ライフサイエンスコーパス: gyrus

1 superior frontal gyrus, and middle temporal gyrus).

2 e junction of the right lingual and fusiform gyrus.

3 association fibers that course through this gyrus.

4 temporal lobe, precuneus cortex, and angular gyrus.

5 ior CA1, parahippocampal cortex, and angular gyrus.

6 ls and the majority of spines in the dentate gyrus.

7 yrus and the left posterior superior frontal gyrus.

8 ed in the activation of the inferior frontal gyrus.

9 en the right amygdala and the middle frontal gyrus.

10 emporal cortex, precuneus, and supramarginal gyrus.

11 s, and in both planum temporale and Heschl's gyrus.

12 a larger interindividual variability in the gyrus.

13 y enriched in granule neurons of the dentate gyrus.

14 ortices, as well as the left middle temporal gyrus.

15 ranule cells and PV interneurons per dentate gyrus.

16 nesis and synaptic plasticity in the dentate gyrus.

17 ssion in mature granule cells in the dentate gyrus.

18 d by PD except for a decrease in the dentate gyrus.

19 rs II-III, IV, and V, as well as the dentate gyrus.

20 unction of neurogenesis in the adult dentate gyrus.

21 lobes and decrease in the superior temporal gyrus.

22 selectivity to arise in the lateral fusiform gyrus.

23 e, superior/mid-temporal, and middle frontal gyrus.

24 the HC and increases in the parahippocampal gyrus.

25 es with blood sinus and folds of the rostrum gyrus.

26 otor cortex and left medial superior frontal gyrus.

27 ortical thickness of the transverse temporal gyrus (0.90[0.86; 0.96]; p = 5 x 10(-4)), educational at

28 thickness (maximum Cohen's d (left fusiform gyrus) = -0.33).

29 cortex, 0.24 ug . g(-1) +/- 0.04 in dentate gyrus, 0.17 ug . g(-1) +/- 0.04 in hippocampus) and subc

30 active for reelin and project to the dentate gyrus [17, 18].

31 choline was increased in left middle frontal gyrus (18 voxels, CCLAV = 0.04).

32 current density in the right middle frontal gyrus, a region associated with attentional engagement.

33 netfeedback inhibition in the mouse dentate gyrus, a region critically involved in pattern separatio

34 te that dopamine D1 receptors in the dentate gyrus act as a pivotal mediator of antidepressant action

35 orrelation network analysis revealed lingual gyrus activation during self-criticism, a marker of visu

36 emporoparietal junction and inferior frontal gyrus activation with compassion during emotionally prov

37 attached individuals showed greater lingual gyrus activation, and more avoidantly attached individua

38 ttachment positively correlated with lingual gyrus activation, whilst avoidant attachment was negativ

39 tly attached individuals showed less lingual gyrus activation.

40 hment was negatively correlated with lingual gyrus activation.

41 s in the dentate hilus that regulate dentate gyrus activity and function.

42 tamen, globus pailldus, and inferior frontal gyrus after donepezil treatment (p < 0.001).

43 riptomic-wide changes in the ventral dentate gyrus after SDS.

44 ions to the occipital lobe from the fusiform gyrus along with longer association fibers that course t

45 t neural network including the supramarginal gyrus also involved in emotional and visual perspective

46 e middle temporal gyrus (MTG), paracingulate gyrus, amygdala, hippocampus, putamen, thalamus, and bra

47 d observed decisions in the inferior frontal gyrus and a dissociation in the anterior prefrontal cort

48 e schizophrenia, including superior temporal gyrus and anterior cingulate cortex, were most abnormal

49 of hippocampal function suggest that dentate gyrus and CA(2,3) (DG/CA(2,3)) are biased to differentia

50 we find this distributed code in the dentate gyrus and CA1 subregions of the hippocampus.

51 hanged the conductances of simulated dentate gyrus and CA3 hippocampal neurons according to our measu

52 the synaptic connections between the dentate gyrus and CA3, which are thought to be critical for enab

53 uronal cytoplasmic inclusions in the dentate gyrus and cornu ammonis regions 1 and 2 of patients with

54 us, orbital frontal cortex, inferior frontal gyrus and dorsomedial prefrontal cortex (IFG, dmPFC).

55 ) on excitability of the hippocampal dentate gyrus and epileptogenesis after brain injury.

56 ated in ASD, including the superior temporal gyrus and inferior frontal sulcus.

57 ippocampus and exemplars in inferior frontal gyrus and lateral parietal cortex.

58 Differences were prominent in the fusiform gyrus and lateral temporal lobe.

59 ghlighting the role of left inferior frontal gyrus and left anterior temporal lobe in the process of

60 ts evoked responses in left inferior frontal gyrus and left anterior temporal lobe that related to ou

61 s altered) connectivity between left angular gyrus and left frontal pole predicted better response to

62 nections between left rostral medial frontal gyrus and left nucleus accumbens as well as right fronta

63 with decreased FC between the right fusiform gyrus and left superior occipital cortex.

64 primary motor cortex (M1), IPL/supramarginal gyrus and middle occipital gyrus (MOG) during action exe

65 inferior frontal, middle frontal and angular gyrus and parahippocampus) and reward systems (orbital g

66 ng (superior temporal and medial postcentral gyrus and parahippocampus) were the main post-training h

67 yrus, and bilaterally in the middle temporal gyrus and precuneus.

68 ted with risk for SCZ, in left supramarginal gyrus and right frontal regions with risk for BD, and in

69 ld potentials from both the inferior frontal gyrus and subthalamic nucleus in 21 subjects.

70 rdirect pathway between the inferior frontal gyrus and subthalamic nucleus is hypothesized to mediate

71 dorsolateral prefrontal cortex/supramarginal gyrus and supramarginal gyrus/middle temporal gyrus was

72 ight ACC-seeded FC with the right precentral gyrus and the bilateral middle and posterior cingulate g

73 f the activation of the left parahippocampal gyrus and the left fusiform gyrus, recruited during faci

74 ypometabolism in the right superior temporal gyrus and the left inferior parietal lobule.

75 Network, including the left inferior frontal gyrus and the left posterior superior frontal gyrus.

76 of primates and that the anterior cingulate gyrus and the mSTS support these computations.

77 e scan and activation of the parahippocampal gyrus and the right hippocampus yielded to loss anticipa

78 t pathway that connects the inferior frontal gyrus and the subthalamic nucleus.

79 ic connectivity between the inferior frontal gyrus and ventral subthalamic nucleus.

80 a group of inferior parietal (supramarginal gyrus) and superior parietal (intraparietal and superior

81 egions with foveal tendencies (e.g. fusiform gyrus), and activations of layer-units with selectivity

82 ngular gyrus, right amygdala/parahippocampal gyrus, and bilaterally in the middle temporal gyrus and

83 being highest in the olfactory bulb, dentate gyrus, and cerebellum.

84 ncy in the left superior and middle temporal gyrus, and individuals with psychotic BD did not show si

85 patterns within the visual cortex, fusiform gyrus, and lateral temporal lobe.

86 at the mesial frontal lobes, parahippocampal gyrus, and lateral temporal neocortex were at least twic

87 solateral prefrontal cortex/superior frontal gyrus, and left medial orbitofrontal cortex.

88 anterior cingulate cortex, inferior frontal gyrus, and middle frontal gyrus was significantly increa

89 tus, orbital segment of the superior frontal gyrus, and middle temporal gyrus).

90 nivariate responses in left inferior frontal gyrus, and multivariate responses in left anterior tempo

91 yrus, inferior frontal gyrus, middle frontal gyrus, and operculum, indicating a similar neural networ

92 rbitofrontal cortex, right inferior temporal gyrus, and right frontal pole.

93 ofrontal gyri (LOFG), left superior temporal gyrus, and right insular, lingual and superior parietal

94 sistent activation of the amygdala, fusiform gyrus, and thalamus than emerging adults, who showed mor

95 ions, including the precuneus, the cingulate gyrus, and the hippocampus, regions commonly associated

96 on was applied to the right inferior frontal gyrus/anterior insula node of the salience network, whic

97 In the banded mongoose the dentate gyrus appears to be comprised of up to seven lamina, thr

98 and geometry of the rostrum and the rostrum gyrus are similar, albeit with a collapsed nostril and a

99 fferences in the bordering landmarks of each gyrus as well as in the manner in which variability was

100 inly connected to the ipsilateral precentral gyrus as well as to both cerebellar hemispheres and the

101 mouth opening was found in the right angular gyrus at <1 Hz, and in early visual cortices at 1-8 Hz.

102 6, and 38), in the right frontal subcallosal gyrus (BA 34) and caudate body, and in the cerebellar to

103 in the right superior and precentral frontal gyrus (BA 6) in the patient group, compared with the con

104 compared to patients in the parahippocampal gyrus (BA27) and perirhinal cortex (BA36).

105 visual cortex and the right superior frontal gyrus based on the conjunction of the first two analyses

106 e spectroscopy in the right inferior frontal gyrus, because of its strong association with response i

107 ntly expressed on the neurons of the dentate gyrus, but its role in mediating behavioral responses to

108 ersus controls in the right inferior frontal gyrus, but not the occipital lobe.

109 ions for overlapping memories in the dentate gyrus/CA(2,3) and subiculum subfields of the hippocampus

110 st effects on the CA3 region and the dentate gyrus (CA3-DG) of the hippocampus, alongside associated

111 nct neuron type pairs throughout the dentate gyrus, CA3, CA2, CA1, subiculum, and entorhinal cortex.

112 ng pyramidal cells, but not putative dentate gyrus/CA3-projecting stellate cells, represented speed p

113 right cerebellum, and right superior frontal gyrus, compared with HC.

114 ual fear memory engrams in the mouse dentate gyrus contain functionally distinct neuronal ensembles,

115 oped more neuronal inclusions in the dentate gyrus, cornu ammonis regions 1, 2 and 4, and the subicul

116 uronal cytoplasmic inclusions in the dentate gyrus, cornu ammonis regions 1-4 and entorhinal cortex.

117 amate concentrations in the inferior frontal gyrus correlated inversely with stop-signal reaction tim

118 n signaling in the postmortem middle frontal gyrus cortex.

119 R-expressing cells within the dorsal dentate gyrus (dDG), but not the dorsal CA1 (dCA1).

120 NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellular proc

121 bation expressed only in hippocampal dentate gyrus (DG) and assessed its association with hippocampal

122 entations for unexpected items, with dentate gyrus (DG) and CA3 being more sensitive to expectation v

123 ses instantiated upstream within the dentate gyrus (DG) and CA3 subregions.

124 computational circuits involving the dentate gyrus (DG) and proximal CA3.

125 Mossy cells (MCs) of the dentate gyrus (DG) are a major group of excitatory hilar neurons

126 The dentate gyrus (DG) controls information flow into the hippocampu

127 The dentate gyrus (DG) has a key role in hippocampal memory formatio

128 ithin the mammalian hippocampus, the dentate gyrus (DG) has the unique characteristic of exhibiting n

129 egions and layers of the hippocampus dentate gyrus (DG) in an electric stimulation rodent model which

130 The reorganization of the dentate gyrus (DG) in TLE may create pathological conduction pat

131 The hippocampal dentate gyrus (DG) is a unique brain region maintaining neural s

132 pairments.SIGNIFICANCE STATEMENT The dentate gyrus (DG) is important for learning, memory, pattern se

133 the supramammillary nucleus (SuM) to dentate gyrus (DG) is needed for contextual memory, social memor

134 tau in GABAergic interneurons in the dentate gyrus (DG) of AD patients and mice.

135 ronal hyperactivity was found in the dentate gyrus (DG) of leuprolide-treated females, but not males,

136 and neuronal differentiation in the dentate gyrus (DG) of the hippocampus and significantly impaired

137 l analog of ECT, neurogenesis in the dentate gyrus (DG) of the hippocampus is observed.

138 he subventricular zone (SVZ) and the dentate gyrus (DG) of the hippocampus, whereas the implantation

139 Dentate gyrus (DG) of the mammalian hippocampus gives rise to ne

140 The dentate gyrus (DG) plays a central role in the process of memory

141 The CA3 and dentate gyrus (DG) regions of the hippocampus are considered key

142 Neural stem cells (NSCs) in the dentate gyrus (DG) reside in a specialized local niche that supp

143 oliferation in the adult hippocampus dentate gyrus (DG) subgranular zone.

144 Acute neuronal activation of the dentate gyrus (DG) using cFos immunohistochemistry was measured

145 Dentate gyrus (DG), a "gate" that controls information flow into

146 n the hippocampus and especially the dentate gyrus (DG), a vulnerable brain region and one of the two

147 paired GABAergic transmission in the dentate gyrus (DG), accompanied by schizophrenia-like behavior i

148 major cell type in the hilus of the dentate gyrus (DG), are unique in providing extensive longitudin

149 e three major hippocampal subfields, dentate gyrus (DG), CA3, and CA1, has a unique function in memor

150 nputs from the entorhinal cortex and dentate gyrus (DG), the proximal CA3 region of aged rats may swi

151 but whether, and to what extent can dentate gyrus (DG)-resident neural stem cells drive regeneration

152 en behavior and transcription in the dentate gyrus (DG).

153 nction of neurons in the hippocampal dentate gyrus (DG).

154 rofile the granule cell layer of the dentate gyrus (DG-GCL) in human hippocampus and contrast these d

155 Neuroblasts within the aged dentate gyrus display a senescence-associated secretory phenotyp

156 nse in the human posterior superior temporal gyrus, enhancing the efficiency of auditory speech proce

157 The dentate gyrus expressed synaptic function and neurogenesis genes

158 e-XR by an increase in NAc-inferior temporal gyrus FC (p < 0.005).

159 t research indicates that the human fusiform gyrus (FG), which is a hominoid-specific structure criti

160 thalamus for physical, and NAc-paracingulate gyrus for social domains (p < 0.001).

161 eport that human tau accumulation in dentate gyrus GABAergic interneurons disrupts AHN and strengthen

162 We recorded populations of dentate gyrus granule cells (DG GCs) and lateral entorhinal cort

163 ive (DCX(+)) ABGCs as well as DCX(-) dentate gyrus granule cells 2 weeks after a stroke or sham opera

164 rexcitability phenotype displayed in dentate gyrus granule neurons derived from patients with bipolar

165 previously studied the phenotype of dentate gyrus granule neurons, we turned our attention to studyi

166 terior cingulate cortex and inferior frontal gyrus) helped dishonest participants to be honest, where

167 ntly associated with smaller CA3 and dentate gyrus hippocampal subfield volumes but not with CA1 or s

168 This region, comprised of the dentate gyrus, hippocampus proper, subiculum, presubiculum, para

169 In the left inferior frontal gyrus, however, prior knowledge leads to integration, an

170 ve functions and neurogenesis (e.g., dentate gyrus, hypothalamus, olfactory areas, cerebellum) in the

171 d reduced rsFC between left inferior frontal gyrus (IFG) and clusters in the left insula (LINS), lent

172 l prefrontal cortex (DLPFC)/inferior frontal gyrus (IFG) and posterior cingulate cortex (PCC)/precune

173 left anterior or posterior inferior frontal gyrus (IFG) in post-stroke patients with left temporo-pa

174 ncreased feedback from left inferior frontal gyrus (IFG) region to the left occipital (OCC) region.

175 ivity in the portion of the inferior frontal gyrus (IFG) specific to the ventral attention network (V

176 t impairments in a DPFC and inferior frontal gyrus (IFG) system may be important in suicide attempt b

177 e auditory cortex, the left inferior frontal gyrus (IFG), and the bilateral superior temporal gyrus (

178 Inferior frontal gyrus (IFG), ventral premotor cortex (PMv) and inferior

179 tex, and positively in the inferior temporal gyrus; (ii) abnormal CSF amyloid-beta42 (<1098) correlat

180 idely accepted model posits that the dentate gyrus improves learning and memory by enhancing discrimi

181 ateral intraparietal sulcus and left angular gyrus in both adolescents and adults with PTSD.

182 tate-related variables in the medial frontal gyrus in both healthy subjects and smokers, suggesting t

183 terneuron firing between the CA1 and dentate gyrus in epileptic mice.

184 ted timeline suggests that the supramarginal gyrus in IPL links decision regions in prefrontal cortex

185 ltaneously recorded from the CA1 and dentate gyrus in pilocarpine-treated epileptic mice with silicon

186 erior cingulate cortex, and inferior frontal gyrus in response to a high-fat/low-sugar compared with

187 and knob area of premotor cortex (precentral gyrus) in people with tetraplegia.

188 medial prefrontal cortex and middle temporal gyrus increase across the age range.

189 ncorporation of neurons in the adult dentate gyrus increases after chronic stress and suggest that su

190 e cortex (aMCC), anterior insula, precentral gyrus, inferior frontal gyrus, middle frontal gyrus, and

191 t stimulation of D1 receptors in the dentate gyrus is a potential adjunctive approach to improve ther

192 The fusiform gyrus is an important region implicated in such tasks as

193 sized that adult neurogenesis in the dentate gyrus is an ongoing process that maintains normal hippoc

194 est the hypothesis that aging of the dentate gyrus is linked to impaired beacon discrimination and co

195 The fusiform gyrus is understood to be involved in the processing of

196 two primary brain regions (inferior temporal gyrus [ITG] and middle frontal gyrus [MFG]), we tested a

197 t the strength of rsFC between left fusiform gyrus (L-FG) and higher-order language systems predicts

198 dition, ablation of Shh in the adult dentate gyrus led to increased neural precursor cell proliferati

199 yrus, right striatum, right inferior frontal gyrus, left thalamus, bilateral insula, right cerebellum

200 ifferentiated these into hippocampal dentate gyrus-like neurons and astrocytes.

201 form gyrus (rFG) and left inferior occipital gyrus (lIOC), regions associated with face processing.

202 With all that, the rostrum gyrus looks like a model of the pig rostrum at a scale o

203 cal regions, including left superior frontal gyrus (LSFG), and right middle frontal gyrus (RMFG).

204 pha/beta power in the left superior temporal gyrus (lSTG).

205 rior temporal gyrus [ITG] and middle frontal gyrus [MFG]), we tested associations between brain tissu

206 r insula, precentral gyrus, inferior frontal gyrus, middle frontal gyrus, and operculum, indicating a

207 cortex/supramarginal gyrus and supramarginal gyrus/middle temporal gyrus was associated with response

208 The rostrum gyrus mimics rostrum geometry in great detail.

209 IPL/supramarginal gyrus and middle occipital gyrus (MOG) during action execution, and in pars opercul

210 hway-tracing experiments showing the dentate gyrus mossy fiber projection, and its relationship to th

211 al that post-tetanic potentiation at dentate gyrus mossy fiber synapses is induced by natural activit

212 pes, stronger activations of middle temporal gyrus (MT/V5), and hippocampus were found in the aesthet

213 The middle temporal gyrus (MTG) has been shown to be recruited during the pr

214 poral cortices including the middle temporal gyrus (MTG), paracingulate gyrus, amygdala, hippocampus,

215 rior parietal lobe and right middle temporal gyrus (MTG).

216 the bilateral middle and posterior cingulate gyrus (N = 187).

217 deficits are specifically linked to dentate gyrus neurogenesis since cyclin D2(-/-) mice also have a

218 erebellum and cortex besides reduced dentate gyrus neurogenesis.

219 e innate immune system reside in the dentate gyrus neurogenic niche of aged brains in humans and mice

220 The computationally simulated BD dentate gyrus neurons had a hyperexcitability phenotype similar

221 screen task and (56)Fe decreased new dentate gyrus neurons relative to Sham.

222 ar to what we previously reported in dentate gyrus neurons.

223 parahippocampus) and reward systems (orbital gyrus, nucleus accumbens and putamen) in driving pre-tra

224 munohistochemistry) cells within the dentate gyrus of adult Egyptian fruit bats from three distinct e

225 roteins are present in the inferior temporal gyrus of human brains; (2) Deltatau314 proteins are gene

226 Elevated MAALIN in the dentate gyrus of impulsive-aggressive suicides was associated wi

227 -selective responses in the lateral fusiform gyrus of individual blind participants during haptic exp

228 AMY), anterior hippocampus (aHIP) and middle gyrus of temporal neocortex (CX) were determined with we

229 Adult neurogenesis in the dentate gyrus of the hippocampus is highly regulated by a number

230 he action of antidepressants, in the dentate gyrus of the hippocampus.

231 amygdala and the rostral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expr

232 Furthermore, deletion of Bdnf in the dentate gyrus, or specifically in LepRb-expressing neurons, abol

233 frontal gyrus (p = 0.004), and supramarginal gyrus (p = 0.003).

234 .010), caudate (p = 0.008), inferior frontal gyrus (p = 0.004), and supramarginal gyrus (p = 0.003).

235 eation in SUVr between groups in the dentate gyrus (p = 0.009).

236 rrected) < 0.05, SBC = -0.32), left fusiform gyrus (P(FDR) < 0.01, SBC = -0.51).

237 replicated in sample 2: right supramarginal gyrus (p(uncorrected) < 0.05, SBC = -0.32), left fusifor

238 fractional anisotropy in the left cingulate gyrus part of the cingulum, left posterior thalamic radi

239 th decreased size of the hippocampal dentate gyrus, partial agenesis of the corpus callosum, and vent

240 ndary auditory cortex (posterior ectosylvian gyrus, PEG).

241 larity in posterior middle/inferior temporal gyrus (pMTG/ITG) and precuneus (PC) and additionally obs

242 terolateral nucleus (VL/VPL) and postcentral gyrus (PoCG) and between the dorsal/ventral medial nucle

243 d decreases in activation in the postcentral gyrus, prefrontal cortex, insula, and anterior cingulate

244 Neurons in the anterior cingulate gyrus, previously implicated in vicarious reinforcement

245 expressing interneurons (PVs) in the dentate gyrus provide activity-dependent regulation of adult neu

246 female) over the posterior superior temporal gyrus (pSTG), a brain area known to be important for spe

247 d activation in mid-insula, superior frontal gyrus, putamen, dorsal anterior cingulate, posterior cin

248 nnel agonist, we studied the role of dentate gyrus PV cells in regulating anxiety-like behavior and r

249 Activation of the Kv3.1 channel in dentate gyrus PV cells may represent a target for the developmen

250 or, whereas upregulation of Kv3.1 in dentate gyrus PV cells or acute activation of Kv3.1 using a spec

251 The activity of dentate gyrus PV cells plays a major role in the behavioral resp

252 capacity of high-frequency firing in dentate gyrus PV cells, and altered short-term plasticity at syn

253 the function and mechanism of p11 in dentate gyrus PV cells.

254 ncorrected) = 0.049) and right supramarginal gyrus (r = -0.19, p(uncorrected) = 0.043) in the HCMV+ g

255 was correlated with GMV in the left fusiform gyrus (r = -0.19, P(uncorrected) = 0.049) and right supr

256 The pig's cortical rostrum gyrus receives dense thalamic innervation, has a thin La

257 parahippocampal gyrus and the left fusiform gyrus, recruited during facial expression processing, we

258 and decreased cortical thickness in others (gyrus rectus, orbital segment of the superior frontal gy

259 ng on the medial and orbital surfaces of the gyrus rectus, this study addresses a key question of cau

260 rradiation improved performance on a dentate gyrus-reliant pattern separation task; irradiated mice l

261 as the middle temporal and superior frontal gyrus, represented state- and trait-related markers of d

262 last century mapped a somatosensory cortical gyrus representing the pig's rostrum.

263 classically place-selective parahippocampal gyrus, retrosplenial complex, and transverse occipital s

264 odulated BOLD activity in the right fusiform gyrus (rFG) and left inferior occipital gyrus (lIOC), re

265 ht: p = 0.001; left: p = 0.001), and angular gyrus (right: p = 0.011; left: p = 0.001).

266 right superior frontal gyrus, right angular gyrus, right amygdala/parahippocampal gyrus, and bilater

267 ng as children in the right superior frontal gyrus, right angular gyrus, right amygdala/parahippocamp

268 y matter abnormalities in left supramarginal gyrus, right striatum, right inferior frontal gyrus, lef

269 ontal gyrus (LSFG), and right middle frontal gyrus (RMFG).

270 coefficient (SBC) = -0.26) and left fusiform gyrus (SBC = -0.25) in sample 1 were replicated in sampl

271 Chronometric stimulation of Heschl's gyrus selectively disrupts speech perception, while stim

272 In dogs, the bilateral mid suprasylvian gyrus showed conspecific-preference, no regions exhibite

273 parietal cortex (specifically supramarginal gyrus [SMG]) integrates saccade and visual signals to up

274 mygdala and precuneus and superior occipital gyrus (SOG).

275 reductions in GMV of the right supramarginal gyrus (standardized beta coefficient (SBC) = -0.26) and

276 , and caspase-like) in the superior temporal gyrus (STG) of 25 SZ and 25 comparison subjects using fl

277 s (IFG), and the bilateral superior temporal gyrus (STG).

278 k performance in posterior superior temporal gyrus (STGp) that was observed in healthy subjects.

279 eled maturing newborn neurons in the dentate gyrus subgranular zone, and a single-Reelin infusion inc

280 ippocampal formation (cornu Ammonis, dentate gyrus, subicular complex, and entorhinal cortex) were re

281 in the hippocampus (CA1, CA2/3, CA4, dentate gyrus, subiculum) and presubiculum layers (PSB1, PSB3) w

282 like neural stem cells (RGLs) in the dentate gyrus subregion of the hippocampus give rise to dentate

283 four different brain regions (medial frontal gyrus, superior temporal gyrus, thalamus, and subventric

284 ment of glutamatergic perforant path-dentate gyrus synapses, but not in commonly studied in Schaffer

285 a control site (vertex) or to a left angular gyrus target region.

286 ons (medial frontal gyrus, superior temporal gyrus, thalamus, and subventricular zone).

287 mentalizing (i.e. the left superior temporal gyrus) than joy.

288 T1w/T2w ratios in the right parahippocampal gyrus, the executive part of both putamina, both thalami

289 in region overlaps with the inferior frontal gyrus, the frontal eye field, and the dorsolateral prefr

290 rticulatory lip movements; the right angular gyrus then extracts slower features of lip movements, ma

291 ms, likely a proxy of right inferior frontal gyrus; then, at 140 ms, there was a broad skeletomotor s

292 ibe the extraordinary correspondence of this gyrus to the rostrum.

293 rgent thinking following cTBS to the angular gyrus versus vertex but not during the nonepisodic contr

294 yrus and supramarginal gyrus/middle temporal gyrus was associated with response to sertraline and ven

295 , inferior frontal gyrus, and middle frontal gyrus was significantly increased in the BD group compar

296 he bilateral temporal poles and the fusiform gyrus were associated with prosopagnosia in rtvFTD.

297 eurogenesis was nearly absent in the dentate gyrus, which was due to inhibited proliferation of neura

298 GN1 decreased neuronal counts in the dentate gyrus, which was not the case in wild-type animals, and

299 CA1 and CA3 fields, the hilus of the dentate gyrus (with sparing of granule cells), and the entorhina

300 enhanced the recovery of NPCs in the dentate gyrus, with sex-dependent effects on neurogenesis and co