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1 as well as CMAr, SMA, and the supplementary sensory area.
2 st circuit-level analysis of BLA inputs to a sensory area.
3 ple senses, even at the level of the primary sensory areas.
4 onic in vivo two-photon imaging in different sensory areas.
5 adaptation has been little studied in higher sensory areas.
6 s expressed in epithelia adjacent to the pro-sensory areas.
7 ion of responses in functionally specialized sensory areas.
8 cal association areas but extends to primary sensory areas.
9 there are few projections from other primary sensory areas.
10 e in cortex to determine the organization of sensory areas.
11 x of primitive mammals was composed of a few sensory areas.
12 in mechanisms of development between the two sensory areas.
13 ansverse 5-HT-IR axons running to peripheral sensory areas.
14 which are generally conceived as high-order sensory areas.
15 a/alpha band (7-9 Hz) oscillations in visual sensory areas.
16 , and highlight an important difference from sensory areas.
17 o a spatial window of integration in primary sensory areas.
18 pectral and laminar profile in each of these sensory areas.
19 resentation of fine-grained details in early sensory areas.
20 order association areas and to spare primary sensory areas.
21 at closely matches that observed in cortical sensory areas.
22 erties and connections similar to layer 4 in sensory areas.
23 of cholinergic projections to task-relevant sensory areas.
24 raphic maps, which are so helpful in primary sensory areas.
25 put circuits like those of the L4 neurons in sensory areas.
26 tion that it is organized similarly to other sensory areas.
27 a general modulatory function across primary sensory areas.
28 rcuitry similar to those observed in primary sensory areas.
29 ation of evolving sinks to those reported in sensory areas.
30 velopment of inhibitory cortical circuits in sensory areas.
31 operties that have been measured in cortical sensory areas.
32 li are often represented in proximity in the sensory areas.
33 physiologically derived maps of neocortical sensory areas.
34 bout how it shapes information processing in sensory areas.
35 ty of surround suppression and adaptation in sensory areas.
36 ty varies across the cortical layers in many sensory areas.
37 a 3 is mainly connected to medial and dorsal sensory areas 3, 1, 2, 5, and SSA and to areas 4 and 6 a
39 terior cingulate cortex, and several primary sensory areas (all r > 0.58; P < 0.05, corrected for fam
42 ssing: representation of evidence from early sensory areas and accumulation of evidence to a decision
43 Catecholaminergic (CA) neurons innervate sensory areas and affect the processing of sensory signa
44 (CD), motor signals that send information to sensory areas and allow for prediction of sensory states
48 iprocal connections with widespread cortical sensory areas and with other memory-related structures,
49 knowledge is skewed markedly toward primary sensory areas, and in fact, it has been difficult to dem
50 ts of WM-related sustained activity in early sensory areas are rare, and typically lack stimulus spec
51 t the hypothesis that the ERP responses from sensory areas arising after aware stimulus detection can
52 children with and without ADHD, with primary sensory areas attaining peak cortical thickness before p
56 evealed here suggests the presence of NOS in sensory areas both in the CNS and the peripheral organs
57 ing neurons was also examined and related to sensory areas by making small injections of wheat germ a
58 mation in birds takes place in the forebrain sensory area called the Wulst, as it does in the primary
59 cortex, most pronounced in the frontal motor-sensory area, can be detected by histological and immuno
60 her cognitive areas and delivered to earlier sensory areas, can support attentional gain modulation.
61 ion showed predominance of midline motor and sensory area CBF in KO mice over WILD mice that received
63 oughout this tubular system are six separate sensory areas composed of hair cells and support cells t
64 pyramidal network commonly found in primary sensory areas, consisting of accommodating pyramidal cel
65 caudal neocortex of hedgehogs has only a few sensory areas, corresponding to those commonly found in
66 frontal cortex and suggest how processing in sensory areas could be altered in mental disorders invol
70 structures, which was greater in the primary sensory areas during the encoding (Wilcoxon rank sum tes
71 or outputs are appropriate), while posterior sensory areas encode continuous or analog feature repres
73 s that in higher cortical areas, as in early sensory areas, experience drives functional clustering a
75 h the columnar organization in other primary sensory areas (i.e., where periodically arranged sets of
76 Current knowledge suggests that cortical sensory area identity is controlled by transcription fac
77 n several ways with previous observations in sensory areas, illuminate the basic circuit organization
79 ata indicate that agranular cortex resembles sensory areas in certain respects, but the cortical micr
82 lopment should be revisited even for primary sensory areas, in that the connectivity basis for visual
83 Several computational neuroscience models of sensory areas, including Olshausen & Field's Sparse Codi
84 h the number of neurons imaged regardless of sensory area, indicating that circuit size is not tied t
85 odality combinations suggests that low-level sensory areas integrate multisensory information at earl
86 idence for bottom-up processing from primary sensory areas into higher association areas during AV in
87 stening, ongoing neural activity in auditory sensory areas is dominated by the attended speech stream
88 r areas lack the visual selectivity of early sensory areas, it has remained unclear how observers can
89 ents are commonly overrepresented in diverse sensory areas like the olfactory, photic, and acoustico-
93 and increase signal passing from lower level sensory area MT+/V5, which is responsive to all motion,
99 The responses of neural elements in many sensory areas of the brain vary systematically with thei
104 uronal and non-neuronal cells in the primary sensory areas of the neocortex of a South American marsu
105 can influence neural activity in 'unimodal' sensory areas of the neocortex, but whether this 'extra-
106 the frontal and parietal lobes and unimodal sensory areas of the occipital and temporal lobes appear
107 nimals can discriminate signals delivered to sensory areas of their brains using electrical microstim
108 a electrical or optical stimulation of brain sensory areas offers a promising treatment for sensory d
109 nsory integration emerges already in primary sensory areas or is deferred to higher-order association
110 e how hedgehog cortex is organized, how much sensory areas overlap, and to compare results with recen
111 c thalamic calcium waves coordinate cortical sensory area patterning and plasticity prior to sensory
112 to translate the blueprints into functional sensory area properties in cortical neurons postmitotica
115 rtex (SMC), primary motor area (M1), primary sensory area (S1), premotor cortex (PMC) and supplementa
116 he view that intermingled neurons in primary sensory areas send specific stimulus features to differe
117 e, attention can amplify neural responses in sensory areas (sensory gain), mediate neural variability
119 mescales naturally emerges from this system: sensory areas show brief, transient responses to input (
123 uted codes similar to those seen in cortical sensory areas such as visual area V1, but they can also
124 anisms of cross-modal integration in primary sensory areas, such as the primary visual cortex (V1), a
126 Cortical-feedback projections to primary sensory areas terminate most heavily in layer 1 (L1) of
127 ollary discharge (CD), motor signals sent to sensory areas that allow for the prediction of impending
129 ventris) with microelectrode recordings from sensory areas that were later correlated with cytochrome
130 n different brain regions and networks, from sensory areas to large-scale frontoparietal systems, hav
131 levels of alpha- (8-12 Hz) power in relevant sensory areas to predict whether a stimulus will be cons
132 nscription factor Ctip1 functions in primary sensory areas to repress motor and activate sensory prog
133 correlations, and found that data from early sensory areas were compatible with optimal linear readou
134 ciples that differ from those in neocortical sensory areas where cells responsive to similar stimulus
135 s the principal target for thalamic input in sensory areas, which raises the question of how thalamoc
136 erebral cortex is organized into specialized sensory areas, whose initial territory is determined by
137 of the pit membrane into three well-defined sensory areas with largely separated innervations by the
138 ocortex rather than those typical of primary sensory areas with which it has been traditionally class
139 ct prey, we investigated the organization of sensory areas within grasshopper mouse neocortex and qua
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