ライフサイエンスコーパス: memory task

1 ut the previously visited arm in the working memory task.

2 ed attention task and a whole-report working memory task.

3 performing a virtual-reality object-location memory task.

4 an (SD) = 22.12 (2.16)] during a declarative memory task.

5 er BOLD PSC across three levels of a working memory task.

6 in the dlPFC of monkeys performing a working memory task.

7 lectrode arrays, who performed a recognition memory task.

8 mice successfully perform a spatial working memory task.

9 ic task, the perceptual task, but not in the memory task.

10 rol subjects, during a visuo-spatial working memory task.

11 connectivity with the hippocampus during the memory task.

12 lated with memory impairments in the working memory task.

13 k with a similar structure to the multi-task memory task.

14 a prefrontal cortex-dependent T-maze working memory task.

15 1 while rats performed a nonspatial sequence memory task.

16 transfer of learning to a different type of memory task.

17 cortex (PFC) of monkeys performing a working memory task.

18 erformed a visuospatial and a verbal working memory task.

19 epilepsy patients who performed an episodic memory task.

20 stently prevented transfer to the subsequent memory task.

21 erbal compared with the visuospatial working memory task.

22 g, water maze training and a spatial working memory task.

23 s performed a hippocampus-dependent sequence-memory task.

24 raging task and a context-object associative memory task.

25 human participants performed an associative memory task.

26 ocampal function was assessed using a verbal memory task.

27 ed the interaction effect in the free recall memory task.

28 ance imaging during the self-ordered working memory task.

29 ic doses of ketamine in a rule-based working memory task.

30 as IT and FEF of the monkey during a working memory task.

31 while nonhuman primates performed a working memory task.

32 g participated in a verbal paired-associates memory task.

33 the cue-encoding phase of a spatial working memory task.

34 ca mulatta) performed an audiovisual working memory task.

35 transfer-of-benefit to an untrained working memory task.

36 rest, during an attention task, and during a memory task.

37 ice performed a reward-based spatial working memory task.

38 erformed a paired-associates episodic verbal memory task.

39 al effects of HT-0712 were seen in a spatial memory task.

40 entorhinal deactivations during an episodic memory task.

41 e they performed a spatial Sternberg working memory task.

42 1.2) and also performed worse on the verbal memory task.

43 ents performed a hybrid spatial and episodic memory task.

44 activity in monkeys performing a recognition memory task.

45 ing acquisition and performance of a working memory task.

46 MRI) data collected during an n-back working memory task.

47 erent amounts of reward in a spatial working memory task.

48 ncoding and retrieval in an odor recognition memory task.

49 MN deactivation induced by an n-back working memory task.

50 tional MRI while performing a verbal working memory task.

51 ng in primate dlPFC during a spatial working memory task.

52 Participants completed a delayed recognition memory task.

53 connectivity (d = 0.57) during a recognition memory task.

54 age were impaired in a hippocampal-dependent memory task.

55 e time and fewer mistakes made in the visual memory task.

56 e neurosurgical patients performed a spatial memory task.

57 ing Treasure Hunt, a virtual-reality spatial-memory task.

58 ngle-trial EEG data from a Sternberg working memory task.

59 115 patients performing a free recall verbal memory task.

60 ts during a free-foraging task and a spatial memory task.

61 died mice performing a whisker-based working memory task.

62 cognitive function, as measured in a working memory task.

63 ution while participants completed a working memory task.

64 e supportive for decision-making and working memory tasks.

65 o-noise ratio in decision making and working memory tasks.

66 tor states of networks of neurons performing memory tasks.

67 ctive impairment in EC-dependent associative memory tasks.

68 ed behavior, and performance in learning and memory tasks.

69 ing and cognitive performance during working memory tasks.

70 but decreased learning of sequential spatial memory tasks.

71 trodes performed spatial and verbal-episodic memory tasks.

72 activation produced by attention and working memory tasks.

73 ar focused on area CA1 in animals performing memory tasks.

74 rk responses to visual attention and working memory tasks.

75 ential to enhance performance in recognition memory tasks.

76 on and performance on hippocampally mediated memory tasks.

77 icates that women outperform men in episodic memory tasks.

78 ing the delay period of object-based working memory tasks.

79 nd assessed cognitive performance by working memory tasks.

80 -term depression and performances on spatial memory tasks.

81 h familiar from novel objects in recognition memory tasks.

82 the spatial tasks and impaired on all of the memory tasks.

83 s while mice performed hippocampus-dependent memory tasks.

84 tion included other non-spatial learning and memory tasks.

85 gical tests as the monkeys performed working memory tasks.

86 campus and impairment on cued and contextual memory tasks.

87 ehavioral function of the PFC during working memory tasks.

88 n several hippocampal-dependent learning and memory tasks.

89 mined by the Barnes maze and object location memory tasks.

90 to substantial biases in basic learning and memory tasks.

91 stem is important for spatial and relational memory tasks.

92 ike memory deficits in hippocampus-dependent memory tasks.

93 esearch in predicting performance on working memory tasks.

94 also perform better than WT in learning and memory tasks.

95 improved performance in spatial and working memory tasks.

96 isms are engaged by males and females during memory tasks.

97 phalogram data recorded during 2 associative memory tasks.

98 bsequently, subjects performed a recognition memory task 10 min and 24 h after encoding.

99 althy adults completed a challenging working memory task (2-back task) while receiving painful therma

100 ncephalography and a hybrid spatial-episodic memory task (29 subjects, 15 female) to determine how sp

101 h response times during the most challenging memory task (3-back; p = 0.005).

102 tasks and then they learned another type of memory task 6 h later, either with or without the same s

103 T) cortical disconnection on two recognition memory tasks, a "constant negative" task, and delayed no

104 ted this idea by creating different types of memory task: a sequence of words or actions that either

105 nance imaging while they performed a working memory task, along with 23 controls.

106 ese agonists to monkeys performing a working memory task also produced an inverted-U dose-response, w

107 Difficulty in the simulation and memory tasks also increased after TMS to the left angula

108 icipants performed a virtual reality spatial memory task analogous to the Morris water maze and a mir

109 duced disruption of performance in a working memory task and a spatial memory task in rodents and non

110 assessed in a delay-match-to-sample working memory task and a spatial recognition task.

111 with indwelling electrodes perform a verbal memory task and asked how encoding or retrieval correlat

112 performed four blocks of a difficult working memory task and four blocks of a control task during fMR

113 elated to children's performance on a source memory task and hippocampal subfield volumes.

114 d ~200 genetically diverse mice on a working memory task and identified a genetic locus on chromosome

115 We trained mice in an auditory long-term memory task and measured learning-related dynamic change

116 romagnetic fields (ELF MFs) on a recognition memory task and morphological changes of hippocampal neu

117 nia, who were mildly impaired at the spatial memory task and no better than chance on the memory inte

118 sonance imaging while performing an episodic memory task and psychological testing.

119 lated with slower performance on the working memory task and slower cognitive speed on the Symbol Dig

120 e significantly less accurate on the working memory task and their neuronal dynamics indicated that e

121 ty during sustained attention and short-term memory tasks and enhance memory retrieval.

122 g led to improvement on (non)trained working memory tasks and generalization to tasks of reasoning an

123 y of different neuron types in the DG during memory tasks and have provided exciting new insights int

124 e present during the delay period of working memory tasks and may therefore reflect the representatio

125 ervention/control period, subjects underwent memory tasks and neuroimaging to assess volume, microstr

126 Participants learned one of these memory tasks and then they learned another type of memor

127 c resonance imaging (during ann-back working-memory task) and positron emission tomography using the

128 ee conditions: pretask rest, spatial working-memory task, and posttask rest.

129 Here we trained rats on a spatial memory task, and showed that subsequent sleep periods wh

130 8 subjects, who performed picture rating and memory tasks, and corresponding fMRI data from up to 696

131 n hippocampal-dependent spatial learning and memory tasks, and on the production of endocannabinoid a

132 and novel faces: (1) a standard recognition memory task; and (2) a task wherein they attempted to co

133 s suggest that PFC activation during working memory task anticipation and performance may be an impor

134 ly where stimuli relevant to the associative memory task appeared.

135 DLPFC and PPC neuron activity during working memory tasks are associated with diversity in the cellul

136 iveness of the DMN but can perform a working memory task as well as healthy subjects, without demonst

137 nt in aging rats, allowing them to perform a memory task as well as young rats.

138 I, participants then completed a recognition memory task, as well as a recall phase in which they wer

139 ced performance on the novel object location memory task, as well as reduced anhedonic behavior.

140 logical assessment, three verbal recognition memory tasks assessing familiarity and recollection each

141 Analysis of working memory-task BOLD PSC revealed a similar interaction betw

142 ectories of the next chosen arm in reference memory tasks but the previously visited arm in the worki

143 asticity had no deficit in spatial reference memory tasks, but were impaired in an associative task w

144 We apply our method to a working memory task by synthesizing a network that implements a

145 te recall and the 2-Back and spatial working memory tasks (CogState Battery), without significantly a

146 D activation during the self-ordered working memory task compared with the control task, and the corr

147 ynamic responses assessed during the working memory task demonstrated a strong positive correlation w

148 Accuracy improvements on the object working memory task did not differ between groups.

149 er single-task conditions, though as working memory task difficulty increased, stimulation disrupted

150 Following two hippocampus-dependent memory tasks, DSW occurrence rates, ripple frequencies,

151 When engaging in a secondary memory task during driving, their performance deteriorat

152 All individuals performed the 2-back working memory task during functional magnetic resonance imaging

153 Participants performed an associative memory task during hr-fMRI in which they encoded and lat

154 infected controls performed a verbal working memory task during magnetoencephalography (MEG).

155 I) scans while performing the n-back working memory task during three hormone conditions: ovarian sup

156 ocampal-prefrontal theta coupling: a spatial memory task (during magnetoencephalography) and a memory

157 We demonstrate-in the spatial memory task, during memory recall-that theta power incre

158 icity or spatial and contextual learning and memory tasks employed in our study, consistent with the

159 isk participants performing a verbal working memory task exhibited altered brain activation compared

160 rest and while performing the 2-back working memory task five times each, with task state alternating

161 ansgenic mice, indicating a higher rating in memory tasks for GSK3beta-overexpressing mice compared w

162 cult to link individual networks to specific memory tasks, for example a learned behavior.

163 specific moments in a temporally structured memory task have so far been observed only in area CA1,

164 went extinction paired with a 2-back working memory task (High-Load).

165 Here, we used taste memory tasks, highly dependent on glutamatergic transmis

166 living sleep may negatively impact difficult memory tasks, however the relationship between free-livi

167 items during early portions of a relational memory task (i.e., relational binding task: P-trend = 0.

168 nts completed a pitch and rhythm recognition memory task immediately after tDCS.

169 ditions exhibited similar performance on the memory task immediately following learning (before intox

170 accuracy improvements on the spatial working memory task in a delay-dependent manner.

171 ation would improve performance of a working memory task in a nonhuman primate model.

172 performed a classical goal-directed spatial memory task in a rectangular chamber.

173 ity during a food-reinforced spatial working memory task in a reward-based alternate trajectory maze.

174 psy patients performing a self-paced spatial memory task in a virtual environment.

175 cted worse performance on the T-maze working memory task in adulthood (Experiment 3).

176 16 e4 carriers (aged 45-55) on a subsequent memory task in conjunction with MRI to assess how hippoc

177 vity was recorded from rats doing an working memory task in control sessions and under the influence

178 functional network recruitment in a working memory task in controls.

179 s (ACE) on brain activation during a working memory task in menopausal women.

180 Using a contextual fear memory task in mice, we demonstrate that fear learning i

181 Using an everyday memory task in mice, we sought the neurons mediating thi

182 mpal IEDs on single-neuron activity during a memory task in patients with medically refractory epilep

183 l magnetic resonance imaging studies using a memory task in patients with mild cognitive impairment h

184 ic module' hypothesis was based on a working-memory task in rats which suggested that spontaneous reo

185 mance in a working memory task and a spatial memory task in rodents and nonhuman primates, respective

186 between baseline activation during a working memory task in the stimulated prefrontal region and symp

187 We created a memory task in which children were required to recall th

188 The current study applied a novel memory task in which moderate drinkers (N = 30) and trea

189 operceptual task and an attention-to-working-memory task in which one or two stimuli were cued before

190 participants performing a retro-cue working memory task in which the selection rule and the memory c

191 23) were scanned while performing a working memory task in which they had to first anticipate perfor

192 on performance of spatial and object working memory tasks in adolescent monkeys.

193 ciated with LC integrity across a variety of memory tasks in both younger (n = 66) and older adults (

194 n infancy impairs performance in recognition memory tasks in mammalian animals, but it is unknown if

195 ted by social cognition and autobiographical memory tasks in prior fMRI data and significantly coloca

196 performance of smooth pursuit and a working memory task increased the diagnostic performance of purs

197 All participants completed a declarative memory task involving incidental encoding of neutral vis

198 teral prefrontal cortex during a declarative memory task involving learning a set of words.

199 onal MR imaging response during a short-term memory task involving the prefrontal, parietal, and occi

200 turn, mice lacking SynCAM 1 were impaired in memory tasks involving CA3.

201 participants completed episodic and semantic memory tasks involving unimodal (auditory or visual) and

202 egies are evident even when performance on a memory task is similar between females and males.

203 ctivity in LPFC recorded during some working memory tasks is a reflection of sensory storage, the not

204 Human performance on memory tasks is severely limited; however, the two major

205 activity during the delay of spatial working memory tasks is thought to maintain spatial location in

206 FC occurs during the delay period of working memory tasks: it might serve to maintain the current con

207 rats performing a continuous spatial working memory task known to require hippocampal-prefrontal inte

208 tisol), parenting stress, and performance on memory tasks known to engage the hippocampus.

209 In working memory tasks, LB speakers were better than RB speakers a

210 in younger and older adults during a working memory task (letter n-back).

211 went extinction paired with a 1-back working memory task (Low-Load), and a third group underwent exti

212 tices, respectively, whereas for the working memory task, maximum and minimum responses were observed

213 Subjects performed a multilevel working-memory task (N-back) during fMRI.

214 ormation during the performance of a working memory task (N-back).

215 Despite learning a spatial memory task normally and displaying normal brain glucose

216 ic oxide (INO) was evaluated by a short term memory task (object recognition task) and immunohistoche

217 In a memory task, objects can be differentiated by their to-b

218 Participants then undertook an anterograde memory task of alcohol impairment when intoxicated.

219 incidental and not required for the working-memory task of judging stimulus orientation.

220 Although working memory tasks often engage dorsolateral prefrontal cortex

221 halamus and performed a visuospatial working memory task outside the scanner.

222 equential memory during a deferred imitation memory task (P-trend = 0.048), and toddlers with more ex

223 th impaired vigilance) and was predictive of memory task performance and symptom severity.

224 e examine COMT in relation to N-Back working memory task performance in a large population-based coho

225 Learning and memory task performance were impaired in Arg-61 mice at

226 ham' groups did not differ in online working memory task performance, but the transcranial direct cur

227 fferences in modularity were correlated with memory task performance, such that lower modularity leve

228 nd significantly improved brief visuospatial memory task performance.

229 ed during an individually calibrated working memory task performed by individuals of both sexes.

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

232 ias the behavior of animals during a spatial memory task, providing causal evidence that hippocampal

233 In the olfactory memory task, rats chose a novel odor from a gradually in

234 In the spatial memory task, rats searched for a depleting food source a

235 Here we report that monkeys perform working memory tasks reliably during puberty and show modest imp

236 up's metacognitive accuracy on an equivalent memory task remained unimpaired (meta-d'/d', 95% confide

237 TUNL, a working memory task, requires animals to 'nonmatch' to a sample

238 of unilateral LPFC lesions during a working memory task requiring monkeys to compare directions of t

239 the task switched every two trials between a memory task (retrieving information from the study phase

240 tasks; moreover, the analysis of one of the memory tasks revealed a marginally significant correspon

241 Evidence from a new recognition memory task reveals that infants are sensitive to this p

242 NMDARs to persistent activity during working memory tasks.SIGNIFICANCE STATEMENT Working memory enabl

243 isodes such as those observed during working memory tasks, suggesting a significant functional impact

244 tly with performance in episodic and working memory tasks, suggesting its role in human disease patho

245 e recordings in monkeys performing a working memory task tested for D1R-HCN channel interactions in v

246 performed better on a demanding recognition memory task that assesses participants' ability to discr

247 We designed a flexible spatial working memory task that required rats to navigate - after distr

248 A while subjects performed a virtual-reality memory task that required them to learn the spatial loca

249 ticipants perform a verbal paired associates memory task that requires the encoding of distinct word

250 ation were assessed using an object-location memory task that segregated recollection precision from

251 Here, we show that during a working memory task the brain uses an oscillatory mechanism for

252 erformance on hippocampus-dependent episodic memory tasks the next morning (beta-values from 0.290 to

253 rmed a reliable and validated visual working memory task (the "Discrete Whole Report task", 90 trials

254 nimals were tested on a self-ordered spatial memory task, the Hamilton Search Task.

255 ecorded in monkeys during an object sequence memory task to identify a role of mixed selectivity in s

256 monitoring during a partial-cue recognition memory task to index reinstatement of lure images behavi

257 nt study used rTMS and fMRI during a working memory task to test this hypothesis.

258 d a battery of working memory and short-term memory tasks to adult native speakers of four LB and fou

259 ty Task (MST), a modified object recognition memory task, to be highly sensitive to hippocampal funct

260 urrent neural networks on several short-term memory tasks under a wide range of circuit and task mani

261 ctivity during the delay period of a working memory task using EEG.

262 onship between hippocampal activity during a memory task using fMRI and subsequent longitudinal chang

263 ith brain activity during the n-back working memory task using functional magnetic resonance imaging,

264 tical regions were assessed during a working memory task using NIRS.

265 y during performance of a subsequent working memory task (ventromedial prefrontal cortex, r = -0.66,

266 Performance on the memory task was better during adolescence.

267 g recovery the following day when no working memory task was executed.

268 Performance on spatial and object memory tasks was assessed 23 or 71 hours after drug admi

269 Performance on the memory tasks was assessed with both direct (accuracy) an

270 Here, using a paired-associates verbal memory task, we combine behavioural data, computational

271 lected from IT as monkeys performed a visual memory task, we demonstrate that variation in a compleme

272 Using an incidental memory task, we find that blocking dopamine (400 mg amis

273 y recorded FEF and IT neurons during working memory task, we observed significant Granger causality i

274 A1 while mice performed an olfactory working-memory task, we recorded stimulus-specific sequences of

275 tes have been reported following training on memory tasks, we hypothesized that SPW-R activity follow

276 mance, their metacognitive judgements in the memory task were as accurate as the control group.

277 e imaging responses during an N-back working memory task were assessed at baseline and at the end of

278 Both memory tasks were completed again the following day.

279 y for nonspatial features of the associative memory task when they were visually available (perceptua

280 hy, age-matched controls performed a working memory task where they encoded, maintained, and actively

281 formance on an associative spatial long-term memory task, whereas right CA3 silencing had no effect.

282 ting long-term memory for an object location memory task, whereas sedentary and adol ELE mice did not

283 to hippocampal theta oscillations in spatial memory tasks, whether and how theta oscillations mediate

284 elevated coupling with each other during the memory task, which correlated with the global reduction

285 ed a selective deficit on an object location memory task, which requires objection-location pairing.

286 5 young adults performed an object and scene memory task while functional MRI data were acquired.

287 ty-one participants completed an associative memory task while undergoing simultaneous EEG-fMRI recor

288 participants who performed a verbal episodic memory task while we recorded high gamma (62-100 Hz) act

289 n task and a more difficult auditory working memory task, while continuously exposed to the same test

290 tive efficiency separately in a visual and a memory task, while taking variations in basic task perfo

291 hich 95 individuals, aged 18-75, performed a memory task with a similar structure to the multi-task m

292 triatum of rats performing a spatial working memory task with delays up to 10 s.

293 entence comprehension than during a sequence memory task with nonwords, or a symbolic math task.

294 s were scanned during an Old/New recognition memory task with only the line-drawings presented as ret

295 ctivity can vary markedly between short-term memory tasks with different cognitive demands.

296 nd performance on easy vs. difficult working memory tasks with emotional stimuli contributes to discr

297 anticipation and performance on the working memory tasks with fearful and neutral faces as variables

298 First, we assessed memory tasks with low (Auditory Verbal Learning Test (AV

299 g task, embedded within an emotional working memory task, with some blocks under unpredictable threat

300 ) details produced during the simulation and memory tasks, with a concomitant increase in external de