ライフサイエンスコーパス: primary visual cortex

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

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

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

4 emarkably similar to that of simple cells in primary visual cortex.

5 sures of response variability for neurons in primary visual cortex.

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

7 or OFF) in the superficial layers of ferret primary visual cortex.

8 neuronal population recordings from macaque primary visual cortex.

9 and well-characterized feature of neurons in primary visual cortex.

10 ral gyrus and failed to be predictive in the primary visual cortex.

11 f spatially separated populations within the primary visual cortex.

12 cient to train reward timing activity in the primary visual cortex.

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

14 formation transmitted from the retina to the primary visual cortex.

15 endent development of neural circuits in the primary visual cortex.

16 f vision, commonly believed to emerge in the primary visual cortex.

17 pecifically to the superficial layers of the primary visual cortex.

18 roperties match closely to those measured in primary visual cortex.

19 s been shown to enhance sensory responses in primary visual cortex.

20 it competes for limited termination zones in primary visual cortex.

21 the population activity structure in macaque primary visual cortex.

22 vision that occurs after destruction of the primary visual cortex.

23 ecordings from superficial layers of macaque primary visual cortex.

24 eriod impairs binocular integration in mouse primary visual cortex.

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

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

27 ature expression of direction selectivity in primary visual cortex.

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

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

30 on enhances GABAergic synaptic inhibition in primary visual cortex.

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

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

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

34 response variability and correlations in the primary visual cortex.

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

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

37 of rs-FC among the same regions (e.g., LA in primary visual cortex accounts for approximately 50%, an

38 In the primary visual cortex, adjacent neurons in iso-orientati

39 The primary visual cortex also exhibited more severe functio

40 opulations of up to 500 neurons in the mouse primary visual cortex and characterized the structure of

41 back interactions between higher centers and primary visual cortex and have been held to index the ef

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

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

44 ecific domains of the orientation map in cat primary visual cortex and imaged their dendritic trees i

45 tivating excitatory neurons in alert macaque primary visual cortex and measuring changes in neuronal

46 ty and function of these cell types in mouse primary visual cortex and reveal a new subtype.

47 s of magnocellular LGN inputs to the macaque primary visual cortex and successfully derived orientati

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

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

50 these effects we focused on the responses of primary visual cortex and the middle temporal area, crit

51 he behavioural results were mirrored in both primary visual cortex and the middle temporal area, with

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

53 The mismatch between the status of the primary visual cortex and visual behavior, both during v

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

55 contrast adaptation, which arise largely in primary visual cortex, are not maintained after approxim

56 In primary visual cortex (area V1), the density and subunit

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

58 were first identified in the thalamic area, primary visual cortex, as well as higher cortical areas

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

60 tions (pixels, V1+; models of the retina and primary visual cortex) but is shared with a state-of-the

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

62 Images are processed in the primary visual cortex by neurons that encode different s

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

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

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

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

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

68 The PACAP in the primary visual cortex did not correlate with the Judgmen

69 ch increases the gain of visual responses in primary visual cortex, dramatically enhances recovery in

70 v, and EBA increased their coupling with the primary visual cortex during congruent visuo-propriocept

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

72 r that pyramidal cells in layer 2/3 of mouse primary visual cortex each receive inhibition in a simil

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

74 rally in a computational model of a patch of primary visual cortex endowed with realistic plasticity

75 ion of astrocytes with channelrhodopsin-2 in primary visual cortex enhances both excitatory and inhib

76 Primary visual cortex exhibits two types of gamma rhythm

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

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

79 the emergence of orientation selectivity in primary visual cortex has been attributed to a complex i

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

81 nctional properties of individual neurons in primary visual cortex have been studied intensely, littl

82 rectly to the orientation tuned responses of primary visual cortex in a way that optimizes the stimul

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

84 More vision is preserved after removal of primary visual cortex in infant than adult primates.

85 f the distinctive organizational features of primary visual cortex in many mammalian species.

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

87 cs of spikelets measured in neurons from cat primary visual cortex in vivo.

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

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

90 Here we demonstrate that in rat primary visual cortex inhibitory synaptic plasticity is

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

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

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

94 The primary visual cortex is organized in a way that assigns

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

96 imates, the functional connectivity of adult primary visual cortex is susceptible to be modified by s

97 ceptive field properties of complex cells in primary visual cortex, it has been concluded that the sa

98 visual cortex, delineating nine known areas (primary visual cortex, lateromedial area, anterolateral

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

100 es the critical period for plasticity in the primary visual cortex, linking this effect to increased

101 Our data demonstrate that the primary visual cortex may contribute to the instruction

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

103 We show here, in primary visual cortex of anaesthetized cats under neurom

104 In the primary visual cortex of anesthetized mice, activation o

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

106 -cell recordings from neurons in upper-layer primary visual cortex of awake mice during locomotion an

107 m imaging of populations of neurons from the primary visual cortex of awake mice during visual stimul

108 cord the activity of neuronal populations in primary visual cortex of awake mice in the presence and

109 alertness on two cell classes in layer 4 of primary visual cortex of awake rabbits: presumptive exci

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

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

112 el of cortical hierarchy, we recorded in the primary visual cortex of cats while controlling synaptic

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

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

115 The primary visual cortex of higher mammals is organized int

116 om the dendrites of pyramidal neurons in the primary visual cortex of lightly anaesthetized and awake

117 activity with two-photon calcium imaging in primary visual cortex of mice performing a go/no-go visu

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

119 focus on the heterogeneous responses in the primary visual cortex of rodents trained with a predicta

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

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

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

123 y of proteins) suppresses LTP and LTD in the primary visual cortex of the mouse.

124 Here we demonstrate these properties in the primary visual cortex of the rhesus macaque (Macaca mula

125 etworks before and after local inhibition of primary visual cortex or FEF.

126 ing from lateral geniculate nucleus (LGN) to primary visual cortex, OS responses have now been found

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

128 ping of cortical topography in the region of primary visual cortex representing the lesioned part of

129 Phosphorylated tau was not detected in primary visual cortex, similar to the pattern observed i

130 we have generated bi-directional changes in primary visual cortex size in vivo and have used it as a

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

132 e present a new subunit model for neurons in primary visual cortex that significantly outperforms thr

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

134 ive their primary inputs from the retina and primary visual cortex, the deep layers receive inputs fr

135 ibitory neurons in superficial layers of cat primary visual cortex to answer two questions: for a giv

136 ording electrophysiology in L4 and L6 of rat primary visual cortex to determine the organization and

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

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

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

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

141 intermediate filaments within cat and human primary visual cortex (V1) across development to determi

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

143 Here we show that both primary visual cortex (V1) and extrastriate area V5/MT a

144 We recorded from all layers of the primary visual cortex (V1) and found that gamma-waves ar

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

146 imaging of approximately 100-300 neurons in primary visual cortex (V1) and lateromedial (LM) visual

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

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

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

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

151 by recording simultaneously from neurons in primary visual cortex (V1) and the middle temporal area

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

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

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

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

156 At eye opening, neurons in primary visual cortex (V1) are selective for stimulus fe

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

158 The firing rates of neurons in primary visual cortex (V1) are suppressed by large stimu

159 Using the mouse primary visual cortex (V1) as a model, we demonstrate th

160 Previous work implicates human primary visual cortex (V1) as the neural substrate media

161 r 2/3 (L2/3) excitatory neurons in the mouse primary visual cortex (V1) as well as L4 excitatory neur

162 nputs to layer 4 excitatory neurons in mouse primary visual cortex (V1) at a developmental stage clos

163 selectivity is present in all layers of the primary visual cortex (V1) at eye opening in the awake m

164 ing DSGCs with the superficial layers of the primary visual cortex (V1) by using viral trans-synaptic

165 Although damage to the primary visual cortex (V1) causes hemianopia, many patie

166 isual angle and activates a larger region of primary visual cortex (V1) compared with the same sphere

167 We construct a laminar neural-field model of primary visual cortex (V1) consisting of a superficial l

168 cular dominance (OD) plasticity in the mouse primary visual cortex (V1) declines during aging and is

169 Ocular dominance (OD) plasticity in mouse primary visual cortex (V1) declines during postnatal dev

170 Neural responses in primary visual cortex (V1) depend on stimulus context in

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

172 activity in the frontal eye fields (FEF) and primary visual cortex (V1) during a curve-tracing task i

173 learning modifies neural representations in primary visual cortex (V1) during acquisition of a visua

174 response properties of excitatory neurons in primary visual cortex (V1) during active exploration and

175 task, we show that activity generated by the primary visual cortex (V1) embodies the target interval

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

177 ed the refinement of feedback projections to primary visual cortex (V1) from multiple sources in juve

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

179 e and mode of computation performed in mouse primary visual cortex (V1) given the physiology of L5 py

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

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

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

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

184 As a result, studies of primary visual cortex (V1) have been performed almost en

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

186 experiments in the main input layer (L4) of primary visual cortex (V1) have shown that excitatory an

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

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

189 Here, we report FUS sonication of the primary visual cortex (V1) in humans, resulting in elici

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

191 , superior colliculus, pulvinar complex, and primary visual cortex (V1) in tree shrews (Tupaia belang

192 When the human primary visual cortex (V1) is damaged, the dominant geni

193 Notably, the visual response of mouse primary visual cortex (V1) is enhanced by locomotion, a

194 ying the representation of color surfaces in primary visual cortex (V1) is not well understood.

195 Layer 1 (L1) of primary visual cortex (V1) is the target of projections

196 Mammalian primary visual cortex (V1) is topographically organized

197 The primary visual cortex (V1) is widely regarded as faithfu

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

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

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

201 ates functionally distinct subpopulations of primary visual cortex (V1) neurons.

202 layer 2/3 (L2/3) pyramidal neurons in mouse primary visual cortex (V1) obeys a simple rule--the few

203 2/1, 2/5, 2/7, 2/8, and 2/9) injected in the primary visual cortex (V1) of adult C57Bl/6J mice.

204 in the lateral geniculate nucleus (LGN) and primary visual cortex (V1) of alert macaque monkeys view

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

206 g in postrhinal association cortex (POR) and primary visual cortex (V1) of behaving mice.

207 ompared the spike activity of neurons in the primary visual cortex (V1) of cats with that of their af

208 hippocampal place cells, many neurons in the primary visual cortex (V1) of freely moving rats selecti

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

210 the cortex of behaving monkeys, focusing on primary visual cortex (V1) of monkeys performing a visua

211 chitecture of iso-orientation domains in the primary visual cortex (V1) of placental carnivores and p

212 observation of reward-timing activity in the primary visual cortex (V1) of rodents, wherein neural re

213 reviously that cholinergic modulation in the primary visual cortex (V1) of the macaque monkey is stro

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

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

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

217 Damage to the primary visual cortex (V1) or its immediate afferents re

218 ssociated with juvenile experience-dependent primary visual cortex (V1) plasticity, yet little is kno

219 The primary visual cortex (V1) receives its main thalamic dr

220 Neurons in rodent primary visual cortex (V1) relate operantly conditioned

221 n hypothesized that neural activities in the primary visual cortex (V1) represent a saliency map of t

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

223 Neurons in the primary visual cortex (V1) respond near instantaneously

224 Neurons in the primary visual cortex (V1) respond to stimuli within a r

225 tes of figure-ground (FG) segregation in the primary visual cortex (V1) showed enhanced activity in t

226 erfully influences sensory processing in the primary visual cortex (V1) through long-range projection

227 ate the contribution of ascending input from primary visual cortex (V1) to beta oscillation dynamics

228 integrates visual inputs from the retina and primary visual cortex (V1) to regulate goal-directed eye

229 mporal response properties of neurons in the primary visual cortex (V1) to stimuli whose luminance an

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

231 l projections from layer 5 (L5) of the mouse primary visual cortex (V1) to the superior colliculus (S

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

233 Injury to the primary visual cortex (V1) typically leads to loss of co

234 esponses and haemodynamic signals in macaque primary visual cortex (V1) using fMRI (7T) and intracort

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

236 Here we examine this question in primary visual cortex (V1) using receptive-field-based m

237 The LGN projects mainly to primary visual cortex (V1) while the SC targets the thal

238 m identified L6 principal cells in the mouse primary visual cortex (V1) with modified rabies virus-ba

239 rrespondence between early MEG responses and primary visual cortex (V1), and later MEG responses and

240 ses in the lateral geniculate nucleus (LGN), primary visual cortex (V1), and visual motion area (V5)

241 lls, two classes of principal neurons in the primary visual cortex (V1), are generally thought to be

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

243 In primary visual cortex (V1), connectivity between layer 2

244 model-based eye tracking, to recordings from primary visual cortex (V1), finding that standard approa

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

246 ount for several physiological properties of primary visual cortex (V1), including the shapes of simp

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

248 nce between excitation and inhibition in the primary visual cortex (V1), measured at rest, modulates

249 In primary visual cortex (V1), neuronal responses are sensi

250 In primary visual cortex (V1), neuronal responses to stimul

251 In the primary visual cortex (V1), orientation-selective neuron

252 In the primary visual cortex (V1), Simple and Complex receptive

253 In macaque primary visual cortex (V1), simple cell responses can be

254 out the anatomy and physiology of neurons in primary visual cortex (V1), the large numbers of inputs

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

256 In the primary visual cortex (V1), visual responses of pyramida

257 In mouse primary visual cortex (V1), we discovered that orientati

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

259 eas receive functionally specific input from primary visual cortex (V1), we used two-photon calcium i

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

261 visual and prosthetic activations of the rat primary visual cortex (V1).

262 ation of binocular correlation by neurons in primary visual cortex (V1).

263 influenced by its rich connectivity with the primary visual cortex (V1).

264 ificantly limits information encoding in the primary visual cortex (V1).

265 omputations such as binocular integration in primary visual cortex (V1).

266 der lateral prefrontal cortex (LPFC) and the primary visual cortex (V1).

267 and also strengthens intracortical inputs to primary visual cortex (V1).

268 ime of expected future reward emerges in the primary visual cortex (V1).

269 rastriate activity requires the integrity of primary visual cortex (V1).

270 igger antidromic spikes in a local region of primary visual cortex (V1).

271 lamocortical (TC) synapses in A1, but not in primary visual cortex (V1).

272 cs of hundreds of neurons in slices of mouse primary visual cortex (V1).

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

274 use visual system: visual thalamus (LGN) and primary visual cortex (V1).

275 g was identified in pyramidal neurons of the primary visual cortex (V1).

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

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

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

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

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

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

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

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

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

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

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

287 people who are blind due to damage to their primary visual cortex, V1, can discriminate stimuli pres

288 for black over white stimuli in the macaque primary visual cortex, V1.

289 we show that, in rat monocular and binocular primary visual cortex (V1m and V1b), postsynaptic streng

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

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

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

293 ference in the cholinergic effectors for the primary visual cortex, we have conducted a comparative s

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

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

296 tion in direction-selective cells in macaque primary visual cortex, where specific hypotheses have be

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

298 ntessential contextual influence, in macaque primary visual cortex with natural images.

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

300 s orientation is a key feature of neurons in primary visual cortex, yet the underlying mechanisms gen