ライフサイエンスコーパス: auditory cortex

1 maging (fMRI) response patterns in the human auditory cortex.

2 e coding in posteromedial and posterolateral auditory cortex.

3 peech, where coherence is strongest over the auditory cortex.

4 axons innervating different layers of mouse auditory cortex.

5 ponse to sound onset, which is found in left auditory cortex.

6 oor concordance in areas outside traditional auditory cortex.

7 in that transmits vocal motor signals to the auditory cortex.

8 auditory-object-based representations in the auditory cortex.

9 ing sound onsets and offsets in the marmoset auditory cortex.

10 l responses to speech outside of the primary auditory cortex.

11 ined to very specific but large areas of the auditory cortex.

12 influencing phonetic representations in the auditory cortex.

13 The opposite was observed in primary auditory cortex.

14 nt effects of binaural timing cues in either auditory cortex.

15 behavioral impact and ERP responses from the auditory cortex.

16 weighting of phonetic representations at the auditory cortex.

17 emporal areas, consistent with generation in auditory cortex.

18 ded by PNNs and area occupied by them in the auditory cortex.

19 ented in separate hierarchical stages of the auditory cortex.

20 ct phonemic maps of their native language in auditory cortex.

21 l-scale processing likely implemented in the auditory cortex.

22 le increasing activity in high-gamma in left auditory cortex.

23 activation of direct inputs from the primary auditory cortex.

24 -scale topographic organization across human auditory cortex.

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

26 d to the activity of the right supratemporal auditory cortex.

27 recordings obtained directly from the human auditory cortex.

28 s in memory is associated with activation in auditory cortex.

29 scriminant neurons are revealed in the avian auditory cortex.

30 rneurons and was stronger in lower layers of auditory cortex.

31 y cortex, and high-frequency rhythms in left auditory cortex.

32 notopic representations in core areas of the auditory cortex.

33 e frequency tuning of neurons in rat primary auditory cortex.

34 enabled long-term synaptic plasticity in the auditory cortex.

35 ation of phonological representations within auditory cortex.

36 g tracers into one or more regions of ferret auditory cortex.

37 n of the neural coding dichotomy observed in auditory cortex.

38 nger for left auditory cortex than for right auditory cortex.

39 ocessing dysfunction at the level of primary auditory cortex.

40 sensory encoding and top-down modulation of auditory cortex.

41 g of the two dimensions bilaterally in human auditory cortex.

42 majority of tonotopically mapped nonprimary auditory cortex.

43 ented in distinct hierarchical stages of the auditory cortex.

44 pairing reduced gamma band activity in left auditory cortex.

45 notopic signal across a number of regions in auditory cortex.

46 f modulated noise (envelope coding) in human auditory cortex.

47 eviously reported face-evoked FPs in macaque auditory cortex.

48 of speech from modulated background noise in auditory cortex.

49 to the Field L2 in the forebrain, the avian auditory cortex.

50 otemporal cortex and volume-conducted to the auditory cortex.

51 ting that their generators are located below auditory cortex.

52 ting normal fMRI responses to pitch in their auditory cortex: (1) individual neurons within the pitch

53 and Arc/Arg3.1 immunoreactive neurons in the auditory cortex 15 days after permanent auditory depriva

54 In the auditory cortex, a combination of large-scale electrophy

55 inciple projections arising from the primary auditory cortex (A1) and the ventral division of the med

56 me or separate neural populations in primary auditory cortex (A1) are perceived as one or two streams

57 Feedback signals from the primary auditory cortex (A1) can shape the receptive field prope

58 ed firing in previous studies of the primary auditory cortex (A1) in anesthetized animals.

59 Primary auditory cortex (A1) responses were acquired from 11 rat

60 pared directly neuronal responses in primary auditory cortex (A1) to time-varying acoustic and CI sig

61 netic activation of projections from primary auditory cortex (A1) to V1.

62 quency-tuned neuronal populations in primary auditory cortex (A1), respectively.

63 ith unusually specific plasticity in primary auditory cortex (A1).

64 We recorded neural activity in auditory cortex (AC) and hippocampus of rats as they lea

65 Recording neural activity from the auditory cortex (AC) and medial geniculate body (MGB) si

66 ive effects remain unknown, it is known that auditory cortex (AC) corticocollicular neurons projectin

67 Auditory cortex (AC) layer 5B (L5B) contains both cortic

68 he resulting sensory deprivation jeopardizes auditory cortex (AC) maturation.

69 ive effects remain unknown, it is known that auditory cortex (AC) neurons projecting from layer 5B (L

70 along a central ascending pathway leading to auditory cortex (AC).

71 al responses: in the normally sighted group, auditory cortex activation increased with increasing noi

72 ed by increased postsynaptic gain in primary auditory cortex activity as well as modulation of feedfo

73 Auditory cortex activity showed characteristic P1-N1-P2

74 und tokens relative to the phase of rhythmic auditory cortex activity.

75 athway from the lateral amygdala (LA) to the auditory cortex (ACx) and found that selective silencing

76 The emergent properties of the Auditory Cortex (ACx) have been difficult to unravel par

77 itory temporal resolution that relies on the auditory cortex (ACx), and early auditory deprivation al

78 ible that impairments in pitch coding within auditory cortex also contribute to the disorder, in part

79 ntext primes phonetic representations at the auditory cortex, altering the auditory percept, evidence

80 l generator contribution to the visual FP in auditory cortex, although we did note an increase in the

81 ntial recorded simultaneously in the primary auditory cortex and a higher-order area, the posterior a

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

83 also reduced the phase coherence between the auditory cortex and areas associated with tinnitus distr

84 during maintenance was demonstrated between auditory cortex and both the hippocampus and inferior fr

85 However, projections from the auditory cortex and central nucleus of the inferior coll

86 unction of different cortical neurons in the auditory cortex and discuss a computational framework fo

87 To test this, we inactivate auditory cortex and find acceleration of adaptation with

88 tial (LFP) responses to faces in the macaque auditory cortex and have suggested that such face-LFPs m

89 potentials (AEPs) were recorded from primary auditory cortex and hippocampus in freely moving rats.

90 n the thalamus rejuvenates plasticity in the auditory cortex and improves auditory perception.

91 he spiking activity of individual neurons in auditory cortex and in the activity of neuronal populati

92 tion technique, we show that activity in the auditory cortex and inferior frontal gyrus is specific t

93 analysis showed that patterns of activity in auditory cortex and left inferior frontal gyrus distingu

94 GABAergic interneurons in layer 2/3 of mouse auditory cortex and measured tone-evoked membrane potent

95 r sensory stimuli and behavioural choices in auditory cortex and posterior parietal cortex as mice pe

96 Although auditory cortex and posterior parietal cortex coded info

97 unique neural network that originates in the auditory cortex and projects to the cochlear receptor th

98 m is a neural network that originates in the auditory cortex and projects to the cochlear receptor th

99 related functional connectivity to secondary auditory cortex and regions of the frontoparietal attent

100 rplay between higher-order components of the auditory cortex and the amygdala via synchrony in the th

101 rease in functional connectivity between the auditory cortex and the dorsal visual cortex, no such ef

102 ect influence of compromised audition on the auditory cortex and the potential impact of long duratio

103 ith a reduction in the interplay between the auditory cortex and the subcortical reward network, indi

104 ctral components of speech-brain coupling in auditory cortex and use causal connectivity analysis (tr

105 ed functional connectivity between the right auditory cortex and ventral striatum (including the NAcc

106 ors, including the piriform cortex, the left auditory cortex, and CA2 of the hippocampus.

107 : low-frequency rhythms predominate in right auditory cortex, and high-frequency rhythms in left audi

108 r temporal sulcus (STS) that lies within the auditory cortex, and is activated by auditory feedback d

109 human superior temporal gyrus, a high-order auditory cortex, and studied the changes in the cortical

110 band noise enhances signal representation in auditory cortex, and that prolonged exposure to noise is

111 Neural responses in the auditory cortex are dynamic, nonlinear, and hard to pred

112 Circuits in the auditory cortex are highly susceptible to acoustic influ

113 esponse patterns in separate portions of the auditory cortex are informative of distinctive sets of s

114 ts indicate that face-evoked FP responses in auditory cortex are not generated locally but are volume

115 ggested that neocortical regions adjacent to auditory cortex are primarily responsible for word compr

116 he acute regulation of sensory coding by the auditory cortex as demonstrated by electrophysiological

117 sociated with speech processing in the human auditory cortex-as an evolutionarily conserved biologica

118 so a right-lateralized contribution from the auditory cortex at the fundamental frequency.

119 We found enhanced neural response in the auditory cortex at the pulse frequency.

120 In auditory cortex, auditory field maps (AFMs) are defined

121 Cells in auditory cortex believed to be integral to ILD processin

122 es have examined the projections from MGN to auditory cortex, but most have focused on the caudal cor

123 segregation (SSS) has been described in the auditory cortex, but the mechanisms leading to those cor

124 e revealed tonotopic organization in primary auditory cortex, but the use of pure tones or noise band

125 uld be decoded in primary visual and primary auditory cortex, but these regions did not sustain gener

126 l representation of frequency in rat primary auditory cortex by constructing tonal frequency response

127 tenance of sound-specific representations in auditory cortex by projections from higher-order areas,

128 y task enhances population coding in primary auditory cortex by selectively reducing deleterious r(no

129 Furthermore, activation of auditory cortex by visual and auditory speech developed

130 In short, our data expose early auditory cortex chiefly as a frequency analyzer, and spe

131 In auditory cortex, cholinergic systems have been shown to

132 , we show that the primary-like areas in the auditory cortex contain dominantly spectrotemporal-based

133 n we investigated whether L2/3 of male mouse auditory cortex contains discrete subpopulations of cell

134 ed that semantic representations outside the auditory cortex contribute to diagnostic accuracy in car

135 tend the prediction from MEG data of a right auditory cortex contribution to the FFR.

136 contrast, delayed eyelid opening extends the auditory cortex CPs by several additional days.

137 Early eyelid opening closes the auditory cortex CPs precociously and dark rearing preven

138 ect of manipulating visual experience during auditory cortex critical periods (CPs) by assessing the

139 METHOD: Primary auditory cortex deep layer 3 spine density and volume wa

140 They observed gains in firing rate in auditory cortex despite nearly absent auditory nerve and

141 ull FIR filter in both primary and secondary auditory cortex, despite requiring fewer than 30 paramet

142 arge-scale topographical organization of the auditory cortex develop in people deaf from birth?

143 plus corpus striatum as well into the IC and auditory cortex did not reveal any double labeling.

144 -band event-related desynchronization in the auditory cortex differentiates between beat positions, s

145 linergic and motor cortical afferents to the auditory cortex display distinct activity patterns and p

146 h magnified envelope coding in posteromedial auditory cortex disrupts the segregation of speech from

147 ogenetic perturbation to selectively silence auditory cortex during early noise processing, we show t

148 rtex as the source of signal modification in auditory cortex during perception of self-generated soun

149 Transient opsin-mediated silencing of auditory cortex during the priming period almost complet

150 cending auditory pathway from the cochlea to auditory cortex; efferent connections provide descending

151 speech, electrophysiological oscillations in auditory cortex entrain to slow ([Formula: see text]8 Hz

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

153 that the two types of rate-coding neurons in auditory cortex exhibited distinct subthreshold response

154 l frequency response areas (FRAs) in primary auditory cortex for different SNRs, tone levels, and noi

155 deafness leads to functional deficits in the auditory cortex for which early cochlear implantation ca

156 and auditory-responsive neurons in the deaf auditory cortex formed two distinct populations that did

157 RTp distinguished this rostral extension of auditory cortex from the adjacent auditory-related corte

158 Cholinergic inputs to the auditory cortex from the basal forebrain (BF) are import

159 In contrast, auditory cortex had a code with rapid fluctuations in st

160 ss-modal plasticity in the deaf higher-order auditory cortex had limited effects on auditory inputs.

161 sound in working memory based on activity in auditory cortex, hippocampus, and frontal cortex, and fu

162 demonstrates an interaction between primary auditory cortex, hippocampus, and inferior frontal gyrus

163 The GM volume decreases in the primary auditory cortex (i.e., superior temporal gyrus and Hesch

164 ound features in the inferior colliculus and auditory cortex in adult mice with a near-complete loss

165 ses indicated dominant activity in the right auditory cortex in both groups but limited ITD processin

166 recorded neural responses directly from the auditory cortex in both species in response to novel leg

167 that the visual task robustly activated the auditory cortex in deaf subjects, peaking in the posteri

168 Here we show a direct role for mouse auditory cortex in detection and segregation of acoustic

169 ines are lost in deep layer 3 of the primary auditory cortex in subjects with schizophrenia, while la

170 aries in the mouse, by the border of primary auditory cortex in the rat and by layers IIIa/b and Cyto

171 ity with linear array multielectrodes across auditory cortex in three macaques (one female), and appl

172 at the acoustic-phonetic level in bilateral auditory cortex, in real-time.

173 We found that the posterior auditory cortex, including A1 and the surrounding caudal

174 tion-induced activation in most parts of the auditory cortex, including A1, but not in circumscribed

175 ture in the congenitally deaf throughout the auditory cortex, including in the language areas.

176 on of either the most anterior region of the auditory cortex, including the primary (Te1) cortex, or

177 The BOLD responses from auditory cortex increased with increasing sequence varia

178 In the auditory cortex, increased spontaneous cross-unit synchr

179 In the primate auditory cortex, information flows serially in the medio

180 nd presynaptic partners, indicating that the auditory cortex integrates bottom-up cholinergic signals

181 ) response peak with reduced activity in the auditory cortex ipsilateral to the leading ITD.

182 remains controversial, however, whether the auditory cortex is also required for fearful memories re

183 studies observed that gamma activity in the auditory cortex is correlated with tinnitus loudness, we

184 sults suggest that the organization of human auditory cortex is driven primarily by its response to s

185 circuits.SIGNIFICANCE STATEMENT Layer 2/3 of auditory cortex is functionally diverse.

186 eural activity at the pulse frequency in the auditory cortex is internally generated rather than stim

187 While the encoding of speech in the auditory cortex is modulated by selective attention, it

188 Although auditory cortex is necessary for sound localization, our

189 neurons throughout the auditory system, and auditory cortex is necessary for sound localization.

190 Together, these data show that the auditory cortex is necessary for the consolidation of au

191 mical studies have clearly demonstrated that auditory cortex is populated by multiple subfields.

192 imaging, we show that activity in the right auditory cortex is related to individual differences in

193 thalamus and that feedback from the primary auditory cortex is required for the normal ability of fe

194 ighting which phonetic representation in the auditory cortex is strengthened or weakened.

195 ic regulation of PNN expression in the adult auditory cortex is vital for fear learning and consolida

196 Sensory cortex, such as the auditory cortex, is involved in the formation of fearful

197 t has also been shown to modify responses in auditory cortex, it is not even clear whether the source

198 ctivity (FC) structure in humans in the core auditory cortex, its extending tonotopic gradients in th

199 tudies on deafness have involved the primary auditory cortex; knowledge of higher-order areas is limi

200 n to one person in a "cocktail party," their auditory cortex mainly follows the attended speech strea

201 uggest that the harmonic template neurons in auditory cortex may play an important role in processing

202 ed, endogenous delta (14 Hz) oscillations in auditory cortex may shift their timing so that higher-ex

203 ecordings within a given brain region (e.g., auditory cortex) may be "contaminated" by activity gener

204 as rapidly reshaped interactions in primary auditory cortex, measured in three different ways: as ch

205 Furthermore, a decision-augmented auditory cortex model accounted for performance and reac

206 In auditory cortex, neuronal responses are less selective i

207 In primary auditory cortex neurons can be characterized by their sp

208 arollia perspicillata, the spike activity of auditory cortex neurons does not track the temporal info

209 al recordings in young ferrets, we show that auditory cortex neurons respond to sound at very young a

210 over long time lags, whereas coupling among auditory cortex neurons was weak and short-lived.

211 e of dendritic spines in deep layer 3 of the auditory cortex of 20 schizophrenia and 20 matched compa

212 monic template neurons in the core region of auditory cortex of a highly vocal New World primate, the

213 ity from large populations of neurons in the auditory cortex of anesthetized rats across different br

214 uestion by analyzing neural responses in the auditory cortex of anesthetized rats using stimulus-resp

215 cortical maps and individual neurons in the auditory cortex of awake adult mice and is associated wi

216 responses to acoustic and CI stimulation in auditory cortex of awake marmoset monkeys, we discovered

217 Here, using single-unit recordings in auditory cortex of awake mice, we show that this may not

218 underlying auditory motion processing in the auditory cortex of awake monkeys using functional magnet

219 dally amplitude modulated (SAM) tones in the auditory cortex of awake squirrel monkeys, we show that

220 In a common view, the "unused" auditory cortex of deaf individuals is reorganized to a

221 l predictions to recordings from the primary auditory cortex of ferrets and found that: (1) the decod

222 we recorded spatial receptive fields in the auditory cortex of freely moving ferrets.

223 We recorded telemetrically from the core auditory cortex of gerbils, both while they engaged in a

224 , we recorded the activity of neurons in the auditory cortex of mice in response to sounds generated

225 le dynamics of this mechanism in the primary auditory cortex of nonhuman primates, and hypothesized t

226 Here we record from single units in auditory cortex of rats performing a self-initiated go/n

227 e roles that neural oscillations play in the auditory cortex of the human brain are becoming clearer.

228 Redox states in the auditory cortex of young and aged animals were similar,

229 the first time, that single neurons, in the auditory cortex of zebra finches, are capable of discrim

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

231 ation of core and noncore areas within human auditory cortex on Heschl's gyrus that process natural h

232 But how is auditory cortex organization affected by congenital, pre

233 ividual principal neurons in the adult mouse auditory cortex over a 50-day period surrounding either

234 ansmission time, whereas grey matter (GM) in auditory cortex partially mediates auditory delay, sugge

235 ly ineffective at activating many neurons in auditory cortex, particularly in the hemisphere ipsilate

236 he cortex, and that different regions of the auditory cortex play complementary but different roles i

237 cortical regions to encompass almost all of auditory cortex, plus large parts of temporal, parietal,

238 Finally, the removal of auditory cortex PNNs resulted in a deficit in fear learn

239 rtical envelope coding in left posteromedial auditory cortex predict speech identification in modulat

240 tion in all of the respective systems (right auditory cortex, prefrontal cortex, and the salience net

241 We found that the integration in auditory cortex preserves the independence of the differ

242 Our findings suggest that early auditory cortex primarily represents sound source locati

243 ated to simple auditory stimuli requires the auditory cortex, provided that the inactivation encompas

244 tamatergic signaling is believed to underlie auditory cortex pyramidal neuron dendritic spine loss an

245 organized along acoustic features similar to auditory cortex, rather than along articulatory features

246 cascade of corticocortical connections, the auditory cortex receives parallel thalamocortical projec

247 Here we show that auditory cortex receptive field models benefit from a no

248 In auditory cortex, regular sequences with smaller alphabet

249 Auditory cortex-related potentials showed no response to

250 Certain neurons in the auditory cortex release zinc to influence how the brain

251 -modally (visually) reorganized higher-order auditory cortex remained auditory in congenital deafness

252 and the area-specific characteristics in the auditory cortex remained unchanged in animals with conge

253 s to affect cortical plasticity: the primary auditory cortex reorganized in a manner that was unusual

254 How the auditory cortex represents temporally modulated CI stimu

255 Instead, auditory cortex responded as though it were processing a

256 ty of speech sound discrimination tasks, and auditory cortex responses were acquired following traini

257 The auditory cortex selectively expands neural representatio

258 ual speech modifies phonetic encoding at the auditory cortex.SIGNIFICANCE STATEMENT The current study

259 scene up through the hierarchy of the human auditory cortex.SIGNIFICANCE STATEMENT Using magnetoence

260 ency preferences across tonotopically mapped auditory cortex spatially correlate with R1-estimated my

261 We show that auditory cortex stores information by persistent changes

262 genital deafness causes large changes in the auditory cortex structure and function, such that withou

263 tential recordings from the human nonprimary auditory cortex (superior temporal gyrus) while subjects

264 diction error responses in bilateral primary auditory cortex, superior temporal gyrus, and lateral pr

265 conclude that in deaf humans the high-level auditory cortex switches its input modality from sound t

266 examined neural activity in the higher-order auditory cortex Te2 and basolateral amygdala (BLA) and t

267 signals are significantly stronger for left auditory cortex than for right auditory cortex.

268 uditory stimulus information was stronger in auditory cortex than in posterior parietal cortex, and b

269 epresentation of auditory space in the human auditory cortex that at least partly integrates the spec

270 e a functional projection from the visual to auditory cortex that could mediate these effects.

271 Neurons in the midbrain and auditory cortex that exhibit stimulus-specific adaptatio

272 transient epoch of inhibitory plasticity in auditory cortex that is dysregulated in Mecp2(het).

273 ve response in the right and an area in left auditory cortex that is sensitive to individual differen

274 dual face coding in a specific region of the auditory cortex that is typically specialized for voice

275 Here we show in the murine auditory cortex that juvenile plasticity can be reestabl

276 scovered, using direct recordings from human auditory cortex, that surprise due to prediction violati

277 nt a model of neural responses in the ferret auditory cortex (the IC Adaptation model), which takes i

278 ith short integration windows, such as early auditory cortex, the differences in neural responses bet

279 ion is transmitted from the brainstem to the auditory cortex, through several stages of processing, w

280 or tonotopy, extend along two axes in human auditory cortex, thus reconciling historical accounts of

281 at neural mechanisms are used by the primate auditory cortex to extract these biologically important

282 Third, we show long-range connectivity of auditory cortex to hippocampus and frontal cortex, which

283 hension partly depends on the ability of the auditory cortex to track syllable boundaries with theta-

284 ) and anterolateral (AL) belt regions of the auditory cortex, to auditory decisions have not been ful

285 background, whereas the right supratemporal auditory cortex tracked 4-8 Hz modulations during both n

286 We show that the primary-like areas in the auditory cortex use a dominantly spectrotemporal-based r

287 nhibition shapes frequency tuning in primary auditory cortex via an unconventional mechanism: non-pre

288 nces in slice health, the redox state in the auditory cortex was assessed by measuring the FAD+/NADH

289 Downstream of the auditory cortex, we found that responses of hippocampal

290 esponses are indeed generated within macaque auditory cortex, we recorded FPs and concomitant multiun

291 aging showed that many excitatory neurons in auditory cortex were suppressed during behavior, while s

292 nificantly greater activation across most of auditory cortex when best frequency is attended, versus

293 mplitude of envelope coding in posteromedial auditory cortex, whereas it enhances the fidelity of env

294 e," we observed a lack of the suppression of auditory cortex, which is commonly seen as a neural corr

295 ) within small neural populations in primary auditory cortex while rhesus macaques performed a novel

296 nguishable from that described previously in auditory cortex, while global suppression was unique to

297 garding the functional organization of early auditory cortex will inform our growing understanding of

298 nature of topographic organization in human auditory cortex with fMRI.

299 nous stream-brain phase entrainment in human auditory cortex with non-invasive transcranial alternati

300 1 AFMs across core and belt regions of human auditory cortex, with likely homology to those of macaqu