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Therefore, genes associated with human episodic memory identified in whole-genome association studies could provide new insights into the mechanisms underlying memory formation and storage.
The types of explicit memory identified in humans and in animals studied are episodic (event) memory and semantic (fact) memory.
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Figure 5 shows the performance of younger adults as a function of the performance of older adults for conditions with focal vs. non-focal cues, for prospective memory proper and for vigilance (no studies of event cued habitual prospective memory were identified in the review, see Uttl [2], for a more extensive discussion of this point), for confound free age-contrasts only.
These results help to narrow a long-standing gap between memory research in humans and data and models based on the temporally fine grained dynamics of memory mechanisms identified in animals.
Further, consistent with previous studies, the main effect of source memory was identified in the left dorsolateral and superior frontal cortex, which are areas that have been noted for their roles in memory associations [ 11, 12, 34].
As shown in Table 4, other regions reflecting a quasiexponential function for the subsequent retrieval success of source memories were identified in the lateral and medial prefrontal regions, lateral temporal, parietal, and occipital regions, basal ganglia, and cerebellum.
It adds to evidence he and others first presented last year in the journal Nature that the physical trace of a specific memory can be identified in a group of brain cells as it forms, and activated later by stimulating those same cells.
Drosophila, with easy accessibility to genetic, molecular, and behavioral analyses, was also employed in olfactory learning studies and many key genes underlying memory formation were identified in these studies (Bellen et al., 2010).
Moderate effects on memory outcomes were identified in seven trials.
Early alterations in CC may be relevant to differences in psychomotor speed and visual memory that were identified in seroconversion and to longer term deterioration in cognitive function.
This is the first study to investigate effective connectivity in non-clinically identified, non-help-seeking young people with PEs, and the same frontoparietal network underlying working memory function was identified in all the 3 groups.
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