ライフサイエンスコーパス: inferotemporal

1 with the best AUCs were the minimum (0.959), inferotemporal (0.956), average (0.935), superotemporal

2 ommotio retinae, in order of frequency, were inferotemporal (37%), temporal (17%), and superotemporal

3 her the control monkeys nor the monkeys with inferotemporal ablations found acquisition more difficul

4 to consecutively, although the monkeys with inferotemporal ablations found acquisition under both th

5 It is suggested that large inferotemporal ablations in monkeys produce a visual agn

6 Inferotemporal ablations in the New World monkey, the co

7 uggests that the severe impairment caused by inferotemporal ablations on concurrent learning measured

8 the hippocampal formation were added to the inferotemporal ablations, a further impairment on retent

9 nemonic, to discrimination performance after inferotemporal ablations.

10 Here we show that this effect occurs because inferotemporal acetylcholine facilitates recovery of fun

11 lion cell/inner plexiform layer thickness at inferotemporal and inferonasal macular sectors (rho = 0.

12 tivity in higher-order prefrontal, parietal, inferotemporal and lateral occipital areas supports visu

13 In contrast, regions of the inferotemporal and parietal cortex were selectively tune

14 eceptor subunit, NMDAR1, was investigated in inferotemporal and prefrontal association neocortices of

15 All of them (except the rostral inferotemporal and superior temporal gyrus cortices) are

16 rhages and disinsertions were located in the inferotemporal and superotemporal sectors.

17 (nasal, superonasal and temporal) and 0.89 (inferotemporal), and macular between 0.56 (nasal) and 0.

18 cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the superior tempora

19 Regions in the lateral-occipital, inferotemporal, and parahippocampal cortices showed stro

20 ina, biopsy specimens were obtained from the inferotemporal arcade region, approximately 2 mm from th

21 elective modulation of this language-related inferotemporal area for the maintenance of words is acco

22 Maintenance activity in this inferotemporal area showed an effect of memory load for

23 pond to the dorsal and the ventral posterior inferotemporal areas (PITd and PITv, respectively) as id

24 ower superior temporal, and dorsal posterior inferotemporal areas.

25 hout all cell-dense layers of prefrontal and inferotemporal association cortex.

26 rt that neurons in prefrontal, parietal, and inferotemporal association cortices show robust sustaine

27 ntal cells that receive inputs from anterior inferotemporal cells, and medial orbitofrontal cells tha

28 ng the fusiform face area (FFA) and anterior inferotemporal cortex (aIT), whose roles in the process

29 his idea, we recorded from neurons in monkey inferotemporal cortex (IT) and assessed visual search pe

30 omputations, we recorded neural responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) a

31 ual targets, we recorded neural responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) a

32 Neurons in primate inferotemporal cortex (IT) are clustered into patches of

33 owever, whereas neuronal responses in monkey inferotemporal cortex (IT) can show robust tolerance to

34 ly inhibits visual object representations in inferotemporal cortex (IT) during reversal learning by s

35 ces, scrambled faces, and objects in macaque inferotemporal cortex (IT) from 1 month to 2 years of ag

36 Inferotemporal cortex (IT) has long been studied as a si

37 refrontal cortex (PFv+o) in 1 hemisphere and inferotemporal cortex (IT) in the other, thus completing

38 Inferotemporal cortex (IT) is believed to be directly in

39 nvolved in visual spatial selection, and the inferotemporal cortex (IT), which is involved in object

40 imensional shape responses in macaque monkey inferotemporal cortex (IT).

41 object part integration in macaque posterior inferotemporal cortex (IT).

42 sual pathway, which in monkeys culminates in inferotemporal cortex (IT).

43 tion in primates is thought to depend on the inferotemporal cortex (IT).

44 macaque visual cortex, including V2, V4, and inferotemporal cortex (IT).

45 a correlate and possible mechanism in monkey inferotemporal cortex (IT).

46 el of the primate ventral visual stream [the inferotemporal cortex (IT)], both properties are highly

47 es appear in fixed sequence, then neurons of inferotemporal cortex (ITC) come to exhibit prediction s

48 dorsal stream and, surprisingly, also in the inferotemporal cortex (ITC) in the ventral visual stream

49 al posterior parietal area (VPP), and caudal inferotemporal cortex (ITc), but these connections were

50 al stream areas V4d and the dorsal posterior inferotemporal cortex (PITd) did.

51 t than expected from direct projections from inferotemporal cortex [16, 18].

52 microstimulation of face patches in macaque inferotemporal cortex affects perception of faces and ob

53 For example, the primate inferotemporal cortex also contains a set of body-select

54 ng extrastriate visual cortex extending into inferotemporal cortex and left dorsal prefrontal cortex,

55 high-order visual processing regions in the inferotemporal cortex and posterior parietal cortex, hig

56 d) critically depends on a circuit involving inferotemporal cortex and the ANC.

57 e-FPs are indeed generated in the underlying inferotemporal cortex and volume-conducted to the audito

58 t is commonly thought that neurons in monkey inferotemporal cortex are conjunction selective--that a

59 Regions of the left inferotemporal cortex are involved in visual word recogn

60 inds that separate populations of neurons in inferotemporal cortex code for perceptual predictions an

61 scheme is extended by existing reports that inferotemporal cortex connects to the caudomedial pole o

62 Here we show that the macaque inferotemporal cortex contains face-selective cells that

63 the population of single units recorded from inferotemporal cortex during these same trials.

64 The powerful neural representations found in Inferotemporal cortex form a remarkably rapid and robust

65 single-unit electrophysiology recordings in inferotemporal cortex in monkeys and fMRI studies of obj

66 These results demonstrate an involvement of inferotemporal cortex in verbal working memory and provi

67 Primate inferotemporal cortex is subdivided into domains for bio

68 responsive pattern-selective neurons in the inferotemporal cortex of macaque monkeys responded more

69 d by cooling of the topologically equivalent inferotemporal cortex of monkeys and provides evidence t

70 in neurons in the ventral pathway leading to inferotemporal cortex of monkeys.

71 he fact that depletion of acetylcholine from inferotemporal cortex on its own has no effect on episod

72 coeruleus, and dorsal raphe nuclei, but not inferotemporal cortex or cerebellum of AD cases.

73 in high-level object cortex (macaque monkey inferotemporal cortex or IT).

74 tivated the lateral cerebellum and the right inferotemporal cortex relative to age-matched controls (

75 in the strength with which neurons in monkey inferotemporal cortex respond to it.

76 odel consistent with physiological data from inferotemporal cortex that accounts for this complex vis

77 en monitored the responses of neurons in the inferotemporal cortex to image sequences that obeyed or

78 Thus, stimulus-specific adaptation in inferotemporal cortex units is not required for recognit

79 extra-retinal origin, in medial temporal and inferotemporal cortex with each saccade (even in the dar

80 face-selective area exists in human anterior inferotemporal cortex, comprising the apparent homologue

81 ted by prior depletion of acetylcholine from inferotemporal cortex, despite the fact that depletion o

82 , and curvature preferences: for example, in inferotemporal cortex, face- and curvature-preferring do

83 Areas TE and TEO of the inferotemporal cortex, portions of the superior temporal

84 the absence of acetylcholine innervation to inferotemporal cortex, this recovery is impaired and the

85 a given area, such as visual area V4 or the inferotemporal cortex, tolerance has been found to be in

86 In the underlying inferotemporal cortex, we found polarity inversions of t

87 orded from face-selective neurons in macaque inferotemporal cortex, while presenting a face-like coll

88 domain formation in stereotyped locations in inferotemporal cortex, without requiring category-specif

89 five visual areas--V1, V2, V3A, MT, and the inferotemporal cortex.

90 tex in one hemisphere from the contralateral inferotemporal cortex.

91 of input to the basal ganglia is area TE, in inferotemporal cortex.

92 mplex stimulus configurations in the macaque inferotemporal cortex.

93 that are largely separated within the monkey inferotemporal cortex.

94 jects normally represented in other parts of inferotemporal cortex.

95 sights into the organizing principles of the inferotemporal cortex.

96 ed over a large portion of the occipital and inferotemporal cortex.

97 n from posterior to anterior face patches in inferotemporal cortex.

98 emotor cortex, inferior parietal cortex, and inferotemporal cortex.

99 es in the hippocampus, amygdala and anterior inferotemporal cortex.

100 eas within the superior temporal sulcus, and inferotemporal cortex.

101 frontal gyri and decreased activity in right inferotemporal cortical areas.

102 We apply the method to recordings of inferotemporal cortical neurons of primates presented wi

103 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal cortices (area TE, n = 5), plus one addit

104 ocaudal intraparietal, ventral premotor, and inferotemporal cortices.

105 e patch (PL) is located within the posterior inferotemporal dorsal (PITd) retinotopic area.

106 ield development occurs predominately in the inferotemporal field.

107 d a presumably more bilateral or right-sided inferotemporal/fusiform object recognition network, whic

108 ior, superonasal, inferonasal, inferior, and inferotemporal GCIPL.

109 or temporal sulcus (STSv) and dorsal/ventral inferotemporal gyrus (TEd, TEv).

110 microelectrode studies, and on the posterior inferotemporal gyrus.

111 view adaptation, we studied the responses of inferotemporal (IT) cortex neurons before and after face

112 ultielectrodes from visual areas V2, V4, and inferotemporal (IT) cortex of two macaque monkeys during

113 cent discovery of "color patches" in macaque inferotemporal (IT) cortex, the part of the brain respon

114 ation of category-specific subregions in the inferotemporal (IT) cortex.

115 es to parts of images and to whole images in inferotemporal (IT) cortex.

116 Inferotemporal (IT) neurons are known to exhibit persist

117 activity in higher-level, category-selective inferotemporal (IT) visual areas.

118 al magnetic resonance imaging to localize an inferotemporal language area and to demonstrate that thi

119 re 2 incidents of conjunctival erosion and 1 inferotemporal macula-on retinal detachment, which were

120 The inferotemporal meridian (324 degrees -336 degrees ) 2.0

121 obal and regional (temporal, superotemporal, inferotemporal, nasal, superonasal, and inferonasal) BMO

122 Inferotemporal neurons exhibited a transitional surprise

123 Our findings embed adaptation effects of inferotemporal neurons into the context of a broader neu

124 Inferotemporal neurons responded more strongly to famili

125 Inferotemporal neurons signal the global content of a hi

126 ellular projections linking early visual and inferotemporal object recognition regions with the orbit

127 ce was explained by a single pattern showing inferotemporal, (para-)hippocampal, and cerebellar loadi

128 human anteroventral temporal areas including inferotemporal, perirhinal, and entorhinal cortices.

129 ory we tested rhesus monkeys with prefrontal-inferotemporal (PFC-IT) cortical disconnection on two re

130 4 (V4) with occipital visual area 2 (V2) and inferotemporal posterior inferotemporal ventral area (PI

131 ter proportion of guttae were present in the inferotemporal quadrant of the cornea (P < 0.001), an ef

132 nferonasal, superonasal, superotemporal, and inferotemporal quadrant, respectively.

133 The superonasal and inferotemporal quadrants were involved in 341 (40%) and

134 were seen between superonasal VF cluster and inferotemporal RA (R(2) = 0.16) in dB scale or RNFL thic

135 een superonasal VF cluster (in dB scale) and inferotemporal RA (R(2) = 0.26, 95% CI: 0.15-0.40) or in

136 l sulcus (areas MT, MST, FST, V4t, and IPa), inferotemporal region (areas TEO and TE1-TE3), and parah

137 ignificant increase in guttae density in the inferotemporal region (P = 0.016) was observed, a patter

138 Area TL receives afferents from the inferotemporal region including visual areas TE1 and TE2

139 hypothesis that the amygdala and associated inferotemporal regions are involved in the integration o

140 This activation pattern matched lateral inferotemporal regions classically associated with visua

141 of six eyes, and equatorial superonasal, and inferotemporal regions of a further six eyes.

142 Fundoscopy of the RE revealed a chronic inferotemporal retinal detachment and peripheral neovasc

143 poral RA (R(2) = 0.26, 95% CI: 0.15-0.40) or inferotemporal RNFL thickness (R(2) = 0.24, 95% CI: 0.13

144 inear and logarithmic associations) to 0.26 (inferotemporal RNFL, superonasal VF; logarithmic associa

145 RNFL, nasal VF; linear association) to 0.38 (inferotemporal RNFL, superonasal VF; logarithmic associa

146 RNFL, nasal VF; linear association) to 0.21 (inferotemporal RNFL, superonasal VF; logarithmic associa

147 onships generally were strongest between the inferotemporal RNFL-optic disc sector and the superonasa

148 In the peripapillary region, the inferotemporal sector exhibited the highest tensile stra

149 with visible RNFL defects were inferior and inferotemporal sectors, followed by superior and superte

150 istribution in the temporal, superotemporal, inferotemporal, superonasal, and inferonasal fields was

151 mages in the HL revealed the superotemporal, inferotemporal, superonasal, and inferonasal major choro

152 emporal, and nasal regions and higher in the inferotemporal, superonasal, and inferonasal regions.

153 or six RNFL/optic disc regions (inferonasal, inferotemporal, temporal, superotemporal, superonasal, a

154 Extramacular commotio occurs mostly in an inferotemporal to temporal location, consistent with dir

155 relationship ranged from moderate (r = 0.45, inferotemporal) to nonexistent (r = 0.01, temporal).

156 ual area 2 (V2) and inferotemporal posterior inferotemporal ventral area (PITv) was investigated thro

157 imulus-evoked activity in category-selective inferotemporal visual areas, and that these modulations

158 a input to the spatial attention network and inferotemporal visual areas, facilitating the rapid dete

159 Results show that amygdala and inferotemporal visual cortex differentiate emotional fro