalamus.

192 the consequences on visual responses in the lateral geniculate nucleus (LGN) of the thalamus.

193 llular layers of their target structure, the lateral geniculate nucleus (LGN) of the thalamus.

194 tion reaching cerebral cortex is through the lateral geniculate nucleus (LGN) of the thalamus.

195 the brain passes from the retina through the lateral geniculate nucleus (LGN) of the thalamus.

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

197 brain to functionally map the koniocellular lateral geniculate nucleus (LGN) projection to primary v

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

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

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

201 that parallel visual pathways in the dorsal lateral geniculate nucleus (LGN) show distinct patterns

202 eniculate neurones make more synapses in the lateral geniculate nucleus (LGN) than retinal ganglion c

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

204 ied an OS mechanism in selective wiring from lateral geniculate nucleus (LGN) to primary visual corte

205 ransfer of spikes between the retina and the lateral geniculate nucleus (LGN) with the goal of determ

206 the spectral response curves of cells in the lateral geniculate nucleus (LGN) with the reflectance sp

207 c responses in the superior colliculus (SC), lateral geniculate nucleus (LGN), and two retinotopic pu

208 eurons in the main thalamic input to V1, the lateral geniculate nucleus (LGN), are considered to be o

209 ures from which they receive afferences: the lateral geniculate nucleus (LGN), due to optic neuritis

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

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

212 amage to the primary visual cortex (V1), the lateral geniculate nucleus (LGN), or the optic tract wer

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

214 imulus dependence of neural responses in the lateral geniculate nucleus (LGN), primary visual cortex

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

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

217 ed the effects of the adaptive mechanisms in lateral geniculate nucleus (LGN), the direct recipient o

218 r/surround receptive field of neurons in the lateral geniculate nucleus (LGN), there is an extraclass

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

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

221 essed not only in visual cortex, but also in lateral geniculate nucleus (LGN), where protein localiza

222 are transmitted to cortex via neurons in the lateral geniculate nucleus (LGN), where they are process

223 he driving (main signature) activity for the lateral geniculate nucleus (LGN), which in turn drives t

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

225 om different classes of relay neurons in the lateral geniculate nucleus (LGN).

226 l circuit or the feedforward inputs from the lateral geniculate nucleus (LGN).

227 GN), and principal visual relay nucleus, the lateral geniculate nucleus (LGN).

228 e first relay between retina and cortex, the lateral geniculate nucleus (LGN).

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

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

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

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

233 t to individual principal cells in the mouse lateral geniculate nucleus (LGN).

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

235 nchronous, rhythmic firing of neurons in the lateral geniculate nucleus (LGN).

236 ly labeled following tracer injection in the lateral geniculate nucleus (LGN).

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

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

239 ic response to electrical stimulation of the lateral geniculate nucleus (LGN, 3+ spikes at >600 Hz),

240 right visual thalamus (especially the right lateral geniculate nucleus [LGN]), right caudate nucleus

241 in ongoing spiking activity in subcortical (lateral geniculate nucleus, LGN) and cortical (area MT)

242 nnectivity between the left visual thalamus (lateral geniculate nucleus, LGN) and V5/MT, a cerebral c

243 ine connectivity of single thalamic neurons (lateral geniculate nucleus, LGN) onto putative fast-spik

244 e behavior of retinotopically aligned dorsal lateral geniculate nucleus (LGNd) neurons, usually recor

245 of individual sustained and transient dorsal lateral geniculate nucleus (LGNd) neurons.

246 SMI-32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat.

247 g the SCN, IGL, OPN, ventral division of the lateral geniculate nucleus (LGv), and preoptic area, but

248 The lateral geniculate nucleus, like all thalamic nuclei, ha

249 blue-ON) cells in recordings from the dorsal lateral geniculate nucleus of anesthetized cats.

250 siological recordings from retina and dorsal lateral geniculate nucleus of cone-deficient and visuall

251 In the lateral geniculate nucleus of macaque, we recorded from

252 der anaesthesia with checkerboards activated lateral geniculate nucleus of monkey S, while full-field

253 lly increasing or decreasing the size of the lateral geniculate nucleus of the mouse thalamus resulte

254 stem, where neurons in the retina and dorsal lateral geniculate nucleus of the thalamus (dLGN) are mo

255 ex: the superior colliculus (SC), the dorsal lateral geniculate nucleus of the thalamus (dLGN), and t

256 y-evoked discharges of neurons in the dorsal lateral geniculate nucleus of the thalamus (dLGN).

257 ion from the retina is relayed to the dorsal lateral geniculate nucleus of the thalamus (LGd).

258 Even though the lateral geniculate nucleus of the thalamus (LGN) is asso

259 c properties of the synaptic inputs from the lateral geniculate nucleus of the thalamus (LGN) onto L4

260 The dorsal lateral geniculate nucleus of the thalamus (LGN) receive

261 mined whether microstimulation of the dorsal lateral geniculate nucleus of the thalamus can generate

262 0% of geniculocortical axons from the dorsal lateral geniculate nucleus of the thalamus innervate lay

263 Inhibitory interneurons of the dorsal lateral geniculate nucleus of the thalamus modulate the

264 ging studies have shown that activity in the lateral geniculate nucleus of the thalamus strongly refl

265 n by electrically stimulating neurons in the lateral geniculate nucleus of the thalamus while simulta

266 n is also accompanied by degeneration of the lateral geniculate nucleus of the thalamus, and 90% of b

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

268 he retina sends to the visual cortex via the lateral geniculate nucleus of the thalamus.

269 rborize in discrete laminar zones within the lateral geniculate nucleus or superior colliculus, demon

270 the number of c-Fos-ir neurons in the dorsal lateral geniculate nucleus or suprachiasmatic nucleus (S

271 mprises the suprachiasmatic nucleus, ventral lateral geniculate nucleus, pretectal nuclear complex an

272 e segregation of eye-specific retinal dorsal lateral geniculate nucleus projections commences.

273 r colliculus, visual dorsal thalamus (dorsal lateral geniculate nucleus, pulvinar and lateral posteri

274 The dorsal lateral geniculate nucleus receives projections from vis

275 ontrol in the retinal ganglion cells and the lateral geniculate nucleus reduces variation in the pres

276 culate (PGN) or thalamocortical cells in the lateral geniculate nucleus resulted in depolarization an

277 innervate the superior colliculus and dorsal lateral geniculate nucleus, retinotopically organized nu

278 length of the visual pathway and on into the lateral geniculate nucleus, superior colliculus, and oth

279 order to investigate the architecture of the lateral geniculate nucleus, superior colliculus, and pri

280 nal modeling, we investigated how rat dorsal lateral geniculate nucleus thalamocortical neurons integ

281 nction delay, in the these nuclei and in the lateral geniculate nucleus, the superior colliculus, and

282 ur opponency, the giant cells project to the lateral geniculate nucleus, the thalamic relay to primar

283 behaving rhesus monkeys in first-order (the lateral geniculate nucleus, the ventral posterior nucleu

284 populations project similarly to the dorsal lateral geniculate nucleus, they project differently to

285 ecorded the responses of single cells in cat lateral geniculate nucleus to a vertical bar stimulus th

286 cterize the adaptation of neurons in the cat lateral geniculate nucleus to changes in stimulus contra

287 al analyses of receptive fields in the cat's lateral geniculate nucleus to describe how inhibition he

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

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

290 onse latencies of 20 ms and a mean estimated lateral geniculate nucleus to primary visual cortex tran

291 r in thalamocortical neurons projecting from lateral geniculate nucleus to visual cortex.

292 rophysiological activity in the mouse dorsal lateral geniculate nucleus under exposure to a simulated

293 on connectivity distribution, with decreased lateral geniculate nucleus V2 density (F, -8.28; P < .05

294 that project to the pretectum (PT), ventral lateral geniculate nucleus (vLGN) or parabigeminal nucle

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

296 Using seed voxels antero-lateral to the lateral geniculate nucleus, we applied this technique to

297 Projections from M6 cells to the dorsal lateral geniculate nucleus were confirmed by retrograde

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

299 rlying this measure of contrast in the cat's lateral geniculate nucleus, which relays signals from re

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