ライフサイエンスコーパス: remote memory

1 on and restrains the formation of recent and remote memory.

2 -like accuracy and hippocampus dependency of remote memory.

3 gement of mechanisms specific for processing remote memory.

4 cocaine memory, without affecting recall of remote memory.

5 g fear extinction, and for the expression of remote memory.

6 ippocampal neurogenesis in the expression of remote memory.

7 methylation 1 month after learning disrupted remote memory.

8 ential drug target site to improve long-term remote memory.

9 s known about signaling events important for remote memory.

10 orward conclusions about the neuroscience of remote memory.

11 tion of new memory but typically spares very remote memory.

12 by a null alpha-CaMKII mutation that blocks remote memory.

13 ations concerning hippocampal involvement in remote memory.

14 neuropsychological tests of anterograde and remote memory.

15 the initial aversive conditioning normalized remote memories.

16 n the BLA and animals are unable to retrieve remote memories.

17 e acetylation, such plasticity is absent for remote memories.

18 ingful association with emotionally salient, remote memories.

19 pathway may open the door for modulation of remote memories.

20 evertheless contained more information about remote memories.

21 respected the distinction between recent and remote memories.

22 rers often complain of irretrievable loss of remote memories.

23 pocampus, which was associated with enhanced remote memories.

24 tant level of activity during recall of more remote memories.

25 s) as well as for the stable organization of remote memories.

26 ion of hippocampal CA1 excitatory neurons to remote memory and find that contextual fear memory recal

27 ling to cAMP contributes to the stability of remote memory and identifies AC1 as a potential drug tar

28 that the anterior cingulate is activated by remote memory and that this activation is impaired by a

29 given 10 tone-shock pairings in one context (remote memory) and 10 tone-shock pairings in a distinct

30 rest in the organization and neurobiology of remote memory, and the pace of work in this area has acc

31 rn of findings has been that both recent and remote memory are impaired after hippocampal lesions whe

32 ively and reversibly modulated the recall of remote memories as silencing COMT Val overexpression sta

33 C, but not ACC or DH, abolished retrieval of remote memory, as revealed by lack of freezing to the co

34 For many tasks and species, remote memory (but not recent memory) is spared after da

35 hibitor (HDACi) during reconsolidation, even remote memories can be persistently attenuated.

36 yed versions of the game, demonstrating that remote memories can influence the images from recent wak

37 ests to clarify the extent and nature of the remote memory deficits in patients with transient epilep

38 activation of these areas produces selective remote memory deficits.

39 n-spatial, but not for the retrieval of very remote memories, either spatial or non-spatial.

40 ed of 10 tone-shock pairings in one context (remote memory), followed 16 months later by 10 additiona

41 or cingulate cortex plays a critical role in remote memory for contextual fear conditioning.

42 Remote memory for factual knowledge (from 11-30 years be

43 iation in executive functions, its impact on remote memory formation and recall is still poorly explo

44 T-Val gene (COMT-Val-tg) present exaggerated remote memories (>50 days) while having unaltered recent

45 Accelerated long-term forgetting and remote memory impairment are common amongst patients wit

46 sturbance: accelerated long-term forgetting, remote memory impairment, especially affecting autobiogr

47 d memories fade over days to weeks and (iii) remote memory impairment, in which there is loss of memo

48 t overtraining and were tested at recent and remote memory intervals.

49 slowly and shows substantial forgetting when remote memory is tested.

50 n teasing apart neural mechanisms underlying remote memory loss.

51 arge medial temporal lobe lesions had intact remote memory, markedly impaired recent memory, and also

52 ion task, but exhibit impairments during the remote memory phase of testing.

53 her, our findings suggest a role for PNNs in remote memory processing by stabilizing the neural netwo

54 ntage of time Te2 theta leads the BLA during remote memory recall correlates with a faster latency to

55 ns in Arc expression modulated by recent and remote memory recall could guide future inactivation and

56 ceptors was sufficient to rescue the altered remote memory recall in COMT-Val-tg mice and increased P

57 s in neuronal activity underlying recent and remote memory recall is unknown but essential for deciph

58 ds to deficits in synaptic plasticity and in remote memory recall using conditional knockout of Cdc42

59 An effective remote memory recall was accompanied by fewer strengthen

60 eurons, which contribute to the capacity for remote memory recall.

61 uisition, but instead significantly impaired remote memory recall.

62 ir interactions during learning and tests of remote memory retention for whisker-signaled trace eyebl

63 ty during the trace interval during tests of remote memory retention, suggesting its involvement in r

64 ygdala of stress-susceptible male mice after remote memory retrieval.

65 critical contribution of the hippocampus to remote memory retrieval.

66 increases in activity specifically following remote memory retrieval.

67 s using flies trained to have both early and remote memories showed that the alpha'/beta' MBNs have a

68 Moreover, bexarotene treatment improved remote memory stabilization in fear conditioned mice and

69 cise HPC circuits and mechanisms involved in remote memory storage remain poorly understood.

70 t to occur weeks to months later to subserve remote memory storage.

71 n healthy older adults taking a famous faces remote memory test.

72 rating novel associations between recent and remote memories that are then instantiated during non-RE

73 genetic variations modulate the retrieval of remote memories through the dysregulation of the endocan

74 dal cells blocked extinction learning at the remote memory time-point.

75 stingly, we also found that while recent and remote memories were both represented within anterior an

76 d remote autobiographical memories, although remote memories were more readily detected there, indica

77 s, fewer functional disabilities, and intact remote memory were associated with unrecognized dementia

78 pocampus is not involved in the retrieval of remote memories, whereas others assert that it is necess

79 on of this structure in normal mice disrupts remote memory without affecting recent memory.

80 of pyramidal cells facilitated extinction of remote memory, without affecting recent memory, inhibiti