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CA1 pyramidal cells organize an episode by segmented and ordered events

https://doi.org/10.1101/565689
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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/10.1016/0006-8993(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.cell.2014.04.009openalex-snapshot
Successful Execution of Working Memory Linked to Synchronized High-Frequency Gamma Oscillations
inferredcites →https://doi.org/10.1016/j.neuron.2007.08.017openalex-snapshot
Gradual Changes in Hippocampal Activity Support Remembering the Order of Events
inferredcites →https://doi.org/10.1016/j.neuron.2009.08.009openalex-snapshot
Automated Analysis of Cellular Signals from Large-Scale Calcium Imaging Data
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.2017.05.024openalex-snapshot
Temporal and Rate Coding for Discrete Event Sequences in the Hippocampus
inferredcites →https://doi.org/10.1016/j.neuron.2018.10.002openalex-snapshot
What Is a Cognitive Map? Organizing Knowledge for Flexible Behavior
inferredcites →https://doi.org/10.1016/j.tics.2018.07.006openalex-snapshot
Space and Time: The Hippocampus as a Sequence Generator
inferredcites →https://doi.org/10.1016/s0306-4522(00)00258-xopenalex-snapshot
Convergence of head direction and place information in the CA1 region of hippocampus
inferredcites →https://doi.org/10.1016/s0306-4522(02)00509-2openalex-snapshot
Coding of auditory temporal and pitch information by hippocampal individual cells and cell assemblies in the rat
inferredcites →https://doi.org/10.1016/s0896-6273(00)00018-0openalex-snapshot
Trajectory Encoding in the Hippocampus and Entorhinal Cortex
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/10.1038/17605openalex-snapshot
The global record of memory in hippocampal neuronal activity
inferredcites →https://doi.org/10.1038/nature05601openalex-snapshot
Hippocampal remapping and grid realignment in entorhinal cortex
inferredcites →https://doi.org/10.1038/nature12354openalex-snapshot
Ultrasensitive fluorescent proteins for imaging neuronal activity
inferredcites →https://doi.org/10.1038/nature21692openalex-snapshot
Mapping of a non-spatial dimension by the hippocampal–entorhinal circuit
inferredcites →https://doi.org/10.1038/nn.3236openalex-snapshot
Spontaneous persistent activity in entorhinal cortex modulates cortico-hippocampal interaction in vivo
inferredcites →https://doi.org/10.1038/nn.3329openalex-snapshot
Long-term dynamics of CA1 hippocampal place codes
inferredcites →https://doi.org/10.1038/s41586-018-0459-6openalex-snapshot
Integrating time from experience in the lateral entorhinal cortex
inferredcites →https://doi.org/10.1038/s41586-019-0919-7openalex-snapshot
Discrete attractor dynamics underlies persistent activity in the frontal cortex
inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00446.xopenalex-snapshot
Sustained activation of hippocampal pyramidal cells by ‘space clamping’ in a running wheel
inferredcites →https://doi.org/10.1126/science.1086872openalex-snapshot
Representation of Action Sequence Boundaries by Macaque Prefrontal Cortical Neurons
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.1159775openalex-snapshot
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
inferredcites →https://doi.org/10.1126/science.1210125openalex-snapshot
Entorhinal Cortex Layer III Input to the Hippocampus Is Crucial for Temporal Association Memory
inferredcites →https://doi.org/10.1126/science.1232655openalex-snapshot
Multisensory Control of Hippocampal Spatiotemporal Selectivity
inferredcites →https://doi.org/10.1126/science.1244634openalex-snapshot
Island Cells Control Temporal Association Memory
inferredcites →https://doi.org/10.1126/science.aaf7003openalex-snapshot
Ventral CA1 neurons store social memory
inferredcites →https://doi.org/10.1126/science.aan8869openalex-snapshot
Space and time in the brain
inferredcites →https://doi.org/10.1136/jnnp.20.1.11openalex-snapshot
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
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.17-11-04302.1997openalex-snapshot
The Fusiform Face Area: A Module in Human Extrastriate Cortex Specialized for Face Perception
inferredcites →https://doi.org/10.1523/jneurosci.2874-15.2016openalex-snapshot
Nonspatial Sequence Coding in CA1 Neurons

What points at this work

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

inferred← citeshttps://doi.org/10.1002/hipo.23272openalex-snapshot
Hippocampal spatial memory representations in mice are heterogeneously stable
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2019.101717openalex-snapshot
Structure learning and the posterior parietal cortex
inferred← citeshttps://doi.org/10.1038/s41467-021-22559-5openalex-snapshot
Clone-structured graph representations enable flexible learning and vicarious evaluation of cognitive maps
inferred← citeshttps://doi.org/10.1101/864421openalex-snapshot
Learning cognitive maps as structured graphs for vicarious evaluation
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