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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 temporal area of the monkey and from the cat lateral geniculate nucleus.

19 and extracellular neural activity in the cat lateral geniculate nucleus.

20 ntained in the separate layers of the Galago lateral geniculate nucleus.

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

22 te transporters VGLUT1 and VGLUT2 in the rat lateral geniculate nucleus.

23 he visual thalamic relay nucleus, the dorsal lateral geniculate nucleus.

24 source of VGLUT2-containing synapses in the lateral geniculate nucleus.

25 ion cell axons from the retina to the dorsal lateral geniculate nucleus.

26 e prethalamic neuroepithelium to the ventral lateral geniculate nucleus.

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

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

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

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

31 The lateral geniculate nucleus, a reciprocal region, had ret

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

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

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

35 ade labeling in the thalamus, chiefly in the lateral geniculate nucleus and lateral posterior-pulvina

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

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

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

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

40 The lateral geniculate nucleus and pulvinar are examples of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 d nonspecific, and convergent input from the lateral geniculate nucleus confers cortical cells with o

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

63 o give rise to axonal collaterals within the lateral geniculate nucleus, constituting another route f

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

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

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

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

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

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

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

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

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

73 gled left and right eye inputs to the dorsal lateral geniculate nucleus (DLGN) during development is

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

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

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

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

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

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

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

81 sual cortex to principal cells in the dorsal lateral geniculate nucleus (dLGN) is markedly enhanced w

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

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

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

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

86 t interneurons in the A lamina of the dorsal lateral geniculate nucleus (dLGN) of the cat.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 ce and at the level of the retina and 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 The balance between lateral connections and lateral geniculate nucleus drive determines whether indi

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

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

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

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

125 iological studies of cells in the retina and lateral geniculate nucleus find far fewer OFF-center tha

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

127 hough a very small number reaches the dorsal lateral geniculate nucleus from the caudal ganglionic em

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

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

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

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

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

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

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

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

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

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

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

139 Relay neurons of the lateral geniculate nucleus innervate visual cortex, but

140 entation columns specified by the convergent lateral geniculate nucleus inputs are arranged in a pinw

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

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

143 The lateral geniculate nucleus is intensely immunoreactive f

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

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

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

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

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

149 ional connections between the retina and the lateral geniculate nucleus (LGN) and between LGN and vis

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

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

152 cortical or retinal origin in the rat dorsal lateral geniculate nucleus (LGN) and lateral posterior n

153 tinued following birth into adulthood 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 tion in which connectivity between the mouse lateral geniculate nucleus (LGN) and primary visual cort

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

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

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

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

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

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

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

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

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

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

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

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

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

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

170 ibution profiles of which differentiated the lateral geniculate nucleus (LGN) from the associated per

171 hes the koniocellular neurons of the primate lateral geniculate nucleus (LGN) from the primary parvo-

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

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

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

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

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

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

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

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

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

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

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

183 model, which include non-DS simple cells and lateral geniculate nucleus (LGN) neurons, by examination

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

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

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

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

188 n the contrast sensitivity of neurons in the lateral geniculate nucleus (LGN) of macaque.

189 As in other primates, the lateral geniculate nucleus (LGN) of owl monkeys contains

190 en and blue/yellow inputs are relayed by the lateral geniculate nucleus (LGN) of thalamus to primary

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

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

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

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

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

196 The role of the lateral geniculate nucleus (LGN) of the thalamus in visu

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

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

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

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

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

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

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

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

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

206 raphe nucleus (DRN) and Fluoro-Gold into the lateral geniculate nucleus (LGN) revealed double-labeled

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

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

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

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

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

212 ct projection in the macaque monkey from the lateral geniculate nucleus (LGN) to the motion-selective

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

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

215 te axons into ON/OFF sublayers in the ferret lateral geniculate nucleus (LGN), and in the formation o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

241 ns in the visual cortex areas V1 and V2, and lateral geniculate nucleus (LGN).

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

243 te the retinotopic organization of the human lateral geniculate nucleus (LGN).

244 ctal area (PTA), and the IGL division of the lateral geniculate nucleus (LGN).

245 ls in the macaque retina that project to the lateral geniculate nucleus (LGN).

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

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

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

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

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

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

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

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

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

255 Here we show that, in slices of the lateral geniculate nucleus maintained in vitro, activati

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

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

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

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

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

261 icular nucleus axons in the highly laminated lateral geniculate nucleus of the prosimian primate Gala

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

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

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

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

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

267 0% of geniculocortical axons from the dorsal lateral geniculate nucleus of the thalamus innervate lay

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

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

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

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

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

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

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

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

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

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

278 ual thalamic reticular nucleus influence the lateral geniculate nucleus retinotopically, with little

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

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

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

282 Retinal ganglion cells and neurons in the lateral geniculate nucleus, superior colliculus, and vis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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