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1 old age as well as individual differences in behavioral performance.
2 hese same features also had an impact on the behavioral performance.
3 ity, attentional focus, neural activity, and behavioral performance.
4 reliance on interference control and reduced behavioral performance.
5 een the provision of monetary incentives and behavioral performance.
6 and the size of this effect correlated with behavioral performance.
7 tterns depends on task demands and subject's behavioral performance.
8 te visual and auditory cues to enhance their behavioral performance.
9 nses were predictive of different aspects of behavioral performance.
10 ference-control processes results in reduced behavioral performance.
11 emains untested how sparse coding relates to behavioral performance.
12 ng rate, and had a tighter relationship with behavioral performance.
13 were often sufficiently sensitive to support behavioral performance.
14 TCN --> DMN, are positively correlated with behavioral performance.
15 mpal-prefrontal synchrony is correlated with behavioral performance.
16 to improved sensory perception and enhanced behavioral performance.
17 DMN --> TCN, are negatively correlated with behavioral performance.
18 ying cognition, such as fMRI, rather than in behavioral performance.
19 nhibitory motorcortical network and level of behavioral performance.
20 rfere with task control, leading to degraded behavioral performance.
21 ameters have been associated with changes in behavioral performance.
22 ether picture presentation was contingent on behavioral performance.
23 ral-parietal lobe positively correlated with behavioral performance.
24 lternatives solely on the basis of subjects' behavioral performance.
25 ssess the role of neurogenesis on subsequent behavioral performance.
26 ially perturb MSTd activity while monitoring behavioral performance.
27 tical locking was predictive of the animals' behavioral performance.
28 in critical task-relevant areas and improved behavioral performance.
29 h other cognitive components associated with behavioral performance.
30 strategies may be used to improve perceived behavioral performance.
31 may result in stimulus-locked periodicity in behavioral performance.
32 timuli contributed independently to impaired behavioral performance.
33 ce in the VWFA and relates VWFA responses to behavioral performance.
34 n the MD system were accompanied by impaired behavioral performance.
35 Fmr1 KO mice and are partly correlated with behavioral performance.
36 evant points in time, resulting in optimized behavioral performance.
37 related patterns in PPC predicted subsequent behavioral performance.
38 systems-level process that in turn enhances behavioral performance.
39 re accompanied by correlated improvements in behavioral performance.
40 early stages of vestibular processing limit behavioral performance.
41 ocal dynamic competition that was related to behavioral performance.
42 emble codes are better suited to account for behavioral performance.
43 on in the absence of eye movements, improves behavioral performance.
44 echanism underlying its beneficial effect on behavioral performance.
45 esponses was closely related to single-trial behavioral performance.
46 task correlated positively with the monkeys' behavioral performance.
47 y and synaptic efficacy and thus influencing behavioral performance.
48 ient, that is, those that cannot account for behavioral performance.
49 mediate-tier areas was predictive of correct behavioral performance.
50 versus correct rejects were correlated with behavioral performance.
51 ferences between individuals in area size on behavioral performance.
52 sed parietal activity, which correlated with behavioral performance.
53 ion are stimulated by sensory experience and behavioral performance.
54 stable, intrinsic networks of the brain and behavioral performance.
55 and only the most sensitive neurons rivaled behavioral performance.
56 Finally, we compare neural performance with behavioral performance.
57 of estrogen on Abeta accumulation but not on behavioral performance.
58 s and show they are required for appropriate behavioral performance.
59 ment and deficits in subsequent cognitive or behavioral performance.
60 under study, which can in turn be related to behavioral performance.
61 both sensory and motor accuracy to optimize behavioral performance.
62 sly invisible, influences brain activity and behavioral performance.
63 gnitude of pre-stimulus modulations predicts behavioral performance.
64 s have sufficient sensitivity to account for behavioral performance.
65 representations was associated with enhanced behavioral performance.
66 correct responses, indicating more efficient behavioral performance.
67 negative consequences of the distracters on behavioral performance.
68 lso graded as a function of cue validity and behavioral performance.
69 network organization were related to better behavioral performance.
70 e abrupt and occurred before the recovery of behavioral performance.
71 y phase of local ensemble activity predicted behavioral performance.
72 of networks for the task at hand, improving behavioral performance.
73 the attended feature can in principle limit behavioral performance.
74 ween brain FCD and individual differences in behavioral performance.
75 lowing a post-cue, and this recovery tracked behavioral performance.
76 ates, reducing processing demands to improve behavioral performance.
77 from rest nonetheless contribute strongly to behavioral performance.
78 dictability during the memory delay affected behavioral performance.
79 gical defects correlate with deficiencies in behavioral performance.
80 mblies among cortical areas is essential for behavioral performance.
81 ortantly, these interactions correlated with behavioral performance.
82 arning in parallel with the crows' increased behavioral performance.
83 g in task-related areas and deterioration of behavioral performance.
84 ivity in HD may have compensatory effects on behavioral performance.
85 brain development is essential for optimized behavioral performance.
86 neural processing stages leading to enhanced behavioral performance.
87 classification was strongly correlated with behavioral performance.
88 functional connectivity may shape subsequent behavioral performance.
89 strength of the response was correlated with behavioral performance.
90 ntrol levels when animals reached asymptotic behavioral performance.
91 activity patterns during behavior, and basic behavioral performance.
92 critically important in modulating multiple behavioral performances.
93 emed to contribute to their improved LTP and behavioral performances.
96 ons, aging, functional brain activations and behavioral performance across key cognitive functions, r
97 these regions were associated with improved behavioral performance across participants and followed
98 bserved were not explained by differences in behavioral performance across rules and thus cannot be a
99 T regrowth and the recovery of CST-dependent behavioral performance after both T10 lateral spinal hem
100 d correlating Granger causal influences with behavioral performance and blood oxygen level-dependent
104 lacebo vs Nicorette gum) and time-on-task on behavioral performance and brain functional network metr
105 nstruction technique, we identified impaired behavioral performance and degraded mnemonic representat
106 owledge of cue-reward probabilities improves behavioral performance and diminishes reinforcement lear
107 d indirect-pathway neurons and disrupted the behavioral performance and electroencephalography-relate
110 The effect of psychopathology dimensions on behavioral performance and executive system recruitment
111 cognitive coupling', the association between behavioral performance and FCD (indexing brain activity)
114 have been inhibited, patients showed reduced behavioral performance and increased activation in mid-V
116 These functional changes may relate to both behavioral performance and measures of brain structure (
117 stimuli to guide visual perception, although behavioral performance and neural representations were l
118 eward learning captures the patterns of both behavioral performance and neural responses during a ran
119 peptide (VIP)-positive interneurons enhanced behavioral performance and neuronal action plan represen
123 lso in the decay of temporal correlations in behavioral performance and ongoing oscillations in human
124 r reinforcer devaluation that are related to behavioral performance and outcome value, respectively.
126 eliabilities and task relevance in line with behavioral performance and principles of statistical opt
127 tates is related to both general measures of behavioral performance and relative differences in task-
128 multiple sites in the striatum as induced by behavioral performance and reward-related stimuli, by di
129 d glutamate in human volunteers predict both behavioral performance and the dynamics of a neural valu
130 one discrimination task on relations between behavioral performance and the magnitude of auditory eve
131 ts have been limited by both their assays of behavioral performance and their use of lesions to chang
132 duced striatal dopamine loss, despite normal behavioral performance and unaltered N-methyl-D-aspartat
133 at VK-28 and M30 both significantly improved behavioral performances and attenuated lactacystin-induc
135 object-selective responses of IT neurons and behavioral performance are affected by changes in fronta
137 ral activity that mature in conjunction with behavioral performance are more likely to subserve detec
139 tivation in early visual cortex and improved behavioral performance as a function of the affective si
140 as shown to predict the multisensory gain in behavioral performance at a time lag of approximately 25
142 The strength of this response parallels behavioral performance: auditory cortical mechanisms are
144 ity were observed even though differences in behavioral performance between MTBI patients and control
145 representations of remembered locations and behavioral performance both decreased with increasing me
146 eover, trained networks can achieve the same behavioral performance but differ substantially in their
148 ation of activation predicted task-switching behavioral performance, but with hemispherically dissoci
149 ing of noncholinergic BF neurons may improve behavioral performance by affecting the activity of wide
151 Attention is commonly thought to improve behavioral performance by increasing response gain and s
152 Recent studies argue that attention improves behavioral performance by shaping of the noise distribut
153 sociation between repetition attenuation and behavioral performance by varying the task performed on
154 ild up sleep pressure, which results in slow behavioral performance (cognitive lapses) typically attr
155 responses from two frontal regions mirrored behavioral performance, consistent with their role in de
162 ttended stimuli, which correlated with their behavioral performance deficits and clinical symptoms.
163 to perform a practiced spatial task leads to behavioral performance deficits, and that synaptic plast
164 n from psychology linking arousal state with behavioral performance, demonstrating neural correlates
169 l ensembles from rat motor cortex to predict behavioral performance during a reaction time task.
172 ves acquisition of knowledge and team leader behavioral performance during subsequent simulated cardi
174 endent (BOLD) functional activity as well as behavioral performance during working memory was examine
175 ponses typically decline, yet perception and behavioral performance either stay constant or improve.
178 er memantine would be effective at improving behavioral performance following embolic strokes in rabb
179 ns of ventral temporal cortex correlate with behavioral performance for face or place processing, res
180 am at a low dose shown previously to improve behavioral performance fully restored hilar SOM expressi
181 fect of target-distractor similarity on VSTM behavioral performance, further challenging the role of
182 ce, visual-discrimination problems, and once behavioral performance had stabilized, they received pos
183 -to-trial fluctuations in brain activity and behavioral performance have only tested a monotonic rela
185 between Arc expression in a brain region and behavioral performance implicates that brain region in t
187 , when reward increased spatial selectivity, behavioral performance improved, whereas when reward dec
190 ed human fMRI with computational modeling of behavioral performance in a delayed color-estimation WM
191 all, our findings demonstrate a link between behavioral performance in a demanding WM task and large-
195 of Abeta(1-40) and Abeta(1-42), and improved behavioral performance in a Y-maze test of spontaneous a
196 ocampal long-term potentiation, and improved behavioral performance in aged PDAPP mice with substanti
199 ly weaker and contributed to lower levels of behavioral performance in children compared to adults.
200 e speedup of response times) is largest when behavioral performance in corresponding unisensory condi
201 on between theta power in the MTL source and behavioral performance in decision making, supporting a
203 MN) has been traditionally assumed to hinder behavioral performance in externally focused, goal-direc
204 ns in the DG and led to the full recovery of behavioral performance in fear conditioning, object loca
205 of a mechanistic model and linking these to behavioral performance in humans, these findings identif
209 omolog of primary auditory cortex, can match behavioral performance in the discrimination of conspeci
210 tical areas is that single neurons can match behavioral performance in the discrimination of sensory
211 ogenesis improves hippocampal plasticity and behavioral performance in the multifactorial context of
212 Using a mouse model system, we examined behavioral performance in the open field and elevated ze
213 ning is associated with trait motivation and behavioral performance in the post-learning test phase.
215 mplitude and instantaneous frequency predict behavioral performance in the same visual discrimination
216 with the CDK5 inhibitor roscovitine improved behavioral performance in the water maze test and reduce
217 g-term potentiation (LTP) and memory-related behavioral performance in transgenic mice overexpressing
220 The two tasks produced opposite patterns of behavioral performance: in the scene task, responses wer
221 across-trial variability can correlate with behavioral performance independent of trial-averaged act
222 orineural modulation with attention, despite behavioral performance indicating that they were perform
223 on the most sensitive neurons, then immature behavioral performance is best explained by an immature
225 ing conditions and found that neutrally cued behavioral performance is generally intermediate to that
229 data further demonstrate that periodicity in behavioral performance is strongly influenced by the pro
231 Whereas the hidden factor failed to affect behavioral performance, it significantly modulated brain
232 havioral speed and accuracy, suggesting that behavioral performance limits arise downstream of aPC.
233 s 3.6% [2.3%-4.7%]; P = .04) and team leader behavioral performance (median [interquartile range (IQR
234 ortical activity or any evidence of atypical behavioral performance; moreover, this pattern of typica
235 ion information over time than expected from behavioral performance; neurons driven by the amblyopic
238 ical parameters in the network such that the behavioral performance of the entire model is optimized
240 tion, there was a significant improvement in behavioral performance of the minocycline-treated Tg-SwD
241 transitive inference task fully supports the behavioral performance of the two monkeys that we tested
242 al discrimination was highly correlated with behavioral performance on 11 consonant-discrimination ta
244 ess their individual and additive effects on behavioral performance on a perceptual learning task.
245 tensive experience with reversals and stable behavioral performance on a probabilistic two-arm bandit
246 decomposed electroencephalographic data, and behavioral performance on a response-choice arrow flanke
247 compare the differential effects of age and behavioral performance on changes in self-regulatory con
250 healthy adults are related to variability in behavioral performance on the conceptual combination tas
251 Neural measures were associated with better behavioral performance on the Hearing in Noise Test (HIN
254 tient group, which-in the presence of normal behavioral performance on the Stroop task-suggests that
255 n into the task, a positive association with behavioral performance only during this interval, and ac
259 aws are correlated with those characterizing behavioral performance or whether neuronal LRTCs and ava
260 20 min per subject and can be used offline (behavioral performance) or with fMRI, positron emission
261 higher DLPFC activation (P = .02) and better behavioral performance (P = .02) than the unmedicated pa
265 subjective response to the drug, changes in behavioral performance (reaction time and accuracy), and
270 regions that may contribute to the improved behavioral performance seen with choline supplementation
271 est that all previously reported measures of behavioral performance should be viewed as amalgamations
273 patterns that correlated differentially with behavioral performance, strongly suggesting that intact
274 ion of the prefrontal cortex does not affect behavioral performance, suggesting that this structure i
275 re of this synchrony and its relationship to behavioral performance suggests an important role in the
276 he brain among control subjects with similar behavioral performance, suggests individual analysis is
277 netic basal forebrain inactivation decreased behavioral performance, synchronized cortical activity a
279 shell) neurons reliably predicted subsequent behavioral performance; that is, the greater the percent
282 ts of irradiation, 5-iodotubercidin restored behavioral performance to that of unirradiated animals.
286 5 d delay, against no change at a 5 d delay; behavioral performance was comparable at both delays.
289 stand how this neural variability constrains behavioral performance, we need to be able to measure th
295 activity reflected learning in parallel with behavioral performance, whereas HPC neurons reflected fe
296 DMN regulate the activity in DMN to enhance behavioral performance, whereas signals from DMN to TCN,
297 in V2 and V4 was negatively correlated with behavioral performance, whereas the opposite was true in
298 sk-relevant information that correlated with behavioral performance, whereas this type of encoding wa
299 at are critical for adjusting and optimizing behavioral performance, which may provide a biomarker fo
300 tial for precise and accurate perception and behavioral performance, yet the reliability of sensory s
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