ライフサイエンスコーパス: short-term memory

1 ision-making, attention, planning and verbal short term memory.

2 y pattern transitions to the next, forming a short-term memory.

3 ntion, processing speed, working memory, and short-term memory.

4 n impaired locomotor function, learning, and short-term memory.

5 ortant computational roles and contribute to short-term memory.

6 ) complexes are associated with reduction in short-term memory.

7 program may temporarily improve visuospatial short-term memory.

8 eneral dynamical properties that instantiate short-term memory.

9 roup had a similar ability for the recall of short-term memory.

10 mmation-induced and Fg-mediated reduction in short-term memory.

11 rsistent activity, a potential substrate for short-term memory.

12 formation processing, by transiently erasing short-term memory.

13 suospatial short-term memory; and (3) verbal short-term memory.

14 e left or right CA3 was sufficient to impair short-term memory.

15 o impaired understanding sentences involving short-term memory.

16 P), a form of plasticity thought to underlie short-term memory.

17 ation during visual detection but not during short-term memory.

18 circuit interactions capable of maintaining short-term memory.

19 dor discrimination, perceptual learning, and short-term memory.

20 r suitable for comparative studies of visual short-term memory.

21 on of stimulus traces in the passive form of short-term memory.

22 us presentation is a biological correlate of short-term memory.

23 t that sensory areas may play a role also in short-term memory.

24 nism that may contribute to diverse forms of short-term memory.

25 ministering dehydroepiandrosterone (DHEA) on short-term memory.

26 over how perceptual information is stored in short-term memory.

27 fear memory consolidation without affecting short-term memory.

28 Postreactivation mifepristone did not impair short-term memory.

29 istone injection to measure postreactivation short-term memory.

30 n (LTD), and led to deficits in learning and short-term memory.

31 to young mice while others exhibited poorer short-term memory.

32 mental impact on prior information stored in short-term memory.

33 ble for holding integrated objects in verbal short-term memory.

34 expense of accuracy on tasks of working and short-term memory.

35 uating information about multiple objects in short-term memory.

36 or MWM platform location, indicating intact short-term memory.

37 rom internal representations coded in visual short-term memory.

38 0.81) and with a slightly lesser benefit in short-term memory.

39 standing higher cognitive function including short-term memory.

40 ngaged in a delayed free recall task to test short-term memory.

41 ed that persistent neural activity underlies short-term memory.

42 may contribute to the maintenance of visual short-term memories.

43 posure to violence was associated with lower short-term memory abilities and lower cognitive control

44 esses: visual recognition, long-term memory, short-term memory, action selection, and motor control.

45 VPr also shows sustained short-term memory activity after target stimulus offset,

46 long-term effects of exposure to violence on short-term memory and aspects of cognitive control.

47 VO2Max was associated with better scores on short-term memory and cognitive processing speed by 0.21

48 cellular and synaptic mechanisms underlying short-term memory and demonstrates how the anatomical st

49 eceptors (AMPARs) for memory acquisition and short-term memory and extracellular regulated kinase (ER

50 Long short-term memory and gated recurrent unit recurrent neu

51 l EAAT2, deletion leads to early deficits in short-term memory and in spatial reference learning and

52 However, in short-term memory and integrator networks, where noise a

53 ons about the functional anatomy of auditory short-term memory and its role in language comprehension

54 this pattern of connectivity for theories of short-term memory and long-term associative memory.

55 for saliency coding, spatial attention, and short-term memory and occur in conjunction with nonspati

56 ty was associated with better performance in short-term memory and processing speed.

57 phonological loop linking speech perception, short-term memory and production remains elusive.

58 is to test the relationship between auditory short-term memory and speech comprehension.

59 Ca(2+)-dependent gene expression shows both short-term memory and strong synergy, where two pulses o

60 y an orphan receptor as a potent modifier of short-term memory and supplement classical PFC-based mod

61 creased activity and risk taking, diminished short term memory, and decreased cognitive function.

62 l, attentional weighting, capacity of visual short term memory, and processing speed.

63 rised by impairments in morphosyntax, verbal short-term memory, and explicit long-term memory.

64 ctivity-silent states merely support passive short-term memory, and provide a cautionary note for pur

65 gene knockout impairs reversal learning and short-term memory, and Rdx phosphorylation in wild-type

66 attention is known to gate entry into visual short-term memory, and some evidence suggests that spati

67 ependent cohort for ability to predict state short-term memory, and trait future positive neuropsycho

68 yzed: (1) visual detection; (2) visuospatial short-term memory; and (3) verbal short-term memory.

69 Here, we used two established short-term memory approaches to test the hypothesis that

70 using convolutional neural network and long short-term memory architectures was trained to classify

71 Short-term memories are correlated with slow neural dyna

72 These results indicate that short-term memories are represented by large-scale patte

73 or retention of visual information in visual short-term memory are considered separate from those of

74 blood gene expression biomarkers that track short term memory as measured by the retention measure i

75 gnature deficits within the domain of visual short-term memory associated with GBA mutation and with

76 rtship behavior and can function as cues for short-term memory associated with the mating experience.

77 However, visuospatial short-term memory, associative learning, and implicit lo

78 efficient cell-intrinsic implementation for short-term memories at the voltage level.

79 ed elevated avoidance behavior and decreased short-term memory at either one or three months after a

80 ttention) and delayed match-to-sample tasks (short-term memory) before and 1 hour after administratio

81 ing memory outcomes, 1 outcome (visuospatial short-term memory) benefited the children at 6 months (e

82 previous state-of-the-art bidirectional long-short-term memory (bi-LSTM) plus conditional random fiel

83 ecture, which integrates bi-directional Long Short-Term Memory (Bi-LSTM), Convolutional Neural Networ

84 L might be associated with decline in visual short-term memory binding (VSTMB), a potential biomarker

85 This suggests that visual short-term memory binding deficits may be a preclinical

86 However, only short-term memory binding has been found to be affected

87 genu of corpus callosum which accounted for short-term memory binding impairments and in the hippoca

88 Short-term memory binding is a memory function that unde

89 Whether short-term memory binding is also impaired in familial A

90 The short-term memory binding task required participants to

91 The current study uses a visual short-term memory binding task, measuring both behaviora

92 carriers differed from controls only in the short-term memory binding task.

93 Visual short-term memory binding tasks are a promising early ma

94 rectional recurrent neural network with long short-term memory (BLSTM) to capture the long-range inte

95 es of models: Associative Linking Models and Short-Term Memory Buffer Models.

96 ing-Buffer Model, the masked word disrupts a short-term memory buffer, causing associative links of w

97 jecting to the basolateral amygdala restored short-term memory but not long-term memory or shock sens

98 at these mice had normal basic behaviors and short-term memory, but exhibited broad long-term memory

99 t produce either acute or chronic effects on short-term memory, but experimenter administration of WI

100 en comprehensively studied in the context of short-term memory, but little is known about how DA regu

101 A short-term memory can be evoked by different inputs and

102 such as sensory information accumulation and short-term memory can be modulated by tonic NE levels, a

103 hat mechanisms of information processing and short-term memory can be studied using cultured neuronal

104 in EEG indices of individual differences in short-term memory capacity and in visual search performa

105 at posit a shared substrate between auditory short-term memory capacity and speech comprehension abil

106 Using digit span as an index of auditory short-term memory capacity we found that the structural

107 temporal gyrus and sulcus predicted auditory short-term memory capacity, even when performance on a r

108 ), a region previously shown to track visual short-term memory capacity, we found object identity rep

109 included measures of attention, impulsivity, short-term memory, cognitive processing speed, and verba

110 involvement in working memory, an essential short-term memory component of cognition dependent on th

111 A short-term memory component temporally separated tactile

112 an approach based on deep convolutional long short term memory (ConvLSTM) to predict biological age,

113 des evidence for a large-capacity conceptual short-term memory (CSTM) that momentarily provides rich

114 The pattern of visual short-term memory deficit potentially provides a cogniti

115 specific synaptic ROS production may predict short-term memory deficits with age.

116 re and after the development of CAA, negated short-term memory deficits, as assessed by object-recogn

117 Here we examined visual short-term memory deficits--long associated with Parkins

118 include locomotion, synapse morphology, and short-term memory deficits.

119 ese seasonal records can be characterized by short-term memory described by an autoregressive process

120 to assess the neural correlates of a form of short-term memory during a dot cancellation task.

121 Short-term memory dysfunction is a key early feature of

122 neurons maintain spatial information during short-term memory, even when that information is irrelev

123 Verbal short-term memory, F(3,33) 3.69; P=0.038, and visuospati

124 ory, F(3,33) 3.69; P=0.038, and visuospatial short-term memory, F(6,64) 2.97; P=0.013, show a more fl

125 G (PKG) (for(R)) do not display deficits in short-term memory following 12 h of sleep deprivation.

126 or(s), for(s2)) show substantial deficits in short-term memory following sleep deprivation but retain

127 In this study, we investigated visual short-term memory for coherent motion in action video ga

128 of objects in a scene, and we propose that a short-term memory for object layout is important in prov

129 Furthermore, short-term memory for object recognition was intact in K

130 and delay periods was predictive of accurate short-term memory for object-location relationships.

131 Visual short-term memory for sequentially presented coloured ba

132 release are essential for long-term but not short-term memory formation, and for the maintenance of

133 ophila brain protects against locomotion and short-term memory function deficits in multiple NDs.

134 locking neutrophil adhesion improved CBF and short-term memory function in APP/PS1 mice, even when fe

135 Competing theories of short-term memory function make specific predictions abo

136 nstrated that improving CBF rapidly enhanced short-term memory function.

137 le of gene expression during learning and in short-term memories has been studied extensively(1-3), b

138 iative or 'binding' deficit is also found in short-term memory has not yet been explored.

139 2 years with a 3-year history of progressive short-term memory impairment and depression.

140 3Dq prevented the pro-depressive effects and short-term memory impairment of MS.

141 Pups of FASD mothers displayed short-term memory impairment, decreased hippocampal size

142 We examined whether visual short-term memory impairments, long associated with pati

143 mal cognitive performance disrupts long- and short-term memories in an age-like manner.

144 rammatic variant PPA, the supporting role of short-term memory in a discussion of logopenic variant P

145 s we investigated binding deficits in verbal short-term memory in Alzheimer's disease.

146 using the term "working memory" to describe short-term memory in animals, it is not known whether mu

147 complexes were correlated with reduction in short-term memory in HFg mice.

148 evidence for the importance of phonological short-term memory in language acquisition.

149 impaired long-term memory but did not impact short-term memory in mice.

150 activity models are two prominent models of short-term memory in neural circuits.

151 eatment with A-801195 significantly improved short-term memory in rat social recognition that was not

152 Short-term memory in the brain cannot in general be expl

153 data show that FS reduced long-term but not short-term memory in the WM paradigm.

154 othesized to support pattern recognition and short-term memory in vivo, exist in vitro.

155 work illustrates a mechanism for maintaining short-term memory in which both feedforward and feedback

156 kedly reduced brain plaque load and improved short-term memory in younger and older APP "plaque-produ

157 weaker mnemonic process we will call passive short-term memory, in which a given stimulus trace is hi

158 Errors in short-term memory increase with the quantity of informat

159 pendent consolidation period that converts a short-term memory into a long-term memory.

160 conversion of early LTP into late LTP and of short-term memory into long-term memory.

161 uronal information about two objects held in short-term memory is enhanced at specific phases of unde

162 However, short-term memory is significantly disrupted when for(R)

163 n the "synaptic tagging hypothesis." Initial short-term memory is sustained by a transient plasticity

164 Short-term memory is the ability to store information.

165 robust relationships between working memory, short-term memory, language skills, and fluid intelligen

166 three convolution layers followed by a long short-term-memory layer achieves an accuracy of 96%.

167 Short-term memories link events separated in time, such

168 ented with a 5-year history of predominantly short-term memory loss and functional impairment.

169 treatment-responsive disorder with prominent short-term memory loss and seizures.

170 revealed significant, gradually progressive short-term memory loss in the absence of any history of

171 tage II included depression, explosivity and short-term memory loss.

172 component, which mainly consists of an Long-short Term Memory (LSTM) model that estimates the associ

173 A deep learning algorithm, Long-Short Term Memory (LSTM), was used to represent each pat

174 e artificial neural networks (ANN), and long-short term memory (LSTM), were compared.

175 lutional neural networks for images and long short-term memory (LSTM) for text were used to extract p

176 This challenge prompted us to use a long short-term memory (LSTM) language model to understand th

177 In this study, we developed a long short-term memory (LSTM) model that integrates heterogen

178 as recurrent neural network (RNN) with long short-term memory (LSTM) models for LV pressure and volu

179 ibility prediction with a convolutional Long Short-Term Memory (LSTM) network with k -mer embedding.

180 s work, we investigated the capacity of Long Short-Term Memory (LSTM) networks to predict food allerg

181 Here we employ long short-term memory (LSTM) networks, a class of recurrent

182 sess the performance of a convolutional long short-term memory (LSTM) neural network.

183 nal recurrent neural network (RNN) with long short-term memory (LSTM) to detect DNA modifications.

184 CNN) and recurrent neural networks with long short-term memory (LSTM) units.

185 The goal is accomplished using CNN with long short-term memory (LSTM).

186 As a variant of RNN, long short term memory(LSTM) solved the problem in some exten

187 It also plays a critical role in short-term memory maintenance.

188 ith those for optimal storage, implying that short-term memory may be co-localized with sensory repre

189 les, and is another example of an intrinsic "short-term memory" mechanism.

190 sequential versus persistent activity-based short-term memory mechanisms in the brain.

191 Rats were tested in a short-term memory model, social recognition, and in a se

192 r parietal cortex, a brain region supporting short-term memory, multisensory integration, and decisio

193 and on increased engagement of a distributed short-term memory network in neocortex.

194 We demonstrate how training the long short-term memory network is equivalent to learning a pa

195 frontal cortex is a crucial component of the short-term memory network, and activation of its VIP neu

196 w that recurrent networks, specifically long short-term memory networks can also capture the temporal

197 onsequences: Despite the persistence time of short-term memory networks, it does not pay to accumulat

198 Here we present a Long Short-Term Memory neural network for detection of spikes

199 In a delayed response task that requires short-term memory, neurons in the mouse anterior lateral

200 as artificial implantation and expression of short-term memory occur in satiated flies, formation and

201 These findings imply operational short-term memory of bacteria while moving through compl

202 Short-term memory of mice was assessed by novel object r

203 nserved but largely overlooked mechanism for short-term memory of neural network function.

204 gesting that the locomotor network retains a short-term memory of previous output.

205 stem is necessary for long-term, but not for short-term memory of step-down inhibitory avoidance (IA)

206 ll-to-cell variability in protein levels), a short-term memory of stimulation, and high Hill coeffici

207 The resulting short-term memory of the membrane potential allows to ge

208 Models of short-term memory often assume that the input fluctuatio

209 cell divisions in the absence of an inducer (short-term memory) or for >6 cell divisions (long-term m

210 on in individual cell cycles, which displays short-term memory, or epigenetic inheritance, from the m

211 Thus, it is short-term memory, or transient hysteresis, in CDK4/6 ac

212 effect on attention or executive functions, short-term memory, or verbal and nonverbal learning afte

213 rformance on sustained attention (P = .004), short-term memory (P = .001), long-term memory (P = .006

214 ylcholine from prefrontal cortex can disrupt short-term memory performance and is reminiscent of Alzh

215 ved to be significantly associated with poor short-term memory performance.

216 such networks behaves differently from human short-term memory performance.

217 Short-term memory persists within one cell generation or

218 CMIP and ATP2C2 act to modulate phonological short-term memory primarily in the context of language i

219 trend represents a transition from long- to short-term memory processes when examined in terms of th

220 n a generative deep-learning model: the long-short-term memory recurrent neural network (LSTM-RNN).

221 hybrid convolutional and bi-directional long short-term memory recurrent neural network framework for

222 ysine PTMs), using deep, bidirectional, long short-term memory recurrent neural networks for accurate

223 Short-term memory refers to the ability to store small a

224 dFmr1 and Atx2 function in long-term but not short-term memory, regulating translation of at least so

225 ow that discrete attractor dynamics underlie short-term memory related to motor planning.

226 ired long term memory consolidation, whereas short-term memory remained unaltered.

227 ion, frequency-specific suppression protects short-term memory representations from being overwritten

228 Investigating short-term memory representations within regions of huma

229 Short-term memory requires communication between multipl

230 In contrast, short-term memory requires the SWI/SNF chromatin-remodel

231 we investigated the effect of two aspects of short term memory (STM) (alpha, tau) and their interplay

232 did however exhibit a significant deficit in short term memory (STM) and strong inflammatory reaction

233 Behaviorally, weak training, which induces short-term memory (STM) but not LTM, can be consolidated

234 leiotropic effect for the epsilon4 allele in short-term memory (STM) but the findings have been incon

235 female PDE11 knockout (KO) mice show normal short-term memory (STM) for social odor recognition (SOR

236 t trafficking in vivo to synapses to support short-term memory (STM) formation.

237 detection is a popular task to study visual short-term memory (STM) in humans [1-4].

238 Auditory short-term memory (STM) in the monkey is less robust tha

239 ation' of an auditory Pavlovian fear memory; short-term memory (STM) is intact, whereas long-term mem

240 Short-term memory (STM) or long-term memory (LTM) was ev

241 vidual self-construal priming on recall in a short-term memory (STM) task.

242 l cortical areas has been causally linked to short-term memory (STM), but whether this activity is ne

243 tingly, we observe that spatial and temporal short-term memory (STM), respectively, recruit visual an

244 Short-term memory (STM), the brief maintenance of inform

245 Appetitive short-term memory (STM), which in wild-type (WT) is time

246 t which was lost externally but preserved in short-term memory (STM).

247 nformation is represented in auditory-verbal short-term memory (STM).

248 s that severely disrupted previous models of short-term memory storage.

249 ed sleep is critical in early learning; when short-term memory stores are limited, memory consolidati

250 nhaled nitric oxide (INO) was evaluated by a short term memory task (object recognition task) and imm

251 ealthy controls) were assessed with a visual short-term memory task and a neuropsychological battery.

252 The short-term memory task assessed the recognition of shape

253 gated brain activation during an associative short-term memory task in two human patient groups match

254 and functional MR imaging response during a short-term memory task involving the prefrontal, parieta

255 ctivity (SUA) in monkeys performing a visual short-term memory task.

256 ging activity during sustained attention and short-term memory tasks and enhance memory retrieval.

257 we presented a battery of working memory and short-term memory tasks to adult native speakers of four

258 raining recurrent neural networks on several short-term memory tasks under a wide range of circuit an

259 se patients using two newly developed visual short-term memory tasks with a sensitive, continuous mea

260 ersistent activity can vary markedly between short-term memory tasks with different cognitive demands

261 fects of DHEA administration on episodic and short-term memory tasks, the current experiment demonstr

262 enotype on BDE-47 exposure was observed in a short-term memory test of social novelty that correspond

263 ek-old) fear memory; that is, post-retrieval short-term memory, tested at 3 h after retrieval, is int

264 lecularly distinct mechanisms, which lead to short-term memories that last for seconds to minutes and

265 Working memory is a form of short-term memory that involves maintaining and updating

266 onword repetition, a measure of phonological short-term memory that is commonly impaired in SLI.

267 n the literature, produced acute deficits in short-term memory that recovered with abstinence.

268 persistence of spatial signals during object short-term memory, the activity of neurons in the fronta

269 Although all groups were impaired in visual short-term memory, there was a double dissociation betwe

270 ging the sleep homeostat impaired subsequent short-term memory, thus providing evidence that neural c

271 gh which single-cycle conditioning allocates short-term memory to a specific subset of eligible neuro

272 ng systems utilize dynamic reservoirs having short-term memory to project features from the temporal

273 video game players form a more robust visual short-term memory trace for coherent moving stimuli duri

274 ost with age, whereas the capacity to form a short-term memory trace in the alpha'/beta' mushroom bod

275 hrough heterogeneous APD restitution and the short-term memory, underscoring the genotype-specific tr

276 During the short-term memory, unilateral inhibition of anterior lat

277 convolutional layers and bi-directional long-short-term memory units in a residual structure.

278 ic activation while sounds are maintained in short-term memory using high-resolution functional MRI (

279 Visual short-term memory (VSTM) briefly maintains a limited sam

280 It is commonly believed that visual short-term memory (VSTM) consists of a fixed number of "

281 ts regarding where in the human brain visual short-term memory (VSTM) content is stored, with strong

282 The limits of human visual short-term memory (VSTM) have been well documented, and

283 t is stored in the human brain during visual short-term memory (VSTM) is still an open question.

284 of adult subjects performing either a visual short-term memory (vSTM) task consisting of holding in m

285 Individual differences in visual short-term memory (VSTM) were linked to variability in t

286 rage for a limited number of items in visual short-term memory (VSTM).

287 use we can represent those objects in visual short-term memory (VSTM).

288 hibition of GluT4 impaired long-term memory, short-term memory was enhanced.

289 ealistic levels learnt more slowly and their short-term memory was significantly impaired following e

290 The alpha(2) (short-term memory) was negative in LQT2 while positive i

291 omeostatic plasticity at the NMJ also impair short-term memory when central neurons are targeted, sug

292 rentially with visceral control, affect, and short-term memory, whereas the dorsomedial module resemb

293 ging, has been described as a form of local, short term memory which may influence the ability of the

294 Except for short-term memory, which had a direct effect on self-car

295 ty induces a mutual-inhibition mechanism for short-term memory, which is robust to noise and where fi

296 campal glucose and enhanced both working and short-term memory while also impairing long-term memory.

297 strongly suggesting that intact associative short-term memory with hippocampal dysfunction is indeed

298 ns available to the brain for sensory and/or short-term memory with no need of synaptic learning.

299 n's disease demonstrated a deficit in visual short-term memory, with recall precision significantly w

300 tworks can rapidly add neurons as they build short-term memories, yet little is known about the princ