ライフサイエンスコーパス: default

1 whether to present that target option as the default.

2 expectations, promoters exhibit low noise by default.

3 on average, even in cases where they do use defaults.

4 large errors in the probability of systemic defaults.

5 edback, they still do not systematically use defaults.

6 s (UHCAs), which are currently identified by default, a high risk of bleeding remains a clinical issu

7 ed to continue to adopt radial access as the default access site for percutaneous coronary interventi

8 transradial access (TRA) site has become the default access site for percutaneous coronary interventi

9 of participants set the target option as the default across 11 samples (n = 2,844), consistent with p

10 PFC spontaneous default activity is altered in neuropsychiatric disorder

11 When default amino acid substitution matrix in the Psi-blast

12 m, choices are framed as comparisons between default and alternative options, which might save some r

13 dels controlled for all time-stable factors (default) and several time-varying covariates as potentia

14 recognition at this memory checkpoint blocks default apoptosis and programs their transition to long-

15 needs that may differ significantly from the default approach described.

16 3) Clinicians should use as their "default" approach a shared decision making process that

17 an pre-ART VL, 3.99 copies/mL; 3% previously defaulted ART; 24% with previous exposure to short-cours

18 The default assumption has been that volatiles passively dif

19 This is problematic as the default assumption is that FPs originate from local acti

20 than strong innate constraints should be the default assumption.

21 experimental data are lacking, resulting in default assumptions being used to account for variabilit

22 sistent with people not systematically using defaults at all.

23 of the reproductive system is established by default because the male reproductive tracts (Wolffian d

24 in present-day ESL estimates, which have by default been ignored in broad-scale sea-level rise impac

25 FGF and Nodal, neural progenitors exhibit a default behavior of sequential cell divisions, and fail

26 sions was more significantly associated with default behaviors (and the absence of executive control)

27 th activation associated with the resting or default brain, while activation during choices inconsist

28 Default branch-length priors in some Bayesian phylogenet

29 es followed by novelty were more dominant by default but liable to interference, whereas sleep engage

30 ro susceptibility to ubiquitin-independent ("default") cleavage by the 20S core proteasome was unchan

31 This flexible tool provides a default clonal resolution using the change point of PSD

32 from one of two customizable databases; the default databases contain 14068 unique entries.

33 compete for BiP and restore IRE1(LD) to its default, dimeric, and active state.

34 tamin K antagonists (VKA) have long been the default drugs for anticoagulant management in venous thr

35 fects, yet most people do not believe in the default effect on average, even in cases where they do u

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

37 Third, we investigate beliefs related to the default effect.

38 eem to anticipate some mechanisms that drive default effects, yet most people do not believe in the d

39 g a mesenchymal-epithelial transition to the default epithelial phenotype.

40 mental Panel on Climate Change (IPCC) Tier 1 default estimates of carbon storage with this tree cover

41 We show that the default fate of Lgr5(+) ISCs is to differentiate, unless

42 Our results suggest that the default for all DSBs is to recruit 53BP1 and RIF1.

43 As an example, the recommended default for small-molecule samples is 5% increase in the

44 Only 1 CrAg-positive patient, who defaulted from care, died from cryptococcal meningitis (

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

46 erns to emerge over time in cells undergoing default, gradient, and true mating responses.

47 The default growth pattern of primary roots of land plants i

48 and the dark zone: Light-zone B cells die by default if they are not positively selected, whereas dar

49 c changes that result in interruption of the default immunologic state of tolerance.

50 of high-level cognitive judgments relying on default implicit representations of possibility rather t

51 explicit reasoning about possibilities from default implicit representations, demonstrate that human

52 ot investigated whether or how people have a default, implicit representation of which events are pos

53 re (connect, separate, or order) will be the default in ambiguous situations, and (c) it facilitates

54 the cGAS-STING-NLRP3 pathway constitutes the default inflammasome response during viral and bacterial

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

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

57 Ontobee is also the default linked data server for publishing and browsing b

58 quantification at heterozygous sites versus default mapping methods and also performs well compared

59 Our data suggest that default mechanical ventilator settings should include PE

60 nisotropy and cytokinesis without disrupting default membrane trafficking.

61 tivation of neural components and decreasing default mode (DM) suppression.

62 rties of interactions between salience (SN), default mode (DMN), and central executive (CEN) networks

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

64 tional connectivity were detected within the default mode (h2 = 0.36; SE, 0.16; cluster level signifi

65 orsal attentional (exogenously-oriented) and default mode (internally-oriented) networks.

66 n their identification as "hub" areas of the default mode and cortical salience networks, respectivel

67 ed within-network functional connectivity of default mode and dorsal/ventral attention networks, as w

68 hin a reward-related network, and across the default mode and executive control networks.

69 ing-state neural activity in reward-related, default mode and executive control networks.

70 ns in key paralimbic and limbic nodes of the default mode and salience networks that support attentio

71 works with known age-related susceptibility (default mode and visual association networks) was associ

72 ampal decoupling from anterior and posterior default mode hubs in TLE-HS, whereas TLE-G did not diffe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 The default mode network has distinct subsystems with unique

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 enerally overlapped with the distribution of default mode network.

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

164 aused by functional disconnection within the default mode network.

165 whereas the dorsomedial module resembles the default mode network.

166 decreased functional connectivity within the default mode network.

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

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

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

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

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

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

173 stically, although habits are the efficient, default mode of response.

174 mbers' needs; and the use of e-learning as a default mode of training delivery.

175 control network and dorsal striatum, whereas default mode regions depicted increased activation in th

176 Flexible default mode regions dynamically switch community member

177 analyses revealed both context-free (greater default mode segregation) and context-specific (greater

178 ns to cognitive systems, we observe that the default mode system imparts large global change despite

179 brain regions typically associated with the 'default mode' or 'task negative' network.

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

181 stronger segregation of internal cognition (default mode) and environmentally driven control (salien

182 uted for regions from the ventral attention, default mode, and salience networks.

183 nally-guided, higher-order mental functions (default mode, central executive and salience networks) a

184 ited atypical functional connectivity in the default mode, cognitive control, and affective networks.

185 entified 5 canonical resting-state networks (default mode, executive control, left and right frontopa

186 enhanced functional connectivity within the default mode, frontal-parietal, and motor control networ

187 Spatial overlap was fair to moderate for the default mode, left central executive, primary and second

188 eech-production (motor activity regulation), default-mode (attention regulation), and emotional-memor

189 gest that domain-specific musical expertise, default-mode cognitive processing style, and intensity o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 yes open, a decreased CMRGlu was observed in default-mode regions (P < 0.05, familywise error-correct

208 ion cortices (partially overlapping with the default-mode, salience, and frontoparietal attention net

209 n between dorsal attention/motor regions and default-mode/frontoparietal regions, particularly in the

210 r of the 21st century onward compared to the default model with fixed traits.

211 r higher sensitivity compared to the aligner default modes, therefore significantly boosting the dete

212 search tool that accelerates MegaBLAST--the default module of NCBI-BLASTN.

213 The default motion simulated by SimGen is a Brownian-like di

214 However, this default myelination process can be modulated by changes

215 We discuss implications of default neglect for decision making, social influence, a

216 faults to influence others, i.e., they show "default neglect." First, in one-shot default-setting gam

217 The default network (DN) has been consistently associated wi

218 The default network (DN) has been consistently associated wi

219 l pulses to fMRI pre-identified nodes of the default network (DN), frontoparietal network (FPN), and

220 three large-scale networks of the brain, the default network (DN), frontoparietal network (FPN), and

221 ed that the distributed network known as the default network is comprised of two separate networks po

222 demonstrate steady-state deactivation of the default network under acute hypoxia, which become more p

223 Activation of the default network was not related to internally directed a

224 d was typified by reduced segregation in the default network with increasing reward value and increas

225 regions of parahippocampal gyrus within the default network, a pattern related to sustained positive

226 lthy speech/language network, but not in the default network, correlated with longitudinal grey matte

227 tively related to R.MFG connections with the default network, which has been largely overlooked in th

228 al prefrontal cortical (MPFC) regions of the default network.

229 specific spatial patterns were reinstated in default-network, medial-temporal, and high-level visual

230 uding the sensorimotor, dorsal attention and default networks, but with increased connectivity betwee

231 canonical somatomotor, ventral attention and default networks, with a differential pattern of engagem

232 ain their undifferentiated state and prevent default neural fate.

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

234 tiation during the third trimester, previous defaulting on ART, and postpartum follow-up.

235 ion within quartz or feldspar; it relies, by default, on destructive read-out of the stored chronomet

236 Cell Line Ontology (CLO) is selected as the default ontology for LINCS cell line representation and

237 activity in the same regions scaled with the default option value, irrespective of the eventual choic

238 en and more rapidly, which qualified them as default options.

239 ns using the other three approaches with the default or available HMMs.

240 direction of future research to support new default or site-specific bioavailability adjustments for

241 urable outcomes (treatment failure, relapse, default, or death despite treatment with a regimen based

242 oscillations with remarkable periodicity, a default output state likely to affect sensory processing

243 from -92 up to +5705%) when compared with a default parameter set available at GNPS.

244 We have optimized the default parameters of NaviSE to facilitate its use.

245 ch as 1.42x compared to the results from the default parameters; (iii) attain good scalability on a h

246 Remyelination is the default pathway after myelin loss in all mammalian speci

247 The osteogenic default pathway may be subverted during pathological con

248 in oligodendrocyte progenitors that favor a default pathway of differentiation.

249 se with early endosomes, thus overriding the default pathway to the Golgi.

250 relative tooth size in mammals, produces the default pattern of tooth sizes for all lower primary pos

251 e results could be improved, compared to the default patterns of the program.

252 Overall, these findings challenge our default perceptions of multihost parasite persistence, a

253 Strikingly, lipid recognition by the default PI(4,5)P2 lipid sensor, phospholipase C delta 1

254 Default plot methods for both layouts for easy use are a

255 ve a priori on their preferences that create default policies and shape the neural comparison process

256 nylation rather than uridylation, which is a default post-trimming modification characteristic of rib

257 ision of the precursor, and resetting of the default prediction to expect tinnitus.

258 layed an epigenetic pattern that suggested a default preference for the osteogenic pathway; however,

259 robability of one institution depends on the default probability of all of the other institutions in

260 As a result, the default probability of one institution depends on the de

261 The default random forest algorithm allows interactions betw

262 The default response of most cells to TNF is survival and NF

263 In some contexts, default rules, simplification, and social norms have had

264 A default rvarphi at which the analysis time is contained

265 These studies thus unravel the default self-organization rules governing early embryoge

266 y show "default neglect." First, in one-shot default-setting games, we find that only 50.8% of partic

267 ular plexuses using manufacturer-recommended default settings are likely to be biased.

268 tion process revealed that autoclave factory default settings are potentially ineffective for certain

269 ms for most metrics, particularly when using default settings.

270 th a previous model of condensin suppressing default somatic pairing.

271 Flattened leaf architecture is not a default state but depends on positional information to p

272 ed in brief, variable bursts but reflected a default state interrupted by encoding and decoding.

273 This suggests that the neuroepithelial default state is IPC-like, whereas OPC identity is deriv

274 Intrinsic forgetting may be the default state of the brain, constantly promoting memory

275 g the LFP, EEG, MEG or fMRI suggest that the default state of the cortex is critical, manifested by s

276 of receptors in extrasynaptic membranes is a default state or is actively controlled remains essentia

277 se state of extrasynaptic receptors is not a default state that is simply explained by the lack of sy

278 As a novel default state, infraslow autorhythmicity is likely to af

279 The default strategy should be to offer anticoagulant thromb

280 ithin taxa that have seed dispersal as their default strategy.

281 ectric properties can stably override genome-default target morphology, and provide a tractable contr

282 ively sanitary conditions early in life to a default Th2 response and increasing allergic phenomena.

283 thm used is fully customisable with sensible defaults that are easily overridden by custom algorithms

284 progressive improvements until it became the default therapy for inoperable patients, and a recommend

285 tations, demonstrate that human adults often default to treating immoral and irrational events as imp

286 makers use the first option they attend as a default to which they compare the second.

287 tegies, we also found that VS lesion monkeys defaulted to an action-based choice strategy.

288 t people often fail to understand and/or use defaults to influence others, i.e., they show "default n

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

290 Whilst Nature almost by default (transiently) organises her components at multip

291 We propose default transition rates for metals to avoid overestimat

292 article equilibrium partitioning theory as a default treatment of gas-aerosol transfer, despite quest

293 The default vaccination policy considered was routine vaccin

294 to high dengue endemicity (SP9 >/= 50%), the default vaccination policy would reduce the burden of de

295 , which are 58-7% of the current IPCC Tier 1 default value for all fires.

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

297 is to calculate N sufficiency index with the default vegetation indices and then to estimate N nutrit

298 semi-empirical approaches using the sensor's default vegetation indices, normalized difference vegeta

299 search suggests that targets are detected by default, whereas distractors are processed in considerab

300 nd exon junction-level accuracy and compared default with optimized parameters.