ライフサイエンスコーパス: geniculate

1 ves interhemispheric suppression from retino-geniculate afferents in intact visual cortex that repres

2 is pathway is not a collateral branch of the geniculate and collicular projecting RGCs.

3 n of spiking responses in the dorsal lateral geniculate and of the local field potentials in their re

4 ed at the anterior end of the dorsal lateral geniculate and superior colliculus, suggestive of a pauc

5 evelopment, prior to the formation of retino-geniculate and thalamocortical pathways.

6 om each eye first map to their target in the geniculate and then segregate into eye-specific layers b

7 ions with a peak at 60 Hz in retina, lateral geniculate, and primary visual cortex of the mouse visua

8 By E11.5, geniculate axons have just reached the tongue and do not

9 Structurally, geniculate axons innervated excitatory cortical targets

10 at carry visual information from the lateral geniculate bodies to the visual cortex.

11 tion for the anterior nucleus, pulvinar, and geniculate bodies.

12 The medial geniculate body (MG) receives a large input from the ips

13 ex, but no detectable response in the medial geniculate body (MGB) and inferior colliculus (IC).

14 However, the putative role of the medial geniculate body (MGB) in tinnitus has not been previousl

15 The medial geniculate body (MGB) integrates ascending inputs with d

16 w of auditory information through the medial geniculate body (MGB) is regulated, in part, by choliner

17 lus (IC), the ventral division of the medial geniculate body (MGB) of the thalamus, and the primary a

18 on of the projections from either the medial geniculate body (MGB) or primary auditory cortex (ACx) t

19 ity from the auditory cortex (AC) and medial geniculate body (MGB) simultaneously with electrical sti

20 of the brachium of the IC (BIN), the medial geniculate body (MGB), and the primary auditory cortex (

21 tions from the three subnuclei of the medial geniculate body (MGB), namely, its ventral (MGv), dorsal

22 Gv) and dorsal divisions (MGd) of the medial geniculate body (MGB), the reticular thalamic nucleus an

23 r increase of GABAergic inhibition in medial geniculate body (MGB).

24 he human inferior colliculus (IC) and medial geniculate body (MGB).

25 rtex (AC) and its thalamic input, the medial geniculate body (MGB).

26 bitory neurotransmitter acting in the medial geniculate body (MGB).

27 function in auditory thalamus or the medial geniculate body (MGB).

28 of the auditory sensory thalamus, the medial geniculate body (MGB).

29 were recorded from auditory thalamus [medial geniculate body (MGB)] of young awake, aged awake, young

30 n homeostasis, possibly convergent on medial geniculate body (MGB, auditory thalamus) and related neu

31 died learning-related activity in the medial geniculate body (MGB; Auditory thalamus), targeting main

32 pose that the ventral division of the medial geniculate body (MGBv) is a single functionally homogeno

33 nucleus (SG) and ventral division of medial geniculate body (MGBv), respectively.

34 (A1) and the ventral division of the medial geniculate body (MGBv).

35 eurons in the ventral division of the medial geniculate body (MGBv).

36 i.e., the ventral subdivision of the medial geniculate body (MGv).

37 e more rostral structures such as the medial geniculate body (P6) were prolonged 2h after NTG adminis

38 s observed in auditory cortex and the medial geniculate body of the thalamus in the absence of any ex

39 ntral and the dorsal divisions of the medial geniculate body of the thalamus, but they also branched

40 The present findings demonstrate that medial geniculate body units from awake rats show an age-relate

41 teral lemniscus, inferior colliculus, medial geniculate body, and auditory cortex all being in their

42 2 in the midbrain tegmental nuclei, lateral geniculate body, and thalamus for nonsmokers (n = 9) but

43 0.07 in the anteroventral thalamus, lateral geniculate body, frontal cortex, and subiculum, respecti

44 include the anteroventral thalamus, lateral geniculate body, frontal cortex, subiculum, and cerebell

45 ponses in the left auditory thalamus (medial geniculate body, MGB) during speech processing in contra

46 processing in the auditory thalamus (medial geniculate body, MGB) is poorly understood.

47 In particular, the auditory thalamus (medial geniculate body, MGB) response is modulated by speech re

48 e circuitry of the auditory thalamus (medial geniculate body, MGB).

49 f the auditory thalamus including the medial geniculate body, suprageniculate nucleus, and reticular

50 not polysensory) subdivisions of the medial geniculate body.

51 on to A1, the ventral division of the medial geniculate body.

52 nsitive planum temporale and the left medial geniculate body.

53 ) IPSPs in the ventral nucleus of the medial geniculate body.

54 the segregated excitatory input from X and Y geniculate cells to A17 and A18.

55 terpreted as originating from a subtype of Y geniculate cells.

56 ment in the inferior colliculus (IC), medial geniculate complex (MGC), and auditory cortex (auditory

57 Several distinct subnuclei in the geniculate complex and the pretectum contain labeled ret

58 ning were identified in the SCN, the lateral geniculate complex including the pregeniculate nucleus,

59 Equivalent enhancement of medial geniculate excitability robustly drove auditory cortical

60 ere, we study subcortical projections to the geniculate from the superior colliculus (SC) and parabig

61 ification of chemosensory neurons within the geniculate ganglion (GG).

62 5-HT(3A) promoter, a subset of cells in the geniculate ganglion and nerve fibers in taste buds are G

63 ve, and general somatosensory neurons in the geniculate ganglion are greatly reduced by mid-gestation

64 Functional studies show that only those geniculate ganglion cells expressing 5-HT3A-driven GFP r

65 The mouse geniculate ganglion contains chemosensory neurons innerv

66 non-oral somatosensory neurons (58%) in the geniculate ganglion did not.

67 iated cell death, which was increased in the geniculate ganglion in Bdnf(-/-) mice, was rescued in Bd

68 mining a published RNA-sequencing dataset of geniculate ganglion neurons and by in situ hybridization

69 nously applied ATP in fura-2 loaded isolated geniculate ganglion neurons from wild-type and P2X3 knoc

70 ere, we report single cell RNA sequencing of geniculate ganglion neurons.

71 3/Znrf3, is expressed in nodose-petrosal and geniculate ganglion neurons.

72 Some neurons in the geniculate ganglion project to taste regions in the oral

73 al taste system, oral sensory neurons of the geniculate ganglion project via the chorda tympani nerve

74 We used mice expressing GCaMP3 in geniculate ganglion sensory neurons to investigate taste

75 The number of neurons in the geniculate ganglion that are available to innervate tast

76 entify oral cavity-projecting neurons in the geniculate ganglion.

77 nfirmed the presence of 5-HT(3A) mRNA in the geniculate ganglion.

78 t gene expression profiles in the gustatory (geniculate) ganglion.

79 nd likely reflect the effect of V1-bypassing geniculate input into extrastriate areas.

80 cerebral cortex are believed to rely on the geniculate input to the primary visual cortex (V1).

81 de () introduced the idea that koniocellular geniculate layers (rather than the parvocellular and mag

82 Furthermore, the koniocellular geniculate layers in marmosets, unlike those in the geni

83 ateral SC, PBG, and NOT to the koniocellular geniculate layers.

84 est that peculiarities of SMI-32 staining at geniculate level could reflect the heterogeneity of Y ce

85 tetrodes in the medial nucleus of the medial geniculate (MGm) and suprageniculate (SG) and trained on

86 The medial division of the medial geniculate (MGM) and the posterior intralaminar nucleus

87 ues as the number of afferent inputs to each geniculate neuron decreases from many to a few.

88 ived cells (P0-Cre; p75(fx/fx)) and examined geniculate neuron development.

89 and mechanism of NT-4-mediated regulation of geniculate neuron number during development.

90 ered that NT-4 mutant mice lose 33% of their geniculate neuronal cells between E10.5 and E11.5.

91 hether the developmental functions of p75 in geniculate neurons are cell autonomous, we deleted p75 s

92 trast to p75(-/-) mice, there was no loss of geniculate neurons in either Phox2b-Cre; p75(fx/fx) or P

93 In germline p75(-/-) mice half of all geniculate neurons were lost.

94 and branching deficits, leading to a loss of geniculate neurons.

95 organization of the optic chiasm and lateral geniculate nuclei (LGN) in human albinism.

96 halamic ventral posterior medial and lateral geniculate nuclei followed cortical active states with m

97 ans-synaptic degeneration across the lateral geniculate nuclei has been suggested as a mechanism of t

98 thalamocortical visual relay in the lateral geniculate nuclei, a number of other thalamic regions co

99 e primary ventral posterior and dorsolateral geniculate nuclei, respectively, and less with the assoc

100 tic atrophy with delamination of the lateral geniculate nuclei.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

244 The dorsal lateral geniculate nucleus receives projections from visuotopica

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 other forms of selectivity in rodent lateral geniculate nucleus.

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

279 lamic neuroepithelium to the ventral lateral geniculate nucleus.

280 ventral basal nucleus and the dorsal lateral geniculate nucleus.

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

282 nogeniculate axon segregation in the lateral geniculate nucleus.

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

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

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

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

287 te anatomical recovery in the dorsal lateral geniculate nuclues (dLGN) from long-term MD started at t

288 ntracranial potentials, reminiscent of ponto-geniculate-occipital waves.

289 ate layers in marmosets, unlike those in the geniculate of commonly studied diurnal Old World monkeys

290 targeted to the koniocellular layers in the geniculates of four marmosets.

291 fferential circuit with the canonical retino-geniculate pathway to achieve context-dependent sharpeni

292 es accelerate the developmental reduction of geniculate receptive field sizes.

293 The development of geniculate receptive fields after receiving these increa

294 Importantly, the augmentation of geniculate responses to retinal input was not associated

295 lso associated with infection of the lateral geniculate, suprachiasmatic nuclei, and superior collicu

296 lly, but studies in macaques have shown that geniculate synapses are lost in striate cortex (V1).

297 stimated that 1-3 RGCs converge onto a mouse geniculate TC neuron.

298 ressed, but results in marked defects in the geniculate (VII) ganglion.

299 Following damage to the human post-geniculate visual pathway retrograde trans-synaptic dege

300 From the recorded responses of geniculate X-cells in the anesthetized cat, we synthesiz