Differential Control of Learning and Anxiety along the Dorsoventral Axis of the Dentate Gyrus
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The dentate gyrus (DG), in addition to its role in learning and memory, is increasingly implicated in the pathophysiology of anxiety disorders. Here, we show that, dependent on their position along the dorso-ventral axis of the hippocampus, DG granule cells (GCs) control specific features of anxiety and contextual learning. Using optogenetic techniques to either elevate or decrease GC activity, we demonstrate that GCs in the dorsal DG control exploratory drive and encoding, not retrieval, of contextual fear memories. In contrast, elevating the activity of GCs in the ventral DG has no effect on contextual learning but powerfully suppresses innate anxiety. These results suggest that strategies aimed at modulating the excitability of the ventral DG may be beneficial for the treatment of anxiety disorders.
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The dorsal hippocampus encodes context more specifically, while the ventral hippocampus includes affective information as well.
“The hippocampus itself appears to have a dorsal-ventral functional gradient, with the dorsal hippocampus encoding context more specifically, while the ventral hippocampus (vHPC) includes affective information as well [37].”
From Prefrontal cortex, amygdala, and threat processing: implications for PTSD (2022) · cites this paper as [37]
The Discussion reports that dorsal dentate gyrus granule cells are required for rapid contextual encoding, while ventral dentate gyrus activity influences anxiety-like behavior. It does not establish that the ventral hippocampus encodes context together with affective information; the Discussion says whether contextual information is represented in the ventral dentate gyrus remains unknown. (LLM, conf=0.86)
Experimental — accuracy not yet measuredThe hippocampus encodes context-specific information of a threat trace.
“The canonical role of the hippocampus in threat circuitry is to encode context-specific information of a threat trace, as it is crucial for an organism to be able to distinguish threats as belonging to a particular context.”
From Prefrontal cortex, amygdala, and threat processing: implications for PTSD (2022) · cites this paper as [37]
The dorsal hippocampus supports spatial navigation learning and memory, and the ventral hippocampus is important for anxiety and stress regulation.
“Studies have shown that different parts of the hippocampus serve these different functions, with the dorsal hippocampus supporting spatial navigation learning and memory, and the ventral hippocampus as important for anxiety and stress regulation (Fanselow and Dong, 2010; Kheirbek et al., 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Kheirbek et al., 2013
Direct photostimulation of ventral dentate gyrus granule cells suppresses anxiety-like behaviors in the EPM and OFT.
“however, direct photostimulation of ventral dentate gyrus granule cells has been in fact found to suppress anxiety-like behaviors in the EPM and OFT91.”
From Resolving the neural circuits of anxiety (2015) · cites this paper as [91]
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Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 4,886 · see citing works
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477 · see citing works
Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants
Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321 · see citing works
Self-citationDeep Brain Stimulation for Treatment-Resistant Depression
Mayberg, H. S., Lozano, A. M., Voon, V., McNeely, H. E., Seminowicz, D., Hamani, C., Schwalb, J. M., & Kennedy, S. H. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.014 · Cited by 4,059 · see citing works
Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus
van Praag, H., Kempermann, G., & Gage, F. H. (1999) · Nature Neuroscience · doi:10.1038/6368 · Cited by 3,880 · see citing works
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358 · see citing works
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.
Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292 · see citing works
Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.
Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.2.274 · Cited by 3,262 · see citing works
Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus
Malberg, J. E., Eisch, A. J., Nestler, E. J., & Duman, R. S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-24-09104.2000 · Cited by 3,111 · see citing works
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401 · see citing works
STRESS AND HIPPOCAMPAL PLASTICITY
McEwen, B. S. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.105 · Cited by 2,087 · see citing works
Multimodal fast optical interrogation of neural circuitry
Zhang, F., Wang, L., Brauner, M., Liewald, J. F., Kay, K., Watzke, N., Wood, P. G., Bamberg, E., Nagel, G., GOTTSCHALK, A. R., et al. (2007) · Nature · doi:10.1038/nature05744 · Cited by 1,742 · see citing works
Smaller hippocampal volume predicts pathologic vulnerability to psychological trauma
Gilbertson, M. W., Shenton, M. E., Ciszewski, A., Kasai, K., Lasko, N. B., Orr, S. P., & Pitman, R. K. (2002) · Nature Neuroscience · doi:10.1038/nn958 · Cited by 1,635 · see citing works
Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus
Leutgeb, J. K., Leutgeb, S., Moser, M.-B., & Moser, E. I. (2007) · Science · doi:10.1126/science.1135801 · Cited by 1,601 · cited 1× · see citing works
“GCs are characterized by a sparse activation pattern (Leutgeb et al., 2007); a behavioral experience (such as exposure to a novel environment or contextual fear conditioning) induces expression of activity dependent immediate early”
BackgroundSwanson, L. W., & Cowan, W. M. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720104 · Cited by 1,571 · see citing works
Adult hippocampal neurogenesis buffers stress responses and depressive behaviour
Snyder, J. S., Soumier, A., Brewer, M., Pickel, J., & Cameron, H. A. (2011) · Nature · doi:10.1038/nature10287 · Cited by 1,473 · see citing works
Regional dissociations within the hippocampus-memory and anxiety
Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462 · see citing works
A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing
Madisen, L., Mao, T., Koch, H., Zhuo, J.-M., Berenyi, A., Fujisawa, S., Hsu, Y.-W. A., Garcia, A. J., Gu, X., Zanella, S., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3078 · Cited by 1,398 · see citing works
Self-citationAmygdala circuitry mediating reversible and bidirectional control of anxiety
Tye, K. M., Prakash, R., Kim, S.-Y., Fenno, L. E., Grosenick, L., Zarabi, H., Thompson, K. R., Gradinaru, V., Ramakrishnan, C., & Deisseroth, K. (2011) · Nature · doi:10.1038/nature09820 · Cited by 1,289 · see citing works
David, D. J., Samuels, B. A., Rainer, Q., Wang, J.-W., Marsteller, D., Mendez, I., Drew, M., Craig, D. A., Guiard, B. P., Guilloux, J.-P., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.017 · Cited by 1,267 · see citing works
Self-citationAdult hippocampal neurogenesis in depression
Sahay, A., & Hen, R. (2007) · Nature Neuroscience · doi:10.1038/nn1969 · Cited by 1,206 · see citing works
Self-citationLower Hippocampal Volume in Patients Suffering From Depression: A Meta-Analysis
Campbell, S., Marriott, M., Nahmias, C., & MacQueen, G. M. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.4.598 · Cited by 1,156 · see citing works
Requirement for Hippocampal CA3 NMDA Receptors in Associative Memory Recall
Nakazawa, K., Quirk, M. C., Chitwood, R. A., Watanabe, M., Yeckel, M. F., Sun, L. D., Kato, A., Carr, C. A., Johnston, D., Wilson, M. A., et al. (2002) · Science · doi:10.1126/science.1071795 · Cited by 1,090 · see citing works
Dentate gyrus NMDA receptors mediate rapid pattern separation in the hippocampal network
McHugh, T. J., Jones, M. W., Quinn, J. J., Balthasar, N., Coppari, R., Elmquist, J. K., Lowell, B. B., Fanselow, M. S., Wilson, M. A., & Tonegawa, S. (2007) · Science · doi:10.1126/science.1140263 · Cited by 958 · see citing works
Dannlowski, U., Stuhrmann, A., Beutelmann, V., Zwanzger, P., Lenzen, T., Grotegerd, D., Domschke, K., Hohoff, C., Ohrmann, P., Bauer, J., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.10.021 · Cited by 954 · see citing works
Measuring normal and pathological anxiety-like behaviour in mice: a review
Belzung, C., & Griebel, G. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00291-1 · Cited by 912 · see citing works
Reduced fear expression after lesions of the ventral hippocampus
Kjelstrup, K. G., Tuvnes, F. A., Steffenach, H.-A., Murison, R., Moser, E. I., & Moser, M.-B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152112399 · Cited by 912 · see citing works
Spatial learning with a minislab in the dorsal hippocampus.
Moser, M., Moser, E. I., Forrest, E., Andersen, P. N., & Morris, R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9697 · Cited by 902 · see citing works
Cerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846 · see citing works
Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat
Jung, M. W., Wiener, S. I., & McNaughton, B. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07347.1994 · Cited by 818 · see citing works
Nakashiba, T., Cushman, J. D., Pelkey, K. A., Renaudineau, S., Buhl, D. L., McHugh, T. J., Barrera, V. R., Chittajallu, R., Iwamoto, K. S., McBain, C. J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.01.046 · Cited by 805 · see citing works
Finite scale of spatial representation in the hippocampus
Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2008) · Science · doi:10.1126/science.1157086 · Cited by 760 · see citing works
Adhikari, A., Topiwala, M. A., & Gordon, J. A. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.002 · Cited by 729 · see citing works
Treves, A., & Rolls, E. T. (1992) · Hippocampus · doi:10.1002/hipo.450020209 · Cited by 702 · see citing works
Place cells and place recognition maintained by direct entorhinal-hippocampal circuitry
Brun, V. H., Otnæss, M. K., Molden, S., Steffenach, H.-A., Witter, M. P., Moser, M.-B., & Moser, E. I. (2002) · Science · doi:10.1126/science.1071089 · Cited by 606 · see citing works
Overgeneralization of conditioned fear as a pathogenic marker of panic disorder
Lissek, S., Rabin, S., Heller, R. E., Lukenbaugh, D., Geraci, M., Pine, D. S., & Grillon, C. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.09030410 · Cited by 565 · see citing works
Neurogenesis and generalization: a new approach to stratify and treat anxiety disorders
Kheirbek, M., Klemenhagen, K. C., Sahay, A., & Hen, R. (2012) · Nature Neuroscience · doi:10.1038/nn.3262 · Cited by 543 · see citing works
Self-citationPattern separation: a common function for new neurons in hippocampus and olfactory bulb
Sahay, A., Wilson, D. A., & Hen, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.012 · Cited by 514 · see citing works
Self-citationAntidepressants recruit new neurons to improve stress response regulation
Surget, A., Tanti, A., Leonardo, E. D., Laugeray, A., Rainer, Q., Touma, C., Palme, R., Griebel, G., Ibarguen-Vargas, Y., Hen, R., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.48 · Cited by 471 · see citing works
Self-citationLinking context with reward: a functional circuit from hippocampal CA3 to ventral tegmental area
Luo, A. H., Tahsili-Fahadan, P., Wise, R. A., Lupica, C. R., & Aston-Jones, G. (2011) · Science · doi:10.1126/science.1204622 · Cited by 425 · see citing works
Kitayama, N., Vaccarino, V., Kutner, M., Weiss, P., & Bremner, J. D. (2005) · Journal of Affective Disorders · doi:10.1016/j.jad.2005.05.014 · Cited by 423 · see citing works
Bannerman, D. M., Yee, B. K., Good, M. A., Heupel, M. J., Iversen, S. D., & Rawlins, J. N. P. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1170 · Cited by 397 · see citing works
Construction of implantable optical fibers for long-term optogenetic manipulation of neural circuits
Sparta, D. R., Stamatakis, A. M., Phillips, J. L., Hovelsø, N., van Zessen, R., & Stuber, G. D. (2012) · Nature Protocols · doi:10.1038/nprot.2011.413 · Cited by 394 · see citing works
Chawla, M. K., Guzowski, J. F., Ramı́rez-Amaya, V., Lipa, P., Hoffman, K. L., Marriott, L. K., Worley, P. F., McNaughton, B. L., & Barnes, C. A. (2005) · Hippocampus · doi:10.1002/hipo.20091 · Cited by 375 · see citing works
Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.
Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M. S., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.5.884 · Cited by 357 · see citing works
Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.
Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.5.884 · Cited by 357 · see citing works
Richmond, M. A., Yee, B. K., Pouzet, B., Veenman, L., Rawlins, J. N. P., Feldon, J., & Bannerman, D. M. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1189 · Cited by 332 · see citing works
Adult‐born hippocampal neurons promote cognitive flexibility in mice
Burghardt, N. S., Park, E. H., Hen, R., & Fenton, A. A. (2012) · Hippocampus · doi:10.1002/hipo.22013 · Cited by 311 · see citing works
Self-citationMcNish, K. A., Gewirtz, J. C., & Davis, M. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09353.1997 · Cited by 281 · see citing works
Maren, S., & Holt, W. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.97 · Cited by 272 · see citing works
Lee, I., & Kesner, R. P. (2004) · Hippocampus · doi:10.1002/hipo.10177 · Cited by 268 · see citing works
Lee, I., & Kesner, R. P. (2004) · Hippocampus · doi:10.1002/hipo.10167 · Cited by 253 · see citing works
Lassalle, J., Bataille, T., & Halley, H. (2000) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1999.3931 · Cited by 213 · see citing works
Experience Dictates Stem Cell Fate in the Adult Hippocampus
Dranovsky, A., Picchini, A. M., Moadel, T., Sisti, A. C., Yamada, A., Kimura, S., Leonardo, E. D., & Hen, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.022 · Cited by 207 · see citing works
Self-citationDeep brain stimulation for treatment-resistant depression
Holtzheimer, P. E., & Hamani, C. (2014) · doi:10.2217/ebo.13.577 · Cited by 172 · see citing works
Bienvenu, T., Busti, D., Magill, P. J., Ferraguti, F., & Capogna, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.022 · Cited by 168 · see citing works
Gilbert, P. E., & Brushfield, A. M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.037 · Cited by 164 · see citing works
Hunsaker, M. R., & Kesner, R. P. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.08.016 · Cited by 156 · see citing works
Cimadevilla, J. M., Wesierska, M., Fenton, A. A., & Bureš, J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051628398 · Cited by 155 · see citing works
Self-citationKishi, T., Tsumori, T., Yokota, S., & Yasui, Y. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20919 · Cited by 150 · see citing works
Reduced amygdalar and hippocampal size in adults with generalized social phobia
Irle, E., Ruhleder, M., Lange, C., Seidler-Brandler, U., Salzer, S., Dechent, P., Weniger, G., Leibing, E., & Leichsenring, F. (2010) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.090041 · Cited by 148 · see citing works
Dissecting spatial knowledge from spatial choice by hippocampal NMDA receptor deletion
Bannerman, D. M., Bus, T., Taylor, A. M., Sanderson, D. J., Schwarz, I., Jensen, V., Hvalby, Ø., Rawlins, J. N. P., Seeburg, P. H., & Sprengel, R. (2012) · Nature Neuroscience · doi:10.1038/nn.3166 · Cited by 142 · see citing works
Dorsal vs Ventral Hippocampal Neurogenesis: Implications for Cognition and Mood
Kheirbek, M. A., & Hen, R. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.148 · Cited by 140 · see citing works
Self-citationGilbertson, M. W., Williston, S. K., Paulus, L. A., Lasko, N. B., Gurvits, T. V., Shenton, M. E., Pitman, R. K., & Orr, S. P. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.12.023 · Cited by 114 · see citing works
Czerniawski, J. L., Ree, F., Chia, C., & Otto, T. (2011) · Hippocampus · doi:10.1002/hipo.20992 · Cited by 91 · see citing works
Dynamic synapse: A new concept of neural representation and computation
Liaw, J., & Berger, T. W. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:6 · Cited by 89 · see citing works
Functional inactivation of dorsal hippocampus impairs active place avoidance in rats
Cimadevilla, J. M., Fenton, A. A., & Bureš, J. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01019-3 · Cited by 76 · see citing works
Self-citationDorsal hippocampus is necessary for novel learning but sufficient for subsequent similar learning
Wang, S., Finnie, P. S. B., Hardt, O. M., & Nader, K. (2012) · Hippocampus · doi:10.1002/hipo.22036 · Cited by 34 · see citing works
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Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738 · see citing works
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Deisseroth, K. A. (2015) · Nature Neuroscience · doi:10.1038/nn.4091 · Cited by 1,286 · see citing works
Madisen, L., Garner, A. R., Shimaoka, D., Chuong, A. S., Klapoetke, N. C., Li, L., van der Bourg, A., Niino, Y., Egolf, L., Monetti, C., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.022 · Cited by 1,114 · see citing works
Self-citationAdult hippocampal neurogenesis and cognitive flexibility — linking memory and mood
Anacker, C., & Hen, R. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.45 · Cited by 1,014 · see citing works
Self-citationIn vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9
Swiech, L., Heidenreich, M., Banerjee, A., Habib, N., Li, Y., Trombetta, J., Sur, M., & Zhang, F. (2015) · Nature Biotechnology · doi:10.1038/nbt.3055 · Cited by 772 · see citing works
Resolving the neural circuits of anxiety
Calhoon, G. G., & Tye, K. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4101 · Cited by 766 · see citing works
The role of adult hippocampal neurogenesis in brain health and disease
Toda, T., Parylak, S. L., Linker, S. B., & Gage, F. H. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0036-2 · Cited by 719 · see citing works
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 · see citing works
CRH Engagement of the Locus Coeruleus Noradrenergic System Mediates Stress-Induced Anxiety
McCall, J. G., Al-Hasani, R., Siuda, E. R., Hong, D. Y., Norris, A. J., Ford, C. P., & Bruchas, M. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.002 · Cited by 666 · see citing works
Kempadoo, K. A., Mosharov, E. V., Choi, S. J., Sulzer, D., & Kandel, E. R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1616515114 · Cited by 647 · see citing works
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Aimone, J. B., Li, Y., Lee, S. W., Clemenson, G. D., Deng, W., & Gage, F. H. (2014) · Physiological Reviews · doi:10.1152/physrev.00004.2014 · Cited by 635 · see citing works
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Adamsky, A., Kol, A., Kreisel, T., Doron, A., Ozeri-Engelhard, N., Melcer, T., Refaeli, R., Horn, H., Regev, L., Groysman, M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.002 · Cited by 631 · see citing works
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Jimenez, J., Su, K., Goldberg, A., Luna, V. M., Biane, J. S., Ordek, G., Zhou, P., Ong, S. K., Wright, M. A., Zweifel, L. S., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.016 · Cited by 606 · see citing works
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Tonegawa, S., Liu, X., Ramirez, S., & Redondo, R. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.002 · Cited by 613 · see citing works
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Anacker, C., Luna, V. M., Stevens, G. S., Millette, A., Shores, R., Jimenez, J. C., Chen, B., & Hen, R. (2018) · Nature · doi:10.1038/s41586-018-0262-4 · Cited by 605 · see citing works
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Felix-Ortiz, A. C., Beyeler, A., Seo, C., Leppla, C. A., Wildes, C. P., & Tye, K. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.016 · Cited by 592 · see citing works
Hill, A. S., Sahay, A., & Hen, R. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.85 · Cited by 557 · see citing works
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Denny, C. A., Kheirbek, M. A., Alba, E. L., Tanaka, K. F., Brachman, R. A., Laughman, K. B., Tomm, N. K., Turi, G. F., Losonczy, A., & Hen, R. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.018 · Cited by 558 · see citing works
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Lovett-Barron, M., Kaifosh, P., Kheirbek, M. A., Danielson, N., Zaremba, J. D., Reardon, T. R., Turi, G. F., Hen, R., Zemelman, B. V., & Losonczy, A. (2014) · Science · doi:10.1126/science.1247485 · Cited by 509 · see citing works
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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 474 · see citing works
Izquierdo, I., Furini, C. R. G., & Myskiw, J. C. (2016) · Physiological Reviews · doi:10.1152/physrev.00018.2015 · Cited by 453 · see citing works
Treatment resistant depression: A multi-scale, systems biology approach
Akil, H., Gordon, J. A., Hen, R., Javitch, J. A., Mayberg, H. S., McEwen, B. S., Meaney, M. J., & Nestler, E. J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.08.019 · Cited by 443 · see citing works
Self-citationFunctions and Dysfunctions of Adult Hippocampal Neurogenesis
Christian, K. M., Song, H., & Ming, G. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014134 · Cited by 395 · see citing works
Behavioral and neurobiological mechanisms of pavlovian and instrumental extinction learning
Bouton, M. E., Maren, S., & McNally, G. P. (2020) · Physiological Reviews · doi:10.1152/physrev.00016.2020 · Cited by 399 · see citing works
Parallel emergence of stable and dynamic memory engrams in the hippocampus
Hainmueller, T., & Bartos, M. (2018) · Nature · doi:10.1038/s41586-018-0191-2 · Cited by 383 · see citing works
Miller, O. H., Yang, L., Wang, C.-C., Hargroder, E. A., Zhang, Y., Delpire, E., & Hall, B. J. (2014) · eLife · doi:10.7554/elife.03581 · Cited by 358 · see citing works
Distinct contribution of adult-born hippocampal granule cells to context encoding
Danielson, N. B., Kaifosh, P., Zaremba, J. D., Lovett-Barron, M., Tsai, J., Denny, C. A., Balough, E. M., Goldberg, A. R., Drew, L. J., Hen, R., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.019 · Cited by 352 · see citing works
Self-citationPrefrontal cortex, amygdala, and threat processing: implications for PTSD
Alexandra Kredlow, M., Fenster, R. J., Laurent, E. S., Ressler, K. J., & Phelps, E. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01155-7 · Cited by 346 · see citing works
“The hippocampus itself appears to have a dorsal-ventral functional gradient, with the dorsal hippocampus encoding context more specifically, while the ventral hippocampus (vHPC) includes affective information as well [37].”
BackgroundLuczynski, P., Whelan, S. O., O'SULLIVAN, C. T. D., Clarke, G. A., Shanahan, F., Dinan, T. G., & Cryan, J. F. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13291 · Cited by 345 · see citing works
Kundaković, M., & Rocks, D. (2022) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2022.101010 · Cited by 333 · see citing works
Anacker, C., Cattaneo, A., Musaelyan, K., Zunszain, P. A., Horowitz, M., Molteni, R., Luoni, A., Calabrese, F., Tansey, K., Gennarelli, M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300886110 · Cited by 319 · see citing works
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 · see citing works
Control of Stress-Induced Persistent Anxiety by an Extra-Amygdala Septohypothalamic Circuit
Anthony, T. E., Dee, N., Bernard, A., Lerchner, W., Heintz, N., & Anderson, D. J. (2014) · Cell · doi:10.1016/j.cell.2013.12.040 · Cited by 310 · see citing works
Adult Neurogenesis: Beyond Learning and Memory
Cameron, H. A., & Glover, L. R. (2014) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015006 · Cited by 302 · see citing works
Encouraging an excitable brain state: mechanisms of brain repair in stroke
Joy, M. T., & Carmichael, S. T. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00396-7 · Cited by 284 · see citing works
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 · see citing works
Functionally Distinct Neuronal Ensembles within the Memory Engram
Sun, X., Bernstein, M. J., Meng, M., Rao, S., Sørensen, A. T., Yao, L., Zhang, X., Anikeeva, P., & Lin, Y. (2020) · Cell · doi:10.1016/j.cell.2020.02.055 · Cited by 270 · see citing works
Hippocampal Somatostatin Interneurons Control the Size of Neuronal Memory Ensembles
Stefanelli, T., Bertollini, C., Lüscher, C., Müller, D., & Méndez, P. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.024 · Cited by 255 · see citing works
Review: adult neurogenesis contributes to hippocampal plasticity
Toda, T., & Gage, F. H. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2735-4 · Cited by 262 · see citing works
Heterogeneity within classical cell types is the rule: lessons from hippocampal pyramidal neurons
Cembrowski, M. S., & Spruston, N. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0125-5 · Cited by 258 · see citing works
The Corticohippocampal Circuit, Synaptic Plasticity, and MemoryPreprint
Basu, J., & Siegelbaum, S. A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021733 · Cited by 244 · see citing works
Engram Cell Excitability State Determines the Efficacy of Memory Retrieval
Pignatelli, M., Ryan, T. J., Roy, D. S., Lovett, C., Smith, L. M., Muralidhar, S., & Tonegawa, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.029 · Cited by 259 · see citing works
Parfitt, G. M., Nguyen, R., Bang, J. Y., Aqrabawi, A. J., Tran, M. M., Seo, D. K., Richards, B. A., & Kim, J. C. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.56 · Cited by 229 · see citing works
Dentate gyrus mossy cells control spontaneous convulsive seizures and spatial memory
Bui, A. D., Nguyen, T. M., Limouse, C., Kim, H. K., Szabo, G. G., Felong, S., Maroso, M., & Soltész, I. (2018) · Science · doi:10.1126/science.aan4074 · Cited by 241 · see citing works
Adult neurogenesis, glia, and the extracellular matrix
Cope, E. C., & Gould, E. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.03.023 · Cited by 236 · see citing works
Adult Hippocampal Neurogenesis, Fear Generalization, and Stress
Besnard, A., & Sahay, A. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.167 · Cited by 226 · see citing works
Tanti, A., & Belzung, C. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.017 · Cited by 220 · see citing works
Ko, J. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00041 · Cited by 212 · see citing works
O’Leary, O. F., & Cryan, J. F. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.09.011 · Cited by 212 · see citing works
DNA repair factor BRCA1 depletion occurs in Alzheimer brains and impairs cognitive function in mice
Suberbielle, E., Djukic, B., Evans, M., Kim, D. H., Taneja, P., Wang, X., Finucane, M. M., Knox, J. A., Ho, K., Devidze, N., et al. (2015) · Nature Communications · doi:10.1038/ncomms9897 · Cited by 202 · see citing works
5-HT1A receptors on mature dentate gyrus granule cells are critical for the antidepressant response
Samuels, B. A., Anacker, C., Hu, A., Levinstein, M. R., Pickenhagen, A., Tsetsenis, T., Madroñal, N., Donaldson, Z. R., Drew, L. J., Dranovsky, A., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4116 · Cited by 200 · see citing works
Self-citationAdult Neurogenesis and Psychiatric DisordersPreprint
Kang, E., Wen, Z., Song, H., Christian, K. M., & Ming, G. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a019026 · Cited by 187 · see citing works
Recalibrating the Relevance of Adult Neurogenesis
Snyder, J. S. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2018.12.001 · Cited by 183 · see citing works
Human Hippocampus Arbitrates Approach-Avoidance Conflict
Bach, D. R., Guitart‐Masip, M., Packard, P. A., Miró, J., Falip, M., Fuentemilla, L., & Dolan, R. J. (2014) · Current Biology · doi:10.1016/j.cub.2014.01.046 · Cited by 179 · see citing works
Pentkowski, N. S., Rogge-Obando, K., Donaldson, T. N., Bouquin, S. J., & Clark, B. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.005 · Cited by 169 · see citing works
Ito, R., & Lee, A. C. H. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.039 · Cited by 173 · see citing works
From Probiotics to Psychobiotics: Live Beneficial Bacteria Which Act on the Brain-Gut Axis
Bermúdez‐Humarán, L. G., Salinas, E., Ortíz, G. G., Ramírez-Jirano, L. J., Morales, J. A., & Bitzer-Quintero, O. K. (2019) · Nutrients · doi:10.3390/nu11040890 · Cited by 172 · see citing works
Activation of local inhibitory circuits in the dentate gyrus by adult-born neurons
Drew, L. J., Kheirbek, M. A., Luna, V. M., Denny, C. A., Cloidt, M. A., Wu, M. V., Jain, S., Scharfman, H. E., & Hen, R. (2016) · Hippocampus · doi:10.1002/hipo.22557 · Cited by 169 · see citing works
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 · see citing works
Neuroanatomic differences associated with stress susceptibility and resilience
Anacker, C., Scholz, J., O’Donnell, K. J., Allemang-Grand, R., Diorio, J., Bagot, R. C., Nestler, E. J., Hen, R., Lerch, J. P., & Meaney, M. J. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.08.009 · Cited by 167 · see citing works
Self-citationAdult Hippocampal Neurogenesis: Regulation and Possible Functional and Clinical Correlates
Baptista, P., & Andrade, J. P. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00044 · Cited by 162 · see citing works
Contextual fear memory retrieval by correlated ensembles of ventral CA1 neurons
Jimenez, J., Berry, J. E., Lim, S. C., Ong, S. K., Kheirbek, M. A., & Hen, R. (2020) · Nature Communications · doi:10.1038/s41467-020-17270-w · Cited by 157 · see citing works
Self-citationSun, Q., Sotayo, A. O., Cazzulino, A. S., Snyder, A. M., Denny, C. A., & Siegelbaum, S. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.012 · Cited by 159 · see citing works
Entorhinal Cortical Ocean Cells Encode Specific Contexts and Drive Context-Specific Fear Memory
北村, 貴., Sun, C., Martin, J., Kitch, L. J., Schnitzer, M. J., & Tonegawa, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.036 · Cited by 156 · see citing works
Circuit and molecular architecture of a ventral hippocampal network
Gergues, M. M., Han, K. J., Choi, H. S., Brown, B., Clausing, K. J., Turner, V. S., Vainchtein, I. D., Molofsky, A. V., & Kheirbek, M. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0705-8 · Cited by 158 · see citing works
Self-citationCRISPR interference-based specific and efficient gene inactivation in the brain
Zheng, Y., Shen, W., Zhang, J., Yang, B., Liu, Y., Qi, H., Yu, X., Lu, S., Chen, Y., Xu, Y., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0077-5 · Cited by 157 · see citing works
FUS regulates AMPA receptor function and FTLD/ALS-associated behaviour via GluA1 mRNA stabilization
Udagawa, T., Fujioka, Y., Tanaka, M., Honda, D., Yokoi, S., Riku, Y., Ibi, D., Nagai, T., Yamada, K., Watanabe, H., et al. (2015) · Nature Communications · doi:10.1038/ncomms8098 · Cited by 156 · see citing works
Anxiety and hippocampal neuronal activity: Relationship and potential mechanisms
Ghasemi, M., Navidhamidi, M., Rezaei, F., Azizikia, A., & Mehranfard, N. (2021) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-021-00973-y · Cited by 167 · see citing works
Functional Dissociation of Adult-Born Neurons Along the Dorsoventral Axis of the Dentate Gyrus
Wu, M. V., & Hen, R. (2014) · Hippocampus · doi:10.1002/hipo.22265 · Cited by 156 · see citing works
Self-citationOptogenetic insights on the relationship between anxiety-related behaviors and social deficits
Allsop, S. A., Vander Weele, C. M., Wichmann, R., & Tye, K. M. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00241 · Cited by 150 · see citing works
An excitatory ventral hippocampus to lateral septum circuit that suppresses feeding
Sweeney, P., & Yang, Y. (2015) · Nature Communications · doi:10.1038/ncomms10188 · Cited by 147 · see citing works
Prefrontal neuronal circuits of contextual fear conditioning
Rozeske, R. R., Valério, S., Chaudun, F., & Herry, C. (2014) · Genes Brain & Behavior · doi:10.1111/gbb.12181 · Cited by 144 · see citing works
Hippocampus: Molecular, Cellular, and Circuit Features in Anxiety
Shi, H., Wang, S., Wang, X., Zhang, R.-X., & Zhu, L. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01020-1 · Cited by 144 · see citing works
The vagus nerve modulates BDNF expression and neurogenesis in the hippocampus
O’Leary, O. F., Ogbonnaya, E. S., Felice, D., Levone, B. R., C. Conroy, L., Fitzgerald, P., Bravo, J. A., Forsythe, P., Bienenstock, J., Dinan, T. G., et al. (2018) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.12.004 · Cited by 139 · see citing works
Adult neurogenesis in the mammalian hippocampus: Why the dentate gyrus?Preprint
Drew, L., Fusi, S., & Hen, R. (2013) · Learning & Memory · doi:10.1101/lm.026542.112 · Cited by 141 · see citing works
Self-citationKirouac, G. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.627633 · Cited by 136 · see citing works
Hippocampal astrocytes modulate anxiety-like behavior
Cho, W.-H., Noh, K., Lee, B. H., Barcelon, E. E., Jun, S. B., Park, H. Y., & Lee, S. J. (2022) · Nature Communications · doi:10.1038/s41467-022-34201-z · Cited by 131 · see citing works
Adult Neurogenesis and the Future of the Rejuvenating Brain Circuits
Lepousez, G., Nissant, A., & Lledo, P. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.002 · Cited by 129 · see citing works
Re-evaluating the link between neuropsychiatric disorders and dysregulated adult neurogenesis
Yun, S., Reynolds, R. P., Masiulis, I., & Eisch, A. J. (2016) · Nature Medicine · doi:10.1038/nm.4218 · Cited by 127 · see citing works
Serotonin in fear conditioning processes
Bauer, E. P. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.028 · Cited by 127 · see citing works
Acoustically targeted chemogenetics for the non-invasive control of neural circuits
Szablowski, J. O., Lee‐Gosselin, A., Lue, B., Malounda, D., & Shapiro, M. G. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0258-2 · Cited by 127 · see citing works
On How the Dentate Gyrus Contributes to Memory Discrimination
van Dijk, M. T., & Fenton, A. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.018 · Cited by 126 · see citing works
Self-citationSurget, A., & Belzung, C. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01136-8 · Cited by 122 · see citing works
You, R., Ho, J. Y. S., Hung, C. H.-L., Liu, Y., Huang, C.-X., Chan, H., Ho, S., Lui, S.-Y., Li, H., & Chang, R. C. (2018) · Particle and Fibre Toxicology · doi:10.1186/s12989-018-0263-3 · Cited by 120 · see citing works
Lateral septum as a nexus for mood, motivation, and movement
Wirtshafter, H. S., & Wilson, M. A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.029 · Cited by 122 · see citing works
Hippocampal-amygdala memory circuits govern experience-dependent observational fear
Terranova, J. I., Yokose, J., Osanai, H., Marks, W. D., Yamamoto, J., Ogawa, S. K., & Kitamura, T. (2022) · Neuron · doi:10.1016/j.neuron.2022.01.019 · Cited by 117 · see citing works
Zhang, D., Wang, X., Wang, B., Garza, J. C., Fang, X., Wang, J., Scherer, P., Brenner, R., Zhang, W., & Lu, X.-Y. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.58 · Cited by 115 · see citing works
de Bartolomeis, A., Barone, A., Vellucci, L., Mazza, B., Austin, M. C., Iasevoli, F., & Ciccarelli, M. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02976-3 · Cited by 113 · see citing works
Dorsal and Ventral Hippocampal Sharp-Wave Ripples Activate Distinct Nucleus Accumbens Networks
Sosa, M., Joo, H. R., & Frank, L. M. (2019) · Neuron · doi:10.1016/j.neuron.2019.11.022 · Cited by 106 · see citing works
Artificially Enhancing and Suppressing Hippocampus-Mediated Memories
Chen, B. K., Murawski, N. J., Cincotta, C., McKissick, O. P., Finkelstein, A. B., Hamidi, A., Merfeld, E., Doucette, E., Grella, S. L., Shpokayte, M., et al. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.065 · Cited by 109 · see citing works
Neuronal types in the mouse amygdala and their transcriptional response to fear conditioning
Hochgerner, H., Singh, S., Tibi, M., Lin, Z., Skarbianskis, N., Admati, I., Ophir, O., Reinhardt, N., Netser, S., Wagner, S., et al. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01469-3 · Cited by 110 · see citing works
Effects of early-life stress on cognitive function and hippocampal structure in female rodents.
Loi, M., Mossink, J. C. L., Meerhoff, G. F., Den Blaauwen, J. L., Lucassen, P. J., & Joëls, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.024 · Cited by 109 · see citing works
Preez, A. D., Law, T., Onorato, D., Lim, Y. M., Eiben, P., Musaelyan, K., Egeland, M. T., Hye, A., Zunszain, P. A., Thuret, S., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01000-3 · Cited by 111 · see citing works
Grégoire, C., Bonenfant, D., Nguyen, A. L., Aumont, A., & Fernandes, K. J. L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086237 · Cited by 106 · see citing works
Fu, C.-H., Iascone, D. M., Petrof, I., Hazra, A., Zhang, X., Pyfer, M. S., Tosi, U., Corbett, B. F., Cai, J., Lee, J., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.101 · Cited by 107 · see citing works
Paradoxical somatodendritic decoupling supports cortical plasticity during REM sleep
Aime, M., Calcini, N., Borsa, M., Campelo, T., Rusterholz, T., Sattin, A., Fellin, T., & Adamantidis, A. (2022) · Science · doi:10.1126/science.abk2734 · Cited by 106 · see citing works
Stimulation of entorhinal cortex-dentate gyrus circuitry is antidepressive
Yun, S., Reynolds, R. P., Petrof, I., White, A., Rivera, P. D., Segev, A., Gibson, A. D., Suarez, M., DeSalle, M. J., Ito, N., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0002-1 · Cited by 120 · see citing works
Ramanathan, K. R., Ressler, R. L., Jin, J., & Maren, S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1429-18.2018 · Cited by 106 · see citing works
Adult hippocampal neurogenesis and its impairment in Alzheimer’s disease
Kim, T. A., Syty, M. D., Wu, K., & Ge, S. (2022) · 动物学研究 · doi:10.24272/j.issn.2095-8137.2021.479 · Cited by 113 · see citing works
- Authors
- Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., Zeng, H., Fenton, A. A., & Hen, R.
- Affiliations
- New York State Psychiatric Institute (US)
- Allen Institute for Brain Science (US)
- SUNY Downstate Health Sciences University (US)
- Corresponding author
- Hen, René
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2013-03
- Volume
- 77
- Issue
- 5
- Pages
- 955-968
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC3595120
- OpenAlex
- W2069281265
- Semantic Scholar
- 3c538be529a4c5c54e7172e30f4e8504564c6a8d
- Cited by
- 713
- References
- 67
- Citations by year
- 2026: 29 · 2025: 62 · 2024: 46 · 2023: 39 · 2022: 63 · 2021: 59 · 2020: 67 · 2019: 74 · 2018: 65 · 2017: 50 · 2016: 46 · 2015: 43 · 2014: 51 · 2013: 19
- FWCI
- 28.95
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institute of Mental Health (R37MH068542, K01MH099371, T32MH015174, K08MH087718)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- dentate gyrus, granule cells, dorsal-ventral axis, anxiety, contextual fear memory, contextual learning, memory encoding, memory retrieval, hippocampus, anxiety disorders, optogenetics
- MeSH terms
- Animals, Anxiety, Avoidance Learning, Behavior, Animal, Conditioning, Psychological, Fear, Immunohistochemistry, Learning, Male, Mental Recall, Stereotaxic Techniques, Dentate Gyrus, Mice, Optical Fibers, Opsins, Electrophysiological Phenomena, In Vitro Techniques
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