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

3 vision and somatosensation are processed in primary auditory cortex.

4 hibitory and excitatory synapse pathology in primary auditory cortex.

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

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

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

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

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

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

11 The opposite was observed in primary auditory cortex.

12 ate impairments of sensory processing within primary auditory cortex.

13 effects increased coupling within the right primary auditory cortex.

14 demonstrating sound location sensitivity in primary auditory cortex.

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

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

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

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

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

20 ateralization may occur even at the level of primary auditory cortex.

21 nge is specifically represented posterior to primary auditory cortex.

22 t than right Heschl's gyrus, the location of primary auditory cortex.

23 formation of tonotopic and binaural maps in primary auditory cortex.

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

25 rior colliculus, medial geniculate body, and primary auditory cortex.

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

27 rs in the ventral medial geniculate body and primary auditory cortex.

28 e left superior temporal cortex posterior to primary auditory cortex.

29 patial tuning properties than neurons in the primary auditory cortex.

30 nalysis shape the functional organization of primary auditory cortex.

31 e is a distributed network distinct from the primary auditory cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 onotopic maps' of sound frequency in the rat primary auditory cortex (A1) arises from parallel develo

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

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

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

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

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

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

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

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

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

62 Neurons in the rat primary auditory cortex (A1) generally cannot respond to

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

64 Furthermore, primary auditory cortex (A1) has traditionally been desc

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

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

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

68 Behavioural deficits observed when primary auditory cortex (A1) is damaged have led to the

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

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

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

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

73 he refinement of response selectivity in the primary auditory cortex (A1) long beyond normal developm

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Primary auditory cortex (A1) responses were acquired fro

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

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

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

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

103 In primary auditory cortex (A1), although the most common e

104 direction-selective neurons are found in the primary auditory cortex (A1), but their topography and t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 es of Thorndike's law may be observed in the primary auditory cortex, A1.

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

125 cus fuscus, by electrical stimulation in the primary auditory cortex (AC).

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

127 Primary auditory cortex activity, as measured by the aud

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

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

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

131 of the cochleotopic (frequency) maps of the primary auditory cortex (AI) and the inferior colliculus

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

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

134 Many response properties in primary auditory cortex (AI) are segregated spatially an

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

136 In the primary auditory cortex (AI) dopamine release has been o

137 conditioning do, electric stimulation of the primary auditory cortex (AI) evokes reorganization of th

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

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

140 thalamus (cross-modal rewiring) results in a primary auditory cortex (AI) that resembles the primary

141 thalamus (cross-modal rewiring) results in a primary auditory cortex (AI) that resembles visual corte

142 cture of layer V neuronal populations in cat primary auditory cortex (AI) were analyzed in Golgi, Nis

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

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

145 ced spontaneous discharge correlation in the primary auditory cortex (AI), as examined under anesthes

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

147 In the primary auditory cortex (AI), the development of tone fr

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

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

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

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

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

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

154 d representations of the paired sound in the primary auditory cortex (AI).

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

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

157 tes depends on anterior projections from the primary auditory cortex, an auditory pathway analogous t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 the ventral division to some primary fields (primary auditory cortex and posterior auditory cortex) h

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

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

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

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

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

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

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

182 ay, visually responsive neurons in 'rewired' primary auditory cortex are also organized into orientat

183 ivision of the medial geniculate body to the primary auditory cortex are also patchy.

184 Neurons in primary auditory cortex are known to be sensitive to the

185 Neurons in the primary auditory cortex are tuned to the intensity and s

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

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

188 ngle- and multiunit activity was recorded in primary auditory cortex as the animals performed a nonsp

189 of activity moves anterolaterally away from primary auditory cortex as the processing of melodic sou

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

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

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

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

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

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

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

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

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

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

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

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

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

203 Consistent with previous studies, the primary auditory cortex contained a clear cochleotopic o

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

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

206 nn's areas 42 and 22, as well as in area 41 (primary auditory cortex), demonstrating that early deafn

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

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

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

210 neuronal processing/decoding circuits in the primary auditory cortex during a critical period.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

225 erentation does not lead to cell loss within primary auditory cortex in humans.

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

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

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

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

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

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

232 lane activates brain areas distinct from the primary auditory cortex, in parietal and frontal lobes a

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

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

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

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

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

238 This functional lateralization for primary auditory cortex is distinct from the contralater

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

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

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

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

243 reactivity are present in primary visual and primary auditory cortex long before thalamocortical syna

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

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

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

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

248 n the caudomedial field are also better than primary auditory cortex neurons at predicting the sound

249 In primary auditory cortex neurons can be characterized by

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

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

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

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

254 We recorded neuronal responses in the primary auditory cortex of behaving ferrets that were tr

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

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

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

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

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

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

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

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

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

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

265 risingly, neuronal responses recorded in the primary auditory cortex of trained monkeys were globally

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

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

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

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

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

271 Primary auditory cortex plays a crucial role in spatiall

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

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

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

275 6 appears to affect cortical plasticity: the primary auditory cortex reorganized in a manner that was

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

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

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

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

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

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

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

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

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

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

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

292 Primary auditory cortex volume was assessed using Cavali

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

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

295 However, TCA projections to (+/-) primary auditory cortex were not as clearly defined.

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

297 ange is specifically represented anterior to primary auditory cortex, whereas height change is specif

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