The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Traces of Experience in the Lateral Entorhinal Cortex
Open accessAbstract
A growing body of evidence suggests that memories are stored in the hippocampus by integrating spatial information from specialized cell types in the medial entorhinal cortex (MEC) with nonspatial information from cells in the lateral entorhinal cortex (LEC). LEC neurons show little spatial modulation when rats run in empty open-field environments but fire in the vicinity of discrete objects, suggesting that they provide information about the specific content of the spatial environment. It is unclear, however, whether firing at objects is elicited purely by stimulus properties, in a sensory-like manner, or whether any higher-order property, such as the history of experience, is also relevant. To address this question, we recorded from LEC neurons in an open field where objects were present on a subset of the trials. Whereas some neurons fired at the objects, other cells developed specific firing at places where objects had been located on previous trials, providing a readout of past experience in the environment. The latter cells generally did not respond to the object when it was present, suggesting that object cells and object-trace cells are independent cell classes. These findings identify LEC as a component of the hippocampal-cortical circuit for object-place memory.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Behavioral, imaging and electrophysiological recording data suggest that LEC preferentially processes object-associated information, e.g., the past and current locations of objects (Beer et al., 2013; Deshmukh and Knierim, 2011; Tsao et al., 2013; Van Cauter et al., 2013), and the context of the objects (Wilson et al., 2013b; Wilson et al., 2013c).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Tsao et al., 2013
Citations
Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
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
Self-citationReactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
Place Cells, Grid Cells, and the Brain's Spatial Representation System
Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934
Place units in the hippocampus of the freely moving rat
O'Keefe, J. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90055-8 · Cited by 1,836
Two-stage model of memory trace formation: A role for “noisy” brain states
Buzsáki, G. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90423-5 · Cited by 1,709
Retrograde amnesia and memory consolidation: a neurobiological perspective
Squire, L. R., & Alvarez, P. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80023-9 · Cited by 1,412
Studies on single neurons in dorsal hippocampal formation and septum in unrestrained rats
Ranck, J. B. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90290-2 · Cited by 1,322
Cited by
Sorted by citations
Items 101–200 of 289
Neuronal chemo‐architecture of the entorhinal cortex: A comparative review
Kobro‐Flatmoen, A., & Witter, M. P. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14511 · Cited by 35
Repeating Spatial Activations in Human Entorhinal Cortex
Miller, J. F., Fried, I., Suthana, N., & Jacobs, J. (2015) · Current Biology · doi:10.1016/j.cub.2015.02.045 · Cited by 40
Object and place information processing by CA1 hippocampal neurons of C57BL/6J mice
Ásgeirsdóttir, H. N., Cohen, S. J., & Stackman, R. W. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00278.2019 · Cited by 35
Assessing mild cognitive impairment using object‐location memory in immersive virtual environments
Castegnaro, A., Howett, D., Li, A., Harding, E. M., Chan, D., Burgess, N., & King, J. A. (2022) · Hippocampus · doi:10.1002/hipo.23458 · Cited by 37
From the GPS to HM: Place cells, grid cells, and memory
Knierim, J. J. (2015) · Hippocampus · doi:10.1002/hipo.22453 · Cited by 37
Salimi, M., Tabasi, F., Abdolsamadi, M., Dehghan, S., Dehdar, K., Nazari, M., Javan, M., Mirnajafi‐Zadeh, J., & Raoufy, M. R. (2022) · Scientific Reports · doi:10.1038/s41598-022-08528-y · Cited by 40
Rutigliano, G., Stazi, M., Arancio, O., Watterson, D. M., & Origlia, N. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.06.006 · Cited by 34
Locations in the Neocortex: A Theory of Sensorimotor Object Recognition Using Cortical Grid Cells
Lewis, M., Purdy, S., Ahmad, S., & Hawkins, J. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00022 · Cited by 38
Advanced Age Dissociates Dual Functions of the Perirhinal Cortex
Burke, S. N., Maurer, A. P., Nematollahi, S., Uprety, A. R., Wallace, J. L., & Barnes, C. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2875-13.2014 · Cited by 37
Pilkiw, M., Insel, N., Cui, Y., Finney, C. A., Morrissey, M. D., & Takehara‐Nishiuchi, K. (2017) · eLife · doi:10.7554/elife.28611 · Cited by 37
Insular projections to the parahippocampal region in the rat
Mathiasen, M. L., Hansen, L., & Witter, M. P. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23742 · Cited by 34
Postsynaptic integrative properties of dorsal CA1 pyramidal neuron subpopulations
Masurkar, A. V., Tian, C., Warren, R., Reyes, I., Lowes, D. C., Brann, D. H., & Siegelbaum, S. A. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00397.2019 · Cited by 34
Entorhinal cortex–hippocampal circuit connectivity in health and disease
Hernández‐Frausto, M., & Vivar, C. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1448791 · Cited by 41
Neural circuits for goal-directed navigation across species
Basu, J., & Nagel, K. I. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.09.005 · Cited by 35
Yoo, S., & Lee, I. (2017) · eLife · doi:10.7554/elife.21543 · Cited by 30
Structural modularity and grid activity in the medial entorhinal cortex
Naumann, R. K., Preston‐Ferrer, P., Brecht, M., & Burgalossi, A. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00574.2017 · Cited by 37
Guthman, E. M., Garcia, J. D., Ma, M., Chu, P., Baca, S. M., Smith, K. R., Restrepo, D., & Huntsman, M. M. (2020) · eLife · doi:10.7554/elife.50601 · Cited by 35
Dynamic neural representations of memory and space during human ambulatory navigation
Maoz, S. L., Stangl, M., Topalovic, U., Batista, D., Hiller, S., Aghajan, Z. M., Knowlton, B. J., Stern, J. M., Langevin, J., Fried, I., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42231-4 · Cited by 30
Beyond hippocampus: Thalamic and prefrontal contributions to an evolving memory
Yadav, N., Toader, A. C., & Rajasethupathy, P. (2024) · Neuron · doi:10.1016/j.neuron.2023.12.021 · Cited by 31
Environmental boundaries as a mechanism for correcting and anchoring spatial maps
Giocomo, L. M. (2015) · The Journal of Physiology · doi:10.1113/jp270624 · Cited by 32
Cox, B. M., Cox, C. D., Gunn, B. G., Le, A. A., Inshishian, V. C., Gall, C. M., & LYNCH, G. S. (2019) · Communications Biology · doi:10.1038/s42003-019-0494-3 · Cited by 30
Object and object‐memory representations across the proximodistal axis of CA1
Vandrey, B., Duncan, S., & Ainge, J. A. (2021) · Hippocampus · doi:10.1002/hipo.23331 · Cited by 28
Local projections of layer Vb-to-Va are more prominent in lateral than in medial entorhinal cortex
Ohara, S., Blankvoort, S., Nair, R. R., Nigro, M. J., Nilssen, E. S., Kentros, C. G., & Witter, M. P. (2021) · eLife · doi:10.7554/elife.67262 · Cited by 31
Mental navigation in the primate entorhinal cortex
Neupane, S., Fiete, I., & Jazayeri, M. (2024) · Nature · doi:10.1038/s41586-024-07557-z · Cited by 36
Park, S., Lim, H., Lee, E., Yoo, S.-W., Jung, H.-S., Lee, E., Sun, W., & Lee, I. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102217 · Cited by 29
Prefrontal and lateral entorhinal neurons co-dependently learn item–outcome rules
Jun, H., Lee, J. Y., Bleza, N. R., Ichii, A., Donohue, J. D., & Igarashi, K. M. (2024) · Nature · doi:10.1038/s41586-024-07868-1 · Cited by 26
From grid cells to place cells with realistic field sizes
Neher, T., Azizi, A. H., & Cheng, S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181618 · Cited by 27
Fiorilli, J., Bos, J. J., Grande, X., Lim, J., Düzel, E., & Pennartz, C. M. A. (2021) · Hippocampus · doi:10.1002/hipo.23304 · Cited by 25
Lateral entorhinal cortex lesions impair odor‐context associative memory in male rats
Persson, B. M., Ambrozova, V., Duncan, S., Wood, E. R., O’Connor, A. R., & Ainge, J. A. (2022) · Journal of Neuroscience Research · doi:10.1002/jnr.25027 · Cited by 27
Vandrey, B., Armstrong, J., Brown, C. M., Garden, D. L. F., & Nolan, M. F. (2022) · eLife · doi:10.7554/elife.83008 · Cited by 28
Event structure sculpts neural population dynamics in the lateral entorhinal cortex
Kanter, B. R., Lykken, C. M., Polti, I., Moser, M., & Moser, E. I. (2025) · Science · doi:10.1126/science.adr0927 · Cited by 30
Hippocampal Contribution to Ordinal Psychological Time in the Human Brain
Gauthier, B., Prabhu, P., Karunakar, A. K., & van Wassenhove, V. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01586 · Cited by 28
Ohara, S., Yoshino, R., Kimura, K., Kawamura, T., Tanabe, S., Zheng, A., Nakamura, S., Inoue, K., Takada, M., Tsutsui, K., et al. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.790116 · Cited by 23
Igarashi, K. M. (2016) · Brain Research · doi:10.1016/j.brainres.2015.10.041 · Cited by 25
Li, A. Y., Fukuda, K., & Barense, M. D. (2022) · Cognition · doi:10.1016/j.cognition.2022.105024 · Cited by 24
Distinct spatial maps and multiple object codes in the lateral entorhinal cortex
Huang, X., Schlesiger, M. I., Barriuso-Ortega, I., Leibold, C., MacLaren, D. A. A., Bieber, N., & Monyer, H. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.020 · Cited by 20
Pathfinder: open source software for analyzing spatial navigation search strategies
Cooke, M. B., O’Leary, T. P., Harris, P., Ma, R., Brown, R. E., & Snyder, J. S. (2019) · F1000Research · doi:10.12688/f1000research.20352.2 · Cited by 31
Involvement of a lateral entorhinal cortex engram in episodic-like memory recall
Tozzi, F., Guglielmo, S., Paraciani, C., van den Oever, M. C., Mainardi, M., Cattaneo, A., & Origlia, N. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114795 · Cited by 24
Unpacking the navigation toolbox: insights from comparative cognition
Jeffery, K. J., Cheng, K., Newcombe, N. S., Bingman, V. P., & Menzel, R. (2024) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2023.1304 · Cited by 26
Suter, E. E., Weiss, C., & Disterhoft, J. F. (2018) · Hippocampus · doi:10.1002/hipo.23041 · Cited by 23
Role of dopamine neurons in familiarity
Fleury, S., Kolaric, R., Espera, J., Ha, Q. H., Tomaio, J. N., Gether, U., Sørensen, A. T., & Mingote, S. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16326 · Cited by 21
Neural Responses in Retrosplenial Cortex Associated With Environmental Alterations
Carstensen, L. C., Alexander, A. S., Chapman, G. W., Lee, A. J., & Hasselmo, M. E. (2021) · iScience · doi:10.1016/j.isci.2021.103377 · Cited by 20
Structural connectivity-based segmentation of the human entorhinal cortex
Syversen, I. F., Witter, M. P., Kobro‐Flatmoen, A., Goa, P. E., Schröder, T. N., & Doeller, C. F. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118723 · Cited by 22
Goal‐directed interaction of stimulus and task demand in the parahippocampal region
Lee, S., Jin, S., Park, S., Park, E., Lee, C., Lee, H., Lim, H., Yoo, S., Ahn, J. R., Shin, J., et al. (2021) · Hippocampus · doi:10.1002/hipo.23295 · Cited by 21
Gaussier, P., Banquet, J. P., Cuperlier, N., Quoy, M., Aubin, L., Jacob, P.-Y., Sargolini, F., Save, É., Krichmar, J. L., & Poucet, B. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.186932 · Cited by 20
Binicewicz, F. Z. M., van Strien, N. M., Wadman, W. J., van den Heuvel, M. P., & Cappaert, N. L. M. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-0992-0 · Cited by 21
The neural ingredients for a language of thought are available
Kazanina, N., & Poeppel, D. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.07.012 · Cited by 25
Ku, S.-P., Nakamura, N. H., Maingret, N., Mahnke, L., Yoshida, M., & Sauvage, M. M. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00051 · Cited by 18
Lateral entorhinal cortex lesions impair both egocentric and allocentric object–place associations
Kuruvilla, M. V., Wilson, D. I. G., & Ainge, J. A. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820939463 · Cited by 23
Wang, C., Lee, H., Rao, G., Yoganarasimha, D., Savelli, F., & Knierim, J. J. (2023) · Hippocampus · doi:10.1002/hipo.23528 · Cited by 18
Egocentric processing of items in spines, dendrites, and somas in the retrosplenial cortex
Cheng, N., Dong, Q., Zhang, Z., Wang, L., Chen, X., & Wang, C. (2023) · Neuron · doi:10.1016/j.neuron.2023.11.018 · Cited by 20
Atucha, E., Karew, A., Kitsukawa, T., & Sauvage, M. M. (2017) · Hippocampus · doi:10.1002/hipo.22754 · Cited by 17
Scaplen, K. M., Ramesh, R. N., Nadvar, N., Ahmed, O. J., & Burwell, R. D. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00040 · Cited by 16
Intact memory for local and distal cues in male and female rats that lack adult neurogenesis
Seib, D. R., Chahley, E. R., Princz‐Lebel, O., & Snyder, J. S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197869 · Cited by 17
Vyleta, N. P., & Snyder, J. S. (2021) · PLoS ONE · doi:10.1371/journal.pone.0253642 · Cited by 19
Brandon, M. P., Koenig, J., & Leutgeb, S. (2013) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1272 · Cited by 19
Spatial Cognition: Grid Cells Support Imagined Navigation
Jacobs, J., & Lee, S. A. (2016) · Current Biology · doi:10.1016/j.cub.2016.02.032 · Cited by 14
Novel types of frequency filtering in the lateral perforant path projections to dentate gyrus
Quintanilla, J., Jia, Y., Lauterborn, J. C., Pruess, B. S., Le, A. A., Cox, C. D., Gall, C. M., LYNCH, G. S., & Gunn, B. G. (2022) · The Journal of Physiology · doi:10.1113/jp283012 · Cited by 13
Circuit dynamics of the olfactory pathway during olfactory learning
Zhang, Y. J., Lee, J. Y., & Igarashi, K. M. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1437575 · Cited by 15
Dynamics of spontaneous local field potentials in the anterior claustrum of freely moving rats
Jankowski, M. M., Islam, M. N., & O’Mara, S. M. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.021 · Cited by 14
Limbic progesterone receptors regulate spatial memory
Joshi, S., Williams, C. L., & Kapur, J. (2023) · Scientific Reports · doi:10.1038/s41598-023-29100-2 · Cited by 15
Soma, S., Ohara, S., Nonomura, S., Suematsu, N., Yoshida, J., Pastalkova, E., Sakai, Y., Tsutsui, K., & Isomura, Y. (2023) · Communications Biology · doi:10.1038/s42003-023-04958-0 · Cited by 13
Representations of tactile object location in the retrosplenial cortex
Lande, A. S., Garvert, A. C., Ebbesen, N. C., Jordbræk, S. V., & Vervaeke, K. (2023) · Current Biology · doi:10.1016/j.cub.2023.09.019 · Cited by 15
The neural representation of 3-dimensional objects in rodent memory circuits
Burke, S. N., & Barnes, C. A. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.001 · Cited by 13
A spatial code in the dorsal lateral geniculate nucleusPreprint
Hok, V., Jacob, P.-Y., Bordiga, P., Truchet, B., Poucet, B., & Save, É. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/473520 · Cited by 12
Waveform-based classification of dentate spikes
Santiago, R. M. M., Lopes‐dos‐Santos, V., Jones, E. A. A., Huang, Y., Dupret, D., & Tort, A. B. L. (2024) · Scientific Reports · doi:10.1038/s41598-024-53075-3 · Cited by 14
Poitreau, J., Buttet, M., Manrique, C., Poucet, B., Sargolini, F., & Save, E. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113448 · Cited by 10
Minute-scale periodicity of neuronal firing in the human entorhinal cortex
Aghajan, Z. M., Kreiman, G., & Fried, I. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113271 · Cited by 13
Dynamic embedding of salience coding in hippocampal spatial mapsPreprint
Sato, M., Mizuta, K., Islam, T., Kawano, M., Takekawa, T., Gómez-Domínguez, D., Kim, K., Yamakawa, H., Ohkura, M., Fukai, T., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/266767 · Cited by 10
Oulé, M., Atucha, E., Wells, T. M., Macharadze, T., Sauvage, M. M., Kreutz, M. R., & Lopez‐Rojas, J. (2021) · iScience · doi:10.1016/j.isci.2021.102876 · Cited by 10
Yu, X., Yu, J. C., Choi, A., & Takehara‐Nishiuchi, K. (2021) · Hippocampus · doi:10.1002/hipo.23389 · Cited by 10
Sensory feedback in a bump attractor model of path integration
Poll, D. B., Nguyen, K., & Kilpatrick, Z. P. (2016) · Journal of Computational Neuroscience · doi:10.1007/s10827-015-0588-y · Cited by 12
Dabaghian, Y. A. (2016) · Neural Computation · doi:10.1162/neco_a_00840 · Cited by 13
Effect of aging differs for memory of object identity and object position within a spatial contextPreprint
Tran, T., Tobin, K. E., Block, S. H., Puliyadi, V., Gallagher, M., & Bakker, A. (2021) · Learning & Memory · doi:10.1101/lm.053181.120 · Cited by 11
Neural signatures for temporal order memory in the macaque medial posterior parietal cortexPreprint
Zuo, S., Wang, C., Wang, L., Jin, Z., Zhou, X., Su, N., Liu, J., McHugh, T. J., Makoto Kusunoki, A., & Kwok, S. C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.17.553665 · Cited by 10
Cortical glutamatergic and GABAergic inputs support learning-driven hippocampal stability
Robert, V., O’Neil, K., Moore, J. J., Rashid, S. K., Johnson, C. D., Delatorre, R. G., Zemelman, B. V., Clopath, C., & Basu, J. (2025) · Science · doi:10.1126/science.adn0623 · Cited by 13
Spatial and Nonspatial Representations in the Lateral Entorhinal Cortex
Deshmukh, S. S. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_6 · Cited by 9
Yeung, L., Hale, C., Rizvi, B. M., Igwe, K. C., Sloan, R. P., Honig, L. S., Small, S. A., & Brickman, A. M. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.10.031 · Cited by 10
Input/Output Relationships for the Primary Hippocampal Circuit
Gunn, B. G., Pruess, B. S., Gall, C. M., & LYNCH, G. S. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0130-24.2024 · Cited by 8
Multiplexing of temporal and spatial information in the lateral entorhinal cortex
Wang, C., Lee, H., Rao, G., & Knierim, J. J. (2024) · Nature Communications · doi:10.1038/s41467-024-54932-5 · Cited by 12
Jacobsen, B., Kleven, H., Gatome, W., Las, L., Ulanovsky, N., & Witter, M. P. (2023) · Hippocampus · doi:10.1002/hipo.23517 · Cited by 8
Chen, Y., Branch, A., Shuai, C., Gallagher, M., & Knierim, J. J. (2023) · Hippocampus · doi:10.1002/hipo.23591 · Cited by 8
Lateral Entorhinal Cortex Suppresses Drift in Cortical Memory Representations
Pilkiw, M., Jarovi, J., & Takehara‐Nishiuchi, K. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1439-21.2021 · Cited by 12
Memory deficits in Sprague Dawley rats with spontaneous ventriculomegaly
Luna‐Munguía, H., Gasca‐Martínez, D., Marquez‐Bravo, L., & Concha, L. (2020) · Brain and Behavior · doi:10.1002/brb3.1711 · Cited by 7
A hippocampal population code for rapid generalizationPreprint
Tang, W., Chang, H., Liu, C., Perez-Hernandez, S., Zheng, W. Y., Park, J., Oliva, A., & Fernández‐Ruiz, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.15.643456 · Cited by 10
Aoun, A., Shetler, O., Raghuraman, R., Rodriguez, G. A., & Hussaini, S. A. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1273283 · Cited by 8
The Role of Hierarchical Dynamical Functions in Coding for Episodic Memory and Cognition
Dannenberg, H., Alexander, A. S., Robinson, J. C., & Hasselmo, M. E. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01439 · Cited by 7
Bnip3 expression is strongly associated with reelin-positive entorhinal cortex layer II neurons
Omholt, S. W., Lejneva, R., Lagartos-Donate, M. J., Caponio, D., Fang, E. F., & Kobro‐Flatmoen, A. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02816-1 · Cited by 6
Allison, E. A. M. A., Moore, J. W., Arkell, D., Thomas, J., Dudchenko, P. A., & Wood, E. R. (2023) · Hippocampus · doi:10.1002/hipo.23506 · Cited by 6
Schiltz, E., Broux, M., Aydın, Ç., Gonçalves, P. J., & Haesler, S. (2024) · eLife · doi:10.7554/elife.103373 · Cited by 6
Ananth, M. R., Gardus, J. D., Huang, C., Palekar, N., Slifstein, M., Záborszky, L., Parsey, R. V., Talmage, D. A., DeLorenzo, C., & Role, L. W. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115249 · Cited by 8
Ardanaz, C. G., Ezkurdia, A., Bejarano, A., Echarte, B., Smerdou, C., Martišová, E., Martínez-Valbuena, I., Luquín, M. R., Ramírez, M. J., & Solas, M. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00092 · Cited by 5
Facial Nerve Axotomy Induces Changes on Hippocampal CA3-to-CA1 Long-term Synaptic Plasticity
Torrado-Arévalo, R., Troncoso, J., & Múnera, A. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.08.023 · Cited by 5
Scleidorovich, P., Fellous, J., & Weitzenfeld, A. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.1039822 · Cited by 5
Johnson, T. D., Keefe, K. R., & Rangel, L. M. (2023) · Hippocampus · doi:10.1002/hipo.23490 · Cited by 3
Introduction to the special issue on the ontogeny of hippocampal functions
Ohana, O., Alberini, C. M., & Donato, F. (2022) · Hippocampus · doi:10.1002/hipo.23406 · Cited by 3
Zuo, S., Wang, C., Wang, L., Jin, Z., Zhou, X., 苏宁, Liu, J., McHugh, T. J., Kusunoki, M., & Kwok, S. C. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003759 · Cited by 14
Okamura-Oho, Y., Shimokawa, K., Nishimura, M., Takemoto, S., Sato, A., Furuichi, T., & Yokota, H. (2014) · Scientific Reports · doi:10.1038/srep06969 · Cited by 4
Assessing episodic memory in rodents using spontaneous object recognition tasks
Barbosa, F. F., & Castelo‐Branco, R. (2022) · Emerging Topics in Life Sciences · doi:10.1042/etls20220010 · Cited by 4
Five discoveries of Volodymyr Betz. Part one. Betz and the islands of entorhinal cortex
Medvediev, V. V., Cherkasov, V., Vaslovych, V. V., & Tsymbaliuk, V. (2023) · Ukrainian Scientific Medical Youth Journal · doi:10.32345/usmyj.1(136).2023.30-59 · Cited by 5
Metadata
- Authors
- Tsao, A., Moser, M.-B., & Moser, E. I.
- Affiliations
- Norwegian University of Science and Technology (NO)
- Corresponding author
- Tsao, Albert
- Moser, Edvard I.
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2013-03
- Volume
- 23
- Issue
- 5
- Pages
- 399-405
- ISSN
- 0960-9822 (ISSN-L)
- OpenAlex
- W2166846124
- Cited by
- 290
- References
- 46
- Citations by year
- 2026: 13 · 2025: 18 · 2024: 35 · 2023: 24 · 2022: 23 · 2021: 25 · 2020: 23 · 2019: 22 · 2018: 24 · 2017: 29 · 2016: 11 · 2015: 17 · 2014: 15 · 2013: 10
- FWCI
- 9.65
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Current Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- lateral entorhinal cortex, spatial memory, memory traces, hippocampus
- MeSH terms
- Animals, Male, Memory, Entorhinal Cortex, Rats, Long-Evans, 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 ›
Are you an author, or do you see a problem with this page? Request a review