ライフサイエンスコーパス: memory consolidation

1 nhancing both object recognition and spatial memory consolidation.

2 onally regulates contextual fear and spatial memory consolidation.

3 proteinase-9 inhibition appears to attenuate memory consolidation.

4 and accordingly, it may also be involved in memory consolidation.

5 ity (<1 Hz) and are thought to be related to memory consolidation.

6 Arc is a synaptic protein essential for memory consolidation.

7 romote semantic memory formation via systems memory consolidation.

8 nk between ABN activity during REM sleep and memory consolidation.

9 ess hormone and emotional arousal effects on memory consolidation.

10 24 h, indicating that it is not dependent on memory consolidation.

11 o identify transcriptome changes specific to memory consolidation.

12 s effects of 17beta-estradiol on hippocampal memory consolidation.

13 rience and activate dopaminergic neurons for memory consolidation.

14 he brain and play a critical role in offline memory consolidation.

15 affect working memory but impaired long-term memory consolidation.

16 efrontal cortex and amygdala are involved in memory consolidation.

17 or structural synapse remodeling involved in memory consolidation.

18 e the prioritization of events for long-term memory consolidation.

19 epressor enriched in CA1 cells important for memory consolidation.

20 tent to which this influence is dependent on memory consolidation.

21 noafferents had been shown to play a role in memory consolidation.

22 otions and in procedural motor and emotional memory consolidation.

23 nt (NREM) sleep has been proposed to support memory consolidation.

24 C inhibition of PV+ interneurons blocks fear memory consolidation.

25 p and seizures specifically impair long-term memory consolidation.

26 ion of PV(+) cells disrupted contextual fear memory consolidation.

27 activity under hippocampal guidance leads to memory consolidation.

28 n is thought to promote memory by supporting memory consolidation.

29 controlling molecular processes required for memory consolidation.

30 pportunity for causal manipulations of human memory consolidation.

31 nes whether sleep spindles can promote motor memory consolidation.

32 rmalities were most likely to interfere with memory consolidation.

33 tanding of the role of REM and NREM sleep in memory consolidation.

34 g navigational planning to one geared toward memory consolidation.

35 ), which have been shown to be important for memory consolidation.

36 believed to support synaptic changes during memory consolidation.

37 anges in synaptic morphology associated with memory consolidation.

38 ity of postencoding markers of systems-level memory consolidation.

39 the dominant neurobiological theory of human memory consolidation.

40 , exhibit impoverished sleep-dependent motor memory consolidation.

41 in performance, a hallmark of motor sequence memory consolidation.

42 ion during sleep, which underlie human motor memory consolidation.

43 f Setd6 in the rat dorsal hippocampus during memory consolidation.

44 ns in the hippocampus is thought to underlie memory consolidation.

45 al receptors mediate the impact of stress on memory consolidation.

46 anism of the deleterious effect of stress on memory consolidation.

47 o promote long-term potentiation and enhance memory consolidation.

48 al population events with a critical role in memory consolidation.

49 us that play a prominent role in theories of memory consolidation.

50 red subtly during SWS to selectively enhance memory consolidation.

51 ciated with the effect of prior knowledge on memory consolidation.

52 ory reactivation (TMR), selectively enhances memory consolidation.

53 e long-lasting consequences such as impaired memory consolidation.

54 of groups of neurons and play a key role in memory consolidation.

55 al mechanism by which reward could influence memory consolidation.

56 hat correlates with impaired sleep-dependent memory consolidation.

57 , a process that may play a critical role in memory consolidation.

58 Sleep plays a role in memory consolidation.

59 ancing/inhibiting perception, attention, and memory consolidation.

60 ations that may form the neural substrate of memory consolidation.

61 Sleep has a profound impact on memory consolidation.

62 in major brain functions such as learning or memory consolidation.

63 n synthesis processes that enhance selective memory consolidation.

64 l spikes during sleep would impair long-term memory consolidation.

65 g asymptotic levels of fear learning or fear memory consolidation.

66 e was proposed to be a neuronal substrate of memory consolidation.

67 ly emerged as a key metabolite necessary for memory consolidation.

68 nges in oligodendrogenesis are important for memory consolidation.

69 ortex information transduction hypothesis of memory consolidation.

70 butes independently to successful extinction memory consolidation.

71 n the human brain that is thought to promote memory consolidation.

72 ably drives synaptic plasticity and promotes memory consolidation.

73 anced endocannabinoid signaling and impaired memory consolidation.

74 nction in CA1 and BLA in different phases of memory consolidation.

75 ghted the important role that sleep plays in memory consolidation.

76 r regulating hippocampal ripple activity and memory consolidation.

77 works following learning and is required for memory consolidation.

78 tostimulation of MnR neurons interfered with memory consolidation.

79 ld potentials that are thought to facilitate memory consolidation.

80 ion, and enhanced short-term contextual fear memory consolidation.

81 t active rehearsal increases the efficacy of memory consolidation.

82 BDNF-TrkB signaling, regulating hippocampal memory consolidation.

83 dialog that is necessary for sleep-dependent memory consolidation.

84 nce-dependent synapse remodeling and promote memory consolidation.

85 Os) both appear to play an important role in memory consolidation.

86 eling of spines on ABN dendrites and impairs memory consolidation.

87 of H3K9me2 changes in the hippocampus during memory consolidation.

88 failed to enhance sleep-dependent procedural memory consolidation.

89 cal example of a complex network involved in memory consolidation.

90 re hippocampal network phenomena involved in memory consolidation.

91 the role of sleep in synaptic plasticity and memory consolidation.

92 ggesting that they are a better biomarker of memory consolidation.

93 ch may have further contributed to deficient memory consolidation.

94 y reinforcement, or by inhibiting extinction-memory consolidation.

95 ntribution of awake time periods to episodic memory consolidation.

96 Sleep is pivotal for memory consolidation.

97 s-postulated as physiological substrates for memory consolidation.

98 2 non-rapid eye movement sleep (N2), mediate memory consolidation.

99 s a fundamental mechanism of sleep-dependent memory consolidation.

100 n the hippocampus of male mice that promotes memory consolidation.

101 g coordinated activity that is important for memory consolidation.

102 nting the adverse effect of excessive LTD on memory consolidation.

103 receptors elevates cAMP levels and modulates memory consolidation.

104 pal communication, such as working memory or memory consolidation.

105 oscillations responsible for sleep-dependent memory consolidation.

106 way and many cortical structures involved in memory consolidation.

107 al reactivation of dopaminergic neurons, and memory consolidation.

108 aves have competing roles in sleep-dependent memory consolidation.

109 dy (MB) alpha'beta' cells that link sleep to memory consolidation [11].

110 Ripples are ideally suited for memory consolidation [14, 15], since the reactivation of

111 e hippocampus after learning interferes with memory consolidation [24-26].

112 indle-ripple events that are associated with memory consolidation [6, 7].

113 Reactivation and replay may underlie memory consolidation [6-10].

114 Whether such distal interactions on memory consolidation also depend on BLA activity is not

115 pus and that SETD6 knockdown interferes with memory consolidation, alters gene expression patterns, a

116 the importance of deficient sleep-dependent memory consolidation among the cognitive deficits of SZ

117 s) have been hypothesized as a mechanism for memory consolidation and action planning.

118 eurons during fear acquisition enhanced fear memory consolidation and drove action potential firing i

119 , is required for hippocampus-dependent fear memory consolidation and extinction in mice.

120 ience and neuropsychiatry literature on fear memory consolidation and extinction, stress, and PTSD.

121 Sleep has been implicated in both memory consolidation and forgetting of experiences.

122 sleep serving as markers of sleep-dependent memory consolidation and hippocampal reactivation.

123 s further associated with impaired overnight memory consolidation and impoverished hippocampal-neocor

124 stablishes the role of gamma oscillations in memory consolidation and introduces a versatile method f

125 w wave-spindle coupling, impairing overnight memory consolidation and leading to forgetting.

126 pal replay has been hypothesized to underlie memory consolidation and navigational planning, yet the

127 mmobility and rest has been linked with both memory consolidation and navigational planning.

128 l sensory function and that it blocked motor memory consolidation and not the ability to retrieve a c

129 for cognitive functions such as declarative memory consolidation and perceptual learning.

130 would reveal important circuit mechanisms in memory consolidation and provide novel insights into mem

131 dependent formation of myelin contributes to memory consolidation and recall, possibly by increasing

132 ristic for the hippocampus and implicated in memory consolidation and recall.

133 investigate the impact of acute exercise on memory consolidation and retrieval-related neural proces

134 urons show response patterns consistent with memory consolidation and spontaneous recovery, the hallm

135 mance-dependent regulation in the service of memory consolidation and storage.

136 is known to affect the dynamic processes of memory consolidation and strengthening.

137 rojection between HC and mPFC contributes to memory consolidation and support an important functional

138 exercise after learning to exogenously boost memory consolidation and thus long-term memory.

139 ciated with NPTP, stress-response signaling, memory consolidation, and cortical neural remodeling.SIG

140 ion specifically within the DG engram during memory consolidation, and identify a novel group of CREB

141 GPER in mediating hippocampal morphology and memory consolidation, and may suggest first steps toward

142 ation, prediction error, incentive salience, memory consolidation, and response output.

143 ed in the integrative activity necessary for memory consolidation, and that intense training facilita

144 ous hippocampal IEDs correlate with impaired memory consolidation, and that they are precisely coordi

145 t confers a small but significant benefit on memory consolidation, and that this benefit requires the

146 NIFICANCE STATEMENT Sleep benefits learning, memory consolidation, and the integration of new with ol

147 the underlying mechanisms of sleep dependent memory consolidation are poorly understood.

148 play leads to synaptic changes that underlie memory consolidation are still poorly understood.

149 tion of sleep to cognitive functions such as memory consolidation are undermined by growing evidence

150 e mechanistic relationship between sleep and memory consolidation, arguing for a significant role of

151 f hippocampus-to-cortex information flow for memory consolidation as well as reciprocal interaction b

152 transients may promote systems and synaptic memory consolidation as well as synaptic homeostasis.

153 s (SPW-Rs) in the hippocampus are implied in memory consolidation, as shown by observational and inte

154 icates that treatments that typically impair memory consolidation become ineffective when animals are

155 research suggesting that amyloid beta helps memory consolidation, before it impairs memory.

156 stigation into the possible role of sleep in memory consolidation began with the early studies of Jen

157 STATEMENT Systems mechanisms of declarative memory consolidation beyond the hippocampal-prefrontal i

158 sufficient for stress-induced impairment of memory consolidation, but CB1 receptors present in other

159 IGF2R is necessary for hippocampus-dependent memory consolidation, but dispensable for learning, memo

160 tive conditioning needed increased sleep for memory consolidation, but flies starved after training d

161 rb2 in Drosophila was recently implicated in memory consolidation, but it remains unclear what featur

162 spine densities during a period of presumed memory consolidation, but only when paired with new lear

163 raphic (EEG) signatures, have been linked to memory consolidation, but underlying mechanisms are poor

164 d extinction before we manipulated nocturnal memory consolidation by a split-night protocol with 80 h

165 ocampal CIM6P/IGF2R plays a critical role in memory consolidation by controlling the rate of training

166 coordinator of IEG expression and subsequent memory consolidation by directing temporally specific ch

167 Deletion of PDE11A may impair memory consolidation by impairing requisite protein tran

168 o the hypothesis that hippocampus can assist memory consolidation by reactivating and broadcasting ex

169 during slow-wave sleep (SWS) may facilitate memory consolidation by regulating interactions between

170 functions in brain development, learning and memory consolidation by selectively eliminating and main

171 Local translation can support memory consolidation by supplying new proteins to synaps

172 n rodents and humans suggests that long-term memory consolidation can be enhanced by the exploration

173 mory encoding and then reapplied during SWS, memory consolidation can be enhanced, an effect that is

174 Memory consolidation can be promoted via targeted memory

175 ar environment showed significantly impaired memory consolidation compared to typically developing pe

176 n endophenotype that impairs sleep-dependent memory consolidation, contributes to symptoms, and is a

177 amic sleep spindles in hippocampus-dependent memory consolidation, conveyed through triple coupling o

178 Memory consolidation crucially depends on sharp-wave rip

179 t GPER-mediated hippocampal spinogenesis and memory consolidation depend on JNK and cofilin signaling

180 ng-lasting memories-a process referred to as memory consolidation-depends on the reactivation of newl

181 is, synaptogenesis, synaptic plasticity, and memory consolidation during development.

182 provide the global physiological context for memory consolidation during non-REM sleep.

183 mic activity are thought to be essential for memory consolidation during sleep and the efficient remo

184 te whether young ABN activity contributes to memory consolidation during sleep using Ca(2+) imaging i

185 nce of an optimal slow-oscillation phase for memory consolidation during sleep, supporting the idea t

186 w oscillations-is thought to be critical for memory consolidation during sleep, the role spindles pla

187 d sleep spindle activity promotes successful memory consolidation during sleep.

188 the putamen has a central role in procedural memory consolidation during sleep.

189 mechanisms behind the role of stimulation in memory consolidation during slow-wave sleep.

190 activation of wake patterns that may support memory consolidation during SWS.

191 erve to enhance sensory-motor processing and memory consolidation during these states.

192 irect activation of the amygdala can enhance memory consolidation even during nonemotional events.

193 he potential for avBST activity to influence memory consolidation following an emotionally arousing l

194 vioral tagging might only be able to improve memory consolidation for weakly encoded information.

195 The role of Arc in synaptic plasticity and memory consolidation has been investigated for many year

196 However, the role of ANS in sleep-dependent memory consolidation has never been examined.

197 pindle coupling are necessary for successful memory consolidation has not been tested directly.

198 While hippocampal and cortical mechanisms of memory consolidation have long been studied, their inter

199 ngrams and circuits that support neocortical memory consolidation have thus far been unknown.

200 vidence that glucocorticoid hormones enhance memory consolidation, helping to ensure that emotionally

201 ical Abeta to impaired hippocampus-dependent memory consolidation; (iii) the potential diagnostic uti

202 CA1 dendritic spine density and hippocampal memory consolidation in a manner dependent on actin poly

203 ovel environment led to significantly better memory consolidation in children and adolescents with AD

204 ave ripple events (SWRs) is thought to drive memory consolidation in hippocampal and cortical circuit

205 prefrontal cortex (mPFC) in sleep-dependent memory consolidation in male mice.

206 sensitive electrophysiological biomarker of memory consolidation in mice.

207 te these activity patterns and sleep-related memory consolidation in nine male and seven female human

208 siological mechanism(s) explaining why motor memory consolidation in older adults fails to benefit fr

209 s (or lack thereof) of sleep-dependent motor memory consolidation in older adults.

210 As with memory consolidation in our previous work (Kim et al., 2

211 evant brain oscillations and improves visual memory consolidation in patients with MCI.

212 n humans during events that are critical for memory consolidation in rodents.SIGNIFICANCE STATEMENT H

213 llations are promising targets for improving memory consolidation in schizophrenia, but enhancing spi

214 l influence of sleep spindles on motor skill memory consolidation in the elderly.

215 ') activate the LC to trigger strong initial memory consolidation in the hippocampus, resulting in vi

216 cal dialogue, which is of key importance for memory consolidation in the mammalian brain.

217 anism which may contribute to impairments in memory consolidation in this model of dementia.

218 y proposes a synaptic-level mechanism of how memory consolidation is affected by sensory stimulation

219 y proposes a synaptic-level mechanism of how memory consolidation is affected by sensory stimulation

220 merous studies have demonstrated that system memory consolidation is an active, selective, and sleep-

221 System memory consolidation is conceptualized as an active proc

222 ritical for learning-related plasticity, and memory consolidation is correlated with hippocampal shar

223 Memory consolidation is hypothesized to involve the dist

224 Declarative memory consolidation is hypothesized to require a two-st

225 Behavioral work suggests that motor memory consolidation is initiated upon the attainment of

226 rtex, direct evidence for its involvement in memory consolidation is limited.

227 encephalographic (EEG) rhythms are linked to memory consolidation is poorly understood.

228 The dynamic of fearful memory consolidation is poorly understood.

229 Another factor that influences memory consolidation is sleep and growing evidence sugge

230 Memory consolidation is the process by which a newly for

231 Systems-level memory consolidation is thought to be dependent on the c

232 wave activity (SWA) and associated overnight memory consolidation is unknown.

233 ve importance of SWRs from these regions for memory consolidation is unknown.

234 t a critical mechanism for BLA influences on memory consolidation is via effects on activity-regulate

235 w-wave sleep (SWS) is known to contribute to memory consolidation, likely through the reactivation of

236 Hippocampal sharpwave ripples, essential for memory consolidation, mark when hippocampal neurons repl

237 ke and active(4), the ability to switch to a memory consolidation mechanism that is not contingent on

238 that awake SWRs and associated planning and memory consolidation mechanisms are engaged specifically

239 Thus, we hypothesized that impaired memory consolidation mechanisms in hippocampal-cortical

240 Mechanistic support for the DMN's role in memory consolidation might come from investigation of la

241 y circuits for memory.SIGNIFICANCE STATEMENT Memory consolidation necessitates synthesis of new prote

242 It is unknown whether the process of memory consolidation occurs exclusively through the stab

243 that M-current suppression is important for memory consolidation of specific types of memories.SIGNI

244 affecting existing oligodendrocytes impaired memory consolidation of water maze, as well as contextua

245 This raises the possibility that memory consolidation or other sleep-dependent processes

246 nt of the infant brain, which would preclude memory consolidation, or to deficits in memory retrieval

247 d of quiet, eyes-closed waking rest benefits memory consolidation, others have reported null effects.

248 ought to provide a window of opportunity for memory consolidation, particularly conducive to cortical

249 l agonism of the ghrelin receptor during the memory consolidation period reduced fear memory strength

250 inhibitor, XE991, when delivered during the memory consolidation phase.

251 zed importance of ripple-spindle coupling in memory consolidation, post-training inhibition of PV(+)

252 campus to mPFC contribute to sleep-dependent memory consolidation, potentially by affecting the tempo

253 This functional connectivity is a result of memory consolidation processes and is characterized by a

254 This functional connectivity stems from memory consolidation processes because it is present dur

255 d in the hippocampus have been implicated in memory consolidation processes critical to memory stabil

256 ocal field potential (LFP) signatures during memory consolidation processes in non-rapid eye movement

257 ses suggest that reactivation contributes to memory consolidation processes, but whether awake and sl

258 nd strictly related to the interference with memory consolidation processes.

259 suggest that the DG is directly affected by memory consolidation processes.

260 ave indicated that the amygdala can modulate memory-consolidation processes in other brain regions su

261 es activated by learning experiences enhance memory consolidation provided strong evidence supporting

262 amnesia may not result from a disruption of memory consolidation/reconsolidation.

263 ults show impoverished overnight motor skill memory consolidation relative to young adults, with the

264 ram-specific molecular mechanisms underlying memory consolidation remain largely unknown.

265 e conformational transitions associated with memory consolidation remain unknown.

266 These results indicate that successful memory consolidation requires coherent hippocampal-neoco

267 hic factor (BDNF) expression is required for memory consolidation, retrieval engages PL BDNF to regul

268 us have been hypothesized to be important in memory consolidation, retrieval, and the pathophysiology

269 ement SWRs as a hippocampal LFP biomarker of memory consolidation.SIGNIFICANCE STATEMENT Awake experi

270 ion at the same site, which is necessary for memory consolidation.SIGNIFICANCE STATEMENT How does the

271 nts and advance our understanding of offline memory consolidation.SIGNIFICANCE STATEMENT In the light

272 nisms through which spindle nesting supports memory consolidation.SIGNIFICANCE STATEMENT Our analysis

273 sentations necessary for REM sleep-dependent memory consolidation.SIGNIFICANCE STATEMENT Sawtooth wav

274 ed spindle-slow oscillation events predicted memory consolidation significantly better than spindle d

275 ese subfields are differentially involved in memory consolidation, spatial navigation and pattern sep

276 rticularly because of its roles in conscious memory consolidation, spatial navigation, emotion, and m

277 Memory consolidation subsequently results in spatial reo

278 stress-dependent regulation of nonemotional memory consolidation, suggesting new potential avenues f

279 ctive during PS and could play a key role in memory consolidation taking place during this state.

280 tion caused significant enhancement of motor memory consolidation that correlated with the stimulatio

281 the potential functions of REM sleep (e.g., memory consolidation), the neural circuits that control

282 races outward to the neocortex to facilitate memory consolidation there.

283 precise and widespread synchronization, and memory consolidation; therefore, the SWRs reported here

284 ripheral acyl-ghrelin robustly inhibits fear memory consolidation through actions in the amygdala and

285 is supposed to play a key role in long-term memory consolidation transferring information from hippo

286 r excitatory synaptic inputs and hippocampal memory consolidation, uncovering a role of mTORC1 in inh

287 ms behind the role of sensory stimulation on memory consolidation using computational models implemen

288 IF2alpha-dependent mRNA translation controls memory consolidation via autonomous mechanisms in excita

289 downstream effector in VGF/TLQP-62-mediated memory consolidation was further revealed by posttrainin

290 pathology and impaired hippocampus-dependent memory consolidation was not direct, but instead statist

291 TEMENT Contrary to expectations from systems memory consolidation, we find that in the absence of a f

292 he importance of post-encoding processing in memory consolidation, we investigated the effects of a b

293 Because of the importance of sleep for memory consolidation, we investigated the role of SHARP1

294 e connection between ripple oscillations and memory consolidation, we investigated whether the struct

295 otonin 2C receptor (5-HT2CR) activity during memory consolidation were necessary for stress enhanceme

296 Slow waves in neural activity contribute to memory consolidation, whereas cerebrospinal fluid (CSF)

297 ar learning significantly impaired long term memory consolidation, whereas short-term memory remained

298 imulation during SWS can selectively enhance memory consolidation with the effect depending on the ph

299 y expression revealed a convergent center of memory consolidation within the mushroom body (MB) impli

300 (E(2)) on hippocampal CA1 spine density and memory consolidation, yet the cell-signaling mechanisms