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1 ates also revealed deactivations in the left angular gyrus.
2 n the left parietal lobule that included the angular gyrus.
3 temporal pole, temporal fusiform cortex, and angular gyrus.
4 fects of memory and content were additive in angular gyrus.
5 a, as well as the inferior frontal gyrus and angular gyrus.
6 ngulate cortex and the intra-parietal sulcus/angular gyrus.
7 pocampus, medial prefrontal cortex, and left angular gyrus.
8 d connectivity between frontal areas and the angular gyrus.
9 ory retrieval, including the hippocampus and angular gyrus.
10 d to the left lateral parietal cortex in the angular gyrus.
11  mesial temporal lobe, precuneus cortex, and angular gyrus.
12 n posterior CA1, parahippocampal cortex, and angular gyrus.
13 nterior and posterior midline structures and angular gyrus.
14 rk, including posterior cingulate cortex and angular gyrus.
15  middle and inferior frontal gyri, and right angular gyrus.
16 eased, particularly with respect to the left angular gyrus.
17 terior piriform cortex to, among others, the angular gyrus, a known multisensory integration area.
18                             In the posterior angular gyrus, a neural priming effect was observed for
19 or parietal lobule that was localized to the angular gyrus, a structure belonging to the heteromodal
20                                          The angular gyrus accounted for this difference in asymmetry
21                                   We suggest angular gyrus activation reflects the experiences of age
22 o structures in left temporoparietal cortex, angular gyrus (AG) and posterior middle temporal gyrus (
23  a novel functional dissociation between the angular gyrus (AG) and posterior middle temporal gyrus (
24 ial/posterior cingulate cortex (RSC/PCC) and angular gyrus (AG) in the high-frequency broadband (HFB,
25        Here, we test the hypothesis that the angular gyrus (AG) is critical for integrating semantic
26                                     The left angular gyrus (AG) is reliably activated across a wide r
27 tion (cTBS)-induced disruption of M1 and the angular gyrus (AG) of the IPL on learning a probabilisti
28                                          The angular gyrus (AG) region of lateral parietal cortex has
29 associated with a buildup of activity in the angular gyrus (AG) that predicted memory 24 h later.
30 ree of exodeviation and the FC value of left angular gyrus (AG) within FPN (P < 0.05).
31 uding the intraparietal sulcus (IPS) and the angular gyrus (AG), and a fronto-parietal network.
32 or temporal gyrus and sulcus (pSTG/STS), and angular gyrus (AG).
33  such as the anterior temporal lobe (ATL) or angular gyrus (AG).
34                                          The angular gyrus also is thought to have functional links w
35 pocampus, medial prefrontal cortex, and left angular gyrus, among other regions.
36 volved during spatial attention and the left angular gyrus and anterior cingulate cortex during motor
37 0.05) with atrophy of left planum temporale, angular gyrus and anterior cingulate gyrus: a cortical n
38 tive and positively modulated FC was between angular gyrus and hippocampus, while the greatest overal
39 arge left-right asymmetry was present in the angular gyrus and inferior occipital gyrus.
40 ontrast, classifier performance for both the angular gyrus and insular cortex was reliably enhanced b
41 ter (less altered) connectivity between left angular gyrus and left frontal pole predicted better res
42 ts, only target-specific semantic effects in angular gyrus and MTG.
43           Instead, our results implicate the angular gyrus and parahippocampal region in this role.
44 mantic (inferior frontal, middle frontal and angular gyrus and parahippocampus) and reward systems (o
45 ding results were found in DMN, including in angular gyrus and posterior cingulate cortex, indicating
46 y in the default mode network, including the angular gyrus and posterior cingulate cortex.
47                                      Whereas angular gyrus and posterior cingulate/precuneus were sig
48 o long events in high-order areas (including angular gyrus and posterior medial cortex), which repres
49 eft-hemisphere language regions, such as the angular gyrus and the banks of the intraparietal sulcus.
50 l cortex, the intraparietal sulcus, the left angular gyrus and the inferior temporal gyrus.
51 in the left anterior temporal lobe, the left angular gyrus and the posterior bank of the left postcen
52 pontaneous neuronal excitability in both the angular gyrus and the primary motor cortex caused the re
53 for RRB, while connectivity between the left angular gyrus and the right middle temporal gyrus show k
54 poral gyrus, precuneus, posterior cingulate, angular gyrus) and some areas of the medial temporal lob
55 FG) and of semantic competition in MTG, left angular gyrus, and IFG.
56 osterior middle temporal gyrus (LpMTG), left angular gyrus, and left intraparietal sulcus (LIPS), in
57 Rolandic operculum, superior parietal gyrus, angular gyrus, and middle temporal pole.
58  of agency, no priming-related activation of angular gyrus, and no priming-related changes in fronto-
59 uding precuneus, posterior cingulate cortex, angular gyrus, and parahippocampal cortex.
60 n in posterior regions (Wernicke's area, the angular gyrus, and striate cortex) and relative overacti
61 refrontal-cortex (mPFC), precuneus, the left angular gyrus, and superior parietal cortex of the DMN,
62 efault-mode network, including precuneus and angular gyrus, and the salience network, including insul
63 ctional connectivity with the precuneus, the angular gyrus, and the temporal visual cortex Brodmann a
64 rieval precision scaled with activity in the angular gyrus, and vividness judgments tracked activity
65 yglucose hypometabolism in the precuneus and angular gyrus; and greater 11C-Pittsburgh compound B bin
66 licity of processes that are associated with angular gyrus (AnG) activation during encoding and retri
67 nce that functionally distinct subregions of angular gyrus (AnG) contribute to the retrieval of episo
68 f investigation indicates the involvement of angular gyrus (AnG) in the retrieval of both episodic an
69              Much evidence suggests that the angular gyrus (AnG) is involved in episodic memory, but
70 coding and retrieval can be decoded from the angular gyrus (ANG), a subregion of posterior lateral pa
71                               Therefore, the angular gyrus appears to recombine consolidated schema c
72 ilateral middle temporal gyri, and bilateral angular gyrus, are distinctly related to these four late
73 d microstructural changes, identify the left angular gyrus as a structure that rapidly adapts to newl
74  BA 38 (anterior temporal cortex) and BA 39 (angular gyrus)--as discriminant variables, classified pa
75                            A further test of angular gyrus asymmetry showed a reversal of the normal
76 ment to mouth opening was found in the right angular gyrus at <1 Hz, and in early visual cortices at
77 ctivity in midline cortical, prefrontal, and angular gyrus, at retrieval.
78                                          The angular gyrus (BA39) was functionally correlated with BA
79 erior cingulate (BA31), precuneus (BA7m) and angular gyrus (BA39).
80  this difference in asymmetry, with the left angular gyrus being significantly larger (18.7%) than th
81 tion level-dependent signal in the posterior angular gyrus bilaterally, left occipitotemporal cortex,
82 n area 10, 32), right hippocampus, bilateral angular gyrus (Brodmann area 39), left posterior cingula
83 shifted the amplitude of tuning functions in angular gyrus but did not change the selectivity of tuni
84 posterior nodes of the DMN, particularly the angular gyrus, but also more anterior and dorsal parieta
85  and escitalopram-induced increased amygdala-angular gyrus connectivity at week 2 predicted the magni
86 tex (vmPFC) and positive left amygdala-right angular gyrus connectivity during emotion processing.
87            Our results show that cTBS to the angular gyrus decreased memory for the linking events an
88 chema components, which converged within the angular gyrus during retrieval.
89 rtificial neural networks, we identified the angular gyrus encoding responses across face-, body-, ar
90 hat the anatomical disconnection of the left angular gyrus from other brain regions that are part of
91  the bilateral intraparietal sulcus and left angular gyrus in both adolescents and adults with PTSD.
92  are consistent with a critical role for the angular gyrus in conceptual combination.
93 entations in left inferior frontal gyrus and angular gyrus in coordination with either hippocampal ac
94  temporal cortex in males and with the right angular gyrus in females.
95 elated in intensity with deactivation of the angular gyrus in females; no such relationships were obs
96 dividual differences in the structure of the angular gyrus in healthy adults are related to variabili
97 ndings demonstrate a causal role of the left angular gyrus in insight-related memory reconfigurations
98 ndings demonstrate a causal role of the left angular gyrus in lexical-semantic integration and provid
99 hypothesizes functional linkages between the angular gyrus in the left hemisphere and visual associat
100 articularly evident in areas of LPC (namely, angular gyrus) in which activity scaled with subjective
101  in dynamic functional connectivity from the angular gyrus, individuals with acquired anosmia had str
102 encoding, identifying medial precuneus, left angular gyrus, intraparietal sulcus, ventral occipitotem
103 ed in the sense of self and agency), and the angular gyrus (involved in language) is thus related to
104 ivity among the orbitofrontal cortex and the angular gyrus (involved in mentalizing).
105                   We demonstrate that the RH angular gyrus is active during ASL processing only in na
106 s are the first to demonstrate that the left angular gyrus is critical for both episodic simulation a
107                        In contrast, the left angular gyrus is functionally disconnected from these re
108 , we found that the degree of atrophy in the angular gyrus is specifically related to impaired perfor
109               Here, we hypothesized that the angular gyrus, known to be involved in episodic memory a
110 ulate cortex/precuneus (PCC/Precun) and left angular gyrus (lANG).
111 trated that temporary disruption of the left angular gyrus leads to impairments in simulation and mem
112 raphy scans showed regions in left and right angular gyrus, left mid-temporal gyrus, and left middle
113 luding bilateral middle temporal gyrus, left angular gyrus, left middle and inferior frontal gyrus.
114 er training in a network including the right angular gyrus, left superior temporal sulcus, right supe
115 etrosplenial cortex, lateral parietal cortex/angular gyrus, medial prefrontal cortex, superior fronta
116 hology averaged from three cerebral regions (angular gyrus, mid-frontal cortex, and anterior cingulat
117 ivation in anterior and posterior cingulate, angular gyrus, middle frontal gyrus, and cuneus.
118 verlap in encoding and retrieval activity in angular gyrus, midline cortical regions, and prefrontal
119 ed contributions of the vmPFC, precuneus and angular gyrus network to the more efficient encoding of
120 pecifically modulates neural activity in the angular gyrus of healthy adults, independent of the moda
121 rea involved in all neglect patients was the angular gyrus of the inferior parietal lobe (IPL).
122 e inferior parietal lobule, particularly the angular gyrus of the inferior parietal lobule, and the p
123 theta burst stimulation (cTBS) over the left angular gyrus or sham stimulation before gaining insight
124 y associated with hypoperfusion of the right angular gyrus (p < 0.0001).
125                             Responses in the angular gyrus, parahippocampal gyrus, and subregions of
126 in areas including the left parietal cortex [angular gyrus/parallel sulcus (area 39)], left anterior
127 rietal sulcus (hIP1, hIP2, and hIP3) and the angular gyrus (PGa, and PGp), bilaterally.
128 or supramarginal gyrus and adjacent anterior angular gyrus, planum temporale, and posterior superior
129 oral lobe, lateral inferior parietal cortex (angular gyrus), posterior cingulate cortex, dorsomedial
130 ior frontal gyrus, medial prefrontal cortex, angular gyrus, posterior MTG, and medial temporal lobes.
131 s of individual regions demonstrated thinner angular gyrus, precuneus and superior parietal lobule in
132 res, particularly the middle temporal gyrus, angular gyrus, precuneus, and cingulate cortex.
133 s; DMN: temporal pole, middle frontal gyrus, angular gyrus, precuneus, posterior cingulate cortex, pa
134 lso regionally specific; connectivity of the angular gyrus predicted poorer performance in both group
135      At the neural level, cTBS targeting the angular gyrus reduced centro-temporal coupling with fron
136 (e.g., occipital cortex) and semantic (e.g., angular gyrus) regions in the cortex, but not in the hip
137 y tasks also increased after TMS to the left angular gyrus relative to the vertex.
138 ivity in the superior temporal gyrus and the angular gyrus, respectively.
139  bank of the intraparietal sulcus and on the angular gyrus, responds selectively to cues for differen
140 men (right: p = 0.001; left: p = 0.001), and angular gyrus (right: p = 0.011; left: p = 0.001).
141 n in the right superior frontal gyrus, right angular gyrus, right amygdala/parahippocampal gyrus, and
142  of the error: this network, including right angular gyrus, right supplementary motor area, and bilat
143  show that parietal cortex, particularly the angular gyrus, robustly combines memory- and content-rel
144 nical stage, and a biphasic influence of the angular gyrus-seeded default mode metabolic network on m
145 e. episodic memory: medial temporal lobe and angular gyrus; semantic memory: left anterior temporal r
146 ocessing areas such as superior temporal and angular gyrus showed no delay or width difference for ro
147 other set, including the hippocampus and the angular gyrus, showed a nonmonotonic response profile tr
148 rtificial neural networks, we found that the angular gyrus shows joint statistical dependence with mu
149 hat regional cerebral blood flow in the left angular gyrus shows strong within-task, across-subjects
150 ontrol site (vertex), disruption of the left angular gyrus significantly reduced the number of intern
151   Within the IPL, although supramarginal and angular gyrus (SMG; AG) regions both demonstrated invali
152 tures (dorsal and ventral PFC, amygdala, and angular gyrus) subserving moral cognition and emotion.
153 erior parietal areas located anterior to the angular gyrus such as AIP and VIP are less medially disp
154  a subregion of lateral parietal cortex, the angular gyrus, supported successful reconstruction of pe
155 , white matter region proximate to the right angular gyrus (Tailerach coordinates 35, -71, 19) and wh
156  either a control site (vertex) or to a left angular gyrus target region.
157 ombined stimulation of the supramarginal and angular gyrus than an isolated PFm stimulation.
158 sociated with increased activity in the left angular gyrus, the medial and left lateral prefrontal co
159  match articulatory lip movements; the right angular gyrus then extracts slower features of lip movem
160 d anosmia had stronger connectivity from the angular gyrus to areas primary responsible for basic vis
161 ng that recollection-related activity in the angular gyrus tracked the period over which recollected
162 r middle/inferior temporal gyrus (pMTG/ITG), angular gyrus, ventral temporal cortex, posterior cingul
163 and divergent thinking following cTBS to the angular gyrus versus vertex but not during the nonepisod
164 tween inferior prefrontal region volumes and angular gyrus volumes.
165 ly self-evaluated traits in the network, and angular gyrus was associated with greater certainty for
166                   Among parietal subregions, angular gyrus was characterized by robust and overlappin
167  cortex, orbital prefrontal cortex, and left angular gyrus, was involved in the neural interaction be
168            On the other hand, lesions in the angular gyrus were associated with persistent allocentri
169 rietal region, area 45 is connected with the angular gyrus, whereas area 44 is connected with the sup
170 nd radial diffusivity reductions in the left angular gyrus, which are significantly correlated with b
171 GG-homozygotes) in the right middle temporal/angular gyrus while subjects were viewing negative versu
172 ation by nicotine in posterior cingulate and angular gyrus with performance improvements under INT(hi
173 gaged the supplementary motor area and right angular gyrus within the social network, but only social
174 ion of heteromodal association cortex in the angular gyrus would be critical for conceptual combinati
175 ess whether temporary disruption of the left angular gyrus would impair both episodic simulation and

 
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