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1 ) and remember episodes from the past (i.e., episodic memory).
2 on, including attention, working memory, and episodic memory.
3 n imitate recently encountered actions using episodic memory.
4 e representation of "schemas," in studies of episodic memory.
5 arning and have been assumed to also support episodic memory.
6 ns are one of the core mechanisms underlying episodic memory.
7 ization ability was associated with stronger episodic memory.
8 r sequences of events, a defining feature of episodic memory.
9 the PAI paradigm results in a marked loss of episodic memory.
10 and later recall some of these events using episodic memory.
11 w the two systems interact in the service of episodic memory.
12 on between hippocampal D2DR availability and episodic memory.
13 ept and greater rates of decline on tests of episodic memory.
14 tical for spatial information processing and episodic memory.
15 anterior with reward, social processing, and episodic memory.
16 er animals remember many unique events using episodic memory.
17 contexts in which the events occurred using episodic memory.
18 specialized measure of verbal and nonverbal episodic memory.
19 y cues, rats relied on item in context using episodic memory.
20 important role in strengthening and updating episodic memory.
21 he hippocampus is seen as the most vital for episodic memory.
22 that aging is associated with impairments in episodic memory.
23 ent differences in brain activity related to episodic memory.
24 the hippocampus have complementary roles in episodic memory.
25 e over the longer scales necessary for human episodic memory.
26 animal's capacity to recollect the complete episodic memory.
27 ecollection is thought to be the hallmark of episodic memory.
28 ved in spatial processing, and necessary for episodic memory.
29 3 without HS was separately related to lower episodic memory.
30 pports short-timescale sequential firing and episodic memory.
31 al cognitive map consistent with its role in episodic memory.
32 atrophy can lead to profound impairments in episodic memory.
33 underlie specific mental processes of human episodic memory.
34 lded proteins, and impairment of spatial and episodic memory.
35 ct speech-dependent retrieval of voices from episodic memory.
36 ncoding of ongoing experiences necessary for episodic memory.
37 lity that might explain its critical role in episodic memory.
38 further investigations on the development of episodic memory.
39 are meaningful in the context of real-world episodic memory.
40 eimer's disease, and their relationship with episodic memory.
41 ons are critical for episodic simulation and episodic memory.
42 ind that a reminder can renew flexibility of episodic memory.
43 ng of the relationship between pathology and episodic memory.
44 ce cells represent the cellular substrate of episodic memory.
45 dal episodic memories compared with unimodal episodic memories.
46 ucture that is critical for the formation of episodic memories.
47 pples and contribute to the consolidation of episodic memories.
48 ions, which are crucial for the formation of episodic memories.
49 tem and context information together to form episodic memories.
50 Hippocampal place cells are key to episodic memories.
51 crucial role selectively in the retrieval of episodic memories.
52 What brain regions underlie retrieval from episodic memory?
53 0.04], p=0.0096) and four cognitive domains (episodic memory -0.10 [0.04], p=0.017; semantic memory -
54 te -0.10 [0.03], p=0.0015) and four domains (episodic memory -0.12 [0.04], p=0.00090; semantic memory
56 on crucial for spatial navigation [6-12] and episodic memory [13-18], has been associated with attrac
59 al role of the medial temporal lobe (MTL) in episodic memory, age-related changes in MTL structure an
60 t with, in part, by endowing RL systems with episodic memory, allowing them to (a) efficiently approx
62 d in formation of spatiotemporal contexts in episodic memory, also represents gradually diverging nar
63 es in functioning of an MTL-based system for episodic memory and a striatum-based system for stimulus
64 Normal aging is associated with a decline in episodic memory and also with aggregation of the beta-am
66 inent, both for their vital contributions to episodic memory and for how these same nuclei appear vul
68 ghts into the intricate relationship between episodic memory and generalization, and constrains theor
69 he hippocampus has long been associated with episodic memory and is commonly thought to rely on neuro
70 d their implications for the organization of episodic memory and its contribution to functions in oth
72 brain region subserving roles of spatial and episodic memory and learning, is sensitive to the detrim
74 A greater than expected effect of ageing on episodic memory and motor function with advanced stages
75 ontexts in which these events occurred using episodic memory and support the view that rats may be us
76 irment.SIGNIFICANCE STATEMENT Alterations in episodic memory and the accumulation of Alzheimer's path
78 associated inversely with midlife visual and episodic memory and visuospatial associative learning (-
79 amental understanding of the neurobiology of episodic memory and will serve as a foundation for our c
80 g with this dynamic perspective, research on episodic memory (and the hippocampus) has infiltrated do
81 ork can use memories for specific locations (episodic memories) and statistical patterns of locations
82 gher-order functions such as theory-of-mind, episodic memory, and attention, causing debate about the
83 to brain aging outcomes (hippocampal volume, episodic memory, and executive function) using a general
85 Post-surgical change in visual and verbal episodic memory, and semantic memory at follow-up were e
86 ying the encoding of verbal information into episodic memory, and separately supported later remember
91 uggest that generalized threat responses and episodic memories are less susceptible to be modified by
95 findings suggest that the contents of human episodic memory are often constructed in the service of
96 heir relation with cerebral amyloid load and episodic memory as a function of estimated years to symp
99 t preferentially impact cognitive domains of episodic memory, attention, working memory, verbal seman
100 and executive function among VitD-deficient (episodic memory: beta = -0.04 [SE = 0.02], P = .049; exe
101 [SE = 0.02], P = .01) and VitD-insufficient (episodic memory: beta = -0.06 [SE = 0.02], P < .001; exe
102 availability was positively associated with episodic memory but not with working memory or speed.
103 mpal area CA1 is essential for consolidating episodic memories, but it is unclear how CA1 activity pa
105 ips between different events is essential to episodic memory, but little is currently known about its
106 line SUVR predicted an increasing decline in episodic memory, but other effects on cognition were mor
107 ial temporal lobes play an important role in episodic memory, but over time, hippocampal contribution
108 The hippocampus is thought to contribute to episodic memory by creating, storing, and reactivating p
109 stems, and the evolving conceptualization of episodic memory, can further neuroscientifically informe
110 hat memory for order, a core component of an episodic memory, capitalizes on the ubiquitous physiolog
111 cumab group and -0.93 in the placebo group), episodic memory (change in raw score, -1.53 and -1.53, r
113 ed during retrieval of integrated multimodal episodic memories compared with unimodal episodic memori
114 performance accuracy and speed in executive, episodic memory, complex cognition, social cognition and
116 analyses revealed that individual multimodal episodic memories could be differentiated in AnG, with c
118 howed that SAR218645 improved MK-801-induced episodic memory deficits in rats and attenuated working
124 he concurrent context reward value, enabling episodic memory for past experience to support future ad
125 that a reminder can retroactively strengthen episodic memory for Pavlovian threat-conditioned events,
127 essential for the formation and retrieval of episodic memory for which individual hippocampal subfiel
128 the early stages of AD is mostly limited to episodic memory, for which the hippocampus has a crucial
131 The mammalian hippocampus is crucial for episodic memory formation and transiently retains inform
134 dings provide the first direct evidence that episodic memory formation in humans relies on a theta-sp
136 rning computational model that accounted for episodic memory formation in single events for group ave
137 ecause emotional arousal typically increases episodic memory formation, the females' memory advantage
141 "SuperAgers," 80+-year-old individuals with episodic memory function at a level equal to, or better
143 torhinal circuit is a critical mechanism for episodic memory function, which is typically impaired in
144 esults demonstrate, for the first time, that episodic memory functionally relies on very rapid reacti
145 ution of the hippocampus to memory is not to episodic memory generally but to allocentric spatial mem
148 However, evidence of pathological effects on episodic memory has largely been limited to beta-amyloid
150 , imagining specific future experiences) and episodic memory (i.e., remembering specific past experie
151 rning in model-free and model-based systems, episodic memory, imagery, and planning, including some o
152 ult that is consistent with navigational and episodic memory impairments following damage to this reg
153 at it involves multiple events, and notably, episodic memory impairments in human diseases are not li
154 n supported by clinical reports of long-term episodic memory impairments in psychiatric conditions wi
155 al phenotypes, including motor coordination, episodic memory impairments, and synaptic plasticity def
157 fter right temporal lobe surgery, and visual episodic memory improved after left temporal lobe surger
159 medial temporal lobe instigates the loss of episodic memory in Alzheimer's disease, one of the earli
161 egions, Abeta, and MTL atrophy contribute to episodic memory in cognitively normal older adults (n =
162 combined evidence indicates that the loss of episodic memory in early Alzheimer's disease reflects mu
164 est whether similar techniques could improve episodic memory in humans, we implemented a microstimula
169 we offer a comprehensive characterization of episodic memory in representational terms, and propose a
170 unt of the metarepresentational structure of episodic memory in terms of its role in communicative in
171 m underlying spatial and temporal aspects of episodic memory in the hippocampus and shed new light on
172 a suggest a common mechanism for spatial and episodic memory in the hippocampus by providing an abstr
173 in vivo activation of Wnt signaling improves episodic memory, increases excitatory synaptic transmiss
176 l tagging occurs in humans to transform weak episodic memories into stable long-term memories is unkn
177 ts suggest that spontaneous recall of verbal episodic memories involves a spatiotemporal pattern of s
178 ifying the underlying cellular mechanisms of episodic memory is an important challenge, since this me
179 findings suggest that encoding of long-term episodic memory is associated with early remodeling of n
182 ploring the molecular underpinnings of human episodic memory is key to the understanding of hippocamp
183 e data provide neurobiological evidence that episodic memory is not a single construct, challenging t
184 ion of hippocampal circuits to high-capacity episodic memory is often attributed to the large number
185 cently learned events.SIGNIFICANCE STATEMENT Episodic memory is often discussed as a solitary constru
189 , the inability of adults to recollect early episodic memories, is associated with the rapid forgetti
191 brain networks, but the act of retrieving an episodic memory may place especially heavy demands for c
192 ablished brain-behaviour relationships (i.e. episodic memory: medial temporal lobe and angular gyrus;
193 rmation represents an important component of episodic memory, mediated by the parahippocampal-hippoca
194 le in declarative memory function, including episodic memory (memory for events) and semantic memory
196 esults were obtained for the analysis of the episodic memory network whether it was defined in a data
197 rtant implications for theoretical models of episodic memory, neurocognitive models of self, embodied
200 struct a meaningful association modeling the episodic memory of meeting a person in a particular plac
204 mechanism critical for a major component of episodic memory, opening a new and noncanonical research
205 nds to minutes) that characterize individual episodic memories, our results provide compelling eviden
207 o be nominally significantly associated with episodic memory (P = .009 and P = .013, respectively).
208 episodic memory (p = 0.010), delayed verbal episodic memory (p = 0.007), selective attention (p < 0.
209 nificant improvement in the immediate verbal episodic memory (p = 0.010), delayed verbal episodic mem
211 on effects were also noted in the domains of episodic memory (p=0.03) and motor function (p=0.02).
212 elve deeply into the structures that mediate episodic memory, particularly the hippocampus, and to tr
214 hese AGTR1 risk alleles also predicted worse episodic memory performance but were not related to othe
219 lyses of model parameters estimated from the episodic memory performance of 1,765 healthy young adult
221 essing in the visual cortex led to decreased episodic memory performance specifically for items encod
222 and high genetic risk indirectly influenced episodic memory performance through cortical thickness,
226 in vivo MTL tau pathology is associated with episodic-memory performance and MTL atrophy in cognitive
227 affected in old age as the best predictor of episodic-memory performance independent of Abeta status.
230 rtant for hippocampal synchronization during episodic memory processing; thus, it is assumed that the
231 lded significant SUVR x time interactions in episodic memory, processing speed, vocabulary, and Mini-
234 ntrol ( r = .34), working memory ( r = .28), episodic memory ( r = .26), and crystallized IQ ( r = .1
236 yloid over time (SUVR x time interaction) on episodic memory, reasoning, processing speed, vocabulary
237 ith hippocampal volume and activation during episodic memory recall, as measured by blood-oxygen-leve
238 Fos and Zif268 brain activation reveals that episodic memory recollection recruits a specific, distri
239 discrepancy in findings leaves it unclear if episodic memories reconsolidate, or only Pavlovian respo
240 y leaves out many aspects of memory, such as episodic memory, related to the traces of individual eve
242 variate pattern classifier could distinguish episodic memory representations in AnG according to whet
246 otemporal dynamics of parietal cortex during episodic memory retrieval and provide clear neurophysiol
247 Moreover, converging evidence suggests that episodic memory retrieval involves the reinstatement of
250 twork segregation-is markedly reduced during episodic memory retrieval relative to closely matched an
251 understand the cognitive and neural bases of episodic memory retrieval, as well as the extent to whic
252 twork of brain regions have been linked with episodic memory retrieval, but limited progress has been
253 brain is reduced when individuals engage in episodic memory retrieval, relative to other cognitive t
256 retrieval to dissociate three components of episodic memory: retrieval success, precision, and vivid
257 he ability to dissociate these components of episodic memory reveals the benefit afforded by measurin
258 ion score 15.4 versus 15.2, p = 0.68; verbal episodic memory score 4.4 versus 4.3, p = 0.79; semantic
259 site scores: beta estimate, -0.11; P = .001; episodic memory scores: beta estimate, -0.18; P < .001;
260 with lower scores indicating fewer errors), episodic memory (scores range from 0 to 70, with lower s
261 easures of global cognitive function, verbal episodic memory, semantic fluency, and calculation as we
262 n clusters using longitudinal assessments of episodic memory, semantic memory, executive function, an
263 perirhinal cortices during the retrieval of episodic memories, shaping how humans revisit the past.
265 rgence reflects an optimal ensemble size for episodic memories.SIGNIFICANCE STATEMENT One primary fac
266 is critical for both episodic simulation and episodic memory.SIGNIFICANCE STATEMENT Humans have the a
267 is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stres
268 gining (episodic simulation) or remembering (episodic memory) specific events also supports a willing
271 ted with functional alterations, often in an episodic memory system with a particular emphasis on med
273 is in 34 participants who performed a verbal episodic memory task while we recorded high gamma (62-10
274 better performance on hippocampus-dependent episodic memory tasks the next morning (beta-values from
277 ight of fixation at encoding, followed by an episodic memory test with centrally presented retrieval
278 y that suggests those details are bound into episodic memories that the rats use when faced with a fo
279 Across the domains of spatial navigation and episodic memory, the hippocampus is thought to play a cr
280 hile deactivation of either pathway impaired episodic memory, the resulting pattern of mnemonic defic
281 ucial for the formation and consolidation of episodic memory, their neurophysiological mechanisms are
282 model of how the brain supports non-spatial episodic memory, these findings suggest that EC neuronal
283 here is a switch from a reliance on detailed episodic memories to generalized schematic memories.
285 e functions, ranging from working memory and episodic memory to goal-directed learning and decision m
286 However, experimental traditions examining episodic memory use very different approaches, and these
287 ons, which suggests that nonhumans represent episodic memories using a structure similar to that of p
288 volumes and cognitive assessment to evaluate episodic memory using the verbal paired associates test.
289 nces were present in trained rats even after episodic memory was impaired and after other internal se
293 rises the true "state" of the task), and for episodic memory (where memories are believed to be organ
294 thy population with intellectual ability and episodic memory, whose impairment contributes to key sym
296 n hippocampus supports functions beyond just episodic memory, with human lesion studies suggesting a
297 ed the amount of neural interference between episodic memories within CA3, which in turn predicted ho
298 mation processing speed, executive function, episodic memory, working memory, and motor function.
299 ge who underwent comprehensive assessment of episodic memory, working memory, and processing speed, a
300 hrenia including general cognitive function, episodic memory, working memory, attentional control, an
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