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Nicotine shifts the temporal activation of hippocampal protein kinase A and extracellular signal-regulated kinase 1/2 to enhance long-term, but not short-term, hippocampus-dependent memory

Gould, T. J., Wilkinson, D. S., Yildirim, E., Poole, R. L., Leach, P. T., & Simmons, S. J. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.01.009 · Cited by 24 · see citing works

Sex differences in contextual pattern separation, neurogenesis, and functional connectivity within the limbic system

Yagi, S., Lee, A. J., Truter, N., & Galea, L. A. M. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00450-2 · Cited by 24 · see citing works

Role of orexin-1 receptors in the dorsal hippocampus (CA1 region) in expression and extinction of the morphine-induced conditioned place preference in the rats

Farahimanesh, S., Karimi, S., & Haghparast, A. (2017) · Peptides · doi:10.1016/j.peptides.2017.12.017 · Cited by 23 · see citing works

Dopaminergic system in CA1 modulates MK-801 induced anxiolytic-like responses

Zarrindast, M., Nasehi, M., Pournaghshband, M., & Yekta, B. G. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2012.07.016 · Cited by 23 · see citing works

Neuronal loss and β-amyloid removal in the amygdala of people with Down syndrome☆

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Hippocampus long‐axis specialization throughout development: A meta‐analysis

Nichols, E. S., Blumenthal, A., Kuenzel, E., Skinner, J. K., & Duerden, E. G. (2023) · Human Brain Mapping · doi:10.1002/hbm.26340 · Cited by 24 · see citing works

Emotional- and cognitive-like responses induced by social defeat stress in male mice are modulated by the BNST, amygdala, and hippocampus

da Costa, V. F., Ramírez, J. C. C., Ramírez, S. V., Avalo-Zuluaga, J. H., Baptista‐de‐Souza, D., Canto‐de‐Souza, L., Planeta, C. S., Rico, J. L., & Nunes‐de‐Souza, R. L. (2023) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2023.1168640 · Cited by 23 · see citing works

Learning Promotes Subfield-Specific Synaptic Diversity in Hippocampal CA1 Neurons

Sakimoto, Y., Mizuno, J., Kida, H., Kamiya, Y., Ono, Y., & Mitsushima, D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz022 · Cited by 22 · see citing works

Dietary restriction reduces hippocampal neurogenesis and granule cell neuron density without affecting the density of mossy fibers

Staples, M. C., Fannon, M. J., Mysore, K. K., Dutta, R. R., Ongjoco, A. T., Quach, L. W., Kharidia, K. M., Somkuwar, S. S., & Mandyam, C. D. (2017) · Brain Research · doi:10.1016/j.brainres.2017.02.028 · Cited by 18 · see citing works

Representations of stimulus features in the ventral hippocampus

Biane, J. S., Ladow, M. A., Fan, A., Choi, H. S., Zhou, L. Z., Hassan, S., Apodaca-Montano, D. L., Kwon, A. O., Bratsch-Prince, J. X., & Kheirbek, M. A. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.007 · Cited by 19 · see citing works

Involvement of the ventral, but not dorsal, hippocampus in anxiety-like behaviors in mice exposed to the elevated plus maze: participation of CRF1 receptor and PKA pathway

Bertagna, N. B., dos Santos, P. G. C., Queiroz, R. M., Fernandes, G. J. D., Cruz, F. C., & Miguel, T. T. (2020) · Pharmacological Reports · doi:10.1007/s43440-020-00182-3 · Cited by 19 · see citing works

Dendrites of the dorsal and ventral hippocampal CA1 pyramidal neurons of singly housed female rats exhibit lamina‐specific growths and retractions during adolescence that are responsive to pair housing

Chen, Y., Akad, A., Aderogba, R., Chowdhury, T. G., & Aoki, C. J. (2018) · Synapse · doi:10.1002/syn.22034 · Cited by 17 · see citing works

Migratory Response of Cells in Neurogenic Niches to Neuronal Death: The Onset of Harmonic Repair?

Geribaldi‐Doldán, N., Carrascal, L., Pérez-García, P., Oliva, J. M., Pardillo-Díaz, R., Domínguez‐García, S., Utrera, C. B., Gómez‐Oliva, R., Martínez‐Ortega, S., Verástegui, C., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076587 · Cited by 15 · see citing works

Age- and location-dependent differences in store depletion-induced h-channel plasticity in hippocampal pyramidal neurons

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Cyclin-Dependent Kinase Inhibitor 1a (p21) Modulates Response to Cocaine and Motivated Behaviors

Scholpa, N. E., Briggs, S. B., Wagner, J. J., & Cummings, B. S. (2016) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.230888 · Cited by 14 · see citing works

Cartography of teneurin and latrophilin expression reveals spatiotemporal axis heterogeneity in the mouse hippocampus during development

Liakath‐Ali, K., Refaee, R., & Südhof, T. C. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002599 · Cited by 13 · see citing works

Ventral Hippocampal Kappa Opioid Receptors Mediate the Renewal of Fear following Extinction in the Rat

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Neuroimmunogastroenterology: At the Interface of Neuroimmunology and Gastroenterology

Sanchez, J. M. S., McNally, J. S., Cortez, M. M., Hemp, J., Pace, L., & Clardy, S. L. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00787 · Cited by 13 · see citing works

Interleukin-18 levels in the hippocampus and behavior of adult rat offspring exposed to prenatal restraint stress during early and late pregnancy

Chen, M.-X., Liu, Q., Chen, M.-X., Lei, L., Lin, A., Lei, L., Hui, T. C. K., Li, Q., Ao, L., & Sham, P. C. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.276358 · Cited by 11 · see citing works

Discrete hippocampal projections are differentially regulated by parvalbumin and somatostatin interneurons

Lodge, D. J., Reiley, H. B., Boley, A. M., & Donegan, J. J. (2023) · Nature Communications · doi:10.1038/s41467-023-42484-z · Cited by 9 · see citing works

Harmaline potentiates morphine-induced antinociception via affecting the ventral hippocampal GABA-A receptors in mice

Alijanpour, S., Jafaripour, S., Ghasemzadeh, Z., Khakpai, F., & Zarrindast, M. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173806 · Cited by 9 · see citing works

Systems genetic analysis of nicotine withdrawal deficits in hippocampus‐dependent learning

Goldberg, L. R., Kutlu, M. G., Zeid, D., Seemiller, L. R., & Gould, T. J. (2021) · Genes Brain & Behavior · doi:10.1111/gbb.12734 · Cited by 9 · see citing works

Socioeconomic status and subdivisions of the amygdala and hippocampus in children and adolescents

Hanson, J. L., Adkins, D. J., Nacewicz, B. M., & Barry, K. R. (2026) · Brain and Environment · doi:10.1016/j.braen.2026.100022 · Cited by 10 · see citing works

The role of hippocampal CaMKII in resilience to trauma-related psychopathology

Hazra, S., Hazra, J. D., Bar-On, R. A., Duan, Y., Edut, S., Cao, X., & Richter‐Levin, G. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100506 · Cited by 9 · see citing works

Topography of inputs into the hippocampal formation of a food‐caching bird

Applegate, M. C., Gutnichenko, K. S., & Aronov, D. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25533 · Cited by 8 · see citing works

The sphingosine 1‐phosphate analogue, FTY720 , modulates the lipidomic signature of the mouse hippocampus

Magalhães, D. M., Stewart, N. A., Mampay, M., Rolle, S. O., Hall, C. M., Moeendarbary, E., Flint, M. S., Sebastião, A. M., Valente, C. A., Dymond, M. K., et al. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16073 · Cited by 7 · see citing works

A novel targeted approach to delineate a role for estrogen receptor-β in ameliorating murine mammary tumor-associated neuroinflammation

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Differential expression of the neuronal CB1 cannabinoid receptor in the hippocampus of male Ts65Dn Down syndrome mouse model

Franco, N. D., Drutel, G., Roullot, V., Julio‐Kalajzić, F., Lalanne, V., Grel, A., Lesté-Lasserre, T., Matias, I., Cannich, A., Gonzales, D., et al. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103705 · Cited by 7 · see citing works

Loss of HCN2 in Dorsal Hippocampus of Young Adult Mice Induces Specific Apoptosis of the CA1 Pyramidal Neuron Layer

Deutsch, M., Stegmayr, C., Balfanz, S., & Baumann, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136699 · Cited by 6 · see citing works

Physical Activity Dynamically Regulates the Hippocampal Proteome along the Dorso-Ventral Axis

Frey, S., Schieweck, R., Forné, I., Imhof, A., Straub, T., Popper, B., & Kiebler, M. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103501 · Cited by 7 · see citing works

Dynamic θ Frequency Coordination within and between the Prefrontal Cortex-Hippocampus Circuit during Learning of a Spatial Avoidance Task

Dickson, C. R., Holmes, G. L., & Barry, J. M. (2022) · eNeuro · doi:10.1523/eneuro.0414-21.2022 · Cited by 5 · see citing works

Stress ulcer modulation by limbic system structures.

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Amygdala is critical for stress-induced modulation of hippocampal long-term potentiation and learning

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M (2001) Amygdala is critical for stressinduced modulation of hippocampal long-term potentiation and learning

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Granule cell potentials in the dentate gyrus of the hippocampus: Coping behavior and stress ulcers in rats

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Potentiation of inputs from the posterolateral amygdala to the dentate gyrus and resistance to stress ulcers formation in rats

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