ライフサイエンスコーパス: associative memory

1 ion processing speed, executive function and associative memory.

2 APPL, the fly APP ortholog, is required for associative memory.

3 ective role of FMRP in hippocampus-dependent associative memory.

4 encoding and retrieval of olfactory-spatial associative memory.

5 d noninvasively, demonstrating their role in associative memory.

6 fect cognitive performance or discriminative associative memory.

7 nal impairment in the areas of attention and associative memory.

8 cuit and impaired the formation of long-term associative memory.

9 significantly decreases the ability to form associative memory.

10 itive ability (P = .01) but not attention or associative memory.

11 tex plays a critical role in recognition and associative memory.

12 ate two spatially distinct stimuli to encode associative memory.

13 that zebrafish larvae can exhibit long-term associative memory.

14 theories of short-term memory and long-term associative memory.

15 is involved in a specific component of late associative memory.

16 est predicts individual differences in later associative memory.

17 reas in mediating innate odour preference or associative memory.

18 aptic plasticity that underlies drug-induced associative memory.

19 tivity predicts subsequent familiarity-based associative memory.

20 suggesting deficits in non-aversive and non-associative memory.

21 ory, indicating a stable neural correlate of associative memory.

22 ) signaling is required for the formation of associative memory.

23 n mushroom body neurons for the formation of associative memory.

24 wed low levels of freezing, indicative of no associative memory.

25 types of cognitive processing, particularly associative memory.

26 aired with NB stimulation induced behavioral associative memory.

27 te the central brain structure for olfactory associative memory.

28 her stimulation of the NB induces behavioral associative memory.

29 ring induction, consolidation and storage of associative memory.

30 in structures involved in the storage of the associative memory.

31 g-term facilitation, a cellular model of non-associative memory.

32 oupling closer to the peak is beneficial for associative memory.

33 perlocomotion without affecting drug-context associative memory.

34 for hippocampal theta oscillations in human associative memory.

35 he sampling of a taste can also lead to such associative memory.

36 which were regulated during consolidation of associative memory.

37 as cardinal centers that in insects mediate associative memory.

38 e of the hippocampus in scene processing vs. associative memory.

39 Presynaptic PUMILIOs regulate associative memory.

40 e found that reward motivation enhanced 24 h associative memory.

41 arning and memory, as well as in working and associative memory.

42 e mammalian piriform cortex and a center for associative memory.

43 Overexpression of DISC1 impairs associative memory.

44 ction of temporal plasticity, and deficit in associative memory.

45 s contributes to the integration of rewarded associative memories.

46 sychiatric condition perpetuated by unwanted associative memories.

47 ctional neuronal networks capable of storing associative memories.

48 he hippocampus and the formation of temporal associative memories.

49 ted in the expression and reconsolidation of associative memories.

50 reconsolidation of context-response-cocaine associative memories.

51 nces of externally triggered reactivation of associative memories.

52 es to a sensory stimulus are often guided by associative memories.

53 are involved in the initial formation of new associative memories.

54 or consolidation of short-term and long-term associative memories.

55 encoding of subjectively arousing, positive associative memories.

56 timing of encoding and recall of cue-object associative memories.

57 scillatory activity enables the formation of associative memories.

58 ontrast, all control conditions did not form associative memories.

59 g were reflected by increased specificity of associative memories.

60 mPFC) during the formation of opiate-related associative memories.

61 for the availability of previously acquired associative memories.

62 he consolidation, retrieval or extinction of associative memories.

63 es the retrieval of context-response-cocaine associative memories.

64 s of rewarding or aversion-related emotional associative memories.

65 or overall cognitive ability, attention, and associative memory 1 week after discharge and 6 and 12 m

66 e-induced gamma predicted the acquisition of associative memory 24 h later and ceased to predict subs

67 docannabinoid signaling facilitated temporal associative memory acquisition and, after training anima

68 ty of the plasticity and generalizability of associative memories across odors.

69 mponents of hippocampal-dependent visuomotor associative memories after variable retention intervals,

70 ions preferentially support the formation of associative memories, although we also observed memory-r

71 ructure for the processing of opiate-related associative memories and is functionally linked to the m

72 the selective consolidation of object-based associative memories and provide support for the notion

73 iative memory networks that includes a Dense Associative Memory and a Transformer as two limiting cas

74 functions than previously thought, including associative memory and emotional memory, as well as cons

75 s functional connection correlated with both associative memory and information processing speed and

76 Associative memory and item memory are differentially af

77 Associative memory and item memory are dramatically affe

78 oAbeta- and oTau-induced defects in spatial/associative memory and LTP.

79 s were not previously identified in positive associative memory and may specifically regulate aversiv

80 geneous autoassociative network critical for associative memory and pattern completion.

81 ovide structural storage sites for long-term associative memory and sites for memory-specific synapto

82 The hippocampus is implicated in associative memory and spatial navigation.

83 rirhinal cortex (PER), which is critical for associative memory and stimulus discrimination, has been

84 that was actively maintained during both the associative memory and working memory tasks.

85 l or nonspatial), process (working memory or associative memory), and mode of response (oculomotor or

86 at specificity, maximize storage capacity of associative memories, and provide an energy efficient in

87 ts on cognition, formation of discriminative associative memory, and emotional behavior in vivo.

88 ical role of CRTC1 in the hippocampus during associative memory, and provide evidence that CRTC1 dere

89 lay integrative roles in emotional learning, associative memory, and sensory perception.

90 However, less is known about how item and associative memories are consolidated.

91 In a standard model, associative memories are represented by assemblies of st

92 r networks is the leading hypothesis for how associative memories are stored and recalled.

93 This suggests that in humans associative memories are stored in balanced excitatory-i

94 ed performance in the courtship conditioning associative memory assay, but it was unknown whether the

95 dy, we investigated whether the formation of associative memory (associations between items) and sour

96 use it has all of the cardinal attributes of associative memory: associativity, specificity, rapid in

97 ttery comprised tests of associative and non-associative memory, attention, language, visuospatial an

98 ce, make the strong case that CA3 constructs associative memories based on attractor dynamics.

99 Context-drug associative memories become destabilized on retrieval an

100 ed a paradigm in which participants acquired associative memories before taking a nap.

101 e outcome z scores over 2-year follow-up for associative memory (beta coefficient, -0.31 [95% confide

102 sly to be necessary for the formation of the associative memory between a neutral stimulus (tone [CS]

103 hen the mouse has the opportunity to form an associative memory between the cocaine-paired context an

104 These associative memory biases were especially pronounced for

105 Here, we investigate associative memory binding during PTA and test the hypot

106 la complex (BLA) mediates the acquisition of associative memories, both positive and negative.

107 city are crucial for the initial encoding of associative memories but likely insufficient to enable t

108 t (REM) sleep enhances hippocampus-dependent associative memory, but REM deprivation has little impac

109 t sea anemone Nematostella vectensis to form associative memories by using a classical conditioning a

110 e animals were further tested for changes in associative memory by employing a passive avoidance cond

111 uential notion that the hippocampus supports associative memory by interacting with functionally dist

112 nyon cells, the neurons that store olfactory associative memories, by ectopically expressing NaChBac,

113 Such associative memories can be weakened through interferenc

114 he release of innate responses and recall of associative memories can occur through focused disinhibi

115 Associative memory can be rendered malleable by a remind

116 re we show that fear conditioning, a type of associative memory, can be inactivated and reactivated b

117 The Drosophila mushroom body (MB) is a key associative memory center that has also been implicated

118 speckle tracking echocardiography variables, associative memory classifier achieved a diagnostic area

119 Furthermore, the associative memory classifier demonstrated greater accur

120 ceiver operating characteristic curve of the associative memory classifier was evaluated for differen

121 e cardiomyopathy were used for developing an associative memory classifier-based machine-learning alg

122 This associative memory component has previously been propose

123 pus; instead, both source discrimination and associative memory correlated highly with performance on

124 sessed: item memory (object recognition) and associative memory (cued recognition of scenes associate

125 nsmission as well as working, reference, and associative memory deficits for at least 2 months after

126 ial learning and memory and conditioned fear-associative memory deficits.

127 s strongly indicate that irradiation impairs associative memories dependent on hippocampus and this d

128 nd CA1 selectively correlated with long-term associative memory, despite subjects actively engaging i

129 Associative memory enables the encoding and retrieval of

130 a, had structural MRI, functional MRI during associative memory encoding and novel viewing and contro

131 g, structural MRI, and functional MRI during associative memory encoding and resting-state and cognit

132 dentify hippocampal correlates of successful associative memory encoding and retrieval in patients (1

133 tive processes support MOGS, predicting that associative memory encoding during inter-trial periods w

134 s in the hippocampus selectively involved in associative memory encoding.

135 ts: complex figure drawing and the face-name associative memory exam (FNAME).

136 expert system (FuRES) and the fuzzy optimal associative memory (FOAM) for the first time, were used

137 hat is, orthogonal basis (OB), fuzzy optimal associative memory (FOAM), and polynomial fitting (PF),

138 that underlies the formation of long-lasting associative memories for environmental cues paired with

139 n primary auditory cortex modulates both the associative memory for an auditory stimulus during class

140 Within regions predicting subsequent associative memory for directly learned associations, en

141 e VTA and the anterior hippocampus predicted associative memory for high- but not low-reward memories

142 ptive social decision-making requires intact associative memory for previous social interactions.

143 moderate drinkers (p < 0.001), but enhanced associative memory for scenes paired with alcohol (p = 0

144 y bias in AUD, and uncover the importance of associative memory for understanding real-world heavy al

145 This represents the first demonstration that associative memory formation after single-trial appetiti

146 Associative memory formation and recall in the fruit fly

147 the observed non-random network structure on associative memory formation and recall.

148 C) is a classical laboratory task that tests associative memory formation and recall.

149 , in the posterior cingulate cortex predicts associative memory formation at encoding.

150 naptic strengths, is dispensable for initial associative memory formation but crucial for the establi

151 midlarval zebrafish brain that occur during associative memory formation by imaging excitatory synap

152 unction of GluA4 for synaptic excitation and associative memory formation in the cerebellum.

153 ivo functional imaging studies revealed that associative memory formation is coupled to a cascade of

154 Associative memory formation is essential for an animal'

155 A central feature of models of associative memory formation is the reliance on informat

156 Associative memory formation requires that animals choos

157 s neural plasticity is the physical basis of associative memory formation, and although the intracell

158 re essential for motor and sensory learning, associative memory formation, and the vestibular ocular

159 stand the patterns of neural activity during associative memory formation, we recorded the activity o

160 a results in the impaired aversive olfactory associative memory formation.

161 across spatiotemporal discontiguities during associative memory formation.

162 ly affected by, and potentially involved in, associative memory formation.

163 er to the phase of the theta rhythm supports associative memory formation.

164 ural activity during dentate spikes disrupts associative memory formation.

165 ons is necessary for cellular plasticity and associative memory formation.

166 When incorporated into a simple associative memory framework, we show that TILT predicts

167 ncoding in terms of increased specificity of associative memories from the first to the second cued a

168 ding brain mechanisms that support long-term associative memory from childhood to adulthood in human

169 Associative memories guide behavioural adaptation by bin

170 Additionally, we show that the associative memory Hamiltonian is also capable of reprod

171 amine both approaches using a version of the associative memory Hamiltonian that incorporates the inf

172 tein structure prediction codes based on the associative memory Hamiltonian were used to probe the bi

173 sequence separation the energy functions are associative memory Hamiltonians constructed from a datab

174 for the optimal energy functions, which are associative memory hamiltonians using a database of fold

175 ever, the role of CaN in regulating drug-cue associative memories has not been investigated.

176 t to the mushroom bodies that play a role in associative memories has proved challenging.

177 diagram of a higher-order circuit supporting associative memory has not been previously available.

178 pus-a brain structure critical to relational/associative memory-has remarkable plasticity as a result

179 In AD, deficits in episodic and associative memory have been linked to structural and fu

180 urface trafficking sustains the formation of associative memory, however, remains unknown.

181 studies of the cortical substrates of visual associative memory, I propose a specific functional proc

182 Associative memory impairment is an early clinical featu

183 spatial working memory only in females while associative memory impairments are reversed in males and

184 ALKBH8 null animals also exhibit associative memory impairments that are reversed by phar

185 provide evidence for reinstatement of unique associative memories in early visual cortex and suggest

186 we show that the formation of reward-related associative memories in rats upregulates key plasticity

187 cellular mechanisms that underlie long-term associative memories in several forebrain circuits (invo

188 ere, we study the formation and retention of associative memory in a computational model based on Heb

189 on processing speed, executive function, and associative memory in a group of 70 heterogeneous patien

190 lations were uniquely linked with successful associative memory in both the anterior and posterior hi

191 e, we show for the first time that olfactory associative memory in Drosophila requires signaling by P

192 led a temporal dissociation between item and associative memory in hippocampus and PPC, with earlier

193 sing factor (Pdf) and its receptor, Pdfr, on associative memory in male and female Drosophila Loss of

194 specific theta phase underlie the decline of associative memory in normal cognitive aging.SIGNIFICANC

195 suggest that the formation and expression of associative memories increase the availability of dendri

196 Long-term associative memory induced by a single associative trial

197 Embedding such associative memories into the network revealed that, whe

198 Defining the molecular and neuronal basis of associative memories is based upon behavioral preparatio

199 Retrograde amnesia of learned associative memories is elicited by inducible neuron-spe

200 term memory, but how neural ensembles encode associative memories is unknown.

201 onal valence, and the age-related decline in associative memory is faster for negative than for posit

202 evidence that they play an important role in associative memory is lacking.

203 hesis, the identity of proteins critical for associative memory is largely unknown.

204 hippocampus are selectively associated with associative memory judgments.

205 Building on Hebbian neural associative memories, like Hopfield networks, we first p

206 onal mRNA pool during an olfactory long-term associative memory (LTAM) in Caenorhabditis elegans herm

207 ugh some patients showed impaired source and associative memory, many performed as well as control pa

208 We have investigated how associative memory mechanisms, synaptic tagging and capt

209 esses in association retrieval suggests that associative memory might be particularly affected by dop

210 Classical theories of associative memory model CA3 as a homogeneous attractor

211 The method is based on an associative memory model for short to intermediate range

212 model are discussed, including the search of associative memory model, the perturbation model, precat

213 on to prospection, which taps into long-term associative memory--more enduring.

214 he model developed here leads to a family of associative memory networks that includes a Dense Associ

215 ks following the acquisition of two distinct associative memories, neuron firing in the rat prelimbic

216 pecifically, DAN-i1 activation can establish associative memories of opposite valence after paired an

217 d with improved working memory (P = .01) and associative memory (P = .02) in amyloid precursor protei

218 ability (P < .001), attention (P = .02), and associative memory, (P = .002).

219 orks that activated or deactivated during an associative memory paradigm.

220 Together with impairments in associative memory, patients in post-traumatic amnesia d

221 forms of learning and memory (e.g., semantic associative memory, Pavlovian conditioning, and instrume

222 sion-like symptoms, and impaired spatial and associative memory performance (p < 0.05).

223 related to both immediate and 24 h item and associative memory performance.

224 l network regions and concomitantly improved associative memory performance.

225 sociative encoding task are related to later associative memory performance.

226 ed task accuracy as well as poorer name-face associative memory performance.

227 e functions, activities of daily living, and associative memory performances was observed.

228 egions, and enhancements of connectivity and associative memory persisted for ~24 hours after stimula

229 othesized that acquisition of such long-term associative memories proceeds via the strengthening of c

230 CONTEXT Abnormalities in associative memory processes, such as Pavlovian fear con

231 0.64), executive function (R(2) = 0.56) and associative memory (R(2) = 0.25).

232 This pattern reversed during associative memory recall, with reaction times and brain

233 vidence for CA3 NMDA receptor involvement in associative memory recall.

234 In addicts, associative memories related to the rewarding effects of

235 yed a causal role in the creation of lasting associative memory representations during one-trial lear

236 e artificial neural networks, and on dynamic associative memory responses to stimuli.

237 ost-encoding TMS to LOC selectively impaired associative memory retention compared to multiple contro

238 a(13-15) has previously been shown to affect associative memory retention in fruit flies(14)(,)(16) a

239 emory, visual recognition and short-term non-associative memory retention.

240 rior temporal cortex, but that goal-directed associative memory retrieval additionally depends on top

241 ment of fronto-striatal circuits in item and associative memory retrieval as well as in the stabiliza

242 hippocampus was specifically enhanced during associative memory retrieval.

243 goal and thus used internal context to guide associative memory retrieval.

244 internal contextual information for flexible associative memory retrieval.

245 brain to examine how memorability influences associative memory retrieval.

246 it allows for increased storage capacity in associative memories; second, it makes the structure in

247 ulata, NMDARs are involved in the storage of associative memories (see references in text).

248 ave systematically studied how four types of associative memories (short- and long-term memories, eac

249 The substrates of associative memory should therefore be identifiable by n

250 odel that implements a high-capacity general associative memory, spatial memory and episodic memory.

251 yramidal cells may function as a network for associative memory storage and recall.

252 g a direct role for the prefrontal cortex in associative memory storage for temporally separated even

253 se readily from the requirement of efficient associative memory storage.

254 ecessary for the cellular changes underlying associative memory storage.

255 These defects reflect a true lessening of associative memory strength, as distortions in nonassoci

256 ening of overlapping memories based on their associative memory strength.

257 e shaped during sleep as a function of their associative memory strength.SIGNIFICANCE STATEMENT Numer

258 Theories of associative memory suggest that successful memory storag

259 tinction was observed together with enhanced associative memory, suggesting increased cortical-depend

260 n taken as evidence for distinct "rule" and "associative" memory systems in morphology and against th

261 pp)-based executive functioning tasks and an associative memory task 3 times over 2 weeks.

262 activity during the performance of a visual associative memory task and a visual working memory task

263 , particularly where stimuli relevant to the associative memory task appeared.

264 Participants performed an associative memory task during hr-fMRI in which they enc

265 ncluding a resting-state scan followed by an associative memory task encompassing encoding and retrie

266 ) experiments, participants completed an ABC associative memory task using pictures of objects, faces

267 o selectivity for nonspatial features of the associative memory task when they were visually availabl

268 Twenty-one participants completed an associative memory task while undergoing simultaneous EE

269 le subjects performed different phases of an associative memory task, learning to associate faces wit

270 anial EEG as human participants performed an associative memory task.

271 during a foraging task and a context-object associative memory task.

272 electroencephalogram data recorded during 2 associative memory tasks.

273 with a selective impairment in EC-dependent associative memory tasks.

274 and electrophysiological signatures of using associative-memory templates to guide perception, while

275 sed both a source monitoring paradigm and an associative memory test to evaluate the ability of patie

276 During subsequent associative memory tests cued by A items, reactivation o

277 Analogous to an associative memory that encodes memory in neuronal conne

278 ter the rules of synaptic plasticity to form associative memories through the use of 'tagged' synapse

279 l activity represents a long-term cue-reward associative memory to support behavioral adaptation.

280 networks, we first propose threshold phasor associative memory (TPAM) networks.

281 to encoding, and on consistent processing of associative memory traces in midline structures that are

282 ficant in acquiring, storing, and retrieving associative memory traces of repeatedly co-occurring neu

283 ive evidence that both reward processing and associative memory undergo dynamic change across develop

284 tested this in rats by creating interlinked associative memories using a second-order fear-condition

285 Associative memory was predicted in the left inferior pr

286 tive coarse-grained protein force field, the associative memory water-mediated structure and energy m

287 fragments encoded by HTT exon 1 by using the associative memory, water-mediated, structure and energy

288 Using the associative memory, water-mediated, structure and energy

289 We extend a protein folding model, the associative memory, water-mediated, structure, and energ

290 edictive coarse-grained protein force field [associative memory, water-mediated, structure, and energ

291 Using the associative-memory, water-mediated, structure and energy

292 te folding of multidomain proteins using the associative-memory, water-mediated, structure and energy

293 tigate protein-protein association using the associative-memory, water-mediated, structure, and energ

294 Associative memories were defined as "weak" if they were

295 dge as schemas and tested item or nonspatial associative memory, whereas animal studies have used int

296 (ii) theta oscillations specifically support associative memory, whereas the spectral tilt reflects a

297 ship between hippocampal representations and associative memory: whereas hippocampal signatures of di

298 ular events that have been implicated during associative memory which are also altered or defective i

299 that they sustain neural firing and produce associative memory, which may underpin maintaining and b

300 roach even allows us to implement a Hopfield associative memory with four fully connected artificial