ライフサイエンスコーパス: extrastriate cortex

1 d to its pallial target, the entopallium (E, extrastriate cortex).

2 egregated M-P streams in four areas of human extrastriate cortex.

3 principle appears to lose prominence in the extrastriate cortex.

4 hat attention modulates visual processing in extrastriate cortex.

5 ], left cerebellum, left thalamus and medial extrastriate cortex.

6 edict expression-specific neural activity in extrastriate cortex.

7 iculus, anterior cingulate, and parts of the extrastriate cortex.

8 rtex, including areas 17, 18, and the nearby extrastriate cortex.

9 he functional organization in this region of extrastriate cortex.

10 istribution of retrogradely labeled cells in extrastriate cortex.

11 ons and organization of topographic areas in extrastriate cortex.

12 stellate cells, and interneurons within the extrastriate cortex.

13 also distinguish drivers from modulators in extrastriate cortex.

14 ely confined to acallosal regions throughout extrastriate cortex.

15 ree adjacent functionally localized areas in extrastriate cortex.

16 ns; the latter likely involves feedback from extrastriate cortex.

17 ift attention influence sensory responses in extrastriate cortex.

18 " (odd-symmetric) tuning becomes dominant in extrastriate cortex.

19 down biasing effects on pooling processes in extrastriate cortex.

20 n fused (versus flicker) trials in occipital extrastriate cortex.

21 in disparity processing) between striate and extrastriate cortex.

22 etition in favor of the attended stimulus in extrastriate cortex.

23 rpatches differ in the output they convey to extrastriate cortex.

24 istribution of retrogradely labeled cells in extrastriate cortex.

25 uces expectation-driven selective biasing of extrastriate cortex.

26 "matching" computation possibly performed in extrastriate cortex.

27 xtual cueing in V1, V2 and other portions of extrastriate cortex.

28 related with increased volume in the lateral extrastriate cortex.

29 tches explicit are most likely elaborated in extrastriate cortex.

30 alian visual pathway, from the retina to the extrastriate cortex.

31 do category-selective regions arise in human extrastriate cortex?

32 whereas pulvinar projections are confined to extrastriate cortex [2--8].

33 results of less left posterior cingulate and extrastriate cortex activation in alcoholics than contro

34 at cholinesterase inhibition enhances visual extrastriate cortex activity during stimulus encoding, e

35 hout each K layer are neurons that innervate extrastriate cortex and that are likely to sustain some

36 significance of overlapping fMRI activity in extrastriate cortex and, by extension, elsewhere in the

37 ression of ignored-object representations in extrastriate cortex, and patterns of spatial and nonspat

38 nnections, direct subcortical projections to extrastriate cortex, and residual inputs from V1 near th

39 asurements suggest that regions within human extrastriate cortex are specialized for different percep

40 ts suggest that different regions of ventral extrastriate cortex are specialized for processing the p

41 y reflecting vasodilation), developed within extrastriate cortex (area V3A).

42 s to posterior and ventral areas of temporal extrastriate cortex, areas TP and TPI.

43 processing within specialized regions of the extrastriate cortex as a function of attention.

44 cortical organization may begin to differ in extrastriate cortex at, or beyond, V3A and V4.

45 produced fMRI activity in the right or left extrastriate cortex (BA18), respectively.

46 tivity increased from early visual cortex to extrastriate cortex but then decreased in anterior regio

47 on enhances activity in specialized areas of extrastriate cortex, but mechanisms of attentional modul

48 content-related activation during imagery in extrastriate cortex, but this activity was restricted to

49 hat global motion sensitivity, a property of extrastriate cortex, can be altered by early visual depr

50 sidered the preserve of "category-selective" extrastriate cortex, can nevertheless emerge in retinoto

51 ite matter most prominently in right ventral extrastriate cortex, close to an area previously implica

52 object enhances its neural representation in extrastriate cortex, compared with those of unattended o

53 tinct areas: the striate cortex (V1) and the extrastriate cortex, consisting of V2 and numerous highe

54 g that the overall category-selective map in extrastriate cortex develops independently from visual e

55 also increased the participation of ventral extrastriate cortex during memory maintenance and decrea

56 In extrastriate cortex (from V2 to LO), on the other hand,

57 s visual attention by increasing activity in extrastriate cortex generally, it accomplishes this in a

58 It is controversial whether mouse extrastriate cortex has a "simple" organization in which

59 monstrate that direct LGN projections to the extrastriate cortex have a critical functional contribut

60 to develop robust visual function in primate extrastriate cortex, highlighting a likely mechanism for

61 atomically restricted lesions in striate and extrastriate cortex, highly informative deficits of visu

62 led studies of the thalamic relationships of extrastriate cortex in apes and humans.

63 ulted in equivalent activations in V1/V2 and extrastriate cortex in both groups.

64 -mm voxels), we identified a small region of extrastriate cortex in most participants that responds s

65 rst extensive study of how amblyopia affects extrastriate cortex in nonhuman primates.

66 pathway by which visual information reaches extrastriate cortex in the absence of V1.

67 e differing proposals on the organization of extrastriate cortex in three species of New World monkey

68 Activation in extrastriate cortex increased after a shift of attention

69 effects, we infer that back-projections from extrastriate cortex influence information content in V1,

70 The most direct pathway identified to the extrastriate cortex is a disynaptic one that provides ro

71 of visual-selective processing in posterior extrastriate cortex is disrupted in schizophrenia.

72 lternative explanation, which is that intact extrastriate cortex is required for mediating voluntary

73 re altered, the functional specialization of extrastriate cortex is retained regardless of visual exp

74 al cortex, but its contribution to coding in extrastriate cortex is unexplored.

75 area (FFA), a face-selective region in human extrastriate cortex, is a matter of active debate.

76 extran amine (BDA) injections into the SG or extrastriate cortex labeled inputs terminating primarily

77 f participation of the left posterior insula/extrastriate cortex, left superior frontal and right ant

78 , the large-scale organization of high-level extrastriate cortex likely reflects the need for both sp

79 pport the notion that population activity in extrastriate cortex limits the precision of both visual

80 level information but this diminished in the extrastriate cortex (LO-1/LO-2/LOC), in which the abstra

81 We conclude that cortical activity in the extrastriate cortex may be a modulating factor in the ma

82 -related activation during imagery in visual extrastriate cortex may be implemented by "top-down" mec

83 ns in the middle temporal area (MT or V5) of extrastriate cortex of alert macaque monkeys.

84 Electrophysiological recording from the extrastriate cortex of non-human primates has revealed n

85 of intrinsic responses to visual stimuli in extrastriate cortex of owl monkeys provided evidence for

86 cal task that is performed by neurons in the extrastriate cortex of the primate brain.

87 hey receive from the retina to virtually all extrastriate cortex, parsing this information into dorsa

88 PFC disruption decreased the tuning of extrastriate cortex responses, coinciding with decrement

89 In the macaque extrastriate cortex, robust correlations between percept

90 ific columns in early/middle stages of human extrastriate cortex.SIGNIFICANCE STATEMENT The magnocell

91 nhibitors can improve memory is by enhancing extrastriate cortex stimulus selectivity at encoding, in

92 and intraparietal clusters with frontal and extrastriate cortex suggested correspondences with areas

93 , EphA3 is only expressed in the prospective extrastriate cortex, suggesting that cortical cells harb

94 Large islands of extrastriate cortex that are enriched for color-tuned ne

95 initial gain enhancement in anterior ventral extrastriate cortex that is coarsely selective for the t

96 , and individual patches receive inputs from extrastriate cortex, the medial temporal lobe, and three

97 the topography of feedback projections from extrastriate cortex to macaque area 17.

98 Feedback connections from extrastriate cortex to primary visual cortex (V1) in the

99 The spatial scale of feedback circuits from extrastriate cortex to V1 is, instead, commensurate with

100 patches and the topographic organization of extrastriate cortex using biologically relevant, phase-e

101 , areas at intermediate processing stages in extrastriate cortex (V4, V3A, MT and V7) showed object-s

102 vity in motion- and color-sensitive areas of extrastriate cortex was enhanced by selective attention

103 owed that modulation of neural processing in extrastriate cortex was significantly enhanced by attent

104 ecting an attentional selection mechanism in extrastriate cortex, was reduced in amplitude with advan

105 of brain activation in the left frontal and extrastriate cortex were made in adults and children (ag

106 ant simultaneous targets, activations in the extrastriate cortex were observed in a patient with call

107 greater connectivity between this region and extrastriate cortex were the most resistant to PFC disru

108 tion in the absence of visual stimulation in extrastriate cortex when subjects covertly directed atte

109 ons among multiple stimuli are eliminated in extrastriate cortex when they are presented in the conte

110 cal terminals are densely distributed in the extrastriate cortex where they form synaptic connections

111 plex" in having a string of areas in lateral extrastriate cortex, which receive direct V1 input.

112 However, one additional region, extrastriate cortex, which was highly active when watchi

113 icit initial category-specific processing in extrastriate cortex while minimizing semantic processing

114 ct varied substantially across subregions of extrastriate cortex, with some showing a twofold increas

115 matching was found to originate from ventral extrastriate cortex, with the former being generated in