ライフサイエンスコーパス: temporoparietal

1 ability statistically comparable to that of temporoparietal (18)F-FDG glucose metabolism.

2 volume in orbitofrontal, cingulate, insular, temporoparietal and cerebellar cortex, and with a more l

3 Brain glucose metabolism in temporoparietal and frontal brain regions was measured u

4 HO-connected network, encompassing bilateral temporoparietal and frontal brain regions, and metabolic

5 aque deposition and neurodegeneration within temporoparietal and hippocampal regions may indicate inc

6 (GMV) in developmental dyslexia in bilateral temporoparietal and left occipitotemporal cortical regio

7 Elevated posterior temporoparietal and occipital AV-1451 uptake in probable

8 rebellum, posterior brainstem, and posterior temporoparietal and occipital brain regions.

9 had greater AV-1451 uptake in the posterior temporoparietal and occipital cortex compared to clinica

10 HIV-1-infected subjects, involving the left temporoparietal and right parietal cortices and bilatera

11 ell as multimodal association regions of the temporoparietal and temporo-occipito-parietal junction,

12 [11C](R)-PK11195 binding in the entorhinal, temporoparietal, and cingulate cortex.

13 rTMS applied at the right temporoparietal area was not superior to sham treatment.

14 rTMS applied at the left temporoparietal area with a frequency of 1 Hz yielded a

15 rTMS, especially when applied at the left temporoparietal area with a frequency of 1 Hz, is effect

16 efrontal cortex or regions in and around the temporoparietal area; this condition, which transcends t

17 rhythm amusia and in posterior temporal and temporoparietal areas in pitch amusia.

18 e brain surface were detected in frontal and temporoparietal areas in the BN compared with control pa

19 These analyses showed that neuronal loss in temporoparietal areas, traditionally included within Wer

20 nd white matter volume in the left and right temporoparietal as well as the left inferior frontal bra

21 ignificant grey matter loss, whereas lateral temporoparietal association cortex displayed both signif

22 widespread pattern of GM loss involving the temporoparietal association cortices and the medial temp

23 lvement of the medial temporal lobes and the temporoparietal association cortices and, for the first

24 trophy was associated with tau mutations and temporoparietal atrophy was associated with progranulin

25 ms, and more focal pattern of left posterior temporoparietal atrophy.

26 Furthermore, left occipitotemporal and temporoparietal brain activity correlates positively wit

27 (-)), in bilateral occipitotemporal and left temporoparietal brain regions.

28 A temporoparietal-brainstem network was coherent with the

29 Temporoparietal CBV was reduced even in mildly affected

30 Temporoparietal cerebral blood volume, expressed as a pe

31 Grey matter volumes in right temporoparietal clusters were greater in stroke survivor

32 sal pathways in semantic variant, and in the temporoparietal component of the dorsal bundles in logop

33 th fractional anisotropy altered only in the temporoparietal component of the dorsal pathway.

34 ted across electrodes, revealing frontal and temporoparietal components for latency and amplitude, re

35 cortical atrophy sites variably encompassing temporoparietal components of Wernicke's area, Broca's a

36 amarginal, frontoangular, frontotemporal and temporoparietal components, (referred to as the dorsal p

37 ferences, (B) modulated to a large extent by temporoparietal connectivity, and (C) accompanied by bra

38 id histology: 15.1%+/-1.5%), followed by the temporoparietal cortex (11C-PIB BPND: 0.75+/-0.08; amylo

39 ses in the P(i)/beta-ATP ratio were found in temporoparietal cortex (P = 0.002 right and P = 0.014 le

40 of the midbrain, substantia innominata (SI), temporoparietal cortex and hippocampus between the group

41 reas in CBS due to AD, atrophy extended into temporoparietal cortex and precuneus (p < 0.001 uncorrec

42 ion and motor intention task, with the right temporoparietal cortex being involved during spatial att

43 sets and offsets of the stimuli, whereas the temporoparietal cortex exhibited sustained activity thro

44 The temporoparietal cortex has been directly implicated in d

45 th a relative sparing of the hippocampus and temporoparietal cortex is, therefore, suggestive of DLB

46 s, grey matter volumes in parts of the right temporoparietal cortex positively related to spontaneous

47 ominantly posterior set of regions including temporoparietal cortex showed reduced source activity 25

48 of 4-day administration of 1-Hz rTMS to left temporoparietal cortex were superior to those of sham st

49 es), visuospatial function (occipital, right temporoparietal cortex) and language (left > right tempo

50 oparietal cortex) and language (left > right temporoparietal cortex).

51 received a 10-day TMS treatment to the left temporoparietal cortex, and 15 received the standard tre

52 etabolism, mostly in the left prefrontal and temporoparietal cortex, and areas of decreased metabolis

53 Two structures in left temporoparietal cortex, angular gyrus (AG) and posterior

54 s suggest that posterior cortex, perhaps the temporoparietal cortex, calculates and represents the pe

55 ng such displays evokes strong activation in temporoparietal cortex, including areas in and near the

56 oth patient groups, mainly involving lateral temporoparietal cortex, precuneus, posterior cingulate c

57 In the right temporoparietal cortex, there was also a significant inc

58 hitectonically defined areas of parietal and temporoparietal cortex, with emphasis on areas in the in

59 c changes in right parahippocampal gyrus and temporoparietal cortex.

60 anism of AHs involves activation of the left temporoparietal cortex.

61 l language comprehension regions in the left temporoparietal cortex.

62 potential evolutionary advances of enhanced temporoparietal cortical connections with the laryngeal

63 In summary, temporoparietal cortical hypometabolism was seen in non-

64 bes, but also showed posterior cingulate and temporoparietal cortical losses at presymptomatic stage.

65 ls, with posterior cingulate and neocortical temporoparietal cortical losses, and medial temporal-lob

66 hological studies implicate both frontal and temporoparietal cortices when humans reason about the me

67 n BN in tracts extending through frontal and temporoparietal cortices, especially in those with the m

68 (PiB-PET), usually affecting prefrontal and temporoparietal cortices, with less occipital involvemen

69 Temporoparietal eDED or ePiB brain perfusion measurement

70 AP subtypes displayed better preservation of temporoparietal FDG metabolism (mean [SD] FDG: Abeta-N+,

71 disease-associated neurodegeneration status (temporoparietal glucose metabolism determined by fluorod

72 Spectra were acquired from midfrontal and temporoparietal gray matter with a double spin-echo sequ

73 The results indicate highly significant temporoparietal gyral asymmetries in both diagnostic gro

74 mispheres, respectively) and correlated with temporoparietal gyrification differences, classified via

75 e focal and varied by PPA subtype, with left temporoparietal hypometabolism in LPA, left frontal hypo

76 biomarkers, namely hippocampal volume loss, temporoparietal hypometabolism, and neocortical beta-amy

77 ntal (ICCU = 0.18; P =.04; lambda = 3.4) and temporoparietal (ICCU = 0.24; P =.01; lambda = 1.7) P300

78 grey matter volume loss, with more extensive temporoparietal involvement in the early-onset group, an

79 was found after virtual lesions to the left temporoparietal junction (control site).

80 idence that neural computations in the right temporoparietal junction (rTPJ) and interconnected struc

81 cal evidence suggesting a role for the right temporoparietal junction (RTPJ) in belief attribution.

82 we show the causal involvement of the right temporoparietal junction (rTPJ) in updating probabilisti

83 Here, we provide evidence that the right temporoparietal junction (rTPJ) is causally involved in

84 Moreover, activity in the right temporoparietal junction (RTPJ) reflects only ES and cor

85 Here, we test the hypothesis that the right temporoparietal junction (RTPJ), an area involved in men

86 igher-order computational nodes in the right temporoparietal junction (rTPJ), right dorsolateral and

87 ponse to accordance with others in the right temporoparietal junction (rTPJ).

88 level processing because the left posterior temporoparietal junction (TP) emphasizes processing of l

89 h this task was found bilaterally within the temporoparietal junction (TPJ) among other areas.

90 target determined BOLD responses in the left temporoparietal junction (TPJ) and inferior frontal gyru

91 entral frontoparietal network comprising the temporoparietal junction (TPJ) and ventral frontal corte

92 others, are associated with activity in the temporoparietal junction (TPJ) area.

93 gest cluster of activity was obtained in the temporoparietal junction (TPJ) bilaterally.

94 ial direct current stimulation (tDCS) of the temporoparietal junction (TPJ) has previously been shown

95 The temporoparietal junction (TPJ) is a key node within the

96 The human temporoparietal junction (TPJ) is a topic of intense res

97 However, although rarely emphasized, the temporoparietal junction (TPJ) is frequently recruited d

98 eye fields (FEFs), intraparietal sulcus, and temporoparietal junction (TPJ) of both hemispheres showe

99 get-evoked activation increases in the right temporoparietal junction (TPJ) of the ventral attentiona

100 ked high-frequency gamma oscillations in the temporoparietal junction (TPJ), a brain region associate

101 The right temporoparietal junction (TPJ), a core region of the ven

102 poral correlation between vPMC and the right temporoparietal junction (TPJ), a region strongly implic

103 e anterior cingulate cortex (ACC), thalamus, temporoparietal junction (TPJ), and areas near or along

104 istent group of brain regions: the bilateral temporoparietal junction (TPJ), medial prefrontal cortex

105 Right temporoparietal junction (TPJ), the posterior core of a

106 ngaged ventral parietal cortex-specifically, temporoparietal junction (TPJ)-and was also more active

107 evoked right-hemisphere dominant activity in temporoparietal junction (TPJ).

108 We found that generous choices engaged the temporoparietal junction (TPJ).

109 sponses in the anterior insula (AI) (but not temporoparietal junction [TPJ]) encoded trial-wise empat

110 increased right supplementary motor area and temporoparietal junction activity.

111 orrelated with emotional appraisals, whereas temporoparietal junction and dorsomedial prefrontal cort

112 correlation between activation in the right temporoparietal junction and expected payoff that was ab

113 gical characteristics between groups, in the temporoparietal junction and its connection with the ven

114 ized to right lateral parietal cortex in the temporoparietal junction and long-term memory (LTM) retr

115 g left superior temporal and parietal lobes, temporoparietal junction and paracentral lobule, right s

116 A separate network, including right temporoparietal junction and parahippocampal gyrus, was

117 highlighted the role of connectivity of the temporoparietal junction as a multimodal area crucial fo

118 that includes both of these regions and the temporoparietal junction bilaterally is involved in proc

119 This suggests that the right temporoparietal junction contributes to controlling sele

120 We found that activation levels in the right temporoparietal junction correlate with the sensory repr

121 Second, only patients with temporoparietal junction damage showed a congruent under

122 e left superior frontal cortex and bilateral temporoparietal junction in both groups, with additional

123 sk, we did not find functional evidence of a temporoparietal junction in macaques.

124 This suggests that the right temporoparietal junction is involved in controlling atte

125 o involvement of the frontal lobes, the left temporoparietal junction is necessary for reasoning abou

126 ity, we found that variability in insula and temporoparietal junction is reflected in reaction time v

127 icits in timing and spatial orientation with temporoparietal junction lesions could be functionally l

128 ld be functionally linked, implying that the temporoparietal junction may act as a cortical temporal

129 to indicate synchronized flow between right temporoparietal junction networks (previously shown to h

130 Third, despite clear evidence of the temporoparietal junction node of the ventral attention n

131 ity; in that directional influences from the temporoparietal junction on the frontal eye fields and t

132 ation) and position perception, seen only in temporoparietal junction patients, may reflect a common

133 sterior inferior temporal and left and right temporoparietal junction regions (controls more than pat

134 location distinct from activations in right temporoparietal junction reported in previous social cog

135 d, only the four patients with damage to the temporoparietal junction showed impaired spatial orienta

136 may reflect a common neural substrate in the temporoparietal junction that mediates the encoding of m

137 visual-target presentation, but in the right temporoparietal junction when the target was detected, p

138 ow-frequency 2-4 Hz phase reset in the right temporoparietal junction with concurrent increases in lo

139 fective empathy (whereas bilateral damage to temporoparietal junction would be required to disrupt em

140 gions putatively involved in theory of mind (temporoparietal junction), pain processing (anterior ins

141 n (dorsomedial prefrontal cortex, precuneus, temporoparietal junction), respectively.

142 nd body schema (supplementary motor area and temporoparietal junction).

143 plicated previously in social cognition (the temporoparietal junction).

144 tivation than both other groups in the right temporoparietal junction, a cluster that also demonstrat

145 ude of sustained BOLD responses in the right temporoparietal junction, a core region of the ventral a

146 the medial prefrontal and parietal cortices, temporoparietal junction, and anterior temporal lobes du

147 errors activation was seen in the striatum, temporoparietal junction, and inferior frontal gyrus.

148 l cortex, posterior superior temporal sulcus/temporoparietal junction, and intraparietal sulcus-and w

149 regions, including the medial temporal lobe, temporoparietal junction, and posterior cingulate/precun

150 prefrontal cortex, anterior cingulate gyrus, temporoparietal junction, and precuneus-represented or u

151 right superior temporal and parietal lobes, temporoparietal junction, and precuneus.

152 l prefrontal cortex, right hippocampus, left temporoparietal junction, and right fusiform gyrus, with

153 me, and neural response in ventral striatum, temporoparietal junction, and ventromedial prefrontal co

154 rontal cortex, inferior parietal lobule, and temporoparietal junction, as well as the insula, cingula

155 was most prominent in the temporal lobe and temporoparietal junction, but extended more broadly into

156 and in the default-mode network (precuneus, temporoparietal junction, medial prefrontal cortex, post

157 s as theory of mind and brain activations in temporoparietal junction, posterior cingulate cortex, an

158 e left dorsolateral prefrontal cortex, right temporoparietal junction, right premotor and right entor

159 s engage a neural network which includes the temporoparietal junction, superior temporal sulcus, and

160 mentalizing network, including the MPFC, the temporoparietal junction, the superior temporal sulcus,

161 attentional reorienting system in the right temporoparietal junction, two additional brain networks

162 sions to any one of these structures, except temporoparietal junction, would cause impaired affective

163 olism bias in the inferior parietal lobe and temporoparietal junction.

164 be and thematic errors localized to the left temporoparietal junction.

165 scrimination selectively activated the right temporoparietal junction.

166 esponse enhancement to visual targets in the temporoparietal junction.

167 right ventral putamen and claustrum and the temporoparietal junction.

168 ion flow between the sender's and receiver's temporoparietal junction.

169 ingulate cortex, temporal pole, amygdala and temporoparietal junction.

170 Right temporoparietal junction/posterior superior temporal sul

171 ls were (1) the existence of left hemisphere temporoparietal language areas outside the traditional "

172 nt function analysis based on left and right temporoparietal measures correctly classified 88.5% of t

173 was intentional; when harm was unintended, a temporoparietal-medial-prefrontal circuit suppressed amy

174 g/mL increase) was associated with increased temporoparietal metabolism (0.005; 95% CI, 0.000-0.010)

175 m (-0.048; 95% CI, -0.067 to -0.029) but not temporoparietal metabolism (0.010; 95% CI, -0.010 to 0.0

176 e association of greater WMHs with increased temporoparietal metabolism (0.051; 95% CI, 0.027-0.076).

177 he positive association of greater WMHs with temporoparietal metabolism suggests that these pathologi

178 ypically associated with focal injury to the temporoparietal or ventral frontal cortex.

179 were significant correlations between right temporoparietal P(i)/beta-ATP ratios and estimated reduc

180 Left temporoparietal P(i)/beta-ATP ratios correlated with ful

181 For the frontal and temporoparietal P300 amplitude and latency components, t

182 iblings showed significant reductions in the temporoparietal P300 amplitude component.

183 Temporoparietal P300 amplitude reduction and frontal P30

184 ility of event-related potential frontal and temporoparietal P300 changes as intermediate phenotypes

185 In contrast, temporoparietal (posterior segment) connections are righ

186 s disease presentations are distinguished by temporoparietal-predominant atrophy.

187 by additional blood flow increases in a left temporoparietal region previously implicated in the rete

188 related with gray matter volumes in the left temporoparietal region, whereas DB scores correlated wit

189 tal region, but MI was elevated (+8%) in the temporoparietal region.

190 ienced outcomes, whereas lateral frontal and temporoparietal regions adapted to observed social outco

191 ienced outcomes, whereas lateral frontal and temporoparietal regions adapted to observed social outco

192 ontrols revealed marked atrophy in bilateral temporoparietal regions and only limited atrophy in the

193 hey also shared cortical atrophy of the left temporoparietal regions and precuneus (P < .05, family-w

194 jor depression group showed abnormalities in temporoparietal regions associated with orienting to une

195 man brain regions composed of prefrontal and temporoparietal regions have been associated with stimul

196 atrophy, and asymmetric involvement of left temporoparietal regions in logopenic variant primary pro

197 ter volume reduction in the left frontal and temporoparietal regions was consistent with left frontot

198 ied primarily in posterior cortex, including temporoparietal regions, extending into occipital and ce

199 or frontoinsular, anterior temporal and left temporoparietal regions, respectively.

200 In temporoparietal regions, significant gyral asymmetries w

201 the classic pattern of hypometabolism in the temporoparietal regions.

202 from the left anterior temporal to the left temporoparietal regions.

203 ng-range connections between the frontal and temporoparietal regions.

204 451 retention in medial temporal and lateral temporoparietal regions.

205 eech sound categorization: they suggest that temporoparietal responses in passive paradigms such as t

206 with greater N2 amplitude at left than right temporoparietal sites.

207 visual memory test, followed by time-varying temporoparietal thickness (standardized beta = 0.21, P =

208 sburgh compound B uptake was associated with temporoparietal thinning, which correlated with memory d

209 t self-awareness and agency, mediated by the temporoparietal (TPJ) area and the prefrontal cortex, ar

210 te deactivation, whereas OCD patients showed temporoparietal underactivation.

211 so been linked to normal variability of left temporoparietal white matter volume connecting the middl

212 ecreased diffusion anisotropy bilaterally in temporoparietal white matter.