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The delay in visual memory exhibited a non-linear two-stage trajectory: a lagging period during childhood followed by a recuperation period from adolescence until adulthood, as supported by a significant Group x Age Periods interaction.
For cell survival, whereas expanded T cells maintained expression of genes seen in acute infection, contracted memory exhibited a similar expression profile to that of naive CD8+ T cells.
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In particular, the nonvolatile memory exhibited an excellent programming characteristic, e.g., a large threshold voltage shift of 8.03 V was obtained after being programmed at 17 V for 5 ms.
The memory exhibits a notable hot hole program characteristic, and hence, a much higher erase speed is achieved.
The memory exhibits a high programming efficiency and a large programming window, which should be attributed to high-density Ni NPs.
Although the ferroelectric probe memory exhibits a capability of providing densities of multi-Tbit/in2, its destructive readout mechanism requires data to be refreshed after readout and this would cumulate read/write cycles and eventually causes severe fatigue.
Magnetic probe memory exhibits an analogous recording/readout mechanism to the conventional HDD.
It has been demonstrated that BE-SONOS memories exhibit a good performance in terms of programming and erasing (P/E) speed and data retention.
The flash memory exhibits a noteworthy hot hole trapping characteristic and excellent electrical properties regarding memory window, program/erase speeds, and charge retention.
Appetitive memory exhibits a more definitive role for neurotransmission from γ neurons [127].
The persistence of cellular memory exhibited by the galactose regulatory network is a system-level property which results from the interactions of several species in multiple nested feedback loops.
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CEO of Professional Science Editing for Scientists @ prosciediting.com