ライフサイエンスコーパス: declarative

1 (PTSD) of sensory intrusive hypermnesia and declarative amnesia for the same traumatic event.

2 results are consistent with the notion that declarative and habit learning compete to mediate task p

3 When learned in quick succession, declarative and motor skill tasks interfere with one ano

4 Because of the competitive nature of declarative and nondeclarative memory during consolidati

5 al predictor of performance on memory tasks (declarative and nondeclarative) than previously thought.

6 d may mediate conversion of memories between declarative and procedural forms.

7 eral CPU, or control lesions were trained on declarative and procedural knowledge variants of a novel

8 uning of corticostriatal systems involved in declarative and procedural learning, a capacity potentia

9 eep's capacity to boost the consolidation of declarative and procedural memories, nor sleep's quality

10 e organization predicts interference between declarative and procedural memories.

11 ning or injury; second, the knowledge of how declarative and procedural memory operates and how this

12 the disengagement of an interaction between declarative and procedural memory systems.

13 which are regions assumed to play a role in declarative and procedural memory, provides an anatomica

14 established broadly in humans, appearing in declarative and procedural tasks.

15 rom multiple cognitive domains, particularly declarative and working memory and executive function.

16 better performance than placebo on tests of declarative and working memory.

17 odulate the engagement of hippocampus-based "declarative" and striatum-based "procedural" memory syst

18 ippocampus, a structure involved in spatial, declarative, and contextual memory, after seizures or is

19 with panic disorder suffer from a deficit in declarative associative learning.

20 categorization, which in humans is linked to declarative cognition and consciousness.

21 We disrupted this latter, declarative component by having participants learn a wor

22 during consolidation, impairment of the fast/declarative component leads to improvements in the slow/

23 Furthermore, we find that the fast/declarative component plays a major role in the consolid

24 targeting the pathologic emotional, but not declarative, component of a memory would be ideal for cl

25 ay abolish the pathologic emotional, but not declarative, component of memories allowing alleviation

26 information, which is ordinarily learned as declarative (conscious) knowledge and with the participa

27 ment, the reciprocal relationship was found: declarative consolidation was blocked by procedural lear

28 A novel GraphQL-based API provides flexible, declarative data retrieval along with a simple-to-use RE

29 Transport reactions are declarative descriptions of transporter activities, and

30 Neural circuits associated with motivated declarative encoding and active threat avoidance have bo

31 ber of disorders, accompanied by deficits in declarative episodic, spatial, and contextual memory per

32 res of processing speed, working memory, and declarative (facial) memory as candidate endophenotypes

33 f items recalled from auditory word lists or declarative facts.

34 ntly, the relationship between awareness and declarative (hippocampus-dependent) memory has been ques

35 human data supporting a benefit of sleep for declarative (hippocampus-mediated) memory in humans (for

36 amidal cells are less critically involved in declarative human memory acquisition compared to dentate

37 The acquisition of declarative (i.e., facts) and procedural (i.e., skills)

38 their WT littermates in situations in which declarative (i.e., place-based) and procedural (i.e., re

39 for developers as well as a straightforward declarative interface that lets users easily share and e

40 a translational schema for NLP that contains declarative knowledge about genes and their associated b

41 We found that stress reduced declarative knowledge about the learning task and change

42 ity was correlated with task performance and declarative knowledge after learning under single-task c

43 Being formal, declarative knowledge representation models, ontologies

44 earning, programming accuracy, and post-test declarative knowledge were used as outcome measures in 3

45 e importance of considering the influence of declarative knowledge when interpreting age-associated c

46 he latter, including functions as diverse as declarative knowledge, episodic memory, word learning, a

47 endency to acquire information as conscious (declarative) knowledge.

48 on a residual ability to acquire conscious (declarative) knowledge.

49 fications at a high level via a standardized declarative language, for example connectivity rules, to

50 ot reduce accuracy but reduced the amount of declarative learning about the task.

51 association of top-down signals relevant for declarative learning and spatially precise ascending tac

52 t cells in the hippocampus appear to support declarative learning by distinguishing novel and familia

53 findings further suggest a brain system for declarative learning motivated by punishment that is dis

54 e motor skill improvement, can be blocked by declarative learning over wake, but not over a night of

55 cits in dyslexia are attributed to an intact declarative learning system combined with an impaired pr

56 Declarative learning was assessed by performance on 3 ta

57 Based on the results of studies in declarative learning, it is likely that phase synchroniz

58 the striatum as being of importance for non-declarative learning.

59 ning is an experimentally tractable model of declarative learning.

60 nd is considered a simple model paradigm for declarative learning.

61 The formation of enduring declarative-like memories engages a dialog between the h

62 in S-R learning from those of a cognitive or declarative medial temporal lobe memory system that incl

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

64 Declarative memories are thought to be stored within ana

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

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

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

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

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

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

71 Consolidation of declarative memories requires hippocampal-neocortical co

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

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

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

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

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

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

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

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

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

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

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

83 ical processes within sleep actively enhance declarative memories.

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

85 cessary for the acquisition and retrieval of declarative memories.

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

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

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

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

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

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

92 Declarative memory (story recall) and selective attentio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 Declarative memory consolidation is hypothesized to requ

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

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

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

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

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

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

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

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

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

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

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

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

128 Declarative memory for rapidly learned, novel associatio

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

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

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

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

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

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

135 tion preceding stimulus encoding can predict declarative memory formation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Declarative memory is enabled by circuits in the entorhi

155 Declarative memory is known to depend on the medial temp

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

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

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

159 Declarative memory is thought to rely on two processes:

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

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

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

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

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

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

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

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

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

169 matter volume were significant predictors of declarative memory performance.

170 Declarative memory permits an organism to recognize stim

171 Declarative memory recall is thought to involve the rein

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

173 Declarative memory relies on a medial temporal lobe syst

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

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

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

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

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

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

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

181 The declarative memory system allows us to accurately recogn

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

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

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

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

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

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

188 rise without important contribution from the declarative memory system.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 lementary MTL encoding computations subserve declarative memory.

247 endent procedural over hippocampus-dependent declarative memory.

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

249 renicline group scored higher on working and declarative memory.

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

251 sociated with improvements in procedural and declarative memory.

252 in associative learning tasks that depend on declarative memory.

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

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

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

256 s learned is a fundamental characteristic of declarative memory.

257 cally enables the relational organization of declarative memory.

258 mental cognitive processes in the service of declarative memory.

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

260 elated with performance on clinical tests of declarative memory.

261 thought to promote systems consolidation of declarative memory.

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

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

264 be acquired implicitly and independently of declarative memory.

265 thesizing dose-dependent decreases in verbal declarative memory.

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

267 s linked to demyelination and impairments in declarative memory.

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

269 s in orthogonalization of representations in declarative memory.

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

271 resulted in robust, reliable enhancements in declarative memory.

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

273 The declarative nature of ASP-G comes at the expense of bein

274 ppocampal region of the brain is crucial for declarative or episodic memory for a broad range of mate

275 g depending upon whether the task emphasized declarative or nondeclarative memory, even when the to-b

276 ort of incidental/observational learning in "declarative" or "episodic" memory versus the striatal su

277 fewer instances of word use, vocalizations, declarative pointing, social gaze, and orienting to name

278 The Declarative/Procedural Model of Pinker, Ullman and colle

279 production, in contrast to the claims of the Declarative/Procedural Model.

280 ional data processing-to-visualizations with declarative querying capabilities is needed.

281 o be expressed and might therefore reflect a declarative rather than procedural form of memory.

282 f reconsolidation-updating theory by using a declarative recall task and sequences similar to phone n

283 The decrease in declarative recall was correlated to participants' proce

284 icated the hippocampal formation in spatial, declarative/relational and episodic types of memory.

285 e subject (S), verb (V), and object (O) in a declarative sentence of the type "the man (S) killed (V)

286 essing egocentric-procedural and allocentric-declarative sequential information, respectively.

287 ed learning strategy from a single-cue-based declarative strategy to a multicue-based procedural stra

288 decay) that are usually associated with the declarative system.

289 t to be distinct from those that support the declarative system.

290 performance, whereas attempts to engage the "declarative" system disrupt performance.

291 sk and allocentric spatial cues to solve the declarative task.

292 pal formation participates in acquisition of declarative tasks but is not the site of their long-term

293 Posttraining direct (declarative) tests of sequence knowledge revealed that c

294 form of FOXP2 promotes faster switching from declarative to procedural learning strategies when the t

295 r of a transition during skill learning from declarative to procedural learning.

296 es the view of taste memory as a type of non-declarative unconscious memory.

297 xia syndrome-affected participants with poor declarative verbal memory would have pronounced abnormal

298 onsolidation was correlated to participants' declarative word recall.

299 ts underwent polysomnography and performed a declarative word-pair learning task.

300 Before and after sleep declarative word-pair memories were tested.