Models that contain the Model Concept : Grid cell

(Grid cells are pyramidal cells found in the entorhinal cortex that fire when an animal moves through the verticies of (non-existent except as detected by the cell firing) regularly spaced equilateral triangles. )
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    Models   Description
1.  An attractor network model of grid cells and theta-nested gamma oscillations (Pastoll et al., 2013)
A two population spiking continuous attractor model of grid cells. This model combines the attractor dynamics with theta-nested gamma oscillatory activity. It reproduces the behavioural response of grid cells (grid fields) in medial entorhinal cortex, while at the same time allowing for nested gamma oscillations of post-synaptic currents.
2.  Development of modular activity of grid cells (Urdapilleta et al 2017)
This study explores the self-organization of modular activity of grid cells
3.  Grid cell model with compression effects (Raudies & Hasselmo, 2015)
We present a model for compression of grid cell firing in modules to changes in barrier location.
4.  Grid cell oscillatory interference with noisy network oscillators (Zilli and Hasselmo 2010)
To examine whether an oscillatory interference model of grid cell activity could work if the oscillators were noisy neurons, we implemented these simulations. Here the oscillators are networks (either synaptically- or gap-junction--coupled) of one or more noisy neurons (either Izhikevich's simple model or a Hodgkin-Huxley--type biophysical model) which drive a postsynaptic cell (which may be integrate-and-fire, resonate-and-fire, or the simple model) which should fire spatially as a grid cell if the simulation is successful.
5.  Grid cell spatial firing models (Zilli 2012)
This package contains MATLAB implementations of most models (published from 2005 to 2011) of the hexagonal firing field arrangement of grid cells.
6.  Grid cells from place cells (Castro & Aguiar, 2014)
" ...Here we present a novel model for the emergence of gridlike firing patterns that stands on two key hypotheses: (1) spatial information in GCs is provided from PC activity and (2) grid fields result from a combined synaptic plasticity mechanism involving inhibitory and excitatory neurons mediating the connections between PCs and GCs. ..."
7.  Hybrid oscillatory interference / continuous attractor NN of grid cell firing (Bush & Burgess 2014)
Matlab code to simulate a hybrid oscillatory interference - continuous attractor network model of grid cell firing in pyramidal and stellate cells of rodent medial entorhinal cortex
8.  MEC layer II stellate cell: Synaptic mechanisms of grid cells (Schmidt-Hieber & Hausser 2013)
This study investigates the cellular mechanisms of grid field generation in Medial Entorhinal Cortex (MEC) layer II stellate cells.
9.  Models of Vector Navigation with Grid Cells (Bush et al., 2015)
Four models of vector navigation in large scale 2D space using grid cell representations of location are included: (1) The 'Distance Cell' model, which directly decodes absolute start and goal locations in allocentric space from rate-coded grid cell representations before computing the displacement between them; (2) The 'Rate-coded Vector Cell' model, which directly decodes the displacement between start and goal locations from rate-coded grid cell representations; (3) The 'Phase-coded Vector Cell' model, which directly decodes the displacement between start and goal locations from the temporally-coded grid cell representations provided by phase precession; (4) The 'Linear Look-ahead' model, which uses a directed search through grid cell representations, initiated at the start location and then moving along a specific axis at a constant speed, to compute the displacement between start and goal locations.
10.  Modular grid cell responses as a basis for hippocampal remapping (Monaco and Abbott 2011)
"Hippocampal place fields, the local regions of activity recorded from place cells in exploring rodents, can undergo large changes in relative location during remapping. This process would appear to require some form of modulated global input. Grid-cell responses recorded from layer II of medial entorhinal cortex in rats have been observed to realign concurrently with hippocampal remapping, making them a candidate input source. However, this realignment occurs coherently across colocalized ensembles of grid cells (Fyhn et al., 2007). The hypothesized entorhinal contribution to remapping depends on whether this coherence extends to all grid cells, which is currently unknown. We study whether dividing grid cells into small numbers of independently realigning modules can both account for this localized coherence and allow for hippocampal remapping. ..."
11.  Noise promotes independent control of gamma oscillations and grid firing (Solanka et al 2015)
"Neural computations underlying cognitive functions require calibration of the strength of excitatory and inhibitory synaptic connections and are associated with modulation of gamma frequency oscillations in network activity. However, principles relating gamma oscillations, synaptic strength and circuit computations are unclear. We address this in attractor network models that account for grid firing and theta-nested gamma oscillations in the medial entorhinal cortex. ..."
12.  Spiking GridPlaceMap model (Pilly & Grossberg, PLoS One, 2013)
Development of spiking grid cells and place cells in the entorhinal-hippocampal system to represent positions in large spaces
13.  Synthesis of spatial tuning functions from theta cell spike trains (Welday et al., 2011)
A single compartment model reproduces the firing rate maps of place, grid, and boundary cells by receiving inhibitory inputs from theta cells. The theta cell spike trains are modulated by the rat's movement velocity in such a way that phase interference among their burst pattern creates spatial envelope function which simulate the firing rate maps.

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