The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Engram cells retain memory under retrograde amnesia
Open accessAbstract
Experimental recovery from retrograde amnesia: When memory researchers induce amnesia, they normally assume that the manipulations prevent the memory engram from effective encoding at consolidation. In accordance with this, Ryan et al. found that after the injection of protein synthesis inhibitors, animals could not retrieve a memory. However, to their surprise, the memory could nevertheless be reactivated by light-induced activation of the neurons tagged during conditioning. Increased synaptic strength that is the result of cellular consolidation is thus not a critical requisite for storing a memory. Science , this issue p. 1007
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706
The Neurobiology of Consolidations, Or, How Stable is the Engram?
Dudai, Y. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.55.090902.142050 · Cited by 1,671
Creating a False Memory in the Hippocampus
Ramirez, S., Liu, X., Lin, P.-A., Suh, J., Pignatelli, M., Redondo, R. L., Ryan, T. J., & Tonegawa, S. (2013) · Science · doi:10.1126/science.1239073 · Cited by 968
Self-citationMisanin, J. R., Miller, R. R., & Lewis, D. J. (1968) · Science · doi:10.1126/science.160.3827.554 · Cited by 872
Translational Regulatory Mechanisms in Persistent Forms of Synaptic Plasticity
Kelleher, R. J., Govindarajan, A., & Tonegawa, S. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.013 · Cited by 592
Self-citationBidirectional switch of the valence associated with a hippocampal contextual memory engram
Redondo, R. L., Kim, J., Arons, A. L., Ramirez, S., Liu, X., & Tonegawa, S. (2014) · Nature · doi:10.1038/nature13725 · Cited by 512
Self-citation
Cited by
Memory engrams: Recalling the past and imagining the future
Josselyn, S. A., & Tonegawa, S. (2020) · Science · doi:10.1126/science.aaw4325 · Cited by 1,087
Self-citationEngrams and circuits crucial for systems consolidation of a memory
Kitamura, T., Ogawa, S. K., Roy, D. S., Okuyama, T., Morrissey, M. D., Smith, L. M., Redondo, R. L., & Tonegawa, S. (2017) · Science · doi:10.1126/science.aam6808 · Cited by 1,104
Self-citationSynaptic Plasticity Forms and Functions
Magee, J. C., & Grienberger, C. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-090919-022842 · Cited by 806
Activity-Regulated Transcription: Bridging the Gap between Neural Activity and Behavior
Yap, E.-L., & Greenberg, M. E. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.013 · Cited by 706
Integration of optogenetics with complementary methodologies in systems neuroscience
Kim, C. K., Adhikari, A., & Deisseroth, K. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.15 · Cited by 690
Ventral CA1 neurons store social memory
Okuyama, T., Kitamura, T., Roy, D. S., Itohara, S., & Tonegawa, S. (2016) · Science · doi:10.1126/science.aaf7003 · Cited by 657
Self-citationMicroglial Remodeling of the Extracellular Matrix Promotes Synapse Plasticity
Nguyen, P. T., Dorman, L. C., Pan, S., Vainchtein, I. D., Han, R. T., Nakao-Inoue, H., Taloma, S. E., Barron, J. J., Molofsky, A. B., Kheirbek, M. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.05.050 · Cited by 615
Dentate gyrus circuits for encoding, retrieval and discrimination of episodic memories
Hainmueller, T., & Bartos, M. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0260-z · Cited by 506
Izquierdo, I., Furini, C. R. G., & Myskiw, J. C. (2016) · Physiological Reviews · doi:10.1152/physrev.00018.2015 · Cited by 453
The hippocampus and related neocortical structures in memory transformation
Sekeres, M. J., Winocur, G., & Moscovitch, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.05.006 · Cited by 370
Insular cortex neurons encode and retrieve specific immune responses
Koren, T., Yifa, R., Amer, M., Krot, M., Boshnak, N., Ben-Shaanan, T. L., Azulay-Debby, H., Zalayat, I., Avishai, E., Hajjo, H., et al. (2021) · Cell · doi:10.1016/j.cell.2021.10.013 · Cited by 334
Raven, F., Van der Zee, E. A., Meerlo, P., & Havekes, R. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2017.05.002 · Cited by 331
Distinct hippocampal engrams control extinction and relapse of fear memory
Lacagnina, A. F., Brockway, E. T., Crovetti, C. R., Shue, F., McCarty, M. J., Sattler, K. P., Lim, S. C., Santos, S. L., Denny, C. A., & Drew, M. R. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0361-z · Cited by 311
Encoding of contextual fear memory in hippocampal–amygdala circuit
Kim, W. B., & Cho, J.-H. (2020) · Nature Communications · doi:10.1038/s41467-020-15121-2 · Cited by 289
Functional and structural underpinnings of neuronal assembly formation in learning
Holtmaat, A., & Caroni, P. (2016) · Nature Neuroscience · doi:10.1038/nn.4418 · Cited by 239
Keiser, A. A., Turnbull, L. M., Darian, M. A., Feldman, D. E., Song, I., & Tronson, N. C. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.174 · Cited by 237
The neurobiological foundation of memory retrieval
Frankland, P. W., Josselyn, S. A., & Köhler, S. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0493-1 · Cited by 228
Forgetting as a form of adaptive engram cell plasticity
Ryan, T. J., & Frankland, P. W. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00548-3 · Cited by 182
Self-citationBernier, B. E., Lacagnina, A. F., Ayoub, A., Shue, F., Zemelman, B. V., Krasne, F. B., & Drew, M. R. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3029-16.2017 · Cited by 168
Migues, P. V., Liu, L., Archbold, G. E. B., Einarsson, E. Ö., Wong, J., Bonasia, K., Ko, S. H., Wang, Y. T., & Hardt, O. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.3333-15.2016 · Cited by 153
Inhibitory engrams in perception and memory
Barron, H. C., Vogels, T. P., Behrens, T. E., & Ramaswami, M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701812114 · Cited by 147
Translational Control in the Brain in Health and Disease
Sossin, W. S., & Costa-Mattioli, M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a032912 · Cited by 138
Trem2 deletion enhances tau dispersion and pathology through microglia exosomes
Zhu, B., Liu, Y., Hwang, S., Archuleta, K., Huang, H., Campos, A., Murad, R., Piña-Crespo, J., Xu, H., & Huang, T. Y. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00562-8 · Cited by 127
Hippocampal Place Fields Maintain a Coherent and Flexible Map across Long Timescales
Kinsky, N. R., Sullivan, D. W., Mau, W., Hasselmo, M. E., & Eichenbaum, H. B. (2018) · Current Biology · doi:10.1016/j.cub.2018.09.037 · Cited by 105
New learning and unlearning: strangers or accomplices in threat memory attenuation?
Clem, R. L., & Schiller, D. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.03.003 · Cited by 90
Clawson, B. C., Pickup, E. J., Ensing, A., Geneseo, L., Shaver, J., Gonzalez-Amoretti, J., Zhao, M., York, A. K., Kuhn, F. R., Swift, K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21471-2 · Cited by 73
Place field assembly distribution encodes preferred locations
Mamad, O., Stumpp, L., McNamara, H. M., Ramakrishnan, C., Deisseroth, K., Reilly, R. B., & Tsanov, M. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2002365 · Cited by 73
Hippocampal Deficits in Amyloid-β-Related Rodent Models of Alzheimer’s Disease
Vyas, Y., Montgomery, J. M., & Cheyne, J. E. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00266 · Cited by 66
In vivo ephaptic coupling allows memory network formation
Pinotsis, D. A., & Miller, E. K. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad251 · Cited by 62
Spatiotemporally resolved protein synthesis as a molecular framework for memory consolidation
Shrestha, P., & Klann, E. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.01.004 · Cited by 54
Memory corticalization triggered by REM sleep: mechanisms of cellular and systems consolidation
Almeida-Filho, D. G., Queiroz, C. M., & Ribeiro, S. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2886-9 · Cited by 38
Beyond dimension reduction: stable electric fields emerge from and allow representational drift
Pinotsis, D. A., & Miller, E. K. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119058 · Cited by 37
Tiam1 is Critical for Glutamatergic Synapse Structure and Function in the Hippocampus
Rao, S., Kay, Y., & Herring, B. E. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1566-19.2019 · Cited by 35
Gershman, S. J., Fiete, I., & Irie, K. (2025) · arXiv · doi:10.48550/arxiv.2501.02950 · Cited by 21
Wixted, J. T. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201332119 · Cited by 13
Metadata
- Authors
- Ryan, T. J., Roy, D. S., Pignatelli, M., Arons, A., & Tonegawa, S.
- Venue
- Science
- Published
- 2015-05-29
- Volume
- 348
- Issue
- 6238
- Pages
- 1007-1013
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1937980604
- Cited by
- 743
- References
- 6
- FWCI
- 32.08
- Type
- journal article
- Language
- en
- Open access
- green
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.