Laminar organization of encoding and memory reactivation in the parietal cortex
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Abstract
Egocentric neural coding has been observed in parietal cortex (PC), but its topographical and laminar organization is not well characterized. We used multi-site recording to look for evidence of local clustering and laminar consistency of linear and angular velocity encoding in multi-neuronal spiking activity (MUA) and in the high-frequency (300-900 Hz) component of the local field potential (HF-LFP), believed to reflect local spiking activity. Rats were trained to run many trials on a large circular platform, either to LED-cued goal locations or as a spatial sequence from memory. Tuning to specific self-motion states was observed and exhibited distinct cortical depth-invariant coding properties. These patterns of collective local and laminar activation during behavior were reactivated in compressed form during post-experience sleep and temporally coupled to cortical delta waves and hippocampal sharp-wave ripples. Thus, PC neuron motion encoding is consistent across cortical laminae, and this consistency is maintained during memory reactivation.
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Reactivations in extrahippocampal/cortical areas tend to coincide with oscillatory hallmarks of memory consolidation during sleep, such as SOs and spindles, and with hippocampal SPW-Rs.
“Reactivations in extrahippocampal/cortical areas tend to coincide with oscillatory hallmarks of memory consolidation during sleep, such as SOs and spindles, 65,88,90,96 but also with hippocampal SPW-Rs, 96,99,101,103”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [96]
The Discussion reports enhanced reactivation of behavioral templates in rat parietal cortex simultaneously with cortical delta waves and hippocampal CA1 sharp-wave ripples during sleep. This supports the cortical-reactivation and hippocampal-ripple portions, but our copy does not establish coincidence with sleep spindles or specifically identify the delta waves as slow oscillations (SOs). (LLM, conf=0.86)
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Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
Investigating causal relations by econometric models and cross-spectral methods
Granger, C. W. J. (1969) · Econometrica · doi:10.2307/1912791 · Cited by 22,989 · see citing works
Oostenveld, R., Fries, P., Maris, E., & Schoffelen, J.-M. (2011) · Computational Intelligence and Neuroscience · doi:10.1155/2011/156869 · Cited by 10,323 · see citing works
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,497 · see citing works
A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.
Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284 · see citing works
The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes
Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068 · see citing works
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118 · see citing works
Self-citationReverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727 · see citing works
Selective suppression of hippocampal ripples impairs spatial memory
Girardeau, G., Benchenane, K., Wiener, S. I., Buzsáki, G., & Zugaro, M. B. (2009) · Nature Neuroscience · doi:10.1038/nn.2384 · Cited by 1,560 · see citing works
Frequency of gamma oscillations routes flow of information in the hippocampus
Colgin, L. L., Denninger, T., Fyhn, M., Hafting, T., Bonnevie, T., Jensen, O. B., Moser, M., & Moser, E. I. (2009) · Nature · doi:10.1038/nature08573 · Cited by 1,425 · see citing works
Encoding of Spatial Location by Posterior Parietal Neurons
Andersen, R., Essick, G. K., & Siegel, R. M. (1985) · Science · doi:10.1126/science.4048942 · Cited by 1,413 · see citing works
Schemas and Memory Consolidation.
Tse, D., Langston, R. F., Kakeyama, M., Bethus, I., Spooner, P. A., Wood, E. R., Witter, M. P., & Morris, R. G. M. (2007) · Science · doi:10.1126/science.1135935 · Cited by 1,244 · see citing works
Forward and reverse hippocampal place-cell sequences during ripples
Diba, K., & Buzsáki, G. (2007) · Nature Neuroscience · doi:10.1038/nn1961 · Cited by 1,205 · see citing works
Spence, S. (1996) · BMJ · doi:10.1136/bmj.312.7024.193 · Cited by 1,177 · see citing works
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173 · see citing works
Self-citationHarris, K. D., Henze, D. A., Csicsvari, J. L., Hirase, H., & Buzsáki, G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.401 · Cited by 1,153 · see citing works
Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep
Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148 · see citing works
Brovelli, A., Ding, M., Ledberg, A., Chen, Y., Nakamura, R., & Bressler, S. L. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308538101 · Cited by 1,065 · see citing works
Truccolo, W., Eden, U. T., Fellows, M. R., Donoghue, J. P., & Brown, E. N. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00697.2004 · Cited by 1,063 · see citing works
Coordinated interactions between hippocampal Ripples and Cortical Spindles during Slow-Wave Sleep
Siapas, A. G., & Wilson, M. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80629-7 · Cited by 1,052 · see citing works
The MVGC multivariate Granger causality toolbox: A new approach to Granger-causal inference
Barnett, L., & Seth, A. K. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.10.018 · Cited by 1,017 · see citing works
Different Origins of Gamma Rhythm and High-Gamma Activity in Macaque Visual Cortex
Ray, S., & Maunsell, J. H. R. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1000610 · Cited by 1,012 · see citing works
Remembering the past and imagining the future: A neural model of spatial memory and imagery.
Byrne, P., Becker, S., & Burgess, N. (2007) · Psychological Review · doi:10.1037/0033-295x.114.2.340 · Cited by 1,011 · see citing works
The columnar organization of the neocortex.
Mountcastle, V. B. (1997) · Brain : a journal of neurology · doi:10.1093/brain/120.4.701 · Cited by 941 · see citing works
Organizing conceptual knowledge in humans with a gridlike code
Constantinescu, A. O., O’Reilly, J. X., & Behrens, T. E. J. (2016) · Science · doi:10.1126/science.aaf0941 · Cited by 937 · see citing works
Replay and Time Compression of Recurring Spike Sequences in the Hippocampus
Nádasdy, Z., Hirase, H., Czurkó, A., Csicsvari, J., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09497.1999 · Cited by 932 · see citing works
Choice-specific sequences in parietal cortex during a virtual-navigation decision task
Harvey, C. D., Coen, P., & Tank, D. W. (2012) · Nature · doi:10.1038/nature10918 · Cited by 916 · see citing works
Benchenane, K., Peyrache, A., Khamassi, M., Tierney, P. L., Gioanni, Y., Battaglia, F. P., & Wiener, S. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.013 · Cited by 872 · see citing works
Evidence for grid cells in a human memory network
Doeller, C. F., Barry, C., & Burgess, N. (2010) · Nature · doi:10.1038/nature08704 · Cited by 828 · see citing works
The reorganization and reactivation of hippocampal maps predict spatial memory performance
Dupret, D., O'Neill, J., Pleydell-Bouverie, B., & Csicsvari, J. (2010) · Nature Neuroscience · doi:10.1038/nn.2599 · Cited by 769 · see citing works
Replay of rule-learning related neural patterns in the prefrontal cortex during sleep
Peyrache, A., Khamassi, M., Benchenane, K., Wiener, S. I., & Battaglia, F. P. (2009) · Nature Neuroscience · doi:10.1038/nn.2337 · Cited by 767 · see citing works
Zilles, K. (1985) · Springer eBooks · doi:10.1007/978-3-642-70573-1 · Cited by 756 · see citing works
The Functional Organization of the Barrel Cortex
Petersen, C. C. H. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.017 · Cited by 732 · see citing works
Preplay of future place cell sequences by hippocampal cellular assemblies
Dragoi, G., & Tonegawa, S. (2011) · Nature · doi:10.1038/nature09633 · Cited by 716 · see citing works
Pavlides, C., & Winson, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02907.1989 · Cited by 684 · see citing works
Hippocampo-cortical coupling mediates memory consolidation during sleep
Maingret, N., Girardeau, G., Todorova, R., Goutierre, M., & Zugaro, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4304 · Cited by 667 · see citing works
Sleep promotes branch-specific formation of dendritic spines after learning
Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B. (2014) · Science · doi:10.1126/science.1249098 · Cited by 616 · see citing works
The ‘module-concept’ in cerebral cortex architecture
Szentágothai, J. (1975) · Brain Research · doi:10.1016/0006-8993(75)90122-5 · Cited by 614 · see citing works
Spontaneous Events Outline the Realm of Possible Sensory Responses in Neocortical Populations
Luczak, A., Barthó, P., & Harris, K. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.014 · Cited by 593 · see citing works
Fast-Forward Playback of Recent Memory Sequences in Prefrontal Cortex During Sleep
Euston, D. R., Tatsuno, M., & McNaughton, B. L. (2007) · Science · doi:10.1126/science.1148979 · Cited by 586 · see citing works
Self-citationMcNaughton, B. L., O'Keefe, J. M., & Barnes, C. A. (1983) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(83)90097-3 · Cited by 571 · see citing works
Self-citationA high-performance neural prosthesis enabled by control algorithm design
Gilja, V., Nuyujukian, P., Chestek, C. A., Cunningham, J. P., Yu, B. M., Fan, J. M., Churchland, M. M., Kaufman, M. T., Kao, J. C., Ryu, S. I., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3265 · Cited by 564 · see citing works
Chen, L. L., Lin, L.-H., Green, E. J., Barnes, C. A., & McNaughton, B. L. (1994) · Experimental Brain Research · doi:10.1007/bf00243212 · Cited by 543 · see citing works
Self-citationOverlapping memory replay during sleep builds cognitive schemata
Lewis, P. A., & Durrant, S. J. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.06.004 · Cited by 512 · see citing works
Area map of mouse visual cortex
Wang, Q., & Burkhalter, A. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21286 · Cited by 498 · see citing works
The minicolumn hypothesis in neuroscience
Buxhoeveden, D. P., & Casanova, M. F. (2002) · Brain · doi:10.1093/brain/awf110 · Cited by 496 · see citing works
Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence
McNamara, C. G., Tejero-Cantero, Á., Trouche, S., Campo-Urriza, N., & Dupret, D. (2014) · Nature Neuroscience · doi:10.1038/nn.3843 · Cited by 486 · see citing works
Distinct relationships of parietal and prefrontal cortices to evidence accumulation
Hanks, T. D., Kopec, C. D., Brunton, B. W., Duan, C. A., Erlich, J. C., & Brody, C. D. (2015) · Nature · doi:10.1038/nature14066 · Cited by 486 · see citing works
THE CIRCUITRY OF V1 AND V2: Integration of Color, Form, and Motion
Sincich, L. C., & Horton, J. C. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135731 · Cited by 433 · see citing works
Wang, Q., Sporns, O., & Burkhalter, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6063-11.2012 · Cited by 410 · see citing works
Rewarded Outcomes Enhance Reactivation of Experience in the Hippocampus
Singer, A. C., & Frank, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.016 · Cited by 385 · see citing works
Tsunoda, K., Yamane, Y., Nishizaki, M., & Tanifuji, M. (2001) · Nature Neuroscience · doi:10.1038/90547 · Cited by 359 · see citing works
Dynamic Analysis of Neural Encoding by Point Process Adaptive Filtering
Eden, U. T., Frank, L. M., Barbieri, R., Solo, V., & Brown, E. N. (2004) · Neural Computation · doi:10.1162/089976604773135069 · Cited by 351 · see citing works
Grid cells and cortical representation
Moser, E. I., Roudi, Y., Witter, M. P., Kentros, C., Bonhoeffer, T., & Moser, M.-B. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3766 · Cited by 335 · see citing works
Local Field Potential in Cortical Area MT: Stimulus Tuning and Behavioral Correlations
Liu, J., & Newsome, W. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5052-05.2006 · Cited by 332 · see citing works
Memory reprocessing in corticocortical and hippocampocortical neuronal ensembles
Qin, Y., McNaughton, B. L., Skaggs, W. E., & Barnes, C. A. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0139 · Cited by 308 · see citing works
Self-citationJung, M. W., Qin, Y. F., McNaughton, B. L., & Barnes, C. A. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.5.437 · Cited by 307 · see citing works
Self-citationCortical Representation of Motion during Unrestrained Spatial Navigation in the Rat
McNaughton, B. L., Mizumori, S. J. Y., Barnes, C. A., Leonard, B. W., Marquis, M., & Green, E. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.1.27 · Cited by 224 · see citing works
Self-citationTracking Route Progression in the Posterior Parietal Cortex
Nitz, D. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.037 · Cited by 209 · see citing works
Goard, M. J., Pho, G. N., Woodson, J., & Sur, M. (2016) · eLife · doi:10.7554/elife.13764 · Cited by 207 · see citing works
Cortical gamma responses: Searching high and low
Crone, N. E., Korzeniewska, A., & Franaszczuk, P. J. (2011) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2010.10.013 · Cited by 201 · see citing works
Interaction of Egocentric and World-Centered Reference Frames in the Rat Posterior Parietal Cortex
Wilber, A. A., Clark, B. J., Forster, T. C., Tatsuno, M., & McNaughton, B. L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0511-14.2014 · Cited by 200 · see citing works
Self-citationXing, J., & Andersen, R. A. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900562363 · Cited by 188 · see citing works
Anatomy of the cortex, statistics and geometry
Bruyn, G. W. (1991) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(91)90179-b · Cited by 184 · see citing works
Save, É., & Poucet, B. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00173-4 · Cited by 177 · see citing works
Battaglia, F. P., Sutherland, G. R., & McNaughton, B. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4896-03.2004 · Cited by 176 · see citing works
Self-citationConnections between pyramidal neurons in layer 5 of cat visual cortex (area 17)
Gabbott, P. L. A., Martin, K. A. C., & Whitteridge, D. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902590305 · Cited by 175 · see citing works
Spatial updating: how the brain keeps track of changing object locations during observer motion
Wolbers, T., Hegarty, M., Büchel, C., & Loomis, J. M. (2008) · Nature Neuroscience · doi:10.1038/nn.2189 · Cited by 174 · see citing works
Johnson, L. A., Euston, D. R., Tatsuno, M., & McNaughton, B. L. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1617-09.2010 · Cited by 160 · see citing works
Self-citationMountcastle, V. B. (2002) · Cerebral Cortex · doi:10.1093/cercor/13.1.2 · Cited by 158 · see citing works
Functional Split between Parietal and Entorhinal Cortices in the Rat
Whitlock, J. R., Pfuhl, G., Dagslott, N. C., Moser, M., & Moser, E. I. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.028 · Cited by 158 · see citing works
Posterior Parietal Cortex Guides Visual Decisions in Rats
Licata, A., Kaufman, M. T., Raposo, D. C., Ryan, M., Sheppard, J. P., & Churchland, A. K. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0105-17.2017 · Cited by 148 · see citing works
Bower, M. R., Euston, D. R., & McNaughton, B. L. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2901-04.2005 · Cited by 124 · see citing works
Self-citationEuston, D. R., & McNaughton, B. L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3803-06.2006 · Cited by 101 · see citing works
Self-citationSpaces within spaces: rat parietal cortex neurons register position across three reference frames
Nitz, D. A. (2012) · Nature Neuroscience · doi:10.1038/nn.3213 · Cited by 95 · see citing works
Micro-drive array for chronic in vivo recording: drive fabrication
Kloosterman, F., Davidson, T. J., Gomperts, S. N., Layton, S. P., Hale, G., Nguyen, D. P., & Wilson, M. A. (2009) · Journal of Visualized Experiments · doi:10.3791/1094 · Cited by 94 · see citing works
Parietal Cortex Codes for Egocentric Space beyond the Field of View
Schindler, A., & Bartels, A. (2012) · Current Biology · doi:10.1016/j.cub.2012.11.060 · Cited by 91 · see citing works
Tatsuno, M., Lipa, P., & McNaughton, B. L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3317-06.2006 · Cited by 86 · see citing works
Self-citationCortical connectivity maps reveal anatomically distinct areas in the parietal cortex of the rat
Wilber, A. A., Clark, B. J., Demecha, A. J., Mesina, L., Vos, J. M., & McNaughton, B. L. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00146 · Cited by 85 · see citing works
Self-citationEffects of inhibition and dendritic saturation in simulated neocortical pyramidal cells
Bush, P. C., & Sejnowski, T. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.6.2183 · Cited by 83 · see citing works
Geostatistics applied to best-fit interpolation of orientation data
Gumiaux, C., Gapais, D., & Brun, J. (2003) · Tectonophysics · doi:10.1016/j.tecto.2003.08.008 · Cited by 59 · see citing works
Save, É., Paz‐Villagràn, V., Alexinsky, T., & Poucet, B. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03882.x · Cited by 58 · see citing works
Auditory Spatial Discriminatory and Mnemonic Neurons in Rat Posterior Parietal Cortex
Nakamura, K. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2503 · Cited by 54 · see citing works
Multi-neuronal activity and functional connectivity in cell assemblies
Roudi, Y., Dunn, B. A., & Hertz, J. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.10.011 · Cited by 52 · see citing works
Head-centered representation and spatial memory in rat posterior parietal cortex
Chen, L. L., & Nakamura, K. (1998) · Psychobiology · doi:10.3758/bf03330599 · Cited by 26 · see citing works
Analysis and Modeling of Coordinated Multi-neuronal Activity
Tatsuno, M. (2015) · Springer Series in Computational Neuroscience · doi:10.1007/978-1-4939-1969-7 · Cited by 19 · see citing works
Associative Reactivation of Place–Reward Information in the Hippocampal–Ventral Striatal Circuitry
Lansink, C., & Pennartz, C. (2015) · Springer series in computational neuroscience · doi:10.1007/978-1-4939-1969-7_4 · Cited by 6 · see citing works
Mesina, L., Wilber, A. A., Clark, B. J., Dube, S. T. A., Demecha, A. J., Stark, C. E. L., & McNaughton, B. L. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.03.021 · Cited by 6 · see citing works
Self-citation
Flagged first, then by citations
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Klinzing, J. G., Niethard, N., & Born, J. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0467-3 · Cited by 1,176 · see citing works
The hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430 · see citing works
Learning-enhanced coupling between ripple oscillations in association cortices and hippocampus
Khodagholy, D., Gelinas, J. N., & Buzsáki, G. (2017) · Science · doi:10.1126/science.aan6203 · Cited by 357 · see citing works
Sleep—A brain-state serving systems memory consolidation
Brodt, S., Inostroza, M., Niethard, N., & Born, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.005 · Cited by 343 · see citing works
Shin, J. D., Tang, W., & Jadhav, S. P. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.012 · Cited by 199 · see citing works
Electrophysiological mechanisms of human memory consolidation
Zhang, H., Fell, J., & Axmacher, N. (2018) · Nature Communications · doi:10.1038/s41467-018-06553-y · Cited by 164 · see citing works
Yang, M., Logothetis, N. K., & Eschenko, O. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.2107-18.2018 · Cited by 57 · see citing works
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Weber, F. D., Supp, G. G., Klinzing, J. G., Mölle, M., Engel, A. K., & Born, J. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2020.117452 · Cited by 29 · see citing works
- Authors
- Wilber, A. A., Skelin, I., Wu, W., & McNaughton, B. L.
- Affiliations
- Florida State University (US)
- University of Lethbridge (CA)
- Corresponding author
- Wilber, Aaron A.
- Skelin, Ivan
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 95
- Issue
- 6
- Pages
- 1406-1419.e5
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC5679317
- OpenAlex
- W2952334031
- Cited by
- 95
- References
- 90
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 11 · 2023: 10 · 2022: 7 · 2021: 13 · 2020: 14 · 2019: 15 · 2018: 15 · 2017: 4
- FWCI
- 7.54
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- NIH National Institute on Aging (AG049090)
- NIH National Institute for Mental Health (MH4682316)
- Alberta Innovates Health Solutions Fellowship
- Alberta Innovates Health Solutions Polaris Award
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
- Keywords
- parietal cortex, laminar organization, memory reactivation, sleep, delta oscillations, sharp-wave ripples, hippocampus, local field potentials, spatial navigation, rats
- MeSH terms
- Animals, Hippocampus, Locomotion, Male, Memory, Neurons, Parietal Lobe, Self Stimulation, Sleep, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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