ライフサイエンスコーパス: resting state

1 mic activity during a task-free period (the "resting state").

2 two oxidation equivalents above the Fe(III) resting state.

3 ively degraded through the proteasome in the resting state.

4 here CMHs are the catalyst spent form or its resting state.

5 , and bromide efficiently restore the ferric resting state.

6 correlates to the global fMRI signal in the resting state.

7 ur data posits a proton-bound, but occluded, resting state.

8 rements during substrate turnover and in the resting state.

9 s with successive oxidations from the cubane resting state.

10 ls with leaky gates that conduct ions in the resting state.

11 at two oxidation levels above an all-Co(III) resting state.

12 activating histone modifications even in the resting state.

13 working state and functional connectivity at resting state.

14 regulated by Fic-mediated AMPylation during resting states.

15 nd determined to be interconverting catalyst resting states.

16 By correlating spontaneous activity during "resting states" [1], studies of intrinsic brain networks

17 tial correlation analysis of cross-sectional resting-state (18)F-fluorodeoxyglucose positron emission

18 Multiecho resting-state acquisition, combined with micromovement c

19 Additional measurements of resting state activity (eyes closed) tested for segregat

20 ter life, reinforcing the functional role of resting-state activity for effective cognitive processin

21 Connectivity mapping based on resting-state activity in mice has revealed functional m

22 Furthermore, the frontocentral resting-state activity predicted the individual magnitud

23 Nevertheless, the functional role of resting-state activity remains unclear.

24 cumulating data suggest that some cerebellar resting-state alterations may constitute a key candidate

25 In the resting-state analysis, the ventral ATL (vATL) and anter

26 quency, [Na(+)]sm is bounded between 9 mM at resting state and 11.5 mM; and 3) the cells can maintain

27 participants underwent fMRI scanning during resting state and a response inhibition task that robust

28 tional magnetic resonance imaging included a resting state and an experimental paradigm focusing on t

29 s shown to enhance mPFC/ACC activity even at resting state and improve cognitive function in patients

30 s of an enzyme from Neurospora crassa in the resting state and of a copper(II) dioxo intermediate com

31 from Mycobacterium tuberculosis: one in its resting state and one at an intermediate state during tu

32 ctional roles of PCC-ACC connectivity in the resting state and provides insights into the dynamic rel

33 e and allowed identification of the catalyst resting state and turnover-rate limiting step.

34 at cognitive dissonance is reflected in both resting-state and choice-related activity of the prefron

35 Functional resting-state and diffusion magnetic resonance imaging d

36 experiment in the laboratory, together with resting-state and localizer fMRI scans, after the baseli

37 Specifically, resting-state and null-task demand conditions were assoc

38 ssessed the effects of acute cocaine on both resting-state and stimulation responses to investigate c

39 Here we combined resting-state and task-driven functional magnetic resona

40 t as an additive upon the reaction, catalyst resting state, and turnover-rate limiting step has been

41 and local correlations of BOLD signals in a resting state, and whether these spatial relationships v

42 n architecture reverted to a more segregated resting-state architecture both immediately before and a

43 hed controls with fMRI during both task-free resting state baseline and active memory encoding.

44 Long-term effects of metreleptin on resting state brain connectivity in treatment-naive pati

45 e that the global directionality patterns in resting state brain networks can be predicted solely by

46 We hypothesized that resting state brain oscillations will show unique defici

47 Although changes in resting-state brain connectivity are a transdiagnostic k

48 The resting-state brain regional connectivity had no signifi

49 e base and metal open site are masked in the resting state but revealed within the catalytic cycle by

50 a-ball and thumb domains reside apart in the resting state but that they become closer to each other

51 Such chelates are the major catalyst resting states but are in rapid equilibrium with ethylen

52 roducing adenomas conducts omega-currents in resting state, but not during voltage-sensing domain act

53 ggest that NEMO may be auto-inhibited in the resting state by intramolecular interactions and that du

54 bipolar disorder was associated with reduced resting-state cohesiveness of the sensorimotor network i

55 Activity flow over resting-state connections thus provides a large-scale ne

56 Moreover, changes in ASD resting state connectivity following the training were c

57 ssed adolescents show limited task-evoked vs resting-state connectivity (termed 'inflexibility') betw

58 Individual differences in baseline resting-state connectivity can predict idiosyncratic com

59 or memories could be predicted from baseline resting-state connectivity in locomotor-related networks

60 encourage testing of the clinical utility of resting-state connectivity in PET data.

61 proach on two independent publicly-available resting-state connectome data sets (the Human Connectome

62 the human brain, spontaneous activity during resting state consists of rapid transitions between func

63 vations and the local profiles of intervoxel resting state correlations for both high-resolution BOLD

64 , functional clustering based on independent resting state data revealed that DMN and shift regions c

65 ) in the same group of subjects, we analyzed resting-state data from the core of the default-mode net

66 atum was indicated by seed-based analyses on resting-state data.

67 In two independent "resting-state" datasets (electroencephalography surface

68 em cells out of the proliferative and into a resting state during muscle growth.

69 se functional connectivity using the average resting state EEG of 311 tinnitus patients and 256 healt

70 dren with ASD were abnormally organized with resting state EEG.

71 Exploratory resting-state EEG analyses before and after the tDCS pro

72 In 65 unmedicated depressed patients 15-min resting-state EEGs were recorded off medication (baselin

73 ranger causality in the alpha band) during a resting state (eyes open) and a passive, serial picture

74 ed a genome-wide association study (GWAS) on resting-state fast beta EEG power.

75 w (the spread of activation amplitudes) over resting-state FC networks allowed prediction of cognitiv

76 we investigate how the switching behavior of resting-state FC relates with cognitive performance in h

77 The resting state Fe(III) is unreactive oxidatively.

78 rs-fMRI connectivity.SIGNIFICANCE STATEMENT Resting state fMRI (rs-fMRI) has become an important too

79 Resting state fMRI (rs-fMRI) is commonly used to study t

80 om the theory of complex networks to analyze resting state fMRI data of the brains of human subjects

81 Resting state fMRI data were collected and seed based fu

82 In the present study, 37 smokers completed resting state fMRI scans during both satiated and 24-h a

83 roups among 80 depressed patients completing resting state fMRI.

84 f the time-shift analysis (TSA) approach for resting-state fMRI (rs-fMRI) blood oxygenation level-dep

85 the brain's functional connectivity (FC) is resting-state fMRI (rs-fMRI).

86 lts suggest that the neural origin of global resting-state fMRI activity is the broadband power fluct

87 As previously reported, seed-based resting-state fMRI analyses revealed that the LC was fun

88 Here we use resting-state fMRI data from 176 subjects to show that s

89 We analyse resting-state fMRI data from 98 healthy adults previousl

90 The current study used resting-state fMRI data from a large sample of male and

91 To investigate this issue, we used resting-state fMRI data from a single individual to iden

92 o apply these privacy methods to human brain resting-state fMRI data from a study of major depressive

93 those obtained from simultaneously acquired resting-state fMRI data in 22 middle-aged healthy subjec

94 To test this hypothesis, we acquired resting-state fMRI data in right-handed healthy voluntee

95 Task-based and resting-state fMRI data were acquired in healthy human a

96 erative matching procedure on each subject's resting-state fMRI data.

97 sing an energy-landscape analysis applied to resting-state fMRI data.

98 ere, we performed a series of task-based and resting-state fMRI experiments to investigate cerebellar

99 Human resting-state fMRI has revealed that infraslow fluctuati

100 ration when studying brain organization with resting-state fMRI in the future.

101 Spontaneous activity observed with resting-state fMRI is used widely to uncover the brain's

102 Fine-grained resting-state fMRI mapping, graph theory, and intergroup

103 ply the proposed strategy to the analysis of resting-state fMRI measurements-a prototypic data modali

104 that altered brain connectivity detected by resting-state fMRI might serve as an early disease bioma

105 le different mathematical representations of resting-state fMRI patterns can embed diverse informatio

106 ffects of cognitive ability, which makes the resting-state fMRI promising as a translational bridge b

107 d wandering, which occurs unavoidably during resting-state fMRI scans and may induce variability of t

108 All the subjects underwent resting-state fMRI scans and the data were analyzed by t

109 Laminar resting-state fMRI showed directional functional connect

110 The current resting-state fMRI study examined the neural correlates

111 This resting-state fMRI study suggests that the changed spont

112 Resting-state fMRI was administered to 33 cirrhotic pati

113 ng functional connectivity (FC) derived from resting-state fMRI with gold standard structural connect

114 normal controls were recruited and underwent resting-state fMRI, DTI scans, and cognitive assessments

115 d cingulate network connectivity measured by resting-state fMRI, even in the absence of hypometabolis

116 In resting-state fMRI, hemodynamic fluctuations have been f

117 rns of functional connectivity observed with resting-state fMRI, respectively.

118 missing hand, as evidenced by task-based and resting-state fMRI.

119 in the context of locomotor adaptation using resting-state fMRI.

120 tal of 637 children 6-12 years old underwent resting-state fMRI.

121 ndering in particular thought domains during resting-state fMRI.

122 nal connectivity analysis indicated impaired resting-state FPCN connectivity in patients, but normal

123 can modulate mental control functionand the resting state functional connectivity (rsFC) of the cogn

124 nt-related spectral decomposition (ERSP) and resting state functional connectivity (rsfcMRI) approach

125 We examined the whole-brain resting state functional connectivity as measured by ima

126 Using resting state functional connectivity in healthy young a

127 Resting state functional connectivity is defined in term

128 connectome data (diffusion tractography and resting state functional connectivity) to identify conne

129 icate in humans (154 healthy controls) using resting state functional connectivity, tracing studies c

130 nted for measures of volume and as seeds for resting state functional connectivity.

131 igate the organization of the amygdala using resting state functional magnetic resonance imaging (rsf

132 FOR A SCIENTIFIC COMMENTARY ON THIS ARTICLE: Resting state functional magnetic resonance imaging dysf

133 nectivity between different brain areas with resting state functional magnetic resonance imaging in h

134 ar MRI research-particularly structural MRI, resting--state functional MRI, and diffusion tensor imag

135 Published MRI evidence of structural and resting-state functional brain abnormalities in MDD has

136 We then employed a measure of global resting-state functional brain connectivity and follow-u

137 ivoxel pattern analysis, and high-resolution resting-state functional connectivity (RSFC) analyses, w

138 l, specificity, and clinical utility of fMRI resting-state functional connectivity (RSFC) and task-ac

139 CBF) and blood oxygen-level dependent (BOLD) resting-state functional connectivity (RSFC) were measur

140 disorder (MDD) is characterized by abnormal resting-state functional connectivity (RSFC), especially

141 METHOD: Functional MRI resting-state functional connectivity analyses using a b

142 Whole brain resting-state functional connectivity analyses with thes

143 I/II during semantic prediction and enhanced resting-state functional connectivity between hubs of th

144 ifferences in cortical thickness and related resting-state functional connectivity between NTSCUs and

145 ings was also correlated with an increase in resting-state functional connectivity between the mid-in

146 were interrelated, and functional MRI-based resting-state functional connectivity between the ventra

147 e-function relationship, suggesting that the resting-state functional connectivity depends on direct

148 ging-based depression subtypes defined using resting-state functional connectivity differentially ide

149 ed consequences of structural differences on resting-state functional connectivity in cocaine addicti

150 kinson disease (PD) by analyzing whole-brain resting-state functional connectivity in PD patients wit

151 Resting-state functional connectivity magnetic resonance

152 Capitalizing on recent advances in resting-state functional connectivity magnetic resonance

153 d the subgenual cingulate was assessed using resting-state functional connectivity magnetic resonance

154 rbation on global network organization using resting-state functional connectivity MRI.

155 ion The findings show a PD-related effect on resting-state functional connectivity of posterior and p

156 AC4 expression, fear-potentiated startle and resting-state functional connectivity of the amygdala in

157 The resting-state functional connectivity of the following t

158 vity in cocaine addiction and tested whether resting-state functional connectivity of the identified

159 ortical thickness of the identified regions, resting-state functional connectivity of the identified

160 Here, we studied resting-state functional connectivity of the left IFG in

161 ccessful antipsychotic drug treatment alters resting-state functional connectivity of the striatum.

162 visceral interoceptive attention task and a resting-state functional connectivity scan.

163 In the present study, we used seed-based resting-state functional connectivity to examine the imp

164 cale of the Behavioral Activation Scale) and resting-state functional connectivity using multivariate

165 Resting-state functional connectivity was unrelated to m

166 ning and cognitive flexibility to underlying resting-state functional connectivity.

167 s have described the spatial overlap between resting-state functional correlation (RSFC) subnetworks

168 Moreover, resting-state functional coupling was decreased during a

169 examine the dimensional relationship between resting-state functional dysconnectivity and severity of

170 rpose To prospectively investigate, by using resting-state functional magnetic resonance (MR) imaging

171 matched healthy controls were compared using resting-state functional Magnetic Resonance Imaging (fMR

172 Major advances in resting-state functional magnetic resonance imaging (fMR

173 We performed a longitudinal resting-state functional magnetic resonance imaging (fMR

174 Resting-state functional magnetic resonance imaging (fMR

175 we used magnetic resonance spectroscopy and resting-state functional magnetic resonance imaging (MRI

176 er FC, estimates temporal correlation of the resting-state functional magnetic resonance imaging (rs-

177 As a noninvasive and "task-free" technique, resting-state functional magnetic resonance imaging (rs-

178 tructure and functional connectivity through resting-state functional magnetic resonance imaging (rsf

179 (D2R) antagonist amisulpride] in humans with resting-state functional magnetic resonance imaging and

180 We used resting-state functional magnetic resonance imaging and

181 functional and structural connectivity using resting-state functional magnetic resonance imaging and

182 n, graph theory-based method, was applied to resting-state functional magnetic resonance imaging data

183 Subsequently, we collected resting-state functional magnetic resonance imaging data

184 rbitofrontal cortex of MAM rats showed lower resting-state functional magnetic resonance imaging func

185 vioral measures, psychiatric assessment, and resting-state functional magnetic resonance imaging in a

186 s used to disclose the effects of DBS during resting-state functional Magnetic Resonance Imaging in t

187 on (AD signature cortical thickness; ADSCT), resting-state functional magnetic resonance imaging of f

188 We performed resting-state functional magnetic resonance imaging of p

189 Resting-state functional magnetic resonance imaging scan

190 We acquired resting-state functional magnetic resonance imaging scan

191 ctroscopy to quantify GABA levels as well as resting-state functional magnetic resonance imaging to a

192 Resting-state functional magnetic resonance imaging was

193 Using resting-state functional magnetic resonance imaging we c

194 Using resting-state functional magnetic resonance imaging, we

195 participants underwent cognitive testing and resting-state functional magnetic resonance imaging.

196 rticipants from 13 to 30 years old underwent resting-state functional magnetic resonance imaging.

197 activation by c-Fos immunohistochemistry and resting-state functional magnetic resonance imaging; and

198 linical placebo response is predictable from resting-state functional magnetic-resonance-imaging (fMR

199 20 healthy control subjects underwent a 3-T resting-state functional MR imaging and static posturogr

200 Resting-state functional MR imaging connectivity network

201 ICA of group resting-state functional MR imaging data revealed promin

202 etwork (ECN) by using seed-based analysis of resting-state functional MR imaging data.

203 Reproducibility analysis of resting-state functional MR imaging maps from four repea

204 ement of hemispheric language dominance with resting-state functional MR imaging was highly concordan

205 ating-current stimulation (tACS) [8-12] with resting-state functional MRI (fMRI) [13] to follow both

206 The authors used resting-state functional MRI (fMRI) to develop a prognos

207 a distributed reward network, assessed using resting-state functional MRI (fMRI), to predict the onse

208 Diffusion tensor imaging (DTI) and resting-state functional MRI (rfMRI) data were acquired

209 o identify constituents of the rat DMN using resting-state functional MRI (rs-fMRI) and diffusion ten

210 etworks by applying a clustering analysis on resting-state functional MRI (RSfMRI) data from white-ma

211 ow-up functional connectivity analyses using resting-state functional MRI collected in the same parti

212 in network topology in head-motion-corrected resting-state functional MRI data acquired from 78 patie

213 Here, using a large multisite study, resting-state functional MRI data were examined in young

214 Resting-state functional MRI may represent a promising t

215 We used resting-state functional MRI recordings in 27 patients w

216 We applied novel fetal resting-state functional MRI to measure brain function i

217 typically developing (TD) controls underwent resting-state functional MRI, and functional connectivit

218 halamo-frontal functional connectivity using resting-state functional MRI.

219 transfer mapping-to test the hypothesis that resting-state functional network topology describes the

220 e to conduct a quantitative meta-analysis of resting-state functional neuroimaging studies of PTSD th

221 Our data demonstrated that the resting-state GABA concentration predicts neural changes

222 signal changes during sematic processing and resting-state GABA concentrations in the ATL.

223 ficant, duration-dependent decrease in local resting-state GABAA inhibition, as quantified by short i

224 s the G protein complex by keeping it in the resting state (GDP-bound).

225 that these networks are highly correlated to resting-state gray-matter networks, highlighting their f

226 Characteristic patterns of resting-state hemodynamics were accompanied by more rapi

227 Here we assess LRTCs in resting state human EEG data during a 40-hour sleep depr

228 ate alterations of brain activity during the resting state in chronic smokers using fractional amplit

229 s assessed brain spontaneous activity in the resting state in chronic smokers.

230 ibition maintains a low-correlation striatal resting state in the presence of cortical neuronal avala

231 hich is considered the hallmark of the brain resting state, in photosensitive patients and in people

232 related with spontaneous activity during the resting state indexed by the Power Law Exponent (PLE) in

233 a suggest that reversible protonation of the resting state is likely occurring, and we term this stat

234 Individuals with stronger resting-state long-range temporal correlations demonstra

235 ional magnetic resonance imaging (fMRI) with resting-state magnetic resonance spectroscopy (MRS) to m

236 Patients (n = 28) underwent resting-state magnetoencephalography and neuropsychologi

237 his in a cross-sectional sample, we recorded resting-state magnetoencephalography from 134 children a

238 inherent problem with side-by-side turnover/resting state measurements, i.e., the difficulty to desi

239 isorders [5], highlighting the importance of resting-state measurements for understanding brain funct

240 To this end, resting-state MEG data of 22 healthy adults was analysed

241 red by diffusion tensor imaging and increase resting-state midline frontal theta activity.

242 ations alone are sufficient in understanding resting-state modularity.

243 reasoning complexity resulted in merging of resting-state modules.

244 Classification based on resting-state MRI (85% sensitivity, 83% specificity) and

245 cts on the strength and spatial structure of resting-state MRI functional connectivity.

246 functional magnetic resonance imaging [MRI], resting-state MRI, or diffusion tensor imaging) in combi

247 ent brain locations but localize to a unique resting state network, providing insight into the neurob

248 that hippocampal glutamatergic elevation and resting-state network alterations may arise from NMDAR h

249 ted based on estimated activity flow through resting-state network connections.

250 Resting-state network connectivity has been associated w

251 in, demonstrating the cognitive relevance of resting-state network topology.

252 d was applied to identify the cerebellar DNs resting-state network; first-level and high-level analys

253 rks are modest when compared with intrinsic "resting-state" network architecture.

254 ndard deviation of BOLD signal amplitude) in resting state networks (RSNs) associated with cognitive

255 cific spatiotemporal patterns in the form of resting state networks (RSNs).

256 of this activity is spatially correlated to resting state networks derived from rs-fMRI.

257 ce of abnormal connectivity patterns between resting state networks in neuropsychiatric disorders, in

258 al MRI (fMRI) studies reported disruption of resting-state networks (RSNs) in several neuropsychiatri

259 Spontaneous brain activity is organized into resting-state networks (RSNs) involved in internally-gui

260 stantly active as they interact in so-called resting-state networks (RSNs).

261 We first identified canonical resting-state networks at the individual subject level u

262 ehavioural impairment and the segregation of resting-state networks empirically measured.

263 sults in the net behavior of nodes composing resting-state networks identified using functional magne

264 identifies a need for studies investigating resting-state networks in the human brain to measure and

265 althy controls, particularly at the level of resting-state networks.

266 latency patterns within and across cortical resting-state networks.

267 Neurovascular coupling between resting-state neural activity and hemodynamics was robus

268 more rapidly changing bilateral patterns of resting-state neural activity.

269 cterize the spatial and temporal patterns of resting state neuronal synchronizations in primary progr

270 ted copper(I) dihydridoborate complex is the resting state of the catalyst in this case.

271 The resting state of the catalyst is an NHC-Ni(eta(6)-arene)

272 With DTBM-SEGPHOS as the ligand, the resting state of the catalyst, which is also a catalytic

273 (2+) affinity of the RyR (or "stabilize" the resting state of the channel) and suggest that the accum

274 iron-borohydrido-hydride complex as a likely resting state of the P3(B)Fe catalyst system.

275 roach, we reveal that the human brain during resting state operates at maximum metastability, i.e. in

276 ing fear extinction have been observed using resting-state or functional activation measures.

277 It is unknown, however, whether endogenous resting state oscillations are similarly lateralized in

278 mmunocytochemical staining revealed that, at resting state, p47phox colocalizes with NOX2, whereas NO

279 Arterial spin labelling was used to index resting-state perfusion and high-resolution anatomical i

280 ree period (WFP) is considered essential for resting-state physiological assessment of coronary steno

281 Resting-state regional cerebral blood flow (CBF) can be

282 Resting-state (rs)-fMRI and diffusion weighted imaging (

283 1 males and 28 females) underwent an initial resting-state scan, followed by a cognitive reasoning ta

284 t levels of complexity, followed by a second resting-state scan.

285 ntipsychotic drugs (<2 years), who underwent resting state scanning while entering 12 weeks of prospe

286 t five functional magnetic resonance imaging resting state scans during treatment.

287 >10(4) faster than the unobserved IET in the resting state, showing that CuZ degrees is the catalytic

288 also displayed a greater variety of temporal resting-state signal pattern changes after treatment.

289 Resting-state signals in blood-oxygenation-level-depende

290 rrelated with tinnitus loudness, we assessed resting-state source-localized EEG before and after one

291 The typical resting-state structure consisted of a high-frequency oc

292 xample, older adults exhibit less segregated resting-state subnetworks relative to younger adults.

293 anization was stable across task-engaged and resting states, suggesting that abstract context represe

294 effects, and identification of the catalyst resting state support turnover limiting C-H activation f

295 mode network connectivity during a separate resting-state task.

296 t enables restoration of the receptor to its resting state, thereby completing the gating cycle.

297 MecA converts this resting state to an active planar ring structure by bind

298 These results indicate that the post-task, resting-state topology of the brain network is dynamical

299 s demonstrate that intrinsic fluctuations in resting-state variability exhibit unique maturation traj

300 uring catalysis, the presence of two anionic resting states was revealed, Ru-dihydride (3(-)) and Ru-