ライフサイエンスコーパス: visual cortical area

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

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

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

4 port specialized perceptual roles for higher visual cortical areas.

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

6 sequential replay of multistep sequences in visual cortical areas.

7 wn influence on sensory responses in primate visual cortical areas.

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

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

10 ionship between connectivity and function in visual cortical areas.

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

12 receive prominent inputs from virtually all visual cortical areas.

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

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

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

16 or driving the functional differentiation of visual cortical areas.

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

18 of these projections to the pulvinar across visual cortical areas.

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

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

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

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

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

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

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

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

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

28 r responsiveness to relative depth in higher visual cortical areas, again consistent with the finding

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

30 V4 is extensively interconnected with other visual cortical areas along the ventral and dorsal visua

31 t learned value modulates spatial signals in visual cortical areas, an effect that correlates with VD

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

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

34 We conclude that early visual cortical areas and DNN layers deploy different ge

35 to deficits arising from alterations in all visual cortical areas and even in nonvisual cortical reg

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

37 n offsets that presumably originate in early visual cortical areas and then transform these sensory i

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

39 isual responses less than V1 lesions, and no visual cortical area appears to entirely rely on SC inpu

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

41 Visual cortical areas are interconnected via layer-speci

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

43 It is unknown whether early visual cortical areas are necessary for this improvement

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

45 a visual stimulus) affects the activities in visual cortical areas as early as in V1.

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

47 ther such coding fluctuations occur in early visual cortical areas; (b) how coding fluctuations are c

48 at these changes are reflected in high-level visual cortical areas before they become apparent in ear

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

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

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

52 how that visual responses in a mouse lateral visual cortical area called the postrhinal cortex are in

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

54 The results suggest that responses from visual cortical areas can be classified effectively usin

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

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

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

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

59 hat guides the functional differentiation of visual cortical areas during development.

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

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

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

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

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

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

66 measured the concentration of GABA in early visual cortical areas in a time-resolved fashion before,

67 s of neural activity traveling across entire visual cortical areas in awake animals.

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

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

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

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

72 Visual cortical areas in the mammalian brain are linked

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

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

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

76 onse profiles were similar in both motor and visual cortical areas, indicating that LC axons broadcas

77 responses in the postrhinal cortex (POR), a visual cortical area, instead depend on the tecto-thalam

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

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

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

81 gher (motor or associative) areas in primate visual cortical areas is crucial for transforming sensor

82 but its role in modulating activity in early visual cortical areas is less well understood.

83 y unknown how visual information from higher visual cortical areas is translated into such a semantic

84 s of how communication, particularly between visual cortical areas, is instantiated and modulated, hi

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

86 we sought to determine whether higher order visual cortical areas lateromedial (LM), anterolateral (

87 dels suggests that visual responses in early visual cortical areas may be modulated by top-down influ

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

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

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

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

92 vity) are distributed between prefrontal and visual cortical areas, respectively.

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

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

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

96 Visual cortical areas subserve cognitive functions by in

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

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

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

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

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

102 ural prediction accuracy in multiple ventral visual cortical areas that equals or exceeds that of mod

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

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

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

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

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

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

109 uperficial division is primarily linked with visual cortical areas, the amygdala, and the posterior t

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

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

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

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

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

115 ity of these circuits, we first mapped mouse visual cortical areas using intrinsic signal optical ima

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

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

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

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

120 li were present, some neurons in the macaque visual cortical areas V1 and V4 exhibited fluctuating fi

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

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

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

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

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

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

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

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

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

130 First, we identified visual cortical area V4 as one plausible contributor to

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

132 l populations in prefrontal cortex (PFC) and visual cortical area V4 in rhesus macaque monkeys perfor

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

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

135 We recorded from populations of neurons in visual cortical area V4 while two male rhesus macaque mo

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

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

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

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

140 r visual input drives the differentiation of visual cortical areas, we used two-photon calcium imagin

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

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

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

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

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