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1 otions and in procedural motor and emotional memory consolidation.
2 nt (NREM) sleep has been proposed to support memory consolidation.
3 ion of PV(+) cells disrupted contextual fear memory consolidation.
4 in major brain functions such as learning or memory consolidation.
5 n synthesis processes that enhance selective memory consolidation.
6 g asymptotic levels of fear learning or fear memory consolidation.
7 e was proposed to be a neuronal substrate of memory consolidation.
8 ly emerged as a key metabolite necessary for memory consolidation.
9 ortex information transduction hypothesis of memory consolidation.
10 butes independently to successful extinction memory consolidation.
11 n the human brain that is thought to promote memory consolidation.
12 ably drives synaptic plasticity and promotes memory consolidation.
13 nction in CA1 and BLA in different phases of memory consolidation.
14 ghted the important role that sleep plays in memory consolidation.
15 r regulating hippocampal ripple activity and memory consolidation.
16 tostimulation of MnR neurons interfered with memory consolidation.
17 ld potentials that are thought to facilitate memory consolidation.
18 ion, and enhanced short-term contextual fear memory consolidation.
19 t active rehearsal increases the efficacy of memory consolidation.
20 BDNF-TrkB signaling, regulating hippocampal memory consolidation.
21 ad severe deficits in learning and long-term memory consolidation.
22 al role of the MnR in regulating ripples and memory consolidation.
23 B signaling, and is required for hippocampal memory consolidation.
24 hat sleep facilitates retention by enhancing memory consolidation.
25 might influence neural processes underlying memory consolidation.
26 onal morphology lead to a deficit in spatial memory consolidation.
27 ippocampal synaptic plasticity and long-term memory consolidation.
28 ithin the basolateral amygdala (BLA) in fear memory consolidation.
29 activity under hippocampal guidance leads to memory consolidation.
30 novel and essential regulator of hippocampal memory consolidation.
31 pal CA1 pyramidal layer, are associated with memory consolidation.
32 ein beta (C/EBPbeta) is necessary to mediate memory consolidation.
33 that the endogenously released AEA modulates memory consolidation.
34 r with the initial BDNF requirement, mediate memory consolidation.
35 Akt, and ERK1/2 phosphorylation and impaired memory consolidation.
36 ation regulates emotional arousal effects on memory consolidation.
37 and regulation of the mechanisms underlying memory consolidation.
38 ytic processes opposes synapse growth during memory consolidation.
39 ortical neurons and justify models of system memory consolidation.
40 kely drives synaptic plasticity and promotes memory consolidation.
41 kinase (ERK) cascade, a critical mediator of memory consolidation.
42 n is thought to promote memory by supporting memory consolidation.
43 t Notch signaling in the BLA suppresses fear memory consolidation.
44 ated recruitment of PPARgamma to pERK during memory consolidation.
45 oth correlated with and necessary for normal memory consolidation.
46 ction of anisomycin into this region impairs memory consolidation.
47 ent benefits, including an important role in memory consolidation.
48 controlling molecular processes required for memory consolidation.
49 ct learning and is necessary for hippocampal memory consolidation.
50 n area 32 plays crucial roles in emotion and memory consolidation.
51 ning stimulation of the vagus nerve enhances memory consolidation.
52 protein synthesis in each hemisphere during memory consolidation.
53 odified in this process as the foundation of memory consolidation.
54 e auditory cortex as observed during initial memory consolidation.
55 nism for regulating protein synthesis during memory consolidation.
56 firing and have been behaviourally linked to memory consolidation.
57 gulate the transcriptional program linked to memory consolidation.
58 n mediating the effects of E2 on hippocampal memory consolidation.
59 ted by the M1 receptor (M1R) is critical for memory consolidation.
60 the beneficial effects of E2 on hippocampal memory consolidation.
61 vent to investigate the processes underlying memory consolidation.
62 early gene that plays a significant role in memory consolidation.
63 a possible link between this persistence and memory consolidation.
64 Sleep is known to support memory consolidation.
65 eIF2alpha phosphorylation is implicated in memory consolidation.
66 ess the temporal nature of the modulation of memory consolidation.
67 repetitive aspects of LTM formation, such as memory consolidation.
68 n for the emergence of sharp waves promoting memory consolidation.
69 leep may contribute to hippocampus-dependent memory consolidation.
70 th initial learning and subsequent long-term memory consolidation.
71 evidence that these affective biases involve memory consolidation.
72 ieval of previously acquired trace EBC after memory consolidation.
73 hese early memory lapses in the structure of memory consolidation.
74 sistent with its role in dream formation and memory consolidation.
75 t Wnt signaling is necessary for hippocampal memory consolidation.
76 nd its interactions with the hippocampus, in memory consolidation.
77 ylation after a learning experience enhances memory consolidation.
78 ar stress responses, emotional behaviour and memory consolidation.
79 lay' has been postulated to be important for memory consolidation.
80 assical music may positively affect surgical memory consolidation.
81 long-term synaptic potentiation and spatial memory consolidation.
82 hen memory storage and likely contributes to memory consolidation.
83 CA1 of the rat hippocampus and the EC during memory consolidation.
84 nes whether sleep spindles can promote motor memory consolidation.
85 rmalities were most likely to interfere with memory consolidation.
86 tanding of the role of REM and NREM sleep in memory consolidation.
87 g navigational planning to one geared toward memory consolidation.
88 believed to support synaptic changes during memory consolidation.
89 anges in synaptic morphology associated with memory consolidation.
90 ity of postencoding markers of systems-level memory consolidation.
91 the dominant neurobiological theory of human memory consolidation.
92 , exhibit impoverished sleep-dependent motor memory consolidation.
93 in performance, a hallmark of motor sequence memory consolidation.
94 ion during sleep, which underlie human motor memory consolidation.
95 ns in the hippocampus is thought to underlie memory consolidation.
96 C inhibition of PV+ interneurons blocks fear memory consolidation.
97 al receptors mediate the impact of stress on memory consolidation.
98 anism of the deleterious effect of stress on memory consolidation.
99 o promote long-term potentiation and enhance memory consolidation.
100 us that play a prominent role in theories of memory consolidation.
101 red subtly during SWS to selectively enhance memory consolidation.
102 ciated with the effect of prior knowledge on memory consolidation.
103 ory reactivation (TMR), selectively enhances memory consolidation.
104 e long-lasting consequences such as impaired memory consolidation.
105 of groups of neurons and play a key role in memory consolidation.
106 al mechanism by which reward could influence memory consolidation.
107 , a process that may play a critical role in memory consolidation.
108 Sleep plays a role in memory consolidation.
109 ancing/inhibiting perception, attention, and memory consolidation.
110 ations that may form the neural substrate of memory consolidation.
111 Sleep has a profound impact on memory consolidation.
114 ds to interfere with fear development during memory consolidation after a trauma, and techniques to i
116 pports a role for dopamine in human episodic memory consolidation, albeit operating within a narrow d
118 the importance of deficient sleep-dependent memory consolidation among the cognitive deficits of SZ
119 eurons during fear acquisition enhanced fear memory consolidation and drove action potential firing i
120 inhibition facilitates transcription during memory consolidation and enhances long-lasting forms of
123 roles in spatial information processing and memory consolidation and has also been implicated in tem
125 s further associated with impaired overnight memory consolidation and impoverished hippocampal-neocor
127 ations responsible for the twin processes of memory consolidation and memory erasure that occur durin
128 pal replay has been hypothesized to underlie memory consolidation and navigational planning, yet the
130 would reveal important circuit mechanisms in memory consolidation and provide novel insights into mem
132 d with curcumin is capable of impairing fear memory consolidation and reconsolidation processes, find
134 ociate with deep sleep and are implicated in memory consolidation and replay of cortical responses el
135 investigate the impact of acute exercise on memory consolidation and retrieval-related neural proces
136 ment of ACC and DLPFC areas in REM sleep for memory consolidation and synergism in awake states for c
137 etylation is critical for object recognition memory consolidation and the beneficial effects of E2 on
138 motor learning, but their relationship with memory consolidation and their dependence on the form of
140 t PKR plays a major role in cortex-dependent memory consolidation and, therefore, that pharmacologica
141 rsal hippocampal dopamine in this late-phase memory consolidation and, unexpectedly, differential rol
142 the cortex as a physiological constraint of memory consolidation, and its downregulation serves as c
144 cision making: first, a role for dopamine in memory consolidation, and second, the critical importanc
145 ronal histone acetylation has been linked to memory consolidation, and targeting histone acetylation
146 ed in the integrative activity necessary for memory consolidation, and that intense training facilita
147 SWS replay in the olfactory cortex enhances memory consolidation, and that memory precision is depen
148 ous hippocampal IEDs correlate with impaired memory consolidation, and that they are precisely coordi
149 ay in rodents also promote human hippocampal memory consolidation, and this process can be manipulate
151 e mechanistic relationship between sleep and memory consolidation, arguing for a significant role of
152 f hippocampus-to-cortex information flow for memory consolidation as well as reciprocal interaction b
153 s (SPW-Rs) in the hippocampus are implied in memory consolidation, as shown by observational and inte
154 These increases are essential for long-term memory consolidation, as their blockade via antisense ol
156 icates that treatments that typically impair memory consolidation become ineffective when animals are
157 stigation into the possible role of sleep in memory consolidation began with the early studies of Jen
158 sufficient for stress-induced impairment of memory consolidation, but CB1 receptors present in other
159 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 has been shown to mediate the maintenance of memory consolidation, but the mechanisms of this regulat
164 raphic (EEG) signatures, have been linked to memory consolidation, but underlying mechanisms are poor
165 d extinction before we manipulated nocturnal memory consolidation by a split-night protocol with 80 h
167 tential contribution of nuclear receptors to memory consolidation by measuring the expression of all
168 o the hypothesis that hippocampus can assist memory consolidation by reactivating and broadcasting ex
169 pT305-CaMKII play a role in AMPAR-dependent memory consolidation by reducing proteasomal degradation
171 during slow-wave sleep (SWS) may facilitate memory consolidation by regulating interactions between
172 functions in brain development, learning and memory consolidation by selectively eliminating and main
173 dromically during SPW-Rs might contribute to memory consolidation by sharpening specificity of subseq
174 n endophenotype that impairs sleep-dependent memory consolidation, contributes to symptoms, and is a
175 amic sleep spindles in hippocampus-dependent memory consolidation, conveyed through triple coupling o
176 AMP levels during sleep deprivation prevents memory consolidation deficits associated with sleep loss
179 ng-lasting memories-a process referred to as memory consolidation-depends on the reactivation of newl
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
190 irect activation of the amygdala can enhance memory consolidation even during nonemotional events.
192 fore or after a learning experience enhances memory consolidation for hippocampus-dependent tasks and
193 association, hippocampal activity modulates memory consolidation for that association via a dopamine
194 The role of Arc in synaptic plasticity and memory consolidation has been investigated for many year
199 tein critical for long-term potentiation and memory consolidation has previously been associated with
200 While hippocampal and cortical mechanisms of memory consolidation have long been studied, their inter
202 n acquired neuroprotection (atf3, serpinb2), memory consolidation (homer1, arc), and the development
203 ical Abeta to impaired hippocampus-dependent memory consolidation; (iii) the potential diagnostic uti
204 medial (DPM) neurons, which are required for memory consolidation in Drosophila, are sleep-promoting
205 ave ripple events (SWRs) is thought to drive memory consolidation in hippocampal and cortical circuit
207 Here we assessed the time course of motor memory consolidation in humans, taking early boosts in p
209 te these activity patterns and sleep-related memory consolidation in nine male and seven female human
210 siological mechanism(s) explaining why motor memory consolidation in older adults fails to benefit fr
212 iral vector, a manipulation known to enhance memory consolidation in other circuits, results in spati
214 Stimulation of muscarinic receptors promotes memory consolidation in several conditioning paradigms,
216 ts function as a physiological constraint of memory consolidation in the cortex, the brain structure
223 at dopamine-dependent boosting of extinction memory consolidation is a promising avenue to improving
224 merous studies have demonstrated that system memory consolidation is an active, selective, and sleep-
226 g object, indicating that object recognition memory consolidation is dependent on canonical Wnt signa
236 present experiments investigated whether the memory consolidation is regulated by endogenously releas
240 ovide evidence that the control of sleep and memory consolidation may share common molecular mechanis
241 that awake SWRs and associated planning and memory consolidation mechanisms are engaged specifically
242 Mechanistic support for the DMN's role in memory consolidation might come from investigation of la
246 echanism by which PregS could participate in memory consolidation of relevance to cognitive function.
248 xpression and potently enhances GR-dependent memory consolidation of training on an inhibitory avoida
250 nt of the infant brain, which would preclude memory consolidation, or to deficits in memory retrieval
251 in learning, working memory, and subsequent memory consolidation, our findings provide a mechanism u
252 ought to provide a window of opportunity for memory consolidation, particularly conducive to cortical
253 l agonism of the ghrelin receptor during the memory consolidation period reduced fear memory strength
254 zed importance of ripple-spindle coupling in memory consolidation, post-training inhibition of PV(+)
255 This functional connectivity is a result of memory consolidation processes and is characterized by a
256 vides a fundamental computational reason for memory consolidation processes at the systems level.
257 This functional connectivity stems from memory consolidation processes because it is present dur
258 d in the hippocampus have been implicated in memory consolidation processes critical to memory stabil
259 ses suggest that reactivation contributes to memory consolidation processes, but whether awake and sl
262 ave indicated that the amygdala can modulate memory-consolidation processes in other brain regions su
263 ontrol subjects (each n = 16), under a motor memory consolidation protocol with functional magnetic r
264 es activated by learning experiences enhance memory consolidation provided strong evidence supporting
265 ia and critically challenges the traditional memory consolidation/reconsolidation hypothesis, providi
268 ults show impoverished overnight motor skill memory consolidation relative to young adults, with the
269 ect of changes in histone acetylation during memory consolidation remain restricted to a handful of m
273 hic factor (BDNF) expression is required for memory consolidation, retrieval engages PL BDNF to regul
274 us have been hypothesized to be important in memory consolidation, retrieval, and the pathophysiology
275 nts and advance our understanding of offline memory consolidation.SIGNIFICANCE STATEMENT In the light
277 stress-dependent regulation of nonemotional memory consolidation, suggesting new potential avenues f
278 ctive during PS and could play a key role in memory consolidation taking place during this state.
279 tion caused significant enhancement of motor memory consolidation that correlated with the stimulatio
280 the potential functions of REM sleep (e.g., memory consolidation), the neural circuits that control
281 KII) plays an essential role in learning and memory consolidation, the roles of CaMKII in other brain
282 precise and widespread synchronization, and memory consolidation; therefore, the SWRs reported here
283 ripheral acyl-ghrelin robustly inhibits fear memory consolidation through actions in the amygdala and
286 affeine administration to test its effect on memory consolidation using a behavioral discrimination t
287 gest that the basolateral amygdala modulates memory consolidation via its projections to brain region
288 t 17beta-estradiol (E2) enhances hippocampal memory consolidation via rapid activation of multiple in
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
292 in an engram or cell assembly is crucial for memory consolidation, we also found that post-training s
294 e connection between ripple oscillations and memory consolidation, we investigated whether the struct
295 reduce eIF2alpha phosphorylation and improve memory consolidation, we pharmacologically inhibited one
296 otonin 2C receptor (5-HT2CR) activity during memory consolidation were necessary for stress enhanceme
297 els impair long-term synaptic plasticity and memory consolidation, whereas decreased levels enhance t
298 ar learning significantly impaired long term memory consolidation, whereas short-term memory remained
299 uctions of both spindles and sleep-dependent memory consolidation, which may be causally related.
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