ライフサイエンスコーパス: somatosensory area

1 ensory areas (areas PV and S2), and a caudal somatosensory area.

2 z oscillation in neocortical slices from rat somatosensory areas.

3 fluence onto the posterior primary motor and somatosensory areas.

4 major projections from the primary motor and somatosensory areas.

5 ping and intrinsic signal optical imaging in somatosensory areas.

6 grity of stroke- or lesion-damaged motor and somatosensory areas.

7 sly thought, including autonomic, motor, and somatosensory areas.

8 tex is occupied by the visual, auditory, and somatosensory areas.

9 th the second (S2) and parietal ventral (PV) somatosensory areas.

10 0, 23a and b, and TSA as well as with medial somatosensory areas 3, 1, 2, 5, and SSA.

11 The detailed organization of somatosensory area 3a was examined in macaque monkeys us

12 remotor cortex, SMA, cingulate motor cortex, somatosensory areas 3a and 1, and the rostral half of po

13 otor areas of frontal cortex as well as with somatosensory areas 3a and 1-2 and higher order somatose

14 from the other motor areas, as well as from somatosensory areas 3a and 3b.

15 remainder of the connections originated from somatosensory areas 3a and second somatosensory cortex/p

16 Only the PMV had connections with somatosensory areas 3a, 1, 2, PR, and PV.

17 1, PMD, and frontal cortex and sparsely with somatosensory areas 3a, 1-2, S2, and PV.

18 Anterior parietal somatosensory areas 3a, 3b, 1, and 2 generally contain c

19 of premotor cortex (areas 6DC and 6M), from somatosensory areas 3a, 3b, 1/2, and S2, and from poster

20 c morphology of pyramidal neurons in primary somatosensory (area 3b), primary motor (area 4), prestri

21 ed proteins throughout postnatal life in the somatosensory (areas 3b/3a/1/2), motor (area 4), frontop

22 's area 10], primary motor [area 4], primary somatosensory [area 3b], and prestriate visual cortex [a

23 ons of the fMRI signal time courses in early somatosensory area 3b and iDH revealed very similar hemo

24 termined how cortical representations in the somatosensory area 3b and the ventroposterior (VP) nucle

25 Here we show that reorganization of primary somatosensory area 3b is not accompanied with either an

26 of the parts of the oral cavity and face in somatosensory area 3b of macaque monkeys were identified

27 A(B)R1a, and GABA(B)R1b receptor subunits in somatosensory area 3b, and cuneate nucleus one week afte

28 ode arrays, in functionally distinct primary somatosensory areas 3b and 1 in nonhuman primates.

29 y connected with the hand representations of somatosensory areas 3b, 1, and S2/PV.

30 2 is densely interconnected with the primary somatosensory area (3b), PV, and area 7b of the ipsilate

31 representations mirrors that of the primary somatosensory area, 3b.

32 Bilateral activation of somatosensory areas after unilateral stimulation is assu

33 ad at least four specifically interconnected somatosensory areas, along with at least one multimodal

34 in multiple cortical regions, including the somatosensory area and prefrontal cortex in behaving rat

35 , disrupting communication between motor and somatosensory areas and resulting in impaired reaching a

36 teral somatosensory areas SII (the secondary somatosensory area) and PV (pairetal ventral area).

37 h the lateral somatosensory areas S2 (second somatosensory area) and the parietal ventral area (PV).

38 d through hemispheric-specific activation of somatosensory areas, and that the rehearsal of somatotop

39 ing pathways usually linked in the secondary somatosensory area are rerouted in blind subjects to the

40 This connectivity suggests that the ventral somatosensory areas are involved in sensorimotor activit

41 somatosensory cortex (area 3b), two lateral somatosensory areas (areas PV and S2), and a caudal soma

42 Primary somatosensory cortex and adjoining somatosensory areas can become extensively deactivated b

43 nd the corticotectal arising from the fourth somatosensory area, commingle in patches across the midd

44 Two somatosensory areas contained complete representations o

45 A medial somatosensory area corresponded to S1, the primary somat

46 triatal projections from focal sites in both somatosensory areas exhibited substantial amounts of div

47 triatal projections from focal sites in both somatosensory areas exhibited substantial amounts of div

48 dorsal and ventral banks and also by second somatosensory area, first temporal cortical area, and st

49 1, moderate to strong projections from other somatosensory areas, FM, along with connectivity from th

50 Second-level somatosensory areas have been described in humans, and a

51 Lateral somatosensory areas have not been explored in detail in

52 osensory areas (SC and SR) are homologous to somatosensory areas in eutherian mammals.

53 mptive oral cavity and face regions of other somatosensory areas in the anterior parietal cortex and

54 te transporters, we investigated the primary somatosensory areas in the brainstem, thalamus, and cort

55 nd M1 as well as prefrontal cortex, FEF, and somatosensory areas in the lateral sulcus and areas on t

56 elimb representation in PM, M1, 3a, 1-2, and somatosensory areas in the lateral sulcus and on the med

57 atosensory areas 3a and 1-2 and higher order somatosensory areas in the lateral sulcus.

58 sections to investigate the organization of somatosensory areas in the naked mole-rat.

59 digit representations of areas 3b with other somatosensory areas is less understood.

60 ew cortical areas including medial motor and somatosensory areas (MMA and MSA), three posterior parie

61 dystonia By mapping the human cortical hand somatosensory area of 6 patients with focal dystonia of

62 ne in which the lacZ reporter delineates the somatosensory area of the cerebral cortex where it is ex

63 a few studies have examined and parceled the somatosensory areas of the cebus monkey, mainly using el

64 erentially occurred in the primary motor and somatosensory areas of the injury penumbra as compared t

65 further establish PV as one of at least four somatosensory areas of the lateral sulcus of primates.

66 Here we report on the somatosensory areas of the nervous system of the Califor

67 , we found no obvious abnormalities in other somatosensory areas or primary visual cortex of GAP-43 (

68 A second representation, the second somatosensory area (or S2), was found adjacent and caudo

69 SCm, while prefrontal motor area 2 (M2), and somatosensory areas provide strong input to the SCl.

70 ods were used to define the parietal ventral somatosensory area (PV) on the upper bank of the lateral

71 areas (MIP and AIP), and parietal area PEip; somatosensory areas S1 and S2; and (pre)motor areas F1,

72 representation was identified as the primary somatosensory area (S1) by its relative position, somato

73 The neocortical primary somatosensory area (S1) consists of a map of the body su

74 The primary somatosensory area (S1) contained an orderly representat

75 ical and callosal connections of the primary somatosensory area (S1) in high-contact (HC) and low-con

76 in some primates and carnivores, the primary somatosensory area (S1) was internally subdivided in dis

77 mporal pole; and a large area 3b, or primary somatosensory area (S1), contained a complete representa

78 ted neuroanatomical tracers into the primary somatosensory area (S1), rostral and caudal somatosensor

79 on inhibitory mechanisms within the primary somatosensory area (S1).

80 uch inputs from S1 compared with the lateral somatosensory areas S2 (second somatosensory area) and t

81 ary motor area (SMA), cingulate motor areas, somatosensory areas S2 and PV, and the posterior parieta

82 lateral suprasylvian visual area, as well as somatosensory areas S2 and S4.

83 entified the more dorsal field as the second somatosensory area (S2) and the more ventral field as th

84 he parietal ventral area (PV) and the second somatosensory area (S2) in other mammals.

85 several areas; in contrast, only the second somatosensory area (S2) sent major inputs to area 8C.

86 ateral sulcus of macaque monkeys: the second somatosensory area (S2), and the parietal ventral area (

87 sulcus, including areas 3a, 1, 2, the second somatosensory area (S2), the parietal ventral area (PV),

88 nding to the previously identified secondary somatosensory area (S2).

89 lly identified sites in PV and/or the second somatosensory area (S2).

90 parietal ventral area (PV) and the secondary somatosensory area (S2).

91 iscuss the possibility that these additional somatosensory areas (SC and SR) are homologous to somato

92 identified somatosensory areas: the primary somatosensory area (SI or area 3b), the anterior parieta

93 Cortex rostral and caudal to the primary somatosensory area (SI) contained neurons that responded

94 ine the detailed organization of the primary somatosensory area (SI).

95 que monkey intermediate visual (area V4) and somatosensory (area SII) cortex, using matched shape sti

96 for several pain-related regions, including somatosensory area SII, anterior and posterior insula, a

97 r parietal areas 3a and 1/2, and the lateral somatosensory areas SII (the secondary somatosensory are

98 n and somatotopic organization to the second somatosensory area (SII) and the parietal ventral area (

99 identified in the striped possum, the second somatosensory area (SII) and the parietal ventral area (

100 ng to primary motor cortex (MI) or secondary somatosensory area (SII) were labeled with red fluoresce

101 cytoarchitectonic area OP1 of the secondary somatosensory area (SII), is involved in somatosensory f

102 In the visual and somatosensory areas, staining densities for both enzymes

103 Primary auditory and somatosensory areas tended to have high densities in the

104 oratory designed to determine the network of somatosensory areas that are present in the neocortex of

105 ssing is followed by activation of nonvisual somatosensory areas that contributes to emotion recognit

106 into five electrophysiologically identified somatosensory areas: the primary somatosensory area (SI

107 Area 23c in the lower bank and transitional somatosensory area (TSA) in the upper bank of the cingul

108 for three separate topographically organized somatosensory areas, two visual areas, and a caudolatera

109 ring primate evolution, the emergence of new somatosensory areas underpinned complex manual behaviors

110 a parietal rostral area (PR), and a ventral somatosensory area (VS).

111 of the body, the rostral and caudal ventral somatosensory areas (VSr and VSc), were found in the dor

112 ound in sighted subjects where the secondary somatosensory area was activated while the ventral occip

113 laterally were activated while the secondary somatosensory area was deactivated.

114 eas 3a and 3b, distinction between different somatosensory areas was more evident in myelin-stained s

115 nly cortical activity, mainly in the primary somatosensory area, was significantly correlated with in

116 Two lateral somatosensory areas were identified, each containing a c

117 nnections of the caudal cingulate and medial somatosensory areas were investigated in the rhesus monk

118 adely labeled fibers and terminal patches in somatosensory areas were plotted and quantified with res

119 ateral convexity of the cortex in the facial somatosensory area, where mRNA and protein expression of

120 erns, particularly in the primary visual and somatosensory areas, where they lost sharp boundaries wi

121 sensory area corresponded to S1, the primary somatosensory area, whereas two lateral areas partially

122 ons such as the insula, parietal cortex, and somatosensory areas, which are also activated when we ou

123 s dependent on touch have particularly large somatosensory areas with modular cortical representation

124 , posterior parietal cortex links visual and somatosensory areas with motor fields of frontal cortex.