The neuroanatomical and neurochemical basis of conditioned fear

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(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010

Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.

Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376

The hippocampus as a cognitive map

Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128

Handbook of Chemical Neuroanatomy

Stern, C. D. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90021-5 · Cited by 4,160

The Expression of the Emotions in Man and Animals

Crowley, T. (1957) · Philosophical Studies · doi:10.5840/philstudies1957703 · Cited by 3,625

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

Psychopharmacology: The Fourth Generation of Progress

Bloom, F. E., & Kupfer, D. J. (1995) · Medical Entomology and Zoology · Cited by 2,985

Modality-Specific Retrograde Amnesia of Fear

Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483

Emotion, attention, and the startle reflex

Lang, P. J., Bradley, M. M., & Cuthbert, B. N. (1990) · Psychological Review · doi:10.1037/0033-295x.97.3.377 · Cited by 2,205

Preliminary analysis of functions of the temporal lobes in monkeys

KLÜVER, H. (1939) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1939.02270240017001 · Cited by 1,696

Differential Regulation of Neuropeptide Y in the Amygdala and Prefrontal Cortex during Recovery from Chronic Variable Stress

McGuire, J. L., Larke, L. E., Sallee, F. R., Herman, J. P., & Sah, R. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00054 · Cited by 36

Repeated withdrawal from ethanol spares contextual fear conditioning and spatial learning but impairs negative patterning and induces over‐responding: evidence for effect on frontal cortical but not hippocampal function?

Borlikova, G. G., Elbers, N. A., & Stephens, D. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04901.x · Cited by 35

Prior cocaine exposure disrupts extinction of fear conditioningPreprint

Burke, K. A., Franz, T. M., Gugsa, N., & Schoenbaum, G. M. (2006) · Learning & Memory · doi:10.1101/lm.216206 · Cited by 36

Role of L-type Ca2+channel isoforms in the extinction of conditioned fearPreprint

Busquet, P., Hetzenauer, A., Sinnegger-Brauns, M. J., Striessnig, J., & Singewald, N. (2008) · Learning & Memory · doi:10.1101/lm.886208 · Cited by 36

Early life programming of innate fear and fear learning in adult female rats

Stevenson, C. W., Meredith, J. P., Spicer, C. H., Mason, R., & Marsden, C. A. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.021 · Cited by 34

Behavioral characterization of P311 knockout mice

Taylor, G. A., Rodriguiz, R. M., Greene, R. I., Daniell, X. G., Henry, S. C., Crooks, K., Kotloski, R. J., Tessarollo, L., Phillips, L. E., & Wetsel, W. C. (2008) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2008.00420.x · Cited by 35

Conditioning-specific reflex modification of the rabbit's nictitating membrane response and heart rate: Behavioral rules, neural substrates, and potential applications to posttraumatic stress disorder.

Burhans, L. B., Smith‐Bell, C. A., & Schreurs, B. G. (2008) · Behavioral Neuroscience · doi:10.1037/a0013599 · Cited by 35

Psychiatric Disorders - Trends and Developments

Uehara, T. (2011) · InTech eBooks · doi:10.5772/2330 · Cited by 36

Implicit aversive memory under anaesthesia in animal models: a narrative review

Samuel, N., Taub, A. H., Paz, R., & Raz, A. (2018) · British Journal of Anaesthesia · doi:10.1016/j.bja.2018.05.046 · Cited by 35

Infralimbic cortex activity is required for the expression but not the acquisition of conditioned safety

Kreutzmann, J. C., Jovanović, T., & Fendt, M. (2020) · Psychopharmacology · doi:10.1007/s00213-020-05527-7 · Cited by 31

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Meis, S., Endres, T., & Leßmann, V. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03260-3 · Cited by 40

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Dere, E., Frisch, C. M., Silva, M. A. D. S., Gödecke, A., Schrader, J., & Huston, J. P. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00382-7 · Cited by 35

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Pickens, C. L., Navarre, B. M., & Nair, S. G. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.036 · Cited by 35

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Gallego, J., Nsegbe, É., & Durand, E. (2001) · Behavior Modification · doi:10.1177/0145445501254002 · Cited by 35

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Fendt, M., & Mucha, R. F. (2001) · Psychopharmacology · doi:10.1007/s002130100709 · Cited by 35

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Norrholm, S. D., Anderson, K. M., Olin, I. W., Jovanovic, T., Kwon, C., Warren, V. T., McCarthy, A., Bosshardt, L., Sabree, J., Duncan, E. J., et al. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00077 · Cited by 34

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Wöhr, M., & Schwarting, R. K. W. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374593-4.00012-7 · Cited by 34

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Mohammadi, M., Bergado-Acosta, J. R., & Fendt, M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.06.053 · Cited by 35

Conditioning-specific reflex modification of the rabbit (Oryctolagus cuniculus) nictitating membrane response: Generality and nature of the phenomenon.

Buck, D. L., Seager, M. A., & Schreurs, B. G. (2001) · Behavioral Neuroscience · doi:10.1037//0735-7044.115.5.1039 · Cited by 34

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Jaworski, D. M., Boone, J. Q., Caterina, J. J., Soloway, P. D., & Falls, W. A. (2005) · Brain Research · doi:10.1016/j.brainres.2005.05.057 · Cited by 34

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Yilmazer‐Hanke, D., Wigger, A., Linke, R., Landgraf, R., & Schwegler, H. (2004) · Behavior Genetics · doi:10.1023/b:bege.0000017874.40934.64 · Cited by 34

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d’Isa, R. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00078 · Cited by 34

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Carrive, P. (2002) · Autonomic Neuroscience · doi:10.1016/s1566-0702(02)00039-5 · Cited by 34

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Anagnostaras, S., Craske, M. G., & Fanselow, M. S. (1999) · Nature Neuroscience · doi:10.1038/12146 · Cited by 34

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Imamura, M., & Zhang, Y. B. (2014) · International Journal of Intercultural Relations · doi:10.1016/j.ijintrel.2014.08.018 · Cited by 35

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Park, K., Ribic, A., Gaupp, F. M. L., Coman, D., Huang, Y. H., Dulla, C. G., Hyder, F., & Biederer, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0189-16.2016 · Cited by 33

Membrane excitability and fear conditioning in cerebellar Purkinje cell

Zhu, L., Scelfo, B., Tempia, F., Sacchetti, B., & Strata, P. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.040 · Cited by 33

Less is more: The effects of very brief versus clearly visible exposure.

Siegel, P., & Weinberger, J. (2012) · Emotion · doi:10.1037/a0026806 · Cited by 33

Aversive stimulation of the inferior colliculus changes dopamine and serotonin extracellular levels in the frontal cortex: Modulation by the basolateral nucleus of amygdala

de Macedo, C. E. A., Cuadra, G. R., Molina, V. A., & Brandão, M. L. (2004) · Synapse · doi:10.1002/syn.20094 · Cited by 33

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Febbraro, F., Svenningsen, K., Tran, T. P., & Wiborg, O. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179434 · Cited by 35

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Fellous, J., Armony, J. L., & LeDoux, J. E. (2002) · Cited by 33

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Wang, L., Rodriguiz, R. M., Wetsel, W. C., Sheng, H., Zhao, S., Liu, X., Paschen, W., & Yang, W. (2014) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.130148 · Cited by 32

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Portugal, L. C. L., Pereira, M. G., Alves, R. D. C. S., Tavares, G., Lobo, I., Rocha-Rego, V., Marques‐Portella, C., Mendlowicz, M. V., Coutinho, E. S. F., Fiszman, A., et al. (2012) · Brazilian Journal of Psychiatry · doi:10.1590/s1516-44462012000100011 · Cited by 36

Activation of the brain 5-HT2C receptors causes hypolocomotion without anxiogenic-like cardiovascular adjustments in mice

Stiedl, O., Misane, I., Koch, M., Pattij, T., Meyer, M., & Ögren, S. O. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.10.012 · Cited by 32

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Spanka, C., Glatthar, R., Desrayaud, S., Fendt, M., Orain, D., Troxler, T. J., & Vranesic, I. (2009) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2009.11.001 · Cited by 32

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Bast, T., Zhang, W., & Feldon, J. (2001) · Cited by 32

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Calandreau, L., Desgranges, B., Jaffard, R., & Desmedt, A. (2010) · Learning & Memory · doi:10.1101/lm.1859810 · Cited by 32

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Gifkins, A., Greba, Q., & Kokkinidis, L. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.5.785 · Cited by 31

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Krystal, A. D., Sutherland, J., & Hochman, D. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035417 · Cited by 30

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Baldi, E., Costa, A., Rani, B., Passani, M. B., Blandina, P., Romano, A., & Provensi, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810000 · Cited by 35

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Hendriksen, H., Bink, D. I., Daniels, E. G., Pandit, R., Piriou, C., Slieker, R. C., Westphal, K. G. C., Olivier, B., & Oosting, R. S. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.05.028 · Cited by 32

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Suarez‐Jimenez, B., Bisby, J. A., Horner, A. J., King, J. A., Pine, D. S., & Burgess, N. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714691115 · Cited by 31

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(EFSA), E. F. S. A. (2009) · EFSA Journal · doi:10.2903/j.efsa.2009.954 · Cited by 43

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Rabinak, C. A., & Maren, S. (2008) · Behavioral Neuroscience · doi:10.1037/a0012903 · Cited by 30

Graded fear generalization enhances the level of cfos‐positive neurons specifically in the basolateral amygdala

Rajbhandari, A. K., Zhu, R., Adling, C., Fanselow, M. S., & Waschek, J. A. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23947 · Cited by 32

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Reimer, A. E., de Oliveira, A. R., & Brandão, M. L. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.06.005 · Cited by 29

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Detert, J. A., Kampa, N. D., & Moyer, J. R. (2008) · Behavioral Neuroscience · doi:10.1037/a0013512 · Cited by 29

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Pavesi, E., Heldt, S. A., & Fletcher, M. L. (2013) · Learning & Memory · doi:10.1101/lm.031450.113 · Cited by 29

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Drumond, A., Madeira, N., & Fonseca, R. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.031 · Cited by 29

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Uhernik, A. L., Montoya, Z. T., Balkissoon, C. D., & Smith, J. P. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.02.009 · Cited by 28

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Kellis, D. M., Kaigler, K. F., Witherspoon, E., Fadel, J. R., & Wilson, M. A. (2020) · Neurobiology of Stress · doi:10.1016/j.ynstr.2020.100279 · Cited by 29

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Sui, L., Wang, F., Liu, F., Wang, J., & Li, B. (2006) · Journal of neuroendocrinology · doi:10.1111/j.1365-2826.2006.01480.x · Cited by 23

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Holahan, M. R., & White, N. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.24 · Cited by 29

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Röskam, S., Neff, F., Schwarting, R. K. W., Bacher, M., & Dodel, R. C. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.10.006 · Cited by 29

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Tovote, P., Meyer, M., Pilz, P. K. D., Ronnenberg, A., Ögren, S. O., Spiess, J., & Stiedl, O. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.55 · Cited by 28

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Maldonado, N. M., Martijena, I. D., & Molina, V. A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.06.035 · Cited by 29

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Wood, S. C., & Anagnostaras, S. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.10.006 · Cited by 29

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de la Mora, M. P., Jacobsen, K. X., Crespo‐Ramírez, M., Flores‐Gracia, C., & Fuxé, K. (2008) · Neurochemical Research · doi:10.1007/s11064-008-9722-9 · Cited by 27

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Kindermann, T., Siemers, B. M., & Fendt, M. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.024174 · Cited by 27

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Rodriguiz, R. M., & Wetsel, W. C. (2006) · Frontiers in neuroscience · doi:10.1201/9781420004335.ch12 · Cited by 27

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Pain, L., Angst, M.-J., Gourrier, L. L., & Oberling, P. (2002) · Anesthesiology · doi:10.1097/00000542-200208000-00023 · Cited by 27

5-HT mechanisms of median raphe nucleus in the conditioned freezing caused by light/foot-shock association.

Avanzi, V., Silva, R. C. B., Macedo, C. E., & Brandão, M. L. (2003) · Physiology and Behavior · doi:10.1016/s0031-9384(03)00029-5 · Cited by 25

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Goode, T. D., Kim, J., & Maren, S. (2015) · eNeuro · doi:10.1523/eneuro.0037-15.2015 · Cited by 28

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Sangha, S. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00354 · Cited by 28

Differential effects of prior stress on conditioned inhibition of fear and fear extinction

Woon, E. P., Seibert, T. A., Urbanczyk, P. J., Ng, K. H., & Sangha, S. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112414 · Cited by 26

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Sneddon, L. U., & Brown, C. (2020) · Advances in neuroethics · doi:10.1007/978-3-030-31011-0_4 · Cited by 26

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Binette, A. N., Totty, M. S., & Maren, S. (2022) · PLoS ONE · doi:10.1371/journal.pone.0264797 · Cited by 26

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Durand, E., Dauger, S., Vardon, G., Gressèns, P., Gaultier, C., de Schonen, S., & Gallego, J. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00488.2002 · Cited by 26

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Alves, F. L., Barbosa, A., & Hoffmann, A. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.12.003 · Cited by 29

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Bignante, E. A., Paglini, M. G., & Molina, V. A. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.02.007 · Cited by 25

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Skelly, M. J., Ariwodola, O. J., & Weiner, J. L. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.10.003 · Cited by 24

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Vila, J., Fernández‐Santaella, M. C., Chica, J. P., Vera, M. N., Robles, H., Pérez‐Marfil, M. N., Sánchez, M. B., Ramírez-Uclés, I. M., & Ruiz‐Padial, E. (2003) · The Spanish Journal of Psychology · doi:10.1017/s1138741600005217 · Cited by 26

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Luyten, L., Vansteenwegen, D., van Kuyck, K., Deckers, D., & Nuttin, B. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.11.005 · Cited by 26

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Brignell, C. M., & Curran, H. V. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0363-x · Cited by 26

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Castilho, V. M., Borelli, K. G., Brandão, M. L., & Nobre, M. J. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.03.014 · Cited by 26

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Andreatta, M., & Pauli, P. (2021) · Clinical Psychology Review · doi:10.1016/j.cpr.2021.102095 · Cited by 27

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Ng, K. H., Pollock, M., Escobedo, A., Bachman, B. B., Miyazaki, N. L., Bartlett, E. L., & Sangha, S. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01598-0 · Cited by 25

The expression of fear-potentiated startle during development: Integration of learning and response systems.

Barnet, R. C., & Hunt, P. S. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.861 · Cited by 25

Inactivation of the lateral septum blocks fox odor-induced fear behavior

Endres, T., & Fendt, M. (2008) · Neuroreport · doi:10.1097/wnr.0b013e3282fb78d9 · Cited by 25

P2X7 purinergic receptors participate in the expression and extinction processes of contextual fear conditioning memory in mice

Domingos, L. B., Hott, S. C., Terzian, A. L. B., & Resstel, L. B. M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.08.005 · Cited by 25

Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior

Ponder, C. A., Munoz, M. B., Gilliam, T. C., & Palmer, A. A. (2007) · Mammalian Genome · doi:10.1007/s00335-007-9013-9 · Cited by 25

Bidirectional modulation of classical fear conditioning in mice by 5-HT1A receptor ligands with contrasting intrinsic activities

Youn, J., Misane, I., Eriksson, T. M., Millan, M. J., Ögren, S. O., Verhage, M., & Stiedl, O. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.07.011 · Cited by 24

Chapter 4.4 The glutamatergic system as a potential therapeutic target for the treatment of anxiety disorders

Cryan, J. F., & Dev, K. K. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(07)00013-6 · Cited by 25

Brain Activation by Peptide Pro-Leu-Gly- (MIF-1)

Khan, R. S., Yu, C., Kastin, A. J., He, Y., Ehrensing, R. H., Hsuchou, H., Stone, K. P., & Pan, W. (2010) · International Journal of Peptides · doi:10.1155/2010/537639 · Cited by 24

Limbic system development underlies the emergence of classical fear conditioning during the third and fourth weeks of life in the rat.

Deal, A. L., Erickson, K. J., Shiers, S. I., & Burman, M. A. (2016) · Behavioral Neuroscience · doi:10.1037/bne0000130 · Cited by 25

Fear: Potentiation and Startle

Falls, W. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-045396-5.00137-8 · Cited by 1

Pharmacological and anatomical analysis of fear conditioning using the fear-potentiated startle paradigm.

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The neurobiological basis of fear : a concise review : review article

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The neurobiological basis of fear : a concise review : review article

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Neuroanatomy of human fear conditioning: brain activity specifically related to stimuli processing and memory formation.

Fischer, H., Andersson, J. L. R., Furmark, T., & Fredrikson, M. G. (1998) · NeuroImage · doi:10.1016/s1053-8119(18)31747-6