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Neurons remap to represent memories in the human entorhinal cortex

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9781118597705.ch13openalex-snapshot

Binding Together the Elements of Episodes: Relational Memory and the Developmental Trajectory of the Hippocampus

inferredcites →https://doi.org/10.1002/hbm.22627openalex-snapshot

Automated volumetry and regional thickness analysis of hippocampal subfields and medial temporal cortical structures in mild cognitive impairment

inferredcites →https://doi.org/10.1007/bf00239513openalex-snapshot

Premotor cortex of the rhesus monkey: neuronal activity in anticipation of predictable environmental events

inferredcites →https://doi.org/10.1007/bf00308809openalex-snapshot

Neuropathological stageing of Alzheimer-related changes

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/j.bbr.2012.12.034openalex-snapshot

Place cell activation predicts subsequent memory

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.conb.2006.10.012openalex-snapshot

Item, context and relational episodic encoding in humans

inferredcites →https://doi.org/10.1016/j.cub.2013.01.036openalex-snapshot

Traces of Experience in the Lateral Entorhinal Cortex

inferredcites →https://doi.org/10.1016/j.jns.2005.05.001openalex-snapshot

Neuroimaging as a marker of the onset and progression of Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.jphysparis.2004.01.018openalex-snapshot

Intracranial EEG and human brain mapping

inferredcites →https://doi.org/10.1016/j.neuron.2011.07.012openalex-snapshot

Hippocampal “Time Cells” Bridge the Gap in Memory for Discontiguous Events

inferredcites →https://doi.org/10.1016/j.neuron.2016.09.043openalex-snapshot

Are You Smarter Than a Teenager? Maybe Not When It Comes to Reinforcement Learning

inferredcites →https://doi.org/10.1016/j.neuron.2016.10.062openalex-snapshot

Direct Electrical Stimulation of the Human Entorhinal Region and Hippocampus Impairs Memory

inferredcites →https://doi.org/10.1016/j.neuron.2018.01.039openalex-snapshot

Functional Imbalance of Anterolateral Entorhinal Cortex and Hippocampal Dentate/CA3 Underlies Age-Related Object Pattern Separation Deficits

inferredcites →https://doi.org/10.1016/j.neuron.2018.06.008openalex-snapshot

A Dedicated Population for Reward Coding in the Hippocampus

inferredcites →https://doi.org/10.1016/j.neuropsychologia.2013.01.013openalex-snapshot

Distinct neuroanatomical bases of episodic and semantic memory performance in Alzheimer’s disease

inferredcites →https://doi.org/10.1016/j.tins.2008.06.008openalex-snapshot

Understanding memory through hippocampal remapping

inferredcites →https://doi.org/10.1016/s0896-6273(00)00071-4openalex-snapshot

Hippocampal Neurons Encode Information about Different Types of Memory Episodes Occurring in the Same Location

inferredcites →https://doi.org/10.1038/nature01964openalex-snapshot

Cellular networks underlying human spatial navigation

inferredcites →https://doi.org/10.1038/nature03721openalex-snapshot

Microstructure of a spatial map in the entorhinal cortex

inferredcites →https://doi.org/10.1038/nature14622openalex-snapshot

Speed cells in the medial entorhinal cortex

inferredcites →https://doi.org/10.1038/nn.2599openalex-snapshot

The reorganization and reactivation of hippocampal maps predict spatial memory performance

inferredcites →https://doi.org/10.1038/nn.3304openalex-snapshot

Memory, navigation and theta rhythm in the hippocampal-entorhinal system

inferredcites →https://doi.org/10.1038/nn.3466openalex-snapshot

Direct recordings of grid-like neuronal activity in human spatial navigation

inferredcites →https://doi.org/10.1038/nn.3606openalex-snapshot

Molecular drivers and cortical spread of lateral entorhinal cortex dysfunction in preclinical Alzheimer's disease

inferredcites →https://doi.org/10.1038/nn.4464openalex-snapshot

Subiculum neurons map the current axis of travel

inferredcites →https://doi.org/10.1038/nn.4509openalex-snapshot

Persistently active neurons in human medial frontal and medial temporal lobe support working memory

inferredcites →https://doi.org/10.1038/nn996openalex-snapshot

Associative knowledge controls deployment of visual selective attention

inferredcites →https://doi.org/10.1038/nrn3827openalex-snapshot

Time cells in the hippocampus: a new dimension for mapping memories

inferredcites →https://doi.org/10.1038/s41586-019-1077-7openalex-snapshot

Object-vector coding in the medial entorhinal cortex

inferredcites →https://doi.org/10.1038/s41593-018-0070-zopenalex-snapshot

Structural tract alterations predict downstream tau accumulation in amyloid-positive older individuals

inferredcites →https://doi.org/10.1080/02724980244000224openalex-snapshot

The hippocampus, space, and viewpoints in episodic memory

inferredcites →https://doi.org/10.1088/1741-2560/10/1/016001openalex-snapshot

A statistical method for predicting seizure onset zones from human single-neuron recordings

inferredcites →https://doi.org/10.1097/00006123-199904000-00001openalex-snapshot

Current Results of the Surgical Management of Aneurysms of the Basilar Apex

inferredcites →https://doi.org/10.1098/rstb.2013.0369openalex-snapshot

Functional correlates of the lateral and medial entorhinal cortex: objects, path integration and local–global reference frames

inferredcites →https://doi.org/10.1101/365593openalex-snapshot

What is a cognitive map? Organising knowledge for flexible behaviour

inferredcites →https://doi.org/10.1126/science.1244056openalex-snapshot

Neural Activity in Human Hippocampal Formation Reveals the Spatial Context of Retrieved Memories

inferredcites →https://doi.org/10.1126/science.aac8128openalex-snapshot

Reduced grid-cell–like representations in adults at genetic risk for Alzheimer’s disease

inferredcites →https://doi.org/10.1126/science.aak9589openalex-snapshot

Vectorial representation of spatial goals in the hippocampus of bats

inferredcites →https://doi.org/10.1136/jnnp.20.1.11openalex-snapshot

LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS

inferredcites →https://doi.org/10.1146/annurev.ps.44.020193.002321openalex-snapshot

The Structure and Organization of Memory

inferredcites →https://doi.org/10.1152/jn.00214.2009openalex-snapshot

Neural Correlates of Novel Object and Novel Location Recognition Behavior in the Mouse Anterior Cingulate Cortex

inferredcites →https://doi.org/10.1152/jn.1997.78.2.1062openalex-snapshot

Object and Place Memory in the Macaque Entorhinal Cortex

inferredcites →https://doi.org/10.1371/journal.pone.0166598openalex-snapshot

Reliable Analysis of Single-Unit Recordings from the Human Brain under Noisy Conditions: Tracking Neurons over Hours

inferredcites →https://doi.org/10.1523/jneurosci.07-03-00716.1987openalex-snapshot

Cue-sampling and goal-approach correlates of hippocampal unit activity in rats performing an odor-discrimination task

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.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.1063-07.2007openalex-snapshot

Disambiguation of Overlapping Experiences by Neurons in the Medial Entorhinal Cortex

inferredcites →https://doi.org/10.1523/jneurosci.1378-09.2009openalex-snapshot

Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where

inferredcites →https://doi.org/10.1523/jneurosci.15-11-07079.1995openalex-snapshot

Interactions between location and task affect the spatial and directional firing of hippocampal neurons

inferredcites →https://doi.org/10.1523/jneurosci.16-14-04491.1996openalex-snapshot

Profound Loss of Layer II Entorhinal Cortex Neurons Occurs in Very Mild Alzheimer’s Disease

inferredcites →https://doi.org/10.1523/jneurosci.2028-17.2017openalex-snapshot

Entorhinal Tau Pathology, Episodic Memory Decline, and Neurodegeneration in Aging

inferredcites →https://doi.org/10.1523/jneurosci.3664-16.2017openalex-snapshot

Anterolateral Entorhinal Cortex Volume Predicted by Altered Intra-Item Configural Processing

inferredcites →https://doi.org/10.3171/jns.1999.91.4.0697openalex-snapshot

Cerebral microdialysis combined with single-neuron and electroencephalographic recording in neurosurgical patients

inferredcites →https://doi.org/10.3389/fnbeh.2011.00069openalex-snapshot

Representation of Non-Spatial and Spatial Information in the Lateral Entorhinal Cortex

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1101/449470openalex-snapshot

Predicting the Future with Multi-scale Successor Representations

inferred← citeshttps://doi.org/10.3389/fnins.2023.1200842openalex-snapshot

Accounting for multiscale processing in adaptive real-world decision-making via the hippocampus

inferred← citeshttps://doi.org/10.7554/elife.45333openalex-snapshot

Mapping sequence structure in the human lateral entorhinal cortex

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