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1 rus (area 21) (in the region of the auditory association cortex).
2 tor networks and diminishing in higher-order association cortex.
3 evoked by electrical stimulation of sensory association cortex.
4 signals across a broad extent of sensory and association cortex.
5 al cortical regions such as ventral temporal association cortex.
6 and neurofibrillary tangles in a high-order association cortex.
7 r cortex, but enhanced activation of frontal association cortex.
8 ense layers of prefrontal and inferotemporal association cortex.
9 complex (PM) has widespread connections with association cortex.
10 maps may be a common organizing principle in association cortex.
11 d network involving prefrontal and posterior association cortex.
12 between primary auditory cortex and adjacent association cortex.
13 surprisingly well those found in the primate association cortex.
14 le of fine-scaled functional organization in association cortex.
15 lly defined multisensory regions in temporal association cortex.
16 h has been reported to project to the visual association cortex.
17 imary motor and sensory cortex compared with association cortex.
18 yer-V pyramidal neurons in the mouse frontal association cortex.
19 ferior frontal gyrus, hippocampus and visual association cortex.
20 examine this relationship in human temporal association cortex.
21 he songbird analog of the mammalian auditory association cortex.
22 strated hubs throughout heteromodal areas of association cortex.
23 mus, and to decreases in the fronto-parietal association cortex.
24 staining and amyloid plaques in the frontal association cortex.
25 classically considered as unimodal auditory association cortex.
26 fects during stimulus encoding within visual association cortex.
27 s role as a first-stage (or "belt") auditory association cortex.
28 creased AChE activity only in lateral visual association cortex.
29 y somatic sensory, primary visual and visual association cortex.
30 frontal cortex that is adjacent to olfactory association cortex.
31 he differences were greatest in higher-order association cortex.
32 r morphometric assessment of the heteromodal association cortex.
33 posterior parietal cortex (PPC), and visual association cortex.
34 with smaller volumes of the left heteromodal association cortex.
35 omponent that is generated within the visual association cortex.
38 : a "slow cortical" route through visual and association cortex and a "fast subcortical" route throug
39 tion bundles interconnecting the heteromodal association cortex and in connections between the thalam
40 widespread neurodegeneration throughout the association cortex and limbic system, deposition of amyl
41 nificantly higher variability in heteromodal association cortex and lower variability in unimodal cor
43 ippocampus, and in the right dorsal parietal association cortex and primary somatosensory and motor c
44 ergic interneurons in the cingulate, frontal association cortex, and amygdala but not hippocampus, as
45 ptosomes from samples of cryopreserved human association cortex, and immunolabeled terminals with a p
46 parietal cortex (area 7 bilaterally), visual association cortex (area 18 bilaterally) and left motor/
47 and superior frontal gyri, and right visual association cortex (area 18) compared with CAD patients
48 al gyrus (area 8), temporal pole, and visual association cortex (area 18), and a concomitant decrease
49 t anterior cingulate (area 32), right visual association cortex (area 18), left fusiform gyrus, and c
51 size and cellular composition of prefrontal association cortex (area 46) examined in adults using ma
52 us, a structure belonging to the heteromodal association cortex as well as being part of the semantic
53 PPA revealed gray matter atrophy in auditory association cortex, as defined functionally in a separat
54 te over few tens of milliseconds, whereas in association cortex behavioural choices can require the m
55 Metabolism was most diminished in the visual association cortex (Brodmann area [BA] 18; -20.0% vs. co
56 zed: caudate nucleus, cerebellum, prefrontal association cortex [Brodmann's area 9 (BA9)] and motor c
57 cause it is not only part of the heteromodal association cortex but also is part of the semantic-lexi
58 ed upon the catecholamine innervation of the association cortex by combining ovarian hormone manipula
59 erlapping areas of predominantly heteromodal association cortex, changes that may act synergistically
60 lexibly modulating network strength in young association cortex, confer vulnerability to degeneration
61 matter loss, whereas lateral temporoparietal association cortex displayed both significant PiB retent
62 pS214-tau) in monkey dorsolateral prefrontal association cortex (dlPFC), which specifically targets s
63 situated around the periphery of DCS: visual association cortex dorsomedially, PPC dorsally, AGl late
64 er, briefly deactivating specific regions of association cortex during this period induced long-term
67 l gyrus, a heteromodal auditory and language association cortex, has been found to be smaller in pati
68 at the beta1 frequency band, as found in rat association cortex, has properties complementary to the
69 ected brain areas (ventral striatum, frontal association cortex, hippocampus, primary motor cortex, o
70 fts in a face-selective region of the visual association cortex [i.e., fusiform face area (FFA)].
71 of multisensory processes in an area of cat association cortex [i.e., the anterior ectosylvian sulcu
73 gs suggest an important role of the temporal association cortex in integrating imagined visual stimul
74 anterior cingulate), hippocampus, and visual association cortex in pathological memories of childhood
75 the highly integrative region of heteromodal association cortex in the angular gyrus would be critica
76 During speech comprehension the auditory association cortex in the superior temporal cortex is in
77 asia is related in part to disease in visual association cortex in ventral-medial portions of the lef
78 poral gyrus, supramarginal gyrus, and visual association cortex in women with PTSD relative to women
80 trafficking of phosphorylated tau in normal association cortex--in axons in young dlPFC vs. in spine
81 d large-scale networks interwoven throughout association cortex, interactions (including anticorrelat
83 y showed marked retention of PIB in areas of association cortex known to contain large amounts of amy
84 es of axons were performed in the multimodal association cortex lining the superior temporal sulcus.
85 lamus), along with decreased activity in the association cortex may be crucial for motor manifestatio
86 reveal a window of sensitivity within which association cortex mediates the encoding of cross-modal
87 visual stimuli at the highest level of human association cortex-namely, in the superior part of the p
88 ntal associations, with PSCs in higher-order association cortex networks showing greater changes with
91 of cortex (primary auditory cortex, auditory association cortex, orbital frontal cortex and inferior
93 nic two-photon calcium imaging in postrhinal association cortex (POR) and primary visual cortex (V1)
94 F decreases were seen in the fronto-parietal association cortex, precuneus and cingulate gyrus during
95 of frontal, parietal, temporal and occipital association cortex, primary visual cortex, and in anteri
96 columns was later and faster in higher-order association cortex, proceeding rapidly before becoming u
97 e songbird homolog of the mammalian auditory association cortex, rapidly enhances the effectiveness o
98 task (i.e. cognitive motor dissociation) and association cortex responses during language and music s
99 s demonstrated that stimulus-specific visual association cortex serves as a marker of activation diff
100 d sharply with the response of somatosensory association cortex (SII), in which activity was suppress
101 V1) are commonly assumed to also hold in the association cortex such that neurons within a cortical c
105 ctive activation of fibers from the temporal association cortex (TeA) or the anterior cingulate corte
106 ed alterations in descending influences from association cortex that allowed these midbrain neurons t
107 multisensory neurons in regions of auditory association cortex that are also involved in auditory de
108 ion but also affect parts of the heteromodal association cortex that are related to emotion recogniti
109 ray matter density in the region of auditory association cortex that healthy participants activated w
110 tively affect pyramidal neurons of the aging association cortex that interconnect extensively through
111 istent with the view that OF is a high order association cortex that plays a role both in the memory
112 mergence of specialized functional roles for association cortex, the orbit of its remit began to dimi
113 stereologically based counts in a high-order association cortex, the superior temporal sulcus, of 30
115 no mRNA changes were detected in prefrontal association cortex, thereby revealing subtleties of path
117 posterior parietal cortex (PPC), and visual association cortex to form a cortical-subcortical circui
119 sis revealed that BOLD signal in heteromodal association cortex typically had more widespread and ove
120 ion of ventrolateral prefrontal and parietal association cortex, volumetric increases in which may be
121 stribution of NMDAR1 immunolabeling in human association cortex was similar to that observed in monke
122 stinct from the response of lateral auditory association cortex, which responded to auditory feedback
123 is that individuals with disease in auditory association cortex would have difficulty processing conc
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