ライフサイエンスコーパス: association area

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

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

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

4 tegration windows increasing from sensory to association areas.

5 rimary functional areas but higher values in association areas.

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

7 tex and between visual cortex and prefrontal association areas.

8 unimodal association areas, and heteromodal association areas.

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

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

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

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

13 tor coordination information with multimodal association areas.

14 ispheric activation of parietal and premotor association areas.

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

16 plete absence of intervening higher level or association areas.

17 etrosplenial, posterior parietal, and visual association areas.

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

19 ory connectivity which converges on cortical association areas.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 Modality-specific sensory association areas exhibited corresponding activity durin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 The association areas of the superior temporal gyrus collect

72 nimodal memories were represented in sensory association areas only.

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

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

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

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

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

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

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

80 Neighboring neocortical association area Te3V was analyzed as well.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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