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1 luences from right TPJ to right IPS and IFG (inferior frontal gyrus).
2 e presenting a decreased volume in the right inferior frontal gyrus.
3 luster encompassing the putamen, insula, and inferior frontal gyrus.
4 s (PCN), bilateral premotor cortex, and left inferior frontal gyrus.
5 the right SMA (and right pre-SMA) and right inferior frontal gyrus.
6 caudate, postcentral gyrus, hippocampus, and inferior frontal gyrus.
7 mulus frequencies, were encoded in bilateral inferior frontal gyrus.
8 nt transcranial DCS administered to the left inferior frontal gyrus.
9 ncreased feedback connectivity from the left inferior frontal gyrus.
10 56080411 had greater activation in the right inferior frontal gyrus.
11 ical areas that are heteromodal, such as the inferior frontal gyrus.
12 ht anterior temporal cortices, and the right inferior frontal gyrus.
13 ty in the right inferior parietal cortex and inferior frontal gyrus.
14 anterior temporal lobe, before reaching the inferior frontal gyrus.
15 stem activity within ventral premotor cortex/inferior frontal gyrus.
16 temporal sulcus, the temporal pole, and the inferior frontal gyrus.
17 eft amygdala, left anterior insula, and left inferior frontal gyrus.
18 al cortex, the dorsomedial striatum, and the inferior frontal gyrus.
19 in mPFC, superior temporal sulcus (STS) and inferior frontal gyrus.
20 gher-level language processing areas such as inferior frontal gyrus.
21 ate; the orbitofrontal cortex; and the right inferior frontal gyrus.
22 ontrol participants in the bilateral ventral inferior frontal gyrus.
23 xic group across a large portion of the left inferior frontal gyrus.
24 al frontal cortex, and pars orbitalis of the inferior frontal gyrus.
25 cortex (ACC; BA24/32), anterior insula, and inferior frontal gyrus.
26 spectively) and pars orbitalis (POrb) of the inferior frontal gyrus.
27 an be mapped to a common portion of the left inferior frontal gyrus.
28 y of language processing in the brain toward inferior frontal gyrus.
29 ciated with increased thickness of the right inferior frontal gyrus.
30 jects in the right globus pallidus and right inferior frontal gyrus.
31 ral sulcus, middle intraparietal sulcus, and inferior frontal gyrus.
32 , including the intraparietal sulcus and the inferior frontal gyrus.
33 the striatum, temporoparietal junction, and inferior frontal gyrus.
34 eft dorsolateral prefrontal cortex and right inferior frontal gyrus.
35 nceptual disambiguation also implicating the inferior frontal gyrus.
36 nisotropy in the white matter underlying the inferior frontal gyrus.
37 in the right orbitofrontal cortex and right inferior frontal gyrus.
38 ft language-related regions and in the right inferior frontal gyrus.
39 d activation was observed in hippocampus and inferior frontal gyrus.
40 kness measures of the left temporal pole and inferior frontal gyrus.
41 d increased the evoked response in the right inferior frontal gyrus.
42 erns disclosed involved deactivation of left inferior frontal gyrus.
43 vity to anterior language regions around the inferior frontal gyrus.
44 ing the SMA with the pars opercularis of the inferior frontal gyrus; (4) medial fibres connecting the
45 cluding (n = 8) or not including (n = 9) the inferior frontal gyrus, a core mirror neuron system regi
46 ctivity between the right amygdala and right inferior frontal gyrus, a key region for top-down modula
47 ion and theory of mind deficits in the right inferior frontal gyrus, a region associated with prosodi
48 sociated with increased activity in the left inferior frontal gyrus, a region implicated in speech pr
50 r, we argue that our main finding of greater inferior frontal gyrus activation in both groups with ph
51 tion of potential losses; and increased left inferior frontal gyrus activation when experiencing an a
52 sia have highlighted the importance of right inferior frontal gyrus activation, especially early afte
54 There was an inverse relationship between inferior frontal gyrus activity and ADHD symptoms and be
55 -by-time differences revealed increased left inferior frontal gyrus activity in the CD group during a
58 atients also showed greater than normal left inferior frontal gyrus activity, suggesting a possible '
59 morphometry confirmed significant atrophy of inferior frontal gyrus, alongside insular, orbitofrontal
60 ulatory effect from Heschl's gyrus to dorsal inferior frontal gyrus also showed a developmental incre
62 ation task activated left ventral middle and inferior frontal gyrus, among other regions, to a greate
63 ron system', which consists of the posterior inferior frontal gyrus and adjacent ventral premotor cor
65 ontrol subjects were identified in the right inferior frontal gyrus and anterior temporal lobe, which
66 associated with phonological recoding (i.e., inferior frontal gyrus and basal ganglia) was predictive
67 e left and right IFG, as well as between the inferior frontal gyrus and brain areas involved in langu
68 related with both functional activity in the inferior frontal gyrus and caudate nucleus and performan
69 emporo-parietal lesion occurred in bilateral inferior frontal gyrus and contralateral superior tempor
71 labeling, participants recruited the dorsal inferior frontal gyrus and exhibited decreased amygdala
72 s work, we found that activation in the left inferior frontal gyrus and hippocampus correlated with l
73 th left anterior basal temporal cortex, left inferior frontal gyrus and homotopic cortex in right ant
74 e (GMV) was significantly higher in the left inferior frontal gyrus and insula, while GMV was signifi
75 um has reciprocal connections with both left inferior frontal gyrus and left lateral temporal cortex,
76 volved in phonological processing, i.e. left inferior frontal gyrus and left lateral temporal cortex.
78 owed significant activation over left dorsal inferior frontal gyrus and left premotor cortex, childre
79 ions of frontal regions, including the right inferior frontal gyrus and medial frontal cortex, to att
80 nally, we observed greater activation in the inferior frontal gyrus and nucleus accumbens in younger
81 mbiguous cues elicited activity in posterior inferior frontal gyrus and posterior parietal cortex dur
85 r activity and directly correlated with left inferior frontal gyrus and right precuneus activity.
86 lations between neural activity in the right inferior frontal gyrus and SMA and timing performance co
87 between preSMA and the STN, and between the inferior frontal gyrus and STN, also predicted individua
88 ve to speech was also increased between left inferior frontal gyrus and superior temporal gyrus in au
91 y retrievals correlated with activity in the inferior frontal gyrus and the anterior cingulate, where
94 comprehension displayed focal atrophy of the inferior frontal gyrus and the anterior temporal lobe.
95 on coefficient (CCC) and identified the left inferior frontal gyrus and the bilateral motor cortex wi
96 esponse to the coherence break and the right inferior frontal gyrus and the insula activate, possibly
97 d neuroanatomical abnormalities in the right inferior frontal gyrus and the posterior part of right i
98 reased stimulus-evoked activity in the right inferior frontal gyrus and the right temporal-parietal j
99 lesions to the left pars opercularis in the inferior frontal gyrus and to the white matter adjacent
100 rmalities in gray matter volume in the right inferior frontal gyrus and white matter volume in the ca
101 prediction error signals in anterior insula, inferior frontal gyrus, and anterior cingulate indicate
103 ant users displayed greater anterior insula, inferior frontal gyrus, and dorsal striatum activation t
104 g cocaine exhibited greater anterior insula, inferior frontal gyrus, and dorsal striatum activation t
105 junction (IFJ), middle frontal gyrus (MFG), inferior frontal gyrus, and intraparietal sulcus correla
108 Activity in left ventrolateral PFC, left inferior frontal gyrus, and left superior temporal sulcu
109 twork comprising the inferior parietal lobe, inferior frontal gyrus, and posterior superior temporal
110 implicate a key role of dorsal ACC, pre-SMA, inferior frontal gyrus, and STN in computing the trade-o
112 y in the midventrolateral region of the left inferior frontal gyrus, and the regions activated in eac
113 ss in the right motor strip, the left middle/inferior frontal gyrus, and the right parieto-occipital
114 e left superior and middle temporal gyri and inferior frontal gyrus, and there was no significant dif
115 small frontal lesion were found in bilateral inferior frontal gyrus; and (iii) of a large temporo-par
116 exhibited decreased activity with age: left inferior frontal gyrus/anterior insula for SI thought ma
117 areas within the superior temporal gyrus and inferior frontal gyrus are heavily recruited when indivi
118 th the left inferior temporal gyrus and left inferior frontal gyrus are involved in processing the se
119 es of the role of the ipsi and contralateral inferior frontal gyrus are necessary, and should be long
121 emporal gyrus, inferior parietal lobule, and inferior frontal gyrus as videos were rated as increasin
122 Instead, deactivation was seen in the left inferior frontal gyrus as well as a neural system encomp
124 cluding the medial temporal lobe (MTL), left inferior frontal gyrus, as well as the ventrolateral tem
125 for implied than explicit events in the left inferior frontal gyrus at the coherence break compared t
126 eas), but also specific regions in bilateral inferior frontal gyrus, bilateral anterior insula and or
127 the monetary incentive delay task and lower inferior frontal gyrus BOLD response during the stop sig
128 ADHD symptoms are associated with increased inferior frontal gyrus BOLD response during the stop sig
131 ding pre-supplementary motor area (pre-SMA), inferior frontal gyrus, caudate, and subthalamic nucleus
134 d odour matching to visual cues, whereas the inferior frontal gyrus correlated with both odour naming
135 in both superior temporal sulci and the left inferior frontal gyrus correlated with the amount of spe
136 and planning (e.g., middle frontal gyrus and inferior frontal gyrus), craving and interoceptive proce
138 erns of activity in auditory cortex and left inferior frontal gyrus distinguished the tone that was m
139 ss activation of the right ventrolateral PFC/inferior frontal gyrus during pre-treatment emotion regu
140 face inhibition and greater activity in left inferior frontal gyrus during sad face inhibition, demon
141 r activation in the left anterior insula and inferior frontal gyrus during successful inhibitions, an
143 the supplementary motor area, brainstem, and inferior frontal gyrus, exhibited significant correlatio
144 rtex, the anterior cingulate cortex, and the inferior frontal gyrus extending to the anterior insula.
146 anisotropy correlated with activity in left inferior frontal gyrus for both speech and song conditio
147 data showed spatial convergence in the left inferior frontal gyrus for covert or overt generation ve
148 marginal gyrus or opercular part of the left inferior frontal gyrus has been reported to transiently
149 tral attentional system, including the right inferior frontal gyrus, has been shown to respond to une
150 connectivity in a network involving the left inferior frontal gyrus, hippocampus and visual associati
151 rning in the human brain, and that the right inferior frontal gyrus hosts a confidence-based statisti
152 s in functional connectivity, with the right inferior frontal gyrus (IFG) a critical region for execu
155 ion in a left-lateralized network, including inferior frontal gyrus (IFG) and inferior parietal corte
156 Comparison of superadditive responses in the inferior frontal gyrus (IFG) and IPL (supramarginal) reg
157 n this system, particularly between the left inferior frontal gyrus (IFG) and left subcortical region
158 , left middle temporal gyrus (MTG), and left inferior frontal gyrus (IFG) and of semantic competition
159 interhemispheric functional symmetry of the inferior frontal gyrus (IFG) and superior temporal gyrus
160 uistic groups, several brain areas including inferior frontal gyrus (IFG) and temporo-parietal juncti
161 in this putative stopping network, the right inferior frontal gyrus (IFG) and the primary motor corte
162 irror neuron system (MNS) which includes the inferior frontal gyrus (IFG) and the somotosensory relat
163 hat the right intraparietal cortex (IPC) and inferior frontal gyrus (IFG) are jointly activated by du
165 eater activity than TD children in the right inferior frontal gyrus (IFG) as well as in bilateral tem
167 dorsolateral prefrontal cortex (dlPFC), and inferior frontal gyrus (IFG) have all been implicated in
168 theta burst stimulation (cTBS) over the left inferior frontal gyrus (IFG) in healthy volunteers, then
169 e lateral orbitofrontal cortex (OFC) and the inferior frontal gyrus (IFG) in subjects performing this
171 convoluted and cytoarchitectonically diverse inferior frontal gyrus (IFG) of humans is known to be cr
173 rea, a cerebral cortical area located in the inferior frontal gyrus (IFG) of the human brain, has bee
174 g memory task and increased activity in left inferior frontal gyrus (IFG) of the prefrontal cortex.
176 e pre-supplementary motor area (pre-SMA) and inferior frontal gyrus (IFG) to the subthalamic nucleus
177 oding was selectively impaired when the left inferior frontal gyrus (IFG) was driven at beta (18.7 Hz
178 , including left hippocampus and left dorsal inferior frontal gyrus (IFG), activity at encoding diffe
179 ic resonance imaging, (rs-fcMRI)] with right inferior frontal gyrus (IFG), an anterior component of t
180 ng the anterior and posterior cingulate, the inferior frontal gyrus (IFG), and ventral and lateral te
181 mentalizing and language networks [bilateral inferior frontal gyrus (IFG), bilateral medial prefronta
183 reater activations were observed in the left inferior frontal gyrus (IFG), posterior superior tempora
184 dysregulatory dynamic signatures within the inferior frontal gyrus (IFG), which our prior work has l
185 gulated neurocognitive function in the right inferior frontal gyrus (IFG)-one node in a corticothalam
191 onnecting language pathways occurred in left inferior frontal gyrus; (ii) of a small frontal lesion w
192 sly reported enhanced activation in the left inferior frontal gyrus in both deaf and dyslexic adults
195 ocessing and underline a distinctive role of inferior frontal gyrus in natural speech comprehension.
197 e for the essential contribution of the left inferior frontal gyrus in syntactic analysis and highlig
200 en primary auditory cortex, hippocampus, and inferior frontal gyrus in the process of discovering the
201 g the critical role of the temporal pole and inferior frontal gyrus in transmodal linking and verbali
202 of a subregion of the prefrontal cortex, the inferior frontal gyrus, in children aged 6 to 12 years;
203 e inhibition, a function linked to the right inferior frontal gyrus, in the manifestation of impulsiv
204 , orbital frontal cortex, and two regions of inferior frontal gyrus, including pars opercularis and p
205 been advanced regarding the role of the left inferior frontal gyrus, inferior parietal lobe and poste
206 vation of different regions within the right inferior frontal gyrus/insula to infrequent stimuli asso
207 ], and attention [anterior cingulate cortex, inferior frontal gyrus, intraparietal sulcus (IPS)].
208 healthy participants to ask whether the left inferior frontal gyrus is essential for syntactic proces
209 how that activity in the auditory cortex and inferior frontal gyrus is specific to the maintained ton
210 is unknown, although its human homolog, the inferior frontal gyrus, is known to be important in inte
211 activation for methylphenidate in the right inferior frontal gyrus, left anterior cingulate/suppleme
212 ntral gyrus, bilateral opercular part of the inferior frontal gyrus, left hippocampus, and left middl
214 tant findings on the functional role of left inferior frontal gyrus (LIFG) in phonological and semant
215 psychological evidence suggest that the left inferior frontal gyrus (LIFG) may play a role in resolvi
217 tion affects the selection process, the left inferior frontal gyrus (LIFG) responds to competition am
219 emantic knowledge and juxtaposition, and the inferior frontal gyrus, likely to be involved in languag
220 cross the anxiety spectrum suggests that the inferior frontal gyrus may have a more complex role in e
222 semantic cognition, including bilateral ATL, inferior frontal gyrus, medial prefrontal cortex, angula
224 ontrols; two others had recruitment in right inferior frontal gyrus, middle frontal gyrus and tempora
225 t during successful response inhibition, the inferior frontal gyrus modulates an excitatory influence
228 ics from producing biased choices, the right inferior frontal gyrus, often implicated in inhibiting p
230 gyrus (SMG), anterior intraparietal sulcus, inferior frontal gyrus opercularis (IFGo), and triangula
231 n can be seen by either direct damage to the inferior frontal gyrus, or via damage to dorsal lateral
232 sms: (i) an initial suppression by the right inferior frontal gyrus over regions supporting sensory c
234 on was seen in the right precuneus and right inferior frontal gyrus (P = .013 and P =.019, respective
235 cortex, middle and anterior temporal cortex, inferior frontal gyrus, parahippocampal gyrus, and orbit
236 tivation was found in the left putamen, left inferior frontal gyrus (pars opercularis), left temporal
239 -hemispheric language network, including the inferior frontal gyrus (pars orbitalis and triangularis)
241 ars), differences were observed in bilateral inferior frontal gyrus, pars opercularis and pars triang
242 latency causal interactions of the posterior inferior frontal gyrus (pIFG) and pre-supplementary moto
243 idely accepted that Broca's area in the left inferior frontal gyrus plays an important role in this p
245 id not implicate traditional language areas (inferior frontal gyrus, posterior temporal regions) in s
246 DLPFC), posterior parietal cortex (PPC), and inferior frontal gyrus, precommitment engaged lateral fr
247 and STN, and the degree of modulation by the inferior frontal gyrus, predicted individual differences
248 tegral to fluent speech production including inferior frontal gyrus, premotor cortex, and superior te
249 esented alternative interactions between the inferior frontal gyrus, presupplementary motor area (pre
250 rials showed common recruitment of the right inferior frontal gyrus, presupplementary motor area, and
251 three prefrontal-limbic regions, wherein the inferior frontal gyrus provides evaluation of stimulus m
252 ght precuneus (r = 0.57; P = .026) and right inferior frontal gyrus (r = 0.60; P = .019) and poor WM
253 g evidence suggests that activation of right inferior frontal gyrus (r-IFG) and right presupplementar
255 a (AI), anterior cingulate cortex (ACC), and inferior frontal gyrus, regions associated with empathy
256 ty in left anterior intraparietal sulcus and inferior frontal gyrus, regions involved in the simulati
257 nificantly higher activation within the left inferior frontal gyrus relative to nonanxious controls d
258 d the probability of a risky choice, whereas inferior frontal gyrus responses showed the inverse rela
259 arly in the course of BD showed larger right inferior frontal gyrus (rIFG) volumes than control subje
260 s, less stop-related activation in the right inferior frontal gyrus (RIFG), and weaker functional con
262 at included the presupplementary motor area, inferior frontal gyrus, subthalamic nucleus, and inferio
263 aration for selective inhibition engages the inferior frontal gyrus, supplementary motor area, and st
264 ted areas including the sensorimotor cortex, inferior-frontal gyrus, supplementary motor area, and th
265 rk contained three modules, including a left inferior frontal gyrus/supplementary motor area, which w
266 e error [FWE]-corrected P = .003), the right inferior frontal gyrus (t168 = 3.65; peak MNI coordinate
267 38, z = 12; FWE-corrected P = .04), the left inferior frontal gyrus (t168 = 4.09; peak MNI coordinate
268 onnectivity of the BLA complex with the left inferior frontal gyrus than the PTSD group (p<0.05; corr
269 found in the superior frontal gyrus and the inferior frontal gyrus that could reflect subvocalizatio
270 lity centered on the pars opercularis of the inferior frontal gyrus that was associated with a sulcal
271 l cortex (dorsolateral prefrontal cortex and inferior frontal gyrus), the medial prefrontal cortex, a
272 frontal gyrus, the middle frontal gyrus, the inferior frontal gyrus, the anterior cingulate, the prec
273 included classic language areas such as the inferior frontal gyrus, the posterior superior temporal
276 (i) atomoxetine increases sensitivity of the inferior frontal gyrus to afferent inputs from the pre-s
277 unctionally distinct sub-regions of the left inferior frontal gyrus; to clarify the relationship betw
278 rgence of "coarse" speech representations in inferior frontal gyrus typically associated with high-le
279 ing the function of the left (but not right) inferior frontal gyrus using transcranial magnetic stimu
281 ntal cortex, dorsolateral prefrontal cortex, inferior frontal gyrus, ventromedial prefrontal cortex)
283 tween pre-supplementary motor cortex and the inferior frontal gyrus was absent in Parkinson's disease
285 nnectivity between homologous regions of the inferior frontal gyrus was associated with reduced neura
286 ent with a feedback process: activity in the inferior frontal gyrus was modulated by prior knowledge
288 the right posterior hippocampus to the right inferior frontal gyrus was significantly decreased in bo
289 stimulation experiment: subjects whose right inferior frontal gyrus was temporarily disrupted made bi
290 om posterior superior temporal cortex toward inferior frontal gyrus were associated with linguistic f
291 al terminations of the arcuate fasciculus in inferior frontal gyrus were indistinguishable between au
292 ourses along the superior temporal gyrus and inferior frontal gyrus were remarkably similar for spoke
293 In contrast, frontal regions, including left inferior frontal gyrus, were only engaged when listeners
294 gions of medial prefrontal cortex (mPFC) and inferior frontal gyrus when elicited by emotional stimul
295 c and significant lack of recruitment of the inferior frontal gyrus when inhibiting responses to fear
296 Both signals were combined in the right inferior frontal gyrus, where they operated in agreement
297 n BD was associated with greater activity in inferior frontal gyrus, which also correlated with the p
298 m sLORETA identified cortical sources in the inferior frontal gyrus, which is a part of dorsolateral
299 ecruiting right inferior parietal cortex and inferior frontal gyrus, which may contribute to their in
300 d with fractional anisotropy measures of the inferior frontal gyrus white matter and corpus callosum
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