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 gain control mechanism in striate and extra-striate cortex.

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

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

6 new insights into the local organization of striate cortex.

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

8 gnificantly correlated with decreases in the striate cortex.

9 rom geniculocortical recipient layers of the striate cortex.

10 dulation of visual processing in the primate striate cortex.

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

12 allosal axons in anomalous places within the striate cortex.

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

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

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

16 osally projecting cells in the contralateral striate cortex.

17 ally reshape the tuning of features coded in striate cortex.

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

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

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

21 orted tracers into different loci of lateral striate cortex.

22 Remapping was very rare in striate cortex.

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

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

25 aracteristics of the callosal pathway in cat striate cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 peed and neural activity varies across extra-striate cortex, and is even negative in anterior extra-s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 region in V1 of albino rats includes lateral striate cortex, being therefore about 25% larger in area

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

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

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

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

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

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

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

67 70% of the total) after damage restricted to striate cortex, could be far more extensive after hemisp

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

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

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

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

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

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

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

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

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

77 In primate striate cortex, geniculocortical afferents in layer IVc

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

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

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

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

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

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

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

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

86 passage of ipsilateral eye input to lateral striate cortex, increasing its binocularity.

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

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

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

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

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

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

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

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

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

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

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

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

99 rtex, and is even negative in anterior extra-striate cortex. Nevertheless, across all visual cortices

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 Some striate cortex simple cells also give linear responses,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

147 bino rats, it has been reported that lateral striate cortex (V1) is highly binocular, and that input

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

149 oxidase (CytOx)-rich patches (blobs) in the striate cortex (V1) of normally sighted Homo sapiens.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 s significantly reduced in both V1 and extra-striate cortex, whereas suppressive contributions remain

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

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

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