ライフサイエンスコーパス: primary visual cortex

1 on between connected pairs of neurons in the primary visual cortex.

2 get and activate predictable spatial loci in primary visual cortex.

3 dritic and somatic compartments in the awake primary visual cortex.

4 layer 5 pyramidal neurons in the awake mouse primary visual cortex.

5 tion on layer-2/3 pyramidal neurons in mouse primary visual cortex.

6 vely enhance or reduce neuronal responses in primary visual cortex.

7 and the synaptic inputs perforating them in primary visual cortex.

8 r 2/3 neurons in the binocular zone of mouse primary visual cortex.

9 e of binocular visual responses in the mouse primary visual cortex.

10 foveal magnification, comparable to that in primary visual cortex.

11 matic responses for anomalous trichromats in primary visual cortex.

12 stsynaptic cortical cells in input layers of primary visual cortex.

13 ecordings from superficial layers of macaque primary visual cortex.

14 ature expression of direction selectivity in primary visual cortex.

15 he development of basic sensory detectors in primary visual cortex.

16 ng of eye-specific visual input in binocular primary visual cortex.

17 properties in parallel, from retina through primary visual cortex.

18 eriod impairs binocular integration in mouse primary visual cortex.

19 ning is a fundamental property of neurons in primary visual cortex.

20 ng of layer 5 pyramidal neurons in the mouse primary visual cortex.

21 , result in functional reorganization of the primary visual cortex.

22 nderlying amblyopia begin in the circuits of primary visual cortex.

23 on enhances GABAergic synaptic inhibition in primary visual cortex.

24 e Oxidase (CO)-blobs boundaries in the human primary visual cortex.

25 e similar to simple cell receptive fields in primary visual cortex.

26 response variability and correlations in the primary visual cortex.

27 the visual field have been widely studied in primary visual cortex.

28 g across a variety of systems, including the primary visual cortex.

29 e pathways interact and merge as early as in primary visual cortex.

30 m in local field potential recorded from the primary visual cortex.

31 essing in the lateral geniculate nucleus and primary visual cortex.

32 gration of head and visual signals in rodent primary visual cortex.

33 nctional at or near the time of birth, as is primary visual cortex.

34 ures: the lateral geniculate nucleus and the primary visual cortex.

35 ns within superficial and deep layers of the primary visual cortex.

36 urce of visual inputs to the colliculus, the primary visual cortex.

37 work, cellular, and subthreshold activity in primary visual cortex.

38 ally realistic simulation of the awake mouse primary visual cortex.

39 binocular integration in thalamic inputs to primary visual cortex.

40 or neurons in a computational model of mouse primary visual cortex.

41 diction-error circuits in layer 2/3 of mouse primary visual cortex.

42 ntextual modulation in individual neurons of primary visual cortex.

43 and in the structure of interneurons in the primary visual cortex.

44 change the density of excitatory synapses in primary visual cortex.

45 ltaneously stimulate thousands of neurons in primary visual cortex, a response that may seem unnecess

46 roscope to monitor activity across the mouse primary visual cortex, along with analyses to quantify t

47 The primary visual cortex also exhibited more severe functio

48 We tested this approach in the primary visual cortex, an area where neural inactivation

49 on, with the glutamate measure lowest in the primary visual cortex and highest in the dorsolateral pr

50 ging neural population activity in the mouse primary visual cortex and hippocampus.

51 y and structure of interneurons, both in the primary visual cortex and in the rest of cerebral region

52 imics the processing of depth information in primary visual cortex and that can process disparity dir

53 We recorded simultaneously from neurons in primary visual cortex and the middle temporal area while

54 We recorded simultaneously from neurons in primary visual cortex and the middle temporal area while

55 arrays, we examined binocular interaction in primary visual cortex and V2 of six amblyopic macaque mo

56 as less bilateral in the monocular region of primary visual cortex and, especially during task engage

57 Neurons in primary visual cortex are strongly modulated both by sti

58 The majority of neurons in primary visual cortex are tuned for stimulus orientation

59 e anatomical inputs and outputs to the mouse primary visual cortex, area V1.

60 These correlations became stronger in primary visual cortex as neuronal signals in that area b

61 grasping and is coded preferentially in the primary visual cortex as well as the anterior and poster

62 ciation with response inhibition, and in the primary visual cortex, as a control region.

63 No major differences were found in the primary visual cortex between both groups.

64 study investigated structural differences in primary visual cortex between normally-sighted controls

65 EMENT Thalamocortical afferents segregate in primary visual cortex by eye input and light-dark polari

66 al organization of receptive fields in mouse primary visual cortex by measuring the tuning of pyramid

67 mage projection occurring between retina and primary visual cortex can be mathematically described by

68 htened attention, the population activity in primary visual cortex can support better spatial acuity,

69 monosynaptic rabies tracing to compare mouse primary visual cortex CCPNs projecting to different high

70 The primary visual cortex contains a detailed map of retinal

71 The primary visual cortex contains a detailed map of the vis

72 ocampal and parahippocampal areas as well as primary visual cortex correlate with the speed of accura

73 Conversely, peripherally-responsive primary visual cortex demonstrated significantly increas

74 re we show that contrast adaptation in mouse primary visual cortex depends on the behavioral relevanc

75 em of primates develops hierarchically, with primary visual cortex developing structurally and functi

76 neurons in the mouse superior colliculus and primary visual cortex display striking differences in th

77 rom populations of synaptic boutons in mouse primary visual cortex during locomotion.

78 ts by measuring hemodynamic responses in the primary visual cortex during visual stimulation.

79 eas that, in the rat brain, run laterally to primary visual cortex, encode object information.

80 Primary visual cortex exhibits two types of gamma rhythm

81 hanges in the lateral geniculate nucleus and primary visual cortex following novel visual experiences

82 cortex, anterior cingulate, hippocampus) and primary visual cortex for comparison from 3.5- to 4-year

83 We measured the selectivity of neurons in primary visual cortex for orientation and spatial freque

84 ate this relation in multiple regions of the primary visual cortex from individual animals, and diffe

85 ections onto excitatory neurons in the mouse primary visual cortex generate a second receptive field

86 The primary visual cortex has a map of multiple visual param

87 ually represented across mouse visual areas: primary visual cortex has substantially more surround su

88 Cortical regions as early as primary visual cortex have been implicated in recognitio

89 GCaMP6s, 10 Hz, 100-250 cells, layer 2/3 of primary visual cortex, i.e., V1) in awake head-fixed mic

90 d neural responses and the effects of EBS in primary visual cortex in four patients implanted with in

91 he responses of single neurons in layer 6 of primary visual cortex in male macaque monkeys (Macaca fa

92 ount for several properties of adaptation in primary visual cortex in response to changes in the stat

93 cortex, dorsolateral prefrontal cortex, and primary visual cortex) in human postmortem brain samples

94 a cellular taxonomy of one cortical region, primary visual cortex, in adult mice on the basis of sin

95 neously with local field potentials (LFP) in primary visual cortex, in sufentanil-anaesthetized marmo

96 sumption is supported by observations in the primary visual cortex: inhibitory neurons are broadly tu

97 in thalamorecipient layer 4 simple cells of primary visual cortex is believed to play important role

98 the "critical period," when the circuitry of primary visual cortex is most sensitive to perturbation

99 areas are sensitive to these features, while primary visual cortex is not.

100 ectivity of inhibitory neurons in layer 4 of primary visual cortex is sufficient to explain broad inh

101 us to spiny stellate cells in layer 4 of the primary visual cortex (L4SS).

102 -photon guided whole-cell Vm recordings from primary visual cortex layer 2/3 excitatory and inhibitor

103 Primary visual cortex occupies 35 cm(2) of surface, 10%

104 electrocorticogram (ECoG) electrodes in the primary visual cortex of 2 female macaque monkeys, and a

105 ergic modulation of visual processing in the primary visual cortex of awake behaving macaque monkeys.

106 unctional properties of these neurons in the primary visual cortex of awake mice.

107 aneously map MUA, LFP, and ECoG RFs from the primary visual cortex of awake monkeys (three female Mac

108 ged interneurons of specific subtypes in the primary visual cortex of behaving mice, we show that spi

109 Studies in the primary visual cortex of carnivores and primates have co

110 ectrode arrays in cortical layers 5/6 of the primary visual cortex of chronically instrumented, freel

111 amidal neuron apical dendritic spines in the primary visual cortex of control and AS model mice (Ube3

112 erence (OP) and ocular dominance (OD) in the primary visual cortex of ferrets, cats and monkeys can b

113 lly, it remains an open question whether the primary visual cortex of higher mammals displays the sam

114 The primary visual cortex of higher mammals is organized int

115 to stimuli of varying contrast, recorded in primary visual cortex of male macaques.

116 of oriented gratings is encoded in layer 2/3 primary visual cortex of mouse (with C57BL/6 background,

117 Stimulus orientation in the primary visual cortex of primates and carnivores is mapp

118 sary, consistent with recent findings in the primary visual cortex of rodents.

119 orrelate with the pattern of activity in the primary visual cortex of the human brain.

120 at 60 Hz in retina, lateral geniculate, and primary visual cortex of the mouse visual system.

121 ntation of information in neurons within the primary visual cortex of the mouse.

122 h micro and ECoG electrodes implanted in the primary visual cortex of two female macaques (for some s

123 om sensory signals within specific layers of primary visual cortex, providing insight into the role o

124 expression in the entorhinal cortex (EC) and primary visual cortex (PVC) of aged APOE mice.

125 oupled with aversive experiences, neurons in primary visual cortex rapidly alter their responses in a

126 ritical period in early life, neurons in the primary visual cortex rapidly lose responsiveness to an

127 enia and Alzheimer's disease, while those in primary visual cortex remain relatively resilient.

128 We additionally applied a model predicting primary visual cortex responses to the set of stimuli.

129 Here we develop a new model and test it on primary visual cortex responses.

130 ritical period when binocular neurons in the primary visual cortex sharpen their receptive field tuni

131 We thus identify a collicular primary visual cortex that is independent of the genicul

132 model of an excitatory-inhibitory circuit in primary visual cortex that performed HMC inference, and

133 ner cortex in typically centrally-responsive primary visual cortex - the region of cortex that normal

134 In the primary visual cortex, the selectivity of a neuron in la

135 through two major pathways, one reaching the primary visual cortex through the thalamus, and the othe

136 ns of the information being fed forward from primary visual cortex to extrastriate processing areas a

137 cular and neural responses in cat and rodent primary visual cortex to investigate the limits of neuro

138 nctional impact of L6CT projections from the primary visual cortex to the dorsolateral geniculate nuc

139 connection (probably multisynaptic) from the primary visual cortex to VPM.

140 mean estimated lateral geniculate nucleus to primary visual cortex transfer time of 15 ms, we claim t

141 sharpen orientation tuning of neurons in the primary visual cortex (V1) [6, 7].

142 3D head-orienting movements (HOMs) modulate primary visual cortex (V1) activity in a direction-speci

143 lation responses, recorded simultaneously in primary visual cortex (V1) and area V4 of monkeys, to pe

144 erence, or dominance, toward the open eye in primary visual cortex (V1) and disrupts the normal devel

145 es involving reciprocal interactions between primary visual cortex (V1) and extrastriate visual areas

146 eye-reopening paradigm to enhance firing in primary visual cortex (V1) and found that neurons bidire

147 Imaging of primary visual cortex (V1) and higher visual areas (HVAs

148 perceive stereoscopic depth, and neurons in primary visual cortex (V1) and higher-order, lateromedia

149 expressing GCaMP6s across all layers of the primary visual cortex (V1) and in the subplate.

150 first stages of visual cortical processing: primary visual cortex (V1) and its thalamic inputs from

151 d event-related fMRI BOLD responses in human primary visual cortex (V1) and manipulated certainty via

152 ual system, the emergence of both rhythms in primary visual cortex (V1) and mid-level cortical areas

153 ization of orientation preference in macaque primary visual cortex (V1) and perform causal manipulati

154 tensor structure for multiple datasets from primary visual cortex (V1) and primary motor cortex (M1)

155 tive to anticorrelated stimuli compared with primary visual cortex (V1) and rostrolateral area (RL),

156 Load-dependent BOLD signals in primary visual cortex (V1) and superior intraparietal su

157 o early gateways into the visual system: the primary visual cortex (V1) and the evolutionarily older

158 on increases correlations between neurons in primary visual cortex (V1) and the middle temporal area

159 re receptive fields (RFs) and size-tuning in primary visual cortex (V1) and three downstream higher v

160 We determined the necessity of the primary visual cortex (V1) and three key higher visual a

161 ifier weights suggested early recruitment of primary visual cortex (V1) and ~160-ms recruitment of th

162 The basic organization principles of the primary visual cortex (V1) are commonly assumed to also

163 GNIFICANCE STATEMENT Visual responses in the primary visual cortex (V1) are diverse, in that neurons

164 Neuronal responses in the primary visual cortex (V1) are driven by simple stimuli,

165 The visual responses of neurons in the primary visual cortex (V1) are influenced by the animal'

166 ral geniculate nucleus (LGN) and from LGN to primary visual cortex (V1) are organized into functional

167 rial fluctuations of population responses in primary visual cortex (V1) are related to simultaneously

168 Neurons in mouse primary visual cortex (V1) are selective for particular

169 gests that local motion signals generated in primary visual cortex (V1) are spatially integrated to p

170 ontacting single pyramidal neurons in ferret primary visual cortex (V1) by combining in vivo two-phot

171 Stroke damage to the primary visual cortex (V1) causes a loss of vision known

172 STATEMENT: Conventional diagrams of primate primary visual cortex (V1) depict neuronal connections w

173 shed across many species that neurons in the primary visual cortex (V1) display preference for visual

174 The primary visual cortex (V1) encodes a diverse set of visu

175 l cortex alpha power, and a greatly expanded primary visual cortex (V1) functional connectivity profi

176 n of extrastriate areas located laterally to primary visual cortex (V1) has been assigned to a putati

177 ically.SIGNIFICANCE STATEMENT Traditionally, primary visual cortex (V1) has been regarded as playing

178 Traditionally, human primary visual cortex (V1) has been thought to mature wi

179 Human primary visual cortex (V1) has long been associated with

180 Primary visual cortex (V1) has long been thought to comp

181 Decades of anatomical studies on the primate primary visual cortex (V1) have led to a detailed diagra

182 Since neurons beyond the primary visual cortex (V1) have rarely been studied in n

183 Voltage-sensitive dye imaging experiments in primary visual cortex (V1) have shown that local, orient

184 orms of experience-dependent modification of primary visual cortex (V1) in adult mice: ocular dominan

185 tically manipulated neuronal excitability in primary visual cortex (V1) in mice of both sexes during

186 ed activity with extracellular recordings of primary visual cortex (V1) in nonanesthetized mice.

187 sh the local context in which neurons in the primary visual cortex (V1) interpret stimuli.

188 ines is highly dynamic with more dynamics in primary visual cortex (V1) layer 2/3 (L2/3) neurons than

189 Lesions of primary visual cortex (V1) lead to loss of conscious vis

190 Unilateral damage to the primary visual cortex (V1) leads to clinical blindness i

191 response- and contrast-gain changes and with primary visual cortex (V1) narrowed and broadened attent

192 Spikes in the primary visual cortex (V1) need to occur at the same tim

193 stimulus presentation alone does not affect primary visual cortex (V1) neurons, which show response

194 he extra-classical receptive field (eCRF) in primary visual cortex (V1) neurons.

195 calcium imaging of excitatory neurons in the primary visual cortex (V1) of awake mice raised in three

196 pharmacologically induced focal seizures in primary visual cortex (V1) of awake mice, and compared t

197 ere, we use voltage-sensitive dye imaging in primary visual cortex (V1) of awake monkeys to show that

198 reliability of visually evoked responses in primary visual cortex (V1) of awake, passively behaving

199 urprisingly, mean firing rates of neurons in primary visual cortex (V1) of freely behaving rodents ar

200 sing, we recorded neuronal activity from the primary visual cortex (V1) of macaque monkeys while they

201 gy, and optogenetics, we first show that the primary visual cortex (V1) of male mice responds to Kani

202 ory area called the Wulst, as it does in the primary visual cortex (V1) of mammals.

203 Although VIP neuron activity in the primary visual cortex (V1) of mouse is highly correlated

204 multaneous recordings from all layers in the primary visual cortex (V1) of the behaving mouse reveale

205 arly all of the information that reaches the primary visual cortex (V1) of the brain passes from the

206 A new computational model of the primary visual cortex (V1) of the macaque monkey was con

207 The primary visual cortex (V1) of the mouse and its inputs f

208 s and markers of GABAergic inhibition in the primary visual cortex (V1) of young adult and senescent

209 rence maps (OPMs) are a prominent feature of primary visual cortex (V1) organization in many primates

210 structing the distribution of attention from primary visual cortex (V1) population neuronal activity

211 nt luminance profoundly transforms how mouse primary visual cortex (V1) processes head movements.

212 distribution and morphology of the afferent primary visual cortex (V1) projections.

213 erging body of work challenges the view that primary visual cortex (V1) represents the visual world f

214 al context.SIGNIFICANCE STATEMENT Neurons in primary visual cortex (V1) show tuning for stimulus size

215 ncrease the sparseness of coding, neurons in primary visual cortex (V1) show tuning for stimulus size

216 rts over several decades, our best models of primary visual cortex (V1) still predict spiking activit

217 sal forebrain provides cholinergic inputs to primary visual cortex (V1) that play a key modulatory ro

218 rom each retina in parallel and merge in the primary visual cortex (V1) through the convergence of ip

219 rough two parallel pathways: one reaches the primary visual cortex (V1) through the thalamus and anot

220 ompared how neuronal tuning evolves from rat primary visual cortex (V1) to a downstream visual cortic

221 e recorded populations of neurons in macaque primary visual cortex (V1) to find that perceptually uni

222 o trial-averaged neural responses in macaque primary visual cortex (V1) to study two fundamental, pop

223 Projections from the primary visual cortex (V1) to the SC have been shown to

224 The responses of neurons in mouse primary visual cortex (V1) to visual stimuli depend on b

225 f a visual grating can be decoded from human primary visual cortex (V1) using functional magnetic res

226 ntrinsic-signal optical imaging) from monkey primary visual cortex (V1) while the animals' engagement

227 projections from layers (L)2/3 and 4B of the primary visual cortex (V1), and project to dorsal or ven

228 al field potential (LFP) dynamics in the S1, primary visual cortex (V1), anterior cingulate cortex (A

229 ration in primary sensory areas, such as the primary visual cortex (V1), are still largely unknown.

230 ations of spontaneous activity events in the primary visual cortex (V1), but it did not affect the fr

231 ye remain separated until they arrive in the primary visual cortex (V1), but their exact meeting poin

232 vely small population of cells projecting to primary visual cortex (V1), compared to a much larger po

233 igations on the postnatal development of the primary visual cortex (V1), cortical mechanisms that may

234 For example, in the mammalian primary visual cortex (V1), heterogenous serotonergic mo

235 atial frequency (SF) vary greatly across the primary visual cortex (V1), increasing in a scale invari

236 redictions of the SSN have been confirmed in primary visual cortex (V1), its computational principles

237 For mouse primary visual cortex (V1), MEIs exhibited complex spati

238 Can the primary visual cortex (V1), once wired up in development

239 ocomotion enhances visual responses in mouse primary visual cortex (V1), resembling the effects of sp

240 rovides spatiotemporally distinct signals to primary visual cortex (V1), such that contralateral eye-

241 Here, we show that in primary visual cortex (V1), the earliest stage of cortic

242 in the lateral geniculate nucleus (LGN) and primary visual cortex (V1), to provide the first in vivo

243 a homolog of pulvinar, or its projection to primary visual cortex (V1), we found that LP contributes

244 nation under classical conditioning requires primary visual cortex (V1), we measured, during learning

245 stimulus affects its representation in mouse primary visual cortex (V1), we performed two-photon calc

246 In layer 2/3 of the primary visual cortex (V1), we use two-photon optogeneti

247 ed in various model systems, including mouse primary visual cortex (V1), where excitatory synapses on

248 This effect is drastic in the primary visual cortex (V1), where locomotion profoundly

249 es robust synaptic plasticity in adult mouse primary visual cortex (V1), which allows subsequent reco

250 primates, complex motion processing involves primary visual cortex (V1), which generates local motion

251 This result contrasted sharply with the primary visual cortex (V1), which reflected low-level im

252 pulations in superficial layers (L) of mouse primary visual cortex (V1).

253 enhance the sensory responses of neurons in primary visual cortex (V1).

254 by the auditory cortex neurons projecting to primary visual cortex (V1).

255 as a function of image contrast in the human primary visual cortex (V1).

256 ieved to rely on the geniculate input to the primary visual cortex (V1).

257 age of the robust visual adaptation in mouse primary visual cortex (V1).

258 ing rate nonlinearity of simple cells in the primary visual cortex (V1).

259 of thalamic synapses in layer 4 of the mouse primary visual cortex (V1).

260 field potentials in their recipient zone in primary visual cortex (V1).

261 ads to retinotopic map reorganization in the primary visual cortex (V1).

262 tivity selectively in the deep layers of the primary visual cortex (V1).

263 of interaction with rhythmic activity in the primary visual cortex (V1).

264 high-level visual brain regions, but not in primary visual cortex (V1).

265 ex is altered following extensive lesions of primary visual cortex (V1).

266 has predominantly focused on circuits in the primary visual cortex (V1).

267 teral geniculate nucleus (LGN) projection to primary visual cortex (V1).

268 hroughout cortical layers 2/3-6 in the mouse primary visual cortex (V1).

269 erlying retinal origin with amplification in primary visual cortex (V1).

270 ctional ocular dominance plasticity in adult primary visual cortex (V1).

271 ces ocular dominance plasticity in the adult primary visual cortex (V1).

272 n record from neuronal populations in monkey primary visual cortex (V1).

273 activity in diverse neural systems including primary visual cortex (V1).

274 enduring changes to ocular dominance (OD) in primary visual cortex (V1).

275 ons to increase or decrease neuronal spiking primary visual cortex (V1).

276 d drive plasticity in neural-circuits of the primary visual cortex (V1).

277 are extracted by distinct neurons in primate primary visual cortex (V1).

278 isual pathways beginning at the level of the primary visual cortex (V1).

279 re are three neural feedback pathways to the primary visual cortex (V1): corticocortical, pulvinocort

280 d neuronal activity simultaneously in early [primary visual cortex (V1)] and midlevel (V4) visual cor

281 responses in early visual processing [e.g., primary visual cortex (V1)] reflect primarily the retina

282 ) and as a comparison, an early stage in the primary visual cortex (V1; N = 15) of male monkeys (Maca

283 from neurons in two areas of visual cortex (primary visual cortex, V1, and the middle temporal area,

284 ry important role in the function of macaque primary visual cortex, V1, but not enough is understood

285 A lesion of primary visual cortex, V1, can result in the perceived s

286 The binocular zone of primary visual cortex (V1b) undergoes spine loss and cha

287 Within primary visual cortex, various populations of pyramidal

288 sence of sound sharpens neural tuning in the primary visual cortex via activation of direct inputs fr

289 The LGd then projects topographically to primary visual cortex (VISp) to mediate visual perceptio

290 The thickness of primary visual cortex was assessed using T1-weighted ana

291 The blind spot region in the primary visual cortex was labeled by cytochrome oxidase

292 Using a computational model of layer 2/3 primary visual cortex, we demonstrate how interneuron ci

293 holinergic modulation in visual thalamus and primary visual cortex, we explore potential functional r

294 geniculate nucleus, superior colliculus, and primary visual cortex, we processed brain sections from

295 two-photon holographic optogenetics in mouse primary visual cortex, we tested whether recalling ensem

296 In cat primary visual cortex, where neurons are clustered by th

297 selectivity influences a subset of cells in primary visual cortex which respond to the optic flow as

298 ds relative to their putative targets in the primary visual cortex, which enables the generation of t

299 ipant groups showed comparable activation of primary visual cortex while patient groups showed differ

300 acetylation was developmentally regulated in primary visual cortex, with enhanced levels being detect