ライフサイエンスコーパス: short-term memory

1 ity) and tests cued at long delays (assay of short-term memory).

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

3 circuit interactions capable of maintaining short-term memory.

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

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

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

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

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

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

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

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

12 fear memory consolidation without affecting short-term memory.

13 Postreactivation mifepristone did not impair short-term memory.

14 istone injection to measure postreactivation short-term memory.

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

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

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

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

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

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

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

22 circuits involved in sensorimotor gating and short-term memory.

23 rated, stored and subsequently released from short-term memory.

24 in the regulation of sensorimotor gating and short-term memory.

25 etrieval of relational information in visual short-term memory.

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

27 al cortices relative to other information in short-term memory.

28 firing rates that are a neural correlate of short-term memory.

29 t be addressed by any satisfactory theory of short-term memory.

30 hippocampus, differ from those that underlie short-term memory.

31 e variety of additional functions, including short-term memory.

32 -term memory whereas the gamma lobes support short-term memory.

33 sary for short-term synaptic facilitation or short-term memory.

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

35 a general mechanism underlying many forms of short-term memory.

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

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

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

39 program may temporarily improve visuospatial short-term memory.

40 eneral dynamical properties that instantiate short-term memory.

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

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

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

44 0.81) and with a slightly lesser benefit in short-term memory.

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

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

47 standing higher cognitive function including short-term memory.

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

49 o impaired understanding sentences involving short-term memory.

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

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

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

53 (48-hr retention test) but had no effect on short-term memory (1-hr retention test) for contextual f

54 k is at least on par with measures of verbal short-term memory (a core component of phonological proc

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

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

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

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

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

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

61 e-mediated reverberation could contribute to short-term memory and help to consolidate the transient

62 major psychological theories (the "mind") of short-term memory and how they relate to evidence about

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

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

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

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

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

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

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

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

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

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

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

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

75 Acetylcholine (ACh) influences attention, short-term memory, and sleep/waking transitions, through

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

77 different sorts of access to information in short-term memory, and that access by retrieval operatio

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

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

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

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

82 ory (assessed at 24 h) was impaired, whereas short-term memory (assessed at 1-3 h) of fear conditioni

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

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

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

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

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

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

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

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

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

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

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

94 The short-term memory binding task required participants to

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

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

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

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

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

100 f the fimbria-fornix fiber system in spatial short-term memory but suggest that the cholinergic septo

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

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

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

104 CV restitution and estimated the effects of short-term memory by calculating time constant of action

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

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

107 l research has led to the view that items in short-term memory can be parsed into two categories: a s

108 o questions of capacity and how--or whether--short-term memory can be separated from long-term memory

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

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

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

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

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

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

115 n examining eight cognitive cases--teaching, short-term memory, causal reasoning, planning, deception

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

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

118 A short-term memory component temporally separated tactile

119 treatment with mGluR antagonists can rescue short-term memory, courtship, and mushroom body defects.

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

121 cortex, predicted subsequent accuracy on the short-term memory decision, as did bilateral posterior h

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

123 her severe postural imbalance or an isolated short-term memory deficit.

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

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

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

127 By contrast, other items in short-term memory demand retrieval mechanisms that are r

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

129 perform delayed-matching-to-sample and their short-term memory during such tasks.

130 synaptic labile state and representation of short-term memory during this critical time window.

131 versus dynamic pacing protocols by inducing short-term memory effects related to pacing-dependent Ca

132 cting cavity could also function as a useful short-term memory element.

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

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

135 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

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

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

138 ontrast, animals displayed similar levels of short-term memory for LFI when trained in either the sub

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

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

141 Visual short-term memory for sequentially presented coloured ba

142 und that the formation of long-term, but not short-term, memory for a nonassociative form of learning

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

144 rocesses were modulated by genes involved in short-term memory formation, namely dunce and rutabaga.

145 iate 10 min after learning severely disrupts short-term memory formation.

146 model distinguishing just-read sentences in short-term memory from activated portions of long-term m

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

148 robustly in measures of verbal learning and short-term memory function.

149 The labile state of short-term memory has been known for more than a century

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

151 In a recent experiment on short-term memory, honeybees (Apis mellifera) learned to

152 2 years with a 3-year history of progressive short-term memory impairment and depression.

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

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

155 Extended wakefulness disrupts acquisition of short-term memories in mammals.

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

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

158 torhinal cortex contributes to early loss of short-term memory in Alzheimer's disease.

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

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

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

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

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

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

165 of conduction velocity (CV) restitution and short-term memory in the organization and evolution of a

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

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

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

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

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

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

172 ed in these mice, while the stabilization of short-term memory into long-term memory is impaired.

173 ntal evidence suggests that early responses (short-term memory) involve post-translational modificati

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

175 The capacity of visual short-term memory is highly limited, maintaining only th

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

177 Acquisition of new information and short-term memory is spared in these mice, while the sta

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

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

180 The second mechanism is associated with short-term memory (large tau) and is characterized by sh

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

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

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

184 toms of hippocampal dysfunction (i.e. severe short-term memory loss) and three with extensive limbic

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

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

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

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

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

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

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

192 ssess the daily changes in the decay rate of short-term memory, motivation, and motor ability in rats

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

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

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

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

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

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

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

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

201 h paired visual and vestibular stimuli cause short-term memory of the mollusc Hermissenda that lasts

202 Some polymerases retain a "short-term memory" of replication errors, responding to

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

204 ion test administered 30 min after training (short-term memory) or 48 h after training (long-term mem

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

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

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

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

209 ic reductions typically observed in classic 'short-term memory' patients with perisylvian brain damag

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

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

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

213 Short-term memory persists within one cell generation or

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

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

216 mouse forebrain during various stages of the short-term memory processes.

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

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

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

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

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

222 Investigating short-term memory representations within regions of huma

223 in neuroimaging investigations with similar short-term memory requirements.

224 Short-term memory requires communication between multipl

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

226 ng-term contextual fear memory while sparing short-term memory, retrieval, and extinction.

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

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

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

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

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

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

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

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

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

236 ngthen the activation of a memory set during short-term memory (STM) retention.

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

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

239 Short-term memory (STM), or the ability to hold informat

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

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

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

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

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

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

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

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

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

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

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

251 he representation of a single item through a short-term memory task, describing the biological mechan

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

253 a multi-image delayed match-to-sample (DMS) short-term memory task.

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

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

256 In short-term memory tasks, individual prefrontal cortical

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

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

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

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

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

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

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

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

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

266 found that primary CD8 T cell responses and short-term memory to HIV Env and VSV nucleocapsid (VSV N

267 been shown to disrupt the normal transfer of short-term memory to long-term storage sites.

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

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

270 put stream, biological systems must retain a short-term memory trace of their recent inputs.

271 suggest that a new mechanism associated with short-term memory underlies SDA formation in the heart,

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

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

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

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

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

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

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

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

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

281 in storing single object features in visual short-term memory (VSTM), such as color, orientation, sh

282 orage in a temporary buffer, known as visual short-term memory (VSTM), that sustains attended informa

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

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

285 mental representations are stored in visual short-term memory (VSTM).

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

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

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

289 debate over the reason about forgetting from short-term memory, whether interference or decay is the

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

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

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

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

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

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

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

297 nary changes in psychological theories about short-term memory, with similarly great advances in the

298 examine the evidence for the architecture of short-term memory, with special attention to questions o

299 ance and increased Abeta levels and abnormal short-term memory (working memory).

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