ライフサイエンスコーパス: memory retention

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

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

3 oduces a bidirectional modulation of spatial memory retention.

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

5 going dopaminergic activity, while enhancing memory retention.

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

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

8 stable molecular modifications required for memory retention.

9 sing linked molecular markers and tested for memory retention.

10 e hippocampus, where its activation enhances memory retention.

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

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

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

14 the impairment of overnight sleep-dependent memory retention.

15 s predominant in distal sections can prolong memory retention.

16 stimulus encoding rather than to failures in memory retention.

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

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

19 essor of hippocampal cellular plasticity and memory retention.

20 omitant changes in synaptic transmission and memory retention.

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

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

23 restricted knockdown after training impairs memory retention.

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

25 ing for trace fear conditioning but impaired memory retention.

26 spatial memory training enhanced subsequent memory retention.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 eir sham controls without exhibiting spatial memory retention deficits.

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

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

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

58 Memory retention for the final discrimination was tested

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 NMDAR dependent and necessary for subsequent memory retention performance.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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