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Flexible use of proximal objects and distal cues by hippocampal place cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1996)6:6<654::aid-hipo8>3.0.co;2-gopenalex-snapshot
Considerations arising from a complementary learning systems perspective on hippocampus and neocortex
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1996)6:6<654::aid-hipo8>3.3.co;2-dopenalex-snapshot
Considerations arising from a complementary learning systems perspective on hippocampus and neocortex
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1997)7:6<613::aid-hipo4>3.0.co;2-fopenalex-snapshot
Discordance of spatial representation in ensembles of hippocampal place cells
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1997)7:6<624::aid-hipo5>3.0.co;2-eopenalex-snapshot
Cues that hippocampal place cells encode: Dynamic and hierarchical representation of local and distal stimuli
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1999)9:4<423::aid-hipo8>3.0.co;2-uopenalex-snapshot
Further study of the control of place cell firing by intra-apparatus objects
inferredcites →https://doi.org/10.1002/hipo.10092openalex-snapshot
Distal landmarks and hippocampal place cells: Effects of relative translation versus rotation
inferredcites →https://doi.org/10.1002/hipo.20060openalex-snapshot
Study of CA1 place cell activity and exploratory behavior following spatial and nonspatial changes in the environment
inferredcites →https://doi.org/10.1002/hipo.450010207openalex-snapshot
Experience‐dependent modifications of hippocampal place cell firing
inferredcites →https://doi.org/10.1002/hipo.450040404openalex-snapshot
Spatial information content and reliability of hippocampal CA1 neurons: Effects of visual input
inferredcites →https://doi.org/10.1007/bf00239813openalex-snapshot
Hippocampal place units in the freely moving rat: Why they fire where they fire
inferredcites →https://doi.org/10.1007/bf00255230openalex-snapshot
Single unit activity in the rat hippocampus during a spatial memory task
inferredcites →https://doi.org/10.1007/s00221-002-1013-0openalex-snapshot
Remapping of place cell firing patterns after maze rotations
inferredcites →https://doi.org/10.1007/s004220000172openalex-snapshot
Predictions derived from modelling the hippocampal role in navigation
inferredcites →https://doi.org/10.1016/0006-8993(71)90358-1openalex-snapshot
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
inferredcites →https://doi.org/10.1016/0022-1902(81)80263-1openalex-snapshot
Seven-coordinate mixed-ligand tungsten(II) chelates containing carbonyls, triphenylphosphine, and 8-quinolinolato, picolinato or a quadridentate schiff-base
inferredcites →https://doi.org/10.1016/0023-9690(81)90020-5openalex-snapshot
Spatial localization does not require the presence of local cues
inferredcites →https://doi.org/10.1016/0031-9384(84)90080-5openalex-snapshot
A driveable bundle of microwires for collecting single-unit data from freely-moving rats
inferredcites →https://doi.org/10.1016/j.bbr.2004.03.006openalex-snapshot
Entorhinal cortex lesions impair the use of distal but not proximal landmarks during place navigation in the rat
inferredcites →https://doi.org/10.1016/j.conb.2005.10.002openalex-snapshot
Place cells, spatial maps and the population code for memory
inferredcites →https://doi.org/10.1016/j.neubiorev.2003.12.002openalex-snapshot
A proposed architecture for the neural representation of spatial context
inferredcites →https://doi.org/10.1016/j.neuron.2004.11.003openalex-snapshot
Ensemble Dynamics of Hippocampal Regions CA3 and CA1
inferredcites →https://doi.org/10.1016/j.neuron.2005.09.007openalex-snapshot
Progressive Transformation of Hippocampal Neuronal Representations in “Morphed” Environments
inferredcites →https://doi.org/10.1016/s0166-4328(99)00173-4openalex-snapshot
Involvement of the hippocampus and associative parietal cortex in the use of proximal and distal landmarks for navigation
inferredcites →https://doi.org/10.1037/0735-7044.117.3.588openalex-snapshot
Entorhinal cortex lesions disrupt the transition between the use of intra- and extramaze cues for navigation in the water maze.
inferredcites →https://doi.org/10.1038/416090aopenalex-snapshot
Long-term plasticity in hippocampal place-cell representation of environmental geometry
inferredcites →https://doi.org/10.1038/nature02739openalex-snapshot
Comparison of population coherence of place cells in hippocampal subfields CA1 and CA3
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02154.xopenalex-snapshot
Properties of place cell firing after damage to the visual cortex
inferredcites →https://doi.org/10.1073/pnas.94.1.343openalex-snapshot
Place cells and place navigation
inferredcites →https://doi.org/10.1073/pnas.95.19.11493openalex-snapshot
Both here and there: Simultaneous expression of autonomous spatial memories in rats
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03570.xopenalex-snapshot
Independent coding of connected environments by place cells
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.03882.xopenalex-snapshot
Functional interaction between the associative parietal cortex and hippocampal place cell firing in the rat
inferredcites →https://doi.org/10.1126/science.1071795openalex-snapshot
Requirement for Hippocampal CA3 NMDA Receptors in Associative Memory Recall
inferredcites →https://doi.org/10.1126/science.1108905openalex-snapshot
Attractor Dynamics in the Hippocampal Representation of the Local Environment
inferredcites →https://doi.org/10.1126/science.1114037openalex-snapshot
Independent Codes for Spatial and Episodic Memory in Hippocampal Neuronal Ensembles
inferredcites →https://doi.org/10.1126/science.280.5372.2121openalex-snapshot
Abolition of Long-Term Stability of New Hippocampal Place Cell Maps by NMDA Receptor Blockade
inferredcites →https://doi.org/10.1126/science.8351520openalex-snapshot
Dynamics of the Hippocampal Ensemble Code for Space
inferredcites →https://doi.org/10.1152/jn.1998.80.1.425openalex-snapshot
Interactions Between Idiothetic Cues and External Landmarks in the Control of Place Cells and Head Direction Cells
inferredcites →https://doi.org/10.1152/jn.2001.85.1.105openalex-snapshot
Hippocampal Place-Cell Firing During Movement in Three-Dimensional Space
inferredcites →https://doi.org/10.1523/jneurosci.07-07-01951.1987openalex-snapshot
The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells
inferredcites →https://doi.org/10.1523/jneurosci.09-11-03915.1989openalex-snapshot
Preserved spatial coding in hippocampal CA1 pyramidal cells during reversible suppression of CA3c output: evidence for pattern completion in hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.09-12-04101.1989openalex-snapshot
The firing of hippocampal place cells predicts the future position of freely moving rats
inferredcites →https://doi.org/10.1523/jneurosci.10-06-02008.1990openalex-snapshot
The firing of hippocampal place cells in the dark depends on the rat's recent experience
inferredcites →https://doi.org/10.1523/jneurosci.15-01-00173.1995openalex-snapshot
Influences of vestibular and visual motion information on the spatial firing patterns of hippocampal place cells
inferredcites →https://doi.org/10.1523/jneurosci.15-03-01648.1995openalex-snapshot
Place cells, head direction cells, and the learning of landmark stability
inferredcites →https://doi.org/10.1523/jneurosci.16-02-00823.1996openalex-snapshot
Binding of hippocampal CA1 neural activity to multiple reference frames in a landmark-based navigation task
inferredcites →https://doi.org/10.1523/jneurosci.17-07-02531.1997openalex-snapshot
Failure of Centrally Placed Objects to Control the Firing Fields of Hippocampal Place Cells
inferredcites →https://doi.org/10.1523/jneurosci.17-15-05900.1997openalex-snapshot
Path Integration and Cognitive Mapping in a Continuous Attractor Neural Network Model
inferredcites →https://doi.org/10.1523/jneurosci.18-05-01818.1998openalex-snapshot
Spatial Firing of Hippocampal Place Cells in Blind Rats
inferredcites →https://doi.org/10.1523/jneurosci.18-20-08455.1998openalex-snapshot
Spatial Firing Properties of Hippocampal CA1 Populations in an Environment Containing Two Visually Identical Regions
inferredcites →https://doi.org/10.1523/jneurosci.21-14-j0001.2001openalex-snapshot
Background, But Not Foreground, Spatial Cues Are Taken as References for Head Direction Responses by Rat Anterodorsal Thalamus Neurons
inferredcites →https://doi.org/10.1523/jneurosci.22-14-06254.2002openalex-snapshot
Dynamic Interactions between Local Surface Cues, Distal Landmarks, and Intrinsic Circuitry in Hippocampal Place Cells
inferredcites →https://doi.org/10.1523/jneurosci.3885-05.2006openalex-snapshot
Head Direction Cell Representations Maintain Internal Coherence during Conflicting Proximal and Distal Cue Rotations: Comparison with Hippocampal Place Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4631865openalex-extracted
Relative Cue Precision and Prior Knowledge Contribute to the Preference of Proximal and Distal Landmarks in Human Orientation
inferred← citeshttps://doi.org/10.1002/hipo.22101openalex-snapshot
Influence of local objects on hippocampal representations: Landmark vectors and memory
inferred← citeshttps://doi.org/10.1002/hipo.22154openalex-snapshot
Association rules for rat spatial learning: The importance of the hippocampus for binding item identity with item location
inferred← citeshttps://doi.org/10.1002/hipo.22289openalex-snapshot
Role of self‐generated odor cues in contextual representation
inferred← citeshttps://doi.org/10.1002/hipo.22656openalex-snapshot
Slow stabilization of concurrently acquired hippocampal context representations
inferred← citeshttps://doi.org/10.1002/hipo.23506openalex-snapshot
The medial entorhinal cortex is necessary for the stimulus control over hippocampal place fields by distal, but not proximal, landmarks
inferred← citeshttps://doi.org/10.1002/wcs.1411openalex-snapshot
Spatial cognition in mice and rats: similarities and differences in brain and behavior
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_14openalex-snapshot
How Does the Brain Solve the Computational Problems of Spatial Navigation?
inferred← citeshttps://doi.org/10.1007/s11055-019-00770-8openalex-snapshot
Effects of Fragmentation of Visual Navigational Signals on the Orientation of Rats in a Radial Maze
inferred← citeshttps://doi.org/10.1016/j.bbr.2014.09.001openalex-snapshot
The neural representation of 3-dimensional objects in rodent memory circuits
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Hippocampal-dependent memory in the plus-maze discriminative avoidance task: The role of spatial cues and CA1 activity
inferred← citeshttps://doi.org/10.1016/j.bbr.2023.114355openalex-snapshot
Peg Forest Rehabilitation – A novel spatial navigation based cognitive rehabilitation paradigm for experimental neurotrauma
inferred← citeshttps://doi.org/10.1016/j.brainres.2014.04.023openalex-snapshot
Hippocampal place cell responses to distal and proximal cue manipulations in dopamine D2 receptor-knockout mice
inferred← citeshttps://doi.org/10.1016/j.cognition.2024.105772openalex-snapshot
Relative cue precision and prior knowledge contribute to the preference of proximal and distal landmarks in human orientation
inferred← citeshttps://doi.org/10.1016/j.jphysparis.2011.09.002openalex-snapshot
Stability and variability of place cell activity during behavior: Functional implications for dynamic coding of spatial information
inferred← citeshttps://doi.org/10.1016/j.neuron.2023.04.008openalex-snapshot
Object-centered population coding in CA1 of the hippocampus
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2026.109539openalex-snapshot
Prevalence and modulation of rat off-track head scanning on linear tracks: possible implications for representational and dynamic properties of hippocampal place cells
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.09.004openalex-snapshot
Hippocampal place cell activity during chasing of a moving object associated with reward in rats
inferred← citeshttps://doi.org/10.1016/j.nlm.2012.02.005openalex-snapshot
Selective lesions of the dentate gyrus produce disruptions in place learning for adjacent spatial locations
inferred← citeshttps://doi.org/10.1037/0735-7044.122.4.827openalex-snapshot
Landmark control and updating of self-movement cues are largely maintained in head direction cells after lesions of the posterior parietal cortex.
inferred← citeshttps://doi.org/10.1037/a0022315openalex-snapshot
Looking beyond the boundaries: Time to put landmarks back on the cognitive map?
inferred← citeshttps://doi.org/10.1038/s41583-023-00716-7openalex-snapshot
Interactions between rodent visual and spatial systems during navigation
inferred← citeshttps://doi.org/10.1093/cercor/bht020openalex-snapshot
Medial Entorhinal Grid Cells and Head Direction Cells Rotate with a T-Maze More Often During Less Recently Experienced Rotations
inferred← citeshttps://doi.org/10.1093/czoolo/59.3.317openalex-snapshot
Do females influence paternal responsiveness in male prairie voles Microtus ochrogaster by increasing the salience of infant odors?
inferred← citeshttps://doi.org/10.1093/texcom/tgab052openalex-snapshot
The Role of Idiothetic Signals, Landmarks, and Conjunctive Representations in the Development of Place and Head-Direction Cells: A Self-Organizing Neural Network Model
inferred← citeshttps://doi.org/10.1101/2025.09.25.678702openalex-snapshot
Honeybees acquire a spatial memory by learning landmarks and visual patterns in parallel
inferred← citeshttps://doi.org/10.1101/lm.1315109openalex-snapshot
Visual object pattern separation deficits in nondemented older adults
inferred← citeshttps://doi.org/10.1101/lm.703907openalex-snapshot
Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map
inferred← citeshttps://doi.org/10.1109/ijcnn55064.2022.9892401openalex-snapshot
Context-Dependent Spatial Representations in the Hippocampus using Place Cell Dendritic Computation
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2011.07653.xopenalex-snapshot
Local remapping of place cell firing in the Tolman detour task
inferred← citeshttps://doi.org/10.1152/jn.00731.2007openalex-snapshot
Dominance of the Proximal Coordinate Frame in Determining the Locations of Hippocampal Place Cell Activity During Navigation
inferred← citeshttps://doi.org/10.1152/physrev.00021.2010openalex-snapshot
Framing Spatial Cognition: Neural Representations of Proximal and Distal Frames of Reference and Their Roles in Navigation
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Self-Organizing Sensorimotor Maps Plus Internal Motivations Yield Animal-Like Behavior
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Conflicts between Local and Global Spatial Frameworks Dissociate Neural Representations of the Lateral and Medial Entorhinal Cortex
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Different CA1 and CA3 Representations of Novel Routes in a Shortcut Situation
inferred← citeshttps://doi.org/10.1523/jneurosci.2127-18.2019openalex-snapshot
The Ventral Midline Thalamus Mediates Hippocampal Spatial Information Processes upon Spatial Cue Changes
inferred← citeshttps://doi.org/10.1523/jneurosci.3427-12.2013openalex-snapshot
Prefrontal Cortex Focally Modulates Hippocampal Place Cell Firing Patterns
inferred← citeshttps://doi.org/10.3389/fnbeh.2013.00202openalex-snapshot
Dynamic NMDAR-mediated properties of place cells during the object place memory task
inferred← citeshttps://doi.org/10.3389/fnbeh.2015.00250openalex-snapshot
Dynamics of place, boundary and object encoding in rat anterior claustrum
inferred← citeshttps://doi.org/10.3389/fnbeh.2017.00092openalex-snapshot
Experience-Dependency of Reliance on Local Visual and Idiothetic Cues for Spatial Representations Created in the Absence of Distal Information
inferred← citeshttps://doi.org/10.3389/fnbeh.2017.00109openalex-snapshot
Are Distal and Proximal Visual Cues Equally Important during Spatial Learning in Mice? A Pilot Study of Overshadowing in the Spatial Domain
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Propriétés de la carte cognitive thalamique : étude des caractéristiques du codage spatial dans le thalamus visuel et de son influence sur le codage positionnel de l’hippocampe
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Electrophysiologie de l’hippocampe in vivo pendant le comportement : étude de l'impact de la locomotion sur le potentiel de membrane des cellules pyramidales de CA1 de l'hippocampe chez la souris naviguant dans un environnement virtuel
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Spatial resolution of the cognitive map : investigation on the influence of proximal visual cues on spatial coding resolution in area CA1 of the dorsal hippocampus using virtual reality
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Rôle du cortex entorhinal médian dans le traitement des informations spatiales : études comportementales et électrophysiologiques
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Framing of grid cells within and beyond navigation boundaries
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Dynamic control of hippocampal spatial coding resolution by local visual cues
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An Intranet of Things approach for adaptable control of behavioral and navigation-based experiments
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