ライフサイエンスコーパス: memory retention

1 memory retention) and remote memory (30-day memory retention).

2 ce (as measured by a clinical test of verbal memory retention).

3 restricted knockdown after training impairs memory retention.

4 ronal induction of Arc, and impaired spatial memory retention.

5 ing for trace fear conditioning but impaired memory retention.

6 spatial memory training enhanced subsequent memory retention.

7 supraspan learning, and short- and long-term memory retention.

8 oduces a bidirectional modulation of spatial memory retention.

9 ale C57BL6 mice exhibited improved long-term memory retention.

10 on of crackling noise, slow relaxations, and memory retention.

11 nd SP amplitude, and their relationship with memory retention.

12 d down-regulation of both learning speed and memory retention.

13 ment of unpredictability into the process of memory retention.

14 rm memory whereas its overexpression weakens memory retention.

15 ssociated with improved spatial learning and memory retention.

16 it is essential for spine consolidation and memory retention.

17 , and activation of its VIP neurons improves memory retention.

18 s predominant in distal sections can prolong memory retention.

19 les, the quality of which predicts overnight memory retention.

20 learning, but intact PNNs are necessary for memory retention.

21 /low-beta oscillatory power (9-18 Hz) during memory retention.

22 going dopaminergic activity, while enhancing memory retention.

23 to hours or even years for consolidation and memory retention.

24 ed memory after 72 h, without affecting 24-h-memory retention.

25 stable molecular modifications required for memory retention.

26 sing linked molecular markers and tested for memory retention.

27 e hippocampus, where its activation enhances memory retention.

28 ons and are candidates for the regulation of memory retention.

29 s that were retained in wasps with decreased memory retention.

30 rmed spines that are important for long-term memory retention.

31 the impairment of overnight sleep-dependent memory retention.

32 stimulus encoding rather than to failures in memory retention.

33 al areas were measured at 24h and 1 month in memory retention.

34 essor of hippocampal cellular plasticity and memory retention.

35 omitant changes in synaptic transmission and memory retention.

36 l recognition and short-term non-associative memory retention.

37 ions of the water maze and passive avoidance memory retention.

38 her physical exercise can be used to improve memory retention [15-17].

39 nesis moderately correlated with deficits in memory retention after 24 hours.

40 d male and female mice exhibit a decrease in memory retention after conventional CFC and, 2) alprazol

41 e oxidase activity in the brain and improves memory retention after learning tasks, including fear ex

42 impaired aged rats for 11 d enhanced spatial memory retention (after a 30 min delay between an exposu

43 e, DKO mice showed defective acquisition and memory retention, although the deficits could be attenua

44 There is substantial variation in memory retention among closely related species in the pa

45 rve successful editing of B cells leading to memory retention and bNAb secretion at neutralizing tite

46 -term effects of WBI on spatial learning and memory retention and determined whether voluntary runnin

47 the amnesiac gene in Drosophila affect both memory retention and ethanol sensitivity.

48 ts antagonistically to dopamine; it shortens memory retention and facilitates the rapid updating of m

49 for studying the neural processes underlying memory retention and loss.

50 sphorylation (PO(4)) sites impairs long-term memory retention and maintenance of newly formed postsyn

51 phosphate, like IGF2, significantly enhances memory retention and persistence in a CIM6P/IGF2R-depend

52 ng or memory retrieval significantly enhance memory retention and prevent forgetting.

53 , also known as IGF2) significantly enhances memory retention and prevents forgetting.

54 lyT1 enhances hippocampal NMDAR function and memory retention and protects against an amphetamine dis

55 es a powerful approach to study variation in memory retention and provides a basis for future researc

56 ocampal subdivisions in recent and long-term memory retention and recall are essentially unknown.

57 ding candidate mechanisms thought to support memory retention and stabilization across hippocampal-co

58 more than 10(4) cycles endurance, a 10-year memory retention and sub-5 us program/erase speed are ac

59 dicate that estradiol and progesterone alter memory retention and suggest that these changes may be t

60 and caused selective deficits in hippocampal memory retention and the translation-dependent, transcri

61 phosphatase and tensin homolog inhibitor, on memory retention and underlying synaptic modifications.

62 of contextual fear memory persistence (7-day memory retention) and remote memory (30-day memory reten

63 Impairments in object recognition, spatial memory retention, and network stability following proton

64 ject recognition task significantly enhances memory retention, and that the beneficial effect of intr

65 e importance of examining the time course of memory retention, and they suggest that inbred mouse str

66 echanisms of how learning mediates sleep for memory retention are not clear.

67 st that while species differences in spatial memory retention are present, they do not correlate with

68 re, neither reward nor punishment benefitted memory retention, arguing against the common assumption

69 ampus and that their dopamine release boosts memory retention as well.

70 , n = 10] and were evaluated for deficits in memory retention at 7 days postinjury.

71 tested in the Morris water maze to evaluate memory retention at 7 days postinjury.

72 Arg 3.1 mRNA, a neuronal activity marker, in memory retention at multiple rostrocaudal levels of the

73 y, the results offer novel insights into why memory retention benefits from repeated retrieval, and t

74 this relationship has been mostly limited to memory retention benefits.

75 as the first factor that impaired the verbal memory retention between 30 minutes and 1 week.

76 Lphn2 from the CA1 region increased spatial memory retention but decreased learning of sequential sp

77 t be harnessed not only to enhance overnight memory retention, but also to combat memory decline asso

78 om psychology suggest that sleep facilitates memory retention by stopping ongoing retroactive interfe

79 that medial entorhinal cortex (mEC) supports memory retention by sustaining the sequential activity o

80 TMS to LOC selectively impaired associative memory retention compared to multiple control conditions

81 hat overnight sleep and daytime naps benefit memory retention, compared to comparable amounts of acti

82 Finally, Arc/Arg3.1 knockout mice show memory retention deficits.

83 eir sham controls without exhibiting spatial memory retention deficits.

84 Finally, we show that how memory retention during associative learning can be prol

85 reaming frequency negatively correlated with memory retention during eyes-closed rest.

86 Retrieval practice boosted memory retention following a 24-hour (long-term) but not

87 We also tested autophagic flux and memory retention following autophagy-promoting treatment

88 The limited memory retention for a ferroelectric field-effect transi

89 t (KO) mice and found behavioral deficits in memory retention for temporal dissociative passive avoid

90 Memory retention for the final discrimination was tested

91 ractions during learning and tests of remote memory retention for whisker-signaled trace eyeblink con

92 learned information in determining long-term memory retention has been of central interest.

93 ated female and male mice show a decrease in memory retention in a state dependent CFC timeline with

94 how that mice lacking NEIL1 exhibit impaired memory retention in a water maze test, but no abnormalit

95 estion of a single flavanol improves spatial memory retention in adult mammals.

96 roplasticity in the VLO may be necessary for memory retention in both appetitive and aversive domains

97 previously been shown to affect associative memory retention in fruit flies(14)(,)(16) and honeybees

98 injured controls (P < 0.02), the deficits in memory retention in injured TNF(-/-) mice were significa

99 d that miRNAs play a central role in somatic memory retention in iPSCs.

100 y, inhibition of AMPAR endocytosis prolonged memory retention in normal animals and reduced memory lo

101 amyloid precursor protein mice worsened the memory retention in passive avoidance and novel object r

102 (COX-2) inhibitors have been shown to block memory retention in rodents following Morris water maze

103 m synaptic plasticity, learning ability, and memory retention in TG mice.

104 rst two hidden platform sessions and spatial memory retention in the first probe trial.

105 aRA-treated mice demonstrated better spatial memory retention in the Morris water-maze test compared

106 lly, we develop suitable methods to quantify memory retention in the system.

107 However, E3-HL mice showed reduced spatial memory retention in the water maze and reduced fear lear

108 mpaired novel object recognition and spatial memory retention in the water maze in Apoe-/-, but not a

109 tial learning task; however, their long-term memory retention in this task was impaired.

110 Although testing memory retention in wild animals is difficult, it is imp

111 NAD(+)-induced memory retention is partially dependent on EVA1C, as ade

112 We found that the magnitude of motor memory retention is proportional to the magnitude of occ

113 indles have been associated with benefits in memory retention, it is not well understood how spindles

114 s and complex biological processes including memory retention, its extremely low levels in the mature

115 tosis and memory differentiation dynamics on memory retention (memory stability).

116 ameliorated deficits in spatial learning and memory retention observed in irradiated mice.

117 WBI prevented the marked decline in spatial memory retention observed months after irradiation.

118 f estradiol 72 and 48 hr before testing, the memory retention of ovariectomized rats was improved com

119 bundance of Lactobacillus Firm-5 cluster and memory retention on a visual discrimination task.

120 red fear-potentiated startle to infer threat memory retention on the next day, as well as skin conduc

121 than 13 minutes was associated with impaired memory retention over 1 week.

122 NMDAR dependent and necessary for subsequent memory retention performance.

123 During the memory retention period of the task (delay), many units

124 During the memory retention period, a transient burst of high gamma

125 opsychological tests of attention, learning, memory (retention), psychomotor speed, and motor skills.

126 ctions and have focused on the mechanisms of memory retention rather than utilization.

127 r maze performance and assessment of 24-hour memory retention revealed significant differences betwee

128 ng the trace interval during tests of remote memory retention, suggesting its involvement in retrieva

129 A post-brumation memory retention test revealed that animals from both co

130 e Morris water maze, PTK/ZK impaired spatial memory retention tested 48 h later.

131 Furthermore, overnight memory retention tests suggest that faster learning indi

132 cbl-b null group showed significantly higher memory retention than WT mice, suggesting an enhancement

133 Even though hogs are thought to have long memory retention, they likely relied on recent experienc

134 preserved and provide a structural basis for memory retention throughout the entire life of an animal

135 combine a wide range of memory states, long memory retention times, and protection against unavoidab

136 To test memory retention, two probe trials were used.

137 ependent cognitive task but abnormal working memory retention under neurochemical challenge of three

138 ortem measures of global cognitive function, memory retention, verbal fluency, and dementia severity

139 ual information but also enhances perceptual memory retention via amygdalo-frontal cortical projectio

140 Extinction memory retention was assessed 1 day and 1 week after ext

141 Memory retention was enhanced.

142 one peptide whose sustained increase during memory retention was implicated by microarray analysis,

143 Our results show that memory retention was improved in GMF-KO mice compared to

144 Performance on measures of memory retention was independent of modality.

145 imals navigated between decision points-when memory retention was most needed.

146 This impairment of memory retention was not state dependent in that it was

147 l 8 months old when reduced visual cognitive memory retention was noted in the IDUA(-/-) mice.

148 ic basis of this interspecific difference in memory retention was studied in a backcrossing experimen

149 When extinction memory retention was tested 1 week after learning, the T

150 When extinction memory retention was tested 24 h after learning, the THC

151 arning, and the effects of THC on extinction memory retention when assessed 1 day and 1 week from lea

152 nt 1, we investigated the impact of sleep on memory retention when the temporal gap between training

153 ng the transition from sensory processing to memory retention whereas prefrontal and parietal beta bu

154 he somatosensory cortex is involved in motor memory retention whereas the motor cortex is not, if con

155 f either drug dose-dependently impaired fear memory retention, whereas infusions 6 hr after condition

156 nificantly greater impairment on measures of memory retention, whereas noncarriers were more impaired

157 r part (encompassing the Te2) alone impaired memory retention, whereas the inactivation of the anteri

158 g-term increase in anxiety and impaired fear memory retention, which was paralleled by an imbalance i