An associative memory retrieves a stored pattern from a related cue. An incomplete cue supplies only some coordinates; a corrupted cue supplies some wrong coordinates. A Hopfield network implements retrieval by making intended patterns stable states with surrounding basins of attraction. This turns correction into a collective computation: no unit needs to know the entire desired answer. A cue outside the appropriate basin of attraction can retrieve another pattern or an unintended stable state.
Reinstatement of a stored representation from an incomplete or degraded cue. Recurrent autoassociative memory provides one mechanism; its success depends on the cue entering the correct basin of attraction. Partial-cue deficits after CA3-targeted NMDA receptor deletion support a hippocampal role without identifying a unique weight-update rule.[ref]
A transformation that makes representations of similar inputs less overlapping, helping reduce interference between stored events. It must retain enough information for useful downstream learning and retrieval. The dentate gyrus is a proposed substrate, with quantitative input–output evidence from spatial cue-conflict experiments.[ref]
A memory retrieves a stored pattern from a partial or corrupted version of that pattern. A recurrent Hopfield network supplies a precise idealization through stored attractors and their basins of attraction. Retrieval can fail through interference, ambiguous cues or spurious stable states.
A learned map retrieves an associated output pattern that need not equal its input cue. With normalized cue vectors and targets , Hebbian learning gives . For orthonormal cues, ; taking the matrix product proves exact retrieval. Nonorthogonal cues add interference . Additional context is required if one identical cue should select different outputs on different occasions.

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