ライフサイエンスコーパス: default

1 cooperation as the default (i.e., an opt-out default).

2 D would then need to be more strict than the default.

3 feat the free-riding encouraged by an opt-in default.

4 ng method, FAST, performed better than SPM's default.

5 whether to present that target option as the default.

6 but that it depends on an individual's moral default.

7 ta are lacking, the use of health-protective defaults.

8 provements over the Gini coefficient and the default 50% MWS, especially in datasets with clusters th

9 The model assumes that most people (default 95%, range in variant simulations 60-95%) are "l

10 tions included contextual factors leading to defaulting, a combined multi-country power estimate, and

11 ributions from the hydrophobic effect are by default absent and only the polarity of the side chain d

12 ive intensity binning strategy as opposed to default absolute intensity binning reduces correlation b

13 dependent activity, which is consistent with default activation (and thus controlled repression), a s

14 PFC spontaneous default activity is altered in neuropsychiatric disorder

15 l and functional changes across sites of the default and frontoparietal networks and well-defined imp

16 d structural and functional integrity of the default and frontoparietal networks.

17 mulated in monopolar mode (i.e. the clinical default), and at different modulation depths.

18 3'-UTR reannotation; extending or truncating default annotations based on RNA-Seq read evidence and (

19 The default answer remains that the prettiest males have the

20 find that the possible actions considered by default are those that are both likely to occur and gene

21 phantom perception (tinnitus) occurs when a default auditory prediction is formed to explain spontan

22 pair asymmetrically differentiates into the default AWC(OFF) and induced AWC(ON) subtypes in a stoch

23 t that the awake, conscious state is not the default behavior of an assembly of neurons, but rather a

24 giotensin I-converting enzyme (ACE) from its default biochemical conversion of Ang I to Ang II has be

25 ing zygotic diploidization does not occur by default but is triggered by a combinatorial switch, the

26 It contains QC metrics that are measured by default by the manufacturer, but also calculates other i

27 d system that precludes healthy foods as the default choices.

28 observations support a scenario in which the default configuration of open chromatin enables a networ

29 hen compared to control treatment - since by default controls are not treated.

30 Results: Site default CT protocols were the following: greatest extrac

31 rs identified the organisms present in their default databases from a mock bacterial community of 20

32 comes included cost-effectiveness, coverage, defaulting, death, length of stay, and average daily wei

33 panied by a randomly assigned narrative: the default deficit-focused "Poverty Alleviation" narrative,

34 the tropics and subtropics rely on IPCC 2006 default DeltaAGB rates, which are values per ecological

35 in this study offer references to update the default EF in the IPCC Tier 1 guideline.

36 died bias with special policy relevance: the default effect, which is the tendency to choose whicheve

37 Although veins are often considered the default endothelial state, genetic manipulations can mod

38 By default, essential oral health care does not include the

39 ful approach to testing genetic drift as the default evolutionary mechanism of trait differentiation

40 ineage, suggesting that smooth muscle is the default fate of Flk1(+) mesoderm.

41 te changes suggest that photoreceptors are a default fate outcome in OTX2+ cells and that VSX2 must b

42 on map correlation, rho (AT), was lower when default filters were used (0.60 (0.30-0.71), P=0.053).

43 that release is maximal around the neurons' default firing frequency.

44 eoretical model to analyse cooperation under defaults for cooperation (opt-out) and defection (opt-in

45 imple and intuitive interface (with sensible defaults) for increased usability, and it complies with

46 Given the millions of mortgages still in default, further research clarifying the potential healt

47 phantoms were used for evaluating biases on default/general scanner protocols, followed by developin

48 such mechanism is setting cooperation as the default (i.e., an opt-out default).

49 ptor CD4, which drives transitions through a default intermediate conformation (state 2) into the thr

50 e-triggered conformation (state 1) through a default intermediate conformation (state 2) to a conform

51 e currently derived using poorly constrained default IPCC emission factors (EF5r) which yield unrelia

52 he absence of deceased's preferences and the default is not to remove organs, and oppose donation whe

53 e there is no evidence of preference but the default is to presume consent; in both cases, the decisi

54 XR Avanti, and Triton DRI OCT platforms with default layer segmentations were used to evaluate segmen

55 Data were analyzed using the factory default level 5 referral criteria targeting 80% sensitiv

56 In the two groups, the default lower limit for oxygen saturation as measured by

57 sts that peripheral channel transport is the default mechanism that was adapted in evolution to inclu

58 functional connectivity between social brain default mode (DMN) subsystems in adolescent males, but h

59 d with information processing related to the default mode (DMS), salience/reward (SRS), and frontopar

60 stimate = -0.760 [95% CI = -1.297, -0.224]), default mode (p = 0.012, parameter estimate = -0.417 [95

61 oss individuals and identify fluctuations in default mode and control network activity as the primary

62 ave suggested regulation of activity between default mode and executive control networks play a role

63 greater between-network connectivity of the default mode and executive control networks.

64 ecame increasingly dissociated in transmodal default mode and fronto-parietal networks.

65 e most to the estimation mainly involved the default mode and frontoparietal control networks.

66 ion and visual networks in the pulvinar, and default mode and multiple control networks in the caudat

67 ectivity across several circuits such as the default mode and prefronto-parietal network.

68 verge in transmodal cortex, particularly the default mode and salience networks.

69 nd the inter-network integration between the default mode and sensorimotor networks.

70 tive to HC participants was detected between default mode and task-positive network regions.

71 ments in the year following stimulation, and default mode connectivity could be used to predict longe

72 Slow migration is the default mode in SN-mDA neurons, while fast, laterally-di

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 Because default mode network downregulation is reliant on input

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 transitions between sensory and higher-order default mode regions in a large cohort of individuals wi

175 findings suggest that cingulo-opercular and default mode regions typically implicated in task contro

176 work linking frontoparietal system activity, default mode system activity, and the interactions betwe

177 c analysis,we found that the autonomy of the default mode system and integration among task-positive

178 integration between the fronto-parietal and default mode systems, and integration with the subcortic

179 interactions between the frontoparietal and default mode systems.

180 However, activation in the default mode was less suppressed in older adults in for

181 s of the brain normally associated with the 'default mode' or 'task negative' network.

182 orsal attention, DAN; ventral attention; and default mode), assessed from the resting-state fMRI.

183 itive network system including the salience, default mode, and central executive networks were reduce

184 he motor/sensory network and medial frontal, default mode, and frontoparietal networks.

185 s mainly involve the frontoparietal control, default mode, and hippocampal networks, suggesting that

186 found for limbic, frontoparietal executive, default mode, and salience networks.

187 thin a region located at the intersection of default mode, dorsal attention and frontoparietal networ

188 The findings point to a role for the default mode, frontoparietal and limbic networks in psyc

189 chical clustering analysis revealed that the default-mode and visual networks normally demonstrate ne

190 s, but also show a loss of interplay between default-mode and visual networks.

191 ntion, executive control, motor, visual, and default-mode functions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

208 rk primarily encompassing the visual system, default-mode system, and frontoparietal system.

209 an .05 showed reduced centrality dynamics in default-mode, frontoparietal, and visual network regions

210 sis not only demonstrate reduced dynamics in default-mode, frontoparietal, and visual networks, but a

211 propose a ordinal regression model (MN) as a default model for count data given that this model is sh

212 Neuroimaging evidence implicates the default network (DN) and frontoparietal control network

213 focused thought and relies upon the brain's default network and its interactions with attentional ne

214 roperties of network connectivity, including default network integrity, were preferentially disrupted

215 cquisition and functional integration of the default network is important for autobiographical episod

216 lyses of single individuals suggest that the default network is not a single network, as historically

217 f retrieval) fell primarily within canonical default network regions.

218 time in, and persistence of, a frontoinsular-default network state involving insula, dorsolateral and

219 ontoinsular-default state and a prototypical default network state reported higher depression.

220 ce and transition frequency of frontoinsular-default network states were also associated with higher

221 f network states involving frontoinsular and default network systems.

222 a collection of brain regions known as the 'default network'.

223 lay stronger functional communication in the default network, and greater microstructural integrity o

224 out the association cortex, often called the default network, are suppressed during tasks that demand

225 One network, often called the default network, is positioned at the apex of a gradient

226 prefrontal cortex, and posterior regions of default network, reported more severe symptoms of depres

227 s make it a candidate homologue to the human default network.

228 medial temporal lobe (MTL) subsystem of the default network.

229 Increased rGMV in key default-network regions involved in prospection, socio-e

230 etically-accessible primate, might possess a default-network-like candidate creates opportunities for

231 nd between regions of the frontoparietal and default networks with distinct patterns evident in patie

232 ubregions of the salience, sensorimotor, and default networks) that were significantly related to the

233 methylation, and mRNA expression to induce a default neuronal state.

234 event recall with activity in a network of "default" or "core" brain regions.

235 physiological mechanisms that underlie this default output state, however, remain controversial.

236 he software tools performed best under their default parameter settings, and power varied widely when

237 ng a user-friendly environment and providing default parameters for fast statistical and exploratory

238 specific model is developed by estimation of default parameters, classified qualitative validation, h

239 ndicated that female external anatomy was a "default" pathway of development not requiring steroids,

240 rocircuits, each characterized by a distinct default pattern of infra-slow rhythmicity.SIGNIFICANCE S

241 Site default PET protocols were the following: uniformity was

242 Hydrogen peroxide (H(2)O(2)) is used as the default photo-oxidant.

243 Default pipeline settings allow new users to run MetaLAF

244 ulated the communicative context so that the default pointing response of apes would have indicated a

245 he next cell cycle, at a position called the default polarity site (DS).

246 We challenge the default practice of modeling at the species level, which

247 Moreover, it is not just a default process occurring at the end of genes.

248 This default programme is markedly disturbed under the influe

249 ange contacts by up to 24.4% compared to the default programs.

250 n preclinical PET/CT and absorbed doses with default protocols.

251 between predicted and observed values, with defaults provided for each GLM.

252 her success rates (82% versus 69%) and lower default rates (11% versus 20%).

253 IPCC 2006 default rates come from a handful of studies, provide no

254 n rates across the globe, and indicates that default rates from the Intergovernmental Panel on Climat

255 ansfer (CCT) policy on treatment success and default rates in a prospective cohort of socioeconomical

256 us and traceable refinement of the IPCC 2006 default rates in tropical and subtropical ecological zon

257 in Latin America, with low success and high default rates.

258 The default reactivity scenario, the model with the simplest

259 In 3D-GNOME 2.0, the default reference 3D genome structure is generated using

260 The main conjugation promoter, Pc, is by default repressed by a regulator RcopLS20 involving DNA

261 Although this default response system may be adaptive, these hard-wire

262 This suspension by default resulted in some participants in a trial evaluat

263 less risky overall, as they exhibit similar default risk but lower prepayment risk.

264 n R. dittoSeq is color blindness-friendly by default, robustly documented to power ease-of-use, and a

265 results for 1989-1990 compare well with the default RSC of 20% used in risk assessments for legacy P

266 ies randomized to the intervention adopted a default session duration >=4.25 hours (255 minutes) for

267 ATS (default settings) and ATI (full-range of threshold setti

268 e of conditional cooperation under different default settings.

269 were placed at the correct limb's canonical (default) side of space.

270 Voxels were either left at the default size or resampled to 3-mm isotropic voxels.

271 users with "physics," including an initial (default) slider position and friction.

272 Is fusion truly a default, stable state that only breaks into rivalry for

273 ed more frequently between the frontoinsular-default state and a prototypical default network state r

274 As an intact Glu-343/Arg-378 bridge is the default state in unbound ETS1 and maintained in high-aff

275 urthermore, during V1 hyperpolarization, the default state of the locomotor central pattern generator

276 Third, the default state of vvl expression in the thorax, in the ab

277 Common femoral artery access is the default strategy for large-bore interventional procedure

278 building blocks are combined to generate non-default structures.

279 t pairs and on a network of sovereign credit default swaps (CDS).

280 f patients a provider can absorb when others default (systemic benefit).

281 2.5-85.7) and 76.3 (95% CI 75.4-77.2) at the default threshold probability of 0.2, respectively.

282 Organ fibrosis represents a default tissue program activated when regenerative capac

283 The map would default to an expected value in situations where other a

284 domly assigned to the intervention group who defaulted to routine use of antibiotics because of failu

285 While the human fetal immune system defaults to a program of tolerance, there is concurrent

286 Thus, the user defaults to using inefficient methods for transfer acros

287 mes demands that researchers steer away from default topologies to instead pursue unusual geometries.

288 robabilistic tractography, high b-values and default tractography parameters: these parameters were u

289 We propose default transition rates for metals to avoid overestimat

290 We found that the default uncertainty factor for human variability may be

291 ereas the number of fragments is kept to its default value for coil regions, important and dramatic r

292 not the case for the V system, when a model default value for the SA of FHY of 600 m(2) g(-1) was us

293 h methods were below the current IPCC (2006) default value of 0.0025 and a downward revision to 0.001

294 The default view now uses ontology structure to provide a co

295 The default view on the ClinVar website, the Variation page,

296 ccess was 2.9 (95% CI 2, 4.3, P < 0.001) and default was 0.36 (95% CI 0.23, 0.57, P < 0.001).

297 entrations to the Australian and New Zealand default water quality guideline values (WQGVs) showed no

298 ers two modes, Maximum Compression and Fast (default), which trade-off compression efficiency and spe

299 initial cooperation encouraged by an opt-out default, while 'good shepherds' defeat the free-riding e

300 Fragments of interest are sequenced by default, while DNA deemed non-informative is rejected by