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1 midbrain and (3) the cortical neurons of the somatosensory area.
2 ensory areas (areas PV and S2), and a caudal somatosensory area.
3 ciated percepts via its connections to early somatosensory areas.
4 fluence onto the posterior primary motor and somatosensory areas.
5 z oscillation in neocortical slices from rat somatosensory areas.
6  lead to increased coupling between them and somatosensory areas.
7 major projections from the primary motor and somatosensory areas.
8 ping and intrinsic signal optical imaging in somatosensory areas.
9 grity of stroke- or lesion-damaged motor and somatosensory areas.
10 sly thought, including autonomic, motor, and somatosensory areas.
11 tex is occupied by the visual, auditory, and somatosensory areas.
12 th the second (S2) and parietal ventral (PV) somatosensory areas.
13 ng excitatory input to the secondary whisker somatosensory area 2.
14 0, 23a and b, and TSA as well as with medial somatosensory areas 3, 1, 2, 5, and SSA.
15                 The detailed organization of somatosensory area 3a was examined in macaque monkeys us
16 remotor cortex, SMA, cingulate motor cortex, somatosensory areas 3a and 1, and the rostral half of po
17 otor areas of frontal cortex as well as with somatosensory areas 3a and 1-2 and higher order somatose
18  from the other motor areas, as well as from somatosensory areas 3a and 3b.
19 remainder of the connections originated from somatosensory areas 3a and second somatosensory cortex/p
20            Only the PMV had connections with somatosensory areas 3a, 1, 2, PR, and PV.
21 1, PMD, and frontal cortex and sparsely with somatosensory areas 3a, 1-2, S2, and PV.
22                            Anterior parietal somatosensory areas 3a, 3b, 1, and 2 generally contain c
23  of premotor cortex (areas 6DC and 6M), from somatosensory areas 3a, 3b, 1/2, and S2, and from poster
24 c morphology of pyramidal neurons in primary somatosensory (area 3b), primary motor (area 4), prestri
25 ed proteins throughout postnatal life in the somatosensory (areas 3b/3a/1/2), motor (area 4), frontop
26 's area 10], primary motor [area 4], primary somatosensory [area 3b], and prestriate visual cortex [a
27 ons of the fMRI signal time courses in early somatosensory area 3b and iDH revealed very similar hemo
28 termined how cortical representations in the somatosensory area 3b and the ventroposterior (VP) nucle
29  Here we show that reorganization of primary somatosensory area 3b is not accompanied with either an
30  of the parts of the oral cavity and face in somatosensory area 3b of macaque monkeys were identified
31 A(B)R1a, and GABA(B)R1b receptor subunits in somatosensory area 3b, and cuneate nucleus one week afte
32 ode arrays, in functionally distinct primary somatosensory areas 3b and 1 in nonhuman primates.
33 y connected with the hand representations of somatosensory areas 3b, 1, and S2/PV.
34 2 is densely interconnected with the primary somatosensory area (3b), PV, and area 7b of the ipsilate
35  representations mirrors that of the primary somatosensory area, 3b.
36                      Bilateral activation of somatosensory areas after unilateral stimulation is assu
37 ad at least four specifically interconnected somatosensory areas, along with at least one multimodal
38  in multiple cortical regions, including the somatosensory area and prefrontal cortex in behaving rat
39 , disrupting communication between motor and somatosensory areas and resulting in impaired reaching a
40 are observed for visual (but not auditory or somatosensory) areas and account for auditory-visual con
41 teral somatosensory areas SII (the secondary somatosensory area) and PV (pairetal ventral area).
42 h the lateral somatosensory areas S2 (second somatosensory area) and the parietal ventral area (PV).
43 sponses, weaken cerebellar connectivity with somatosensory areas, and increase this connectivity with
44 d through hemispheric-specific activation of somatosensory areas, and that the rehearsal of somatotop
45 ncluding the primary (S1) and secondary (S2) somatosensory areas, and the medial (MM) and anterolater
46 ing pathways usually linked in the secondary somatosensory area are rerouted in blind subjects to the
47  This connectivity suggests that the ventral somatosensory areas are involved in sensorimotor activit
48  somatosensory cortex (area 3b), two lateral somatosensory areas (areas PV and S2), and a caudal soma
49 s modifies correlation strengths that relate somatosensory areas both to one another and to higher-or
50   Primary somatosensory cortex and adjoining somatosensory areas can become extensively deactivated b
51 nd the corticotectal arising from the fourth somatosensory area, commingle in patches across the midd
52                                          Two somatosensory areas contained complete representations o
53                                     A medial somatosensory area corresponded to S1, the primary somat
54 triatal projections from focal sites in both somatosensory areas exhibited substantial amounts of div
55  dorsal and ventral banks and also by second somatosensory area, first temporal cortical area, and st
56 1, moderate to strong projections from other somatosensory areas, FM, along with connectivity from th
57                                 Second-level somatosensory areas have been described in humans, and a
58                                      Lateral somatosensory areas have not been explored in detail in
59          Intriguingly, other key features of somatosensory area identity are largely preserved, sugge
60 osensory areas (SC and SR) are homologous to somatosensory areas in eutherian mammals.
61 at feedback between primary motor to primary somatosensory areas in mice is disinhibitory, targeting
62 mptive oral cavity and face regions of other somatosensory areas in the anterior parietal cortex and
63 te transporters, we investigated the primary somatosensory areas in the brainstem, thalamus, and cort
64 nd M1 as well as prefrontal cortex, FEF, and somatosensory areas in the lateral sulcus and areas on t
65 elimb representation in PM, M1, 3a, 1-2, and somatosensory areas in the lateral sulcus and on the med
66 atosensory areas 3a and 1-2 and higher order somatosensory areas in the lateral sulcus.
67  sections to investigate the organization of somatosensory areas in the naked mole-rat.
68 digit representations of areas 3b with other somatosensory areas is less understood.
69 ew cortical areas including medial motor and somatosensory areas (MMA and MSA), three posterior parie
70  dystonia By mapping the human cortical hand somatosensory area of 6 patients with focal dystonia of
71 ne in which the lacZ reporter delineates the somatosensory area of the cerebral cortex where it is ex
72 restricted and were predominantly from other somatosensory areas of the anterior parietal cortex (are
73 a few studies have examined and parceled the somatosensory areas of the cebus monkey, mainly using el
74 erentially occurred in the primary motor and somatosensory areas of the injury penumbra as compared t
75 further establish PV as one of at least four somatosensory areas of the lateral sulcus of primates.
76                        Here we report on the somatosensory areas of the nervous system of the Califor
77 al and caudal cingulate motor areas and from somatosensory areas of the parietal cortex.
78 , we found no obvious abnormalities in other somatosensory areas or primary visual cortex of GAP-43 (
79          A second representation, the second somatosensory area (or S2), was found adjacent and caudo
80 SCm, while prefrontal motor area 2 (M2), and somatosensory areas provide strong input to the SCl.
81 ods were used to define the parietal ventral somatosensory area (PV) on the upper bank of the lateral
82  exhibit a pro-active top-down inhibition of somatosensory areas resulting in suppressed processing a
83 areas (MIP and AIP), and parietal area PEip; somatosensory areas S1 and S2; and (pre)motor areas F1,
84 representation was identified as the primary somatosensory area (S1) by its relative position, somato
85                      The neocortical primary somatosensory area (S1) consists of a map of the body su
86                                  The primary somatosensory area (S1) contained an orderly representat
87 ical and callosal connections of the primary somatosensory area (S1) in high-contact (HC) and low-con
88 in some primates and carnivores, the primary somatosensory area (S1) was internally subdivided in dis
89 mporal pole; and a large area 3b, or primary somatosensory area (S1), contained a complete representa
90 ted neuroanatomical tracers into the primary somatosensory area (S1), rostral and caudal somatosensor
91 ojection from medial VP (VPM) to the primary somatosensory area (S1), the wiring of these pathways re
92  on inhibitory mechanisms within the primary somatosensory area (S1).
93 nd neural response properties of the primary somatosensory area, S1.
94 uch inputs from S1 compared with the lateral somatosensory areas S2 (second somatosensory area) and t
95 ary motor area (SMA), cingulate motor areas, somatosensory areas S2 and PV, and the posterior parieta
96 lateral suprasylvian visual area, as well as somatosensory areas S2 and S4.
97 entified the more dorsal field as the second somatosensory area (S2) and the more ventral field as th
98 he parietal ventral area (PV) and the second somatosensory area (S2) in other mammals.
99  several areas; in contrast, only the second somatosensory area (S2) sent major inputs to area 8C.
100 tal cortex (areas 1, 3b, and 3a), the second somatosensory area (S2), and from medial and lateral por
101 ateral sulcus of macaque monkeys: the second somatosensory area (S2), and the parietal ventral area (
102 nnervates heavily and topographically second somatosensory area (S2), but not S1.
103 ion, VPM and Po neurons innervate the second somatosensory area (S2), but the synaptic organization o
104 sulcus, including areas 3a, 1, 2, the second somatosensory area (S2), the parietal ventral area (PV),
105 parietal ventral area (PV) and the secondary somatosensory area (S2).
106 nding to the previously identified secondary somatosensory area (S2).
107 lly identified sites in PV and/or the second somatosensory area (S2).
108 iscuss the possibility that these additional somatosensory areas (SC and SR) are homologous to somato
109  identified somatosensory areas: the primary somatosensory area (SI or area 3b), the anterior parieta
110     Cortex rostral and caudal to the primary somatosensory area (SI) contained neurons that responded
111 ine the detailed organization of the primary somatosensory area (SI).
112 nuation via its functional connectivity with somatosensory areas.SIGNIFICANCE STATEMENT When we touch
113 que monkey intermediate visual (area V4) and somatosensory (area SII) cortex, using matched shape sti
114  for several pain-related regions, including somatosensory area SII, anterior and posterior insula, a
115 r parietal areas 3a and 1/2, and the lateral somatosensory areas SII (the secondary somatosensory are
116 n and somatotopic organization to the second somatosensory area (SII) and the parietal ventral area (
117 identified in the striped possum, the second somatosensory area (SII) and the parietal ventral area (
118 ng to primary motor cortex (MI) or secondary somatosensory area (SII) were labeled with red fluoresce
119  cytoarchitectonic area OP1 of the secondary somatosensory area (SII), is involved in somatosensory f
120                            In the visual and somatosensory areas, staining densities for both enzymes
121 he first postnatal week, the primary whisker somatosensory area starts providing excitatory input to
122 ore than a third of the L5PNs originate from somatosensory areas, such as the barrel field (vS1).
123                         Primary auditory and somatosensory areas tended to have high densities in the
124 oratory designed to determine the network of somatosensory areas that are present in the neocortex of
125 ssing is followed by activation of nonvisual somatosensory areas that contributes to emotion recognit
126  into five electrophysiologically identified somatosensory areas: the primary somatosensory area (SI
127 d across the neuroaxis, from primary sensory/somatosensory areas, through insular-cingulate regions,
128  Area 23c in the lower bank and transitional somatosensory area (TSA) in the upper bank of the cingul
129 for three separate topographically organized somatosensory areas, two visual areas, and a caudolatera
130 ring primate evolution, the emergence of new somatosensory areas underpinned complex manual behaviors
131  a parietal rostral area (PR), and a ventral somatosensory area (VS).
132  of the body, the rostral and caudal ventral somatosensory areas (VSr and VSc), were found in the dor
133 ound in sighted subjects where the secondary somatosensory area was activated while the ventral occip
134 laterally were activated while the secondary somatosensory area was deactivated.
135              Activity in bilateral secondary somatosensory areas was attenuated when the touch was pr
136 ontralateral primary and bilateral secondary somatosensory areas was linearly and positively related
137 eas 3a and 3b, distinction between different somatosensory areas was more evident in myelin-stained s
138 nly cortical activity, mainly in the primary somatosensory area, was significantly correlated with in
139                                  Two lateral somatosensory areas were identified, each containing a c
140 nnections of the caudal cingulate and medial somatosensory areas were investigated in the rhesus monk
141 adely labeled fibers and terminal patches in somatosensory areas were plotted and quantified with res
142 ateral convexity of the cortex in the facial somatosensory area, where mRNA and protein expression of
143 erns, particularly in the primary visual and somatosensory areas, where they lost sharp boundaries wi
144 sensory area corresponded to S1, the primary somatosensory area, whereas two lateral areas partially
145 ons such as the insula, parietal cortex, and somatosensory areas, which are also activated when we ou
146 s dependent on touch have particularly large somatosensory areas with modular cortical representation
147 , posterior parietal cortex links visual and somatosensory areas with motor fields of frontal cortex.
148 n primary motor, secondary motor, or primary somatosensory areas within the overall jaw-opening motor
149 er cortical areas, such as secondary whisker somatosensory area (wS2).

 
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