RGS14 is a natural suppressor of both synaptic plasticity in CA2 neurons and hippocampal-based learning and memory

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Morphological and molecular markers of mouse area CA2 along the proximodistal and dorsoventral hippocampal axes

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Specific Proteomes of Hippocampal Regions CA2 and CA1 Reveal Proteins Linked to the Unique Physiology of Area CA2

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Development of the hippocampal CA2 region and the emergence of social recognition

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Integration of the CA2 region in the hippocampal network during epileptogenesis

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“Disruptor” residues in the regulator of G protein signaling (RGS) R12 subfamily attenuate the inactivation of Gα subunits

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The Ras‐binding domain region of RGS14 regulates its functional interactions with heterotrimeric G proteins

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Hippocampal area CA2: interneuron disfunction during pathological states

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Expression of brain‐derived neurotrophic factor and structural plasticity in the dentate gyrus and CA 2 region correlate with epileptiform activity

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A single-nucleus transcriptomic atlas of the dog hippocampus reveals the potential relationship between specific cell types and domestication

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Competition from newborn granule cells does not drive axonal retraction of silenced old granule cells in the adult hippocampus

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14-3-3γ binds regulator of G protein signaling 14 (RGS14) at distinct sites to inhibit the RGS14:Gαi–AlF4− signaling complex and RGS14 nuclear localization

Gerber, K. J., Squires, K. E., & Hepler, J. R. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002816 · Cited by 16

Projections of hippocampal CA2 pyramidal neurons: Distinct innervation patterns of CA2 compared to CA3 in rodents

Shinohara, Y., & Kohara, K. (2023) · Hippocampus · doi:10.1002/hipo.23519 · Cited by 23

Exercise enhancement by RGS14 disruption is mediated by brown adipose tissue

Vatner, D. E., Oydanich, M. K., Zhang, J., Campbell, S. C., & Vatner, S. F. (2023) · Aging Cell · doi:10.1111/acel.13791 · Cited by 15

Mechanisms of mGluR ‐dependent plasticity in hippocampal area CA2

Samadi, M., Hales, C. A., Lustberg, D. J., Farris, S., Ross, M. R., Zhao, M., Hepler, J. R., Harbin, N. H., Robinson, E. S. J., Banks, P. J., et al. (2023) · Hippocampus · doi:10.1002/hipo.23529 · Cited by 14

Human genetic variants disrupt RGS14 nuclear shuttling and regulation of LTP in hippocampal neurons

Squires, K. E., Gerber, K. J., Tillman, M. C., Lustberg, D. J., Montañez‐Miranda, C., Zhao, M., Ramineni, S., Scharer, C. D., Saha, R. N., Shu, F., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.016009 · Cited by 15

Hippocampal area CA2 activity supports social investigation following an acute social stress

Radzicki, D., McCann, K. E., Alexander, G. M., & Dudek, S. M. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02834-9 · Cited by 18

RGS14 regulates the lifetime of G α ‐GTP signaling but does not prolong G βγ signaling following receptor activation in live cells

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Endogenous RGS14 is a cytoplasmic-nuclear shuttling protein that localizes to juxtanuclear membranes and chromatin-rich regions of the nucleus

Branch, M. R., & Hepler, J. R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184497 · Cited by 15

The transcriptome of rat hippocampal subfields

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FGF21 modulates hippocampal cold-shock proteins and CA2-subregion proteins in neonatal mice with hypoxia–ischemia

Herrmann, J. R., Kochanek, P. M., Vagni, V., Janesko‐Feldman, K. L., Stezoski, J. P., Gorse, K., & Jackson, T. C. (2023) · Pediatric Research · doi:10.1038/s41390-023-02652-9 · Cited by 14

Bi-directional interplay between proximal and distal inputs to CA2 pyramidal neurons

Nasrallah, K., Piskorowski, R. A., & Chevaleyre, V. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.024 · Cited by 15

Specific AAV2/PHP.eB-mediated gene transduction of CA2 pyramidal cells via injection into the lateral ventricle

Okamoto, K., Kamikubo, Y., Yamauchi, K., Okamoto, S., Takahashi, M., Ishida, Y., Koike, M., Ikegaya, Y., Sakurai, T., & Hioki, H. (2023) · Scientific Reports · doi:10.1038/s41598-022-27372-8 · Cited by 17

RGS14 414 treatment induces memory enhancement and rescues episodic memory deficits

Masmudi‐Martín, M., Navarro‐Lobato, I., López‐Aranda, M. F., Delgado, G., Martín‐Montañez, E., Quirós-Ortega, M. E., Carretero‐Rey, M., Narváez, L., Garrido, M. G., Posadas, S. J., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201900429rr · Cited by 13

Regulator of G-protein signalling and GoLoco proteins suppress TRPC4 channel function via acting at Gαi/o

Jeon, J.-P., Thakur, D., Tian, J., So, I., & Zhu, M. X. (2016) · Biochemical Journal · doi:10.1042/bcj20160214 · Cited by 12

Detailed neuronal distribution of GPR3 and its co-expression with EF-hand calcium-binding proteins in the mouse central nervous system

Ikawa, F., Tanaka, S., Harada, K., Hide, I., Maruyama, H., & Sakai, N. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147166 · Cited by 12

CA2 physiology underlying social memory

Oliva, A. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102642 · Cited by 12

RGS14 expression in CA2 hippocampus, amygdala, and basal ganglia: Implications for human brain physiology and disease

Montañez‐Miranda, C., Bramlett, S. N., & Hepler, J. R. (2022) · Hippocampus · doi:10.1002/hipo.23492 · Cited by 12

RGS14 modulates locomotor behavior and ERK signaling induced by environmental novelty and cocaine within discrete limbic structures

Foster, S. L., Lustberg, D. J., Harbin, N. H., Bramlett, S. N., Hepler, J. R., & Weinshenker, D. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05892-x · Cited by 10

Silencing hippocampal CA2 reduces behavioral flexibility in spatial learning

Lehr, A. B., Hitti, F. L., Deibel, S. H., & Stöber, T. M. (2023) · Hippocampus · doi:10.1002/hipo.23521 · Cited by 14

Sodium bicarbonate cotransporter NBCn1/Slc4a7 affects locomotor activity and hearing in mice

Choi, I., Beedholm, K., Dam, V. S., Bae, S., Noble, D. J., Garraway, S. M., Aalkjær, C., & Boedtkjer, E. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113065 · Cited by 13

Structural and Functional Properties of Hippocampal Neurons

Spruston, N., Piskorowski, R. A., Chevaleyre, V., Eyre, M. D., McBain, C. J., & Bartos, M. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0005 · Cited by 11

Machine learning-based segmentation of the rodent hippocampal CA2 area from Nissl-stained sections

Takeuchi, Y., Yamashiro, K., Noguchi, A., Liu, J., Mitsui, S., Ikegaya, Y., & Matsumoto, N. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1172512 · Cited by 10

RGS14 limits seizure-induced mitochondrial oxidative stress and pathology in hippocampus

Harbin, N. H., Lustberg, D. J., Hurst, C. D., Paré, J., Crotty, K. M., Waters, A. L., Yeligar, S. M., Smith, Y., Seyfried, N. T., Weinshenker, D., et al. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106128 · Cited by 12

Classifying visual fatigue severity based on neurophysiological signals and psychophysiological ratings

Wiyor, H. D., Ntuen, C. A., Stephens, J. D. W., Jiang, S. X., & Jiang, Z. (2013) · International Journal of Human Factors and Ergonomics · doi:10.1504/ijhfe.2013.055982 · Cited by 9

Loss of TET Activity in the Postnatal Mouse Brain Perturbs Synaptic Gene Expression and Impairs Cognitive Function

Liu, J., Zhang, Z.-Q., Zhu, Z., Li, K., Xu, Q., Zhang, J., Cheng, X., Li, H., Sun, Y., Wang, J., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01302-2 · Cited by 8

Targeting CA2 Perineuronal Nets Restores Recognition Memory and Theta Oscillations in Aged Mice

Mehak, S. F., Shivakumar, A. B., Jijimon, F., Gupta, A., Pillai, V. G., & Gangadharan, G. (2025) · Aging Cell · doi:10.1111/acel.70139 · Cited by 6

Identification of hippocampal area CA2 in hamster and vole brain

Siegler, P. N., Shaughnessy, E. K., Horman, B. M., Vierling, T. T., King, D. H., Patisaul, H. B., Huhman, K. L., Alexander, G. M., & Dudek, S. M. (2024) · The Journal of Comparative Neurology · doi:10.1002/cne.25603 · Cited by 7

The Enigmatic CA2: Exploring the Understudied Region of the Hippocampus and Its Involvement in Parkinson’s Disease

Zhao, F., & Behnisch, T. (2023) · Biomedicines · doi:10.3390/biomedicines11071996 · Cited by 6

Reversal of Object Recognition Memory Deficit in Perirhinal Cortex-Lesioned Rats and Primates and in Rodent Models of Aging and Alzheimer’s Diseases

Masmudi‐Martín, M., Navarro‐Lobato, I., López‐Aranda, M. F., Browning, P. G. F., Simón, A., Lopez-Tellez, J. F., Jiménez‐Recuerda, I., Martín‐Montañez, E., Pérez‐Mediavilla, A., Frechilla, D., et al. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.08.039 · Cited by 7

Serotonin facilitates late-associative plasticity via synaptic tagging/cross-tagging and capture at hippocampal CA2 synapses in male rats

Benoy, A., Wong, L., Ather, N., & Sajikumar, S. (2022) · Oxford Open Neuroscience · doi:10.1093/oons/kvac002 · Cited by 6

Age-dependent expression pattern in the mammalian brain of a novel, small peptide encoded in the 22q11.2 deletion syndrome region

Kragness, S., Harrison, M. A. A., Westmoreland, J. J., Burstain, A., & Earls, L. R. (2018) · Gene Expression Patterns · doi:10.1016/j.gep.2018.03.004 · Cited by 6

Regular cycling between representations of alternatives in the hippocampusPreprint

Kay, K., Chung, J. E., Sosa, M., Schor, J. S., Karlsson, M. P., Larkin, M. C., Liu, D. F., & Frank, L. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/528976 · Cited by 7

Genomic Characterization of the Istrian Shorthaired Hound

Kušec, I. D., Bošković, I., Zorc, M., Gvozdanović, K., Škorput, D., Dovč, P., & Kušec, G. (2020) · Animals · doi:10.3390/ani10112013 · Cited by 6

Inhibition of the expression of rgs‐3 alleviates propofol‐induced decline in learning and memory in Caenorhabditis elegans

Zhao, A., Jin, H., Fan, G., Li, Y., Li, C., Li, Q., Ma, X., Zhao, T., Sun, S., Liu, S., et al. (2022) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14004 · Cited by 5

Introduction to the special issue on: A new view of hippocampal area CA2

Dudek, S. M., Alexander, G. M., & Farris, S. (2023) · Hippocampus · doi:10.1002/hipo.23514 · Cited by 5

Mineralocorticoid receptor knockout alters hippocampal CA2 neurons to become like those in CA1

Harris, E. P., Kandemir, B., Jones, S. M., Alexander, G. M., Ward, J. M., Wang, T., Proaño, S. B., Xu, X., & Dudek, S. M. (2025) · Communications Biology · doi:10.1038/s42003-025-08378-0 · Cited by 4

Hippocampal CA2 Region: A New Player in Social Dysfunctions

Mou, X. (2016) · Journal of Neurology & Neurophysiology · doi:10.4172/2155-9562.1000357 · Cited by 3

New hues for CA2

Chevaleyre, V., & Piskorowski, R. A. (2022) · Hippocampus · doi:10.1002/hipo.23496 · Cited by 5

Genetic variants disrupt human RGS 14 binding to NHERF 1 and regulation of NPT 2 A-mediated phosphate transportPreprint

Friedman, P. A., Mamonova, T., Magyar, C. E., Squires, K. E., Sneddon, W. B., Emlet, D. R., & Hepler, J. R. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/540781 · Cited by 4

RGS14 is neuroprotective against seizure-induced mitochondrial oxidative stress and pathology in hippocampusPreprint

Harbin, N. H., Lustberg, D. J., Hurst, C. D., Paré, J., Crotty, K. M., Waters, A. L., Yeligar, S. M., Smith, Y., Seyfried, N. T., Weinshenker, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.01.526349 · Cited by 4

Regulator of G-protein signaling 14 (RGS14) promotes cancer growth in hepatocellular carcinoma

Ran, Y., Li, L., Wang, Z., Sun, T., Wen, C., Zhang, Y., Jiang, S., Jiang, S., 郑君杰, Yin, C., et al. (2025) · Cancer Genetics · doi:10.1016/j.cancergen.2025.04.002 · Cited by 3

Gradual transition of pyramidal cell types in the dorsal hippocampal area CA2b of the C57BL/6 mouse

Fellenz, M., Schneider, R. M., Jabra, S., Rietsche, M., Smilović, D., Vukšić, M., Slattery, D. A., & Deller, T. (2025) · Scientific Reports · doi:10.1038/s41598-025-04329-1 · Cited by 3

Regulators of G protein Signaling (RGS) proteins in GtoPdb v.2021.2

Ahlers‐Dannen, K. E., Alqinyah, M., Bodle, C., Dagher, J. B., Chakravarti, B., Choudhuri, S. P., Druey, K. M., Fisher, R. A., Gerber, K. J., Hepler, J. R., et al. (2021) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f891/2021.2 · Cited by 3

SM22α Deletion Contributes to Neurocognitive Impairment in Mice through Modulating Vascular Smooth Muscle Cell Phenotypes

Xu, X., Liu, X., Liu, X.-L., Wang, X., Zhang, W., Huang, X.-F., Jia, F.-Y., Kong, P., & Han, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087117 · Cited by 3

A new AAV tool for highly preferentially targeting hippocampal CA2

Peng, S., Gu, W., Zhu, W., Zhuang, Y., Yang, X., Lv, Y., Meng, S., Xie, W., & Li, M. (2023) · Molecular Brain · doi:10.1186/s13041-023-01038-6 · Cited by 3

The molecular sociology of NHERF1 PDZ proteins controlling renal hormone-regulated phosphate transport

Friedman, P. A., & Mamonova, T. (2024) · Bioscience Reports · doi:10.1042/bsr20231380 · Cited by 3

Endogenous regulator of G protein signaling 14 (RGS14) blunts cocaine-induced emotionally motivated behaviors in female mice

Bramlett, S. N., Foster, S. L., Weinshenker, D., & Hepler, J. R. (2025) · Addiction Neuroscience · doi:10.1016/j.addicn.2025.100203 · Cited by 3

Developing inhibitors of the guanosine triphosphate hydrolysis accelerating activity of Regulator of G protein Signaling-14

Agogo-Mawuli, P. S., Sadiya, I., Abramyan, T. M., Bosch, D. E., Emmitte, K. A., Colón-Pérez, L. M., Kosloff, M., & Siderovski, D. P. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110611 · Cited by 2

Defining hippocampal area CA2 in the fox ( Vulpes vulpes ) brain

Dudek, S. M., Phoenix, A., Scappini, E., Shepeleva, D. V., Herbeck, Y. E., Trut, L. N., Farris, S., & Kukekova, A. V. (2023) · Hippocampus · doi:10.1002/hipo.23546 · Cited by 2

Social play exclusion model in adolescent rats: Monitoring locomotor and emotional behavior associated with social play and examining c-Fos expression in the brain

Byun, Y., & Noh, J. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114379 · Cited by 2

Transcriptome analysis reveals genes associated with stem cell activation by physical exercise in the dentate gyrus of aged p16Ink4a knockout mice

Micheli, L., D’Andrea, G., Creanza, T. M., Volpe, D., Ancona, N., Scardigli, R., & Tirone, F. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1270892 · Cited by 2

Prenatal exposure to the mineralocorticoid receptor antagonist spironolactone disrupts hippocampal area CA2 connectivity and alters behavior in mice

Jones, S. M., Sleiman, S. J., McCann, K. E., Jarmusch, A. K., Alexander, G. M., & Dudek, S. M. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01971-7 · Cited by 3

The relationship of learning and memory disfunction with NEURL1 and RGS14 genes in patients with autism spectrum disorders

Eci̇roglu, H., Şener, E. F., Öztop, D. B., Özmen, S., Kaan, D., & Özkul, Y. (2022) · Acta Medica Alanya · doi:10.30565/medalanya.1136820 · Cited by 2

The fasciola cinereum subregion of the hippocampus is important for the acquisition of visual contextual memoryPreprint

Park, S., Lee, E., Lim, H., Yoo, S.-W., Lee, E., Jung, H.-S., Sun, W., & Lee, I. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/748301 · Cited by 2

PCP4 immunoreactivity suggests the presence of hippocampal region CA2 in solitary, social and eusocial mole-rat speciesPreprint

Stöber, T. M., & Oosthuizen, M. K. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.02.526898 · Cited by 3

RGS14 binds to GNAI3 and regulates the proliferation and apoptosis of human spermatogonial stem cells by affecting PLPP2 expression and MAPK signaling

Liu, B., Deng, A., Liu, L., Peng, L., Liu, X., Chen, X., Zhu, F., Zhang, S., & Zhou, D. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1593595 · Cited by 1

Chemogenetic activation of hippocampal area CA2 promotes acute and chronic seizures in a mouse model of epilepsy

LaFrancois, J. J., Kennedy, M., Rathod, M., Santoro, B., Lisgaras, C. P., Siegelbaum, S. A., & Scharfman, H. E. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107256 · Cited by 1

From Synaptic Plasticity and Critical Periods to Social Behavior and Stress: Getting to, and Staying in, CA2

Dudek, S. M. (2026) · Hippocampus · doi:10.1002/hipo.70068 · Cited by 1

Disruption of the gut microbiota in regulator of G protein signaling 14 knockout (RGS14 KO) mice alters the metabolome and reduces enhanced exercise capacity

Longoria, C. R., DeSio, D. D., Oydanich, M. K., Su, X., Chiles, E. N., Kerkhof, L. J., Ibironke, O. A., Häggblom, M. M., Wages, N. P., Guers, J. J., et al. (2026) · European Journal of Applied Physiology · doi:10.1007/s00421-026-06191-z · Cited by 1

What Is the Potential Relevance of Hippocampal Area CA2 in Neurologic Disorders?

Benarroch, E. E. (2026) · Neurology · doi:10.1212/wnl.0000000000218096 · Cited by 1

EpiPro, a Novel, Synthetic, Activity-Regulated Promoter That Targets Hyperactive Neurons in Epilepsy for Gene Therapy Applications

Burke, C. T., Vitko, I., Straub, J., Nylund, E. O., Gawda, A., Blair, K., Sullivan, K. A., Ergun, L., Ottolini, M., Patel, M. K., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914467 · Cited by 3

Nogo‐A‐mediated constraints on activity‐dependent synaptic plasticity and associativity in rat hippocampal CA2 synapses

Pavón, M. V., Navakkode, S., & Sajikumar, S. (2024) · Hippocampus · doi:10.1002/hipo.23625 · Cited by 2

Regulator of G protein signalling 14 (RGS14) protein expression profile in the adult mouse brain

Bramlett, S. N., Fitzmaurice, S. M., Harbin, N. H., Yan, W., Bandlamudi, C., Doorn, G. E. V., Smith, Y., & Hepler, J. R. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16592 · Cited by 1

Regulators of G protein Signaling (RGS) proteins (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database

Alqinyah, M., Bodle, C., Dagher, J. B., Chakravarti, B., Choudhuri, S. P., Druey, K. M., Fisher, R. A., Gerber, K. J., Hepler, J. R., Hooks, S. B., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f891/2019.4 · Cited by 1

Involvement of the Hypothalamic Nuclei in Forming Object–Place Associations in Neurons of Hippocampal Field CA2 (a hypothetical mechanism)

Silkis, I. G. (2021) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-021-01169-0 · Cited by 1

Morphology of Hippocampal Neurons

Vida, I., Degro, C. E., & Booker, S. A. (2018) · Springer series in computational neuroscience · doi:10.1007/978-3-319-99103-0_2 · Cited by 2

Examining Demographic Factors Impacting Green Marketing Strategies and Consumer Choices

Mohammed Ahmad Alsaggaf, W. A. (2023) · Journal of Informatics Education and Research · doi:10.52783/jier.v3i2.273 · Cited by 1

Structural factors of RGS14 regulating hormone-dependent phosphate transport mediated by NPT2APreprint

Sneddon, W. B., Ramineni, S., Doorn, G. E. V., Hepler, J. R., & Friedman, P. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.29.586499 · Cited by 1

Regulator of G Protein Signaling 14 protein expression profile in the adult mouse brainPreprint

Bramlett, S. N., Fitzmaurice, S. M., Harbin, N. H., Yan, W., Bandlamudi, C., Doorn, G. E. V., Smith, Y., & Hepler, J. R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.22.600169 · Cited by 1

Deciphering causal relationships between cell type-specific genetic factors and brain imaging-derived phenotypes and disordersPreprint

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a balanced mind

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