Cited by 568Memory and Neural MechanismsMemory Processes and InfluencesNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Object recognition memory and the rodent hippocampus

Open access

Broadbent, Nicola J., Gaskin, Stephane, Squire, Larry R., Clark, Robert E.·2010·Learning & Memory

Open this paper in CoChat — free account Open PDF

Abstract

In rodents, the novel object recognition task (NOR) has become a benchmark task for assessing recognition memory. Yet, despite its widespread use, a consensus has not developed about which brain structures are important for task performance. We assessed both the anterograde and retrograde effects of hippocampal lesions on performance in the NOR task. Rats received 12 5-min exposures to two identical objects and then received either bilateral lesions of the hippocampus or sham surgery 1 d, 4 wk, or 8 wk after the final exposure. On a retention test 2 wk after surgery, the 1-d and 4-wk hippocampal lesion groups exhibited impaired object recognition memory. In contrast, the 8-wk hippocampal lesion group performed similarly to controls, and both groups exhibited a preference for the novel object. These same rats were then given four postoperative tests using unique object pairs and a 3-h delay between the exposure phase and the test phase. Hippocampal lesions produced moderate and reliable memory impairment. The results suggest that the hippocampus is important for object recognition memory.

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

Crossref · 10.1101/lm.1650110

Cites

25 of 25 references verified0 citation errors · 0 not checkable

Statistics

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.

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
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 4,501
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
Recognition memory and the medial temporal lobe: a new perspective
Squire, L. R., Wixted, J. T., & Clark, R. E. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2154 · Cited by 1,059
Self-citation
Spatial memory, recognition memory, and the hippocampus
Broadbent, N. J., Squire, L. R., & Clark, R. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406344101 · Cited by 985
Self-citation
Neurotoxic lesions of the dorsal hippocampus and Pavlovian fear conditioning in rats
Maren, S., Aharonov, G., & Fanselow, M. S. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00088-0 · Cited by 765
Impaired Recognition Memory in Rats after Damage to the Hippocampus
Clark, R. E., Zola, S. M., & Squire, L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08853.2000 · Cited by 740
Self-citation
Object recognition memory: Neurobiological mechanisms of encoding, consolidation and retrieval
Winters, B. D., Saksida, L. M., & Bussey, T. J. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.04.004 · Cited by 600
Double Dissociation between the Effects of Peri-Postrhinal Cortex and Hippocampal Lesions on Tests of Object Recognition and Spatial Memory: Heterogeneity of Function within the Temporal Lobe
Winters, B. D., Forwood, S., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1346-04.2004 · Cited by 588
Impaired Recognition Memory in Monkeys after Damage Limited to the Hippocampal Region
Zola, S. M., Squire, L. R., Teng, E., Stefanacci, L., Buffalo, E. A., & Clark, R. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00451.2000 · Cited by 477
Self-citation

Flagged first, then by citations

Show all 24 references

Research works printed but not linked: 1

Squire LR Clark RE Bayley P (2004) in The cognitive neurosciences, Medial temporal lobe functions and memory, ed Gazzaniga M (MIT, Cambridge, MA), 3rd ed, pp 691â708.

Sorted by citations

Items 501–567 of 567

PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO GRANDE DO SUL PROGRAMA DE PÓS-GRADUAÇÃO EM MEDICINA E CIÊNCIAS DA SAÚDE ÁREA DE CONCENTRAÇÃO: NEUROCIÊNCIAS
da Silveira, C. K. B. (2011)
The effect of binge-like ethanol exposure on adolescent performance in non-spatial and spatial forms of the novel object recognition paradigm
Collins, M. (2016) · doi:10.26686/wgtn.17018819
A novel neurotrophic drug for cognitive enhancement and Alzheimer?s disease
Prior, M. (2013) · Journal of Alzheimers Disease & Parkinsonism
Modulation of Memory Consolidation, Retrieval and Extinction by Brain Histamine
Myskiw, J. D. C., Furini, C. R. G., & Izquierdo, I. (2016) · The Receptors · doi:10.1007/978-3-319-40308-3_14
Neurobiology of Recognition Memory
Manns, J. R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21075-4 · Cited by 1
The role of striatal acetylcholine in cognition: Assessment of a novel genetic mouse model
Palmer, D. D. (2013) · The Atrium (University of Guelph)
Avaliação dos efeitos da exposição prolongada às isoflavonas em ratas na senescência: aspectos comportamentais, bioquímicos e anatomopatológicos
Sandini, T. M. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.9.2017.tde-17072017-175123
WITHDRAWN: Gestational and lactational exposure to atrazine affects behavior and cognitive functions in Sprague-Dawley rats
Bai, L., Sun, Y., Li, Y., Jiang, W., Chen, Q., Wu, Y., & Li, B. (2017) · Oncotarget · doi:10.18632/oncotarget.23211
Changes in the Endocannabinoid system in the Brain Following Bilateral Vestibular Damage
Baek, J. (2011) · Otago University Research Archive (University of Otago)
Gut-brain axis: Central impact of gut peptides and metabolic drug on monoamine neurotransmission
Omoloye, A. (2019) · DMU Open Research Archive (De Montfort University)
Estrogenic Regulation of Recognition Memory and Spinogenesis
Luine, V. N., & Frankfurt, M. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190645908.003.0011
Oral Supplementation of Bauhinia variegata affects the Behavior of Albino Mice in a Gender Specific Manner
Ullah, A., Iqbal, S., & Iqbal, F. (2020) · Pakistan Journal of Zoology · doi:10.17582/journal.pjz/20171213171244
Effects of Nanoparticle and Conventional-Size Suspensions of MgO and ZnO on Recognition Memory in Mice
Kesmati, M., Torabi, M., Pourreza, N., Abdollahzadeh, R., Rahiminezhadseta, R., & Banitorof, M. B. (2020) · Neurophysiology · doi:10.1007/s11062-020-09847-4
Evidence that an HDAC2-targeted ASO persistently upregulates cortical acetylcholine and dopamine signaling via a CREB | Gs positive feedback loopPreprint
Sanders, T. H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.24.312264
Physiological synaptic activity and recognition memory are fueled by astroglial glutaminePreprint
Cheung, G. T. Y., Bataveljić, D., Kumar, N., Moulard, J., Dallérac, G. M., Visser, J., Rollenhagen, A., Mongin, C., Chever, O., Bemelmans, A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.06.328823
Novel roles of cell cycle regulator E2F1 in the CNS: Implications for synaptic damage in HIV-associated neurocognitive disorders
Ting, J. H. (2014) · ScholarlyCommons (University of Pennsylvania)
Complementing Subarachnoid Hemorrhage
van Dijk, B. J. (2020) · Utrecht University Repository (Utrecht University) · doi:10.33540/210
Gestational Diabetes Mellitus Induces Neuroinflammation, Synaptic Reduction, Behavioural Changes, and Impaired Memory in the Offspring.
Vuong, B. (2016) · Mspace (University of Manitoba)
Bipolar-associated miR-499-5p controls neuroplasticity by downregulating the Cav1.2 L-type voltage gated calcium channel subunit CACNB2Preprint
C., M., Ö., S., C., G., M., P., S., B., F, G., J., W., M., K. T., N, M., D., B., et al. (2021) · bioRxiv · doi:10.1101/2021.06.09.447782 · Cited by 3
The Expression of Interleukin-1β Is Regulated by DNA Methylation in Microglia of Hippocampus to Participate Postoperative Cognitive Dysfunction in Aged MicePreprint
Gao, Y., Li, Y., Yang, X., Hao, J., Shen, X., Xu, L., Liu, Y., Liu, L., Tong, K., You, Y., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-670804/v1
Histone H3K4 methylation In hippocampal memory formation and In Alzheimer’s disease
Obayashi, Y. (2021) · cIRcle (University of British Columbia) · doi:10.14288/1.0401445
The Expression of Interleukin-1β is Regulated by DNA Methylation in Microglia to Mediate Postoperative Cognitive Dysfunction in Aged MicePreprint
Gao, Y., Yang, L., Yang, X. J., Hao, J., Shen, X., Wang, H.-Y., Li, X., Liu, Y., Liu, L., Tong, K., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-973050/v1
In vitro and in vivo characterization of the E3 ubiquitin ligase RNF157 in the brain
Lee, S.-J. (2015) · doi:10.53846/goediss-5029
Faculty Opinions recommendation of Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress.
Sandi, C. (2014) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718297966.793492714
Análise dos efeitos da oxigenoterapia hiperbárica associada ao tratamento cirúrgico em lesões cerebrais secundárias à hidrocefalia experimental
da Silva, S. C. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2021.tde-28012022-112417
N-truncated Aβ4-x peptides in Alzheimer's disease: generation, degradation, and relationship with neuropathological hallmarks
Zampar, S. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9004
تأثير الميثوتركسيت على ذاكرة التعرف في إناث الفئران البالغة
Elmatoni, W. F., Ahmed, F. H., Ghliwo, H. M., & Drah, M. M. (2022) · AL-MUKHTAR JOURNAL OF SCIENCES · doi:10.54172/mjsc.v37i2.617
A Monte Carlo Simulation of Rat Choice Behavior with Interdependent Outcomes
Frankot, M. A. (2022) · doi:10.33915/etd.11446
WIN-55,212-2-Therapie in einem Modell für die sporadische Alzheimer Erkrankung
Ott, F. W. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9572
The effect of binge-like ethanol exposure on adolescent performance in non-spatial and spatial forms of the novel object recognition paradigm
Collins, M. (2016) · doi:10.26686/wgtn.17018819.v1
Data from Nicotinamide Mononucleotide Prevents Cisplatin-Induced Cognitive Impairments
Yoo, K. H., Tang, J. J., Rashid, M. A., Cho, C. H., Corujo-Ramirez, A. M., Choi, J., Bae, M. G., Brogren, D., Hawse, J. R., Hou, X., et al. (2023) · doi:10.1158/0008-5472.c.6513195.v1
High-THC Cannabis smoke impairs working memory capacity in spontaneous tests of novelty preference for objects and odors in ratsPreprint
Barnard, I. L., Onofrychuk, T. J., Toderash, A. D., Patel, V. N., Glass, A. E., Adrian, J. C., Laprairie, R. B., & Howland, J. G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.06.535880
Endopiriform neurons projecting to ventral CA1 are a critical node for recognition memory
Yamawaki, N., Login, H., Feld-Jakobsen, S. Ø., Molnar, B. M., Kirkegaard, M. Z., Moltesen, M., Okrasa, A., Radulović, J., & Tanimura, A. (2025) · eLife · doi:10.1101/2024.03.17.585387
Prosapip1 in the dorsal hippocampus mediates synaptic protein composition, long-term potentiation, and spatial memoryPreprint
Hoisington, Z. W., Gangal, H., Phamluong, K., Shukla, C., Ehinger, Y., Moffat, J. J., Homanics, G. E., Wang, J., & Dorit Ron, A. (2024) · eLife · doi:10.7554/elife.100653.1
Differences in memory performance: The effects of sex and reproductive experience on object recognition memory in high- and low-yawning Sprague‒Dawley rats
Díaz, L., Cortes, C., Ugarte, A., Trujillo, A., & Eguibar, J. R. (2024) · Physiology & Behavior · doi:10.1016/j.physbeh.2024.114713
Maternal Methyl-Enriched Diet Improves Episodic Memory and Does Not Affect the Conditioned Fear Memory in Offspring of WAG/RIJ Rats
Fedosova, E. A., Shatskova, A. B., & Sarkisova, K. Y. (2024) · Российский физиологический журнал им И М Сеченова · doi:10.31857/s0869813924050097
CaMKII modulates memory destabilization by regulating the interaction of theta and gamma oscillationsPreprint
Cammarota, M., Rossato, J. I., González, M. C., Radiske, A., Souza, J., Apolinário, G., & Baracho, A. L. (2024) · Research Square · doi:10.21203/rs.3.rs-5314185/v1
Endopiriform neurons projecting to ventral CA1 are a critical node for recognition memoryPreprint
Yamawaki, N., Login, H., Feld-Jakobsen, S. Ø., Molnar, B. M., Kirkegaard, M. Z., Moltesen, M., Okrasa, A., Radulović, J., & Tanimura, A. (2024) · eLife · doi:10.7554/elife.99642.2
Endopiriform neurons projecting to ventral CA1 are a critical node for recognition memoryPreprint
Yamawaki, N., Login, H., Feld-Jakobsen, S. Ø., Molnar, B. M., Kirkegaard, M. Z., Moltesen, M., Okrasa, A., Radulović, J., & Tanimura, A. (2025) · eLife · doi:10.7554/elife.99642.3
Theories of Hippocampal Function
McKenzie, S., Gobbo, F., & Morris, R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0014
Medial septum deep brain stimulation enhances memory and hippocampal neurogenesis in the D-galactose induced rat model of aging: behavioral and immunohistochemical study
Kipiani, E. E., Burjanadze, M. A., Dashniani, M. G., Chkhikvishvili, N. C., Naneishvili, T. L., Chighladze, M. R., Nozadze, B. G., & Beselia, G. V. (2025) · Experimental Brain Research · doi:10.1007/s00221-025-07051-6
Prosapip1 in the dorsal hippocampus mediates synaptic protein composition, long-term potentiation, and spatial memoryPreprint
Hoisington, Z. W., Gangal, H., Phamluong, K., Shukla, C., Ehinger, Y., Moffat, J. J., Homanics, G. E., Wang, J., & Dorit Ron, A. (2025) · eLife · doi:10.7554/elife.100653.2 · Cited by 1
Neurodevelopmental impacts of betamethasone administered in the late preterm period: An experimental study in CD-1 mice
Hardy, I. S., Gagnon, A., Croft, E. K., Tremblay, L., Lebel, R., Roy‐Lacroix, M., Takser, L., Ouellet, A., & Gris, D. (2025) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2025.107523
Longitudinal Brain Structural, Neurochemical, and Behavioral Changes Following Traumatic Brain Injury in Immature Rat Brain with ALCAR Treatment
Scafidi, S., Xu, S., Jernberg, J. N., Chu, T., Fiskum, G. M., & McKenna, M. C. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04494-9
PKMζ drives spatial memory reconsolidation but not maintenance
de Oliveira, J. R., Rossato, J. I., Souza, J., Orvate, R., Carneiro, L., Baracho, A. L., & Cammarota, M. (2025) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2025.1638371
Modulation of Memory Consolidation, Retrieval, and Extinction by Brain Histamine
Myskiw, J. D. C., Furini, C. R. G., & Izquierdo, I. (2025) · The Receptors · doi:10.1007/978-3-031-98921-6_9
In Vivo Positron Emission Tomography Imaging of Presynaptic Density Reveals Stress-Associated Synaptic Deficits Related to Behavioral and Molecular Alterations in Rats
Asch, R., Martin, N. H., García-Milian, R., Fowles, K., Dileone, R., Cai, Z., Liston, C. M., & Esterlis, I. (2025) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2025.09.021 · Cited by 1
Dissecting novel object exploration in a fully automated homecage-based novel object recognition test
Ho, H., Kejzar, N., Burton, S., Katsouri, L., Krstulović, M., Arany, E. S., O'Keefe, J. M., Bauža, M., & Krupic, J. (2026) · Cell Reports Methods · doi:10.1016/j.crmeth.2025.101290
Bone Marrow Mesenchymal Stem Cells Improve Cognitive Impairment Induced by Neuropathic Pain Through Blood CXCL12 / CXCR4 Axis in Male Mice
Sun, K., Qi, L., Zhang, H., Wang, L., & Zhang, T. (2026) · Journal of Neuroscience Research · doi:10.1002/jnr.70111
Paternal anabolic-androgenic steroid exposure promotes autism-like behavior in adult mouse offspring of both sexes
Lau, R. D. S., de Souza, J. S., da Conceição, R. R., Giannocco, G., Silva-Almeida, C., Marinho, B. G., da Rocha, F. F., Ahmed, R. G., Côrtes, W. D. S., & Laureano‐Melo, R. (2026) · Hormones and Behavior · doi:10.1016/j.yhbeh.2026.105901
Does hypercholesterolemia worsen cognitive decline in arterial hypertension? Insights from clinical and experimental studies
Betat, A., dos Santos, V., de Oliveira, C. G. A., Alflen, L., Ferreira, C. F., Izídio, G. S., & Lataro, R. M. (2026) · Journal of Hypertension · doi:10.1097/hjh.0000000000004277
Etude des effets de programmes d'endurance de haute intensité et de haut volume sur les performances physiques, cognitives ainsi que sur la plasticité musculaire et cérébrale chez le rat sain et ayant subi une ischémie cérébrale
Constans, A. (2019) · theses.fr (ABES) · doi:10.70675/93486891z6065z449cz992az7390677dca22
Prolonged non-traumatic early auditory deprivation increases hearing thresholds, leads to memory deficits, and reduces doublecortin-positive neurons in mice
Migliaccio, M. M., Benites, N. M., Rodrigues, B., Juliano, R. A., Mendes-Filho, D., Pizzolato, A. L. B., Vanderlei, L. C. A., Pedrazzi, J. F. C., Campos, A. C., & Leão, R. M. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.03.053
Astrocytes in the visual layers of the superior colliculus : properties and role in visual processing
Visser, J. (2022) · theses.fr (ABES) · doi:10.70675/bd2669fdzfb7az41aezb634z91c7e005996c
Astrocytic disruption and cognitive impairment following sub-acute fentanyl administration in male rats
Dolatshahi, S., Omran, H. S., Beirami, A. D., Hasanzadeh, M., Zeynalzadeh, A., Parvardeh, S., Ashtari, S., Abianeh, P. R., Shirvani, P., Shirvani, P., et al. (2026) · 3 Biotech · doi:10.1007/s13205-026-04775-2
NOTCH3 R545C mutation drives vascular-neuronal dysfunction and cognitive impairment in CADASIL pathogenesis
Ping, S., Hu, B., Wu, D., Wan, C., Tang, H., Xiong, X., Long, L., Xu, M., Xiong, H., Wu, Q., et al. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107404
IL-4Rα signalling and Iloprost treatment modulate neuroimmune and neurocognitive responses in Trypanosoma brucei-Infected mice
Olaolu, O. S., Davids, H., Dealtry, G., Morenikeji, O. R., Obishakin, E., Iliyasu, B., & Ajonijebu, D. C. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.04.020
Amyloid Plaques Ameliorate Memory Deficits and Hippocampal Neuron Loss in an Aβ4-42-Driven Alzheimer’s Disease Mouse Model
Zampar, S., Fricke, M., Kremser, F., Talucci, I., Maric, H. M., Klafki, H., Rostagno, A. A., Jahn, O., Weggen, S., Ghiso, J. A., et al. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05912-x
Hippocampal NOP Receptor Activation Impairs Object Recognition Memory Acquisition
Ribeiro, L., Orvate, R., de Souza, J. P., Baracho, A. L., Apolinário, G., Cammarota, M., & Rossato, J. I. (2026) · Hippocampus · doi:10.1002/hipo.70104
Effect of Cosmos Caudatus supplementation and aerobic exercise on selected neurobehaviour, biochemical profile and histology in rats with mild cognitive impairment (MCI) induced by AlCl3: Study Protocol
Joseph, D. K., Ludin, A. F. M., Ibrahim, F. W., Roos, N. A. C., Fairof, M. H. Z., Shahar, S., & Rajab, N. F. (2026) · PLoS ONE · doi:10.1371/journal.pone.0349933
Chronic hypertension and social isolation disrupt the blood-brain barrier and memory in a sex-dependent manner
Thaqi, A., DeMarco, G. M., Schellinger, E. D., Chen, D., Luchetta, J., & Chapman, A. C. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107563
Cinnamaldehyde protects against aluminum oxide nanoparticle–induced cognitive dysfunction in male Swiss mice by attenuating hippocampal ERK/p38 hyperphosphorylation and enhancing
Ahmadi, M., Mehrbeheshti, N., SoukhakLari, R., & Moosavi, M. (2026) · NeuroToxicology · doi:10.1016/j.neuro.2026.103556
Operant behavior is reliably impaired in a mouse model of Angelman syndrome
Guoynes, C. D., Kerr, D. D., Hotait, Z. S., Tanas, J. K., & Sidorov, M. S. (2026) · Scientific Reports · doi:10.1038/s41598-026-71483-5
A novel rat model of ovarian cancer and cisplatin chemotherapy-related cognitive impairment
Lomeli, N., Pearre, D. C., Lepe, J. J., Argueta, D. A., Arellano, M. A., Gupta, K., Taylor, T. H., & Bota, D. A. (2026) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2026.101373
Adolescent Exposure to a THC ‐Rich Cannabis Extract Produces Genotype‐Dependent Effects on Cognition and Glial Morphology in Serine Racemase Mutant Mice
Rangel, I. F., Chaves, M., Pagnoncelli, I. B., Medeiros, I., Pinheiro, F., da Silva, L. F., Branco, L. A. C., Rocha, E. D., Carvalho, V. M., Lima, F. R. S., et al. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70559
Leveraging Preclinical Models to Understand Human Neurobiology and Behavior
Dearborn, J. T., Selmanovic, D., Chaturvedi, S. M., Sarafinovska, S., & Maloney, S. E. (2026) · Current topics in behavioral neurosciences · doi:10.1007/7854_2026_619
Disentangling the Effects of Craniotomy and Traumatic Brain Injury in Experimental Models: A Narrative Review
Gribovskaya, V., Adzhemian, D., Rogozin, P., Nesterova, V., Gureev, A. P., & Silachev, D. N. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27209186

Authors: Broadbent, N. J., Gaskin, S., Squire, L. R., & Clark, R. E.
Affiliations: University of California System (US)
ORCID: Squire, Larry R.
Clark, Robert E.
Venue: Learning & Memory
Publisher: Cold Spring Harbor Laboratory
Published: 2009-12-22
Volume: 17
Issue: 1
Pages: 5-11
ISSN: 1072-0502 (ISSN-L)
1549-5485
DOI: 10.1101/lm.1650110
PMC: PMC2807177
OpenAlex: W2046922635
Cited by: 568
References: 24
Citations by year: 2026: 20 · 2025: 24 · 2024: 31 · 2023: 24 · 2022: 46 · 2021: 44 · 2020: 47 · 2019: 31 · 2018: 47 · 2017: 38 · 2016: 51 · 2015: 34 · 2014: 32 · 2013: 38 · 2012: 21
Type: posted content
Language: en
Open access: bronze
doi.org
Locations: Learning & Memory (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Science Foundation (0542013)
U.S. Department of Veterans Affairs
James S. McDonnell Foundation
Kavli Foundation
National Institute on Aging (P50AG005131, P50-AG05131)
National Institute of Mental Health (P50 AG05131, AG05131, R01MH024600)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: object recognition memory, hippocampus, hippocampal lesions, anterograde amnesia, retrograde amnesia, memory impairment, rats
MeSH terms: Analysis of Variance, Animals, Behavior, Animal, Exploratory Behavior, Hippocampus, Male, Memory, Random Allocation, Time Factors, 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

Object recognition memory and the rodent hippocampus

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks