コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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
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-
17 an pre-ART VL, 3.99 copies/mL; 3% previously defaulted ART; 24% with previous exposure to short-cours
21 experimental data are lacking, resulting in default assumptions being used to account for variabilit
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
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
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
38 eem to anticipate some mechanisms that drive default effects, yet most people do not believe in the d
40 mental Panel on Climate Change (IPCC) Tier 1 default estimates of carbon storage with this tree cover
45 Given the millions of mortgages still in default, further research clarifying the potential healt
48 and the dark zone: Light-zone B cells die by default if they are not positively selected, whereas dar
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
58 quantification at heterozygous sites versus default mapping methods and also performs well compared
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
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
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
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
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
88 ation and functional connectivity within the default mode network (DMN) of the brain while participan
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
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
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.
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
115 creased blood flow to the major nodes of the default mode network became more pronounced and widespre
117 ontrol subjects; chi(2) = 8.6, p = .003) and default mode network connectivity during a separate rest
119 findings of this paper are (i) the posterior default mode network fails before measurable amyloid pla
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
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
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
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
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
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
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
175 control network and dorsal striatum, whereas default mode regions depicted increased activation in th
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
181 stronger segregation of internal cognition (default mode) and environmentally driven control (salien
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
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
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
198 -task-positive) and decreased or "negative" [default-mode network (DMN)] fMRI responses during task p
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
211 r higher sensitivity compared to the aligner default modes, therefore significantly boosting the dete
216 faults to influence others, i.e., they show "default neglect." First, in one-shot default-setting gam
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
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
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
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
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
245 ch as 1.42x compared to the results from the default parameters; (iii) attain good scalability on a h
250 relative tooth size in mammals, produces the default pattern of tooth sizes for all lower primary pos
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
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
266 y show "default neglect." First, in one-shot default-setting games, we find that only 50.8% of partic
268 tion process revealed that autoclave factory default settings are potentially ineffective for certain
272 ed in brief, variable bursts but reflected a default state interrupted by encoding and decoding.
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
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
288 t people often fail to understand and/or use defaults to influence others, i.e., they show "default n
292 article equilibrium partitioning theory as a default treatment of gas-aerosol transfer, despite quest
294 to high dengue endemicity (SP9 >/= 50%), the default vaccination policy would reduce the burden of de
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
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。