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 ht posterior neocortical areas implicated in heteromodal and polysensory integration.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

21 The heteromodal association cortex has been hypothesized to

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

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

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

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

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

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

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

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

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

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

32 The heteromodal association neocortex is believed to be a ma

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

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

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

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

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

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

39 The heteromodal cortex is highly elaborated in humans and is

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

41 ossmodal binding by convergence in the human heteromodal cortex.

42 nceptual information from neural activity in heteromodal cortical areas.

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

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

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

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

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

48 intrinsic networks covering fronto-parietal heteromodal cortices.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 However, while the heteromodal somatosensory consequences of visual looming

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

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