review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | William E. Skaggs | Q46245644 |
P2093 | author name string | Barnes CA | |
McNaughton BL | |||
Knierim JJ | |||
Qin Y | |||
Suster M | |||
Jung MW | |||
Gerrard JL | |||
Gothard K | |||
Kudrimoti H | |||
Weaver KL | |||
P433 | issue | Pt 1 | |
P304 | page(s) | 173-185 | |
P577 | publication date | 1996-01-01 | |
P1433 | published in | The Journal of Experimental Biology | Q1355917 |
P1476 | title | Deciphering the hippocampal polyglot: the hippocampus as a path integration system | |
P478 | volume | 199 |
Q37627192 | A Computational Model for Spatial Navigation Based on Reference Frames in the Hippocampus, Retrosplenial Cortex, and Posterior Parietal Cortex. |
Q41834278 | A Prefrontal-Hippocampal Comparator for Goal-Directed Behavior: The Intentional Self and Episodic Memory |
Q45339547 | A computational model of parallel navigation systems in rodents |
Q49044670 | A controlled attractor network model of path integration in the rat. |
Q34235278 | A neural systems analysis of adaptive navigation |
Q42119375 | A quantitative theory of the functions of the hippocampal CA3 network in memory |
Q33736159 | A simple neural network model of the hippocampus suggesting its pathfinding role in episodic memory retrieval |
Q48395881 | A statistical paradigm for neural spike train decoding applied to position prediction from ensemble firing patterns of rat hippocampal place cells. |
Q34388405 | A topological paradigm for hippocampal spatial map formation using persistent homology |
Q37477284 | A video demonstration of preserved piloting by scent tracking but impaired dead reckoning after fimbria-fornix lesions in the rat. |
Q48116393 | Acetylcholine contributes to the integration of self-movement cues in head direction cells. |
Q43129552 | Acetylcholine efflux from retrosplenial areas and hippocampal sectors during maze exploration |
Q37033023 | Activity dynamics and behavioral correlates of CA3 and CA1 hippocampal pyramidal neurons |
Q41973426 | Acute stress and hippocampal output: exploring dorsal CA1 and subicular synaptic plasticity simultaneously in anesthetized rats |
Q89742656 | An uncertainty principle for neural coding: Conjugate representations of position and velocity are mapped onto firing rates and co-firing rates of neural spike trains |
Q40863259 | Analysis of the connectional organization of neural systems associated with the hippocampus in rats |
Q40151604 | Are new place representations independent of theta and path integration? |
Q33995353 | Attractor-map versus autoassociation based attractor dynamics in the hippocampal network |
Q30478463 | Backward shift of head direction tuning curves of the anterior thalamus: comparison with CA1 place fields |
Q35112687 | Bayesian integration of information in hippocampal place cells |
Q57148240 | Behavioral and Neural Subsystems of Rodent Exploration |
Q36312217 | Both here and there: simultaneous expression of autonomous spatial memories in rats |
Q48679389 | Brain aging: changes in the nature of information coding by the hippocampus. |
Q48679376 | Brain aging: impaired coding of novel environmental cues |
Q35800624 | Building a cognitive map by assembling multiple path integration systems |
Q34434444 | Can we reconcile the declarative memory and spatial navigation views on hippocampal function? |
Q42735768 | Cell assembly sequences arising from spike threshold adaptation keep track of time in the hippocampus |
Q93039710 | Cell type, sub-region, and layer-specific speed representation in the hippocampal-entorhinal circuit |
Q35160440 | Changes in reward contingency modulate the trial-to-trial variability of hippocampal place cells |
Q37381846 | Cholinergic blockade reduces theta-gamma phase amplitude coupling and speed modulation of theta frequency consistent with behavioral effects on encoding. |
Q36029534 | Cholinergic modulation of cognitive processing: insights drawn from computational models |
Q44844961 | Cognitive aging and the hippocampus: how old rats represent new environments. |
Q46884567 | Cognitive disorganization in hippocampus: a physiological model of the disorganization in psychosis. |
Q33385722 | Computation by oscillations: implications of experimental data for theoretical models of grid cells |
Q36436354 | Conjoint control of hippocampal place cell firing by two visual stimuli. I. The effects of moving the stimuli on firing field positions |
Q36832888 | Contextual behavior and neural circuits |
Q39168473 | Continuous attractor network models of grid cell firing based on excitatory-inhibitory interactions |
Q33654156 | Continuous attractors with morphed/correlated maps |
Q37135708 | Cosine directional tuning of theta cell burst frequencies: evidence for spatial coding by oscillatory interference |
Q47868253 | Coupling between place cells and head direction cells during relative translations and rotations of distal landmarks. |
Q41138748 | Cranial irradiation alters the behaviorally induced immediate-early gene arc (activity-regulated cytoskeleton-associated protein) |
Q37231840 | Deficits in landmark navigation and path integration after lesions of the interpeduncular nucleus |
Q37365276 | Development of schemas revealed by prior experience and NMDA receptor knock-out |
Q49072889 | Different CA1 and CA3 representations of novel routes in a shortcut situation. |
Q89321469 | Differential Representation of Landmark and Self-Motion Information along the CA1 Radial Axis: Self-Motion Generated Place Fields Shift toward Landmarks during Septal Inactivation |
Q30493114 | Disruption of the head direction cell signal after occlusion of the semicircular canals in the freely moving chinchilla |
Q40841719 | Dissociation of exteroceptive and idiothetic orientation cues: effect on hippocampal place cells and place navigation. |
Q35690191 | Distinct speed dependence of entorhinal island and ocean cells, including respective grid cells |
Q41252480 | Driving Performance Among Patients with Cirrhosis Who Drove to Their Outpatient Hepatology Clinic Appointments |
Q36250584 | Dual phase and rate coding in hippocampal place cells: theoretical significance and relationship to entorhinal grid cells |
Q48545950 | Dynamic interactions between local surface cues, distal landmarks, and intrinsic circuitry in hippocampal place cells. |
Q52029935 | Dynamics of hippocampal ensemble activity realignment: time versus space. |
Q38579343 | Dynamics of mismatch correction in the hippocampal ensemble code for space: interaction between path integration and environmental cues. |
Q36975968 | Emergence of Cognition from Action |
Q47547458 | Entorhinal fast-spiking speed cells project to the hippocampus |
Q47720988 | Environmental boundaries as a mechanism for correcting and anchoring spatial maps |
Q27320586 | Estimating location without external cues |
Q38716416 | Experience-Dependency of Reliance on Local Visual and Idiothetic Cues for Spatial Representations Created in the Absence of Distal Information. |
Q35767271 | Experience-dependent firing rate remapping generates directional selectivity in hippocampal place cells |
Q34476871 | Firing properties of rat lateral mammillary single units: head direction, head pitch, and angular head velocity |
Q90330796 | For humans navigating without vision, navigation depends upon the layout of mechanically contacted ground surfaces |
Q48257746 | Fragmentation of grid cell maps in a multicompartment environment |
Q37947565 | Framing spatial cognition: neural representations of proximal and distal frames of reference and their roles in navigation |
Q27004002 | From ear to uncertainty: vestibular contributions to cognitive function. |
Q35211746 | From visual affordances in monkey parietal cortex to hippocampo-parietal interactions underlying rat navigation |
Q34537030 | Functional relationships between the hippocampus and dorsomedial striatum in learning a visual scene-based memory task in rats |
Q38219358 | Grid cells and cortical representation |
Q38750183 | Grid cells and theta as oscillatory interference: theory and predictions |
Q21145320 | Grid cells, place cells, and geodesic generalization for spatial reinforcement learning |
Q36533030 | Head direction cell activity in the anterodorsal thalamus requires intact supragenual nuclei |
Q37401345 | Head direction cell instability in the anterior dorsal thalamus after lesions of the interpeduncular nucleus |
Q34421997 | Head direction cell representations maintain internal coherence during conflicting proximal and distal cue rotations: comparison with hippocampal place cells |
Q33870089 | Head direction cells in rats with hippocampal or overlying neocortical lesions: evidence for impaired angular path integration |
Q34450934 | Head direction is coded more strongly than movement direction in a population of entorhinal neurons. |
Q42000186 | Head direction maps remain stable despite grid map fragmentation |
Q30570915 | Hippocampal "time cells": time versus path integration |
Q48159102 | Hippocampal Place Cell Instability after Lesions of the Head Direction Cell Network |
Q71720221 | Hippocampal participation in the sun compass orientation of phase-shifted homing pigeons |
Q38991391 | Hippocampal place cells construct reward related sequences through unexplored space |
Q35681282 | Hippocampal spatial representations require vestibular input. |
Q33494498 | Hippocampus leads ventral striatum in replay of place-reward information. |
Q35805200 | How to avoid going bump in the night: object and place representations in the hippocampus. |
Q36512403 | How vision and movement combine in the hippocampal place code |
Q34703763 | Impairment of the anterior thalamic head direction cell network following administration of the NMDA antagonist MK-801. |
Q93115911 | In a Temporally Segmented Experience Hippocampal Neurons Represent Temporally Drifting Context But Not Discrete Segments |
Q44205911 | Induction and experience-dependent consolidation of stable long-term potentiation lasting months in the hippocampus. |
Q36141447 | Influence of Proximal, Distal, and Vestibular Frames of Reference in Object-Place Paired Associate Learning in the Rat. |
Q34430574 | Influence of boundary removal on the spatial representations of the medial entorhinal cortex |
Q30471074 | Insensitivity of the hippocampus to environmental stimulation during postnatal development. |
Q41814180 | Internally generated cell assembly sequences in the rat hippocampus. |
Q26862523 | Is there a pilot in the brain? Contribution of the self-positioning system to spatial navigation |
Q37407089 | Landmark control and updating of self-movement cues are largely maintained in head direction cells after lesions of the posterior parietal cortex. |
Q34440886 | Lateral entorhinal neurons are not spatially selective in cue-rich environments |
Q52001439 | Learned association of allocentric and egocentric information in the hippocampus. |
Q37719079 | Lesions of the dorsal tegmental nuclei disrupt control of navigation by distal landmarks in cued, directional, and place variants of the Morris water task. |
Q88741203 | Linear Self-Motion Cues Support the Spatial Distribution and Stability of Hippocampal Place Cells |
Q51675439 | Local sensory cues and place cell directionality: additional evidence of prospective coding in the hippocampus. |
Q37365891 | Looking for cognition in the structure within the noise. |
Q30577685 | Medial entorhinal grid cells and head direction cells rotate with a T-maze more often during less recently experienced rotations |
Q27690811 | Memory on time |
Q33837733 | Memory, navigation and theta rhythm in the hippocampal-entorhinal system |
Q34451713 | Millisecond timescale synchrony among hippocampal neurons |
Q38005119 | Models of grid cell spatial firing published 2005-2011 |
Q37912644 | Models of place and grid cell firing and theta rhythmicity |
Q38138991 | Modulation of adult-born neurons in the inflamed hippocampus. |
Q30478065 | Modulation of memory by vestibular lesions and galvanic vestibular stimulation |
Q55173043 | Navigation Patterns and Scent Marking: Underappreciated Contributors to Hippocampal and Entorhinal Spatial Representations? |
Q52587308 | Navigational Strategies and Their Neural Correlates. |
Q57491364 | Neural Mechanisms Involved in Mental Imagery of Slip-Perturbation While Walking: A Preliminary fMRI Study |
Q24625332 | Neural Protein Synthesis during Aging: Effects on Plasticity and Memory |
Q30497706 | Neural Syntax: Cell Assemblies, Synapsembles, and Readers |
Q46726669 | Neural correlates of encoding space from route and survey perspectives. |
Q38204836 | Neural mechanisms of self-location |
Q30491828 | Neurocognitive aging: prior memories hinder new hippocampal encoding |
Q42473123 | Neuroinflammation alters the hippocampal pattern of behaviorally induced Arc expression. |
Q37841810 | Neuroinflammation and the plasticity-related immediate-early gene Arc. |
Q51023067 | Neuroscience: Seeing into the future. |
Q43106440 | New and distinct hippocampal place codes are generated in a new environment during septal inactivation |
Q48414465 | Object recognition and location memory in monkeys with excitotoxic lesions of the amygdala and hippocampus. |
Q33665958 | Optic flow input to the hippocampal formation from the accessory optic system |
Q42788567 | Oscillatory neurocomputing with ring attractors: a network architecture for mapping locations in space onto patterns of neural synchrony |
Q48202541 | Path integration absent in scent-tracking fimbria-fornix rats: evidence for hippocampal involvement in "sense of direction" and "sense of distance" using self-movement cues. |
Q28243541 | Path integration and cognitive mapping in a continuous attractor neural network model |
Q37330851 | Pattern of hippocampal shape and volume differences in blind subjects |
Q34831874 | Place cells in the hippocampus: eleven maps for eleven rooms |
Q37963888 | Place cells, grid cells, attractors, and remapping. |
Q45970839 | Postsynaptic complex spike bursting enables the induction of LTP by theta frequency synaptic stimulation. |
Q48487149 | Rats with fimbria-fornix lesions are impaired in path integration: a role for the hippocampus in "sense of direction". |
Q33861121 | Reactivation of hippocampal cell assemblies: effects of behavioral state, experience, and EEG dynamics |
Q34169558 | Reconceiving the hippocampal map as a topological template |
Q90427486 | Reduced GluN1 in mouse dentate gyrus is associated with CA3 hyperactivity and psychosis-like behaviors |
Q38564308 | Repeating firing fields of CA1 neurons shift forward in response to increasing angular velocity. |
Q33877885 | Replay and time compression of recurring spike sequences in the hippocampus. |
Q34233471 | Retrospectively and prospectively modulated hippocampal place responses are differentially distributed along a common path in a continuous T-maze. |
Q36382186 | Reward cues in space: commonalities and differences in neural coding by hippocampal and ventral striatal ensembles. |
Q36005144 | Running speed alters the frequency of hippocampal gamma oscillations |
Q33820907 | Scale-free topology of the CA3 hippocampal network: a novel method to analyze functional neuronal assemblies |
Q39153654 | Segregated Cell Populations Enable Distinct Parallel Encoding within the Radial Axis of the CA1 Pyramidal Layer. |
Q26828829 | Selection of preconfigured cell assemblies for representation of novel spatial experiences |
Q42004999 | Selective excitotoxic lesions of the hippocampus and basolateral amygdala have dissociable effects on appetitive cue and place conditioning based on path integration in a novel Y-maze procedure |
Q46681415 | Self-motion and the hippocampal spatial metric. |
Q57170283 | Self-motion processing in visual and entorhinal cortices: Inputs, integration, and implications for position coding |
Q37243980 | Sequence reactivation in the hippocampus is impaired in aged rats |
Q91854053 | Space and Time: The Hippocampus as a Sequence Generator |
Q47999129 | Space and time in the brain |
Q38173644 | Space in the brain: how the hippocampal formation supports spatial cognition |
Q41422228 | Sparse orthogonal population representation of spatial context in the retrosplenial cortex |
Q48497791 | Spatial exploration-induced Arc mRNA and protein expression: evidence for selective, network-specific reactivation. |
Q48519683 | Spatial firing of hippocampal place cells in blind rats. |
Q48380121 | Spatial firing properties of hippocampal CA1 populations in an environment containing two visually identical regions. |
Q46076172 | Spatial representation in the hippocampal formation: a history |
Q30435105 | Spatial representations of place cells in darkness are supported by path integration and border information |
Q50791456 | Spatial response properties of homing pigeon hippocampal neurons: correlations with goal locations, movement between goals, and environmental context in a radial-arm arena. |
Q47828403 | Stellate Cells in the Medial Entorhinal Cortex Are Required for Spatial Learning. |
Q37182302 | Synchronous bursts of neuronal activity in the developing hippocampus: modulation by active sleep and association with emerging gamma and theta rhythms |
Q30303876 | Temporal sequence compression by an integrate-and-fire model of hippocampal area CA3. |
Q43610879 | Temporary inactivation of the retrosplenial cortex causes a transient reorganization of spatial coding in the hippocampus. |
Q36722203 | Temporoparietal encoding of space and time during vestibular-guided orientation. |
Q48132574 | The Aging Navigational System |
Q38832825 | The Art of Grid Fields: Geometry of Neuronal Time |
Q21129322 | The anterior thalamus provides a subcortical circuit supporting memory and spatial navigation |
Q37181063 | The hippocampus is required for short-term topographical memory in humans |
Q37074664 | The long-term stability of new hippocampal place fields requires new protein synthesis. |
Q50017965 | The storage and recall of memories in the hippocampo-cortical system. |
Q43256978 | The temporal context model in spatial navigation and relational learning: toward a common explanation of medial temporal lobe function across domains |
Q36338235 | The visual ecology of fiddler crabs |
Q45007400 | Theta sequences are essential for internally generated hippocampal firing fields |
Q47864741 | Theta sequences of grid cell populations can provide a movement-direction signal |
Q43125296 | Theta-modulated place-by-direction cells in the hippocampal formation in the rat. |
Q30101070 | Theta-paced flickering between place-cell maps in the hippocampus: A model based on short-term synaptic plasticity |
Q38830183 | Topological Schemas of Cognitive Maps and Spatial Learning |
Q36979375 | Tracking the course of hippocampal representations during learning: when is the map required? |
Q38066941 | Updating the lamellar hypothesis of hippocampal organization |
Q35211738 | Variable place-cell coupling to a continuously viewed stimulus: evidence that the hippocampus acts as a perceptual system |
Q35841340 | Vestibular and attractor network basis of the head direction cell signal in subcortical circuits |
Q21558385 | Vestibular pathways involved in cognition |
Q44445827 | What grid cells convey about rat location |
Q28728252 | What is comparable in comparative cognition? |
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