ライフサイエンスコーパス: default mode network

1 sk-negative" patterns of activity (e.g., the default mode network).

2 network associated with mind wandering (i.e. default mode network).

3 whereas the dorsomedial module resembles the default mode network.

4 decreased functional connectivity within the default mode network.

5 ithin an intrinsic connectivity network, the default mode network.

6 y regions in the visual cortex and posterior default mode network.

7 ience network, dorsal attention network, and default mode network.

8 esonance imaging with a focus on the brain's default mode network.

9 enerally overlapped with the distribution of default mode network.

10 tentional capacity and tends to activate the default mode network.

11 aused by functional disconnection within the default mode network.

12 es, from the brain's salience network to the default mode network.

13 gnals in multiple expression datasets in the default mode network.

14 , and closely corresponded to regions of the default mode network.

15 beyond the temporal lobe, especially in the default mode network.

16 th greater activity in medial regions of the default mode network.

17 orrelated with activity in the task-negative default mode network.

18 ong with additional areas of the VAN and the default mode network.

19 ted, particularly in the pain matrix and the default mode network.

20 ated to reduced functional activation of the default mode network.

21 d navigation, and is a core component of the default mode network.

22 ateral parietal and precuneus regions of the Default Mode Network.

23 n the frontoparietal control network and the default mode network.

24 yzed resting-state data from the core of the default-mode network.

25 l network and negative correlations with the default-mode network.

26 unctional connectivity mainly located in the default-mode network.

27 ogy, include the structural substrate of the default-mode network.

28 nternal organization, closely related to the default-mode network.

29 fically in the cerebellum, visual areas, and default-mode network.

30 attention, central executive, salience, and default mode networks.

31 s that included dorsal/ventral attention and default mode networks.

32 right-biased ICs was connected to social or default mode networks.

33 mparisons of the salience, sensorimotor, and default mode networks.

34 arietal, subcortical, cingulo-opercular, and default-mode networks.

35 rsal prefrontal and regions of the limbic or default-mode networks.

36 modulate long-range connectivity within the default mode network [15].

37 lacked the typical anticorrelation with the default mode network; 2) hypoconnectivity between left d

38 been shown to be one of the main hubs of the Default Mode Network, a network classically activated du

39 vity disequilibrium between the salience and default-mode networks, a finding of potential pathophysi

40 l beliefs produced increased activity in the default mode network-a set of interconnected structures

41 vision is preferentially correlated with the default mode network; a second is preferentially correla

42 ke, the PCC, consistently a main hub of the "default mode network," activates in response to smoking

43 In addition, anodal stimulation normalized default mode network activation in patients with poor re

44 tive control from difficulties shifting from default mode network activity to task-positive network a

45 nspection of the spatial maps related to the default mode network and a frontoparietal task control n

46 r (greater positive) connectivity within the default mode network and by anticorrelated (greater nega

47 cortex and functional connectivities in the default mode network and central executive network in th

48 ed by cortical patterns of activation in the default mode network and deactivation in the frontoparie

49 nvolving increased cortical thickness in the default mode network and decreased cortical thickness in

50 ngs extend previous research implicating the default mode network and dopaminergic dysfunction in ADH

51 (ii) high connectivity between the posterior default mode network and hubs of high connectivity (many

52 tivity between the nucleus accumbens and the default mode network and increased connectivity between

53 ecreased FNC between these networks (insular-default mode network and insular-cerebellum) was found i

54 rment and in mood and anxiety disorders: the default mode network and negative affective network.

55 s, and show that anticorrelation between the default mode network and parietal regions of the dorsal

56 ortex (vmPFC) is one of the main hubs of the Default Mode Network and plays a central role in value c

57 ht reduced positive connectivity between the default mode network and salience network in attempters

58 ap-like representations in subregions of the default mode network and sentence-like representations o

59 ges, we discovered that brain regions in the default mode network and somatosensory/somatomotor hand,

60 dren exhibited hyperconnectivity between the default mode network and subgenual anterior cingulate co

61 hronization) that affects key regions of the default mode network and temporal areas.

62 The anti-correlation strength between the default mode network and the central executive network w

63 vity and diminished connectivity between the default mode network and the cingulo-opercular network.

64 te aberrant involvement of the insula in the default mode network and the frontal frontoparietal task

65 structural connectivity between nodes of the default mode network and the frontal-thalamo-caudate reg

66 scussed in the context of MPH effects on the default mode network and the possible role of the defaul

67 divergent impact these disorders have on the default mode network and the salience network.

68 first primarily involves the regions of the default mode network and the second comprises the fronta

69 ork disruption, affecting key regions of the default mode network and the temporal cortex.

70 he precentral cortex, prefrontal cortex, and default mode network and these brain hyper-responses wer

71 nal connectivity at rest (coupling with the "default mode network" and "frontoparietal control system

72 e functional connectivities of the posterior default mode network, and positively correlated with fro

73 lts highlight the central role of the sgACC, default mode network, and salience network as predictors

74 er-order cognitive modules: control network, default mode network, and salience/ventral attention net

75 d responsivity in the nucleus accumbens, the default mode network, and the cingulo-opercular network.

76 R sample compared with the HC sample for the default-mode network, and increased covariance was obser

77 s between SN, central executive network, and default mode network are a reproducible feature of child

78 network (SN), central executive network, and default mode network are dysregulated in children with A

79 sis and find that regions of interest within default mode network are encoding task-relevant informat

80 ty between the precuneus and the rest of the default mode network at rest.

81 creased blood flow to the major nodes of the default mode network became more pronounced and widespre

82 l factors shared abnormal RSFC involving the default mode network, but the directionality (hypo- or h

83 Interactions within the default mode network can be assessed using resting state

84 right lateral OFC was more connected to the default mode network compared to the left lateral OFC.

85 ut C9orf72 expansions exhibited increases in default mode network connectivity compared to controls a

86 ontrol subjects; chi(2) = 8.6, p = .003) and default mode network connectivity during a separate rest

87 reas the thalamus-medial visual and thalamus-default mode network connectivity emerged later, at 1 ye

88 ses revealed salience network disruption and default mode network connectivity enhancement in C9orf72

89 nses were found to have less contribution to default mode network connectivity in individuals with au

90 t with previous neuroimaging studies of TMS, default mode network connectivity played an important ro

91 Exploratory neuroimaging revealed default mode network connectivity was predictive of 1-ye

92 salience network connectivity and heightened default mode network connectivity.

93 The default mode network consistently decreases its activity

94 The brain's default mode network consists of discrete, bilateral and

95 network (SN), central executive network, and default mode network contribute to positive symptoms in

96 better text processing, while reductions in default mode network coupling to the visual system may u

97 Regions of the default-mode network demonstrate lower variability in pa

98 Several regions, mostly localized to the default mode network, demonstrated negative subsequent m

99 uences the location of the vmPFC peak of the Default Mode Network, demonstrating that the location of

100 ce the understanding of the PMC in posterior default mode network development.

101 vestigate the functional organization of the Default Mode Network (DMN) - an important subnetwork wit

102 Within the default mode network (DMN) an area of the dorsomedial pr

103 graphy), we examined connectivity within the default mode network (DMN) and between the DMN and the c

104 rinsic functional connectivity in the dorsal default mode network (DMN) and executive control network

105 cific maturational lag in connections within default mode network (DMN) and in DMN interconnections w

106 terize the functional integration within the Default Mode Network (DMN) and its role in self-perceive

107 curring selectively during activation of the default mode network (DMN) and parietal alpha networks.

108 The default mode network (DMN) and semantic network (SN) are

109 between large-scale networks, in particular, default mode network (DMN) and task-positive networks (T

110 bations to individually defined nodes of the default mode network (DMN) and the dorsal attention netw

111 were implanted with CPEs in two nodes of the default mode network (DMN) and two nodes in a lateral co

112 between 'social brain' circuitry such as the default mode network (DMN) and visual and attention netw

113 ns between the Salience Network (SN) and the Default Mode Network (DMN) are thought to be important f

114 r regions, and task-related deactivations in default mode network (DMN) areas.

115 and dorsolateral prefrontal cortex (PFC) in default mode network (DMN) associated with TD in healthy

116 h the IPS overlapped with regions within the default mode network (DMN) but the IPS also showed conne

117 GNIFICANCE STATEMENT Activation of the human default mode network (DMN) can be measured with fMRI whe

118 The topography of the default mode network (DMN) can be obtained with one of t

119 hildhood poverty was associated with reduced default mode network (DMN) connectivity.

120 The default mode network (DMN) consists of several regions t

121 resent study was to research the patterns of Default Mode Network (DMN) deactivation in Obsessive Com

122 PreC; Brodmann area 7), a key hub within the default mode network (DMN) displays amyloid and tau-cont

123 ognitive performance, and suppression of the default mode network (DMN) during executive functioning

124 ts is marked by aberrant connectivity of the default mode network (DMN) during resting state.

125 st prominent effect being attenuation of the default mode network (DMN) during the first half of a 20

126 Neuroimaging evidence suggests that the default mode network (DMN) exhibits antagonistic activit

127 een working memory performance, task-induced default mode network (DMN) functional connectivity chang

128 The default mode network (DMN) has been defined in functiona

129 functional connectivity (FC) of the brain's default mode network (DMN) has been identified within th

130 The default mode network (DMN) has been shown to increase it

131 The default mode network (DMN) has been suggested to support

132 The default mode network (DMN) has been traditionally assume

133 Regions of the default mode network (DMN) have been frequently identifi

134 sotropy), and functional connectivity of the default mode network (DMN) in 54 amnestic mild cognitive

135 terior cingulate cortex (PCC) regions of the default mode network (DMN) in dogs.

136 at had a spatial distribution similar to the default mode network (DMN) in humans, consistent with ea

137 ty indexed with goodness of fit (GOF) of the default mode network (DMN) in the drug group and decreas

138 The default mode network (DMN) is a commonly observed restin

139 The default mode network (DMN) is a complex dynamic network

140 The evolutionarily conserved default mode network (DMN) is a distributed set of brain

141 ., valence and arousal), we propose that the default mode network (DMN) is additionally important for

142 The default mode network (DMN) is associated with a wide ran

143 Reduced deactivation within the default mode network (DMN) is common in individuals with

144 The default mode network (DMN) is critical in this study, gi

145 The brain's default mode network (DMN) is highly active during wakef

146 The brain's default mode network (DMN) is highly heritable and is co

147 ation and functional connectivity within the default mode network (DMN) of the brain while participan

148 Does the default mode network (DMN) reconfigure to encode informa

149 ing that mindfulness meditation may increase default mode network (DMN) resting-state functional conn

150 dent, cognition overlap with key hubs of the default mode network (DMN) that become compromised by am

151 een the functional and structural changes of default mode network (DMN) underlying the cognitive impa

152 The brain default mode network (DMN) was activated, gauged by incr

153 etworks-the cingulo-opercular network (CON), default mode network (DMN), and frontoparietal network-a

154 etal network (FPN), hyperconnectivity in the default mode network (DMN), and increased connection bet

155 , including central executive network (CEN), default mode network (DMN), and salience network (SN).

156 referentially decreased in the thalamus, the Default Mode Network (DMN), and the bilateral Frontopari

157 retrial brain activity in key regions of the default mode network (DMN), but not the dorsal attention

158 influences the way our brain networks [e.g., default mode network (DMN), fronto-parietal network (FPN

159 The brain's default mode network (DMN), having a high rate of basal

160 connectivity between regions involved in the default mode network (DMN), implicated in divergent thin

161 sses, most notably increased activity in the default mode network (DMN), suppressed activity within t

162 rontoparietal control network (FPCN) and the default mode network (DMN), two networks that do not str

163 as been implicated in cognitive function and default mode network (DMN), which has been implicated in

164 A unifying function associated with the default mode network (DMN), which is more active during

165 tional connectivity within the resting state default mode network (DMN), which may signal heightened

166 t, we examine the existence of the so-called default mode network (DMN)--a distributed functional bra

167 N) and the medial prefrontal-medial parietal default mode network (DMN)-are consistent findings in de

168 rest, including hyperconnectivity within the default mode network (DMN).

169 es, i.e., several of the core regions of the default mode network (DMN).

170 erior parietal lobe, a prominent node of the default mode network (DMN).

171 bolic RSN was topographically similar to the default mode network (DMN).

172 resting-state functional connectivity in the default mode network (DMN).

173 uage network (LN) and anti-correlated to the default mode network (DMN).

174 structure and functional connectivity of the default mode network (DMN); and (3) the interactions bet

175 remitters by greater connectivity within the default mode network (DMN); specifically, between the DM

176 n of activation in the posterior node of the default mode network (DMN; p = 0.006).

177 he typical balance of connections within the default mode network (DMN; prominent during introspectiv

178 ortical systems-the multiple-demand (MD) and default mode networks (DMN)-during multistep task episod

179 ortical systems-the multiple-demand (MD) and default mode networks (DMN).

180 Existing evidence suggests that the default-mode network (DMN) and fronto-pariatal network (

181 tive correlation between fluctuations in the default-mode network (DMN) and task-positive networks, w

182 d with the visual system posteriorly and the default-mode network (DMN) anteriorly.

183 erential operations performed by the brain's default-mode network (DMN) has prompted interest in exam

184 pth associated with the FNE was found in the default-mode network (DMN) involved with spontaneous int

185 d that activity in the posterior part of the default-mode network (DMN) is down-regulated by both nor

186 th broad cognitive domains; for example, the Default-mode network (DMN) is engaged during internally

187 The default-mode network (DMN) is known to be dysfunctional,

188 yses, increased RSFC was observed within the default-mode network (DMN) post-treatment.

189 volving the so-called salience network (SN), default-mode network (DMN), and frontoparietal task cont

190 Cognitive brain networks such as the default-mode network (DMN), frontoparietal network, and

191 ent analysis revealed 4 major NCNs: anterior default-mode network (DMN), posterior DMN, salience netw

192 ss four major cortical association networks [default-mode network (DMN), salience network (SAL), dors

193 measured in dorsal attention network (DAN), default-mode network (DMN), salience network (SN), and e

194 ct and functionally antagonistic system--the default-mode network (DMN)--which typically deactivates

195 or network (SMN), salience network (SN), and default-mode network (DMN)-and in neurotransmitters sign

196 al regions that, in humans, are known as the default-mode network (DMN).

197 d connectivity between the precuneus and the default-mode network (DMN).

198 asks are now known to deactivate the brain's default-mode network (DMN).

199 edial prefrontal cortex overlapping with the default-mode network (DMN).

200 -task-positive) and decreased or "negative" [default-mode network (DMN)] fMRI responses during task p

201 tive networks ["external-task positive" and "default-mode network" (DMN)] are responsive to increasin

202 d segregation between anterior and posterior default-mode networks (DMNs).

203 ctivity of four known neural networks (i.e., default mode network, dorsal attention network, salience

204 reative-ideation regions associated with the default mode network (dorsomedial prefrontal cortex, mid

205 Because default mode network downregulation is reliant on input

206 and increases functional connectivity to the default mode network during conditioned heroin withdrawa

207 ger adults, while failing to disengage their default-mode network during learning.

208 However, integration of the default mode network emerged as a key feature differenti

209 Spatially, posterior regions of the brain's default mode network exhibit reductions in both function

210 In contrast, the frontoparietal and default mode networks exhibit similar sharpening of cont

211 findings of this paper are (i) the posterior default mode network fails before measurable amyloid pla

212 In the default mode network, fMRI amplitude was 0.57% (SD 0.26)

213 cognitive control, and a segregation of the default mode network from task-related networks.

214 functional connectivity using seeds from the default mode network, frontoparietal network, and cingul

215 connectivity overlap with structures in the Default Mode Network, Frontoparietal Network, Ventral At

216 Our results of aberrant default mode network functional connectivity and distinc

217 The default mode network has distinct subsystems with unique

218 While medial-visual and default-mode networks have the highest rPWR, frontoparie

219 ired reward responsivity was associated with default mode network hyperconnectivity and diminished co

220 Heterogeneous default mode network hypo- and hyper-RSFC across the fac

221 ing working memory in extensive areas in the default mode network (i.e., greater task-induced deactiv

222 Finally, the default-mode network, identified in a separate resting-s

223 thin two major intrinsic brain networks: the default mode network, implicated in memory encoding, sto

224 among the SN, central executive network, and default mode network in 130 patients with schizophrenia

225 y processing and integration, as well as the default mode network in girls, and with weaker connectiv

226 the functionally distinct inferior parietal default mode network in humans compared to monkeys resul

227 kin to that between the social brain and the default mode network in humans: this overlap specificall

228 and associated vasoconstriction, within the default mode network in hypoxia is supported by increase

229 he face patch resting state networks and the default mode network in monkeys show a pattern of overla

230 lt mode network and the possible role of the default mode network in MPH-mediated improvements in ina

231 nd between temporal pole and elements of the default mode network in NTSCUs.

232 ted decreased functional connectivity in the default mode network in the cognitively normal older adu

233 ectivity between the VL/VPL and PoCG and the default mode network in the more frequent connectivity s

234 onnectivity in the executive control and the default mode networks in the bilingual, compared with th

235 ter is linked to shifts into a task-inactive default-mode network in between task-relevant stimulus o

236 ions belonged to two important networks: the default-mode network, including precuneus and angular gy

237 hey highlight the importance of task control-default mode network interconnections as a major locus o

238 he SN with the central executive network and default mode network is a clinically relevant neurobiolo

239 t stronger intrinsic connectivity within the default mode network is linked to better text processing

240 al connectivity of the ventral attention and default mode networks is associated with behavioral inhi

241 nd that Abeta aggregation within the brain's default mode network leads to regional hypometabolism in

242 duced connectivity between the sgACC and the default mode network, left dorsolateral prefrontal corte

243 usters of coactivated areas with an enlarged default mode network-like posterior region.

244 gher cognitive functions such as the brain's default mode network, may be particularly vulnerable to

245 work, while moxibustion mainly regulated the default mode network of the brain.

246 htened internetwork connectivity between the default mode network, particularly the anterior cingulat

247 inal fasciculus and heritable aspects of the default mode network (phenotypic correlation, rhop = -0.

248 In particular, the default mode network plays a central role in semantic pr

249 The brain's default mode network plays a central role in this work.

250 t of brain regions collectively known as the default mode network plays a crucial role in such "autop

251 ty from the rACC, and key regions within the default mode network (posterior cingulate cortex), front

252 ollows: visual cortex, V3/V3A/V7; within the default mode network, precuneus, and inferior parietal l

253 In general, higher connectivity within the default mode network predicted better outcomes specifica

254 tment connectivity between the sgACC and the default mode network predicted clinical improvement, as

255 The default mode network region (i) had greater connectivity

256 igher FCD in visual and prefrontal cortices, default mode network regions and thalamus, while HD had

257 ere coupled with reduced integration of core default mode network regions in the ventromedial cortex

258 mpal connectivity to multiple prefrontal and default mode network regions, and disrupted the relation

259 uations in brain activity within several key default mode network regions, as well as within the ante

260 rcels/regions included cingulo-opercular and default mode network regions, specifically the anterior

261 characterized by significant deactivation in default mode network regions, suggesting suppression res

262 ive that nAChR agonists suppress activity in default-mode network regions and enhance activity in exe

263 The discovery of the default mode network reignited a longstanding interest i

264 uding regions relevant to cognitive control, default mode network related self-referential thought, b

265 ductions in intranetwork connectivity of the default mode network relative to the HC group (p<0.05 co

266 to the dorsal-attention/fronto-parietal and default-mode networks, respectively.

267 e-scale intrinsic connectivity networks (the default mode network, salience network and central execu

268 left lateral occipital cortex) included the default mode network seed.

269 s well as with parts of the self-referential default-mode network, seemed instrumental in establishin

270 sal prefrontal and regions of the limbic and default-mode networks serves as a significant predictor.

271 regions, including hubs of the executive and default mode networks, showed a robust nonlinear age-by-

272 While applying learned rules, the default mode network shows both greater activity and con

273 orrected ps < .05), which are regions of the default mode network specialized for social and memory f

274 es of the frontoparietal control network and default mode network strengthen their interaction with o

275 Initiative, we characterized the pattern of default mode network subsystem connectivity changes acro

276 ected cortical regions that form most of the default mode network, such as the insula, cingulate cort

277 h four canonical resting-state networks: the default mode network, the dorsal attention network, the

278 resting-state networks (RSNs), including the default mode network, the somato-motor network, the visu

279 intrinsic brain networks in superaging: the default mode network, typically engaged during memory en

280 ate functional connectivity, focusing on the default mode network, ventral and dorsal salience networ

281 Conversely, integration of the default mode network was increased in the sibling group

282 nt VTA/midbrain connectivity strength to the default mode network was negatively correlated.

283 increased correlation of the insula with the default mode network was related to lower attentional ac

284 Higher internal cohesiveness of the default mode network was the single most important posit

285 The default mode network was used as a control network.

286 prefrontal cortices, major components of the default-mode network, was reduced only in patients whose

287 olateral prefrontal cortex and the posterior default mode network were associated with and predictive

288 hat the functional connectivities of (i) the default mode network were greater; (ii) the salience net

289 patterns involving task control networks and default mode network were prominently implicated in pred

290 ife memory test preferentially activated the default mode network, whereas hits in the picture memory

291 ith static brain connectivity in frontal and default mode networks, whereas age showed positive corre

292 within the visual, medial temporal lobe and default mode networks, whereas during task it was driven

293 f cortical areas which are components of the default-mode network, whereas regulation of feedback inh

294 cate a memory-based "autopilot role" for the default mode network, which may have important implicati

295 The rACC is a key hub of the default mode network, which prior studies indicate is hy

296 The failure begins in the posterior default mode network, which then shifts processing burde

297 ample, strong functional connectivity of the default mode network with the superior colliculus in mar

298 hip between rsFC in the anterior salience or default mode networks with inflammation in either study.

299 temporal lobe progressing along the cortical default mode network, with no or minimal involvement of

300 Its anatomy overlaps with the default-mode network, with a network of cognitive contro