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1 ) and remember episodes from the past (i.e., episodic memory).
2 ntributions of noradrenaline and dopamine to episodic memory.
3 ea of the hippocampus, regions important for episodic memory.
4  with nonhuman animals experience human-like episodic memory.
5 ivity did not modify sensorial perception or episodic memory.
6 ts the organization of events across time in episodic memory.
7 fic cognitive deficits and relatively spared episodic memory.
8 irment in multiple cognitive domains but not episodic memory.
9 theta (4-8 Hz) activity underlies successful episodic memory.
10  have been positively associated with verbal episodic memory.
11 ts we reveal their specific contributions to episodic memory.
12 he role of the alEC in representing time for episodic memory.
13 how the hippocampus codes time in support of episodic memory.
14 ng in how hippocampal networks might support episodic memory.
15 on, including attention, working memory, and episodic memory.
16 pocampus lesions suffer profound failures in episodic memory.
17  are meaningful in the context of real-world episodic memory.
18 eimer's disease, and their relationship with episodic memory.
19 nterference between statistical learning and episodic memory.
20 ons are critical for episodic simulation and episodic memory.
21 ind that a reminder can renew flexibility of episodic memory.
22 ng of the relationship between pathology and episodic memory.
23 ce cells represent the cellular substrate of episodic memory.
24  a temporal record of the past in support of episodic memory.
25  to be an electrophysiological biomarker for episodic memory.
26 e role of REM sleep in hippocampal-dependent episodic memory.
27 h may, in turn, be necessary for efficacious episodic memory.
28 l for understanding the neural mechanisms of episodic memory.
29 nce in performance across multiple assays of episodic memory.
30 ompassing its role in spatial navigation and episodic memory.
31 mpletion is a fundamental process supporting episodic memory.
32 ictable patterns of maternal care and poorer episodic memory.
33 lementary but distinct mechanisms supporting episodic memory.
34 (RPEs) as a key factor in the acquisition of episodic memory.
35 nformation in the human brain needed to form episodic memories.
36 t of the mammalian brain that is crucial for episodic memories.
37 x everyday experiences, such as emotions and episodic memories.
38 ocampus, resulting in vivid and long-lasting episodic memories.
39           Hippocampal place cells are key to episodic memories.
40 crucial role selectively in the retrieval of episodic memories.
41 ning theory, are crucial to the formation of episodic memories.
42 emporal integration of individual items into episodic memories.
43 s critical for the encoding and retrieval of episodic memories.
44   What brain regions underlie retrieval from episodic memory?
45 hat we use semantic memory in the service of episodic memory [2, 3].
46 scle mass (+ 1.4%)] and cognitive function [(episodic memory (+ 9.5%), processing efficiency (+ 7.5%)
47                                              Episodic memory, a fundamental component of human cognit
48                                           As episodic memory abilities continue to develop across chi
49 ampus contributes to developmental change in episodic memory abilities remains unclear.
50 broad indicator of individual differences in episodic memory ability.
51 twork aligns with neuroimaging correlates of episodic memory, abnormalities in Alzheimer's disease, a
52  line with previous behavioral observations, episodic memory accuracy increases with the magnitude of
53 es the experimental manipulation of SRPEs on episodic memory accuracy.
54 l predictions related to the role of RPEs in episodic memory acquisition remain to be tested.
55 al role of the medial temporal lobe (MTL) in episodic memory, age-related changes in MTL structure an
56 t with, in part, by endowing RL systems with episodic memory, allowing them to (a) efficiently approx
57                                              Episodic memory allows us to mentally travel through tim
58 es.SIGNIFICANCE STATEMENT The flexibility of episodic memory allows us to remember both the details t
59                     Our results indicate the episodic memories also reconsolidate, allowing strengthe
60 ntegrated into neuronal circuits that encode episodic memories and plays an important role in guiding
61 Normal aging is associated with a decline in episodic memory and also with aggregation of the beta-am
62 igher risk of poor (lowest quartile) midlife episodic memory and associative learning (relative risk
63 gienic parental smoking were nonsignificant (episodic memory and associative learning: RR = 1.19, 95%
64 l, lesion, neuroimaging and sleep studies of episodic memory and contend that forgetting is largely d
65 ion of subjective measures of threat memory, episodic memory and exploration behaviour between the re
66 ement of the CRN to the temporal dynamics of episodic memory and highlight the role of alpha rhythms
67 ries and explain how they are different from episodic memory and how they can guide action in animal
68                       We investigated verbal episodic memory and intrinsic functional connectivity in
69  prompts a reassessment of the definition of episodic memory and its distinction from semantic memory
70 brain region subserving roles of spatial and episodic memory and learning, is sensitive to the detrim
71 er, particularly with tests referable to the episodic memory and motor domains.
72  A greater than expected effect of ageing on episodic memory and motor function with advanced stages
73 have theorized that the hippocampus supports episodic memory and navigation via the theta oscillation
74 re also conducted with composite measures of episodic memory and perceptual speed.
75    Remembering event sequences is central to episodic memory and presumably supported by the hippocam
76  knockdown impaired HPC-dependent contextual episodic memory and reduced HPC brain-derived neurotroph
77                             We conclude that episodic memory and scene imagination share fundamental
78 works to support cognitive abilities such as episodic memory and semantic prediction.
79 ion to support the variable phenomenology of episodic memory and simulation.
80                                           If episodic memory and spatial navigation are 2 sides of th
81 dial temporal lobe (MTL) is known to support episodic memory and spatial navigation, raising the poss
82 on critical for cognitive functions, such as episodic memory and spatial navigation.
83 mation is a crucial functional substrate for episodic memory and spatial representation.
84 irment.SIGNIFICANCE STATEMENT Alterations in episodic memory and the accumulation of Alzheimer's path
85 f cognitive and brain function, particularly episodic memory and the underlying hippocampal function.
86 associated inversely with midlife visual and episodic memory and visuospatial associative learning (-
87 ial temporal lobe are critically involved in episodic memory and, at the same time, affected by tau p
88 ork can use memories for specific locations (episodic memories) and statistical patterns of locations
89 t on the mechanism through which ECT impairs episodic memory, and additionally underline the importan
90   Then I discuss research on working memory, episodic memory, and autobiographical memory as examples
91 gnitive problems, especially disturbances in episodic memory, and hippocampal sclerosis are common in
92 s supporting mesolimbic dopamine activation, episodic memory, and perception.
93              The hippocampus is critical for episodic memory, and synaptic changes induced by long-te
94 ore suggest that internal models formed from episodic memories are generated throughout the visual hi
95                                              Episodic memories are information-rich, often multisenso
96 uggest that generalized threat responses and episodic memories are less susceptible to be modified by
97                                      Because episodic memories are rooted in the space in which they
98                                              Episodic memories are shaped by the representational for
99 ynaptic circuits involved in the encoding of episodic memory are compromised in AD mouse models.
100  findings suggest that the contents of human episodic memory are often constructed in the service of
101 suggests that cognitive processing speed and episodic memory are the most frequently affected cogniti
102 heir relation with cerebral amyloid load and episodic memory as a function of estimated years to symp
103 al memory, a compound capacity incorporating episodic memory, as a case study.
104 c Resonance Imaging, with annual (1999-2010) episodic memory assessment by the California Verbal Lear
105 nt recollection accuracy of one-shot learned episodic memory associations.
106 t preferentially impact cognitive domains of episodic memory, attention, working memory, verbal seman
107 ng Instrument and in five cognitive domains (episodic memory, attention/working memory, executive fun
108  contributions to semantic prediction versus episodic memory based on stimulation rhythm, supporting
109 that is important for spatial navigation and episodic memory, benefits from a rich diversity of neuro
110 /- SE = -0.012 +/- 0.002; P < 0.001), verbal episodic memory (beta +/- SE = -0.009 +/- 0.002; P < 0.0
111 n the hippocampus negatively correlated with episodic memory (beta = -0.24; 95% CI: -0.40, -0.08; P =
112 t death was unrelated to residual decline in episodic memory but was related to residual decline in p
113 mpal area CA1 is essential for consolidating episodic memories, but it is unclear how CA1 activity pa
114  that the angular gyrus (AnG) is involved in episodic memory, but its precise role has yet to be dete
115 line SUVR predicted an increasing decline in episodic memory, but other effects on cognition were mor
116  is known as the locus of spatial coding and episodic memory, but the interaction between these cogni
117 al factors, perhaps involving associative or episodic memory, can exert a dramatic effect on function
118 cumab group and -0.93 in the placebo group), episodic memory (change in raw score, -1.53 and -1.53, r
119 ontextual information to be maintained in an episodic memory circuit.
120 pocampus and other brain regions critical to episodic memory code for the passage of time at a range
121 hin the LEC contribute to the integration of episodic memory components.
122 direct contribution of awake time periods to episodic memory consolidation.
123 mmonly referred to as "autobiographical" or "episodic" memories, critically relies on the hippocampus
124 earned schemas as well as their influence on episodic memory decisions.
125                                  Age-related episodic memory decline is characterized by striking het
126 commentary refers to 'Particulate matter and episodic memory decline mediated by early neuroanatomic
127  dysfunction that underlie the expression of episodic memory decline using fMRI measures of hippocamp
128 l study to examine whether PM2.5 affects the episodic memory decline, and also explored the potential
129 ccumulation and MTL dysfunction may underlie episodic-memory decline in aging and dementia.
130                                              Episodic memory deficits are consistently documented as
131 n resting-state hippocampal connectivity and episodic memory deficits following one night of total sl
132                                              Episodic memories depend on the hippocampus but have bee
133 pocampal maturation can provide insight into episodic memory development, as well as clues to episodi
134  as occurring mainly in the autobiographical-episodic memory domain and this is considered to depend
135 learning) predict the strength of subsequent episodic memory (during recollection).
136 unit activity is temporally organized during episodic memory encoding and retrieval.
137 sexes, cerebellar theta stimulation improved episodic memory encoding but did not influence neural si
138                    First, stimulation during episodic memory encoding impaired subsequent free recall
139 ry activity.SIGNIFICANCE STATEMENT Models of episodic memory encoding predict that theta oscillations
140 ovide converging evidence that action boosts episodic memory encoding via a noradrenergic mechanism.
141 offer causal evidence implicating the PCC in episodic memory encoding.
142 of semantic prediction but did not influence episodic memory encoding.
143 oninvasive brain stimulation have identified episodic memory enhancements and modulation of activity
144 the hippocampus, is jointly recruited during episodic memory, episodic simulation, and divergent crea
145  consolidation and computational theories of episodic memory, evidence from model organisms suggests
146 and reward on two forms of long-term memory: episodic memory for neutral objects and memory for stimu
147 he concurrent context reward value, enabling episodic memory for past experience to support future ad
148 that a reminder can retroactively strengthen episodic memory for Pavlovian threat-conditioned events,
149 essential for the formation and retrieval of episodic memory for which individual hippocampal subfiel
150 eactivation, a neural mechanism critical for episodic memory formation and consolidation, takes place
151         The hippocampus is the main locus of episodic memory formation and the neurons there encode t
152        Models of memory formation posit that episodic memory formation depends critically on the hipp
153                                              Episodic memory formation depends on information about a
154                     Here, we show that human episodic memory formation depends on phase synchrony bet
155 dings provide the first direct evidence that episodic memory formation in humans relies on a theta-sp
156  of experimentally induced theta rhythms and episodic memory formation in humans.
157 uential patterns thought to be important for episodic memory formation.
158 s to reveal the neural substrates underlying episodic memory formation.
159  suggesting a central role of these areas in episodic memory formation.
160 campus is crucial for spatial navigation and episodic memory formation.
161 " gamma (60 to 80 Hz) power increases during episodic memory formation; during episodic memory retrie
162 ng intracranial EEG recordings, we show that episodic memories formed after a single visual experienc
163                         Existing accounts of episodic memory function that have focused on explaining
164 ctable maternal sensory signals and impaired episodic memory function.
165                                On this view, episodic memory has a metarepresentational format and sh
166                                              Episodic memory has been analyzed in a number of differe
167 However, evidence of pathological effects on episodic memory has largely been limited to beta-amyloid
168 ry systems, but the role of these signals in episodic memory has not been fully characterized.
169 tial spatial trajectory learning, a model of episodic memory, has remained equivocal, with proposals
170                                              Episodic memories hinge upon our ability to process a wi
171                             Human studies of episodic memory, however, have provided mixed evidence f
172 , imagining specific future experiences) and episodic memory (i.e., remembering specific past experie
173 reward prediction errors on the formation of episodic memories, (ii) dissociate this influence from s
174                               Prosopagnosia, episodic memory impairment and behavioural changes such
175 itive neuroscience revealed disproportionate episodic memory impairments in schizophrenia (Sz) under
176           However, ECT frequently results in episodic memory impairments, causing many patients to di
177 al connectivity underpinnings of ECT-induced episodic memory impairments.
178 s in the medial temporal lobe (MTL) underlie episodic-memory impairments in AD dementia.
179 the brain shapes the ongoing experience into episodic memories in the real-life.
180  medial temporal lobe instigates the loss of episodic memory in Alzheimer's disease, one of the earli
181 match the two primary approaches to studying episodic memory in an unparalleled manner.
182 egions, Abeta, and MTL atrophy contribute to episodic memory in cognitively normal older adults (n =
183 est whether similar techniques could improve episodic memory in humans, we implemented a microstimula
184 ntifying the effect of the drug on emotional episodic memory in humans.
185 we offer a comprehensive characterization of episodic memory in representational terms, and propose a
186 unt of the metarepresentational structure of episodic memory in terms of its role in communicative in
187 The medial temporal lobe (MTL) is a locus of episodic memory in the human brain.
188                                              Episodic memories initially require rapid synaptic plast
189                                   In adults, episodic memory involves a distributed neural circuit in
190                                   Successful episodic memory involves dynamic increases in activity a
191                       Retrieval of long-term episodic memories is characterized by synchronized neura
192 dicate that the ability to retrieve distinct episodic memories is related to how quickly neural repre
193                                              Episodic memory is believed to be intimately related to
194 ation.SIGNIFICANCE STATEMENT Because loss of episodic memory is considered the cognitive hallmark of
195                                              Episodic memory is critical to human functioning.
196                             Early decline of episodic memory is detectable in preclinical Alzheimer's
197  Together, these data demonstrate that human episodic memory is encoded by specific sequences of neur
198 e data provide neurobiological evidence that episodic memory is not a single construct, challenging t
199 cently learned events.SIGNIFICANCE STATEMENT Episodic memory is often discussed as a solitary constru
200           There is widespread agreement that episodic memory is organized into a timeline of past exp
201                              The hallmark of episodic memory is recollecting multiple perceptual deta
202                                              Episodic memory is sensitive to the influence of neuromo
203                                              Episodic memory is thought to critically depend on inter
204 , the inability of adults to recollect early episodic memories, is associated with the rapid forgetti
205 rved age-sensitive cognitive functions, like episodic memory, is an often-suggested criterion.
206 standing differences between the spatial and episodic memory literatures.
207  human CA3 is necessary for the retrieval of episodic memories long after their initial acquisition a
208 rhinal cortex, as a substrate of age-related episodic-memory loss.
209 oss childhood and into adolescence, studying episodic memory maturation can provide insight into the
210 brain networks, but the act of retrieving an episodic memory may place especially heavy demands for c
211 ablished brain-behaviour relationships (i.e. episodic memory: medial temporal lobe and angular gyrus;
212 NCE STATEMENT For the encoding and recall of episodic memories, nerve cells in the cerebral cortex ar
213 odic sampling, decisions are guided by a few episodic memories of past choices.
214 ting evidence about the dependence of remote episodic memories on the hippocampus.
215  mechanism critical for a major component of episodic memory, opening a new and noncanonical research
216                    Lower risk of poor verbal episodic memory (OR: 0.784; 95% CI: 0.641, 0.959; P = 0.
217  episodic memory (p = 0.010), delayed verbal episodic memory (p = 0.007), selective attention (p < 0.
218 nificant improvement in the immediate verbal episodic memory (p = 0.010), delayed verbal episodic mem
219  in immediate (p = 0.045) and delayed verbal episodic memory (p = 0.040) compared to baseline.
220 on effects were also noted in the domains of episodic memory (p=0.03) and motor function (p=0.02).
221  stronger link between dedifferentiation and episodic memory performance in older than in younger adu
222  and high genetic risk indirectly influenced episodic memory performance through cortical thickness,
223 ther neural differentiation is predictive of episodic memory performance, and whether the relationshi
224 nces were both associated with reductions in episodic memory performance.
225 lt network is important for autobiographical episodic memory performance.
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.
228 cate the posterior cingulate cortex (PCC) in episodic memory processing, making it a potential target
229 n of scene imagery is a crucial component of episodic memory processing.
230 lded significant SUVR x time interactions in episodic memory, processing speed, vocabulary, and Mini-
231 ntrol ( r = .34), working memory ( r = .28), episodic memory ( r = .26), and crystallized IQ ( r = .1
232       Older adults experience impairments in episodic memory, ranging from mild to clinically signifi
233 yloid over time (SUVR x time interaction) on episodic memory, reasoning, processing speed, vocabulary
234 ith hippocampal volume and activation during episodic memory recall, as measured by blood-oxygen-leve
235 discrepancy in findings leaves it unclear if episodic memories reconsolidate, or only Pavlovian respo
236                                              Episodic memories reflect a bound representation of mult
237  specific deficits in component processes of episodic memory reflect impaired activation and connecti
238                                              Episodic memory reflects the ability to recollect the te
239 y leaves out many aspects of memory, such as episodic memory, related to the traces of individual eve
240 new flexibility of threat responses but that episodic memories remain stable.
241 g is largely due to contextual interference, episodic memory remains dependent on the hippocampus acr
242  with age, and contributes to variability in episodic memory, remains unclear.
243                              This identifies episodic memory replay as a dynamic process in which par
244                     Even though there was no episodic memory requirement in the perceptual task, a we
245                                              Episodic memory requires different types of information
246                                              Episodic memory requires linking events in time, a funct
247 it is unclear how the networks that underlie episodic memory respond to vascular constraints that ult
248                      Age-related deficits in episodic memory result, in part, from declines in the in
249 r understanding of dopaminergic processes in episodic memory retrieval and offer new perspectives on
250 constitute the first evidence in humans that episodic memory retrieval and scene imagination rely on
251  Moreover, converging evidence suggests that episodic memory retrieval involves the reinstatement of
252 ns in the hippocampus.SIGNIFICANCE STATEMENT Episodic memory retrieval is characterized by a dialog b
253                                              Episodic memory retrieval is increasingly influenced by
254                                              Episodic memory retrieval is thought to rely on the repl
255 twork segregation-is markedly reduced during episodic memory retrieval relative to closely matched an
256                                              Episodic memory retrieval relies on the recovery of neur
257 us fMRI reports of IPL activity arising from episodic memory retrieval, according to the type of info
258 ses during episodic memory formation; during episodic memory retrieval, however, hippocampal "slow" g
259  brain is reduced when individuals engage in episodic memory retrieval, relative to other cognitive t
260 ment of cortical representations during free episodic memory retrieval.
261       Drawing on recent work that identifies episodic memory's influence on decisions for reward, we
262 ion score 15.4 versus 15.2, p = 0.68; verbal episodic memory score 4.4 versus 4.3, p = 0.79; semantic
263  with lower scores indicating fewer errors), episodic memory (scores range from 0 to 70, with lower s
264 easures of global cognitive function, verbal episodic memory, semantic fluency, and calculation as we
265                                We argue that episodic memory should be understood as a distinctive ep
266 rgence reflects an optimal ensemble size for episodic memories.SIGNIFICANCE STATEMENT One primary fac
267 rts the role of theta-band activity in human episodic memory.SIGNIFICANCE STATEMENT Can noninvasive s
268 is critical for both episodic simulation and episodic memory.SIGNIFICANCE STATEMENT Humans have the a
269 s as key factors subtending the formation of episodic memory.SIGNIFICANCE STATEMENT Recent behavioral
270  is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stres
271 main regarding the role of hippocampal-based episodic memory systems.
272  electroencephalography and a hybrid spatial-episodic memory task (29 subjects, 15 female) to determi
273 is in 34 participants who performed a verbal episodic memory task while we recorded high gamma (62-10
274  27 human epilepsy patients who performed an episodic memory task.
275 predicted improved performance of a separate episodic memory test.
276 were undistinguishable on neuropsychological episodic memory tests.
277 ther hippocampal-dependent processes such as episodic memory that are central to supporting our menta
278 with performance in another cognitive domain-episodic memory-that is also highly vulnerable to aging.
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     The hippocampus plays a critical role in episodic memory: the sequential representation of visite
282 e dopamine had an effect on reward-modulated episodic memory, there was no effect of dopamine on memo
283  is a central concept in current theories of episodic memory: this computation is thought to support
284                  Scientific understanding of episodic memory thus far relied upon separate lines of r
285 hich are thought to be critical for enabling episodic memories to be formed and stored in CA3.
286  consolidation processes may transform novel episodic memories to reflect such regularities.
287 ontaneous thought, semantic memory scaffolds episodic memory to form the content of thought, and drif
288                                              Episodic memories typically comprise multiple elements.
289   However, experimental traditions examining episodic memory use very different approaches, and these
290 volumes and cognitive assessment to evaluate episodic memory using the verbal paired associates test.
291 ssible to toggle cerebellar participation in episodic memory versus semantic prediction by noninvasiv
292 -parietal networks that respectively support episodic memory versus semantic prediction have been ass
293 rk-specific frequencies selectively enhanced episodic memory versus semantic prediction.
294                     The hippocampus supports episodic memory via interaction with a distributed brain
295 mposite scores including executive function, episodic memory, visual-spatial processing, and language
296              Among temporal lobe subregions, episodic memory was most strongly related to tau-tracer
297 n" paradigm based on computational models of episodic memory, we report evidence that the ORE may be
298 n hippocampus supports functions beyond just episodic memory, with human lesion studies suggesting a
299 mation processing speed, executive function, episodic memory, working memory, and motor function.
300 d couple to successfully create and retrieve episodic memories, yet this hypothesis has not been test

 
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