ライフサイエンスコーパス: geniculate

1 and 14 of 60 ciliary, 25 of 48 and 11 of 48 geniculate, 15 of 50 and 8 of 50 otic, 14 of 47 and 4 of

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

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

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

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

8 1aR binding in the auditory thalamus (medial geniculate), binding in structures involved in vocal pro

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

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

11 the inferior colliculus (IC) and the medial geniculate body (MGB) en route to the cortex.

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

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

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

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

16 of retrogradely labeled somas in the medial geniculate body (MGB) were examined as a function of the

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

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

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

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

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

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

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

24 rom the ventral nucleus (MGBv) of the medial geniculate body (MGB).

25 originating in various nuclei of the medial geniculate body (MGB).

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

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

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

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

30 e ventral and medial divisions of the medial geniculate body (MGBv and MGBm) respectively are the lem

31 e ventral and medial divisions of the medial geniculate body (MGBv and MGBm, respectively).

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

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

36 input from the ventral nucleus of the medial geniculate body (MGBv); whereas belt cortex receives pre

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

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

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

40 cleus and the ventral division of the medial geniculate body resulted in three distinct response clas

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

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

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

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

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

49 not polysensory) subdivisions of the medial geniculate body.

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

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

52 ation that alpha oscillations in the lateral geniculate cohere with those in V1.

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

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

55 supramammillary, mammillary, ventral lateral geniculate, deep mesencephalic, red, pedunculopontine an

56 tical structures, such as the dorsal lateral geniculate (dLGN) of thalamus.

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

58 5-HT(3A) promoter, a subset of cells in the geniculate ganglion and nerve fibers in taste buds are G

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

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

61 The mouse geniculate ganglion contains chemosensory neurons innerv

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

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

64 Neurons of the geniculate ganglion innervate taste buds located in two

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

66 ze post-CTX cannot be explained by a loss of geniculate ganglion neurons or degeneration of central a

67 ed neurotrophic factor (BDNF), the number of geniculate ganglion neurons, which innervate taste buds,

68 -)/Ntf4/5(-/-) double mutants lose 90-95% of geniculate ganglion neurons.

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

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

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

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

73 ates the number of neurons in the developing geniculate ganglion.

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

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

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

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

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

79 The ventral and dorsal medial geniculate (MGV and MGD) constitute the major auditory t

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

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

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

83 Thus, BDNF regulates embryonic geniculate neuronal number by preventing cell death rath

84 The axons of geniculate neurons approach their target cells, the fung

85 The loss of geniculate neurons begins at embryonic day 13.5 (E13.5)

86 target cells regulates the survival of early geniculate neurons by inhibiting cell death of different

87 cells and the outputs from connected lateral geniculate neurons in the macaque to examine how visual

88 ce, Bdnf(-/-) mice showed a 50% reduction in geniculate neurons innervating the tongue and a 28% loss

89 e required for neurogenesis, and the loss of geniculate neurons is likely to be the result of increas

90 Although Hmx1 is expressed in geniculate neurons prior to cell cycle exit, it does not

91 We found that geniculate neurons re-encoded multiple temporal stimulus

92 d by the short-term summation of inputs that geniculate neurons require to spike.

93 In lateral geniculate neurons, we show that retinogeniculate and co

94 in excessive retinal innervation of lateral 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 mary and secondary auditory cortices, medial geniculate nuclei, and inferior colliculus.

100 nections with the dorsal and ventral lateral geniculate nuclei, nuclei of the pretectum, and nucleus

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

102 tic atrophy with delamination of the lateral geniculate nuclei.

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

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

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

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 has emerged as a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

278 ventral basal nucleus and the dorsal lateral geniculate nucleus.

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

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

281 6 with identified projections to the lateral geniculate nucleus.

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

283 in interneurons of the mouse dorsal lateral geniculate nucleus.

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

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

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

287 other forms of selectivity in rodent lateral geniculate nucleus.

288 lamic neuroepithelium to the ventral lateral geniculate nucleus.

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

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

291 in humans only where the damage to the post-geniculate pathway occurred prenatally.

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

293 The development of geniculate receptive fields after receiving these increa

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

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

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

297 BA)ergic; 3) are smaller than ventral medial geniculate terminals synapsing in layer IV; 4) make asym

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