ライフサイエンスコーパス: long-term memory

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

2 0 in the MB of adult flies causes defects in long-term memory.

3 , synaptic markers and volume, and protected long-term memory.

4 into late LTP and of short-term memory into long-term memory.

5 memory and in spatial reference learning and long-term memory.

6 some, but not all, learning experiences into long-term memory.

7 ter, which we suspected of being involved in long-term memory.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 s is thought to be essential for maintaining long-term memory.

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

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

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

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

44 eported to be involved in the maintenance of long-term memory.

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

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

47 rophysiological signal hypothesized to index long-term memory.

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

49 nship between perception, working memory and long-term memory.

50 eurons in the lateral amygdala (LA) impaired long-term memory.

51 in synthesis rates, impedes the formation of long-term memory.

52 ierarchical organization of information into long-term memory.

53 ssociated with dopamine, game enjoyment, and long-term memory.

54 ent, thus predictable from schemas stored in long-term memory.

55 is a key player in the epigenetic control of long-term memory.

56 2 and overlapping roles for AKT1 and AKT3 in long-term memory.

57 mplex dynamical networks (CDNs) that exhibit long-term memory.

58 ecular processes for synaptic plasticity and long-term memory.

59 , bolstered synaptic plasticity and enhanced long-term memory.

60 vent to promote its successful encoding into long-term memory.

61 REB target genes involved in the encoding of long-term memory.

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

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

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

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

66 experience is necessary for the formation of long-term memories.

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

68 lateral amygdala during the consolidation of long-term memories.

69 expression are required for the formation of long-term memories.

70 HPC is not obligatory for these features of long-term memories.

71 t with trends towards reduced short-term and long-term memories.

72 ritical for the formation and maintenance of long-term memories.

73 How do neurons encode long-term memories?

74 ecular switch that promotes the formation of long-term memory(1-4).

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

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

77 involvement in the encoding of experience to long-term memory across time and biological levels of or

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

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

80 on of adaptive immune responses endowed with long-term memory against mycobacterial antigens.

81 critical for understanding the evolution of long-term memories and for enabling the development of n

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

83 election for complex dynamical networks with long-term memory and by leveraging the structure of the

84 ural and functional plasticity, formation of long-term memory and cognitive function.

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

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

87 e abstract representations consolidated into long-term memory and how are they integrated with pre-ex

88 rucial for translational control involved in long-term memory and in late long-term potentiation (LTP

89 fore, in this paper, we study the effects of long-term memory and of the topological properties on th

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

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

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

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

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

95 s a major role in encoding and consolidating long-term memories, and undergoes plastic changes during

96 es in working memory and target templates in long-term memory, and consider how searches are terminat

97 roles for dTau in regulation of translation, long-term memory, and footshock habituation are also rev

98 sed seizures, rescued ASD-like behaviors and long-term memory, and normalized metabolic changes in th

99 reduced brain inflammation, restored LTP and long-term memory, and reversed social and communication

100 Long-term memories are believed to be stored in the syna

101 PNNs may be an important substrate by which long-term memories are stored in the central nervous sys

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

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

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

105 ontaining neurons are necessary to establish long-term memories associating predictive stimuli with r

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

107 Stroked animals developed impairment in long-term memory at 4-weeks post-stroke despite recovery

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

109 Here, assuming that CRISPR functions as a long-term memory-based defense against a diverse landsca

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

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

112 quantify changes in the brain mechanisms of long-term memory (BM-LTM).

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

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

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

116 Prior knowledge in long-term memory can aid in efficient encoding of inform

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

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

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

120 ither their short-term effector functions or long-term memory capacity.

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

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

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

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

125 evidence in rodents and humans suggests that long-term memory consolidation can be enhanced by the ex

126 REM) sleep is supposed to play a key role in long-term memory consolidation transferring information

127 ) did not affect working memory but impaired long-term memory consolidation.

128 help guide the prioritization of events for long-term memory consolidation.

129 uring sleep and seizures specifically impair long-term memory consolidation.

130 hippocampal spikes during sleep would impair long-term memory consolidation.

131 that the hippocampus, known for its role in long-term memory, contributes to these flexible aspects

132 loss results in late-onset spatial reference long-term memory deficit.

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

134 sion and rescued the synaptic plasticity and long-term memory deficits in DS mice.

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

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

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

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

139 Persistent long-term memory depends on successful stabilization and

140 TEMENT Awake experience is consolidated into long-term memories during sleep.

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

142 In this work, we leverage the short/long term memory effects due to the electron trapping ev

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

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

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

146 pamine modulation and reward on two forms of long-term memory: episodic memory for neutral objects an

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

148 mid and phage targets and a second providing long-term memory for access to chromosomal sites upon en

149 lus, juv ELE and juv-adol ELE formed lasting long-term memory for an object location memory task, whe

150 used a novel auditory paradigm to assess how long-term memory for auditory scenes facilitates detecti

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

152 has long been known that schemas can enhance long-term memory for related information.

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

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

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

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

157 of its major ligands, IGF2, is critical for long-term memory formation and strengthening.

158 the main function of dentate neurogenesis is long-term memory formation because we assumed that a new

159 he integrated stress response (ISR), impairs long-term memory formation in rodents and birds(11-13).

160 ngle isoform of creb1/crh-1 shows defects in long-term memory formation in the animal and expression

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

162 tically contribute to hippocampus-dependent, long-term memory formation using a combination of transc

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

164 a suggest key roles for Stk11 and Fos in CTA long-term memory formation, dependent at least partly th

165 ranslation-dependent processes necessary for long-term memory formation, entrained by dopamine in CA1

166 extracted Orb2 fibrils, that are involved in long-term memory formation, from Drosophila brains, char

167 tus contain loci annotated with functions in long-term memory formation, mushroom body development, a

168 sting, providing an ideal model for studying long-term memory formation, storage, and retrieval.

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

170 genetic suppressor of hippocampus-dependent, long-term memory formation.

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

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

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

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

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

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

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

178 cognitive deficits, including impairments in long-term memory formation.

179 table and having unique predictive value for long-term memory function, hippocampal volume and traini

180 val in a murine orthotopic PDAC model with a long-term memory immune response.

181 rogenesis participates in the development of long-term memory impairment.

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

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

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

185 tice is a strategy to optimize encoding into long-term memory in both young and elderly humans.

186 ere, we show that consolidation of courtship long-term memory in Drosophila is mediated by reactivati

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

188 We developed tests that measure long-term memory in hamsters.

189 a with the ISR inhibitor ISRIB(11), enhances long-term memory in health and disease(18).

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

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

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

193 2(-/-) mice had robust and sustained loss of long-term memory in two separate behavioral tasks, Morri

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

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

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

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

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

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

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

201 We also show long-term memory-like cytokine responses upon subsequent

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

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

204 on a comparable match-to-sample task with no long-term memory load, suggesting that the effect is not

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

206 hodology to target the mechanisms supporting long term memory (LTM) access/retrieval in language and

207 ositive biological processes that facilitate long-term memories (LTM) but also the suppression of inh

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

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

210 initially require the hippocampus for recent long-term memory (LTM) but then become increasingly inde

211 the general field of molecular processing in long-term memory (LTM) by describing a novel form of pre

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 Long-term memory (LTM) formation is a critical survival

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

221 Forming long-term memory (LTM) often requires repetitive experie

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

223 The formation of spatial long-term memory (LTM) requires the de novo synthesis of

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

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

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

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

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

229 ronal excitability (LTEE), two correlates of long-term memory (LTM).

230 soforms on the ability of C. elegans to form long-term memory (LTM).

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

232 ese findings demonstrate that people rely on long-term memory not only for remembering familiar items

233 with a cGMP-dependent switch from short- to long-term memory observed in vivo after intrahippocampal

234 Long-term memories of fear have been notoriously difficu

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

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

237 tory sensory input with a social cue induces long-term memory of a food odor.

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

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

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

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

242 tend to reside in genomic clusters and that long-term memory of these genes is locally restricted by

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

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

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

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

247 in selective attention, working memory, and long-term memory persist in remission from a major depre

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

249 dence that human hippocampal activity during long-term memory processing is sensitive to temporal dur

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

251 fically enhances protein synthesis-dependent long-term memory (PSD-LTM), but not anesthesia-resistant

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

253 synthesis is crucial for the maintenance of long-term memory-related synaptic plasticity.

254 ENT How new experiences are transformed into long-term memories remains a fundamental question for ne

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

256 central role as the orthographic lexicon-the long-term memory representations of visual word forms.

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

258 both by their current environment and their long-term memory representations.

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

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

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

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

263 ent GR-phosphorylation (PO(4)) sites impairs long-term memory retention and maintenance of newly form

264 g the stopping of action and the stopping of long-term memory retrieval (stopping thoughts), where in

265 We found that male mice exhibit stronger long-term memory retrieval than do female mice, and this

266 in generating explanations (e.g., attention, long-term memory) shape the outputs of this process.

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

268 ive memory stabilization was associated with long-term memory specificity.

269 ion mechanisms have been proposed to mediate long-term memory stabilization and transformation.

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

271 The hippocampal complex (HC) is central to long-term memory storage and retrieval as well as spatia

272 icant insights into the molecular biology of long-term memory storage at the level of the synapse.

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

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

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

276 l node of the neocortical network supporting long-term memory storage) undergoes rapid modifications

277 on retrieval and must be reconsolidated into long-term memory stores to persist.

278 of GABAergic cells, is important to modulate long-term memory strength and precision.

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 We trained mice in an auditory long-term memory task and measured learning-related dyna

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

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

284 emories that last for seconds to minutes and long-term memories that last for hours or longer [1, 2].

285 rd a possible molecular mechanism underlying long-term memory that involves CPEB3's binding to actin,

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

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

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

289 ding of the cellular architecture supporting long-term memory traces has also substantially improved.

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

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

292 or medium (22 [29%]) in size, although three long-term memory variables showed large deficits: g=-0.8

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 presents both classic diauxic behaviors and long-term memory, where the bacteria can pause for >11 h

297 enhances CA1 neuronal excitability, LTP and long-term memory whereas its overexpression weakens memo

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

299 tumor regression, endogenous T cells secured long-term memory with a broad repertoire of antigen spec

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