ライフサイエンスコーパス: long-term memory

1 mory such as working, episodic, spatial, and long term memory.

2 milar context until the link crystallizes in long term memory.

3 estored spine density prevents the rescue of long-term memory.

4 engram cells restores both spine density and long-term memory.

5 resulting in chronic deficits in working and long-term memory.

6 g and short-term memory while also impairing long-term memory.

7 between physical activity during the day and long-term memory.

8 f, generally ineffective training to produce long-term memory.

9 neprilysins are involved in middle-term and long-term memory.

10 tic regulation of gene expression underlying long-term memory.

11 esponsive genes, including those involved in long-term memory.

12 and unstable memory transforms into a stable long-term memory.

13 yonic axis specification to the formation of long-term memory.

14 rophysiological signal hypothesized to index long-term memory.

15 T cell response, promoting the formation of long-term memory.

16 ) it is involved in spontaneous retrieval of long-term memory.

17 he first probe trial, and exhibited impaired long-term memory.

18 e same time enabling self-renewal needed for long-term memory.

19 established LTP and disrupt several forms of long-term memory.

20 ct the B-cell compartment and maintenance of long-term memory.

21 schema congruence has a strong influence on long-term memory.

22 an immediate-early gene that is required for long-term memory.

23 ong-lasting forms of synaptic plasticity and long-term memory.

24 n synthesis necessary for the maintenance of long-term memory.

25 NA plays a critical role in consolidation of long-term memory.

26 d versus massed training in the formation of long-term memory.

27 2 significantly boosted contextual and trace long-term memory.

28 ich are the cellular analogs of two forms of long-term memory.

29 stabilized for consolidation of associative long-term memory.

30 oach to help elucidate the synaptic basis of long-term memory.

31 for both persistent synaptic plasticity and long-term memory.

32 function and improve synaptic plasticity and long-term memory.

33 KII and GluA1 levels and impairs associative long-term memory.

34 oted asynchronous GABA release, and impaired long-term memory.

35 ventral tegmental area predicted associative long-term memory.

36 c plasticity, a cellular mechanism mediating long-term memory.

37 erent kinds of information in the service of long-term memory.

38 ects of CaMKIINtide on both GluA1 levels and long-term memory.

39 specifically improve olfactory learning and long-term memory.

40 to be necessary for both LTP maintenance and long-term memory.

41 impaired the ability of CD8+ T cells to form long-term memory.

42 necessary for the conversion from short- to long-term memory.

43 functional consequence of which is impaired long-term memory.

44 protein synthesis at activated synapses, and long-term memory.

45 nding and intron removal selectively impairs long-term memory.

46 plasticity contributes to the maintenance of long-term memory.

47 ck into working memory during retrieval from long-term memory.

48 consolidating the learned association into a long-term memory.

49 that forms functional amyloids necessary for long-term memory.

50 ole in binding temporally adjacent events in long-term memory.

51 res synapse number, synaptic plasticity, and long-term memory.

52 differed markedly on subsequent measures of long-term memory.

53 wn to be a key component in the formation of long-term memory.

54 JJJ2 enhances the animal's capacity to form long-term memory.

55 vation mediated IEG expression implicated in long-term memory.

56 er, this is at the expense of forming stable long-term memory.

57 N-terminal targeting domain, does not affect long-term memory.

58 genously boost memory consolidation and thus long-term memory.

59 own to be important for Orb2 aggregation and long-term memory.

60 to be crucial for converting experience into long-term memory.

61 KC isoform proposed to maintain late-LTP and long-term memory.

62 involved in the formation and maintenance of long-term memory.

63 crucial for expression and likely storage of long-term memory.

64 imental to the maintenance of information in long-term memory.

65 identified as relating to the maintenance of long-term memory.

66 or, consistent with impaired ability to form long-term memories.

67 ng the synaptic changes required for storing long-term memories.

68 ibutes both to the encoding and retrieval of long-term memories.

69 architecture that supports it and shapes our long-term memories.

70 dependent changes in neural circuits mediate long-term memories.

71 vity via inhibitors is sufficient to enhance long-term memories.

72 ith a decrease in the influence of others on long-term memories.

73 communication aid transformation into stable long-term memories.

74 hallenge the idea that stable synapses store long-term memories.

75 ns during the retrieval of short-term versus long-term memories.

76 uates the formation of hippocampus-dependent long-term memories.

77 % of the responding clones were recruited to long-term memory 3 months postvaccination, (iii) the mos

78 r LTP generation, which may be implicated in long-term memory acquisition and in its deterioration in

79 gle-strand DNA damage, was also required for long-term memory acquisition in a variety of learning pa

80 An enzyme called PKM zeta may have a role in long-term memory after all.

81 areas and mark those synapses for forming a long-term memory after the prion form is established.

82 s) are important for neuronal functions like long-term memory and are well-characterized in mammals b

83 rocess during the formation and retrieval of long-term memory and define general memory-implicated ge

84 priately timed physical exercise can improve long-term memory and highlight the potential of exercise

85 tical role of astrocyte-derived L-lactate in long-term memory and long-term potentiation in vivo.

86 igosaccharide analogs of ST-5 CPS RU induced long-term memory and protective immune responses in rabb

87 mation is buffered when being retrieved from long-term memory and reconcile current theories of memor

88 odic memories are gradually assimilated into long-term memory and this process is strongly influenced

89 lesions may selectively affect orthographic long-term memory and working memory processes, relativel

90 ritical illness in early life are at risk of long-term-memory and attention impairments.

91 this strategy versus exploring new ones from long-term memory, and (ii) another from polar to lateral

92 Understanding the mechanisms by which long-term memories are formed and stored in the brain re

93 Long-term memories are likely stored in the synaptic wei

94 Long-term memories are linked to cortical representation

95 sodic memories, it is not known whether such long-term memories are necessary for particular features

96 Therefore, long-term memories are rapidly replayed during recollect

97 Binding information in short-term and long-term memory are functions sensitive to Alzheimer's

98 and consolidation were prevented by blocking long-term memory arising from the new experiences.

99 bout the word's letters and their order from long-term memory as well as the maintenance and processi

100 increase the precision of hippocampal-based long-term memory associations by assessing the salience

101 f antagonists, and coexistence of short- and long-term memory at loci with weak and strong constituti

102 Some forms of long-term memories become labile and can be reversed wit

103 ependent of alpha'/beta' and gamma MBNs, and long-term memory becomes completely dependent on alpha/b

104 part of cingulum bundle which accounted for long-term memory binding deficits.

105 The long-term memory binding task was a Paired Associates Le

106 ptic remodeling associated with formation of long-term memories, but the mechanisms that regulate thi

107 binding protein Orb2 has been implicated in long-term memory, but how conformational conversion of O

108 to associate different stimuli is vital for long-term memory, but how neural ensembles encode associ

109 Induced CREB activity is a hallmark of long-term memory, but the full repertoire of CREB transc

110 The neocortex in our brain stores long-term memories by changing the strength of connectio

111 e further studied their capacity to maintain long-term memory by measuring cellular and serologic res

112 On retrieval, consolidated long-term memory can be neutralized by extinction if the

113 Retrieving information from long-term memory can result in the episodic forgetting o

114 ll generation or in postmitotic cells, while long-term memory can survive multiple rounds of cell div

115 rapidly forgets, or is not yet able to form long-term memories, can exert such a long-lasting and im

116 mpal synaptic plasticity, and impairments in long-term memory caused by sleep deprivation.

117 ntiation of memory precursor WP T cells into long-term memory cells.

118 m for the discovery of orthologous mammalian long-term memory components.

119 Canonical models suggest that mechanisms of long-term memory consist of a synapse-specific, protein

120 before fear learning significantly impaired long term memory consolidation, whereas short-term memor

121 These increases are essential for long-term memory consolidation, as their blockade via an

122 ese mice had severe deficits in learning and long-term memory consolidation.

123 impaired hippocampal synaptic plasticity and long-term memory consolidation.

124 s and short-term memory, but exhibited broad long-term memory deficits as revealed by several behavio

125 working memory processes, with orthographic long-term memory deficits centred in either the left pos

126 Finally, synaptic tagging and long-term memory deficits in mice lacking translin/trax

127 erexpression in aged animals ameliorated the long-term memory deficits observed in control animals.

128 place cell representations could explain the long-term memory deficits observed in previous behaviora

129 ce showed reduced prepulse inhibition (PPI), long-term memory deficits, and spontaneous locomotor hyp

130 Consolidation of long-term memories depends on de novo protein synthesis.

131 Persistent long-term memory depends on successful stabilization and

132 o internal representations, whether semantic long-term memory (e.g., letters, digits, words), sensory

133 Here we report that long-term memory encoding can elicit early transcription

134 Prevailing theory suggests that long-term memory encoding involves early plasticity with

135 ss the real-time contribution of the mPFC to long-term memory encoding, we performed temporally preci

136 ein (SCOP), a negative ERK regulator, blocks long-term memory encoding.

137 gy switch in the mushroom body that controls long-term memory encoding.

138 re of well-organized relevant information in long-term memory, enhanced attitude extremity and access

139 g-term memory formation and are required for long-term memory enhancement by a class of broad-acting

140 The ability to form long-term memories for novel events depends on informati

141 n the unfolding therapeutic process generate long-term memories for reconsolidated emotional material

142 In addition, we found selectively enhanced long-term memory for contextual but not cued fear memory

143 PHC), and hippocampus differentially support long-term memory for item information, spatial context,

144 that appear critical for morphine reward and long-term memory for natural reward behavior.

145 memory T cells from the bone marrow provide long-term memory for systemic pathogens.

146 rful experience promote the consolidation of long-term memory for that experience.

147 and ends by categorizing the sound based on long-term memory for word meaning.

148 Nr4a nuclear receptors contribute to long-term memory formation and are required for long-ter

149 es histone deacetylase 4, and is involved in long-term memory formation and behavior.

150 tate from astrocytes, which is necessary for long-term memory formation and for underlying molecular

151 lular and molecular mechanisms that regulate long-term memory formation and storage may provide alter

152 n Arc (also known as Arg3.1) is required for long-term memory formation and synaptic plasticity.

153 HT-0712 enhanced long-term memory formation in normal young mice at brain

154 ously uncharacterized in the brain, supports long-term memory formation in the amygdala and suggests

155 le their sucrose intake at an early stage of long-term memory formation initiated the investigation o

156 Our results suggest a model of long-term memory formation that includes a systems-level

157 as an essential and well established role in long-term memory formation throughout a diverse set of o

158 encoding-induced hippocampal activation and long-term memory formation, and have important implicati

159 ement-binding protein, a crucial mediator in long-term memory formation, correlated anatomically and

160 To evaluate what determines the efficacy of long-term memory formation, we developed an extensive se

161 wn-regulation may be implicated in decreased long-term memory formation.

162 the interaction between prior knowledge and long-term memory formation.

163 stration immediately after training enhanced long-term memory formation.

164 egulated transcription that is necessary for long-term memory formation.

165 state to control Orb2A protein abundance and long-term memory formation.

166 slation initiation is a central regulator of long-term memory formation.

167 ux is both necessary and sufficient to drive long-term memory formation.

168 ich directly promotes network plasticity and long-term memory formation.

169 amyloid that plays a key role in Drosophila long-term memory formation.

170 The dissociation of hippocampal long-term memory function between hemispheres suggests t

171 ociation system segregation is predictive of long-term memory function, independent of an individual'

172 rovide constraints for mechanistic models of long-term memory function.

173 lus-guided attention and a symmetric one for long-term memory-guided attention.

174 Although persistence is a key feature of long-term memory, how this occurs, despite the rapid tur

175 amine-depleted rats, hence amnesic, restored long-term memory; however, the time frame of memory resc

176 arliest initiator of synaptic plasticity and long-term memory impairment.

177 lude that caffeine enhanced consolidation of long-term memories in humans.

178 In particular, long-term memories in such paradigms have been extensive

179 ucture suggested to store, at least in part, long-term memories in the mammalian brain.

180 show a severe impairment of both short- and long-term memory in a number of behavioral tasks.

181 d these defects are associated with impaired long-term memory in both the exposed fathers and their o

182 n anti-amyloidogenic peptide interferes with long-term memory in Drosophila.

183 whether caffeine has an enhancing effect on long-term memory in humans.

184 Decreasing the levels of caspase-2 restored long-term memory in mice that had existing deficits.

185 n of astrocytic Gs-coupled signaling reduced long-term memory in mice without affecting learning.

186 ts of eIF2alpha phosphorylation and enhances long-term memory in rodents.

187 is a critical genetic factor in constraining long-term memory in the adult brain.

188 Long-term memory in the brain is thought to arise from a

189 trials, spaced by one hour, produced robust long-term memory in the KOs.

190 stimulation enhanced the short-, but not the long-term memory in the novel-object recognition task.

191 erved, indicating a poor ability to maintain long-term memory in these patients.

192 the formation of amyloid-like aggregates and long-term memory in vivo.

193 econd, PKMzeta is essential for late-LTP and long-term memory in wild-type mice, and PKMzeta-null mic

194 e in hippocampus blocks late-LTP and spatial long-term memory in wild-type mice, but not in PKMzeta-n

195 genetic removal of these receptors enhanced long-term memory in young and aging mice and increased t

196 Sleep is important for the formation of long-term memory, in humans as well as in other animals,

197 of several types of working, short-term and long-term memories, including fear conditioning, object

198 s2(-/-) mice displayed impaired formation of long-term memory, increased risk taking and stimulus see

199 The observed merging of long-term memories is thus similar to the memory conjunc

200 transform weak episodic memories into stable long-term memories is unknown.

201 been assumed that information retrieved from long-term memory is represented in working memory, we la

202 Long-term memory is thought to be mediated by synaptic p

203 The capacity of long-term memory is thought to be virtually unlimited.

204 Significance statement: Long-term memory is thought to rely on the strengthening

205 vivo, and identify the microRNA miR-21 as a long-term memory keeper of the fibrogenic program in MSC

206 l subsets that have been suggested to play a long-term memory-like response to HCMV infection.

207 studies suggested that NK cells may display long-term, memory-like responses to murine cytomegalovir

208 changes using aversive olfactory associative long-term memory (LTAM) and identified three major gene

209 ds have existing representations in subjects long-term memories (LTM) and that face stimuli used in p

210 Both the formation of long-term memory (LTM) and dendritic spine growth that s

211 lly involved in middle-term memory (MTM) and long-term memory (LTM) and that their expression is requ

212 uced performance in Morris Water Maze (MWM), long-term memory (LTM) contextual fear testing, and rota

213 le that activates mTORC2 (A-443654) reverses long-term memory (LTM) deficits in both aged mice and fl

214 the fact that PDE11A is required for social long-term memory (LTM) formation during adolescence and

215 (p38 MAPK), two MAPK isoforms important for long-term memory (LTM) formation.

216 1 expression does not affect contextual fear long-term memory (LTM) formation.

217 Previously, we reported that long-term memory (LTM) in Aplysia can be reinstated by t

218 brain are required for middle-term (MTM) and long-term memory (LTM) in the dorsal paired medial (DPM)

219 l synaptic plasticity.SIGNIFICANCE STATEMENT Long-term memory (LTM) induced by repeated trials spaced

220 Long-term memory (LTM) is believed to be stored in the b

221 ; short-term memory (STM) is intact, whereas long-term memory (LTM) is significantly impaired.

222 f spaced training trials in the formation of long-term memory (LTM) is widely appreciated, surprising

223 Creating long-term memory (LTM) requires new protein synthesis to

224 l cortex in the temporoparietal junction and long-term memory (LTM) retrieval processes are localized

225 Short-term memory (STM) or long-term memory (LTM) was evaluated in rutabaga (rut) a

226 transform a subthreshold learning event into long-term memory (LTM), and hSyn-HM4D completely impaire

227 nduce a more persistent memory identified as long-term memory (LTM).

228 ntenance of long-term potentiation (LTP) and long-term memory (LTM).

229 ryonic development, synaptic plasticity, and long-term memory (LTM).

230 ngs provide initial evidence to suggest that long-term memory may be enhanced by more carefully atten

231 in the storage of target representations in long-term memory may underlie rapid changes in the effic

232 evidence has indicated that, in addition to long-term memory, MTL subregions may similarly contribut

233 Long-term memories of fear have been notoriously difficu

234 ster prefers D- over L- arabinose, but forms long-term memories of L-arabinose more reliably.

235 ced memory reactivation during sleep renders long-term memories of negative experiences more negative

236 both synaptic plasticity and the encoding of long-term memory of a novel, complex environment.

237 mission of food preference (STFP), mice form long-term memory of food odors presented by a social par

238 unclear whether this inheritance can direct long-term memory of individual gene expression states (c

239 on processes from daily movement training to long-term memory of movement pattern.

240 rrent light directionality, rather than by a long-term memory of previous conditions.

241 within hours after Ag exposure, resulting in long-term memory or abortive effector responses, correla

242 be explained easily by hippocampal-dependent long-term memory or spatial cognition.

243 animals are awakened may produce maladaptive long-term memory, or may interrupt consolidation.

244 dren undergoing epilepsy surgery may enhance long-term memory outcome.

245 We report evidence that rats' long-term memory performance is enhanced if they had pre

246 e encoding protein KIBRA, is associated with long-term memory performance, we hypothesized that commo

247 Encoding and retrieval processes enhance long-term memory performance.

248 arily provides rich associated material from long-term memory, permitting rapid chunking.

249 s PKMzeta is essential for wild-type LTP and long-term memory, persistent PKCiota/lambda activation c

250 We show that the observed long-term memory phenomenon in rhythmic synchronization

251 mory CD8 T cells, including acquisition of a long-term memory phenotype (i.e., CD27(hi), CD62L(hi), K

252 lly involved in gene regulation required for long-term memory processes.

253 medial temporal lobe, which is critical for long-term memory processing.

254 Neurobiological models of long-term memory propose a mechanism by which initially

255 reflex, we compared acquisition learning and long-term memory recall of uninfected (control) honey be

256 eep transforms episodic representations into long-term memories, redistributes them toward extrahippo

257 lity and concentration-features relevant for long-term memory-remains unknown.

258 ntenance results from the interactions among long-term memory representations and basic processes, in

259 ive control task if control processes engage long-term memory representations that are supported by t

260 into nested events, which form the basis of long-term memory representations.

261 lies, formation and expression of artificial long-term memory require flies to be hungry.

262 After effective training, long term memory required subsequent transcription and t

263 In contrast, nutrient-dependent long-term memory requires different dopaminergic neurons

264 It is not clear whether the altered long-term memory resides within the T-cell or the B-cell

265 red to induce antibody isotype switching and long-term memory responses.

266 mmunotherapy because of the establishment of long-term memory responses.

267 We propose a model whereby persistence of long-term memory results from the assembly of CPEB3 into

268 g newly formed spines that are important for long-term memory retention.

269 ereas long-term inhibition of GluT4 impaired long-term memory, short-term memory was enhanced.

270 e basic brain processes: visual recognition, long-term memory, short-term memory, action selection, a

271 hought to be a critical mechanism supporting long-term memory stabilization.

272 use its inhibition disrupts LTP in vitro and long-term memory storage in vivo.

273 trong neurobiological evidence suggests that long-term memory storage involves formation of new synap

274 rieved and must undergo reconsolidation into long-term memory storage to be maintained.

275 factor important for synaptic plasticity and long-term memory storage.

276 and promotes a value-based stratification of long-term memory stores.

277 P degradation also prevents the formation of long-term memory, suggesting rapid SCOP breakdown is nec

278 e to NMDA receptor activation is crucial for long term memory, synaptic tagging, and epigenetic signa

279 ed to reflect the use of a separate episodic long-term memory system, rather than working memory.

280 t solely due to the use of separate episodic long-term memory systems.

281 paired performance on an associative spatial long-term memory task, whereas right CA3 silencing had n

282 pite the fact that these mice are amnesic in long-term memory tests when natural recall cues are used

283 id single-colored stimuli and were tested in long-term-memory tests 1 or 3 days later, they only init

284 d stimulus was found in both short-term- and long-term-memory tests.

285 ditioning trial, N. vitripennis consolidates long-term memory that lasts at least 6 days.

286 ynaptic substrate for a socially conditioned long-term memory that operates at the level of the initi

287 tems in prokaryotes and animals give rise to long-term memory through modification of specific genomi

288 promote the storage of new information into long-term memory through the activation of the SN/VTA-Hi

289 apid working memory during ongoing tasks and long-term memory to guide future action, respectively).

290 imulus associations and their retrieval from long-term memory to optimize attention in search.

291 -organized hierarchical peak structure has a long-term memory transmitted across several waves.

292 primates is especially complex and requires long-term memory, value comparison, strategic planning,

293 Moreover, long-term memory was formed immediately after training r

294 found that the retrieval of information from long-term memory was limited to just a few simple object

295 h-frequency stimulation, both the short- and long-term memories were robustly improved in the novel-o

296 However, a striking asymmetry emerged in long-term memory, wherein only left CA3 silencing impair

297 In addition, when the data exhibit long-term memory (which is the case in most climate reco

298 ewed and mentally replayed short videos from long-term memory while undergoing fMRI.

299 the capability to integrate information from long-term memory with information from novel spike input

300 sticity and attenuates hippocampus-dependent long-term memories without affecting anxiety.