ライフサイエンスコーパス: association cortex

1 rus (area 21) (in the region of the auditory association cortex).

2 s role as a first-stage (or "belt") auditory association cortex.

3 creased AChE activity only in lateral visual association cortex.

4 y somatic sensory, primary visual and visual association cortex.

5 frontal cortex that is adjacent to olfactory association cortex.

6 he differences were greatest in higher-order association cortex.

7 r morphometric assessment of the heteromodal association cortex.

8 posterior parietal cortex (PPC), and visual association cortex.

9 with smaller volumes of the left heteromodal association cortex.

10 omponent that is generated within the visual association cortex.

11 evoked by electrical stimulation of sensory association cortex.

12 al cortical regions such as ventral temporal association cortex.

13 and neurofibrillary tangles in a high-order association cortex.

14 r cortex, but enhanced activation of frontal association cortex.

15 ense layers of prefrontal and inferotemporal association cortex.

16 complex (PM) has widespread connections with association cortex.

17 d network involving prefrontal and posterior association cortex.

18 be a critical period for the development of association cortex.

19 ortex, which are kept in check by systems in association cortex.

20 hrough average controllability is crucial in association cortex.

21 tral posterior midline, and lateral parietal association cortex.

22 ortex (Prh), ectorhinal cortex, and temporal association cortex.

23 osterior cingulate cortex, and somatosensory association cortex.

24 interactions with later-maturing aspects of association cortex.

25 face, extending from sensorimotor regions to association cortex.

26 e gradually within sensory-motor cortex than association cortex.

27 sual field maps in visual and frontoparietal association cortex.

28 uman medial temporal lobe (MTL) and temporal association cortex.

29 of widely distributed regions populate human association cortex.

30 ditory system and do not necessarily rely on association cortex.

31 able areas seen in primary visual and visual association cortex.

32 tor networks and diminishing in higher-order association cortex.

33 le of fine-scaled functional organization in association cortex.

34 h has been reported to project to the visual association cortex.

35 signals across a broad extent of sensory and association cortex.

36 maps may be a common organizing principle in association cortex.

37 between primary auditory cortex and adjacent association cortex.

38 surprisingly well those found in the primate association cortex.

39 lly defined multisensory regions in temporal association cortex.

40 imary motor and sensory cortex compared with association cortex.

41 originating from primary motor, sensory, and association cortex.

42 yer-V pyramidal neurons in the mouse frontal association cortex.

43 ferior frontal gyrus, hippocampus and visual association cortex.

44 examine this relationship in human temporal association cortex.

45 he songbird analog of the mammalian auditory association cortex.

46 strated hubs throughout heteromodal areas of association cortex.

47 mus, and to decreases in the fronto-parietal association cortex.

48 ic constraints on the structural topology of association cortex.

49 staining and amyloid plaques in the frontal association cortex.

50 classically considered as unimodal auditory association cortex.

51 fects during stimulus encoding within visual association cortex.

52 signal in a large area of the left parietal association cortex, a region involved in planning.

53 ns that project to the LA or to the auditory association cortex (AAC) is not known.

54 ere, we imaged hundreds of neurons in visual association cortex across days as mice learned a visual

55 : a "slow cortical" route through visual and association cortex and a "fast subcortical" route throug

56 strated that glioma frequency is elevated in association cortex and correlated with multiple graph-th

57 while 3-6 Hz feedback waves originate in the association cortex and flow caudally.

58 oth reduced gray matter volume of the visual association cortex and fractional anisotropy of pontine

59 tion bundles interconnecting the heteromodal association cortex and in connections between the thalam

60 ociated with its reduced covariance with the association cortex and its increased intraconnectivity.

61 development and in aging is greatest in the association cortex and least in the sensorimotor cortex.

62 widespread neurodegeneration throughout the association cortex and limbic system, deposition of amyl

63 nificantly higher variability in heteromodal association cortex and lower variability in unimodal cor

64 blood flow in the lateral parieto-occipital association cortex and precuneus bilaterally.

65 ippocampus, and in the right dorsal parietal association cortex and primary somatosensory and motor c

66 o during adolescence, which were specific to association cortex and related to psychopathology.

67 Disruptive development was characteristic of association cortex and subcortical regions, where connec

68 AD) beta-amyloid (Abeta) deposits throughout association cortex and tau appears in the entorhinal cor

69 ergic interneurons in the cingulate, frontal association cortex, and amygdala but not hippocampus, as

70 ptosomes from samples of cryopreserved human association cortex, and immunolabeled terminals with a p

71 or temporal gyrus, prefrontal cortex, visual association cortex, and primary visual cortex.

72 generalized hyperactivation of ACC, sensory association cortex, and supplementary motor cortex in re

73 iding attention.(27) Neurons in the parietal association cortex are tuned to numerosity, with both a

74 n help reveal how synapses in the prefrontal association cortex are uniquely regulated compared to th

75 parietal cortex (area 7 bilaterally), visual association cortex (area 18 bilaterally) and left motor/

76 and superior frontal gyri, and right visual association cortex (area 18) compared with CAD patients

77 al gyrus (area 8), temporal pole, and visual association cortex (area 18), and a concomitant decrease

78 t anterior cingulate (area 32), right visual association cortex (area 18), left fusiform gyrus, and c

79 he right temporal (area 21) and right visual association cortex (area 19).

80 size and cellular composition of prefrontal association cortex (area 46) examined in adults using ma

81 courage further focus on the CTCC and visual association cortex as core neural substrates and potenti

82 us, a structure belonging to the heteromodal association cortex as well as being part of the semantic

83 PPA revealed gray matter atrophy in auditory association cortex, as defined functionally in a separat

84 connected with a distributed network in the association cortex associated with social cognition, whi

85 We show that rhythmic activity in auditory association cortex at a frequency of ~10 Hz (alpha waves

86 te over few tens of milliseconds, whereas in association cortex behavioural choices can require the m

87 precuneus and lateral temporal and parietal association cortex bilaterally, and in the right amygdal

88 o-thalamo-cortical circuit (CTCC) and visual association cortex, both of which are important for moni

89 Metabolism was most diminished in the visual association cortex (Brodmann area [BA] 18; -20.0% vs. co

90 zed: caudate nucleus, cerebellum, prefrontal association cortex [Brodmann's area 9 (BA9)] and motor c

91 cause it is not only part of the heteromodal association cortex but also is part of the semantic-lexi

92 ntiating the primary sensory cortex from the association cortex, but radiate in parallel with the axe

93 of evidence accumulation are established in association cortex, but the site and mechanism of termin

94 ed upon the catecholamine innervation of the association cortex by combining ovarian hormone manipula

95 Thus, correlations in association cortex can benefit task performance even if

96 erlapping areas of predominantly heteromodal association cortex, changes that may act synergistically

97 lexibly modulating network strength in young association cortex, confer vulnerability to degeneration

98 eriodic timescales increased from sensory to association cortex, decreased during sensory processing

99 matter loss, whereas lateral temporoparietal association cortex displayed both significant PiB retent

100 pS214-tau) in monkey dorsolateral prefrontal association cortex (dlPFC), which specifically targets s

101 situated around the periphery of DCS: visual association cortex dorsomedially, PPC dorsally, AGl late

102 er, briefly deactivating specific regions of association cortex during this period induced long-term

103 sented in overlapping fashion throughout the association cortex, even in the areas that showed the st

104 presentations of numerical zero to posterior association cortex, extending the purview of parietal co

105 items) across cortical depth in the parietal association cortex follows this hypothesis.

106 motor functions, and lower correspondence in association cortex for cognitive functions.

107 ations emphasize the relevance of the visual association cortex for visual snow syndrome.

108 midal neurons in the visual (V1) and frontal association cortex (FrA) of 1-month-old mice.

109 Here, we show that frontal association cortex (FrA) pyramidal neurons of mice integ

110 f consciousness by disrupting how the higher association cortex governs bottom-up sensory signals.

111 patterns occur in resting-state activity in association cortex grouped into high-order cognitive net

112 However, association cortex had faster rates of shrinkage and mye

113 The heteromodal association cortex has been hypothesized to be selective

114 l gyrus, a heteromodal auditory and language association cortex, has been found to be smaller in pati

115 at the beta1 frequency band, as found in rat association cortex, has properties complementary to the

116 ected brain areas (ventral striatum, frontal association cortex, hippocampus, primary motor cortex, o

117 fts in a face-selective region of the visual association cortex [i.e., fusiform face area (FFA)].

118 of multisensory processes in an area of cat association cortex [i.e., the anterior ectosylvian sulcu

119 s of the unimodal cortex with regions in the association cortex implicated in higher-order processes.

120 tex to progressively higher-order transmodal association cortex in both frontal and temporal cortex.

121 ctional organization resembling multisensory association cortex in cats and primates.

122 gs suggest an important role of the temporal association cortex in integrating imagined visual stimul

123 anterior cingulate), hippocampus, and visual association cortex in pathological memories of childhood

124 atching and provide evidence for the role of association cortex in reducing distraction when we watch

125 the highly integrative region of heteromodal association cortex in the angular gyrus would be critica

126 ured from electrodes implanted over auditory association cortex in the posterior superior temporal gy

127 During speech comprehension the auditory association cortex in the superior temporal cortex is in

128 asia is related in part to disease in visual association cortex in ventral-medial portions of the lef

129 poral gyrus, supramarginal gyrus, and visual association cortex in women with PTSD relative to women

130 n networks, including anterior and posterior association cortex, in both groups.

131 trafficking of phosphorylated tau in normal association cortex--in axons in young dlPFC vs. in spine

132 covariance with regions in the higher-order association cortex, including both the default mode and

133 esting potential therapeutics to protect the association cortex, including preventive therapies that

134 d large-scale networks interwoven throughout association cortex, interactions (including anticorrelat

135 are selective to the more plastic regions of association cortex involved in cognition.

136 Association cortex is also 'interdigitated' with adjacen

137 The temporal association cortex is considered a primate specializatio

138 For example, association cortex is located furthest from systems invo

139 In particular, tau pathology in the association cortex is poorly replicated in mouse models.

140 rtical processing, but its presence in human association cortex is unknown.

141 a lower E/I ratio marker (especially in the association cortex) is linked to better cognitive perfor

142 y showed marked retention of PIB in areas of association cortex known to contain large amounts of amy

143 es of axons were performed in the multimodal association cortex lining the superior temporal sulcus.

144 lamus), along with decreased activity in the association cortex may be crucial for motor manifestatio

145 nce that coupled ripples between the MTL and association cortex may underlie successful memory retrie

146 8 [95% CI, 0.19 to 0.77]; P = .009), sensory association cortex (mean difference on left side, 0.54 [

147 reveal a window of sensitivity within which association cortex mediates the encoding of cross-modal

148 visual stimuli at the highest level of human association cortex-namely, in the superior part of the p

149 ntal associations, with PSCs in higher-order association cortex networks showing greater changes with

150 These data indicate that in primate association cortex, NMDA receptors are heterogeneously d

151 The association cortex of the superior temporal gyrus (STG)

152 rate that regions distributed throughout the association cortex, often called the default network, ar

153 of cortex (primary auditory cortex, auditory association cortex, orbital frontal cortex and inferior

154 ons between primary auditory cortex (A1) and association cortex (Par2).

155 k comprises frontopolar and rostral temporal association cortex, parahippocampal areas TH / TF, the v

156 tivity of anterior cingulate cortex, frontal association cortex, parasubiculum, and the superficial l

157 In the association cortex, population activity has a longer tim

158 nic two-photon calcium imaging in postrhinal association cortex (POR) and primary visual cortex (V1)

159 F decreases were seen in the fronto-parietal association cortex, precuneus and cingulate gyrus during

160 of frontal, parietal, temporal and occipital association cortex, primary visual cortex, and in anteri

161 columns was later and faster in higher-order association cortex, proceeding rapidly before becoming u

162 activity - to suppress signaling to parietal association cortex-projecting claustrum neurons.

163 e songbird homolog of the mammalian auditory association cortex, rapidly enhances the effectiveness o

164 sentations, whereas increased variability in association cortex reflects recurrent dynamics that supp

165 task (i.e. cognitive motor dissociation) and association cortex responses during language and music s

166 Notably, projections originating from association cortex resulted in less laterality than prim

167 s demonstrated that stimulus-specific visual association cortex serves as a marker of activation diff

168 d sharply with the response of somatosensory association cortex (SII), in which activity was suppress

169 V1) are commonly assumed to also hold in the association cortex such that neurons within a cortical c

170 stimulation of entorhinal cortex and sensory association cortex (Te3).

171 ral entorhinal=area 28, and ventral temporal association cortex=Te3 region).

172 to active neurons, we find that the temporal association cortex (TeA) in mothers exhibits robust USV

173 We first establish that mouse temporal association cortex (TeA) is required for remote recall o

174 ctive activation of fibers from the temporal association cortex (TeA) or the anterior cingulate corte

175 In temporal association cortex (TeA) terminal distributions below La

176 subset of excitatory neurons in the temporal association cortex (TeA) through in utero electroporatio

177 ventral most auditory field is the temporal association cortex (TeA), which remains largely unstudie

178 sponses in the awake mouse auditory temporal association cortex (TeA).

179 ed alterations in descending influences from association cortex that allowed these midbrain neurons t

180 multisensory neurons in regions of auditory association cortex that are also involved in auditory de

181 ion but also affect parts of the heteromodal association cortex that are related to emotion recogniti

182 xperiences drive activity patterns in visual association cortex that are subsequently reactivated dur

183 al history information in rostrolateral (RL) association cortex that emerges before stimulus presenta

184 ray matter density in the region of auditory association cortex that healthy participants activated w

185 tively affect pyramidal neurons of the aging association cortex that interconnect extensively through

186 istent with the view that OF is a high order association cortex that plays a role both in the memory

187 mergence of specialized functional roles for association cortex, the orbit of its remit began to dimi

188 stereologically based counts in a high-order association cortex, the superior temporal sulcus, of 30

189 beta deposits were assessed in a high-order association cortex, the superior temporal sulcus.

190 no mRNA changes were detected in prefrontal association cortex, thereby revealing subtleties of path

191 Primary and association cortex, therefore, are differentiated by how

192 cal differentiation and the vulnerability of association cortex to be tested.

193 the cerebral cortex in ASD, extending beyond association cortex to broadly involve primary sensory re

194 posterior parietal cortex (PPC), and visual association cortex to form a cortical-subcortical circui

195 connections linking putative hub regions of association cortex to other brain areas.

196 sis revealed that BOLD signal in heteromodal association cortex typically had more widespread and ove

197 ion of ventrolateral prefrontal and parietal association cortex, volumetric increases in which may be

198 stribution of NMDAR1 immunolabeling in human association cortex was similar to that observed in monke

199 olateral prefrontal cortex and left parietal association cortex when compared to controls.

200 stinct from the response of lateral auditory association cortex, which responded to auditory feedback

201 mple and test odors in olfactory sensory and association cortex, which were sufficient to identify th

202 lly functionally connected to other parts of association cortex with like domain preference.

203 ponses across cortical depth in the parietal association cortex with ultra-high field fMRI and popula

204 ts responses in distinct areas of high-level association cortex within the default mode network, span

205 traction emerged when activity in regions of association cortex within the frontoparietal system was

206 is that individuals with disease in auditory association cortex would have difficulty processing conc