Publications by authors named "E C Reifenstein"

Article Synopsis
  • Grid cells in the brain, which help with spatial navigation, typically show a firing pattern in triangular grids, but direct recordings from humans are rare.
  • Previous fMRI studies have tried to measure grid cell activity indirectly by observing changes in brain activity related to a person's movement direction, but the cause of these changes is still debated.
  • The current research suggests that orientation related to the grid's axes may explain observed patterns better than other proposed mechanisms, highlighting the need for further studies on human grid cells and their properties.
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The idea of guidance toward a target is central to axon pathfinding and brain wiring in general. In this work, we show how several thousand axonal growth cones self-pattern without target-dependent guidance during neural superposition wiring in . Ablation of all target lamina neurons or loss of target adhesion prevents the stabilization but not the development of the pattern.

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Spatial navigation and memory rely on neural systems that encode places, distances, and directions in relation to the external world or relative to the navigating organism. Place, grid, and head-direction cells form key units of world-referenced, allocentric cognitive maps, but the neural basis of self-centered, egocentric representations remains poorly understood. Here, we used human single-neuron recordings during virtual spatial navigation tasks to identify neurons providing a neural code for egocentric spatial maps in the human brain.

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Remembering the temporal order of a sequence of events is a task easily performed by humans in everyday life, but the underlying neuronal mechanisms are unclear. This problem is particularly intriguing as human behavior often proceeds on a time scale of seconds, which is in stark contrast to the much faster millisecond time-scale of neuronal processing in our brains. One long-held hypothesis in sequence learning suggests that a particular temporal fine-structure of neuronal activity - termed 'phase precession' - enables the compression of slow behavioral sequences down to the fast time scale of the induction of synaptic plasticity.

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The medial entorhinal cortex (MEC) and the adjacent parasubiculum are known for their elaborate spatial discharges (grid cells, border cells, etc.) and the precessing of spikes relative to the local field potential. We know little, however, about how spatio-temporal firing patterns map onto cell types.

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