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1 gnificant deficits in object recognition and spatial memory.
2 eral assays related to episodic, working and spatial memory.
3 al neurons is a key component of working and spatial memory.
4 -term potentiation and hippocampus-dependent spatial memory.
5 episodic memory generally but to allocentric spatial memory.
6 to the processing of wake and SWS-associated spatial memory.
7 VGF knock-out mice have impaired fear and spatial memory.
8 may be associated with improvement in visual-spatial memory.
9 directly mediated actions of inflammation on spatial memory.
10 ocampus, which could account for deficits of spatial memory.
11 normal performance in hippocampus-dependent spatial memory.
12 splay impairments in contextual learning and spatial memory.
13 is that are linked to age-related decline in spatial memory.
14 on in hippocampal long-term potentiation and spatial memory.
15 ecially important for spatial processing and spatial memory.
16 deleted mice, which also display deficits in spatial memory.
17 IC1a is not required for hippocampal LTP and spatial memory.
18 for the maintenance of reactivated long-term spatial memory.
19 ficits and dysfunction in working memory and spatial memory.
20 activity, and object placement, a measure of spatial memory.
21 l septum alters hippocampal theta rhythm and spatial memory.
22 otentiation and causes selective deficits in spatial memory.
23 sure did not significantly impair adolescent spatial memory.
24 al role in various cognitive tasks including spatial memory.
25 d deficits in synaptic plasticity but not in spatial memory.
26 eurons from FUS toxicity and preserved rats' spatial memory.
27 ribution of the ReRh to the persistence of a spatial memory.
28 brain glucose uptake, GLUT4 expression, and spatial memory.
29 tion deficits and impaired context-dependent spatial memory.
30 bnormal REM sleep propensity and deficits in spatial memory.
31 p, is essential for the proper expression of spatial memory.
32 on measures of immediate and delayed visual spatial memory.
33 e iCA1-->mPFC pathway deactivation disrupted spatial memory.
34 working memory but did not affect long-term spatial memory.
35 ith the strength of the sigmoidal pattern in spatial memory.
36 CTNNB1 in parvalbumin-interneurons enhanced spatial memory.
37 four conceptually different dynamic maps of spatial memory.
38 , including episodic memory, navigation, and spatial memory.
39 receptor to regulate object recognition and spatial memory.
40 overty predicts deficits in adult short-term spatial memory.
41 rhinal region improved the accuracy of human spatial memory.
42 wed treated eFSE rats to encode and retrieve spatial memories.
43 n and/or retrieval of precise contextual and spatial memories.
44 on and therefore prevents them from encoding spatial memories.
45 r encoding or storing long-term, associative spatial memories.
46 and in the encoding of hippocampal-dependent spatial memories.
47 and are associated with the consolidation of spatial memories.
49 ppocampal ACSS2 expression impairs long-term spatial memory, a cognitive process that relies on histo
50 SF) to understand how resource selection and spatial memory affect space use of feral hogs (Sus scrof
51 activation in turn prevented impairments in spatial memory after RSD but did not prevent deficits in
53 y considered crucial substrates of long-term spatial memory, although their precise role remains unce
54 opeptidase (IRAP) enhance fear avoidance and spatial memory and accelerate spatial learning in a numb
58 ce [5-7] in the spatial domain to compromise spatial memory and evaluated the impact of adding an olf
61 histone acetylation, and display deficits in spatial memory and impaired contextual fear extinction.
62 entorhinal cortex (mEC) plays a key role in spatial memory and is one of the first areas to express
63 from dorsal hippocampal networks involved in spatial memory and navigation to neocortical networks in
66 n an area implicated in long-term multimodal spatial memory and representation, even in the absence o
68 hort term, low-dose BPA exposure on anxiety, spatial memory and sucrose preference in adolescent rats
69 he previously demonstrated erasure of stored spatial memory and the disruption of place cell firing a
70 mice were impaired in locomotor activity and spatial memory and were resistant to seizure induction.
72 play a role in the offline consolidation of spatial memories, and in the generation of vivid percept
73 KO) exhibit defects in synaptic plasticity, spatial memory, and increased anxiety-related behaviors-
74 scent development increases anxiety, impairs spatial memory, and increases sucrose consumption indepe
75 on system, we investigated anxious behavior, spatial memory, and metabolic functions of conditional k
76 phisticated behaviors relating to predation, spatial memory, and visual recognition comparable to tho
77 ampus computes diverse information involving spatial memory, anxiety, or reward and directly projects
78 model, hippocampal place fields that support spatial memories are abnormal at old age (7-9 months) wh
81 Both directional coding and flexible use of spatial memory are upended, however, when a rat has to f
83 number of background strains and found that spatial memory assayed by the water maze and contextual
84 els in both cortical regions, the effects on spatial memory, assessed by spontaneous alternation, wer
86 e the spatial specificity of place cells and spatial memories at vastly different running speeds.
89 lexibility and diversity have been linked to spatial memory, attention and task performance, the cell
90 ylase inhibitor vorinostat not only restored spatial memory, but also exerted antiinflammatory action
91 ed G-1 from enhancing object recognition and spatial memory, but the ERK inhibitor U0126 did not.
92 nd of Broca (MSDB) have been associated with spatial memory, but the relationship between the two neu
93 prefrontal cortex, are important for rodent spatial memory, but their potential role in executive fu
95 d Physarum polycephalum constructs a form of spatial memory by avoiding areas it has previously explo
96 In the dentate gyrus - a key component of spatial memory circuits - granule cells (GCs) are known
101 ishment in CD3zeta(-/-) mice did not restore spatial memory defects, suggesting that the cognitive de
102 +) microglial activation correlates with the spatial memory deficit and spread of tau pathology in th
103 the acute compensation of EC lesion-induced spatial memory deficit before a slower glutamatergic rei
105 s old) rescued the early contextual fear and spatial memory deficits and decreased subsequent plaque
106 virus-mediated PGRN overexpression prevented spatial memory deficits and hippocampal neuronal loss in
107 roaggregant Tau transgenic mice restores the spatial memory deficits and normalizes the basic synapti
108 ing of APP/PS1 transgenic mice fully rescues spatial memory deficits and synaptic depletion, without
109 d, in a large sample of wild sea lions, that spatial memory deficits are predicted by the extent of r
111 (+/+) mice had a reduced survival, developed spatial memory deficits at 6 months and motor impairment
112 t acute stresses, which might be relevant to spatial memory deficits described in posttraumatic stres
113 We show that 14 prevents manifestation of spatial memory deficits in chimeric EcoHIV-infected mice
115 548G>T(KI/KI);Psen2(-/-) mice exhibited mild spatial memory deficits in the Morris water maze task.
116 ocampal inflammatory processes contribute to spatial memory deficits in the rodent social defeat mode
117 y found that daily scheduled feeding rescued spatial memory deficits in these arrhythmic animals.
119 ion of S6K1 improved synaptic plasticity and spatial memory deficits, and reduced the accumulation of
120 e model of Alzheimer's disease, JM6 prevents spatial memory deficits, anxiety-related behavior, and s
121 cluding sensory disturbances, and verbal and spatial memory deficits, not only in complicated HSP but
125 However, the extent to which navigational spatial memory depends on hippocampal integrity in human
126 o enhance hippocampal object recognition and spatial memory depends on rapid activation of extracellu
130 n hippocampal acetylcholine (ACh) efflux and spatial memory during tasks that varied in memory demand
131 ute stresses, with potential implications to spatial memory dysfunction in, for example, posttraumati
133 iences, hogs were able to discriminate among spatial memories encoded at different circadian phases o
134 ug-place preference, showing that recoding a spatial memory engram can alleviate associated maladapti
139 gh dose caused bees to make more and earlier spatial memory errors and take longer to complete the ta
141 rments of synaptic plasticity and defects in spatial memory exhibited by the Alzheimer's disease mode
142 Nestin-Cre mice exhibit a severe deficit in spatial memory extinction, whereas acquisition and long
143 a antagonist LY367385 blocked the object and spatial memory facilitation induced by E2, PPT, and DPN,
144 d inflammatory pain and opioid medication on spatial memory for a well-learned task in male Sprague-D
145 we found that TMS to the right OPA impaired spatial memory for boundary-tethered, but not landmark-t
146 condition placed a greater demand on visual-spatial memory for motion extrapolation, and thus partic
147 the MT1-MMP cytoplasmic domain in imprinting spatial memory for podosome reformation via assembly in
148 on of retinotopic to egocentric mappings, 2) spatial memory for the purposes of medium-term inhibitio
149 cal role of Crtc1-dependent transcription on spatial memory formation and provide the first evidence
150 ilarly propose that the known sparing of new spatial memory formation depends on the sparing of new m
151 t DBS of the entorhinal cortex (EC) enhances spatial memory formation in normal (wild-type) mice.
156 self-stress regulation on the development of spatial memory function in Long-Evans hooded rats, we sh
157 ring showed a novelty-induced enhancement in spatial memory function, whereas for mothers with poor s
158 implicated in hippocampal CA3 cell-dependent spatial memory functions that likely rely on dynamic cel
160 as long been implicated in both episodic and spatial memory, however these mnemonic functions have be
161 r1 KO) mice, an animal model of FXS, exhibit spatial memory impairment and synapse malfunctioning in
163 y provides a new murine model of WNV-induced spatial memory impairment, and identifies a potential me
164 y heterozygous BDNF Val66Met females exhibit spatial memory impairment, regardless of acute stress.
168 nimals (both male and female) displayed mild spatial memory impairments and disrupted cingulate netwo
169 1beta-HSD1 deficient mice are protected from spatial memory impairments with aging, but the underlyin
173 -guided focused ultrasound treatments led to spatial memory improvement in a Tg mouse model of AD Alz
176 impairments of pattern separation-associated spatial memory in AD mice are in part caused by degenera
177 s related to poorer attention, cognition and spatial memory in controls and people with PD for single
180 nt a role for hippocampus in nonnavigational spatial memory in macaques and demonstrate the efficacy
184 n protein synthesis, synaptic plasticity and spatial memory in mice that express familial Alzheimer's
188 navigation across species, but its role for spatial memory in nonnavigational tasks is uncertain.
189 agonist G-1 enhanced object recognition and spatial memory in ovariectomized female mice, whereas th
190 iota/lambda-antagonist disrupts late-LTP and spatial memory in PKMzeta-null mice but not in wild-type
191 General anesthesia has been shown to impair spatial memory in rats and this performance is dependent
193 eptide load in the brain, alpha-MSH improves spatial memory in TgCRND8 mice and prevents alterations
197 Aged C57BL/6J control mice showed impaired spatial memory in the Y-maze; this improved with GR bloc
198 that have been implicated in landmark-driven spatial memory in walking flies and memory for visual pa
200 at systemic pools of TIMP2 are necessary for spatial memory in young mice, while treatment of brain s
201 quisition of select types of associative and spatial memories increases the number of these cells tha
203 ransformation of a new hippocampal-dependent spatial memory into a remote one also depending on corti
204 approach has shown how the incorporation of spatial memory into animal movement models can improve e
206 behavioral tests reveal that in PC7 KO mice spatial memory is intact and plasticity of responding is
208 ctivation did enhance object recognition and spatial memory, it did so by activating different cell-s
210 us and CA1 subfields of the hippocampus form spatial memories just as well as wild-type mice, but the
212 w onto cognitive processing in tasks such as spatial memory, linguistic processing, and decision maki
214 , supporting the theory that an externalized spatial memory may be the functional precursor to the in
215 ssment demonstrated impaired recognition and spatial memory, measured by novel object recognition and
216 (Rey Auditory-Verbal Learning Test), visual-spatial memory (Medical College of Georgia Complex Figur
218 lthough CFA, by itself, had little effect on spatial memory, morphine administered to pain-free anima
219 of cognitive function, including deficits in spatial memory, object recognition, and fear conditionin
221 neurons in brain structures that instantiate spatial memory often exhibit firing fields that are stro
226 mining the role of theta phase precession in spatial memory, particularly sequence retrieval, are als
227 restored phosphorylation of beta-CaMKII and spatial memory performance in APP/PS1 Ear2(-/-) mice.
228 activation after psychosocial stress impairs spatial memory performance independent of deficits in ne
230 EB signaling in the hippocampus and impaired spatial memory performance, while optoA2AR activation in
234 the gene avpr1a) in brain regions related to spatial memory predict male space use and sexual fidelit
235 Here we identified significant, enduring spatial memory problems in male rats following experimen
240 beta + EB) groups failed to improve episodic spatial memory relative to oil-treated animals, indicati
243 loss of Lphn2 from the CA1 region increased spatial memory retention but decreased learning of seque
246 ys a key role in the selective regulation of spatial memory retrieval of stressful experience, sheddi
248 endent BDNF expression significantly impairs spatial memory reversal and contextual memory extinction
249 ted in tasks that do not require navigation, spatial memory seems unaffected by lesions of the hippoc
250 ffects of LCPUFAs were not found on tasks of spatial memory, simple inhibition, or advanced problem s
251 shifting structure), the hippocampus (as the spatial memory substrate), and the ventral midline thala
253 on, participants performed a virtual reality spatial memory task analogous to the Morris water maze a
254 vity in rats trained to perform a "standard" spatial memory task in a plus maze and in two new task v
255 nisms, we trained rats to perform a standard spatial memory task in a plus maze and tested how traini
258 f performance in a working memory task and a spatial memory task in rodents and nonhuman primates, re
268 common approach that approaches nonspecific spatial memory tasks to evaluate cognition, but also wou
269 linically relevant given that the object and spatial memory tasks used in monkeys are often translate
271 ficant improvements in performing short-term spatial memory tasks, which upon continued suppression t
275 well as dysfunctional hippocampus-dependent spatial memory tested in the object-placement and the Y-
277 als produced profound detrimental effects on spatial memory that persisted longer than the analgesic
278 cement in long-term depression, and weakened spatial memory, these changes were not observed in oxyto
279 ovide the first evidence that tPA influences spatial memory through its preferential interaction with
280 control hippocampal synaptic plasticity and spatial memory through the hyperpolarization-activated c
281 ve evolved life-histories requiring reliable spatial memories to support the task of provisioning the
284 data suggests that vision, echolocation, and spatial memory together with the possible exercise of an
286 rmining excitatory neuronal architecture and spatial memory via their ability to regulate Arc/Arg3.1.
291 lucocorticoid receptors (GRs)] are involved, spatial memory was measured in aged 11beta-HSD1(-/-) mic
293 sensory input from echolocation, vision, and spatial memory, we conducted an experiment in which bats
295 hippocampus is necessary for nonnavigational spatial memory, we selected a technique that avoids long
296 essing FKBP1b showed dramatic enhancement of spatial memory, which correlated with marked reduction o
297 ing a suite of sensory modalities that blend spatial memory with input from vision, tactile sensing,
298 engaging higher cognitive functions such as spatial memory, with significance for the "nature versus
299 drawn from self-administration and underwent spatial memory (Y-maze) and working memory (T-maze) test
300 .54 [1.67], p = 0.010, respectively), visual-spatial memory (z score = -1.65 [1.37], p = 0.008; z sco
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