ライフサイエンスコーパス: declarative memory

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

2 in associative learning tasks that depend on declarative memory.

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

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

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

6 s learned is a fundamental characteristic of declarative memory.

7 cally enables the relational organization of declarative memory.

8 mental cognitive processes in the service of declarative memory.

9 s linked to demyelination and impairments in declarative memory.

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

11 elated with performance on clinical tests of declarative memory.

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

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

14 be acquired implicitly and independently of declarative memory.

15 thesizing dose-dependent decreases in verbal declarative memory.

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

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

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

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

20 s in orthogonalization of representations in declarative memory.

21 thought to promote systems consolidation of declarative memory.

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

23 resulted in robust, reliable enhancements in declarative memory.

24 lementary MTL encoding computations subserve declarative memory.

25 endent procedural over hippocampus-dependent declarative memory.

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

27 renicline group scored higher on working and declarative memory.

28 sociated with improvements in procedural and declarative memory.

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

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

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

32 ical processes within sleep actively enhance declarative memories.

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

34 cessary for the acquisition and retrieval of declarative memories.

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

36 1.48; 95% CI, 1.08-2.04; P = .02), impaired declarative memory abilities (beta = -0.87; HR, 0.42; 95

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 Declarative memories are thought to be stored within ana

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

77 Declarative memory consolidation is hypothesized to requ

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

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

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

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

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

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

84 Declarative memory enables conscious recollection of the

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

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

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

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

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

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

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

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

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

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

95 Declarative memory for rapidly learned, novel associatio

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

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

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

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

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

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

102 tion preceding stimulus encoding can predict declarative memory formation.

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

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

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

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

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

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

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

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

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

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

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

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

115 These findings show that declarative memory has different operating characteristi

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

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

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

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

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

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

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

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

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

125 The hippocampus is critical to declarative memory in humans.

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

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

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

129 Human declarative memory involves a systematic organization of

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

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

132 Declarative memory is enabled by circuits in the entorhi

133 Declarative memory is known to depend on the medial temp

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

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

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

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

138 Declarative memory is thought to rely on two processes:

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 matter volume were significant predictors of declarative memory performance.

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

161 Declarative memory permits an organism to recognize stim

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

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

164 Declarative memory recall is thought to involve the rein

165 Declarative memory relies on a medial temporal lobe syst

166 Consolidation of declarative memories requires hippocampal-neocortical co

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

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

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

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

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

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

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

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

175 Declarative memory (story recall) and selective attentio

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

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

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

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

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

181 rise without important contribution from the declarative memory system.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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