ライフサイエンスコーパス: gyrus

1 , mid-frontal cortex, and anterior cingulate gyrus).

2 ning and memory (caudate and parahippocampal gyrus).

3 ated in its mid-dorsal part (posterior short gyrus).

4 al ventricle subventricular zone and dentate gyrus.

5 reasing neuronal excitability of the dentate gyrus.

6 gene, in granule cells of the adult dentate gyrus.

7 subventricular zone and hippocampal dentate gyrus.

8 was only found in the precentral/postcentral gyrus.

9 size and decreased thickness of the dentate gyrus.

10 ge processing areas such as inferior frontal gyrus.

11 ventromedial PFC (vmPFC) and left precentral gyrus.

12 bilateral dorsal caudate and left precentral gyrus.

13 obust morphological sprouting in the dentate gyrus.

14 at human pattern separation requires dentate gyrus.

15 cessing in the brain toward inferior frontal gyrus.

16 tivity between frontal areas and the angular gyrus.

17 ased thickness of the right inferior frontal gyrus.

18 f synaptic transmission in the mouse dentate gyrus.

19 led to volume reduction only in the dentate gyrus.

20 erminals (fiber varicosities) in the dentate gyrus.

21 ration and neurogenesis in the adult dentate gyrus.

22 CA3 area bypassing CA1, CA2, and the dentate gyrus.

23 ed activity in the posterior middle temporal gyrus.

24 in the outer GCL of the hippocampal dentate gyrus.

25 , medial prefrontal cortex, and left angular gyrus.

26 he anterior temporal lobe and the precentral gyrus.

27 ntraparietal sulcus and the inferior frontal gyrus.

28 ortex (DLPFC), and bilateral middle temporal gyrus.

29 cingulate cortex and in the superior frontal gyrus.

30 utamatergic rMF sprouting within the dentate gyrus.

31 ght inferior frontal gyrus and supramarginal gyrus.

32 ity was attenuated in the left orbitofrontal gyrus.

33 in and between subregions of CA1 and dentate gyrus.

34 r not including (n = 9) the inferior frontal gyrus, a core mirror neuron system region, and compared

35 othesized that OSAS would affect the dentate gyrus, a hippocampal subdivision essential to neurogenes

36 The hippocampal dentate gyrus, a region with ongoing adult neurogenesis, is sens

37 We suggest angular gyrus activation reflects the experiences of agency, or

38 losses; and increased left inferior frontal gyrus activation when experiencing an actual loss.

39 pproaches that Oxtrs in the anterior dentate gyrus (aDG) and anterior CA2/CA3 (aCA2/CA3) of mice are

40 ed with a buildup of activity in the angular gyrus (AG) that predicted memory 24 h later.

41 , cingulate cortex, caudate, and postcentral gyrus (all regions: p < .001, etap(2) > .06) in both at-

42 , medial prefrontal cortex, and left angular gyrus, among other regions.

43 tory interneurons in the hippocampal dentate gyrus, an important area for seizure propagation.

44 uring spatial attention and the left angular gyrus and anterior cingulate cortex during motor intenti

45 The ECN and DMN had regions (middle temporal gyrus and bilateral middle/inferior temporal/fusiform gy

46 ions and showed trends toward larger dentate gyrus and CA1 regions of the hippocampus.

47 utations ascribed to the hippocampal dentate gyrus and CA3 fields.

48 of years lived in poverty with left dentate gyrus and CA3 hippocampal subfields and left amygdalar v

49 cells in caudate-kindled rats in the dentate gyrus and CA3 hippocampal subfields.

50 calcifications in the basal ganglia, nucleus gyrus and cerebral cortex.

51 in ECN connectivity in the right precentral gyrus and decreases in DMN connectivity in the right inf

52 er, source-localized to the superior frontal gyrus and dorsal cingulate cortex), accompanied by atten

53 ary auditory cortex (i.e., superior temporal gyrus and Heschl's gyrus) correlated with reduced hearin

54 T-ir fibers were seen throughout the dentate gyrus and hippocampus, in the mediodorsal, laterodorsal,

55 l representations past the superior temporal gyrus and how they engage higher-level language processi

56 nhibition and planning (e.g., middle frontal gyrus and inferior frontal gyrus), craving and interocep

57 ficantly higher in the left inferior frontal gyrus and insula, while GMV was significantly lower in t

58 neurogenesis persists in the rodent dentate gyrus and is stimulated by chronic treatment with conven

59 activation over left dorsal inferior frontal gyrus and left premotor cortex, children who stutter exh

60 ss perfusion in the right occipital/fusiform gyrus and left subgenual ACC.

61 n with memory systems in the parahippocampal gyrus and medial temporal lobe, especially involving the

62 target-specific semantic effects in angular gyrus and MTG.

63 f fluoxetine on proliferation in the dentate gyrus and on depressive behavior.

64 vents in high-order areas (including angular gyrus and posterior medial cortex), which represent abst

65 FW decreases in the post-central gyrus and precuneus correlated negatively with balance c

66 sis in the granule cell layer of the dentate gyrus and rescues hippocampal memory defects in a mouse

67 lateral occipital cortex and right fusiform gyrus and sources in a control region (left V1) yielded

68 (TVAs) are regions of the superior temporal gyrus and sulcus that respond more to vocal sounds than

69 Activity in the postcentral gyrus and superior parietal lobule was sensitive to dot

70 N connectivity in the right inferior frontal gyrus and supramarginal gyrus.

71 d with the activity in the superior temporal gyrus and the angular gyrus, respectively.

72 rior parietal lobe (aIPL), bilateral lingual gyrus and the cuneus, as well as with extended deactivat

73 epresentation in the insular posterior short gyrus and the first detailed description of olfactory se

74 Within precuneus, bilateral middle temporal gyrus and the left hippocampus, reinstatement effects be

75 pace in the left posterior inferior temporal gyrus and the left prefrontal cortex.

76 the inferior temporal gyrus, to the fusiform gyrus and to a white matter network including the left p

77 n was mainly detected in the Middle Temporal Gyrus and within regions related to the mirror mechanism

78 romodulation in obesity (ie superior frontal gyrus) and a quantifiable mediator of their effects (ie

79 ., in the caudate, cingulate, and precentral gyrus) and decreased activation in the insula and superi

80 tal regions (medial OFC and superior frontal gyrus) and primary and higher-order visual, somatosensor

81 sorders, including insula, superior temporal gyrus, and anterior/mid-cingulate cortex among non-lapse

82 Young adults' whole hippocampal, dentate gyrus, and CA3 hippocampal subfields as well as amygdala

83 the posterior cingulate, precuneus, lingual gyrus, and cerebellum.

84 the middle temporal gyrus, inferior temporal gyrus, and cingulate cortex, was associated with word co

85 caudate, anterior cingulate, medial frontal gyrus, and dorsolateral prefrontal cortex.

86 us, middle temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encoding reduced

87 r in temporal pole, anterior parahippocampal gyrus, and hippocampus of the schizophrenia patients tha

88 pplementary motor area, left parahippocampal gyrus, and hippocampus; decreased brain activity in righ

89 of semantic competition in MTG, left angular gyrus, and IFG.

90 area, cingulate gyrus, cuneus and occipital gyrus, and insula in response to milkshake receipt predi

91 s in the left caudate, left inferior frontal gyrus, and left frontal pole.

92 operculum, superior parietal gyrus, angular gyrus, and middle temporal pole.

93 cy, no priming-related activation of angular gyrus, and no priming-related changes in fronto-parietal

94 sterior cingulate/precuneus, middle temporal gyrus, and superior occipital cortex during the anticipa

95 ontal gyrus, the posterior superior temporal gyrus, and the inferior parietal lobule, while those of

96 gyrus, Rolandic operculum, superior parietal gyrus, angular gyrus, and middle temporal pole.

97 Finally, we showed that adult dentate gyrus appears similar to immature CA1, demonstrating reg

98 y motor area, and the right inferior frontal gyrus as part of the PFC.

99 local inhibitory function within the dentate gyrus at time points where sparse activation was comprom

100 rons are continually produced in the dentate gyrus but it is unclear whether synaptic integration of

101 al role of the Ptchd1 protein in the dentate gyrus, but indicate that it is not required for structur

102 omatostatin-positive interneurons in dentate gyrus, but no change in density of calretinin interneuro

103 1 and alpha3 were accentuated in the dentate gyrus, CA1 region, and subiculum, whereas alpha5 express

104 ulation was sufficient to elicit the dentate gyrus circuit collapse evident during epilepsy developme

105 local circuit generates the massive dentate gyrus circuit hyperactivation evident in animals during

106 sed in temporal regions, insula and fusiform gyrus, consistent with those areas known to be most affe

107 Mossy cells in the hilus of the dentate gyrus constitute a major excitatory principal cell type

108 st which pathological changes in the dentate gyrus correlate with seizure frequency and help prioriti

109 (i.e., superior temporal gyrus and Heschl's gyrus) correlated with reduced hearing ability.

110 outh stimuli in the right inferior occipital gyrus could be separated with significantly higher accur

111 ., middle frontal gyrus and inferior frontal gyrus), craving and interoceptive processing (anterior i

112 rtex and supplementary motor area, cingulate gyrus, cuneus and occipital gyrus, and insula in respons

113 nvolving the lateral occipital lobe, lingual gyrus, cuneus, precuneus, posterior cingulate, inferior

114 efrontal cortex and right superior occipital gyrus/cuneus and anterior cingulate cortex.

115 s d=-0.293; P=1.71 x 10(-21)), left fusiform gyrus (d=-0.288; P=8.25 x 10(-21)) and left rostral midd

116 n of adult neurogenesis in the mouse dentate gyrus decreases hippocampal network activation and reduc

117 Within the middle frontal gyrus, decrements in linoleic acid, linolenic acid, and

118 ne subcallosal cortex and left paracingulate gyrus demonstrated improved response to BATD.

119 y fiber (mf) connections between the dentate gyrus (DG) and CA3 neurons in vivo are still elusive.

120 pressing-interneurons (SOMIs) in the dentate gyrus (DG) control formation of granule cell (GC) assemb

121 Moreover, we investigated the dentate gyrus (DG) granule cell reactivity and synaptic plastici

122 (IEG) induction in stress-activated dentate gyrus (DG) granule neurons play a crucial role in these

123 nu ammonis (CA) subfields CA1-4, the dentate gyrus (DG) including a granule cell layer (GCL) and a mo

124 bitory interneurons of the mammalian dentate gyrus (DG) initiate the therapeutic response to antidepr

125 Adult neurogenesis in the dentate gyrus (DG) is strongly influenced by drug-taking behavio

126 Dentate gyrus (DG) is widely thought to provide a teaching signa

127 e recently reported that hippocampal dentate gyrus (DG) neurons differentiated from induced pluripote

128 Infusions of adiponectin into the dentate gyrus (DG) of the hippocampus in fear-conditioned mice f

129 influence adult neurogenesis in the dentate gyrus (DG) of the hippocampus, we hypothesized that sele

130 ted in fewer adult-born cells in the dentate gyrus (DG) overall, reducing populations across differen

131 undant evidence that the hippocampal dentate gyrus (DG) plays a critical role in memory, it remains u

132 aried between 6.6 +/- 0.7 muM in the dentate gyrus (DG) region of the hippocampus and 22.1 +/- 4.9 mu

133 Synapses from the dentate gyrus (DG) to the CA3 area of the hippocampus are distin

134 ds cornu ammonis 2/3 (CA2/3) and CA4/dentate gyrus (DG), as well as impaired hippocampal microstructu

135 l stem cells (NSCs) in the postnatal dentate gyrus (DG), drastically increased perinatal apoptosis, a

136 progenitors in the adult hippocampal dentate gyrus (DG), one of the select regions of the mature brai

137 mpal plasticity, particularly in the dentate gyrus (DG).

138 lbindin reduction in the hippocampal dentate gyrus (DG).

139 ongly activated granule cells in the dentate gyrus (DG).

140 albumin (PV) interneurons within the dentate gyrus (DG).

141 ss, and (ii) activity in ERC and the dentate gyrus (DG)/CA3 region.

142 yrus, premotor cortex, and superior temporal gyrus during a picture description task.

143 gyrus, superior temporal gyrus, and fusiform gyrus during memory encoding reduced odds of recall by a

144 y between the left putamen and paracingulate gyrus during reward anticipation.

145 less activation in the right middle frontal gyrus during the inhibition task reported more euphoria

146 ior superior temporal lobe and supramarginal gyrus; executive functions: bilateral frontoparietal reg

147 to investigate the fundamental mechanism of gyrus formation.

148 dendritic spines in newly generated dentate gyrus granule cell neurons of the hippocampus after a cl

149 fied more than 40 lipid species from dentate gyrus granule cells and CA1 pyramidal neurons of the hip

150 ty by modulating tonic inhibition in dentate gyrus granule cells, in a process involving crosstalk be

151 generation of excitatory synapses in dentate gyrus granule cells.

152 opercular part of the left inferior frontal gyrus has been reported to transiently impair the abilit

153 mechanisms involving the hippocampal dentate gyrus have been proposed.

154 n brain, and that the right inferior frontal gyrus hosts a confidence-based statistical learning algo

155 onnectivity, with the right inferior frontal gyrus (IFG) a critical region for executive function.

156 poral gyrus (MTG), and left inferior frontal gyrus (IFG) and of semantic competition in MTG, left ang

157 The inferior frontal gyrus (IFG) is a key cortical hub in the circuits of emo

158 itive function in the right inferior frontal gyrus (IFG)-one node in a corticothalamic inhibitory con

159 e of disrupted microstructure of the dentate gyrus in children with OSAS that may help explain some o

160 strate lower mean diffusivity of the dentate gyrus in children with OSAS, which correlates with a low

161 monstrate distinct roles for CA3 and dentate gyrus in human memory and uncover the variegated effects

162 rline a distinctive role of inferior frontal gyrus in natural speech comprehension.

163 oral gyrus toward anterior superior temporal gyrus in the human brain.

164 the prefrontal cortex, the inferior frontal gyrus, in children aged 6 to 12 years; and emotional awa

165 audate nucleus and bilateral (para)cingulate gyrus increased in patients after real-rTMS when compare

166 refrontal cortex and right inferior temporal gyrus; increased grey matter in right insula, right puta

167 n and its connections to the middle temporal gyrus, inferior temporal gyrus, and cingulate cortex, wa

168 re biased for auditory attention, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal

169 e first to demonstrate that the left angular gyrus is critical for both episodic simulation and episo

170 We tested the hypothesis that human dentate gyrus is critical for pattern separation, whereas, CA3 u

171 Dentate gyrus is intimately connected to CA3 where, in animals,

172 The hippocampal dentate gyrus is often viewed as a segregator of upstream inform

173 ess ECS-induced proliferation in the dentate gyrus, it blocks dendritic outgrowth of immature granule

174 orbitofrontal gyrus, right inferior temporal gyrus (ITG), left postcentral gyrus/precuneus, left supp

175 uneus, right inferior temporal and occipital gyrus(ITG/IOG), while significantly increased fALFF in t

176 ngulate cortex (dACC) and the middle frontal gyrus, key regions for social pain processing.

177 hat temporary disruption of the left angular gyrus leads to impairments in simulation and memory.

178 supramarginal gyrus, left superior temporal gyrus, left middle temporal gyrus (MTG), and left inferi

179 of lexical competition in left supramarginal gyrus, left superior temporal gyrus, left middle tempora

180 ed BDNF release and signaling in the dentate gyrus may account for cognitive and mental deficits some

181 modulations in the ACC and Superior Temporal Gyrus may associate with increases of voluntary control

182 learning score correlated with lower dentate gyrus mean diffusivity (r = 0.54, p = 0.004).

183 as well as potential utility of the dentate gyrus mean diffusivity as an early marker of brain patho

184 Decreased dentate gyrus mean diffusivity correlated with a higher apnea hy

185 Path analysis demonstrated that dentate gyrus mean diffusivity mediates the impact of OSAS on ve

186 uracy of a regression model based on dentate gyrus mean diffusivity reached 85.8% (cross validated).

187 n, including bilateral ATL, inferior frontal gyrus, medial prefrontal cortex, angular gyrus, posterio

188 ivity (iFC), highlighting the middle frontal gyrus (MFG) for both competencies.

189 interference and in the right middle frontal gyrus (MFG) for the double interference condition.

190 veraged from three cerebral regions (angular gyrus, mid-frontal cortex, and anterior cingulate gyrus)

191 dition, spikes in the left inferior temporal gyrus, middle temporal gyrus, superior temporal gyrus, a

192 tral ATL (vATL) and anterior middle temporal gyrus (MTG) were shown to connect to areas responsible f

193 piking activity in the human middle temporal gyrus (MTG), a cortical region supporting the semantic r

194 uperior temporal gyrus, left middle temporal gyrus (MTG), and left inferior frontal gyrus (IFG) and o

195 medial rostral part), right middle temporal gyrus (MTG), and right premotor cortex.

196 In the central hilus (CH) of the dentate gyrus, Nav 1.1 immunoreactivity was selectively expresse

197 ecreased connectivity in left middle frontal gyrus of CEN was associated with clinical severity.

198 tivity was identified in left middle frontal gyrus of CEN, left precuneus and bilateral superior fron

199 eft precuneus and bilateral superior frontal gyrus of DMN, and right anterior insula of SN.

200 l relationship between (i) superior-temporal gyrus of either hemisphere and auditory hallucination; (

201 selective calretinin-ir cells in the dentate gyrus of hippocampal-kindled rats, which suggests a poss

202 tor cells isolated directly from the dentate gyrus of MBD1 mutant (KO) and WT mice showed that gene s

203 ramatic shift in excitability in the dentate gyrus of Pafah1b1(+/-) mice that may contribute to epile

204 s reduced TSPO binding in the middle frontal gyrus of patients with recent-onset schizophrenia, who w

205 hexin5 expression using shRNA in the dentate gyrus of presymptomatic adolescent hAPP mice was suffici

206 1, Nav 1.2, Nav 1.6) in area CA1 and dentate gyrus of rat hippocampus.

207 in neural stem cells residing in the dentate gyrus of the adult hippocampus (aNSCs) and MBD1 deficien

208 Granule cells in the dentate gyrus of the hippocampus are thought to be essential to

209 Exercise signals neurogenesis in the dentate gyrus of the hippocampus.

210 g biased choices, the right inferior frontal gyrus, often implicated in inhibiting prepotent response

211 ed on either the left anterior supramarginal gyrus or opercular part of the left inferior frontal gyr

212 group, with no change in the middle frontal gyrus or parietal cortices.

213 either direct damage to the inferior frontal gyrus, or via damage to dorsal lateral prefrontal cortex

214 tivation in the insula and superior temporal gyrus (P < 0.01 for all).

215 teraction was shown in the superior temporal gyrus (P < 0.01).

216 decreased activation in the inferior frontal gyrus (P < 0.01).

217 creased mean diffusivity of the left dentate gyrus (p = 0.002; false discovery rate corrected; adjust

218 ion of the thalamus and the inferior frontal gyrus (pars triangularis), thalamic volume, T2 lesion lo

219 etwork measures of the left superior frontal gyrus, pars orbitalis (r = -0.40, p = 0.009), left thala

220 to tau-tracer uptake in the parahippocampal gyrus, particularly the posterior entorhinal cortex, whi

221 ains was reduced in CD in the left cingulate gyrus post-cocaine and in the left putamen in the abstin

222 ost-cocaine and in the left superior frontal gyrus post-saline.

223 ation of neural activity in left postcentral gyrus (PostCG), right culmen and, co-varying with narcis

224 tal gyrus, medial prefrontal cortex, angular gyrus, posterior MTG, and medial temporal lobes.

225 ss centrality in the medial superior frontal gyrus, precentral gyrus, Rolandic operculum, superior pa

226 cortices as well as the posterior cingulate gyrus, precuneus, and mesial temporal cortex.

227 plementary motor cortex and left postcentral gyrus/precuneus after ECT.

228 erior temporal gyrus (ITG), left postcentral gyrus/precuneus, left supplementary motor area, and left

229 ivation in the precuneus and middle temporal gyrus predicted lower weight variability.From our study

230 speech production including inferior frontal gyrus, premotor cortex, and superior temporal gyrus duri

231 arily to lateral posterior superior temporal gyrus (pSTG) and modulated binaural-cue response functio

232 sal anterior cingulate cortex/medial frontal gyrus (R dACC/MFG).

233 atory hilar mossy cells (MCs) in the dentate gyrus receive inputs from dentate granule cells (GCs) an

234 operculum (related to speed) and postcentral gyrus (related to dot periodicity).

235 activation within the left inferior frontal gyrus relative to nonanxious controls during the re-incl

236 also increased after TMS to the left angular gyrus relative to the vertex.

237 bilateral middle/inferior temporal/fusiform gyrus, respectively) that showed reversed effects (decre

238 the superior temporal gyrus and the angular gyrus, respectively.

239 ocampus/parahippocampus, right orbitofrontal gyrus, right inferior temporal gyrus (ITG), left postcen

240 he medial superior frontal gyrus, precentral gyrus, Rolandic operculum, superior parietal gyrus, angu

241 FICANCE STATEMENT In the hippocampal dentate gyrus, seizures drive retrograde sprouting of granule ce

242 electrodes over the human superior temporal gyrus selectively represented intonation contours.

243 dic memory: medial temporal lobe and angular gyrus; semantic memory: left anterior temporal regions;

244 ween the DLPFC and the left superior frontal gyrus (SFG) and anterior cingulate cortex; and 3) the Ba

245 prefrontal cortex (rd-mPFC)/superior frontal gyrus (SFG) that was also sensitive to (deactivated by)

246 cortex (ACC) and the right superior frontal gyrus (SFG).

247 s IV/V and VIII), bilateral superior frontal gyrus (SFG, medial rostral part), right middle temporal

248 The dentate gyrus shows a novel phenotype: the infrapyramidal blade

249 ite (vertex), disruption of the left angular gyrus significantly reduced the number of internal (i.e.

250 18 years forecasted diminished left dentate gyrus (simple slope, -14.20; standard error, 5.22; P = .

251 own the importance of the left supramarginal gyrus (SMG) for pitch memory.

252 in hippocampus, precuneus, superior temporal gyrus (STG) and insula.

253 t that the right posterior superior temporal gyrus (STG) in the human brain is specialized for aspect

254 synaptic gain in the left superior temporal gyrus (STG).

255 lated areas of the rostral superior temporal gyrus (STGr) and temporal pole.

256 ulate, inferior parietal lobe, supramarginal gyrus, striatum, and thalamus.

257 nvestigate the relationships between dentate gyrus structure, hippocampus-dependent cognition, and ob

258 were frequently found in the CA3 and dentate gyrus sub-regions, corresponding to large thorny excresc

259 ence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure.

260 eft inferior temporal gyrus, middle temporal gyrus, superior temporal gyrus, and fusiform gyrus durin

261 e modules, including a left inferior frontal gyrus/supplementary motor area, which was most strongly

262 d reduced power of the left superior frontal gyrus (t=-3.386, p=9.56 x 10(-4)) and increased power at

263 d (subiculum, cornu ammonis 1-3, and dentate gyrus) targets of immunomodulation-treated LGI1 VGKC-com

264 f an LPFC region (in the left middle frontal gyrus) that was recruited by both executive and choice t

265 teral prefrontal cortex and inferior frontal gyrus), the medial prefrontal cortex, and the dorsal ant

266 representing three brain regions-the frontal gyrus, the lateral substantia, and the medial substantia

267 he paracentral lobule, the superior temporal gyrus, the middle cingulate gyrus, the putamen and the s

268 A second excitatory cell type in the dentate gyrus, the mossy cell, forms an intricate circuit with g

269 in regions of the precentral and postcentral gyrus, the paracentral lobule, the superior temporal gyr

270 language areas such as the inferior frontal gyrus, the posterior superior temporal gyrus, and the in

271 uperior temporal gyrus, the middle cingulate gyrus, the putamen and the superior parietal lobules.

272 hese pathways: the posterior middle temporal gyrus, thought to serve as a lexical interface and speci

273 A1 of pre-adolescent rodents, and in dentate gyrus throughout maturity.

274 bserved that damage to the inferior temporal gyrus, to the fusiform gyrus and to a white matter netwo

275 s of speech from posterior superior temporal gyrus toward anterior superior temporal gyrus in the hum

276 ssive microstructural changes in the dentate gyrus translate to the severity of hippocampal sclerosis

277 " speech representations in inferior frontal gyrus typically associated with high-level language proc

278 ed in hippocampus region CA3 and the dentate gyrus under both conditions.

279 le for the astroglial xCT in ventral dentate gyrus (vDG) in stress and antidepressant responses.

280 Critically, human dentate gyrus volume decreases with age whereas CA3 volume is ag

281 separation task, we demonstrate that dentate gyrus volume predicts accuracy and response time during

282 Further, decreased dentate gyrus volume, and no other subfield volume, mediates adv

283 fetime alcohol drinking and superior frontal gyrus volume.

284 Smaller inferior frontal gyrus volumes and poor emotional awareness sequentially

285 ng of happy faces, activation in postcentral gyrus was a significant predictor of treatment response.

286 haviour, while hypertrophy in the precentral gyrus was associated with declining behaviour.

287 cells in the subgranular zone of the dentate gyrus was observed.

288 e to the onset of objects in parahippocampal gyrus was predictive of trait differences in creativity.

289 iment: subjects whose right inferior frontal gyrus was temporarily disrupted made biased choices more

290 (cLBP study, thalamus; ALS study, precentral gyrus) was normalized with the SUV from candidate pseudo

291 rior temporal cortex toward inferior frontal gyrus were associated with linguistic features such as v

292 t supplementary motor area, and left lingual gyrus were identified as predictors of ECT response, ach

293 cellularly recorded cells in CA1 and dentate gyrus were modulated by HRR and theta oscillations.

294 cues in the insula, declive, and precentral gyrus were negatively related to appetitive traits (P <

295 were combined in the right inferior frontal gyrus, where they operated in agreement with the confide

296 rules from both levels except for precentral gyrus, which represented only low-level rule information

297 ral stem cell differentiation in the dentate gyrus, with higher expression intensity in neuroblast ce

298 in the medial entorhinal cortex and dentate gyrus, with no frank noradrenergic cell body loss.

299 her temporary disruption of the left angular gyrus would impair both episodic simulation and memory (

300 neus (z score = 3.95, P < .001), the lingual gyrus (z score = 4.31, P < .001), and the crus I/II of t