ライフサイエンスコーパス: superior colliculus

1 optic tectum (TeO, counterpart to mammalian superior colliculus).

2 ing/steering commands from the optic tectum (superior colliculus).

3 aphic information, the retinal EFNAs, to the superior colliculus.

4 so require interaction with signals from the superior colliculus.

5 lar nuclei, as well as select laminae of the superior colliculus.

6 ra pars reticulata to the deep layers of the superior colliculus.

7 e mesencephalic reticular formation, and the superior colliculus.

8 including the lateral geniculate nucleus and superior colliculus.

9 xcitatory input from both the retina and the superior colliculus.

10 he caudate nucleus, both of which target the superior colliculus.

11 f visual responses from neurons in the mouse superior colliculus.

12 eurons to movement commands generated by the superior colliculus.

13 ccurs in the other major visual pathway, the superior colliculus.

14 de is perturbed by a microstimulation in the superior colliculus.

15 pal brain centres: the visual cortex and the superior colliculus.

16 of the ipsilateral intermediate layer of the superior colliculus.

17 sumably via subcortical connections with the superior colliculus.

18 brachium of the superior colliculus, and the superior colliculus.

19 by reducing the innate response bias of the superior colliculus.

20 uts regulate whisker-related activity in the superior colliculus.

21 ked by weak microstimulation of the midbrain superior colliculus.

22 ibuted in anterior and posterior superficial superior colliculus.

23 rge number of visual areas projecting to the superior colliculus.

24 the known topography of these areas and the superior colliculus.

25 provides a major auditory projection to the superior colliculus.

26 ons were shown to project to the ipsilateral superior colliculus.

27 cell loss or substantial alterations in the superior colliculus.

28 motor and attentional mechanisms mediated by superior colliculus.

29 ific predictions for neural circuitry in the superior colliculus.

30 the selective triggering of behaviors by the superior colliculus.

31 he thalamus, and the other projecting to the superior colliculus.

32 massive cerebellar projection to maps in the superior colliculus.

33 the synaptic boutons of retinal axons in the superior colliculus.

34 eniculate nucleus (60% decrease), and to the superior colliculus (49% decrease).

35 c manipulations show that ACC outputs to the superior colliculus, a key midbrain structure for respon

36 we increased neuronal activity in the mouse superior colliculus, a main projection target of rodent

37 The superior colliculus, a major midbrain center for saccade

38 By focusing on the superior colliculus, a major site of topographic map ali

39 The obvious place to investigate is the superior colliculus, a midbrain oculomotor center respon

40 study was to investigate the function of the superior colliculus, a sensorimotor brainstem structure,

41 How do inputs from the superior colliculus, a visuomotor structure, fit into th

42 The projections: to the superior colliculus, accessory optic nuclei, and nucleus

43 Superior colliculus activation during emotionally aversi

44 systems, including pathologically inhibited superior colliculus activity, deficient corollary discha

45 ophic factor (BDNF) in the visual cortex and superior colliculus after single and multiple stimulatio

46 njections that included deeper layers of the superior colliculus also labeled neurons in medial front

47 ocol was used to stimulate and visualize the superior colliculus and 2 other visual structures: the l

48 cross sites, are evident in the inferior and superior colliculus and anterior and posterior cingulate

49 Iv to reveal retrogradely labeled neurons in superior colliculus and anterogradely labeled terminals

50 nglion cells expand the targeted area in the superior colliculus and at the same time increase their

51 ation of anterograde axonal transport to the superior colliculus and degeneration in the optic nerve.

52 transport from retinal ganglion cells to the superior colliculus and degeneration of the axons themse

53 ransiently inactivated either the FOF or the superior colliculus and found that the resulting impairm

54 glect through reversible inactivation of the superior colliculus and frontal eye fields.

55 tracers were placed, respectively, into the superior colliculus and globus pallidus of Sprague-Dawle

56 ior gradient in development and produces the superior colliculus and inferior colliculus.

57 ectively, in sensory-responsive sites in the superior colliculus and posteromedial (POm) thalamus, th

58 ere we demonstrate that neurons in the mouse superior colliculus and primary visual cortex display st

59 Other RGC recipient areas, such as the superior colliculus and suprachiasmatic nucleus, are tar

60 incerta regulates communication between the superior colliculus and the posteromedial thalamus, we h

61 arietal cortices) and subcortical (e.g., the superior colliculus and the pulvinar nucleus of the thal

62 retina through the superficial layers of the superior colliculus and the pulvinar, is poorly understo

63 and sensory roles to ACC projections to the superior colliculus and the visual cortex and demonstrat

64 the cortex, lateral geniculate nucleus, and superior colliculus, and can be used to express optogene

65 and on into the lateral geniculate nucleus, superior colliculus, and other visual centers.

66 g the auditory thalamus, auditory brainstem, superior colliculus, and periaqueductal gray.

67 hitecture of the lateral geniculate nucleus, superior colliculus, and primary visual cortex, we proce

68 i and in the lateral geniculate nucleus, the superior colliculus, and the lateral and intergeniculate

69 leus of the optic tract, the brachium of the superior colliculus, and the superior colliculus.

70 in the visual cortex, but is similar in the superior colliculus, another major retinal target.

71 and whisker-related neural activities in the superior colliculus are under strong inhibitory and neur

72 Overall, these data support the view of the superior colliculus as a selectively addressable and mod

73 esla) fMRI techniques, this study imaged the superior colliculus at high (0.75 mm isotropic) resoluti

74 the eye to the tectum (amphibians and fish)/superior colliculus (birds and mammals) is a paradigm mo

75 Cholinergic stimulation activates the superior colliculus by increasing spontaneous firing and

76 bution of cortical neurons projecting to the superior colliculus by injecting anatomical tracers into

77 Collectively, these results indicate that superior colliculus can activate the inhibitory projecti

78 In vertebrates, the optic tectum (superior colliculus) commands gaze shifts by synaptic in

79 Changes in imaging the superior colliculus could play an important role as a pr

80 is significant because it suggests that the superior colliculus could suppress the interactions betw

81 on, such as deep layers of the contralateral superior colliculus, deep cerebellar and several brainst

82 The visuomotor functions of the superior colliculus depend not only on direct inputs fro

83 ANCE STATEMENT Receptive field refinement in superior colliculus differs from more commonly studied e

84 s to the deep and intermediate layers of the superior colliculus (DLSC) and the pedunculopontine nucl

85 ation of the intermediate and deep layers of superior colliculus (DLSC) in rodents evokes both orient

86 that the deep and intermediate layers of the superior colliculus (DLSC), a key target of nigral proje

87 etinal activity transfer to the thalamus and superior colliculus does not change across the first two

88 Likewise, the superior colliculus, dorsal lateral geniculate nucleus,

89 nduced by brief microstimulation in the deep superior colliculus (dSC).

90 hown that such maintenance involves the deep superior colliculus (dSC).

91 ing simultaneous inactivation of the FOF and superior colliculus during memory maintenance.

92 found that barrel cortex afferents drive the superior colliculus during the middle portion of the ris

93 e we report that inactivation of the primate superior colliculus eliminates the changes in perceptual

94 t with these findings, direct stimulation of superior colliculus evoked neuronal excitation in ZIv an

95 Instead, the superior colliculus favours specific contour orientation

96 from retinal ganglion cells (RGCs) onto the superior colliculus form a precise retinotopic map.

97 it is challenging to discern activity in the superior colliculus from activity in surrounding nuclei

98 ) resolution, which enabled isolation of the superior colliculus from other brainstem nuclei.

99 ke primates, a substantial projection to the superior colliculus from posterior parietal cortex is no

100 This traditional view of superior colliculus function is challenged by the discov

101 activity in premotor neurons of the primate superior colliculus has 'motor potential'.

102 The superior colliculus has been well-studied in humans for

103 ental nucleus, locus coeruleus, inferior and superior colliculus homologs, hypothalamus, preoptic are

104 mates has established the involvement of the superior colliculus in defensive behaviours and visual t

105 ia theory and suggest a crucial role for the superior colliculus in executive control.

106 optic tectum in birds and its homologue the superior colliculus in mammals both send major bilateral

107 In avians, the optic tectum (OT; called the superior colliculus in mammals) and the GABAergic nucleu

108 vertebrates, the pretectum and optic tectum (superior colliculus in mammals) are visuomotor areas tha

109 ial attention network, the optic tectum (OT, superior colliculus in mammals), in awake barn owls.

110 how retinal inputs to the optic tectum (TeO, superior colliculus in mammals), triggered by moving sti

111 ompetitive interactions in the optic tectum (superior colliculus in mammals), which are vital to the

112 ctivity of the default mode network with the superior colliculus in marmosets that was much weaker in

113 le of the connections between cerebellum and superior colliculus in previously observed dynamic coord

114 ration of RGC termination zones in the mouse superior colliculus in vivo, while their topographic tar

115 In the superior colliculus, in which the superficial gray layer

116 s are expected to match the visuotopy of the superior colliculus, injections at different retinotopic

117 (POm) thalamus, the labeled projections from superior colliculus innervated the ZIv regions that cont

118 cerning the circuit connections by which the superior colliculus interacts with the basal ganglia.

119 We go on to argue that the superior colliculus is a candidate neural substrate for

120 The superior colliculus is canonically viewed as a controlle

121 odulated by contrast-based saliency, and the superior colliculus is likely involved in its coordinati

122 The superior colliculus is part of a broader neural network

123 tion would predict that when activity in the superior colliculus is suppressed by reversible inactiva

124 fields (FEFs) and intermediate layers of the superior colliculus (iSC) support such models for saccad

125 standard functional MRI studies of the human superior colliculus, it is challenging to discern activi

126 Small injections in the superior colliculus labeled neurons in locations within

127 ircuits for orienting behaviors, such as the superior colliculus, likely have privileged access to vi

128 These findings suggest that the superior colliculus may play a role in shaping subjectiv

129 se ratio, whereas other regions, such as the superior colliculus, may be involved in processes that i

130 ssociated with target selection, such as the superior colliculus, may have privileged access to visua

131 The superior colliculus mediates a set of innate behaviors,

132 ere, we show how optogenetic inactivation of superior colliculus neurons in awake monkeys leads to cl

133 hibition of cdlSNr neurons and inhibition of superior colliculus neurons.

134 Here, we report the first experiments in the superior colliculus of awake primates with strabismus us

135 s and sensory responsiveness observed in the superior colliculus of behaving animals during distinct

136 Based on neuronal recordings in the superior colliculus of cats, three basic rules were form

137 on for all groups, but only sustained in the superior colliculus of ephrin-A2A5(-/-) mice.

138 anatomical representation of azimuth in the superior colliculus of heterozygous Islet2-EphA3 knockin

139 ilar to neurophysiological recordings in the superior colliculus of nonhuman primates generating anti

140 We investigate motion processing in the superior colliculus of the awake mouse by optically reco

141 In the superficial layers of the superior colliculus of the midbrain, converging projecti

142 eir cell bodies in the eye to targets in the superior colliculus of the midbrain.

143 Here, we show how specific cells in the superior colliculus, one synapse downstream of the retin

144 omotor neurons, possibly at the level of the superior colliculus or omnipause neurons.

145 ucleus (PPT), not by inhibiting cells in the superior colliculus or thalamus.

146 The superior colliculus, or tectum, is a key sensorimotor st

147 Notably, adjacent superior colliculus orientation columns have only limite

148 The superior colliculus plays an evolutionarily conserved ro

149 ave shown that the superficial layers of the superior colliculus project to multiple divisions of the

150 uces learning speed, whereas the ablation of superior colliculus projecting neurons does not impact l

151 ns at different retinotopic locations in the superior colliculus provide information about the locati

152 nsposition of retinal guidance cues into the superior colliculus providing positional information for

153 UT2 in the lateral geniculate nucleus (LGN), superior colliculus, pulvinar complex, and primary visua

154 n in the subcortical face processing system (superior colliculus, pulvinar nucleus of the thalamus an

155 The subcortical pathway, which consists of superior colliculus, pulvinar nucleus of the thalamus, a

156 The intermediate layers of the superior colliculus receive whisker-related excitatory a

157 In mammals, the superior colliculus receives inhibitory gamma-aminobutyr

158 PD patients, there was no modulation of the superior colliculus responses to the luminance contrasts

159 Silencing the visual cortex or superior colliculus revealed that they drive visual tuni

160 The rostral superior colliculus (rSC) encodes position errors for mu

161 (LIP), the frontal eye fields (FEF), and the superior colliculus (SC) (e.g., [1]).

162 us (fSTS), as the primary cortical target of superior colliculus (SC) activity.

163 xation and saccade-generating neurons in the superior colliculus (SC) and can lead to premature gaze

164 two main retinorecipient brain targets, the superior colliculus (SC) and dorsal lateral geniculate n

165 accade initiation.SIGNIFICANCE STATEMENT The superior colliculus (SC) and frontal eye fields (FEFs) a

166 tinal ganglion cell (RGC) projections to the superior colliculus (SC) and lateral geniculate nucleus

167 to map the topographic organization of human superior colliculus (SC) and model how population activi

168 mapped the topographic organization of human superior colliculus (SC) and modeled how population acti

169 tical projections to the geniculate from the superior colliculus (SC) and parabigeminal nucleus (PBG)

170 ns to sensorimotor structures, including the superior colliculus (SC) and regions associated with cer

171 LP regions receive bottom-up input from the superior colliculus (SC) and respond preferably to non-p

172 ions to both the motor-related layers of the superior colliculus (SC) and the lateral posterior nucle

173 deep layers of the macaque (Macaca mulatta) superior colliculus (SC) and the underlying reticular fo

174 finement of visual receptive fields (RFs) in superior colliculus (SC) and visual cortex (V1), but ear

175 intermediate and deep layers of the midbrain superior colliculus (SC) are a key locus for several cri

176 nhuman species indicated that neurons in the superior colliculus (SC) are involved in the control of

177 scaffolds expressed in the young superficial superior colliculus (SC) are synapse-associated protein

178 the lateral geniculate nucleus (LGN) and the superior colliculus (SC) are the major targets of visual

179 and formation of functional synapses in the superior colliculus (SC) but not significant recovery of

180 Surprisingly, the superior colliculus (SC) contained only sparse anterogra

181 Neuronal networks within the superior colliculus (SC) encode locations of intended ey

182 The superior colliculus (SC) follows this pattern as it play

183 et al. describes a dopaminergic input to the superior colliculus (SC) from the zona incerta, as well

184 e behaviors.SIGNIFICANCE STATEMENT The mouse superior colliculus (SC) has become a popular model for

185 The superior colliculus (SC) has long been known to be part

186 x expression patterns in both the retina and superior colliculus (SC) have made it difficult to uncov

187 the representation for eye movements in the superior colliculus (SC) in awake mice.

188 us to the role of ascending signals from the superior colliculus (SC) in monkeys.

189 vity of sensorimotor neurons in the midbrain superior colliculus (SC) in two monkeys.

190 The superior colliculus (SC) is a fundamental structure for

191 The superior colliculus (SC) is a key structure within the e

192 The superior colliculus (SC) is a layered midbrain structure

193 The superior colliculus (SC) is a major center for processin

194 The superior colliculus (SC) is a major site of sensorimotor

195 The superior colliculus (SC) is a midbrain center involved i

196 The superior colliculus (SC) is a midbrain nucleus that inte

197 The superior colliculus (SC) is a midbrain structure central

198 The superior colliculus (SC) is a midbrain structure importa

199 The superior colliculus (SC) is a midbrain structure that in

200 The superior colliculus (SC) is an evolutionarily conserved,

201 The superior colliculus (SC) is arguably the most important

202 The mammalian superior colliculus (SC) is made up of seven distinct la

203 Prior studies of the superior colliculus (SC) neuron as a model suggest that

204 The present study demonstrates that superior colliculus (SC) neurons in animals whose visual

205 of multisensory integration capabilities in superior colliculus (SC) neurons was examined in cats wh

206 patterns of neural activity in the midbrain superior colliculus (SC) of an echolocating bat tracking

207 neural recording experiments in the midbrain superior colliculus (SC) of echolocating bats engaged in

208 uditory stimulus selectivity in the midbrain superior colliculus (SC) of the echolocating bat, an ani

209 al-world contexts.SIGNIFICANCE STATEMENT The superior colliculus (SC) performs a visual-to-motor tran

210 The superior colliculus (SC) plays a highly conserved role i

211 the pulvinar complex in galagos by examining superior colliculus (SC) projections to this structure a

212 The superior colliculus (SC) receives direct input from the

213 fects SC activity.SIGNIFICANCE STATEMENT The superior colliculus (SC) receives visual input from the

214 ells in retino-recipient layers of the mouse superior colliculus (SC) respond selectively to small mo

215 Human superior colliculus (SC) responds in a retinotopically s

216 Its application in superior colliculus (SC) reveals that SC neuron subpopul

217 Previous studies suggested that the superior colliculus (SC) sends error signals to drive sa

218 the mouse primary visual cortex (V1) to the superior colliculus (SC) significantly reduces an SC-dep

219 roaches in MASC, a model of attention in the superior colliculus (SC) that captures known neurophysio

220 In monkeys, a circuit from superior colliculus (SC) through medial-dorsal nucleus o

221 ex (V1) through the thalamus and another the superior colliculus (SC) via direct projections from the

222 ked defensive responses are triggered by the superior colliculus (SC) which receives direct retinal i

223 mined the ultrastructure of the glaucomatous superior colliculus (SC) with three-dimensional serial b

224 ith the activation of neurons in the primate superior colliculus (SC), a midbrain structure associate

225 ive indirect anatomical connections from the superior colliculus (SC), a midbrain structure that is k

226 uch a columnar structure exists in the mouse superior colliculus (SC), a prominent visual center for

227 late nucleus (LGN), pretectal area (PTA) and superior colliculus (SC), and avoid the suprachiasmatic

228 excitation of visual-saccadic neurons in the superior colliculus (SC), and induces contralateral sacc

229 a, dorsal lateral geniculate nucleus (dLGN), superior colliculus (SC), and primary visual cortex (V1)

230 pretectal nuclei, superficial layers of the superior colliculus (SC), and the main nuclei of the acc

231 directly received anatomical input from the superior colliculus (SC), and the neurons showed visual

232 on selectivity in a major visual center, the superior colliculus (SC), are entirely unknown.

233 tical and subcortical areas, for example the superior colliculus (SC), as well as prefrontal areas re

234 ty is initiated by excitatory input from the superior colliculus (SC), but how the tectum's saccade-r

235 formation enters the cortex also through the superior colliculus (SC), but the function of this input

236 lomotor drive command in structures like the superior colliculus (SC), but they also disinhibit the s

237 by specific sensory signals relayed from the superior colliculus (SC), contributing to the maintenanc

238 ically to sensorimotor nuclei, including the superior colliculus (SC), via long-range inhibitory conn

239 of an important murine RGC target area, the superior colliculus (SC), was established via a novel op

240 he complexities of GABAergic circuits in the superior colliculus (SC), we utilized mouse lines that e

241 nal projections from the PMd to the midbrain superior colliculus (SC), which also contains reach-rela

242 ich controls the pupillary light reflex; the superior colliculus (SC), which mediates orienting respo

243 the function of top-down input in the mouse superior colliculus (SC), which receives convergent inpu

244 re and after aspiration of the contralateral superior colliculus (SC), which removed terminals of opt

245 The critical involvement of the superior colliculus (SC)-the central structure in the mi

246 ual cortex (V1) and the evolutionarily older superior colliculus (SC).

247 ey attention-related midbrain structure, the superior colliculus (SC).

248 a-synuclein was detected in the striatum and superior colliculus (SC).

249 for directing saccadic eye movements is the superior colliculus (SC).

250 ), whereas Pro could be mediated by midbrain superior colliculus (SC).

251 port on auditory space encoding in the mouse superior colliculus (SC).

252 ss in deep layer neurons of the ipsilesional superior colliculus (SC).

253 excitatory inputs to the deep layers of the superior colliculus (SC).

254 egulating target selection of the developing superior colliculus (SC).

255 xists in another major visual structure, the superior colliculus (SC).

256 ns receive direct excitatory inputs from the superior colliculus (SC).

257 The projection of the retina to the superior colliculus (SC)/tectum has been an important mo

258 level (2 muL, 40 mug/muL) or at level of the superior colliculus (SC, 1 muL, 40 mug/muL).

259 corticosubcortical feedback projections (to superior colliculus [SC]).

260 the orofacial region of the lateral tectum (superior colliculus, SC).

261 connected to the intermediate layers of the superior colliculus (SCi), evoked robust pupil dilation

262 vity [7-9], and that auditory neurons in the superior colliculus show shifting receptive fields [10-1

263 maps or disrupt binocular convergence in the superior colliculus.SIGNIFICANCE STATEMENT Patients with

264 three main layers, A, A1, and C, while each superior colliculus similarly consisted of seven distinc

265 The superficial superior colliculus (sSC) occupies a critical node in th

266 the specific circuits within the superficial superior colliculus (sSC) that drive orienting and appro

267 etinal axons, which terminate in superficial superior colliculus (sSC), we also found alpha6 subunit

268 ses on individual neurons in the superficial superior colliculus (sSC).

269 eral geniculate, suprachiasmatic nuclei, and superior colliculus, suggesting a commonality for the vi

270 en found upstream of cortex in mouse LGN and superior colliculus, suggesting a possible origin in the

271 ing revealed that M1-M4 cells project to the superior colliculus, suggesting that the contrast and mo

272 ior end of the dorsal lateral geniculate and superior colliculus, suggestive of a paucity of the rele

273 imulus onset was earlier for V1 neurons than superior colliculus superficial visual-layer neurons (SC

274 components that include the retino-recipient superior colliculus, tecto-recipient pulvinar nucleus an

275 s in mice, we show that dLGN inputs from the superior colliculus (tectogeniculate) possess many of th

276 on cell (RGC) axons within their target, the superior colliculus/tectum.

277 l ganglion cells (TGCs), of the optic tectum/superior colliculus (TeO/SC).

278 -tracer experiment, the projections from the superior colliculus terminated densely in the ventral zo

279 eption model with a map of prominence in the superior colliculus that modulates the stimulus signal's

280 on electrophysiological recordings from the superior colliculus, that used a standard adaptive-filte

281 By examining multisensory neurons in cat superior colliculus, the present study demonstrated that

282 isions of the PI, the superior layers of the superior colliculus, the retina, and the lateral genicul

283 e superficial and intermediate layers of the superior colliculus, the thalamic reticular nucleus, and

284 These signals are sent to the superior colliculus through different parts of the subst

285 saccades has been identified extending from superior colliculus through MD thalamus to frontal corte

286 ays previously implicated in blindsight: (i) superior colliculus to hMT+ and (ii) between hMT+ in eac

287 econdary visual pathways (from retina to the superior colliculus to the dorsal thalamus and extrastri

288 A pathway projecting from the superior colliculus to the frontal eye fields (FEFs) via

289 recordings, Zhou and colleagues identified a superior colliculus to ventral tegmental area pathway in

290 cells that project to anterior and posterior superior colliculus undergo cell death during topographi

291 Receptive fields were mapped in the superior colliculus using a sparse noise stimulus while

292 subcortical pathway to the amygdala from the superior colliculus via the pulvinar.

293 Our findings suggest that pathological superior colliculus visual responses in de novo PD patie

294 image-forming visual system consists of the superior colliculus, visual dorsal thalamus (dorsal late

295 anterograde transport from the retina to the superior colliculus was observed 6 weeks after streptozo

296 is of well characterized neural circuitry in superior colliculus, we construct a dynamical model of n

297 s projecting to the visual cortex versus the superior colliculus, we identified two distinct subnetwo

298 1 (55%), whereas neurons that project to the superior colliculus were rarely responsive (6%).

299 ciated with visual processing, including the superior colliculus, zona incerta, and the visual and re

300 g the striatum, associative thalamic nuclei, superior colliculus, zona incerta, pontine nucleus, mult