ライフサイエンスコーパス: visual cortical area

1 ctivity that propagate across the surface of visual cortical areas.

2 ngle-unit and population responses in higher visual cortical areas.

3 in certain extrastriate, but not in striate, visual cortical areas.

4 ionship between connectivity and function in visual cortical areas.

5 -error adjustments by modulating activity in visual cortical areas.

6 receive prominent inputs from virtually all visual cortical areas.

7 e a solid handle on the global topography of visual cortical areas.

8 ions in neural activity, particularly within visual cortical areas.

9 t cannot be attributed to the dysfunction of visual cortical areas.

10 ed on an interaction between polysensory and visual cortical areas.

11 s slowed in migraine for early but not later visual cortical areas.

12 arp and is similar to the tuning observed in visual cortical areas.

13 t the shape integration is mediated by later visual cortical areas.

14 py and spatial frequency tuning, in multiple visual cortical areas.

15 al perception are based on activity in early visual cortical areas.

16 hin the lateral geniculate nucleus (LGN) and visual cortical areas.

17 object and spatial scaling is common to all visual cortical areas.

18 he cat before and after selective lesions in visual cortical areas.

19 procal effects of localized damage to either visual cortical areas 17 and 18, or posteromedial latera

20 Following unilateral removal of all known visual cortical areas, a cat is rendered hemianopic in t

21 e propose that feedback from higher to lower visual cortical areas activates an explicit neural repre

22 s and Arc/Arg3.1 in auditory and neighboring visual cortical areas after bilateral deafness in young

23 injections into somatosensory, auditory, and visual cortical areas almost all produced terminal label

24 Here, we show that prospective visual cortical areas and corresponding thalamic nuclei

25 differences within functionally specialized visual cortical areas and deactivation differences in th

26 deep layers receive inputs from extrastriate visual cortical areas and from auditory, somatosensory,

27 resonance imaging signals to define 12 human visual cortical areas, and then determined whether the r

28 l interactions between primary and secondary visual cortical areas are important for visual processin

29 Visual cortical areas are interconnected via layer-speci

30 that responses in retinotopically organized visual cortical areas are modulated by gain fields quali

31 Dorsal visual cortical areas are thought to be dominated by inp

32 tial attention influences representations in visual cortical areas as well as perception.

33 lvinar nucleus is a major source of input to visual cortical areas, but many important facts are stil

34 criminated eye position in five of the early visual cortical areas by taking advantage of a spatially

35 The innervation of distinct visual cortical areas by the thalamus is especially segr

36 Other studies have also shown that visual cortical areas can be activated by somatosensory

37 connections from a higher- to a lower-order visual cortical area carry predictions of lower-level ne

38 ck connections between primary and secondary visual cortical areas directly, we have performed intrac

39 However, interneuron numbers in piriform and visual cortical areas do not differ from those of normal

40 le difference in cortical activation in many visual cortical areas does not necessarily lead to diffe

41 s showed activation of primary and secondary visual cortical areas during tactile tasks, whereas norm

42 d signal-to-noise ratios were higher in most visual cortical areas for color naming compared to diver

43 eurons progressively increase in neighboring visual cortical areas from 2 weeks after deafness and th

44 Top-down modulation of activity within visual cortical areas has been demonstrated through stud

45 Bottom-up hierarchical processing among visual cortical areas has been revealed in experiments t

46 istage feedforward neural processing between visual cortical areas, ignoring the likely impact of cor

47 binocular disparity are found in a number of visual cortical areas in primates, but there is little e

48 Unilateral removal of all known visual cortical areas in the cat renders the animal hemi

49 ude that the early, visuotopically organized visual cortical areas in the human brain (like their cou

50 he topography and functional organization of visual cortical areas in the human brain.

51 Visual cortical areas in the mammalian brain are linked

52 s useful to any laboratory wishing to target visual cortical areas in this increasingly valuable mode

53 ts can be found both in early and high-order visual cortical areas, in parallel with their stimulus t

54 This was not the case for any of the other visual cortical areas, including V1, although decoding w

55 ormation of visual-feature encoding in early visual cortical areas into more flexible categorical rep

56 lowing an error, activity increased in those visual cortical areas involved in processing task-releva

57 een object perception and neural activity in visual cortical areas is a problem of fundamental import

58 e was strong motion opponency in a secondary visual cortical area known as the human MT complex (MT+)

59 A candidate site for this integration is visual cortical area MT (V5), in which cells with large

60 neurons recorded with a single electrode in visual cortical area MT while monkeys performed a direct

61 Pontine cells that receive inputs from visual cortical areas or the superior colliculus respond

62 aspects of feedback circuitry from multiple visual cortical areas proceeds at a similar rate in all

63 This control biased activity in multiple visual cortical areas, resulting in selective sensory pr

64 Hearing cats and visual cortical areas served as a control.

65 duced by unilateral lesion of all contiguous visual cortical areas spanning occipital, parietal and t

66 Visual cortical areas subserve cognitive functions by in

67 m comparably transient responses recorded in visual cortical areas such as area MT, and represent the

68 ssion appears to be an intrinsic property of visual cortical areas such as inferior temporal cortex a

69 of the SC receive direct inputs from various visual cortical areas such as V1, V2, and middle tempora

70 he organization of amygdaloid projections to visual cortical areas TE and V1 by injecting anterograde

71 s not greatly depend on stimulus contrast in visual cortical areas tested [V1, V2, V3, and MT+ (middl

72 nate similar stimuli and are fully absent in visual cortical areas that feed into the hippocampus.

73 rapid dynamic interplay between auditory and visual cortical areas that is triggered by the second so

74 agnetic resonance imaging data revealed that visual cortical areas that selectively process relevant

75 we found that a well known "scene-selective" visual cortical area (the parahippocampal place area; PP

76 small-scale changes in projections from one visual cortical area, the posterior ectosylvian field (E

77 zone is additionally connected to nonprimary visual cortical areas, the aggressive face zone is not.

78 examine the contribution of early and later visual cortical areas to dynamic shape integration.

79 ttentional filter acts in one or more higher visual cortical areas to restrict the availability of vi

80 monkeys to first measure the response in 12 visual cortical areas to stimuli of varying luminance co

81 tribution of higher-level versus lower-level visual cortical areas to this process.

82 Thus, in the absence of all visual cortical areas unilaterally, disinhibition of the

83 col for mapping retinotopy to identify mouse visual cortical areas using ISI.

84 ties depends on neural activity available at visual cortical area V1.

85 Responses to subjective contours in visual cortical areas V1 and V2 in adult cats were inves

86 In visual cortical areas V1 and V2, the strongest response

87 orrelated activity fluctuations across human visual cortical areas V1 through V4 to the dynamics (rat

88 at successive stages of the ventral pathway [visual cortical areas V1, V2, and V4 and inferior tempor

89 between their retinotopic representations in visual cortical areas V1, V2, and V4.

90 re evident for DF in the ventral portions of visual cortical areas V1, V2, V3, and hV4.

91 ation with spatial attention was observed in visual cortical areas V1-V4 for both tasks.

92 hin many regions of the visual system (e.g., visual cortical areas V1-V4v) not normally associated wi

93 f specialized completion mechanisms in early visual cortical areas (V1/V2), since those areas are lik

94 cepted account of the function of the second visual cortical area (V2), partly because no simple resp

95 tended retinotopic location were enhanced in visual cortical area V4 and throughout visual cortex.

96 Past studies of shape coding in visual cortical area V4 have demonstrated that neurons c

97 euronal responses from individual neurons in visual cortical area V4 to both single and paired stimul

98 ncing blood oxygen level-dependent signal in visual cortical area V4 when it is directed to three sti

99 d the local field potential (LFP) in primate visual cortical area V4.

100 red processing in two ventral stream stages (visual cortical areas V4 and IT) in the rhesus macaque m

101 ranial magnetic stimulation (TMS) applied to visual cortical area V5/MT to reduce the SNR focally and

102 lated modulation of activity occurs in other visual cortical areas, we recorded from individual neuro

103 pathways and subsequently conveyed to higher visual cortical areas, where it could be integrated with

104 Our results suggest that damage to adult visual cortical areas, whether striate or extrastriate,

105 patially global feature enhancement in early visual-cortical areas, which is obligatory and persists

106 ry corresponds to the isolated activation of visual cortical areas with concurrent deactivation of "i

107 nance imaging (fMRI) to show that many human visual cortical areas, with the exception of VO, can dis