ライフサイエンスコーパス: associative memory

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

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

3 est predicts individual differences in later associative memory.

4 reas in mediating innate odour preference or associative memory.

5 aptic plasticity that underlies drug-induced associative memory.

6 tivity predicts subsequent familiarity-based associative memory.

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

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

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

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

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

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

13 types of cognitive processing, particularly associative memory.

14 aired with NB stimulation induced behavioral associative memory.

15 her stimulation of the NB induces behavioral associative memory.

16 ring induction, consolidation and storage of associative memory.

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

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

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

20 Overexpression of DISC1 impairs associative memory.

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

22 ion processing speed, executive function and associative memory.

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

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

25 encoding and retrieval of olfactory-spatial associative memory.

26 d noninvasively, demonstrating their role in associative memory.

27 fect cognitive performance or discriminative associative memory.

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

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

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

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

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

33 reconsolidation of context-response-cocaine associative memories.

34 nces of externally triggered reactivation of associative memories.

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

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

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

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

39 for the availability of previously acquired associative memories.

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

41 s contributes to the integration of rewarded associative memories.

42 sychiatric condition perpetuated by unwanted associative memories.

43 ctional neuronal networks capable of storing associative memories.

44 he consolidation, retrieval or extinction of associative memories.

45 he hippocampus and the formation of temporal associative memories.

46 ted in the expression and reconsolidation of associative memories.

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

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

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

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

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

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

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

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

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

56 Associative memory and item memory are differentially af

57 Associative memory and item memory are dramatically affe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

86 Furthermore, the associative memory classifier demonstrated greater accur

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

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

89 This associative memory component has previously been propose

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

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

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

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

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

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

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

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

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

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

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

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

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

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

104 Associative memory formation is essential for an animal'

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

106 Associative memory formation requires that animals choos

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

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

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

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

111 across spatiotemporal discontiguities during associative memory formation.

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

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

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

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

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

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

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

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

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

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

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

123 Associative memory impairment is an early clinical featu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

150 l network regions and concomitantly improved associative memory performance.

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

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

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

154 0.64), executive function (R(2) = 0.56) and associative memory (R(2) = 0.25).

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

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

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

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

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

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

161 hippocampus was specifically enhanced during associative memory retrieval.

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

163 internal contextual information for flexible associative memory retrieval.

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

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

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

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

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

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

170 ecessary for the cellular changes underlying associative memory storage.

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

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

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

174 Theories of associative memory suggest that successful memory storag

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

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

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

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

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

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

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

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

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

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

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

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

187 Associative memory was predicted in the left inferior pr

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

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

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

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

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

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

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

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

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

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

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