ライフサイエンスコーパス: primary auditory cortex

1 tion (right superior temporal gyrus to right primary auditory cortex).

2 lus-dependent transformation patterns in the primary auditory cortex.

3 ory neurons in layer 2/3 (L2/3) of the mouse primary auditory cortex.

4 eld estimates in the inferior colliculus and primary auditory cortex.

5 ted from neural responses typically found in primary auditory cortex.

6 o an enlarged representation of that tone in primary auditory cortex.

7 gle-unit neural responses recorded in ferret primary auditory cortex.

8 e exposure during the critical period in the primary auditory cortex.

9 ) to enable reliable pitch extraction in non-primary auditory cortex.

10 vision and somatosensation are processed in primary auditory cortex.

11 hibitory and excitatory synapse pathology in primary auditory cortex.

12 contribute to loss of gray matter volume in primary auditory cortex.

13 en hearing ability and gray matter volume in primary auditory cortex.

14 ot observe any significant activation in the primary auditory cortex.

15 , and increases signal-to-noise ratio in the primary auditory cortex.

16 s that visual stimuli influence cells in the primary auditory cortex.

17 als (LFPs)] and spiking responses in macaque primary auditory cortex.

18 ate impairments of sensory processing within primary auditory cortex.

19 effects increased coupling within the right primary auditory cortex.

20 demonstrating sound location sensitivity in primary auditory cortex.

21 and functional disturbances at the level of primary auditory cortex.

22 c mechanisms that underlie processing in the primary auditory cortex.

23 ateral superior temporal region, anterior to primary auditory cortex.

24 tral and temporal response properties in the primary auditory cortex.

25 lus time histogram responses recorded in the primary auditory cortex.

26 resent throughout cortical depths in the non-primary auditory cortex.

27 ation processing dysfunction at the level of primary auditory cortex.

28 el neural responses to speech outside of the primary auditory cortex.

29 The opposite was observed in primary auditory cortex.

30 e secondary auditory cortex, followed by the primary auditory cortex.

31 tex via activation of direct inputs from the primary auditory cortex.

32 the same sound stimuli in layer 4 of the rat primary auditory cortex.

33 el on the frequency tuning of neurons in rat primary auditory cortex.

34 eference is stable through cortical depth in primary auditory cortex.

35 nal subpopulations upon functional images of primary auditory cortex, a model array representing cort

36 found over the left hemisphere, anterior to primary auditory cortex, a network whose instantaneous f

37 nges, and more localized, frequency-specific primary auditory cortex (A1) activation than CI stimulat

38 ies of core auditory fields on contralateral primary auditory cortex (A1) activity.

39 onstrated the high selectivity of neurons in primary auditory cortex (A1) and a highly sparse represe

40 ncy-matched locations in the core areas, the primary auditory cortex (A1) and anterior auditory field

41 models, we studied the interactions between primary auditory cortex (A1) and association cortex (Par

42 hanisms, we recorded single-unit activity in primary auditory cortex (A1) and medial prefrontal corte

43 ecordings of responses to click pairs in rat primary auditory cortex (A1) and offer new insights into

44 ve listening, we recorded neural activity in primary auditory cortex (A1) and secondary auditory cort

45 rest known to be involved with language: the primary auditory cortex (A1) and the superior temporal g

46 h the principle projections arising from the primary auditory cortex (A1) and the ventral division of

47 e the same or separate neural populations in primary auditory cortex (A1) are perceived as one or two

48 Feedback signals from the primary auditory cortex (A1) can shape the receptive fie

49 Neurons in the primary auditory cortex (A1) can show rapid changes in r

50 xperimentally determined milestones in mouse primary auditory cortex (A1) development and characteriz

51 ed response strength and topography in mouse primary auditory cortex (A1) during a brief, 3-d window,

52 mpared activity in ferret frontal cortex and primary auditory cortex (A1) during auditory and visual

53 -temporal receptive fields (STRFs) in ferret primary auditory cortex (A1) during tone detection.

54 fects, we studied sensory representations in primary auditory cortex (A1) during two instrumental tas

55 Although single units in primary auditory cortex (A1) exhibit accurate timing in

56 Recent evidence is reshaping the view of primary auditory cortex (A1) from a unisensory area to o

57 When raised in a quiet environment, the rat primary auditory cortex (A1) has a well-defined 'critica

58 Corticofugal projections from the primary auditory cortex (A1) have been shown to play a r

59 sustained firing in previous studies of the primary auditory cortex (A1) in anesthetized animals.

60 y modulations of LP or its projection to the primary auditory cortex (A1) in awake mice reveal that L

61 s obtained over time scales of 30-120 min in primary auditory cortex (A1) in the quiescent, awake fer

62 ntensive selectivity of neurons in the adult primary auditory cortex (A1) is easily degraded in early

63 Activity in the primary auditory cortex (A1) is essential for normal sou

64 The primary auditory cortex (A1) is involved in sound locali

65 c spine density (DSD) in deep layer 3 of the primary auditory cortex (A1) is lower, due to having few

66 biosonar target shape representation in the primary auditory cortex (A1) is more reliably encoded by

67 The primary auditory cortex (A1) is organized tonotopically,

68 rrets, we show that within-trial activity in primary auditory cortex (A1) is required for training-de

69 In this study, we tested the hypothesis that primary auditory cortex (A1) neurons use temporal precis

70 in excitatory and inhibitory circuits in the primary auditory cortex (A1) of adult mice to promote fe

71 , however, that many of these neurons in the primary auditory cortex (A1) of awake marmoset monkeys w

72 opes in quiet and in background noise in the primary auditory cortex (A1) of awake marmoset monkeys.

73 sed on single-unit responses recorded in the primary auditory cortex (A1) of awake rhesus monkeys lis

74 We recorded multiunit activity from primary auditory cortex (A1) of behaving monkeys elicite

75 population coding of tones and speech in the primary auditory cortex (A1) of gerbils, and found that

76 of ITDs in the inferior colliculus (IC) and primary auditory cortex (A1) of gerbils.

77 The primary auditory cortex (A1) of mice exhibits a critical

78 SSA is strong and widespread in primary auditory cortex (A1) of rats, but is weak or abs

79 In the primary auditory cortex (A1) of rats, refinement of exci

80 niculate body (MGB) of the thalamus, and the primary auditory cortex (A1) of the cat in response to n

81 The responses of neurons within the primary auditory cortex (A1) of the ferret elicited by b

82 ous studies have convincingly shown that the primary auditory cortex (A1) of the rat possesses a post

83 le, selective changes that radically altered primary auditory cortex (A1) organization.

84 The extent to which the primary auditory cortex (A1) participates in instructing

85 The primary auditory cortex (A1) plays a key role for sound

86 adjustments of functional properties in the primary auditory cortex (A1) remain unknown.

87 Primary auditory cortex (A1) responses were acquired fro

88 r training in the sound maze, neurons in the primary auditory cortex (A1) showed greater responses to

89 Here we show in mouse primary auditory cortex (A1) that daily passive sound ex

90 ation of sounds by populations of neurons in primary auditory cortex (A1) that may provide a neural b

91 n cortical layers L4 and L2/3 of awake mouse primary auditory cortex (A1) to characterize the populat

92 to the recipient layer 4 neurons in the rat primary auditory cortex (A1) to determine the developmen

93 mporal information available at the level of primary auditory cortex (A1) to enable reliable pitch ex

94 more accurately for responses of neurons in primary auditory cortex (A1) to natural sounds.

95 we predicted responses of neurons in ferret primary auditory cortex (A1) to stimuli with natural tem

96 The shift in spectral tuning in primary auditory cortex (A1) to the frequency of a tone

97 , we compared directly neuronal responses in primary auditory cortex (A1) to time-varying acoustic an

98 Here, we examined neural responses in monkey primary auditory cortex (A1) to two concurrent HCTs that

99 r optogenetic activation of projections from primary auditory cortex (A1) to V1.

100 We recorded from pairs of neurons in primary auditory cortex (A1) under two conditions: while

101 gate possible homologs of the MMN in macaque primary auditory cortex (A1) using a frequency oddball p

102 d the spatial receptive fields of neurons in primary auditory cortex (A1) while ferrets performed a r

103 n imaging of Ntsr1-Cre+ L6 CT neurons in the primary auditory cortex (A1) while mice were engaged in

104 In primary auditory cortex (A1), a similar auditory-somatos

105 When injecting CTB into the primary auditory cortex (A1), a small number of CTB-posi

106 cell recordings from rat locus coeruleus and primary auditory cortex (A1), pairing sounds with locus

107 inct frequency-tuned neuronal populations in primary auditory cortex (A1), respectively.

108 In primary auditory cortex (A1), so-called "sideband" inhib

109 ly dominant cortical source of inputs is the primary auditory cortex (A1), suggesting strong A1-to-Te

110 In the rat primary auditory cortex (A1), the experience-dependent p

111 neuronal responses at or before the level of primary auditory cortex (A1), the underlying physiologic

112 ), the medial geniculate body (MGB), and the primary auditory cortex (A1).

113 percept competition thought to occur beyond primary auditory cortex (A1).

114 privation leads to functional enhancement in primary auditory cortex (A1).

115 on-related effects have been demonstrated in primary auditory cortex (A1).

116 cal stage of auditory stimulus processing in primary auditory cortex (A1).

117 single neurons and neuronal ensembles in the primary auditory cortex (A1).

118 is known about the intrinsic connectivity of primary auditory cortex (A1).

119 resulted in the abnormal development of the primary auditory cortex (A1).

120 onto presynaptic and postsynaptic nAChRs in primary auditory cortex (A1).

121 neuron responses from awake macaque monkeys' primary auditory cortex (A1).

122 ant role in the encoding of vocalizations in primary auditory cortex (A1).

123 nsory features, including sound frequency in primary auditory cortex (A1).

124 ased release of ACh onto auditory neurons in primary auditory cortex (A1).

125 curred with unusually specific plasticity in primary auditory cortex (A1).

126 ains regarding the neuroplastic potential of primary auditory cortex (A1).

127 rded the spatial tuning of single neurons in primary (auditory cortex, A1) and secondary (caudolatera

128 model that incorporates spiking activity in primary auditory cortex, A1, as input and resolves perce

129 While neurons in the primary auditory cortex (AC) respond differentially to t

130 radigm for monkeys, and recorded activity in primary auditory cortex (AC), dorsolateral prefrontal co

131 explained by increased postsynaptic gain in primary auditory cortex activity as well as modulation o

132 Primary auditory cortex activity, as measured by the aud

133 In the posterior primary auditory cortex, activity of neural ensembles me

134 m either the medial geniculate body (MGB) or primary auditory cortex (ACx) to auditory striatum in mi

135 vestigated sound intensity coding in the rat primary auditory cortex (AI) and describe its plasticity

136 corded simultaneously from all layers in cat primary auditory cortex (AI) and estimated spectrotempor

137 e [central narrow band (cNB)] of cat central primary auditory cortex (AI) and the nontonotopic, broad

138 ntensity receptive fields (RF) of neurons in primary auditory cortex (AI) are heterogeneous.

139 ng-induced representational expansion in the primary auditory cortex (AI) directly encodes the degree

140 Dopaminergic neurotransmission in primary auditory cortex (AI) has been shown to be involv

141 The evolution of left primary auditory cortex (AI) interaural frequency map ch

142 Hemispheric fine-grain maps of primary auditory cortex (AI) were derived from microelec

143 tory thalamic neurons projecting to the IAF, primary auditory cortex (AI), and anterior auditory fiel

144 In primary auditory cortex (AI), broadly correlated firing

145 highly specific frequency information to the primary auditory cortex (AI), whereas nonlemniscal neuro

146 mary visual cortex or fine-scale tonotopy in primary auditory cortex (AI).

147 y experience on sound representations in the primary auditory cortex (AI).

148 e specifically represented by neurons in the primary auditory cortex (AI).

149 erior colliculus (IC) and compared them with primary auditory cortex (AI).

150 lus-synchronized neuronal firing patterns in primary auditory cortex (AI).

151 atures of neuroinflammatory responses-in the primary auditory cortex (AI).

152 ptic receptive field plasticity in the adult primary auditory cortex (also known as AI) using in vivo

153 Such nonlinearities were most prevalent in primary auditory cortex, although they tended to be smal

154 the primary forebrain auditory area field L (primary auditory cortex analog) of zebra finches, previo

155 ective connectivity was observed between the primary auditory cortex and (1) the lateral planum polar

156 eld potential recorded simultaneously in the primary auditory cortex and a higher-order area, the pos

157 ther topographic map plasticity in the adult primary auditory cortex and a secondary auditory area, t

158 Here, we considered interactions between primary auditory cortex and adjacent association cortex.

159 Both responses occur in primary auditory cortex and adjacent nonprimary areas.

160 nses simultaneously across cortical depth in primary auditory cortex and anterior auditory field of C

161 imilar inverse correlation was found between primary auditory cortex and anterior prefrontal cortex,

162 at 800 ms in TVAs, but also at 700 ms in the primary auditory cortex and at 300 ms in the ventral occ

163 for control subjects versus aphasics in left primary auditory cortex and bilateral superior temporal

164 have delineated multiple areas in and around primary auditory cortex and demonstrated connectivity am

165 corticopontine projections originating from primary auditory cortex and detail several potential ext

166 This effect was absent in primary auditory cortex and did not occur for quilts mad

167 st (ritanserin) of 5-HT(2A) receptors to the primary auditory cortex and discovered the following dru

168 -evoked potentials (AEPs) were recorded from primary auditory cortex and hippocampus in freely moving

169 nds enhances the responses of neurons in the primary auditory cortex and improves the accuracy and sp

170 ngly, facial touch-induced inhibition in the primary auditory cortex and off-responses after terminat

171 of temporal selectivity is most prominent in primary auditory cortex and planum temporale, with no su

172 o support a hierarchical process, present in primary auditory cortex and refined in secondary auditor

173 aging to probe the organization of the mouse primary auditory cortex and show that the spatial organi

174 d nonspeech sounds occurs bilaterally within primary auditory cortex and surrounding regions of the s

175 eater damage to two unimodal auditory areas: primary auditory cortex and the planum temporale.

176 obtained, the effective connectivity between primary auditory cortex and the surrounding auditory reg

177 he auditory system (superior temporal versus primary auditory cortex) and in different hemispheres (l

178 region near the anterolateral border of the primary auditory cortex, and is consistent with the loca

179 enhanced representation of acoustic cues in primary auditory cortex, and modulation of inhibitory st

180 Here we show that primary and non-primary auditory cortex are differentiated by their inva

181 res, such as those observed in the mammalian primary auditory cortex, are critical to provide the ric

182 ex (area FI), primary motor cortex (area 4), primary auditory cortex (area 41/42), and the planum tem

183 rom over a thousand neurons in the mammalian primary auditory cortex as well as from simulated cortic

184 undles) were made in four regions of cortex (primary auditory cortex, auditory association cortex, or

185 nvelope of speech is robustly tracked in non-primary auditory cortex (belt areas in particular), and

186 eedback connections from planum temporale to primary auditory cortex bilaterally, while in severe pat

187 As expected, within primary auditory cortex, both moving and stationary stim

188 AP2-IR loss has not been investigated in the primary auditory cortex (Brodmann area 41), a site of co

189 ing the representation of the spatial cue in primary auditory cortex but nevertheless revealed some p

190 been characterized in the auditory nerve and primary auditory cortex, but little is known about inter

191 dies have revealed tonotopic organization in primary auditory cortex, but the use of pure tones or no

192 also could be decoded in primary visual and primary auditory cortex, but these regions did not susta

193 he neural representation of frequency in rat primary auditory cortex by constructing tonal frequency

194 ments to excitatory synaptic strength in rat primary auditory cortex by pairing acoustic stimuli with

195 auditory task enhances population coding in primary auditory cortex by selectively reducing deleteri

196 e whether neurons in field L, the homolog of primary auditory cortex, can match behavioral performanc

197 restingly, for the superficial layers of the primary auditory cortex, consistently linear and locally

198 The decrease in cerebral blood flow in the primary auditory cortex correlated with the decrease in

199 METHOD: Primary auditory cortex deep layer 3 spine density and v

200 Cochlear nucleus, inferior colliculus, and primary auditory cortex did not show significant differe

201 ting that potential crossmodal activation of primary auditory cortex differs depending on the age of

202 se influences temporal processing in the rat primary auditory cortex documented immediately after exp

203 spectrotemporal receptive fields (STRFs) in primary auditory cortex during detection of a target ton

204 sparse set (~5%) of layer 2/3 neurons in the primary auditory cortex, each of which reliably exhibits

205 Single neurons in primary auditory cortex either increased or decreased th

206 zebra finch field L (an analog of mammalian primary auditory cortex) encode source identity.

207 processing impairments that may result from primary auditory cortex excitatory and inhibitory circui

208 The majority of neurons in the primary auditory cortex exhibit SSA, yet little is known

209 ing tonal frequency response areas (FRAs) in primary auditory cortex for different SNRs, tone levels,

210 rrent source density (CSD) profiles in mouse primary auditory cortex from just after hearing onset un

211 rtex, we examined axonal terminations in the primary auditory cortex from nonprimary extrastriate vis

212 display significantly more neuropil, but the primary auditory cortex had a lower neuropil fraction th

213 chemically distinct neuronal subtypes in the primary auditory cortex have different contributions to

214 were observed in response to hearing tones (primary auditory cortex), hearing words (posterior tempo

215 analysis demonstrates an interaction between primary auditory cortex, hippocampus, and inferior front

216 on the responses of neurons in field L, the primary auditory cortex homolog in songbirds, which allo

217 The GM volume decreases in the primary auditory cortex (i.e., superior temporal gyrus a

218 by recording single-unit responses from the primary auditory cortex in awake ferrets exposed passive

219 shold membrane potential fluctuations in rat primary auditory cortex in both the anesthetized and awa

220 early onset of adult-like AChE expression in primary auditory cortex in O. garnetti, suggesting the a

221 midal neuron somal volume, in layer 3 of the primary auditory cortex in subjects with schizophrenia,

222 llest spines are lost in deep layer 3 of the primary auditory cortex in subjects with schizophrenia,

223 el boundaries in the mouse, by the border of primary auditory cortex in the rat and by layers IIIa/b

224 effect of intensive auditory training on the primary auditory cortex in these aged rats by using an o

225 regions of Heschl's gyrus, the site of human primary auditory cortex, in congenitally deaf humans by

226 In the rat primary auditory cortex, in vivo whole-cell recording fr

227 veral functional maps have been described in primary auditory cortex, including those related to freq

228 d from left primary auditory cortex to right primary auditory cortex (interhemispheric).

229 ex, extending from a low-frequency region of primary auditory cortex into a more anterior and less fr

230 Thus, like a radio, human primary auditory cortex is able to tune into attended fr

231 in Fmr1 KO mice, developmental plasticity in primary auditory cortex is grossly impaired.

232 y in the thalamus and that feedback from the primary auditory cortex is required for the normal abili

233 dence indicates that reorganization of adult primary auditory cortex is still possible after removal

234 evious studies on deafness have involved the primary auditory cortex; knowledge of higher-order areas

235 Neurons of primary auditory cortex, many of which are sharply tuned

236 , suggesting that neural networks within non-primary auditory cortex may be involved in early cortica

237 process as rapidly reshaped interactions in primary auditory cortex, measured in three different way

238 was to determine whether gamma activation in primary auditory cortex modulates both the associative m

239 In primary auditory cortex neurons can be characterized by

240 re these neuronal classes, we stimulated cat primary auditory cortex neurons with a dynamic moving ri

241 -related cortical processing deficits in the primary auditory cortex of aging versus young rats that

242 o extracellular recordings of neurons in the primary auditory cortex of anaesthetized ferrets.

243 tory system, we recorded from neurons in the primary auditory cortex of anesthetized and awake adult

244 ngle- and multiple-neuron responses from the primary auditory cortex of anesthetized cats while prese

245 Single-unit activity was recorded from primary auditory cortex of awake ferrets during presenta

246 the model predictions to recordings from the primary auditory cortex of ferrets and found that: (1) t

247 In contrast, responses from neurons in primary auditory cortex of ferrets show that both synchr

248 range 29-90 years) and were not found in the primary auditory cortex of Heschl's gyrus, indicating th

249 lective" neurons have been identified in non-primary auditory cortex of marmoset monkeys.

250 report that response profiles of neurons in primary auditory cortex of monkeys show a similar distin

251 Using extracellular neural recordings in the primary auditory cortex of naturally sleeping common mar

252 -timescale dynamics of this mechanism in the primary auditory cortex of nonhuman primates, and hypoth

253 acteristics similar to those measured in the primary auditory cortex of primates, contain sufficient

254 ere, we record local field potentials in the primary auditory cortex of rats engaged in auditory disc

255 d number were not altered in deep layer 3 of primary auditory cortex of subjects with schizophrenia.

256 hifted constant frequency (DSCF) area of the primary auditory cortex of the mustached bat is highly s

257 sponses to BMLD stimuli were measured in the primary auditory cortex of urethane-anesthetized guinea

258 reflecting increased limbic connectivity in primary auditory cortex of WS.

259 in the posterior auditory field (but not in primary auditory cortex) of deaf cats.

260 mma (70-150 Hz) range, in focal areas of non-primary auditory cortex on superior temporal gyrus (STG)

261 lood flow was significantly decreased in the primary auditory cortex (p </= .001), left Broca's area

262 tabolism of the inferior colliculus (IC) and primary auditory cortex (PAC) in patients with asymmetri

263 Neuronal spiking and LFP responses in primary auditory cortex (PAC) persisted after LOC, while

264 s on sound processing inside and outside the primary auditory cortex (PAC).

265 Primary auditory cortex plays a crucial role in spatiall

266 tical subregion just anterior and lateral to primary auditory cortex predicted accuracy of sound iden

267 The latter were associated with degraded primary auditory cortex receptive fields and a disrupted

268 e is a fundamental auditory feature coded in primary auditory cortex, relevant for perceiving auditor

269 6 appears to affect cortical plasticity: the primary auditory cortex reorganized in a manner that was

270 Neurons in the deep region of primary auditory cortex responded more to conspecific so

271 Here, cell-attached recordings in rat primary auditory cortex revealed that for the majority o

272 hole-cell recordings from neurons in the rat primary auditory cortex revealed that the frequency tuni

273 Single-neuron recordings in primary auditory cortex showed enhanced representation o

274 In primary auditory cortex, slowly repeated acoustic events

275 In the rat primary auditory cortex, such refinement in layer (L)4 i

276 fied prediction error responses in bilateral primary auditory cortex, superior temporal gyrus, and la

277 nded to decreased cerebral blood flow in the primary auditory cortex, supporting its crucial role in

278 bilateral superior temporal gyri (including primary auditory cortex), thalamus, and brainstem.

279 cal periods, were more strongly expressed in primary auditory cortex than inferior colliculus, and di

280 identify a specific population of neurons in primary auditory cortex that are sensitive to the spectr

281 In primary auditory cortex the bulk of MGV axon terminals a

282 atomical differences between primary and non-primary auditory cortex, the associated representational

283 study by Lakatos et al. reveals that, in the primary auditory cortex, the phase of neural oscillation

284 Beyond the primary auditory cortex, there are at least three distin

285 ometry performance was associated with lower primary auditory cortex thickness, but no evidence that

286 temporal gyrus (feed-forward) and from left primary auditory cortex to right primary auditory cortex

287 tronger modulation of connections from right primary auditory cortex to right superior temporal gyrus

288 e compared single-neuron responses in ferret primary auditory cortex to speech and vocalizations in f

289 (Taeniopygia guttata) field L (homologous to primary auditory cortex) to target birdsongs that were e

290 s gyrus (HG), the structure containing human primary auditory cortex, to how this region processes te

291 y in vivo whole-cell recordings in the mouse primary auditory cortex, using pure tones and broadband

292 ateral inhibition shapes frequency tuning in primary auditory cortex via an unconventional mechanism:

293 Primary auditory cortex volume was assessed using Cavali

294 it neural responses to natural sounds in the primary auditory cortex, we found that it is necessary t

295 m excitatory and inhibitory neurons of mouse primary auditory cortex, we report two temporally distin

296 nd number of GAD65-immunoreactive boutons in primary auditory cortex were measured using quantitative

297 along the superior temporal plane closer to primary auditory cortex were not selective for stimulus

298 s the dominant organizational feature in the primary auditory cortex, whereas other feature-based org

299 eled by changes in neuronal responses in the primary auditory cortex, which became relatively more se

300 (rnoise) within small neural populations in primary auditory cortex while rhesus macaques performed