ライフサイエンスコーパス: association area

1 e mouse retrosplenial cortex, a visuospatial association area.

2 l and thalamic region, and the left parietal association area.

3 ge (P180) and compare it with the prefrontal association area.

4 and an 'intermediate' cluster of multimodal association areas.

5 splits posterior sensory areas from anterior association areas.

6 ory connectivity which converges on cortical association areas.

7 l areas and frontal, temporal, and occipital association areas.

8 n sensory areas and slow time integration in association areas.

9 er connectivity between M1 and somatosensory association areas.

10 ing sensorimotor regions to later-developing association areas.

11 nt, reducing segregation between sensory and association areas.

12 nd gradual T1w/T2w increases in higher-order association areas.

13 ty, and were less dense and robust in higher association areas.

14 d pathway that additionally involved sensory association areas.

15 g temporal, parietal, limbic, and prefrontal association areas.

16 ast-slow timescale hierarchy from sensory to association areas.

17 sensory areas or is deferred to higher-order association areas.

18 tegration windows increasing from sensory to association areas.

19 rimary functional areas but higher values in association areas.

20 with a wide range of unimodal and polymodal association areas.

21 tex and between visual cortex and prefrontal association areas.

22 unimodal association areas, and heteromodal association areas.

23 tical thickness before polymodal, high-order association areas.

24 or regions, motor cortex and posterior motor association areas.

25 skill-the latter depends more on neocortical association areas.

26 ps were most significant in the higher-order association areas.

27 tor coordination information with multimodal association areas.

28 ispheric activation of parietal and premotor association areas.

29 tex, and in posterior parietal and occipital association areas.

30 plete absence of intervening higher level or association areas.

31 etrosplenial, posterior parietal, and visual association areas.

32 still lower correlations across heteromodal association areas (0.517, SD=0.226).

33 ificantly lower correlations across unimodal association areas (0.597, SD=0.230) and still lower corr

34 cortex, consisting of V2 and numerous higher association areas [1].

35 eas Abeta load was minimal; (2) in posterior association areas, Abeta deposition was predominant, tog

36 In bilateral middle temporal association areas activated by motion and dominated by m

37 ons of the right occipital and left parietal association areas after adjusting for confounding factor

38 lobe, which are interconnected with cerebral association areas and distinct from the primary and seco

39 motional disorders: expansion of homotypical association areas and expansion of the hippocampus.

40 vation in the occipital and parietal sensory association areas and in the dorsolateral prefrontal cor

41 high levels of GAP-43 persist in neocortical association areas and in the limbic system throughout li

42 f cortical neurons decreases from sensory to association areas and is nearly constant for each neuron

43 ortical organization is especially marked in association areas and likely is related to underlying mi

44 hile transmodal areas, including heteromodal association areas and limbic system, demonstrate the hig

45 with PPC-STR receiving stronger inputs from association areas and PPC-pM2 receiving stronger sensori

46 within the visual pathway and between visual association areas and prefrontal attention areas; increa

47 ion error signal that emerges in both visual association areas and the medial temporal lobe.

48 been suggested to be limited to higher order association areas and to spare primary sensory areas.

49 ing primary sensory-motor cortices, unimodal association areas, and heteromodal association areas.

50 yri; (iii) it arises in extrastriate visual 'association' areas; and (iv) it projects to lateral and

51 s study indicate that paralimbic and sensory association areas are critically implicated in tic gener

52 l prefrontal and other higher-order cortical association areas are distinguished by high proportions

53 Here, we show that social cognitive association areas are intrinsically and selectively conn

54 Association areas are known to multiplex behaviorally re

55 cortex (POR) and neighboring lateral visual association areas are necessary for identifying objects

56 These findings indicate that some visuomotor association areas are organized based on abstract action

57 parietofrontal system, including sensory and association areas, as well as the medial thalamus and su

58 nn areas 22, 39, and 42) and auditory-visual association areas (Brodmann areas 20 and 37) but were ra

59 rly in the right hemisphere, and surrounding association areas (Brodmann's areas 10, 11, 12, and 32).

60 ation is not limited to specialized cortical association areas but extends to primary sensory areas.

61 neurons are added to these three neocortical association areas, but not to a primary sensory area (st

62 umn width was not restricted to higher order association areas, but was also seen in the primary sens

63 metabolic worsening in temporal and parietal association areas, consistent with the expectation that

64 theory that sensory areas develop first and association areas develop last.

65 ont, with sensory areas developing first and association areas developing last.

66 sory areas displaying fast, and higher-order association areas displaying slower timescales.

67 ssing from primary sensory areas into higher association areas during AV integration in humans and su

68 on of extrastriate visual areas and parietal association areas during Braille reading, compared with

69 P = 0.002) and in the higher-order cortical association areas during the recall (Wilcoxon rank sum t

70 Upstream sectors of unimodal association areas encode basic features of sensation suc

71 brain and 4.47cm(3) (2.27-6.67) lower in the association areas, equivalent to 1 to 2 years of brain a

72 In all monkey association areas examined, the laminar distribution pat

73 Modality-specific sensory association areas exhibited corresponding activity durin

74 tically, this error signal emerges in visual association areas first and then propagates to the media

75 st from primary cortical regions to unimodal association areas - from Heschl's gyrus to superior temp

76 nterrupted by a previously undescribed motor association area in the depths of the midlateral aspect

77 centrality of connections linking multimodal association areas in humans compared with chimpanzees, t

78 d movement representations in cortical motor association areas in relation to the direction and degre

79 ncept representation, composed of high-level association areas in the anterior, lateral, and ventral

80 ular gyrus in the left hemisphere and visual association areas in the occipital and temporal lobes.

81 In addition, the blind subjects activated association areas in the right occipital cortex, the foc

82 nces in interactions with posterior auditory association areas in the two species were also present-t

83 th a marked reduction of activity in frontal association areas including lateral orbital and dorsolat

84 appropriate for sensory processing), whereas association areas integrate inputs over time and exhibit

85 coordination between visual and higher-order association areas involved in imagery control.

86 hereas lower coordination across heteromodal association areas is consistent with functional laterali

87 areas providing input to DCS include visual association areas, lateral agranular cortex and orbital

88 he striate cortex, linear increase in visual association areas, linear decrease in many anterior area

89 Neurons in the parietal association area LIP represented the integration of evid

90 hysiological studies suggest that neurons in association areas may be involved in this process.

91 ories in these disorders, while higher-order association areas may be most vulnerable to connectivity

92 y lesion-induced activation of dorsal visual association areas may predispose some patients to the em

93 Under-connectivity between cerebral cortical association areas may underlie cognitive deficits in neu

94 ortices, ventral striatum, temporal/parietal association areas, mediodorsal thalamus and cerebellum.

95 e nidopallium caudolaterale (NCL), a pallial association area of the avian endbrain.

96 great ape brain is present in a multisensory association area of the superior temporal gyrus.

97 In contrast, polysensory and high-order association areas of cortex, the most complex areas in t

98 the left, but not the right, motor cortex or association areas of either hemisphere.

99 correlative functions analogous to those in association areas of neocortex rather than those typical

100 ore aspect of social cognition and relies on association areas of the brain that have expanded dispro

101 tential unifying model in which higher-order association areas of the brain that normally connect to

102 n cases of damage to the peristriate cortex (association areas of the brain).

103 e DLPFC during the WCST and posterior visual association areas of the inferolateral temporal cortex d

104 throughout bilateral primary, secondary, and association areas of the superior temporal cortex, but n

105 The association areas of the superior temporal gyrus collect

106 how increased volumes of several sensory and association areas one day after systemic administration

107 nimodal memories were represented in sensory association areas only.

108 r learned associations stabilize in cortical association areas or continue to change following learni

109 h auditory localization activating occipital association areas originally intended for dorsal-stream

110 d decrease in excitation-inhibition ratio in association areas, paralleled by an increase or lack of

111 We examined this principle in the association areas, PFC, and ventral intraparietal area o

112 ensory cortex, A1 and S1, respectively), and association areas (posterior parietal and prefrontal cor

113 sociated with CT in somatosensory, motor and association areas, precuneus, and insula, primarily in t

114 ot predict target presence, while high-level association areas related to general purpose decision ma

115 time of learning, starting from higher-order association area RL and propagating down (i.e., top-down

116 Specific locations in higher-order association areas showed selectivity to either high or l

117 in primary sensorimotor areas and weaker in association areas such as prefrontal cortex, consistent

118 These data suggest that neuronal loss in association areas such as the superior temporal sulcus c

119 nction mature earliest, whereas higher-order association areas, such as the prefrontal cortex, which

120 ombination of information--modality-specific association areas support sensory, verbal, and motor sou

121 In transmodal/paralimbic association areas, T1w/T2w starts at low levels and incr

122 Neighboring neocortical association area Te3V was analyzed as well.

123 orded the activity of neurons in an endbrain association area termed nidopallium caudolaterale (NCL)

124 tional connectivities are less correlated in association areas than in sensory areas.

125 The perirhinal cortex is a polymodal association area that contributes importantly to normal

126 ings agree with the proposal that BA37 is an association area that integrates converging inputs from

127 lesions of medial agranular cortex (AGm), an association area that is its major source of cortical in

128 bottom-up input may take place in downstream association areas that are proposed to be involved in pe

129 ts, locating MIND reductions in higher-order association areas that mature later.

130 Deactivation of the heteromodal association areas (the orbital, dorsolateral prefrontal

131 With maturation of homotypical association areas, the concrete concerns of childhood ex

132 ons between the prefrontal cortex and visual association areas; the neurons involved can be modulated

133 y sensory-motor cortices versus higher-order association areas, these have not been characterized.

134 ivity, and connectivity of specific cortical association areas through which years of education (YoE)

135 n of connectivity from visual to audiovisual association areas throughout learning.

136 receives polysensory input from distributed association areas throughout the neocortex.

137 res as for dendritic trees shows heteromodal association areas to have larger, more complex white mat

138 ea [STP; including temporo-parieto-occipital association area (TPO), PGa, and IPa], the motion comple

139 erior temporal gyrus, including the auditory association areas TS1-3, and from the middle sector of a

140 ingulate cortex, all of which are high-level association areas typically involved in complex cognitiv

141 from the superior temporal sulcus (STS), an association area, we recorded local field potentials and

142 ering the cortical hierarchy from sensory to association areas, we tested whether neural variability

143 findings show an important characteristic of association areas, where diverse streams of information

144 ns with limbic, parietotemporal, and frontal association areas, whereas parietal area 3 has more rest

145 eads beyond sensory cortex to frontoparietal association areas, which do not serve stimulus identific

146 speed and cortical thickness in heteromodal association areas, which was absent in both CNV groups.

147 hip with activity in default mode and visual association areas while scanning for social information.

148 th selective deactivation of the heteromodal association areas, while activity in primary and seconda

149 The Drosophila mushroom bodies are critical association areas whose role in olfactory associative le

150 PFC occurred in humans in concert with other association areas, with modifications of corticocortical