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To evaluate memory retention, after 2 days rest, we performed a probe trial at the last MWM day.
11β-HSD1 null mice also unexpectedly show reduced memory retention after 24 h in the passive avoidance test (latency 16 ± 2.3 s vs. 63 ± 22.2 s).
A QTL on chromosome 1 (∼5.8 cM in size) and a QTL on chromosome 5 (∼25,5 cM in size) both reduced memory retention after 72 h.
This strain was named 'SIL_LTM1A_gV' and the strain was tested for memory retention after 24 (±2), 72 (±2) and 120 (±2) h after a single conditioning.
These results from the analyses show that both N. vitripennis and N. longicornis have a long-lasting memory retention after a single conditioning, although their PIs decrease over time.
Their female offspring were conditioned and tested for memory retention after 72 (±2) h; this time point was chosen instead of 48 h to match the time point of selection in the initial introgression experiment.
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Rat pups displayed deficits in learning and retention of memory after exposure to the organochlorine insecticide and acaricide endosulfan (6 mg/kg bw) on PND2 25 (Lakshmana and Raju 1994).
Memory-retention tests were performed 3 days after the last training session, that is, 8 days after the discontinuation of drug administration.
By measuring freezing during long-term memory tests, we were able to examine retention of a fear memory after social acquisition and found that a subset of FCbP rats froze in response to the cue on day 3. Taking into consideration the importance of previous experience on social fear transmission, breeding rats in our own colony allowed us to better control for prior life experience.
Of particular note was that he displayed completely normal levels of forced-choice recognition memory after a retention delay of 24 h, which was demonstrably sufficient to eliminate ceiling effects (Vann et al., 2008).
One region on chromosome 1 (spanning ∼5.8 cM) and another on chromosome 5 (spanning ∼25.6 cM) resulted in decreased memory after 72 h, without affecting 24-h-memory retention.
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