| scholarly article | Q13442814 |
| P50 | author | James J Knierim | Q56516883 |
| P2093 | author name string | Francesco Savelli | |
| P2860 | cites work | Intracellular dynamics of hippocampal place cells during virtual navigation | Q24646223 |
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| Progressive increase in grid scale from dorsal to ventral medial entorhinal cortex | Q28301425 | ||
| Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice | Q28589052 | ||
| The medial temporal lobe | Q29615990 | ||
| Interneurons of the hippocampus | Q29618946 | ||
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| Unmasking the CA1 ensemble place code by exposures to small and large environments: more place cells and multiple, irregularly arranged, and expanded place fields in the larger space. | Q34014471 | ||
| The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells | Q34050288 | ||
| A unified model of NMDA receptor-dependent bidirectional synaptic plasticity | Q34076145 | ||
| Place cells and place recognition maintained by direct entorhinal-hippocampal circuitry | Q34134638 | ||
| Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex | Q34277494 | ||
| NMDA receptors, place cells and hippocampal spatial memory | Q34315328 | ||
| A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory | Q34324150 | ||
| Hippocampal plasticity across multiple days of exposure to novel environments. | Q34345190 | ||
| SEE: a tool for the visualization and analysis of rodent exploratory behavior | Q34376197 | ||
| Influence of boundary removal on the spatial representations of the medial entorhinal cortex | Q34430574 | ||
| Differential effects of early hippocampal pathology on episodic and semantic memory | Q34432245 | ||
| The boundary vector cell model of place cell firing and spatial memory | Q34526796 | ||
| Evolution of declarative memory | Q34553104 | ||
| Memory retention--the synaptic stability versus plasticity dilemma | Q34554444 | ||
| Representation of geometric borders in the entorhinal cortex | Q34908018 | ||
| Boundary vector cells in the subiculum of the hippocampal formation | Q34995837 | ||
| Plasticity of the hippocampal place cell representation | Q35969729 | ||
| Dual phase and rate coding in hippocampal place cells: theoretical significance and relationship to entorhinal grid cells | Q36250584 | ||
| Hippocampal place cells: parallel input streams, subregional processing, and implications for episodic memory. | Q36554550 | ||
| Experience-dependent, asymmetric expansion of hippocampal place fields | Q36566694 | ||
| Hippocampal and cortical place cell plasticity: implications for episodic memory | Q36572157 | ||
| Long-term potentiation in rat hippocampal neurons is accompanied by spatially widespread changes in intrinsic oscillatory dynamics and excitability | Q36724721 | ||
| Learning in a geometric model of place cell firing | Q36863666 | ||
| Heterosynaptic depression: a postsynaptic correlate of long-term potentiation | Q40080472 | ||
| Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation | Q40386039 | ||
| Spatial firing patterns of hippocampal complex-spike cells in a fixed environment | Q41460130 | ||
| The input-output transformation of the hippocampal granule cells: from grid cells to place fields. | Q41913178 | ||
| The role of competitive learning in the generation of DG fields from EC inputs | Q41953717 | ||
| Impact of spikelets on hippocampal CA1 pyramidal cell activity during spatial exploration | Q43186613 | ||
| NMDA receptor antagonism blocks experience-dependent expansion of hippocampal "place fields". | Q43730152 | ||
| Experience-dependent modifications of hippocampal place cell firing | Q44364534 | ||
| A double dissociation between hippocampal subfields: differential time course of CA3 and CA1 place cells for processing changed environments. | Q44925615 | ||
| Distinct ensemble codes in hippocampal areas CA3 and CA1. | Q44991781 | ||
| Spatial and behavioral correlates of hippocampal neuronal activity | Q45835647 | ||
| Scale-invariant memory representations emerge from moiré interference between grid fields that produce theta oscillations: a computational model. | Q45932818 | ||
| Sparse, environmentally selective expression of Arc RNA in the upper blade of the rodent fascia dentata by brief spatial experience | Q46514008 | ||
| Independent codes for spatial and episodic memory in hippocampal neuronal ensembles | Q46616106 | ||
| Activity-dependent decrease of excitability in rat hippocampal neurons through increases in I(h). | Q46761730 | ||
| State-dependent dendritic computation in hippocampal CA1 pyramidal neurons. | Q46947152 | ||
| Entorhinal theta phase precession sculpts dentate gyrus place fields. | Q47828412 | ||
| Organization of hippocampal cell assemblies based on theta phase precession | Q47849223 | ||
| Abolition of long-term stability of new hippocampal place cell maps by NMDA receptor blockade | Q47908800 | ||
| Hippocampal place units in the freely moving rat: why they fire where they fire | Q47963837 | ||
| First occurrence of hippocampal spatial firing in a new environment | Q48148664 | ||
| "Heterosynaptic" LTD in the dentate gyrus of anesthetized rat requires homosynaptic activity | Q48151690 | ||
| Experience-dependent rescaling of entorhinal grids | Q48175917 | ||
| Dynamics of the hippocampal ensemble code for space | Q48232012 | ||
| Storing covariance with nonlinearly interacting neurons | Q48257153 | ||
| Pattern separation in the dentate gyrus and CA3 of the hippocampus | Q48271203 | ||
| Beta oscillations and hippocampal place cell learning during exploration of novel environments | Q48286295 | ||
| Spatial selectivity of unit activity in the hippocampal granular layer | Q48314334 | ||
| From grids to places | Q48325417 | ||
| Entorhinal cortex grid cells can map to hippocampal place cells by competitive learning | Q48340587 | ||
| From grid cells to place cells: a mathematical model | Q48375025 | ||
| Spatial firing properties of hippocampal CA1 populations in an environment containing two visually identical regions. | Q48380121 | ||
| Action of brief pulses of glutamate on AMPA/kainate receptors in patches from different neurones of rat hippocampal slices | Q48402561 | ||
| What can the hippocampal representation of environmental geometry tell us about Hebbian learning? | Q48434551 | ||
| Rats and mice share common ethologically relevant parameters of exploratory behavior. | Q48520787 | ||
| Dynamic interactions between local surface cues, distal landmarks, and intrinsic circuitry in hippocampal place cells. | Q48545950 | ||
| Hippocampal place-cell firing during movement in three-dimensional space | Q48691846 | ||
| The dynamics of long-term exploration in the rat. Part II. An analytical model of the kinematic structure of rat exploratory behavior | Q48715366 | ||
| The dynamics of long-term exploration in the rat. Part I. A phase-plane analysis of the relationship between location and velocity | Q48715375 | ||
| Head-anchored whole-cell recordings in freely moving rats. | Q48722962 | ||
| Hippocampal place fields are altered by the removal of single visual cues in a distance-dependent manner | Q48766711 | ||
| How heterogeneous place cell responding arises from homogeneous grids--a contextual gating hypothesis | Q48820509 | ||
| The emergence of grid cells: Intelligent design or just adaptation? | Q48820547 | ||
| Channel kinetics determine the time course of NMDA receptor-mediated synaptic currents | Q48919293 | ||
| Long-term stability of the place-field activity of single units recorded from the dorsal hippocampus of freely behaving rats | Q49097492 | ||
| The fuzzy-boundary arena--a method for constraining an animal's range in spatial experiments without using walls. | Q51902641 | ||
| Differences in hippocampal neuronal population responses to modifications of an environmental context: evidence for distinct, yet complementary, functions of CA3 and CA1 ensembles. | Q51999047 | ||
| Discordance of spatial representation in ensembles of hippocampal place cells. | Q52044626 | ||
| Synapses as associative memory elements in the hippocampal formation. | Q52106325 | ||
| A physiological basis for a theory of synapse modification. | Q52255807 | ||
| Integrative properties of radial oblique dendrites in hippocampal CA1 pyramidal neurons. | Q53746443 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | grid neuron | Q863495 |
| P304 | page(s) | 3167-3183 | |
| P577 | publication date | 2010-03-31 | |
| P1433 | published in | Journal of Neurophysiology | Q1709863 |
| P1476 | title | Hebbian analysis of the transformation of medial entorhinal grid-cell inputs to hippocampal place fields | |
| P478 | volume | 103 |
| Q98735880 | A Brain-Inspired Adaptive Space Representation Model Based on Grid Cells and Place Cells |
| Q46597994 | A model for the differentiation between grid and conjunctive units in medial entorhinal cortex. |
| Q38173647 | Architecture of spatial circuits in the hippocampal region |
| Q34245846 | Beyond the bolus: transgenic tools for investigating the neurophysiology of learning and memory. |
| Q37522495 | CA3 retrieves coherent representations from degraded input: direct evidence for CA3 pattern completion and dentate gyrus pattern separation |
| Q37922313 | Computational models of grid cells |
| Q37106738 | Conflicts between local and global spatial frameworks dissociate neural representations of the lateral and medial entorhinal cortex |
| Q42788571 | Coordinated learning of grid cell and place cell spatial and temporal properties: multiple scales, attention and oscillations |
| Q37135708 | Cosine directional tuning of theta cell burst frequencies: evidence for spatial coding by oscillatory interference |
| Q41121817 | Experience-dependent shaping of hippocampal CA1 intracellular activity in novel and familiar environments |
| Q37610626 | Framing of grid cells within and beyond navigation boundaries. |
| Q37947565 | Framing spatial cognition: neural representations of proximal and distal frames of reference and their roles in navigation |
| Q41153763 | From grid cells to place cells with realistic field sizes |
| Q27013789 | Functional connectivity of the entorhinal-hippocampal space circuit |
| Q58740403 | Functional properties of stellate cells in medial entorhinal cortex layer II |
| Q38219358 | Grid cells and cortical representation |
| Q38158731 | Grid cells and neural coding in high-end cortices |
| Q43544059 | Grid cells require excitatory drive from the hippocampus |
| Q52664166 | Heterogeneity in hippocampal place coding. |
| Q51575833 | Hippocampal Remapping after Partial Inactivation of the Medial Entorhinal Cortex. |
| Q59812605 | Hippocampal place cell encoding of sloping terrain |
| Q47781558 | How do spatial learning and memory occur in the brain? Coordinated learning of entorhinal grid cells and hippocampal place cells |
| Q45341094 | Impaired hippocampal rate coding after lesions of the lateral entorhinal cortex |
| Q37407341 | Influence of local objects on hippocampal representations: Landmark vectors and memory. |
| Q47640441 | Inheritance of Hippocampal Place Fields Through Hebbian Learning: Effects of Theta Modulation and Phase Precession on Structure Formation |
| Q49713443 | Learning place cells, grid cells and invariances with excitatory and inhibitory plasticity |
| Q40962237 | Megamap: flexible representation of a large space embedded with nonspatial information by a hippocampal attractor network |
| Q35625140 | Memory storage fidelity in the hippocampal circuit: the role of subregions and input statistics |
| Q48758630 | Modeling inheritance of phase precession in the hippocampal formation. |
| Q42178760 | Modular realignment of entorhinal grid cell activity as a basis for hippocampal remapping |
| Q52587308 | Navigational Strategies and Their Neural Correlates. |
| Q36836758 | Neuron-specific expression of tomosyn1 in the mouse hippocampal dentate gyrus impairs spatial learning and memory |
| Q43106440 | New and distinct hippocampal place codes are generated in a new environment during septal inactivation |
| Q46070039 | Optogenetic dissection of entorhinal-hippocampal functional connectivity |
| Q39186256 | Pattern separation in the hippocampus through the eyes of computational modeling |
| Q38342222 | Place cells, grid cells, and memory |
| Q34409245 | Representation of geometric borders in the developing rat. |
| Q34295573 | Selective reduction of AMPA currents onto hippocampal interneurons impairs network oscillatory activity |
| Q38586059 | Sensory feedback, error correction, and remapping in a multiple oscillator model of place-cell activity |
| Q27335438 | Social and novel contexts modify hippocampal CA2 representations of space |
| Q47368513 | Spatial Representations of Granule Cells and Mossy Cells of the Dentate Gyrus. |
| Q35876899 | Spatial firing correlates of physiologically distinct cell types of the rat dentate gyrus |
| Q46076172 | Spatial representation in the hippocampal formation: a history |
| Q34663835 | Spiking neurons in a hierarchical self-organizing map model can learn to develop spatial and temporal properties of entorhinal grid cells and hippocampal place cells |
| Q38792532 | Ten Years of Grid Cells |
| Q42107911 | The single place fields of CA3 cells: a two-stage transformation from grid cells |
| Q38977422 | The structure of networks that produce the transformation from grid cells to place cells |
| Q36479852 | Transient optogenetic inactivation of the medial entorhinal cortex biases the active population of hippocampal neurons |
| Q38184137 | What do grid cells contribute to place cell firing? |
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