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1 the attended feature can in principle limit behavioral performance.
2 lowing a post-cue, and this recovery tracked behavioral performance.
3 ates, reducing processing demands to improve behavioral performance.
4 from rest nonetheless contribute strongly to behavioral performance.
5 e amount of information encoded and modulate behavioral performance.
6 dictability during the memory delay affected behavioral performance.
7 gical defects correlate with deficiencies in behavioral performance.
8 mblies among cortical areas is essential for behavioral performance.
9 arning in parallel with the crows' increased behavioral performance.
10 g in task-related areas and deterioration of behavioral performance.
11 brain development is essential for optimized behavioral performance.
12 neural processing stages leading to enhanced behavioral performance.
13 classification was strongly correlated with behavioral performance.
14 functional connectivity may shape subsequent behavioral performance.
15 strength of the response was correlated with behavioral performance.
16 ntrol levels when animals reached asymptotic behavioral performance.
17 activity patterns during behavior, and basic behavioral performance.
18 hese same features also had an impact on the behavioral performance.
19 ity, attentional focus, neural activity, and behavioral performance.
20 reliance on interference control and reduced behavioral performance.
21 een the provision of monetary incentives and behavioral performance.
22 and the size of this effect correlated with behavioral performance.
23 tterns depends on task demands and subject's behavioral performance.
24 te visual and auditory cues to enhance their behavioral performance.
25 nses were predictive of different aspects of behavioral performance.
26 ference-control processes results in reduced behavioral performance.
27 emains untested how sparse coding relates to behavioral performance.
28 ng rate, and had a tighter relationship with behavioral performance.
29 were often sufficiently sensitive to support behavioral performance.
30 TCN --> DMN, are positively correlated with behavioral performance.
31 mpal-prefrontal synchrony is correlated with behavioral performance.
32 to improved sensory perception and enhanced behavioral performance.
33 DMN --> TCN, are negatively correlated with behavioral performance.
34 ying cognition, such as fMRI, rather than in behavioral performance.
35 nhibitory motorcortical network and level of behavioral performance.
36 rfere with task control, leading to degraded behavioral performance.
37 ameters have been associated with changes in behavioral performance.
38 ether picture presentation was contingent on behavioral performance.
39 ral-parietal lobe positively correlated with behavioral performance.
40 lternatives solely on the basis of subjects' behavioral performance.
41 e adult hippocampal neurogenesis and improve behavioral performance.
42 ssess the role of neurogenesis on subsequent behavioral performance.
43 ially perturb MSTd activity while monitoring behavioral performance.
44 tical locking was predictive of the animals' behavioral performance.
45 in critical task-relevant areas and improved behavioral performance.
46 h other cognitive components associated with behavioral performance.
47 strategies may be used to improve perceived behavioral performance.
48 ilor form-function relationships for primate behavioral performance.
49 may result in stimulus-locked periodicity in behavioral performance.
50 timuli contributed independently to impaired behavioral performance.
51 ce in the VWFA and relates VWFA responses to behavioral performance.
52 Fmr1 KO mice and are partly correlated with behavioral performance.
53 evant points in time, resulting in optimized behavioral performance.
54 related patterns in PPC predicted subsequent behavioral performance.
55 systems-level process that in turn enhances behavioral performance.
56 re accompanied by correlated improvements in behavioral performance.
57 early stages of vestibular processing limit behavioral performance.
58 ocal dynamic competition that was related to behavioral performance.
59 emble codes are better suited to account for behavioral performance.
60 on in the absence of eye movements, improves behavioral performance.
61 ctively improves perception and consequently behavioral performance.
62 echanism underlying its beneficial effect on behavioral performance.
63 esponses was closely related to single-trial behavioral performance.
64 task correlated positively with the monkeys' behavioral performance.
65 and the level of suppression correlated with behavioral performance.
66 y and synaptic efficacy and thus influencing behavioral performance.
67 ient, that is, those that cannot account for behavioral performance.
68 mediate-tier areas was predictive of correct behavioral performance.
69 versus correct rejects were correlated with behavioral performance.
70 training may be an effective way to enhance behavioral performance.
71 lume that was associated with improvement in behavioral performance.
72 apy-naive mice results in impaired cognitive behavioral performance.
73 he reduction in GABA, which in turn predicts behavioral performance.
74 t of locomotion with local selection impairs behavioral performance.
75 old age as well as individual differences in behavioral performance.
76 n the MD system were accompanied by impaired behavioral performance.
77 correct responses, indicating more efficient behavioral performance.
78 ween brain FCD and individual differences in behavioral performance.
79 ortantly, these interactions correlated with behavioral performance.
80 ivity in HD may have compensatory effects on behavioral performance.
81 cts on the amount of information encoded and behavioral performance.
82 sed parietal activity, which correlated with behavioral performance.
83 stable, intrinsic networks of the brain and behavioral performance.
84 s and show they are required for appropriate behavioral performance.
85 under study, which can in turn be related to behavioral performance.
86 negative consequences of the distracters on behavioral performance.
87 lso graded as a function of cue validity and behavioral performance.
88 network organization were related to better behavioral performance.
89 e abrupt and occurred before the recovery of behavioral performance.
90 y phase of local ensemble activity predicted behavioral performance.
91 of networks for the task at hand, improving behavioral performance.
92 critically important in modulating multiple behavioral performances.
93 ividuals, but yet achieve remarkably similar behavioral performances.
95 ons, aging, functional brain activations and behavioral performance across key cognitive functions, r
96 these regions were associated with improved behavioral performance across participants and followed
97 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
103 bis involvement were examined in relation to behavioral performance and brain activity in a visual N-
105 lacebo vs Nicorette gum) and time-on-task on behavioral performance and brain functional network metr
106 ages to contain only LSF or HSF and measured behavioral performance and corticospinal excitability (C
107 nstruction technique, we identified impaired behavioral performance and degraded mnemonic representat
108 owledge of cue-reward probabilities improves behavioral performance and diminishes reinforcement lear
109 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 stimuli to guide visual perception, although behavioral performance and neural representations were l
117 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
128 tates is related to both general measures of behavioral performance and relative differences in task-
129 multiple sites in the striatum as induced by behavioral performance and reward-related stimuli, by di
130 d glutamate in human volunteers predict both behavioral performance and the dynamics of a neural valu
131 one discrimination task on relations between behavioral performance and the magnitude of auditory eve
132 ts have been limited by both their assays of behavioral performance and their use of lesions to chang
133 duced striatal dopamine loss, despite normal behavioral performance and unaltered N-methyl-D-aspartat
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
140 as shown to predict the multisensory gain in behavioral performance at a time lag of approximately 25
142 ity were observed even though differences in behavioral performance between MTBI patients and control
143 representations of remembered locations and behavioral performance both decreased with increasing me
144 eover, trained networks can achieve the same behavioral performance but differ substantially in their
146 ation of activation predicted task-switching behavioral performance, but with hemispherically dissoci
148 ermine the amount of encoded information and behavioral performance by combining analytic calculation
149 Attention is commonly thought to improve behavioral performance by increasing response gain and s
150 Recent studies argue that attention improves behavioral performance by shaping of the noise distribut
151 ild up sleep pressure, which results in slow behavioral performance (cognitive lapses) typically attr
156 ttended stimuli, which correlated with their behavioral performance deficits and clinical symptoms.
157 to perform a practiced spatial task leads to behavioral performance deficits, and that synaptic plast
158 n from psychology linking arousal state with behavioral performance, demonstrating neural correlates
159 ring the delay period significantly impacted behavioral performance, demonstrating the importance of
164 temporally precise SC inhibition influenced behavioral performance during a visually guided orientat
167 ves acquisition of knowledge and team leader behavioral performance during subsequent simulated cardi
169 endent (BOLD) functional activity as well as behavioral performance during working memory was examine
170 ponses typically decline, yet perception and behavioral performance either stay constant or improve.
173 , PS, or combined Pb and PS in F1 offspring: behavioral performance [fixed-interval (FI) schedule of
175 ns of ventral temporal cortex correlate with behavioral performance for face or place processing, res
177 am at a low dose shown previously to improve behavioral performance fully restored hilar SOM expressi
178 fect of target-distractor similarity on VSTM behavioral performance, further challenging the role of
179 ce, visual-discrimination problems, and once behavioral performance had stabilized, they received pos
180 -to-trial fluctuations in brain activity and behavioral performance have only tested a monotonic rela
182 between Arc expression in a brain region and behavioral performance implicates that brain region in t
184 d in cortex and cerebellum over learning: as behavioral performance improved, initially dissimilar L5
185 , when reward increased spatial selectivity, behavioral performance improved, whereas when reward dec
187 ered that EFV activates CYP46A1 and improves behavioral performance in 5XFAD mice, an Alzheimer's dis
188 ed human fMRI with computational modeling of behavioral performance in a delayed color-estimation WM
189 all, our findings demonstrate a link between behavioral performance in a demanding WM task and large-
193 model of RT to 46 female human participants' behavioral performance in a simple reaction time task.
198 ly weaker and contributed to lower levels of behavioral performance in children compared to adults.
199 e speedup of response times) is largest when behavioral performance in corresponding unisensory condi
200 on between theta power in the MTL source and behavioral performance in decision making, supporting a
202 MN) has been traditionally assumed to hinder behavioral performance in externally focused, goal-direc
203 ns in the DG and led to the full recovery of behavioral performance in fear conditioning, object loca
204 of a mechanistic model and linking these to behavioral performance in humans, these findings identif
208 ogenesis improves hippocampal plasticity and behavioral performance in the multifactorial context of
209 Using a mouse model system, we examined behavioral performance in the open field and elevated ze
210 ning is associated with trait motivation and behavioral performance in the post-learning test phase.
212 mplitude and instantaneous frequency predict behavioral performance in the same visual discrimination
214 th theta and delta amplitude correlated with behavioral performance in the tasks but in an opposite m
215 with the CDK5 inhibitor roscovitine improved behavioral performance in the water maze test and reduce
216 antities are correlated with fluctuations of behavioral performance in various tasks and brain region
218 During locomotion, selective mice have worse behavioral performance, increased noise correlations in
219 across-trial variability can correlate with behavioral performance independent of trial-averaged act
220 on the most sensitive neurons, then immature behavioral performance is best explained by an immature
222 ing conditions and found that neutrally cued behavioral performance is generally intermediate to that
223 relationship between shared variability and behavioral performance is heterogeneous and complex in f
224 This study provides evidence that rodent behavioral performance is highly flexible in the face of
228 data further demonstrate that periodicity in behavioral performance is strongly influenced by the pro
230 e DMN, ultimately facilitating cognitive and behavioral performance levels that are equivalent to tha
231 havioral speed and accuracy, suggesting that behavioral performance limits arise downstream of aPC.
232 s 3.6% [2.3%-4.7%]; P = .04) and team leader behavioral performance (median [interquartile range (IQR
233 ortical activity or any evidence of atypical behavioral performance; moreover, this pattern of typica
234 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 transitive inference task fully supports the behavioral performance of the two monkeys that we tested
241 reatment, EGCG did not significantly improve behavioral performance of Ts65Dn mice in the multivariat
243 ls the translocation of a reward, predicting behavioral performance on a goal-oriented spatial learni
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 ed that this technique can improve subjects' behavioral performance on a wide range of tasks and amel
249 healthy adults are related to variability in behavioral performance on the conceptual combination tas
250 ive cognitive control, leading to changes in behavioral performance on the DPX task and in activity i
251 Neural measures were associated with better behavioral performance on the Hearing in Noise Test (HIN
253 n into the task, a positive association with behavioral performance only during this interval, and ac
256 aws are correlated with those characterizing behavioral performance or whether neuronal LRTCs and ava
257 higher DLPFC activation (P = .02) and better behavioral performance (P = .02) than the unmedicated pa
261 subjective response to the drug, changes in behavioral performance (reaction time and accuracy), and
264 regions that may contribute to the improved behavioral performance seen with choline supplementation
265 est that all previously reported measures of behavioral performance should be viewed as amalgamations
266 slates into the precision of an individual's behavioral performance.SIGNIFICANCE STATEMENT Which neur
269 patterns that correlated differentially with behavioral performance, strongly suggesting that intact
270 ion of the prefrontal cortex does not affect behavioral performance, suggesting that this structure i
271 re of this synchrony and its relationship to behavioral performance suggests an important role in the
272 he brain among control subjects with similar behavioral performance, suggests individual analysis is
273 netic basal forebrain inactivation decreased behavioral performance, synchronized cortical activity a
275 shell) neurons reliably predicted subsequent behavioral performance; that is, the greater the percent
276 To test the impact of this variability on behavioral performance, these models were used to perfor
279 ts of irradiation, 5-iodotubercidin restored behavioral performance to that of unirradiated animals.
280 itive control function necessary for optimal behavioral performance under cognitively demanding condi
281 ask rule coding also tracked improvements in behavioral performance under high-reward conditions.
284 5 d delay, against no change at a 5 d delay; behavioral performance was comparable at both delays.
286 t for executing the trained motor skill, and behavioral performance was impaired following targeted m
289 stand how this neural variability constrains behavioral performance, we need to be able to measure th
295 inverted-U dose response on cell firing and behavioral performance when given systemically to aged m
296 activity reflected learning in parallel with behavioral performance, whereas HPC neurons reflected fe
297 DMN regulate the activity in DMN to enhance behavioral performance, whereas signals from DMN to TCN,
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