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1 ing task (either a zero- or two-back working memory task).
2 ic doses of ketamine in a rule-based working memory task.
3 as IT and FEF of the monkey during a working memory task.
4 while nonhuman primates performed a working memory task.
5 g participated in a verbal paired-associates memory task.
6 the cue-encoding phase of a spatial working memory task.
7 ca mulatta) performed an audiovisual working memory task.
8 transfer-of-benefit to an untrained working memory task.
9 rest, during an attention task, and during a memory task.
10 ice performed a reward-based spatial working memory task.
11 erformed a paired-associates episodic verbal memory task.
12 al effects of HT-0712 were seen in a spatial memory task.
13 entorhinal deactivations during an episodic memory task.
14 e they performed a spatial Sternberg working memory task.
15 ents performed a hybrid spatial and episodic memory task.
16 in the dlPFC of monkeys performing a working memory task.
17 activity in monkeys performing a recognition memory task.
18 ing acquisition and performance of a working memory task.
19 MRI) data collected during an n-back working memory task.
20 erent amounts of reward in a spatial working memory task.
21 ncoding and retrieval in an odor recognition memory task.
22 MN deactivation induced by an n-back working memory task.
23 tional MRI while performing a verbal working memory task.
24 ng in primate dlPFC during a spatial working memory task.
25 Participants completed a delayed recognition memory task.
26 connectivity (d = 0.57) during a recognition memory task.
27 pilepsy participated in a visual recognition memory task.
28 nd rCBF during resting and an N-back working-memory task.
29 ges associated with performance on a working memory task.
30 14 healthy controls during a 2-back working memory task.
31 enables strong discrimination in the spatial memory task.
32 impaired performance on a trace-conditioning memory task.
33 FC) in humans before performance of a visual memory task.
34 hile participants performed the same working memory task.
35 ferences in neural activity during a working memory task.
36 raphy (EEG) in patients during a recognition memory task.
37 itions, followed by training on a procedural memory task.
38 egion of rats while they performed a spatial memory task.
39 effects predict rat performance in a spatial memory task.
40 xed monkeys performing a free-viewing visual memory task.
41 h the representation of context in a working memory task.
42 rdings from 27 patients performing a working memory task.
43 ty for 20 minutes and then repeated the word memory task.
44 c resonance imaging during a spatial working memory task.
45 ndependent features defining trials during a memory task.
46 A) in monkeys performing a visual short-term memory task.
47 izure rats learned response tasks before the memory task.
48 g specific delay periods as rats performed a memory task.
49 rea TE as monkeys performed a temporal-order memory task.
50 ally trained on a delayed-nonmatch-to-sample memory task.
51 s of brain activity during an N-back working memory task.
52 hildren by means of a videogame-like working memory task.
53 lectrode arrays, who performed a recognition memory task.
54 were severely impaired on a spatial working memory task.
55 mma oscillations as humans perform a working memory task.
56 ted to performance on an item and relational memory task.
57 mice successfully perform a spatial working memory task.
58 onkeys on two variants of an object sequence memory task.
59 ith better memory performance on the imaging memory task.
60 rformance on the relational but not the item memory task.
61 rformance on a hippocampus-dependent spatial memory task.
62 an (SD) = 22.12 (2.16)] during a declarative memory task.
63 ic task, the perceptual task, but not in the memory task.
64 rol subjects, during a visuo-spatial working memory task.
65 connectivity with the hippocampus during the memory task.
66 lated with memory impairments in the working memory task.
67 k with a similar structure to the multi-task memory task.
68 a prefrontal cortex-dependent T-maze working memory task.
69 1 while rats performed a nonspatial sequence memory task.
70 transfer of learning to a different type of memory task.
71 cortex (PFC) of monkeys performing a working memory task.
72 erformed a visuospatial and a verbal working memory task.
73 stently prevented transfer to the subsequent memory task.
74 erbal compared with the visuospatial working memory task.
75 er BOLD PSC across three levels of a working memory task.
76 g, water maze training and a spatial working memory task.
77 s performed a hippocampus-dependent sequence-memory task.
78 human participants performed an associative memory task.
79 ed the interaction effect in the free recall memory task.
80 ance imaging during the self-ordered working memory task.
81 ing the delay period of object-based working memory tasks.
82 nd assessed cognitive performance by working memory tasks.
83 -term depression and performances on spatial memory tasks.
84 h familiar from novel objects in recognition memory tasks.
85 the spatial tasks and impaired on all of the memory tasks.
86 s while mice performed hippocampus-dependent memory tasks.
87 gical tests as the monkeys performed working memory tasks.
88 campus and impairment on cued and contextual memory tasks.
89 ehavioral function of the PFC during working memory tasks.
90 n several hippocampal-dependent learning and memory tasks.
91 mined by the Barnes maze and object location memory tasks.
92 to substantial biases in basic learning and memory tasks.
93 entirely separate and subsequently performed memory tasks.
94 o-noise ratio in decision making and working memory tasks.
95 tor states of networks of neurons performing memory tasks.
96 t prefrontal activity during complex working memory tasks.
97 postnatally-treated animals in learning and memory tasks.
98 perated controls were trained on two working memory tasks.
99 ar mnemonic processes to perform recognition memory tasks.
100 of injury lost the ability to learn spatial memory tasks.
101 riety of hippocampal- and amygdala-dependent memory tasks.
102 ulthood and their controls in the same three memory tasks.
103 o evinced difficulties in the visual working memory tasks.
104 stages of training monkeys on visual working memory tasks.
105 ctive impairment in EC-dependent associative memory tasks.
106 ion during performance of verbal and figural memory tasks.
107 20 neurosurgical patients performed working memory tasks.
108 ed behavior, and performance in learning and memory tasks.
109 ing and cognitive performance during working memory tasks.
110 but decreased learning of sequential spatial memory tasks.
111 e supportive for decision-making and working memory tasks.
112 trodes performed spatial and verbal-episodic memory tasks.
113 activation produced by attention and working memory tasks.
114 ar focused on area CA1 in animals performing memory tasks.
115 rk responses to visual attention and working memory tasks.
116 ential to enhance performance in recognition memory tasks.
117 on and performance on hippocampally mediated memory tasks.
118 icates that women outperform men in episodic memory tasks.
119 T) cortical disconnection on two recognition memory tasks, a "constant negative" task, and delayed no
121 ese agonists to monkeys performing a working memory task also produced an inverted-U dose-response, w
123 in brain function using a social recognition memory task, an assessment of the acquisition and retent
124 icipants performed a virtual reality spatial memory task analogous to the Morris water maze and a mir
126 duced disruption of performance in a working memory task and a spatial memory task in rodents and non
128 performance in a high control demand working memory task and also to exhibit high global connectivity
129 performed four blocks of a difficult working memory task and four blocks of a control task during fMR
130 romagnetic fields (ELF MFs) on a recognition memory task and morphological changes of hippocampal neu
132 lated with slower performance on the working memory task and slower cognitive speed on the Symbol Dig
133 e significantly less accurate on the working memory task and their neuronal dynamics indicated that e
135 g led to improvement on (non)trained working memory tasks and generalization to tasks of reasoning an
136 d significant impairments in spatial working-memory tasks and in the encoding phase of trace fear-con
137 e present during the delay period of working memory tasks and may therefore reflect the representatio
138 ervention/control period, subjects underwent memory tasks and neuroimaging to assess volume, microstr
139 c resonance imaging (during ann-back working-memory task) and positron emission tomography using the
142 8 subjects, who performed picture rating and memory tasks, and corresponding fMRI data from up to 696
144 and novel faces: (1) a standard recognition memory task; and (2) a task wherein they attempted to co
145 , psychostimulant response, and learning and memory tasks are mutated, they produce subtle phenotypes
146 iveness of the DMN but can perform a working memory task as well as healthy subjects, without demonst
148 ced performance on the novel object location memory task, as well as reduced anhedonic behavior.
150 logical assessment, three verbal recognition memory tasks assessing familiarity and recollection each
152 asticity had no deficit in spatial reference memory tasks, but were impaired in an associative task w
153 a contextual component to the odor sequence memory task by training rats to choose the earlier odor
155 te recall and the 2-Back and spatial working memory tasks (CogState Battery), without significantly a
156 D activation during the self-ordered working memory task compared with the control task, and the corr
157 ynamic responses assessed during the working memory task demonstrated a strong positive correlation w
159 er single-task conditions, though as working memory task difficulty increased, stimulation disrupted
162 All individuals performed the 2-back working memory task during functional magnetic resonance imaging
165 I) scans while performing the n-back working memory task during three hormone conditions: ovarian sup
167 isk participants performing a verbal working memory task exhibited altered brain activation compared
168 rest and while performing the 2-back working memory task five times each, with task state alternating
169 ansgenic mice, indicating a higher rating in memory tasks for GSK3beta-overexpressing mice compared w
171 puterized self-ordered spatial search (SOSS) memory task has been adapted from a human neuropsycholog
172 specific moments in a temporally structured memory task have so far been observed only in area CA1,
174 items during early portions of a relational memory task (i.e., relational binding task: P-trend = 0.
176 ditions exhibited similar performance on the memory task immediately following learning (before intox
179 rats trained to perform a "standard" spatial memory task in a plus maze and in two new task variants.
180 e trained rats to perform a standard spatial memory task in a plus maze and tested how training affec
182 ity during a food-reinforced spatial working memory task in a reward-based alternate trajectory maze.
185 vity was recorded from rats doing an working memory task in control sessions and under the influence
187 he present experiment, we used an incidental memory task in humans and obtained valence and arousal r
190 me and neural activation during a relational memory task in patients who were in the early stage of a
191 l magnetic resonance imaging studies using a memory task in patients with mild cognitive impairment h
193 mance in a working memory task and a spatial memory task in rodents and nonhuman primates, respective
194 d animals also performed better on a spatial memory task in the Morris water maze, showing improved l
196 activation during an associative short-term memory task in two human patient groups matched for exte
197 , rats were given a novel object recognition memory task in which initial encounters with some of the
198 operceptual task and an attention-to-working-memory task in which one or two stimuli were cued before
200 thin subjects, combined with a biconditional memory task in which the rat must consider information a
203 n infancy impairs performance in recognition memory tasks in mammalian animals, but it is unknown if
204 All participants completed a declarative memory task involving incidental encoding of neutral vis
206 onal MR imaging response during a short-term memory task involving the prefrontal, parietal, and occi
208 participants completed episodic and semantic memory tasks involving unimodal (auditory or visual) and
209 ctivity in LPFC recorded during some working memory tasks is a reflection of sensory storage, the not
211 activity during the delay of spatial working memory tasks is thought to maintain spatial location in
213 tices, respectively, whereas for the working memory task, maximum and minimum responses were observed
215 ation patterns in response to n-back working memory tasks (n = 1, 2, 3) were assessed with functional
216 processing components of the emotion working memory task (no correlation during the identity task), c
218 ic oxide (INO) was evaluated by a short term memory task (object recognition task) and immunohistoche
220 equential memory during a deferred imitation memory task (P-trend = 0.048), and toddlers with more ex
223 l connectivity to the LPFC predicted working memory task performance and also correlated with LPFC BO
225 hippocampal volumes and superior relational memory task performance compared to lower-fit children.
226 e examine COMT in relation to N-Back working memory task performance in a large population-based coho
228 ham' groups did not differ in online working memory task performance, but the transcranial direct cur
229 fferences in modularity were correlated with memory task performance, such that lower modularity leve
230 working memory and performance on a working memory task performed in a magnetoencephalography scanne
231 aradigms were used: a fractal n-back working memory task probing executive system function and an emo
234 ated neural activity observed during working memory tasks reflect the short-term retention of informa
236 Here we report that monkeys perform working memory tasks reliably during puberty and show modest imp
237 up's metacognitive accuracy on an equivalent memory task remained unimpaired (meta-d'/d', 95% confide
240 a role of the ReRh in strategy shifting in a memory task requiring cortical and hippocampal functions
241 of unilateral LPFC lesions during a working memory task requiring monkeys to compare directions of t
242 tasks; moreover, the analysis of one of the memory tasks revealed a marginally significant correspon
244 isodes such as those observed during working memory tasks, suggesting a significant functional impact
245 tly with performance in episodic and working memory tasks, suggesting its role in human disease patho
246 e recordings in monkeys performing a working memory task tested for D1R-HCN channel interactions in v
247 performed better on a demanding recognition memory task that assesses participants' ability to discr
248 icate that female rats outperform males on a memory task that combines object recognition and locatio
249 an at-risk mental state performing a working memory task that entailed the maintenance and manipulati
250 A while subjects performed a virtual-reality memory task that required them to learn the spatial loca
251 ation were assessed using an object-location memory task that segregated recollection precision from
252 erformance on hippocampus-dependent episodic memory tasks the next morning (beta-values from 0.290 to
253 erformance during a well-established working-memory task (the n-back) in individuals sustaining moder
255 EA administration on episodic and short-term memory tasks, the current experiment demonstrated large
257 early and late adolescence during a working memory task, this recruitment is correlated with behavio
258 ecorded in monkeys during an object sequence memory task to identify a role of mixed selectivity in s
259 approach that approaches nonspecific spatial memory tasks to evaluate cognition, but also would bette
260 separate experiments using an episodic-like memory task, to learn six paired associates (PAs) in an
261 y relevant given that the object and spatial memory tasks used in monkeys are often translated to inv
263 onship between hippocampal activity during a memory task using fMRI and subsequent longitudinal chang
265 y during performance of a subsequent working memory task (ventromedial prefrontal cortex, r = -0.66,
268 y recorded FEF and IT neurons during working memory task, we observed significant Granger causality i
270 tes have been reported following training on memory tasks, we hypothesized that SPW-R activity follow
272 e imaging responses during an N-back working memory task were assessed at baseline and at the end of
275 are not cognitively deficient with temporal memory tasks, when the tasks do not rely heavily upon vi
276 were acquired in the test phase of a verbal memory task where healthy human volunteers made Remember
277 (6 male) completed a continuous recognition memory task where the interval between presentation and
278 hy, age-matched controls performed a working memory task where they encoded, maintained, and actively
279 formance on an associative spatial long-term memory task, whereas right CA3 silencing had no effect.
280 its in Morris water maze and contextual fear memory tasks, whereas mice lacking Itsn2 showed normal l
281 elevated coupling with each other during the memory task, which correlated with the global reduction
282 mprovements in performing short-term spatial memory tasks, which upon continued suppression translate
283 ed control subjects performed a visuospatial memory task while their electroencephalograms were recor
284 participants who performed a verbal episodic memory task while we recorded high gamma (62-100 Hz) act
285 14;10) completed visual and auditory working memory tasks while event-related potentials (ERPs) were
286 n task and a more difficult auditory working memory task, while continuously exposed to the same test
287 tive efficiency separately in a visual and a memory task, while taking variations in basic task perfo
288 or instance, during delay periods in working memory tasks, while stimuli are represented in working m
289 hich 95 individuals, aged 18-75, performed a memory task with a similar structure to the multi-task m
292 entence comprehension than during a sequence memory task with nonwords, or a symbolic math task.
293 nned while performing a serial order working memory task with pictures of common objects and were lat
294 control, we used a delayed response working memory task with pictures of varying content (emotional
295 using two newly developed visual short-term memory tasks with a sensitive, continuous measure of rep
297 g task, embedded within an emotional working memory task, with some blocks under unpredictable threat
298 ) details produced during the simulation and memory tasks, with a concomitant increase in external de
299 pared brain activation response to a working-memory task (WMT) in type 1 diabetic subjects (n = 16) w
300 e 2-Back WM prior to a hippocampal-dependent memory task would impair performance on the latter task.
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