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Single unit activity in the rat hippocampus during a spatial memory task
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00237147openalex-snapshot
The contributions of position, direction, and velocity to single unit activity in the hippocampus of freely-moving rats
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/bf02476084openalex-snapshot
Glass-coated platinum-plated tungsten microelectrodes
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/10.1016/0006-8993(78)90930-7openalex-snapshot
Hippocampal connections and spatial discrimination
inferredcites →https://doi.org/10.1016/0006-8993(80)91214-7openalex-snapshot
Spatial correlates of hippocampal unit activity are altered by lesions of the fornix and entorhinal cortex
inferredcites →https://doi.org/10.1016/0014-4886(73)90290-2openalex-snapshot
Studies on single neurons in dorsal hippocampal formation and septum in unrestrained rats
inferredcites →https://doi.org/10.1016/0014-4886(76)90055-8openalex-snapshot
Place units in the hippocampus of the freely moving rat
inferredcites →https://doi.org/10.1016/0014-4886(78)90058-4openalex-snapshot
First occurrence of hippocampal spatial firing in a new environment
inferredcites →https://doi.org/10.1016/0014-4886(78)90096-1openalex-snapshot
Spatial correlates of hippocampal unit activity
inferredcites →https://doi.org/10.1016/0014-4886(82)90032-2openalex-snapshot
Reliability of the relationship between hippocampal unit activity and sensory-behavioral events in the rat
inferredcites →https://doi.org/10.1016/0028-3932(81)90090-7openalex-snapshot
The role of the right hippocampus in the recall of spatial location
inferredcites →https://doi.org/10.1016/0165-0173(83)90037-1openalex-snapshot
Cellular bases of hippocampal EEG in the behaving rat
inferredcites →https://doi.org/10.1016/0165-0270(83)90097-3openalex-snapshot
The stereotrode: A new technique for simultaneous isolation of several single units in the central nervous system from multiple unit records
inferredcites →https://doi.org/10.1016/0197-4580(83)90034-9openalex-snapshot
Loss of place specificity in hippocampal complex spike cells of senescent rat
inferredcites →https://doi.org/10.1016/0301-0082(79)90005-4openalex-snapshot
A review of the hippocampal place cells
inferredcites →https://doi.org/10.1017/s0140525x00062713openalex-snapshot
Hippocampus, space, and memory
inferredcites →https://doi.org/10.1037/11774-000openalex-snapshot
Statistical principles in experimental design.
inferredcites →https://doi.org/10.1113/jphysiol.1980.sp013435openalex-snapshot
A comparison of distal and proximal dendritic synapses on CA1 pyramids in guinea‐pig hippocampal slices in vitro
inferredcites →https://doi.org/10.1136/jnnp.20.1.11openalex-snapshot
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
inferredcites →https://doi.org/10.1152/jn.1961.24.3.225openalex-snapshot
ELECTROPHYSIOLOGY OF HIPPOCAMPAL NEURONS: I. SEQUENTIAL INVASION AND SYNAPTIC ORGANIZATION
inferredcites →https://doi.org/10.1152/jn.1964.27.4.592openalex-snapshot
LOCATION OF POSTSYNAPTIC INHIBITORY SYNAPSES ON HIPPOCAMPAL PYRAMIDS
inferredcites →https://doi.org/10.1152/jn.1981.46.5.952openalex-snapshot
Synaptic efficacy and EPSP summation in granule cells of rat fascia dentata studied in vitro.
inferredcites →https://doi.org/10.1523/jneurosci.07-07-01935.1987openalex-snapshot
Spatial firing patterns of hippocampal complex-spike cells in a fixed environment
inferredcites →https://doi.org/10.1523/jneurosci.08-11-04159.1988openalex-snapshot
A selective mnemonic role for the hippocampus in monkeys: memory for the location of objects
inferredcites →https://doi.org/10.3758/bf03332854openalex-snapshot
On the trail of the hippocampal engram
inferredcites →https://doi.org/10.4324/9780203710029openalex-snapshot
Cognitive Processes in Animal Behavior
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/(sici)1096-9861(19980222)391:4<456::aid-cne4>3.0.co;2-#openalex-snapshot
Projections from the accessory optic system and pretectum to the dorsolateral thalamus in the pigeon ( Columbia livia ): A study using both anterograde and retrograde tracers
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1996)6:3<247::aid-hipo4>3.0.co;2-kopenalex-snapshot
Theory of rodent navigation based on interacting representations of space
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1996)6:3<271::aid-hipo5>3.0.co;2-qopenalex-snapshot
Population dynamics and theta rhythm phase precession of hippocampal place cell firing: A spiking neuron model
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1996)6:3<281::aid-hipo6>3.0.co;2-qopenalex-snapshot
Hippocampal place fields: Relationship between degree of field overlap and cross-correlations within ensembles of hippocampal neurons
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1996)6:6<735::aid-hipo15>3.0.co;2-1openalex-snapshot
Memory for places: A navigational model in support of Marr's theory of hippocampal function
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1996)6:6<749::aid-hipo16>3.0.co;2-0openalex-snapshot
Neuronal computations underlying the firing of place cells and their role in navigation
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1997)7:1<15::aid-hipo3>3.0.co;2-6openalex-snapshot
Cognitive maps beyond the hippocampus
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1998)8:4<340::aid-hipo4>3.0.co;2-lopenalex-snapshot
Superior colliculus and active navigation: Role of visual and non-visual cues in controlling cellular representations of space
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1998)8:6<608::aid-hipo3>3.0.co;2-7openalex-snapshot
Functional differentiation in the hippocampus
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1998)8:6<651::aid-hipo8>3.0.co;2-lopenalex-snapshot
Plasticity of directional place fields in a model of rodent CA3
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:2<158::aid-hipo7>3.0.co;2-oopenalex-snapshot
Comparison of the timing of hippocampal and subicular spatial signals: Implications for path integration
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:3<206::aid-hipo2>3.0.co;2-hopenalex-snapshot
Head direction cells in the primate pre-subiculum
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:3<235::aid-hipo4>3.0.co;2-3openalex-snapshot
Hippocampal place cells can develop distinct representations of two visually identical environments
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<346::aid-hipo2>3.0.co;2-3openalex-snapshot
Placing hippocampal single-unit studies in a historical context
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<365::aid-hipo4>3.0.co;2-topenalex-snapshot
Hippocampus as a memory map: Synaptic plasticity and memory encoding by hippocampal neurons
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<385::aid-hipo5>3.0.co;2-kopenalex-snapshot
Hippocampal encoding of non-spatial trace conditioning
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<413::aid-hipo7>3.0.co;2-#openalex-snapshot
Is the hippocampus of the rat part of a specialized navigational system?
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<432::aid-hipo9>3.0.co;2-popenalex-snapshot
Complimentary roles for hippocampal versus subicular/entorhinal place cells in coding place, context, and events
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<458::aid-hipo12>3.0.co;2-gopenalex-snapshot
Active Spatial Information Processing in the Septo-Hippocampal System
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:4<481::aid-hipo14>3.0.co;2-sopenalex-snapshot
Attractor neural network models of spatial maps in hippocampus
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(1999)9:6<659::aid-hipo7>3.0.co;2-eopenalex-snapshot
Calibrating space: Exploration is important for allothetic and idiothetic navigation
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(2000)10:1<31::aid-hipo3>3.0.co;2-lopenalex-snapshot
Immunocytochemical mapping of Fos protein following seizures in gerbils indicates the activation of hippocampal neurons
inferred← citeshttps://doi.org/10.1002/(sici)1098-1063(2000)10:1<64::aid-hipo7>3.0.co;2-yopenalex-snapshot
Contribution of multiple sensory information to place field stability in hippocampal place cells
inferred← citeshttps://doi.org/10.1002/1098-1063(2000)10:3<207::aid-hipo1>3.0.co;2-sopenalex-snapshot
Disparate effects of long-term potentiation on evoked potentials and single CA1 neurons in the hippocampus of anesthetized rats
inferred← citeshttps://doi.org/10.1002/1098-1063(2000)10:3<226::aid-hipo3>3.0.co;2-hopenalex-snapshot
Dorsal hippocampal function in unreinforced spatial learning
inferred← citeshttps://doi.org/10.1002/1098-1063(2000)10:3<338::aid-hipo14>3.0.co;2-yopenalex-snapshot
Age-related deficits in the ability to encode contextual change: A place cell analysis
inferred← citeshttps://doi.org/10.1002/9781118650813.ch13openalex-snapshot
The Relation Between Spatial and Nonspatial Learning
inferred← citeshttps://doi.org/10.1002/advs.76661openalex-snapshot
Experience‐Dependent Reorganization of Hippocampal CA3 Neuronal Ensembles Associates With Memory Generalization
inferred← citeshttps://doi.org/10.1002/ajpa.1330350606openalex-snapshot
Evolution of sex difference in spatial ability
inferred← citeshttps://doi.org/10.1002/bies.201500004openalex-snapshot
Neuronal hyperactivity – A key defect in Alzheimer's disease?
inferred← citeshttps://doi.org/10.1002/cne.10167openalex-snapshot
Electrophysiological profile of avian hippocampal unit activity: A basis for regional subdivisions
inferred← citeshttps://doi.org/10.1002/cne.23803openalex-snapshot
Evolution of the hippocampus in reptiles and birds
inferred← citeshttps://doi.org/10.1002/hipo.10021openalex-snapshot
Development of spatial firing in the hippocampus of young rats
inferred← citeshttps://doi.org/10.1002/hipo.10047openalex-snapshot
Preserved performance in a hippocampal‐dependent spatial task despite complete place cell remapping
inferred← citeshttps://doi.org/10.1002/hipo.10056openalex-snapshot
Reward value invariant place responses and reward site associated activity in hippocampal neurons of behaving rats
inferred← citeshttps://doi.org/10.1002/hipo.10062openalex-snapshot
Representation of place by monkey hippocampal neurons in real and virtual translocation
inferred← citeshttps://doi.org/10.1002/hipo.10092openalex-snapshot
Distal landmarks and hippocampal place cells: Effects of relative translation versus rotation
inferred← citeshttps://doi.org/10.1002/hipo.10161openalex-snapshot
Excitotoxic lesions of the pre‐ and parasubiculum disrupt the place fields of hippocampal pyramidal cells
inferred← citeshttps://doi.org/10.1002/hipo.1039openalex-snapshot
Competitive Hebbian learning and the hippocampal place cell system: Modeling the interaction of visual and path integration cues
inferred← citeshttps://doi.org/10.1002/hipo.1052openalex-snapshot
Evidence for a relationship between place‐cell spatial firing and spatial memory performance
inferred← citeshttps://doi.org/10.1002/hipo.1085openalex-snapshot
A view model which accounts for the spatial fields of hippocampal primate spatial view cells and rat place cells
inferred← citeshttps://doi.org/10.1002/hipo.1095openalex-snapshot
Noradrenergic regulation of hippocampal place cells
inferred← citeshttps://doi.org/10.1002/hipo.20023openalex-snapshot
Role of active movement in place-specific firing of hippocampal neurons
inferred← citeshttps://doi.org/10.1002/hipo.20042openalex-snapshot
Stability of hippocampal place cell activity across the rat estrous cycle
inferred← citeshttps://doi.org/10.1002/hipo.20108openalex-snapshot
Place-related neural responses in the monkey hippocampal formation in a virtual space
inferred← citeshttps://doi.org/10.1002/hipo.20196openalex-snapshot
Spatial firing properties of lateral septal neurons
inferred← citeshttps://doi.org/10.1002/hipo.20199openalex-snapshot
Hippocampal place cells: The “where” of episodic memory?
inferred← citeshttps://doi.org/10.1002/hipo.20204openalex-snapshot
Episodic memory—From brain to mind
inferred← citeshttps://doi.org/10.1002/hipo.20209openalex-snapshot
Hippocampal place fields: A neural code for episodic memory?
inferred← citeshttps://doi.org/10.1002/hipo.20277openalex-snapshot
Flexible use of proximal objects and distal cues by hippocampal place cells
inferred← citeshttps://doi.org/10.1002/hipo.20304openalex-snapshot
Processing idiothetic cues to remember visited locations: Hippocampal and vestibular contributions to radial‐arm maze performance
inferred← citeshttps://doi.org/10.1002/hipo.20316openalex-snapshot
Cohesiveness of spatial and directional representations recorded from neural ensembles in the anterior thalamus, parasubiculum, medial entorhinal cortex, and hippocampus
inferred← citeshttps://doi.org/10.1002/hipo.20318openalex-snapshot
Space and context in the temporal cortex
inferred← citeshttps://doi.org/10.1002/hipo.20583openalex-snapshot
Patterns of retrograde amnesia for recent and remote incidental spatial learning in rats
inferred← citeshttps://doi.org/10.1002/hipo.20839openalex-snapshot
Lateral entorhinal neurons are not spatially selective in cue‐rich environments
inferred← citeshttps://doi.org/10.1002/hipo.20919openalex-snapshot
Hippocampal place cells encode intended destination, and not a discriminative stimulus, in a conditional T‐maze task
inferred← citeshttps://doi.org/10.1002/hipo.20977openalex-snapshot
The presence of a second rat has only subtle effects on the location‐specific firing of hippocampal place cells
inferred← citeshttps://doi.org/10.1002/hipo.22002openalex-snapshot
Activity dynamics and behavioral correlates of CA3 and CA1 hippocampal pyramidal neurons
inferred← citeshttps://doi.org/10.1002/hipo.22075openalex-snapshot
Limbic system structures differentially contribute to exploratory trip organization of the rat
inferred← citeshttps://doi.org/10.1002/hipo.22410openalex-snapshot
Otolithic information is required for homing in the mouse
inferred← citeshttps://doi.org/10.1002/hipo.22496openalex-snapshot
Place field repetition and spatial learning in a multicompartment environment
inferred← citeshttps://doi.org/10.1002/hipo.22545openalex-snapshot
Learning by subtraction: Hippocampal activity and effects of ethanol during the acquisition and performance of response sequences
inferred← citeshttps://doi.org/10.1002/hipo.22680openalex-snapshot
The postrhinal cortex is not necessary for landmark control in rat head direction cells
inferred← citeshttps://doi.org/10.1002/hipo.22750openalex-snapshot
Space, time, and episodic memory: The hippocampus is all over the cognitive map
inferred← citeshttps://doi.org/10.1002/hipo.22956openalex-snapshot
Three brain states in the hippocampus and cortex
inferred← citeshttps://doi.org/10.1002/hipo.23143openalex-snapshot
Validating the theoretical bases of sleep reactivation during sharp‐wave ripples and their association with emotional valence
inferred← citeshttps://doi.org/10.1002/hipo.23188openalex-snapshot
The rodent hippocampus as a bilateral structure: A review of hemispheric lateralization
inferred← citeshttps://doi.org/10.1002/hipo.23477openalex-snapshot
Hippocampal cellular functional organization for fear memory: Effects of sleep
inferred← citeshttps://doi.org/10.1002/hipo.23483openalex-snapshot
Significance of visual scene‐based learning in the hippocampal systems across mammalian species
inferred← citeshttps://doi.org/10.1002/hipo.23661openalex-snapshot
Mental Time Travel: A Retrospective
inferred← citeshttps://doi.org/10.1002/hipo.450010207openalex-snapshot
Experience‐dependent modifications of hippocampal place cell firing
inferred← citeshttps://doi.org/10.1002/hipo.450010302openalex-snapshot
The hippocampus and space revisited
inferred← citeshttps://doi.org/10.1002/hipo.450010303openalex-snapshot
An allocentric spatial model for the hippocampal cognitive map
inferred← citeshttps://doi.org/10.1002/hipo.450010305openalex-snapshot
Multiple representations in the hippocampus
inferred← citeshttps://doi.org/10.1002/hipo.450010306openalex-snapshot
The hippocampus as a cognitive graph (abridged version)
inferred← citeshttps://doi.org/10.1002/hipo.450010307openalex-snapshot
Space, the final hippocampal frontier?
inferred← citeshttps://doi.org/10.1002/hipo.450010309openalex-snapshot
The hippocampus and space: Are there “place neurons” in the monkey hippocampus?
inferred← citeshttps://doi.org/10.1002/hipo.450020202openalex-snapshot
Fast (beta) rhythms in the hippocampus: A review
inferred← citeshttps://doi.org/10.1002/hipo.450020208openalex-snapshot
Navigation by fragment fitting: A theory of hippocampal function
inferred← citeshttps://doi.org/10.1002/hipo.450020310openalex-snapshot
Neuronal activity in the hippocampus during delayed non‐match to sample performance in rats: Evidence for hippocampal processing in recognition memory
inferred← citeshttps://doi.org/10.1002/hipo.450030209openalex-snapshot
Spatial selectivity of unit activity in the hippocampal granular layer
inferred← citeshttps://doi.org/10.1002/hipo.450030307openalex-snapshot
Phase relationship between hippocampal place units and the EEG theta rhythm
inferred← citeshttps://doi.org/10.1002/hipo.450030310openalex-snapshot
Learning and memory after adrenalectomy‐induced hippocampal dentate granule cell degeneration in the rat
inferred← citeshttps://doi.org/10.1002/hipo.450030312openalex-snapshot
Maps, routes, and the hippocampus: A neural network approach
inferred← citeshttps://doi.org/10.1002/hipo.450040315openalex-snapshot
Effects of medial septal or unilateral hippocampal inactivations on reference and working spatial memory in rats
inferred← citeshttps://doi.org/10.1002/hipo.450040404openalex-snapshot
Spatial information content and reliability of hippocampal CA1 neurons: Effects of visual input
inferred← citeshttps://doi.org/10.1002/hipo.450050504openalex-snapshot
View‐responsive neurons in the primate hippocampal complex
inferred← citeshttps://doi.org/10.1002/hipo.70044openalex-snapshot
Altered Coding of Environmental Boundaries in Human Aging: An fMRI Study
inferred← citeshttps://doi.org/10.1002/hipo.70052openalex-snapshot
Oscillations and Boundaries in My Route Through the Hippocampal Cognitive Map
inferred← citeshttps://doi.org/10.1002/nadc.19880360809openalex-snapshot
Gedächtnis für Worte und Gesichter
inferred← citeshttps://doi.org/10.1006/nlme.2000.3997openalex-snapshot
Training Method Dramatically Affects the Acquisition of a Place Response in Rats with Neurotoxic Lesions of the Hippocampus
inferred← citeshttps://doi.org/10.1006/nlme.2001.4008openalex-snapshot
Multiple Parallel Memory Systems in the Brain of the Rat
inferred← citeshttps://doi.org/10.1006/nlme.2001.4053openalex-snapshot
Hippocampus Lesions Impair Landmark Array Spatial Learning in Homing Pigeons: A Laboratory Study
inferred← citeshttps://doi.org/10.1007/0-306-46897-2_13openalex-snapshot
Cellular Alterations in Hippocampus During Acquisition and Consolidation of Hippocampus-Dependent Trace Eyeblink Conditioning
inferred← citeshttps://doi.org/10.1007/978-0-387-71978-8_14openalex-snapshot
Spatial Representations in the Rat: Case Study or Perspective on Episodic Memory?
inferred← citeshttps://doi.org/10.1007/978-1-4471-3427-5_5openalex-snapshot
A Connectionist Approach to Spatial Memory and Planning
inferred← citeshttps://doi.org/10.1007/978-1-4612-1302-4_12openalex-snapshot
Septal Modulation of the Working Memory for Voluntary Behavior
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_1openalex-snapshot
Sensory Determinants of Hippocampal Place Cell Firing Fields
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_10openalex-snapshot
Hippocampal Spatial Representations and Navigation in Primates
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_12openalex-snapshot
The Rodent Navigation Circuit
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_2openalex-snapshot
Different Hippocampal Place Cell Maps for Different Environments
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_3openalex-snapshot
The Path-Integration Properties of Hippocampal Place Cells
inferred← citeshttps://doi.org/10.1007/978-1-4615-0887-8_4openalex-snapshot
Hippocampal Place Cell Activity During Overtly Purposeful Behavior
inferred← citeshttps://doi.org/10.1007/978-1-4939-2159-1_5openalex-snapshot
Insights into Age-Related Cognitive Decline: Coupling Neurophysiological and Behavioral Approaches
inferred← citeshttps://doi.org/10.1007/978-1-59259-019-3_2openalex-snapshot
Cellular and Molecular Mechanisms of Learning and Memory
inferred← citeshttps://doi.org/10.1007/978-3-030-30457-7_4openalex-snapshot
Technology-Mediated Memory Impairment
inferred← citeshttps://doi.org/10.1007/978-3-031-54864-2_21openalex-snapshot
Spatial Map: Through the Lens of Behavioral Tag and Capture
inferred← citeshttps://doi.org/10.1007/978-3-319-15759-7_4openalex-snapshot
Pattern Completion and Pattern Separation Mechanisms in the Hippocampus
inferred← citeshttps://doi.org/10.1007/978-3-319-50406-3_3openalex-snapshot
Elements of Information Processing in Hippocampal Neuronal Activity: Space, Time, and Memory
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_1openalex-snapshot
Introduction: A Neural Systems Approach to Space, Time, and Memory in the Hippocampal Formation
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_19openalex-snapshot
Functional Interactions of Prefrontal Cortex and the Hippocampus in Learning and Memory
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_8openalex-snapshot
Models of Path Integration in the Hippocampal Complex
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_9openalex-snapshot
Remapping to Discriminate Contexts with Hippocampal Population Codes
inferred← citeshttps://doi.org/10.1007/978-4-431-73021-7_9openalex-snapshot
Neural Representations Supporting Spatial Navigation and Memory
inferred← citeshttps://doi.org/10.1007/978-94-010-0870-9_53openalex-snapshot
Spatial Representations in Mammals as Topological Networks
inferred← citeshttps://doi.org/10.1007/978-94-011-0091-5_13openalex-snapshot
The Psychobiology of Spatial Behavior: The Hippocampal Formation and Spatial Mapping
inferred← citeshttps://doi.org/10.1007/978-94-011-0091-5_15openalex-snapshot
Dissociation between Basic Components of Spatial Memory in Rats
inferred← citeshttps://doi.org/10.1007/978-94-011-1709-8_7openalex-snapshot
How and Why Sex Differences Evolve, with Spatial Ability as a Paradigm Example
inferred← citeshttps://doi.org/10.1007/978-981-99-7611-9_3openalex-snapshot
More Than the Sum of Its Parts: Visual–Tactile Integration in the Behaving Rat
inferred← citeshttps://doi.org/10.1007/bf00248904openalex-snapshot
Hippocampal granule cells are necessary for normal spatial learning but not for spatially-selective pyramidal cell discharge
inferred← citeshttps://doi.org/10.1007/bf01251004openalex-snapshot
Hippocampal 5-hydroxytryptamine synthesis is greater in female rats than in males and more decreased by the 5-HT1A agonist 8-OH-DPAT
inferred← citeshttps://doi.org/10.1007/bf03284025openalex-snapshot
Granulocyte-macrophage colony-stimulating factor
inferred← citeshttps://doi.org/10.1007/bf03337772openalex-snapshot
Control of place-cell activity in an open field
inferred← citeshttps://doi.org/10.1007/bf03337774openalex-snapshot
Cortical-hippocampal interactions and cognitive mapping: A hypothesis based on reintegration of the parietal and inferotemporal pathways for visual processing
inferred← citeshttps://doi.org/10.1007/bfb0032464openalex-snapshot
Neuronal circuitry in the medial cerebral cortex of lizards
inferred← citeshttps://doi.org/10.1007/pl00005707openalex-snapshot
The effects of disorientation on visual landmark control of head direction cell orientation
inferred← citeshttps://doi.org/10.1007/s00221-002-1013-0openalex-snapshot
Remapping of place cell firing patterns after maze rotations
inferred← citeshttps://doi.org/10.1007/s00221-004-2135-3openalex-snapshot
Spatially selective reward site responses in tonically active neurons of the nucleus accumbens in behaving rats
inferred← citeshttps://doi.org/10.1007/s002210000656openalex-snapshot
Multimodal mechanisms of attention related to rates of spatial shifting in vision and touch
inferred← citeshttps://doi.org/10.1007/s002210050206openalex-snapshot
Directional control of hippocampal place fields
inferred← citeshttps://doi.org/10.1007/s004019900166openalex-snapshot
Neural substrates of spatial and temporal disorientation in Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/s00422-002-0360-zopenalex-snapshot
What can the hippocampal representation of environmental geometry tell us about Hebbian learning?
inferred← citeshttps://doi.org/10.1007/s00422-003-0395-9openalex-snapshot
A recurrent network for landmark-based navigation
inferred← citeshttps://doi.org/10.1007/s10608-007-9128-zopenalex-snapshot
Cognitive Deficits in Depression and Functional Specificity of Regional Brain Activity
inferred← citeshttps://doi.org/10.1007/s10827-005-6558-zopenalex-snapshot
A Controlled Attractor Network Model of Path Integration in the Rat
inferred← citeshttps://doi.org/10.1007/s10827-008-0090-xopenalex-snapshot
Odor supported place cell model and goal navigation in rodents
inferred← citeshttps://doi.org/10.1007/s11055-026-02046-4openalex-snapshot
The Role of Context and Motivation in Cognition of the Surrounding External World
inferred← citeshttps://doi.org/10.1007/s11229-014-0480-8openalex-snapshot
Investigating neural representations: the tale of place cells
inferred← citeshttps://doi.org/10.1007/s13218-010-0038-yopenalex-snapshot
Learning from Nature: Biologically Inspired Robot Navigation and SLAM—A Review
inferred← citeshttps://doi.org/10.1007/s42489-026-00225-4openalex-snapshot
The Contribution of Spatially Tuned Brain Cells to Human Navigation Performance
inferred← citeshttps://doi.org/10.1016/0003-3472(95)80164-2openalex-snapshot
Optimizing visual landmarks: two- and three-dimensional minimal landscapes
inferred← citeshttps://doi.org/10.1016/0006-8993(94)90361-1openalex-snapshot
Reversible inactivation of the lateral dorsal thalamus disrupts hippocampal place representation and impairs spatial learning
inferred← citeshttps://doi.org/10.1016/0006-8993(94)90645-9openalex-snapshot
Spatial, movement- and reward-sensitive discharge by medial ventral striatum neurons of rats
inferred← citeshttps://doi.org/10.1016/0028-3932(95)00107-7openalex-snapshot
Deficits in spatial working memory after unilateral temporal lobectomy in man
inferred← citeshttps://doi.org/10.1016/0028-3932(96)00022-xopenalex-snapshot
Topographical disorientation following unilateral temporal lobe lesions in humans
inferred← citeshttps://doi.org/10.1016/0031-9384(90)90260-bopenalex-snapshot
Perinatal decortication impairs performance on an 8-arm radial maze task
inferred← citeshttps://doi.org/10.1016/0091-3057(90)90140-dopenalex-snapshot
MK-801 and AP5 impair acquisition, but not retention, of the Morris milk maze
inferred← citeshttps://doi.org/10.1016/0091-3057(94)90091-4openalex-snapshot
Milacemide treatment in mice enhances acquisiton of a Morris-type water maze task
inferred← citeshttps://doi.org/10.1016/0163-1047(92)90724-iopenalex-snapshot
The hippocampus—what does it do?
inferred← citeshttps://doi.org/10.1016/0165-0173(91)90005-sopenalex-snapshot
Learning and memory. FESN Study Group.
inferred← citeshttps://doi.org/10.1016/0166-2236(88)90100-2openalex-snapshot
Representation in the hippocampus: what do hippocampal neurons code?
inferred← citeshttps://doi.org/10.1016/0166-2236(88)90143-9openalex-snapshot
Spatial learning and memory processes: the search for their neurobiological mechanisms in the rat
inferred← citeshttps://doi.org/10.1016/0166-4328(90)90028-dopenalex-snapshot
Role of the hippocampus in temporal and spatial navigation
inferred← citeshttps://doi.org/10.1016/0166-4328(90)90038-gopenalex-snapshot
Hippocampus and medial temporal cortex: Neuronal activity related to behavioural responses during the performance of memory tasks by primates
inferred← citeshttps://doi.org/10.1016/0166-4328(90)90175-eopenalex-snapshot
Enhancing the impact of visual extra-maze cues in a spatial orientation task
inferred← citeshttps://doi.org/10.1016/0166-4328(94)00165-copenalex-snapshot
Optimizing distal landmarks: horizontal versus vertical structures and relation to background
inferred← citeshttps://doi.org/10.1016/0196-9781(90)90012-topenalex-snapshot
Vasoactive intestinal peptide (VIP): An amnestic neuropeptide
inferred← citeshttps://doi.org/10.1016/0301-0082(94)00050-ropenalex-snapshot
Spatially selective firing properties of hippocampal formation neurons in rodents and primates
inferred← citeshttps://doi.org/10.1016/0301-0082(95)00037-2openalex-snapshot
Transgenic animals as models in the study of the neurobiological role of polyamines
inferred← citeshttps://doi.org/10.1016/0301-0082(96)00019-6openalex-snapshot
Spatial, behavioral and sensory correlates of hippocampal CA1 complex spike cell activity: Implications for information processing functions
inferred← citeshttps://doi.org/10.1016/0304-3959(93)90104-wopenalex-snapshot
Is TENS purely a placebo effect? A controlled study on chronic low back pain
inferred← citeshttps://doi.org/10.1016/0306-4522(89)90103-6openalex-snapshot
Intrahippocampal grafts of fetal basal forebrain tissue alter place fields in the hippocampus of rats with fimbria-fornix lesions
inferred← citeshttps://doi.org/10.1016/0306-4522(89)90423-5openalex-snapshot
Two-stage model of memory trace formation: A role for “noisy” brain states
inferred← citeshttps://doi.org/10.1016/0376-6357(95)00060-7openalex-snapshot
A comparative analysis of spatial memory processes
inferred← citeshttps://doi.org/10.1016/0920-1211(91)90033-copenalex-snapshot
An analysis of various environmental and specific sensory stimuli on the seizure activity of the Mongolian gerbil
inferred← citeshttps://doi.org/10.1016/0921-8890(95)00051-8openalex-snapshot
A view-based neurocomputational system for relational map-making and navigation in visual environments
inferred← citeshttps://doi.org/10.1016/0926-6410(96)00004-3openalex-snapshot
Maze procedures: the radial-arm and water maze compared
inferred← citeshttps://doi.org/10.1016/b978-0-12-474993-1.50018-3openalex-snapshot
WITHDRAWN: Neurobiological Views of Memory
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21067-5openalex-snapshot
Interactions Among Multiple Parallel Learning and Memory Systems in the Mammalian Brain
inferred← citeshttps://doi.org/10.1016/b978-0-12-812012-5.00005-7openalex-snapshot
Methodological Approaches to the Behavioural Investigation of Visual Perception in Rodents
inferred← citeshttps://doi.org/10.1016/b978-0-12-820480-1.00029-2openalex-snapshot
Electrophysiological recordings in rodents during spatial navigation: Single neuron recordings
inferred← citeshttps://doi.org/10.1016/b978-0-12-820480-1.00072-3openalex-snapshot
Perception and navigation: What is the interface?
inferred← citeshttps://doi.org/10.1016/b978-0-323-89932-1.00001-9openalex-snapshot
Cognitive consequences of experimental febrile status epilepticus
inferred← citeshttps://doi.org/10.1016/b978-0-444-81444-9.50013-4openalex-snapshot
Mazes: their use in delayed conditional discriminations and place discriminations
inferred← citeshttps://doi.org/10.1016/b978-012369391-4/50038-2openalex-snapshot
Memory in the Aging Hippocampus: What Can Place Cells Tell Us?
inferred← citeshttps://doi.org/10.1016/b978-012372540-0/50006-6openalex-snapshot
Mnemonic contributions of hippocampal place cells
inferred← citeshttps://doi.org/10.1016/b978-012475655-7/50011-3openalex-snapshot
Neurobiological Views of Memory
inferred← citeshttps://doi.org/10.1016/b978-012734610-6/50004-xopenalex-snapshot
Spatial Cognition and Functional Alterations of Aged Rat Hippocampus
inferred← citeshttps://doi.org/10.1016/bs.irn.2020.11.009openalex-snapshot
Potential roles of the rodent medial prefrontal cortex in conflict resolution between multiple decision-making systems
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.11.007openalex-snapshot
The role of growth hormone in hippocampal function
inferred← citeshttps://doi.org/10.1016/j.alcohol.2019.03.006openalex-snapshot
Acute alcohol and cognition: Remembering what it causes us to forget
inferred← citeshttps://doi.org/10.1016/j.bbr.2003.09.005openalex-snapshot
Retention of cue-based associations in the water maze is time-dependent and sensitive to disruption by rotating the starting position
inferred← citeshttps://doi.org/10.1016/j.bbr.2005.12.007openalex-snapshot
Specific changes in hippocampal spatial codes predict spatial working memory performance
inferred← citeshttps://doi.org/10.1016/j.bbr.2006.05.034openalex-snapshot
Subicular place cells generate the same “map” for different environments: Comparison with hippocampal cells
inferred← citeshttps://doi.org/10.1016/j.bbr.2009.03.016openalex-snapshot
Incidental (unreinforced) and reinforced spatial learning in rats with ventral and dorsal lesions of the hippocampus
inferred← citeshttps://doi.org/10.1016/j.bbr.2010.03.044openalex-snapshot
Vibrissal paralysis unveils a preference for textural rather than positional novelty in the one-trial object recognition task in rats
inferred← citeshttps://doi.org/10.1016/j.bbr.2010.07.038openalex-snapshot
Inertial stimuli generated by arena rotation are important for acquisition of the active place avoidance task
inferred← citeshttps://doi.org/10.1016/j.bbr.2010.09.021openalex-snapshot
Locomotion-induced hippocampal theta is independent of visual information in rats during movement through a pipe
inferred← citeshttps://doi.org/10.1016/j.bbr.2011.02.008openalex-snapshot
The dorsomedial striatum mediates flexible choice behavior in spatial tasks
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