ライフサイエンスコーパス: heteromodal

1 nd characterizes a spectrum from unimodal to heteromodal activity in a functional metaanalysis.

2 ions have strong network interdigitations in heteromodal and associative areas of the cortical mantle

3 nlemniscal IC, while layer 6 neurons provide heteromodal and limbic modulation diffusely to the nonle

4 that are variably specialized for unimodal, heteromodal and memory-related processing.

5 anterograde horizontal axis from unimodal to heteromodal and paralimbic cortex; a radial axis where v

6 ht posterior neocortical areas implicated in heteromodal and polysensory integration.

7 reasingly rare, heterogeneous and complex in heteromodal and transmodal networks higher in the hierar

8 ignal in mid-to-deeper layers, especially in heteromodal and unimodal association cortices.

9 The first dimension, separating heteromodal and unimodal cortices, showed no differences

10 ographic heritability did not differ between heteromodal and unimodal networks.

11 ex; the Abeta deposits were clustered in the heteromodal areas and rather patchy in distributed regio

12 This is the first demonstration that heteromodal areas involved in semantic processing can di

13 These results indicate that heteromodal areas involved in semantic processing encode

14 s (each n = 24) demonstrated hubs throughout heteromodal areas of association cortex.

15 entation consistently implicate a network of heteromodal areas that seem to support concept retrieval

16 eposits in the temporal lobe and distributed heteromodal areas were tightly nested.

17 andedness in unimodal sensorimotor cortices, heteromodal areas, and cerebellum (P < 0.001) and reprod

18 They also reveal that, in most heteromodal areas, event concepts have more heterogeneou

19 grouped in the temporal lobe, distributed in heteromodal areas, medial and visual regions, and primar

20 D=0.230) and still lower correlations across heteromodal association areas (0.517, SD=0.226).

21 Deactivation of the heteromodal association areas (the orbital, dorsolateral

22 riability, while transmodal areas, including heteromodal association areas and limbic system, demonst

23 rdination, whereas lower coordination across heteromodal association areas is consistent with functio

24 e same measures as for dendritic trees shows heteromodal association areas to have larger, more compl

25 n processing speed and cortical thickness in heteromodal association areas, which was absent in both

26 ssociated with selective deactivation of the heteromodal association areas, while activity in primary

27 or cortices, unimodal association areas, and heteromodal association areas.

28 long association bundles interconnecting the heteromodal association cortex and in connections betwee

29 ex, with significantly higher variability in heteromodal association cortex and lower variability in

30 angular gyrus, a structure belonging to the heteromodal association cortex as well as being part of

31 interest because it is not only part of the heteromodal association cortex but also is part of the s

32 The heteromodal association cortex has been hypothesized to

33 dicted that the highly integrative region of heteromodal association cortex in the angular gyrus woul

34 tion regulation but also affect parts of the heteromodal association cortex that are related to emoti

35 tional analysis revealed that BOLD signal in heteromodal association cortex typically had more widesp

36 tially nonoverlapping areas of predominantly heteromodal association cortex, changes that may act syn

37 was used for morphometric assessment of the heteromodal association cortex.

38 correlated with smaller volumes of the left heteromodal association cortex.

39 The inferior parietal lobule is a heteromodal association cortical region that has been im

40 -hemisphere interaction was prominent in the heteromodal association cortices and minimal in the sens

41 ssociation between activity in higher order, heteromodal association cortices in the frontal and pari

42 frontal, temporal, and parietal regions are heteromodal association cortices that constitute a distr

43 The heteromodal association neocortex is believed to be a ma

44 lity and reduced heritability in the size of heteromodal association networks (h(2) : M = 0.34, SD =

45 s: functional connections within and between heteromodal association networks, including default, lim

46 ate evolution, due to their embedding within heteromodal association networks.

47 Activation changes in this heteromodal association region may be related to an impa

48 ature' of cortical atrophy in paralimbic and heteromodal association regions measured with MRI.

49 usters of both pathologic alterations in the heteromodal association regions.

50 The superior temporal gyrus, a heteromodal auditory and language association cortex, ha

51 include both a single modality-independent (heteromodal) convergence region and spatially discrete m

52 indicate that concept representations in the heteromodal cortex are based, at least in part, on exper

53 view of vOTC organization-the existence of a heteromodal cortex critical to both reading and naming,

54 n of the adaptive asymmetric organization of heteromodal cortex in aging and AD.

55 This strategy identified an area of heteromodal cortex in the left superior temporal sulcus

56 The heteromodal cortex is highly elaborated in humans and is

57 pment of the neocortex, and particularly the heteromodal cortex, are not well understood.

58 , with primary cortex clearly separated from heteromodal cortex.

59 ossmodal binding by convergence in the human heteromodal cortex.

60 were less heritable and typically located in heteromodal cortex.

61 can be reliably decoded from a wide range of heteromodal cortical areas in the frontal, parietal, and

62 antiation of lexical concepts in high-level, heteromodal cortical areas previously associated with se

63 We hypothesized that heteromodal cortical areas typically associated with the

64 nceptual information from neural activity in heteromodal cortical areas.

65 d morphometry further suggests that parietal heteromodal cortical gray matter deficits may underlie v

66 ory by applying focal brain stimulation to a heteromodal cortical hub implicated in semantic processi

67 tomic models of semantic memory propose that heteromodal cortical hubs integrate distributed semantic

68 uld illuminate the basic neurobiology of the heteromodal cortical network.

69 Hypometabolism was observed in heteromodal cortices in dysexecutive Alzheimer's disease

70 sis revealed that relative hypometabolism in heteromodal cortices was associated with worse dysexecut

71 lations were found principally in paramedian heteromodal cortices whereas positive correlations were

72 intrinsic networks covering fronto-parietal heteromodal cortices.

73 trophysiologic evidence that the left ATL is heteromodal for proper-name retrieval.

74 tal abnormalities of anterior paralimbic and heteromodal frontal cortices, key structures in emotiona

75 onnectivity in areas of high connectivity in heteromodal hubs, and particularly in the default mode n

76 This finding supports the idea of heteromodal (i.e., transmodal) dispositions for proper n

77 nd colleagues reported that the temporal and heteromodal insular cortices have a central role in prop

78 s, including the vicinity of the Perisylvian heteromodal language area (Sample 1, n=650).

79 These data indicate a convergence of heteromodal lexical retrieval within the PFC.

80 nt for ongoing cognition, regions supporting heteromodal memory are functionally separated from senso

81 of amyloid-beta on intrinsic connectivity in heteromodal networks is underestimated by conventional a

82 of sensory-fugal processing are occupied by heteromodal, paralimbic and limbic cortices, collectivel

83 ory, upstream unimodal, downstream unimodal, heteromodal, paralimbic and limbic zones of the cerebral

84 erarchical sequence of modality-specific and heteromodal processes.

85 al roles, with pSTS acting as a presemantic, heteromodal region for crossmodal perceptual features, a

86 probability maps suggested that the anterior heteromodal region was more affected in the schizophreni

87 action of posterior perceptual cortices with heteromodal regions in the prefrontal and parietal corti

88 racterized by selective abnormalities of the heteromodal regions involved in the neuroanatomy of lang

89 primary and paralimbic regions, unimodal and heteromodal regions showed higher receptomic diversifica

90 notion that higher-order processing requires heteromodal resources different to those linked to input

91 ormal interhemispheric information transfer, heteromodal sensorimotor processing, and executive contr

92 ocessing of false font throughout visual and heteromodal sensory pathways that support reading, in wh

93 However, while the heteromodal somatosensory consequences of visual looming

94 lmia to the level of cortical areas that are heteromodal, such as the inferior frontal gyrus.

95 looming toward the face predictively enhance heteromodal tactile sensitivity around the expected time