ライフサイエンスコーパス: striate cortex

1 on areas, but not to a primary sensory area (striate cortex).

2 nucleus (LGN) and primary visual cortex (V1, striate cortex).

3 al frequency) are mapped onto the surface of striate cortex.

4 sory area, first temporal cortical area, and striate cortex.

5 new insights into the local organization of striate cortex.

6 cally across the different layers of the cat striate cortex.

7 gnificantly correlated with decreases in the striate cortex.

8 dulation of visual processing in the primate striate cortex.

9 allosal axons in anomalous places within the striate cortex.

10 g 225 microns in width, was found throughout striate cortex.

11 change the width of the callosal zone in the striate cortex.

12 oxidase (CO)-rich puffs of the adult monkey striate cortex.

13 osally projecting cells in the contralateral striate cortex.

14 the projection of the visual field upon the striate cortex.

15 on the first stage of cortical processing in striate cortex.

16 ional selectivity (DS) is first exhibited in striate cortex.

17 orted tracers into different loci of lateral striate cortex.

18 Remapping was very rare in striate cortex.

19 of rat area 17 and pyramidal cells in monkey striate cortex.

20 el, we record from binocular simple cells in striate cortex.

21 rom geniculocortical recipient layers of the striate cortex.

22 aracteristics of the callosal pathway in cat striate cortex.

23 extensive lesion of the corresponding (left) striate cortex.

24 lation-based computation that takes place in striate cortex.

25 al of those areas, including primary visual (striate) cortex.

26 conditions did not differ in the calcarine (striate) cortex.

27 gulated by neuronal activity in adult monkey striate cortex; 2) GABA-IR neurons are much more vulnera

28 mary visual area 17 abnormalities in rostral striate cortex, a region contributing to the dorsal visu

29 ocular disparity through simple cells in the striate cortex: a difference in receptive field (RF) pos

30 brane potential, 78% (45/58) of the cells in striate cortex activated by feedback input showed monosy

31 his fraction was less than the proportion of striate cortex allocated to the representation of the ce

32 rmally associated with vision, including the striate cortex along with frontal and parietal cortical

33 On the other hand, many neurons in striate cortex and a small fraction in the LGN responded

34 ength of long-range correlation between left striate cortex and Broca's area.

35 space-time RF structure of cells in macaque striate cortex and found two subpopulations of (nondirec

36 r of investigations of cortical areas beyond striate cortex and has addressed more complex behavioura

37 such as areas MT and MST) which bypasses the striate cortex and is specialized for analysing 'fast' m

38 ar-related stimuli independently of both the striate cortex and normal phenomenal visual awareness.

39 ons (Wernicke's area, the angular gyrus, and striate cortex) and relative overactivation in an anteri

40 of NRF-2 (NRF-2 alpha) with CO in the monkey striate cortex, and that it can be regulated by neuronal

41 linear manner, although the LGN input to the striate cortex, and the cortical network itself, are hig

42 ng from restricted loci in medial, acallosal striate cortex, and the overall pattern of callosal conn

43 t to be generated in the developing ferret's striate cortex, and, in mature animals, these cells have

44 ished that humans and monkeys with damage to striate cortex are able to detect and localize bright ta

45 hat retinal pathways other than those to the striate cortex are crucially involved in vision.

46 tems of the retina that provide input to the striate cortex are now well described, although certain

47 Pyramidal neurons in layer VI of striate cortex are the source of descending projections

48 ated intrinsic horizontal connections within striate cortex (area V1) of normal and strabismic, adult

49 blindsight, which results from damage to the striate cortex (area V1) of the brain that is sufficient

50 The earliest activity in striate cortex (area V1) was not modulated by contextual

51 y represented in the responses of neurons in striate cortex as part of a neural representation of obj

52 tuning widths of orientation-tuned cells in striate cortex as well as the distribution of oriented e

53 redict the internal, retinotopic function of striate cortex as well.

54 indicated that the initial sensory input to striate cortex at 50-55 milliseconds after the stimulus

55 t and motion; the failure of response in the striate cortex at high but not low frequencies in the Al

56 Reports showing that activity in striate cortex can be dissociated from awareness , where

57 color responses of a large subpopulation of striate cortex cells.

58 t posterior cingulate cortex, lingual gyrus, striate cortex, cerebellar vermis, and left thalamus.

59 otor areas, cingulate sulcus, temporal lobe, striate cortex, cerebellum, thalamus and basal ganglia.

60 In normal rats callosal projections in striate cortex connect retinotopically corresponding, no

61 ated in the superficial and middle layers of striate cortex, consistent with the known anatomy of thi

62 We examined the fine-scale pattern of striate cortex correlations within and between hemispher

63 70% of the total) after damage restricted to striate cortex, could be far more extensive after hemisp

64 Following striate cortex damage in monkeys and humans there can be

65 Simple cells in macaque striate cortex differ in their spatial phases, but evide

66 Next, the retina was warped onto striate cortex, distorting it as necessary to match each

67 We show that correlation-based cells in striate cortex do in fact signal depth here because they

68 s serving each eye segregate in layer IVc of striate cortex during early life into a pattern of alter

69 of striate-extrastriate, but not the size of striate cortex, ends by P6.

70 cortical surface, however, the boundaries of striate cortex fall at a consistent location across indi

71 d to predict the retinotopic organization of striate cortex for an individual with accuracy equivalen

72 ted the right eye and subsequently processed striate cortex for cytochrome oxidase (CO) activity.

73 In primate striate cortex, geniculocortical afferents in layer IVc

74 Disparity selectivity in the striate cortex has generally been studied with uniform d

75 hrome oxidase in patches or blobs of primate striate cortex has never been explained.

76 lumns were reconstructed from flat-mounts of striate cortex in both hemispheres.

77 intracellular recordings from neurons in cat striate cortex in vivo and examined the relationships be

78 of intrinsically bursting pyramidal cells in striate cortex in vivo and the discovery of inhibitory i

79 ding and staining of single cells in the cat striate cortex in vivo, a biophysically distinct class o

80 ate that the recovery after infant damage to striate cortex includes some sensitivity to direction of

81 eral response variables are clustered within striate cortex, including some that have not received mu

82 Functional architecture of the striate cortex is known mostly at the tissue level--how

83 The tree shrew (Tupaia belangeri) striate cortex is reciprocally connected with the dorsal

84 input to the patches in the upper layers of striate cortex is segregated by eye in newborns.

85 Since the striate cortex is the first site along the central visua

86 One of the hallmarks of the primate striate cortex is the presence of cytochrome oxidase (CO

87 Once the visual pathway reaches striate cortex, it fans out to a number of extrastriate

88 rimates but are unique in that sublaminae of striate cortex layer IV respond preferentially to light

89 Three monkeys with unilateral striate cortex lesions sustained in infancy were tested

90 more +S(o) than -S(o) LGN cells, but at the striate cortex level -S(o) input to simple cells is as c

91 included biphasic rising then falling in the striate cortex, linear increase in visual association ar

92 We hypothesize that the striate cortex modulation found with fMRI may represent

93 We conclude that, in monkey striate cortex, more tissue is allocated per ganglion ce

94 properties of this rhythmic activity in the striate cortex of alert cats and to compare this activit

95 vity and tissue oxygen concentrations in the striate cortex of anaesthetized cats while using visual

96 is activity to similar data collected in the striate cortex of anesthetized cats.

97 emporal modulation of binocular disparity in striate cortex of awake monkeys.

98 onous, 20-70 Hz oscillatory responses in the striate cortex of cats that are fully alert and performi

99 labeling in living slices prepared from the striate cortex of ferrets aged 13-35 days postnatal (P13

100 otic evoked responses were recorded from the striate cortex of Long-Evans hooded intact, monocular vi

101 Complex cells in striate cortex of macaque showed a rapid pattern-specifi

102 tial distribution of callosal neurons in the striate cortex of strabismic cats to that in normally re

103 in the lateral geniculate nucleus (LGN) and striate cortex of the macaque monkey.

104 by retinal blood vessels are represented in striate cortex of the squirrel monkey.

105 ound the representations of angioscotomas in striate cortex of the squirrel monkey.

106 at the distribution of callosal cells in the striate cortex of these cats does not differ significant

107 d with linear array multielectrodes from the striate cortex of two macaque monkeys performing an inte

108 lectivity of cells in primary visual cortex (striate cortex or V1) in young adult and very old macaqu

109 in V1 (also known as primary visual cortex, striate cortex, or Brodmann's area 17) was defined in ea

110 extent are spontaneous neural signals within striate cortex organized by vision?

111 on pattern of NRF-2 alpha mRNA in the normal striate cortex paralleled that of CO activity.

112 Lesions of striate cortex [primary visual cortex (V1)] in adult pri

113 rocedures are used, implying that lesions of striate cortex produce a sharp dissociation between visu

114 In the Pv or the dLGN, striate cortex projections are thought to either strongl

115 rum, we compare the synaptic arrangements of striate cortex projections to the dLGN, Pv, and claustru

116 opponent path is doubled at the level of the striate cortex, relative to that at the LGN.

117 nization of neurons within a local region of striate cortex remains unclear.

118 Attention-induced rate enhancement in striate cortex requires cholinergic mechanisms.

119 Simple cells in the striate cortex respond to visual stimuli in an approxima

120 Studies of callosal projections in striate cortex show that the retina is involved in the d

121 Some striate cortex simple cells also give linear responses,

122 vs. L + M cones (S(o) cells), relatively few striate cortex simple cells show chromatic responses alo

123 of direct subcortical inputs that may bypass striate cortex, such as input to V5/MT+.

124 The striate cortex terminals were largest in the Pv (0.94 +/

125 Aergic terminals (0.34 +/- 0.01 mum(2) ) and striate cortex terminals were not significantly differen

126 or source of axon terminals in the layers of striate cortex that receive LGN projections.

127 trastriate visual cortex produced effects in striate cortex that were relatively weak, generally supp

128 vels examined were the optic radiations, the striate cortex, the inferior parietal lobule, and the fu

129 Extracellular recordings were made in striate cortex, the lateral geniculate nucleus (LGN), an

130 ome patients with brain damage affecting the striate cortex, though clinically blind in their field d

131 rgic receptor proteins m1 to m4 were used in striate cortex tissue of normal rhesus monkeys to determ

132 geniculocortical terminals in the tree shrew striate cortex to compare directly the characteristics o

133 rbors of layer 6 pyramidal neurons in ferret striate cortex to determine whether early developing axo

134 conducted acute recording experiments in cat striate cortex to evaluate the recording capabilities of

135 we characterize the responses of neurons in striate cortex to stationary grating patterns presented

136 ponses of binocular complex cells in the cat striate cortex to stimuli of various intra- and interocu

137 d right eye RFs of simple cells in the cat's striate cortex using binary m-sequence noise, and then w

138 ally, and connectionally distinct areas: the striate cortex (V1) and the extrastriate cortex, consist

139 -field (7 T) fMRI, we find that responses in striate cortex (V1) best reflect stimulus position in th

140 ucted from flat-mounts of the left and right striate cortex (V1) in six normal adult macaques (Macaca

141 columns (ODCs) have been well studied in the striate cortex (V1) of macaques, as well defined arrays

142 ubjects with complete destruction of part of striate cortex (V1) retain extensive visual capacities w

143 emonstrate, however, that neurons in the cat striate cortex (V1) show pronounced adaptation-induced s

144 ic subject with damage largely restricted to striate cortex (V1) sometimes reports being 'aware' of t

145 measured the responses of neurons in macaque striate cortex (V1) to dynamic, translational Glass patt

146 l deprivation induced the columns throughout striate cortex (V1) to retract the same distance from th

147 corticogeniculate feedback pathway from the striate cortex (V1) to the lateral geniculate nucleus (L

148 sal lateral geniculate nucleus (dLGN) target striate cortex (V1), a small number project instead to e

149 area (MT): namely, a direct projection from striate cortex (V1), and a set of indirect projections t

150 macaque monkeys with longstanding lesions of striate cortex (V1), sustained in infancy, could discrim

151 In striate cortex (V1), the frontal eye fields (FEF), and t

152 e shown that geniculate synapses are lost in striate cortex (V1).

153 area V5 depends on the amount of activity in striate cortex (V1).

154 on of directionally selective neurons in the striate cortex (V1).

155 tients with lesions to their primary visual (striate) cortex (V1) demonstrate residual visual capacit

156 after damage to a portion of primary visual (striate) cortex, V1.

157 A mean of 53.1% of striate cortex was devoted to the representation of the

158 distribution of lateral interactions within striate cortex was visualized with optical recording, an

159 ions of biocytin into layer VI of tree shrew striate cortex, we identified two sublayers that differ

160 Only in striate cortex were cells found that had responses corre

161 significant alterations in activation in the striate cortex were found.

162 Alternate sections from flat-mounts of striate cortex were then processed either for autoradiog

163 analysis of visual motion takes place in the striate cortex, where directionally selective cells are

164 visual processing is assumed to originate in striate cortex, where single cells exhibit a refinement

165 iculate (LG) nucleus specifically innervates striate cortex, whereas pulvinar projections are confine

166 rded from single neurons in extrastriate and striate cortex while monkeys performed a saccade task.

167 the retina and cortical simple cells in the striate cortex with overlapping receptive fields and eva

168 etween the contralateral and the ipsilateral striate cortex with relation to the MD eye.