Repeated restraint stress facilitates fear conditioning independently of causing hippocampal CA3 dendritic atrophy

SOSW: Stress Sensing With Off-the-Shelf Smartwatches in the Wild

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Translational reciprocity: Bridging the gap between preclinical studies and clinical treatment of stress effects on the adolescent brain

Neigh, G. N., Ritschel, L. A., Kilpela, L. S., Harrell, C. S., & Bourke, C. H. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.075 · Cited by 18

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Pagliaccio, D., & Barch, D. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802456-0.00002-9 · Cited by 16

A life-course, epigenetic perspective on resilience in brain and body

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miR-375 negatively regulates the synthesis and secretion of catecholamines by targeting Sp1 in rat adrenal medulla

Gai, Y., Zhang, J., Wei, C., Cao, W. J., Cui, Y., & Cui, S. (2017) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00345.2016 · Cited by 17

Acute restraint stress alters sound-evoked neural responses in the rat auditory cortex

Ma, L., Zhang, J., Yang, P., Wang, E., & Qin, L. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.074 · Cited by 16

Elevation of BACE in an Aβ rat model of Alzheimer's disease: exacerbation by chronic stress and prevention by nicotine

Alkadhi, K. A., Alzoubi, K. H., Srivareerat, M., & Tran, T. T. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711000162 · Cited by 16

Repeated Neck Restraint Stress Bidirectionally Modulates Excitatory Transmission in the Dentate Gyrus and Performance in a Hippocampus-dependent Memory Task

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Emotionality modulates the impact of chronic stress on memory and neurogenesis in birds

Lormant, F., Ferreira, V. H. B., Meurisse, M., Lemarchand, J., Constantin, P., Morisse, M., Cornilleau, F., Parias, C., Chaillou, É., Bertin, A., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71680-w · Cited by 16

Larger bilateral amygdalar volumes are associated with affective loss experiences

Acosta, H., Jansen, A., & Kircher, T. T. J. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24835 · Cited by 16

Aircraft noise exposure affects rat behavior, plasma norepinephrine levels, and cell morphology of the temporal lobe

Di, G., Zhou, B. Y., Li, Z., & Lin, Q. (2011) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1000439 · Cited by 16

Recent Progress in Some Aircraft Technologies

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Chronic corticosterone-induced impaired cognitive flexibility is not due to suppressed adult hippocampal neurogenesis

Lui, E., Salim, M., Chahal, M., Puri, N., Marandi, E., Quadrilatero, J., & Satvat, E. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.05.060 · Cited by 15

Early sexual experience and stressful conditions affect the response of young ewes to the male

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Tianeptine: A Facilitator of the Reuptake of Serotonin and Norepinephrine as an Antidepressant?

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Relations of Lifetime Perceived Stress and Basal Cortisol With Hippocampal Volume Among Healthy Adolescents and Those at Clinical High Risk for Psychosis: A Structural Equation Modeling Approach

Aberizk, K., Addington, J., Bearden, C. E., Cadenhead, K. S., Cannon, T. D., Cornblatt, B. A., Keshavan, M. S., Mathalon, D. H., Perkins, D. O., Stone, W. S., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.11.027 · Cited by 15

Neurobiology of Interpreting and Responding to Stressful Events: Paradigmatic Role of the Hippocampus

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Excessive Sensory Stimulation during Development Alters Neural Plasticity and Vulnerability to Cocaine in Mice

Ravinder, S., Donckels, E. A., Ramirez, J. S. B., Christakis, D., Ramirez, J., & Ferguson, S. M. (2016) · eNeuro · doi:10.1523/eneuro.0199-16.2016 · Cited by 19

The Psychoneuroimmunology of Stress Regulation in Pediatric Cancer Patients

White, G. E., Caterini, J. E., McCann, V., Rendall, K., Nathan, P. C., Rhind, S. G., Jones, H., & Wells, G. D. (2021) · Cancers · doi:10.3390/cancers13184684 · Cited by 20

Qualitative and quantitative changes in phospholipids and proteins investigated by spectroscopic techniques in animal depression model

Depciuch, J., Sowa-Kućma, M., Nowak, G., Papp, M., Gruca, P., Misztak, P., & Parlińska‐Wojtan, M. (2016) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2016.12.007 · Cited by 14

Stressed rats fail to exhibit avoidance reactions to innately aversive social calls

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History of chronic stress modifies acute stress-evoked fear memory and acoustic startle in male rats

Schmeltzer, S. N., Vollmer, L. L., Rush, J., Weinert, M., Dolgas, C. M., & Sah, R. (2015) · Stress · doi:10.3109/10253890.2015.1016495 · Cited by 16

High frequency stimulation of the infralimbic cortex induces morphological changes in rat hippocampal neurons

Bezchlibnyk, Y. B., Stone, S. S. D., Hamani, C., & Lozano, A. M. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.11.013 · Cited by 16

Effects of chronic forced-swim stress on behavioral properties in rats with neonatal repeated MK-801 treatment

Kawabe, K. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.06.009 · Cited by 14

Timing is everything: differential effects of chronic stress on fear extinction

Chakraborty, P., & Chattarji, S. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5053-y · Cited by 15

Long‐term perturbation of spine plasticity results in distinct impairments of cognitive function

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Non-specific Effect of Fear Conditioning and Specific Effect of Social Defeat on Social Recognition Memory Performance in Female Rats

Penka, L.-L., Bond, T., & Heinrichs, S. (2004) · Stress · doi:10.1080/10253890410001677231 · Cited by 12

A novel adolescent chronic social defeat model: reverse-Resident-Intruder Paradigm (rRIP) in male rats

Manz, K. M., Levine, W. A., Seckler, J. C., Iskander, A. N., & Reich, C. G. (2018) · Stress · doi:10.1080/10253890.2017.1423285 · Cited by 12

Chronic Restraint Stress Decreases the Excitability of Hypothalamic POMC Neuron and Increases Food Intake

Ha, G. E., & Cheong, E. (2021) · Experimental Neurobiology · doi:10.5607/en21037 · Cited by 13

Postnatal exposure to predator odor (TMT) enhances spatial learning in mice adulthood

Hacquemand, R., Jacquot, L., & Brand, G. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.12.032 · Cited by 13

Matrix disequilibrium in Alzheimer’s disease and conditions that increase Alzheimer’s disease risk

Amontree, M., Deasy, S., Turner, R. S., & Conant, K. E. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1188065 · Cited by 13

Repeated social defeat promotes persistent inflammatory changes in splenic myeloid cells; decreased expression of β-arrestin-2 (ARRB2) and increased expression of interleukin-6 (IL-6)

Rajalingam, D., Nymoen, I., Jacobsen, D., Eriksen, M., Dissen, E., Nielsen, M. B., Einarsen, S., & Gjerstad, J. (2020) · BMC Neuroscience · doi:10.1186/s12868-020-00574-4 · Cited by 11

Maternal hypothalamic-pituitary-adrenal axis response to foraging uncertainty: A model of individual vs. social allostasis and the "Superorganism Hypothesis"

Coplan, J. D., Gupta, N. K., Karim, A., Rozenboym, A. V., Smith, E. L., Kral, J. G., & Rosenblum, L. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184340 · Cited by 12

Testosterone prevents synaptic loss in the perineal motoneuron pool in the spinal cord in male rats exposed to chronic stress

Matsumoto, A. (2005) · Stress · doi:10.1080/10253890500140642 · Cited by 12

The Neural Bases of Emotions

Franklin, T. B., & Mansuy, I. M. (2013) · Springer eBooks · doi:10.1007/978-3-642-10769-6_24 · Cited by 12

A dendritic organization of lateral amygdala neurons in fear susceptible and resistant mice

Gomes, V. D. C., Bergstrom, H. C., McGuire, J. L., Parker, C. C., Coyner, J. L., Landeira-Fernández, J., Ursano, R. J., Palmer, A. A., & Johnson, L. R. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.11.010 · Cited by 11

Salivary alpha-amylase enzyme is a non-invasive biomarker of acute stress in Japanese macaques (Macaca fuscata)

Broche, N., Takeshita, R. S. C., Mouri, K., Bercovitch, F. B., & Huffman, M. A. (2019) · Primates · doi:10.1007/s10329-019-00757-6 · Cited by 12

Beneficial Effects of Tianeptine on Hippocampus-Dependent Long-Term Memory and Stress-Induced Alterations of Brain Structure and Function

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Rethinking the role of L-type voltage-gated calcium channels in fear memory extinctionPreprint

Schafe, G. E. (2008) · Learning & Memory · doi:10.1101/lm.996908 · Cited by 11

Behavioral effects of chronic stress in the Fmr1 mouse model for fragile X syndrome

Lemaire, V., Subashi, E., Henkous, N., Béracochéa, D., & Pietropaolo, S. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.11.051 · Cited by 12

Transcriptomics of the depressed and PTSD brain

Zhang, J., Kaye, A. P., Wang, J., & Girgenti, M. J. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100408 · Cited by 11

Different duration of crowding and noise exposure effects on exploratory behavior, cellular immunity and HSP70 expression in rats

Pan, F., Lu, C.-Y., Song, J., Hong, J. L., Li, Q., Hong-luan, Y., & Xiao-yang, C. (2006) · Stress and Health · doi:10.1002/smi.1103 · Cited by 10

PTSD: From Neurons to Networks

Rao, R. P., Suvrathan, A., Miller, M. M., McEwen, B. S., & Chattarji, S. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-329-9_7 · Cited by 11

Sex-dependent long-term effects of prepubescent stress on the posterior parietal cortex

Fariborzi, M., Park, S. B., Ozgur, A., & Lür, G. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100295 · Cited by 8

Prefrontal Regulation of Safety Learning during Ethologically Relevant Thermal Threat

Felix‐Ortiz, A. C., Terrell, J. M., Gonzalez, C., Msengi, H. D., Boggan, M. B., Ramos, A. R., Magalhães, G., & Burgos-Robles, A. (2024) · eNeuro · doi:10.1523/eneuro.0140-23.2024 · Cited by 7

The effect of stress and reward on encoding future fear memories

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Recovery periods during repeated stress impact corticosterone and behavioral responses differently in house sparrows

Gormally, B. M. G., Ramos, S., Yin, H., & Romero, L. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.04.009 · Cited by 9

Structural Plasticity and Molecular Markers in Hippocampus of Male Rats after Acute Stress

Chen, F., Polsinelli, B., Nava, N., Treccani, G., Elfving, B., Müller, H. K., Musazzi, L., Popoli, M., Nyengaard, J. R., & Wegener, G. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.05.001 · Cited by 10

Chronic variable stress and intravenous methamphetamine self-administration – Role of individual differences in behavioral and physiological reactivity to novelty

Taylor, S. B., Watterson, L. R., Kufahl, P. R., Nemirovsky, N. E., Tomek, S. E., Conrad, C. D., & Olive, M. F. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.05.003 · Cited by 9

Perceived stress associations with hippocampal-dependent behavior and hippocampal subfield volume

Grupe, D. W., Barnes, A. L., Gresham, L. K., Kirvin-Quamme, A., Nord, E., Alexander, A. L., Abercrombie, H. C., Schaefer, S. M., & Davidson, R. J. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100469 · Cited by 8

Modest elevation of corticosterone in preweanling rats impairs subsequent trace eyeblink conditioning during the juvenile period

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Repeated unpredictable threats without harm impair spatial working memory in the Barnes maze

Kim, D. J., Louis, N. S., Molaro, R. A., Hudson, G. T., Chorley, R. C., & Anderson, B. J. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.11.014 · Cited by 8

Therapeutic effects of a restraint procedure on posttraumatic place learning in fimbria-fornix transected rats

Rytter, H. M., Castro, M. R., Knippel, J., Kohler, P. J., Lassen, P., & Mogensen, J. (2008) · Brain Research · doi:10.1016/j.brainres.2008.04.005 · Cited by 8

Training level reveals a dynamic dialogue between stress and memory systems in birds

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The co-expression of GluN2B subunits of the NMDA receptors and glucocorticoid receptors after chronic restraint stress in low and high anxiety rats

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Adaptation to Stress and Psychobiological Mechanisms of Resilience

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Corticotrophin-releasing hormone decreases synaptic transmission in rat sensorimotor cortex in vivo

Froc, D. J., & Christie, B. R. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.004 · Cited by 7

A precision medicine approach to pharmacological adjuncts to extinction: A call to broaden research

King, G., Baker, K. D., Bisby, M. A., Chan, D., Cowan, C. S. M., Stylianakis, A. A., Zimmermann, K. S., & Richardson, R. (2019) · Psychopharmacology · doi:10.1007/s00213-018-4999-0 · Cited by 6

Neuritin Controls Axonal Branching in Serotonin Neurons: A Possible Mediator Involved in the Regulation of Depressive and Anxiety Behaviors via FGF Signaling

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The lifetime impact of stress on fear regulation and cortical function

Trask, S., Kuczajda, M. T., & Ferrara, N. C. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109367 · Cited by 6

Using New Approaches in Neurobiology to Rethink Stress-Induced Amnesia

Radulović, J. (2017) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-017-0109-6 · Cited by 6

Adversity in early adolescence promotes an enduring anxious phenotype and increases serotonergic innervation of the infralimbic medial prefrontal cortex

Tao, C. S., Dhamija, P., Booij, L., & Menard, J. L. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.004 · Cited by 7

Opposing Changes in Synaptic and Extrasynaptic N-Methyl-D-Aspartate Receptor Function in Response to Acute and Chronic Restraint Stress

Tse, Y. C., Nath, M., Larosa, A., & Wong, T. P. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.716675 · Cited by 6

Differential effects of chronic adolescent glucocorticoid or methamphetamine on drug-induced locomotor hyperactivity and disruption of prepulse inhibition in adulthood in mice

Schonfeld, L., Jaehne, E. J., Ogden, A. R., Spiers, J. G., Hogarth, S. J., & van den Buuse, M. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110552 · Cited by 5

Aspects of Psychodynamic Neuropsychiatry II: Psychical Locality and Biology—Toward the Neurobiology of Psychotherapy

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Behavioral and Neurobiological Assessments of Predator-Based Fear Conditioning and Extinction

Halonen, J. D., Zoladz, P. R., Park, C. R., & Diamond, D. M. (2016) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2016.68033 · Cited by 6

The effectiveness of extinction training in male rats: temporal considerations and brain mechanisms.

Correia, P., Demeter, K., Varga, J., Urbán, E., Török, B., Balázsfi, D., Bakos, N., Haller, J., & Zelena, D. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114285 · Cited by 5

Long-term potentiation and memory processes in the psychological works of Sigmund Freud and in the formation of neuropsychiatric symptoms

Centonze, D., Siracusano, A., Calabresi, P., & Bernardi, G. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.032 · Cited by 7

Translational Animal Models for the Study of Epigenetics and the Environment

Murgatroyd, C., & Bradburn, S. (2016) · Springer eBooks · doi:10.1007/978-3-319-25325-1_8 · Cited by 7

Animal Models in Psychiatric Disorder Studies

Nani, J. V. S., Rodríguez, B., Cruz, F. C., & Hayashi, M. A. F. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89034 · Cited by 7

The ventral/anterior hippocampus as a central hub for stress-related dopaminergic circuit dysfunction in psychiatric disorders

Grace, A. A., & Uliana, D. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03513-7 · Cited by 5

Mitochondrial Transplantation in Animal Models of Psychiatric Disorders: A Novel Approach to Psychiatric Treatment

Iwata, K., Noguchi, M., & Shintani, N. (2025) · Biomolecules · doi:10.3390/biom15020184 · Cited by 6

Prolonged stress-induced depression-like behaviors in aged rats are mediated by endoplasmic reticulum stress and apoptosis in the hippocampus

Ghaffari‐Nasab, A., Javani, G., Yousefi, H., Sharafkhani, R., & Taghizadeh, S. (2023) · Neuroscience Research · doi:10.1016/j.neures.2023.06.011 · Cited by 4

Chronic stress leads to persistent and contrasting stellate neuron dendritic hypertrophy in the amygdala of male and female rats, an effect not found in the hippocampus

Peay, D. N., Acuña, A. M., Reynolds, C. M., Willis, C., Takalkar, R., Ortiz, J. B., & Conrad, C. D. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137403 · Cited by 5

What Is Stress?

McEwen, B. S., & Karatsoreos, I. N. (2011) · Springer eBooks · doi:10.1007/978-3-642-22272-6_3 · Cited by 5

Stress and Brain Function

Karatsoreos, I. N., & McEwen, B. S. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-375097-6.10021-6 · Cited by 4

Chronic Stress Effects on Corticolimbic Morphology

Wellman, C. L. (2011) · Wiley eBooks · doi:10.1002/9781118083222.ch10 · Cited by 4

Neuronal plasticity in hippocampal neurons due to chronic mild stress and after stress removal in postnatal chicks

Tamta, K., Kumar, A. M., Arya, H., Arya, S., & Maurya, R. C. (2023) · Journal of Anatomy · doi:10.1111/joa.13997 · Cited by 3

Cannabidiol Treatment in a Predator-Based Animal Model of PTSD: Assessing Oxidative Stress and Memory Performance

Jîtcă, G., Stoicescu, R., & Májai, E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104491 · Cited by 3

Neural-Cognitive Effects of Stress in the Hippocampus

Kim, J. J., Pellman, B. A., & Kim, E. J. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_9 · Cited by 3

Effects of Early-Life Stress on the Structural and Functional Development of Central Nervous System : A Review of the Studies Focusing on Animal Models

Kim, M. J., Kim, J., & Seok, J. (2016) · 신경정신의학 · doi:10.4306/jknpa.2016.55.2.75 · Cited by 3

Differential effects of tianeptine on the dorsal hippocampal volume of rats submitted to maternal separation followed by chronic unpredictable stress in adulthood

Pollano, A., Zalosnik, M. I., Durando, P. E., & Suárez, M. M. (2016) · Stress · doi:10.1080/10253890.2016.1224842 · Cited by 3

Repeated corticosterone enhances the acquisition and recall of trace fear conditioning

Marks, W. N., & Kalynchuk, L. E. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.09.022 · Cited by 3

The paradoxical effects of chronic stress on avoidance: a role for amygdala-dorsomedial prefrontal cortex dialogue

Grunfeld, I. S., & Likhtik, E. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01262-5 · Cited by 3

Genome Instability of Hippocampal and Bone Marrow Cells in Male Mice Exposed to Immobilization and Female Pheromone Stressor

Shcherbinina, V., Bakulevskiy, B. V., Glinin, T. S., & Даев, Е. В. (2023) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093023040154 · Cited by 3

The influence of mild stressors on neurons containing interleukin-1β in the central (CeA) and medial (MeA) amygdala in the ageing process of rats

Badowska‐Szalewska, E., Ludkiewicz, B., Spodnik, J. H., Krawczyk, R., & Moryś, J. (2015) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2015-2034 · Cited by 3

Corticotropin releasing factor modulates excitatory synaptic transmission

Joshi, N., McAree, M., & Chandler, D. J. (2020) · Vitamins and hormones · doi:10.1016/bs.vh.2020.04.003 · Cited by 3

Stress and Glucocorticoids as Experience-Dependent Modulators of Huntington's Disease

Mo, C., Renoir, T., & Hannan, A. J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813146-6.00020-5 · Cited by 4

Chronic stress has lasting effects on improved cued discrimination early in extinctionPreprint

Judd, J. M., Smith, E. A., Kim, J., Shah, V. B., Sanabria, F., & Conrad, C. D. (2020) · Learning & Memory · doi:10.1101/lm.051060.119 · Cited by 3

The infralimbic and prelimbic cortical areas bidirectionally regulate safety learning during normal and stress conditionsPreprint

Felix‐Ortiz, A. C., Terrell, J. M., Gonzalez, C., Msengi, H. D., Ramos, A. R., Boggan, M. B., Lopez-Pesina, S. M., Magalhães, G., & Burgos-Robles, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.05.539516 · Cited by 3

Studies of mechanisms involved in neuronal cell death induced by chronic stress in rats

Ayarapetyanz, M. G., Yakovlev, A. A., Levshina, I. P., Vorontsova, O. N., Stepanichev, M. Y., Onufriev, M. V., Лазарева, Н. А., & Gulyaeva, N. V. (2007) · Neurochemical Journal · doi:10.1134/s1819712407010126 · Cited by 2

Unpredictable chronic mild stress shows neuronal remodeling in multipolar projection neurons of hippocampal complex in postnatal chicks

Arya, H., Tamta, K., Kumar, A. M., Arya, S., & Maurya, R. C. (2024) · Anatomical Science International · doi:10.1007/s12565-024-00758-6 · Cited by 2

Effect of chronic alcohol exposure and single-prolonged stress on conditioned fear behavior

Mayberry, H. K., Rinker, J. A., & Chandler, L. J. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.115294 · Cited by 2

Impacts of social isolation stress in safety learning and the structure of defensive behavior during a spatial-based learning task involving thermal threat

Villalon, S. A., Felix‐Ortiz, A. C., Lozano-Ortiz, K., McCarrey, J. R., & Burgos-Robles, A. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1503097 · Cited by 2

Effect of stress on neuronal cell: Morphological to molecular approach

Bhardwaj, I., Singh, S., Ansari, A. H., Rai, S. P., & Singh, D. (2025) · Progress in brain research · doi:10.1016/bs.pbr.2025.01.010 · Cited by 3

Evolutionary medicine and bioastronautics: an innovative approach in addressing adverse mental health effects to astronauts during long term space missions

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