ライフサイエンスコーパス: declarative memory

1 list of semantically associated word pairs (declarative memory).

2 e awareness as expected from a substrate for declarative memory.

3 sociated with improvements in procedural and declarative memory.

4 in associative learning tasks that depend on declarative memory.

5 the MTL function together in the service of declarative memory.

6 ortex may mediate processes beyond long-term declarative memory.

7 al temporal lobe lesions and no capacity for declarative memory.

8 s learned is a fundamental characteristic of declarative memory.

9 cally enables the relational organization of declarative memory.

10 mental cognitive processes in the service of declarative memory.

11 eneral role of the hippocampus in relational/declarative memory.

12 elated with performance on clinical tests of declarative memory.

13 al paired-comparison task measures a form of declarative memory.

14 t ideas about the role of the hippocampus in declarative memory.

15 be acquired implicitly and independently of declarative memory.

16 thesizing dose-dependent decreases in verbal declarative memory.

17 al ganglia, and various neocortical areas in declarative memory.

18 thought to promote systems consolidation of declarative memory.

19 licated in memory, in particular episodic or declarative memory.

20 le memory expression that is the hallmark of declarative memory.

21 hanisms and optimal strategies for improving declarative memory.

22 l striatum, insula, and midbrain can enhance declarative memory.

23 physiology and on overnight consolidation of declarative memory.

24 neural representations capable of supporting declarative memory.

25 epresentations, which may form the basis for declarative memory.

26 s linked to demyelination and impairments in declarative memory.

27 of durable associations, a hallmark of human declarative memory.

28 s in orthogonalization of representations in declarative memory.

29 eas the memory view suggests a broad role in declarative memory.

30 resulted in robust, reliable enhancements in declarative memory.

31 lementary MTL encoding computations subserve declarative memory.

32 endent procedural over hippocampus-dependent declarative memory.

33 r less compelling, especially with regard to declarative memory.

34 renicline group scored higher on working and declarative memory.

35 tion, and the neocortex, the storage site of declarative memories.

36 lly involved in the acquisition of long-term declarative memories.

37 antial and long-lasting benefit of sleep for declarative memories.

38 ical processes within sleep actively enhance declarative memories.

39 cial for the ability to learn and retain new declarative memories.

40 cessary for the acquisition and retrieval of declarative memories.

41 en reported, along with enhanced ability for declarative memories.

42 memories, mirroring the role of the MTL for declarative memories.

43 t that VS and MS neurons are a substrate for declarative memories.

44 ectively the retrieval, but not encoding, of declarative memories.

45 1.48; 95% CI, 1.08-2.04; P = .02), impaired declarative memory abilities (beta = -0.87; HR, 0.42; 95

46 n attention and working memory abilities and declarative memory abilities (Cohen d, approximately 0.8

47 n attention and working memory abilities and declarative memory abilities, is a robust characteristic

48 n attention and working memory abilities and declarative memory abilities.

49 attention and working memory abilities, and declarative memory abilities.

50 approaches to the treatment of psychosis and declarative memory alterations and in novel animal prepa

51 Outcomes were declarative memory and hippocampal subregion volumes.

52 pendently and together, were associated with declarative memory and hippocampal volume in late early

53 for facts and events, collectively known as declarative memory and often studied as spatial memory i

54 unambiguous evidence for the independence of declarative memory and priming.

55 The entorhinal cortex is crucial for declarative memory and spatial cognition.

56 sm for substantial normal variation in human declarative memory and suggest that the basic effects of

57 ies the functional specialization of HCsf in declarative memory and the potential use of MRE measures

58 The hippocampus is crucial for episodic or declarative memory and the theta rhythm has been implica

59 they support the link between aware memory, declarative memory, and hippocampus-dependent memory.

60 d tests of processing speed, working memory, declarative memory, and intelligence, no evidence for pl

61 sitively correlated with psychosis severity, declarative memory, and overall cognitive performance (P

62 lobal cognitive function, verbal and spatial declarative memory, and perceptual-motor speed.

63 emporal lobe damage impairs the formation of declarative memory, and that semantic knowledge is impai

64 esponse to altered scenes reflect conscious, declarative memory, and they support the link between aw

65 s, but the extent to which animals also have declarative memory, and whether inferential expression o

66 ed impairment in the formation of long-term, declarative memory (anterograde amnesia), together with

67 and retrieved, the neural processes by which declarative memories are maintained or forgotten remain

68 e refuting the hypothesis that procedural or declarative memories are processed/consolidated in sleep

69 Declarative memories are thought to be stored within ana

70 Basic issues about the nature of declarative memory are considered in this review from th

71 Human brain pathways supporting language and declarative memory are thought to have differentiated su

72 n, a process that enables the flexibility of declarative memories, are both hippocampus-dependent and

73 The discovery of declarative memory as distinct from other forms of memor

74 or-word subscale score) as well as in verbal declarative memory (as measured by the Paragraph Recall

75 temporal lobes are known to be critical for declarative memory, at present the neural mechanisms sup

76 Performance was examined for tests of verbal declarative memory, attention, and executive function.

77 aration reveals action-independent coding of declarative memory-based familiarity and confidence of c

78 ms underlying systems-level consolidation of declarative memory beyond the hippocampal-prefrontal int

79 are essential for the formation of long-term declarative memories, both spatial and non-spatial, but

80 functionally related system specialized for declarative memory but not for perception.

81 a newly learned rule makes heavy demands on declarative memory, but after thousands of repetitions r

82 mory can be disrupted by a task that engages declarative memory, but the slow motor memory is immune

83 emporal lobe structures are known to support declarative memory, but there is not consensus about wha

84 motivation has been demonstrated to enhance declarative memory by facilitating systems-level consoli

85 hypothesis that circadian arrhythmia impairs declarative memory by increasing the relative influence

86 cortical acetylcholine in a rodent model of declarative memory by infusing the cholinergic muscarini

87 Here we show that existing declarative memories can be selectively impaired by usin

88 These results demonstrate that human declarative memory can be selectively rewritten during r

89 Type 3, n = 5) showed significantly reduced declarative memory capacities (intracarotid amobarbital

90 view that the hippocampus mediates a general declarative memory capacity in animals, as it does in hu

91 vates the hippocampus and other areas of the declarative memory circuit.

92 Alzheimer's disease (AD), the impairment of declarative memory coincides with the accumulation of ex

93 ly related structures that are essential for declarative memory (conscious memory for facts and event

94 mpus dependent because, as in other tasks of declarative memory, conscious knowledge must be acquired

95 eficial role for cognitive functions such as declarative memory consolidation and perceptual learning

96 SIGNIFICANCE STATEMENT Systems mechanisms of declarative memory consolidation beyond the hippocampal-

97 Declarative memory consolidation is hypothesized to requ

98 a direct role for cortical acetylcholine in declarative memory consolidation or retrieval.

99 s followed by an improved procedural but not declarative memory consolidation under conditions of SD.

100 This provides convergent evidence that declarative memory decisions can be regulated via striat

101 on of individual neurons by IEDs to specific declarative memory deficits in specific cell types, ther

102 Individuals with T2DM had specific verbal declarative memory deficits, reduced hippocampal and pre

103 The capacity for declarative memory depends on the hippocampal region and

104 it is unclear whether these findings in the declarative memory domain also apply in the motor memory

105 on have deficits in hippocampal-based verbal declarative memory (e.g., recall of a paragraph) and in

106 Declarative memory enables conscious recollection of the

107 lly known for its role in building long-term declarative memories, enables the spread of value across

108 nce for hippocampal involvement in long-term declarative memory encoding and for the view that the am

109 campal region and the amygdala, in long-term declarative memory encoding was examined by using positr

110 Declarative memory encoding, consolidation, and retrieva

111 Declarative memory encompasses episodic and semantic div

112 e imaging in humans to examine mechanisms of declarative memory enhancement when subjects were motiva

113 During encoding and retrieval of declarative memories, entorhinal and hippocampal circuit

114 Contrary to claims that PRh mediates declarative memory exclusively, previous evidence sugges

115 hat the medial temporal lobe (MTL) subserves declarative memory exclusively, whereas nondeclarative m

116 The role of the amygdala in enhancing declarative memory for emotional experiences has been in

117 a is involved with the formation of enhanced declarative memory for emotionally arousing events.

118 Here we test 6- and 12-mo-old infants' declarative memory for novel actions after a 4-h [Experi

119 Declarative memory for rapidly learned, novel associatio

120 al stimulation to the amygdala could enhance declarative memory for specific images of neutral object

121 SCR to unconditioned stimulus or compromised declarative memory for stimulus-outcome contingencies.

122 Despite impaired declarative memory for the tasks, the amnesic subjects d

123 arning of the task but had severely impaired declarative memory for the training episode.

124 ars to have a complex influence on long-term declarative memory for those stimuli: Whereas emotion en

125 hese two processes are related in supporting declarative memory formation and how they are compromise

126 view that the amygdala is not involved with declarative memory formation for nonemotional material.

127 tion preceding stimulus encoding can predict declarative memory formation.

128 hanisms can be recruited to prevent unwanted declarative memories from entering awareness, and that t

129 rst study to demonstrate that sleep protects declarative memories from subsequent associative interfe

130 during sleep may facilitate the transfer of declarative memories from the hippocampus to the neocort

131 enia, hippocampal perfusion is increased and declarative memory function is degraded.

132 ols; (3) that hippocampal volumes and verbal declarative memory function will be positively correlate

133 associational activity in CA3, with degraded declarative memory function, and with formation of false

134 on are consistently reported; impairments in declarative memory function, especially in the flexible

135 The temporal lobes play a prominent role in declarative memory function, including episodic memory (

136 ed the nature and recovery of procedural and declarative memory functioning in a cocaine-abusing coho

137 Measures of declarative memory functioning, in contrast, were normal

138 performance on 3 tasks that required intact declarative memory functioning.

139 Besides its relevance for declarative memory functions, hippocampal activation has

140 ng memory (g = 0.45, 95% CI: 0.11-0.79), and declarative memory (g = 0.30, 95% CI: 0.02-0.58).

141 These findings show that declarative memory has different operating characteristi

142 premise that the amygdala causally enhances declarative memory has not been directly tested in human

143 ial temporal lobe (MTL), a critical area for declarative memory, have been shown to change their tuni

144 l loss (HS ILAE Type 2; n = 13) did not show declarative memory impairment and were indistinguishable

145 ancing role of sleep in the consolidation of declarative memories in the first year of life.

146 to identify genetic contributions to verbal declarative memory in a community setting.

147 et) substitution is associated with impaired declarative memory in healthy volunteers and patients wi

148 Furthermore, the basic properties of declarative memory in human beings can be viewed as evol

149 The hippocampus is necessary for declarative memory in humans and episodic memory in rode

150 Chronic circadian dysfunction impairs declarative memory in humans but has little effect in co

151 The hippocampus is critical to declarative memory in humans.

152 nto the role of PRs in facilitating spatial, declarative memory in males, which may help with finding

153 , the idea that MTL components contribute to declarative memory in similar ways has also been contrad

154 th lower scores on measures of attention and declarative memory, including several measures of audito

155 pocampus is essential for different forms of declarative memory, including social memory, the ability

156 e relationship between the basal ganglia and declarative memory, including the involvement of striatu

157 Human declarative memory involves a systematic organization of

158 ongest arguments against a role for sleep in declarative memory involves the demonstration that the m

159 Deciphering the mechanisms of declarative memory is a major goal of neuroscience.

160 ally, a medial-temporal system that mediates declarative memory is affected by the late onset of AD.

161 Declarative memory is enabled by circuits in the entorhi

162 Declarative memory is known to depend on the medial temp

163 It is widely believed that declarative memory is mediated by a medial temporal lobe

164 These studies have shown that declarative memory is mediated by a specific brain syste

165 and reproduction, but their role in spatial declarative memory is not understood.

166 tion of cognitive functions supporting human declarative memory is one of the grand challenges of neu

167 the ventral visual stream, whereas long-term declarative memory is supported by the medial temporal l

168 A characteristic usually attributed to declarative memory is that what is learned is accessible

169 One of the most widely studied examples of declarative memory is the capacity to recognize recently

170 Declarative memory is thought to rely on two processes:

171 pisodic and semantic memory (together termed declarative memory) is an unresolved and much-debated to

172 encodes a wide range of non-spatial forms of declarative memory, it is not yet known whether SWRs are

173 daptation of visual neurons and retrieval of declarative memories, largely follow similar rules.

174 patients (n = 8), who have severely impaired declarative memory, learned a probabilistic classificati

175 rast, showed more specific associations with declarative memory, letter fluency and processing speed

176 Factors "declarative memory" (measuring 25% of the common varianc

177 Inspired by the classic finding that for declarative memories, medial temporal lobe (MTL) structu

178 hought to operate together in the service of declarative memory--memory for facts and events--having

179 g their differential roles in procedural and declarative memory more generally.

180 scillations (SOs) and sleep spindles indexes declarative memory network development.

181 nown as consolidation, which, in the case of declarative memories, occurs within the medial temporal

182 ssessing skin conductance response (SCR) and declarative memory of stimulus-outcome contingencies dur

183 In fact, reactivating a declarative memory often makes it more robust and less s

184 ern may well be involved in the formation of declarative memories on places.

185 cortical regions was associated with better declarative memory only in bipolar disorder subjects, an

186 which subjects solve a problem using either declarative memory or habit learning.

187 Some argue that hippocampus supports declarative memory, our capacity to recall facts and eve

188 nitary memory system supporting all types of declarative memory, our conscious memory for facts and e

189 The hippocampus is critical for encoding declarative memory, our repository of knowledge of who,

190 The hippocampus serves a critical role in declarative memory--our capacity to recall everyday fact

191 onance imaging was used with a simple visual declarative memory paradigm to test for differences in n

192 nd memory (Delayed Non-Match to Sample), and declarative memory (Paragraph Recall).

193 inding is minimized, showing that relational/declarative memory per se is not impaired in aging.

194 HC, and PFC over a 5 year period can predict declarative memory performance in healthy adults.

195 pal formation, resulting in decreased verbal declarative memory performance.

196 matter volume were significant predictors of declarative memory performance.

197 Declarative memory permits an organism to recognize stim

198 n hippocampus, traditionally associated with declarative memory, plays a role in motor sequence learn

199 depression) on general intellectual ability, declarative memory, procedural memory, executive functio

200 ess brain patterns related to procedural and declarative memory processes, respectively.

201 tive performance scores, executive function, declarative memory, processing speed, or visuoperception

202 Declarative memory recall is thought to involve the rein

203 st-training eyes-closed waking rest improved declarative memory relative to a distractor task.

204 Declarative memory relies on a medial temporal lobe syst

205 Consolidation of declarative memories requires hippocampal-neocortical co

206 Declarative memory retrieval is thought to involve reins

207 IEDs disrupt medial temporal lobe-dependent declarative memory retrieval processes.SIGNIFICANCE STAT

208 However, the contribution of striatum to declarative memory retrieval remains unknown.

209 dence for the involvement of the striatum in declarative memory retrieval.

210 wo functions of the fronto-parietal network: declarative memory retrievals and updating of working me

211 The meta-analysis showed that declarative memory retrievals correlated with activity i

212 ts, in a fear memory setting, and in a human declarative memory setting.

213 ests could be summarized as four constructs: declarative memory, signal discrimination, working memor

214 igm is a particularly good system to explore declarative memory since humans do not acquire trace con

215 ed to identify the neuroanatomy of long-term declarative memory (sometimes termed explicit memory).

216 gdala is not a site of long-term explicit or declarative memory storage, but serves to influence memo

217 Declarative memory (story recall) and selective attentio

218 Detecting novelty is critical to consolidate declarative memories, such as spatial contextual recogni

219 The declarative memory system allows us to accurately recogn

220 sentation of the trauma in the context-based declarative memory system in favor of its overrepresenta

221 This could represent a shift to the declarative memory system in Parkinson's disease during

222 Here, we explored declarative memory system reorganization in patients wit

223 ask the benefits of sleep by challenging the declarative memory system with competing information (in

224 a significant limitation on the hippocampal declarative memory system, and impaired interference man

225 rovide evidence for an interaction between a declarative memory system, dependent on the medial tempo

226 s, but it shares critical resources with the declarative memory system.

227 rise without important contribution from the declarative memory system.

228 es an important challenge on the hippocampal declarative memory system.

229 al evidence suggests prolonged maturation of declarative memory systems in the human brain from child

230 rate a novel context in which mesolimbic and declarative memory systems interact.

231 detrimental effect on a sensitive nonverbal declarative memory task in cocaine-dependent subjects fo

232 functional magnetic resonance imaging and a declarative memory task in healthy individuals.

233 l functioning during performance of a verbal declarative memory task in subjects with midlife major d

234 All participants completed a declarative memory task involving incidental encoding of

235 left dorsolateral prefrontal cortex during a declarative memory task involving learning a set of word

236 ales; age mean (SD) = 22.12 (2.16)] during a declarative memory task.

237 onal magnetic resonance imagery responses of declarative memory tasks in the medial temporal lobe (MT

238 sia, however, have shown that performance on declarative memory tasks may not always be dependent on

239 the performance of hippocampal-based verbal declarative memory tasks was measured by using positron

240 a causal link between these two features of declarative memory: Temporal binding is a necessary cond

241 re separated in time and may make demands on declarative memory that are beyond the capacity of amnes

242 n function that may use such interactions is declarative memory--that is, memory that can be consciou

243 memory consolidates in a manner analogous to declarative memory--that is, with the formation of a mem

244 ocessing (the paced serial addition task) or declarative memory (the delayed paragraph recall task),

245 osing a coherent large-scale architecture of declarative memory, the integrative memory model would b

246 Declarative memory-the ability to learn, store, and retr

247 a brain region traditionally associated with declarative memory-the hippocampus.

248 l-process theory predicts no effect, whereas declarative memory theory predicts impairment of all typ

249 The latter finding is incompatible with declarative memory theory, whereas the former constrains

250 maturation of the neural systems supporting declarative memory to assess the necessity of early memo

251 ng of the role of hippocampal ripples beyond declarative memory to include enhancing motor procedural

252 ble with a component process model, in which declarative memory types rely on different weightings of

253 Procedural memory, like declarative memory, undergoes a slow, time-dependent per

254 Moreover, visual declarative memory was improved by so-tDCS compared with

255 These findings not only demonstrate enhanced declarative memory when individuals have perceived contr

256 ppocampus plays a broad role in episodic and declarative memory, whereas others argue for a specific

257 nts derives from their general impairment in declarative memory, which affects performance on most 2-

258 The findings support the distinction between declarative memory, which depends on the hippocampus and

259 ve map of space and is critical for encoding declarative memory (who, what, when and where).

260 mation critical for establishing spatial and declarative memories will benefit greatly from determini

261 case for a new brain-based understanding of declarative memory with a focus on hippocampal physiolog

262 executive" functions, and some components of declarative memory with aging, most studies have failed

263 dose produced reversible decreases in verbal declarative memory without effects on nonverbal memory,

264 pt learning (dot pattern classification) and declarative memory (word pair associates) across a 4-hr