Early life experience alters response of adult neurogenesis to stress

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

The role of childhood trauma in the neurobiology of mood and anxiety disorders: preclinical and clinical studies

Heim, C., & Nemeroff, C. B. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01157-x · Cited by 2,791

Learning enhances adult neurogenesis in the hippocampal formation

Gould, E., Beylin, A., Tanapat, P., Reeves, A., & Shors, T. J. (1999) · Nature Neuroscience · doi:10.1038/6365 · Cited by 2,157

Hippocampal Volume Reduction in Major Depression

Bremner, J. D., Narayan, M., Anderson, E. R., Staib, L. H., Miller, H. L., & Charney, D. S. (2000) · American Journal of Psychiatry · doi:10.1176/ajp.157.1.115 · Cited by 1,670

Early, postnatal experience alters hypothalamic corticotropin-releasing factor (CRF) mRNA, median eminence CRF content and stress-induced release in adult rats

Plotsky, P. M., & Meaney, M. J. (1993) · Molecular Brain Research · doi:10.1016/0169-328x(93)90189-v · Cited by 1,638

Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus

Cameron, H. A., & Mckay, R. D. G. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1040 · Cited by 1,585

Neurogenesis in the Dentate Gyrus of the Adult Tree Shrew Is Regulated by Psychosocial Stress and NMDA Receptor Activation

Gould, E., McEwen, B. S., Tanapat, P., Galea, L. A. M., & Fuchs, E. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02492.1997 · Cited by 1,496

Proliferation of granule cell precursors in the dentate gyrus of adult monkeys is diminished by stress

Gould, E., Tanapat, P., McEwen, B. S., Flügge, G., & Fuchs, E. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3168 · Cited by 1,395

Depression Duration But Not Age Predicts Hippocampal Volume Loss in Medically Healthy Women with Recurrent Major Depression

Sheline, Y. I., Sanghavi, M., Mintun, M. A., & Gado, M. H. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05034.1999 · Cited by 1,382 · cited 1×

Enhanced synaptic plasticity in newly generated granule cells of the adult hippocampus

Schmidt-Hieber, C., Jonas, P., & Bischofberger, J. (2004) · Nature · doi:10.1038/nature02553 · Cited by 1,292

Stress and electroconvulsive seizure differentially alter GPR56 expression in the adult rat brain

Suzuki, G., Kanda, Y., Nibuya, M., Hiramoto, T., Tanaka, T., Shimizu, K., Watanabe, Y., & Nomura, S. (2007) · Brain Research · doi:10.1016/j.brainres.2007.09.020 · Cited by 16

An Overview of Psychological and Neurobiological Mechanisms by which Early Negative Experiences Increase Risk of Mood Disorders.

Hassel, S., McKinnon, M. C., Cusi, A. M., & MacQUEEN, G. M. (2011) · Europe PMC (PubMed Central) · Cited by 16

Effects of hindlimb unloading on neurogenesis in the hippocampus of newly weaned rats

Nomura, S., Kami, K., Kawano, F., Oke, Y., Nakai, N., Ohira, T., Fujita, R., Terada, M., Imaizumi, K., & Ohira, Y. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.12.022 · Cited by 16

Stress Neurobiology and Developmental Psychopathology

Jacoby, N., Overfeld, J., Binder, E. B., & Heim, C. M. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy221 · Cited by 16

Maternal separation impairs long term-potentiation in CA3-CA1 synapses in adolescent female rats

heydari, A., Esmaeilpour, K., & Sheibani, V. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112239 · Cited by 16

ISX-9 can potentiate cell proliferation and neuronal commitment in the rat dentate gyrus

Bettio, L. E. B., Patten, A. R., Gil‐Mohapel, J., O’Rourke, N. F., Hanley, R. P., Kennedy, S., Gopalakrishnan, K., Rodrigues, A. L. S., Wulff, J. E., & Christie, B. R. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.06.042 · Cited by 15

Adult Neurogenesis, Chronic Stress and Depression

Lucassen, P. J., Oomen, C. A., Schouten, M., Encinas, J. M., & Fitzsimons, C. P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801977-1.00008-8 · Cited by 15

Genetic predisposition and early life experience interact to determine glutamate transporter (GLT1) and solute carrier family 12 member 5 (KCC2) levels in rat hippocampus

Sterley, T.-L., Howells, F. M., Dimatelis, J. J., & Russell, V. A. (2015) · Metabolic Brain Disease · doi:10.1007/s11011-015-9742-5 · Cited by 16

A Relationship-Based Model for Psychiatric Nursing Practice

Wheeler, K. (2010) · Perspectives In Psychiatric Care · doi:10.1111/j.1744-6163.2010.00285.x · Cited by 15

HCNP precursor protein transgenic mice display a depressive-like phenotype in old age

Matsukawa, N., Furuya, Y., Ogura, H., & Ojika, K. (2010) · Brain Research · doi:10.1016/j.brainres.2010.06.041 · Cited by 15

Early life low intensity stress experience modifies acute stress effects on juvenile brain cell proliferation of European sea bass ( D. Labrax )

Fokos, S., Pavlidis, M. A., Yiotis, T., Tsalafouta, A., Papandroulakis, N., & Dermon, C. R. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.026 · Cited by 15

Early life adversity increases the salience of later life stress: an investigation of interactive effects in the PSID

Saxton, K. B., & Chyu, L. (2019) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174419000308 · Cited by 17

Early Maternal and Social Deprivation Expands Neural Stem Cell Population Size and Reduces Hippocampus/Amygdala-Dependent Fear Memory

Daun, K. A., Fuchigami, T., Koyama, N., Maruta, N., Ikenaka, K., & Hitoshi, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00022 · Cited by 15

Sirt7-p21 Signaling Pathway Mediates Glucocorticoid-Induced Inhibition of Mouse Neural Stem Cell Proliferation

Alnoud, M. A. H., Chen, W., Liu, N., Zhu, W. J., Qiao, J., Chang, S., Wu, Y., Wang, S., Yang, Y., Sun, Q., et al. (2020) · Neurotoxicity Research · doi:10.1007/s12640-020-00294-x · Cited by 14

Absence of neurogenic response following robust predator-induced stress response

Lau, C., Hebert, M. A., Vani, M. A., WALLING, S., Hayley, S. P., Lagace, D. C., & Blundell, J. J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.001 · Cited by 14

Regional Differences in Human Ependymal and Subventricular Zone Cytoarchitecture Are Unchanged in Neuropsychiatric Disease

Comte, I., Kotagiri, P., & Szele, F. G. (2012) · Developmental Neuroscience · doi:10.1159/000338600 · Cited by 14

Chronic Exposure to Light Reverses the Effect of Maternal Separation on Proteins in the Prefrontal Cortex

Dimatelis, J. J., Stein, D. J., & Russell, V. A. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0071-z · Cited by 14

The Impact of Parent-Infant Interaction on Epigenetic Plasticity Mediating Synaptic Adaptations in the Infant Brain

Matas, E., Bock, J., & Braun, K. (2016) · Psychopathology · doi:10.1159/000448055 · Cited by 14

Stress and mental illness

Lee, H.-Y., & Ham, B. (2013) · Journal of Korean Medical Association · doi:10.5124/jkma.2013.56.6.471 · Cited by 14

Cross-tolerance: embryonic heat conditioning induces inflammatory resilience by affecting different layers of epigenetic mechanisms regulating IL6 expression later in life

Rosenberg, T., Kisliouk, T., Ben‐Nun, O., Cramer, T., & Meiri, N. (2020) · Epigenetics · doi:10.1080/15592294.2020.1795596 · Cited by 14

Population Density and Temperature Influence the Return on Maternal Investment in Wild House Mice

Auclair, Y., Gerber, N., König, B., & Lindholm, A. K. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2020.602359 · Cited by 13

Elevated glucocorticoid alters the developmental dynamics of hypothalamic neurogenesis in zebrafish

Eachus, H., Choi, M., Tochwin, A., Kaspareit, J., Ho, M., & Ryu, S. (2024) · Communications Biology · doi:10.1038/s42003-024-06060-5 · Cited by 13

Prenatal immobilization stress and postnatal maternal separation cause differential neuroendocrine responses to fasting stress in adult male rats

Roque, A., Ruiz‐González, R., Pineda, E., Torner, L., & Lajud, N. (2019) · Developmental Psychobiology · doi:10.1002/dev.21947 · Cited by 14

Early Life Stress

Möhler, E., & Resch, F. (2019) · Praxis der Kinderpsychologie und Kinderpsychiatrie · doi:10.13109/prkk.2019.68.7.575 · Cited by 12

Endocrine-disrupting chemicals and the brain

Gore, A. C. (2018) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(17)30436-9 · Cited by 12

Potential role of hippocampal neurogenesis in spinal cord injury induced post-trauma depression

Ma, Y., Qiao, Y., & Gao, X. (2024) · Neural Regeneration Research · doi:10.4103/1673-5374.392855 · Cited by 11

Developmental and adult stress: effects of steroids and neurosteroids

Gore, I. R., & Gould, E. (2024) · Stress · doi:10.1080/10253890.2024.2317856 · Cited by 11

The hippocampal-to-ventricle ratio (HVR): Presentation of a manual segmentation protocol and preliminary evidence

Schoemaker, D., Buß, C., Pietrantonio, S., Maunder, L., Freiesleben, S. D., Hartmann, J., Collins, D. L., LUPIEN, S. J., & Pruessner, J. C. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116108 · Cited by 13

Maternal separation induces retinal and peripheral blood mononuclear cell alterations across the lifespan of female rats

Grigoruţă, M., Chavez-Solano, M., Varela-Ramı́rez, A., Sierra-Fonseca, J. A., Orozco‐Lucero, E., Hamdan, J. N., Gosselink, K. L., & Martı́nez-Martı́nez, A. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147117 · Cited by 11

Activation of D1R signaling in the medial prefrontal cortex rescues maternal separation-induced behavioral deficits through restoration of excitatory neurotransmission

Yang, Y., Zhong, Z., Wang, B., Wang, Y., & Ding, W. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114287 · Cited by 12

Neonatal Maternal Separation Induces Sexual Dimorphism in Brain Development: The Influence on Amino Acid Levels and Cognitive Disorders

Kotlinska, J. H., Grochecki, P., Michalak, A., Pankowska, A., Kochalska, K., Suder, P., Ner‐Kluza, J., Matosiuk, D., & Marszałek‐Grabska, M. (2023) · Biomolecules · doi:10.3390/biom13101449 · Cited by 12

The Stress and Vascular Catastrophes in Newborn Rats: Mechanisms Preceding and Accompanying the Brain Hemorrhages

SEMYACHKINA-GLUSHKOVSKAYA, O. V., Borisova, E. G., Abakumov, M. A., Gorin, D. A., Avramov, L. A., Fedosov, I. V., Александрович, Н. А., Abdurashitov, A. S., Serov, A. N., Павлов, А. Н., et al. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00210 · Cited by 11

Gene-environment interplay in neurogenesis and neurodegeneration

Palomo, T., Archer, T., Beninger, R. J., & Kostrzewa, R. M. (2004) · Neurotoxicity Research · doi:10.1007/bf03033279 · Cited by 11

Effects of prenatal chronic mild stress exposure on hippocampal cell proliferation, expression of GSK‐3α, β and NR2B in adult offspring during fear extinction in rats

Li, M., Li, X., Zhang, X., Ren, J., Jiang, H., Wang, Y., Ma, Y., & Cheng, W. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.02.004 · Cited by 10

Early Life Stress- and Sex-Dependent Effects on Hippocampal Neurogenesis

Lucassen, P. J., Kőrösi, A., Krugers, H. J., & Oomen, C. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802175-0.00013-9 · Cited by 11

The effect of childhood trauma on spatial cognition in adults: a possible role of sex

Syal, S., Ipser, J., Phillips, N. J., Thomas, K. G. F., van Honk, J., & Stein, D. J. (2014) · Metabolic Brain Disease · doi:10.1007/s11011-014-9497-4 · Cited by 11

Silent Vascular Catastrophes in the Brain in Term Newborns: Strategies for Optical Imaging

SEMYACHKINA-GLUSHKOVSKAYA, O. V., Kurths, J., Павлов, А. Н., Borisova, E. G., Abdurashitov, A. S., Zhu, D. Y., Li, P., Luo, Q., & Tuchin, V. V. (2016) · IEEE Journal of Selected Topics in Quantum Electronics · doi:10.1109/jstqe.2016.2523982 · Cited by 10

Effects of stress of postnatal development on corticosterone, serotonin and behavioral changes

Matsui, F., Morimoto, M., Yoshimoto, K., Nakatomi, Y., Syoji, H., Nishimura, A., Isoda, K., Tanda, K., & Hosoi, H. (2009) · Brain and Development · doi:10.1016/j.braindev.2009.09.001 · Cited by 10

Clinical neuroscience and imaging studies of core psychoanalytic constructs

Peterson, B. S. (2005) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2005.03.011 · Cited by 10

Early-Life Stress Induces Prodromal Features of Parkinsonism in Ageing Rats

Ren, C., Wang, F., He, K.-J., Zhang, Y., Li, L.-X., Zhang, J., Chen, J., Mao, C., & Liu, C. (2021) · The Journals of Gerontology Series A · doi:10.1093/gerona/glab253 · Cited by 9

Isoflurane stress induces region-specific glucocorticoid levels in neonatal mouse brain

Hamden, J. E., Gray, K. M., Salehzadeh, M., & Soma, K. K. (2022) · Journal of Endocrinology · doi:10.1530/joe-22-0049 · Cited by 9

How Can Early Stress Influence Later Alzheimer's Disease Risk? Possible Mediators and Underlying Mechanisms

Lucassen, P. J., Kőrösi, A., de Rooij, S. R., Smit, A. B., van Dam, A., Daskalakis, N. P., van Kesteren, R. E., Verheijen, M. H. G., Lesuis, S. L., Kessels, H. W. H. G., et al. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.11.007 · Cited by 9

The effects of early protein malnutrition and environmental stimulation on behavioral and biochemical parameters in rats.

Sampaio, V. D. F., Oliveira, L. M. D., Almeida, S. S., Marchini, J. S., Antunes‐Rodrigues, J., & Elias, L. L. K. (2008) · Psychology & Neuroscience · doi:10.3922/j.psns.2008.2.004 · Cited by 9

Restraint stress in lactating mice alters the levels of sulfur-containing amino acids in milk

Nishigawa, T., NAGAMACHI, S., Ikeda, H., Chowdhury, V. S., & Furuse, M. (2018) · Journal of Veterinary Medical Science · doi:10.1292/jvms.17-0661 · Cited by 9

Adult Neurogenesis and Stress

Briones, B. A., & Gould, E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813146-6.00007-2 · Cited by 9

Monoamine Oxidase A Genotype, Childhood Trauma, and Subclinical Atherosclerosis: A Twin Study

Zhao, J., Bremner, J. D., Goldberg, J., Quyyumi, A. A., & Vaccarino, V. (2013) · Psychosomatic Medicine · doi:10.1097/psy.0b013e318292922a · Cited by 9

Effect of immobilization stress on the appetite and stomach ghrelin expression in maternal mice.

Li, B., Xu, Y., Pan, D., Xiao, Q., Gao, Q., Chen, X., Peng, X., Du, Y., & Gao, P. (2015) · PubMed Central · Cited by 9

Linking the psychosocial aetiology and neurobiology of unipolar depression.

Coulter, L., Ibrahimi, M., Patel, R. J., & Agius, M. A. (2017) · PubMed · Cited by 9

Endocrine-Disrupting Chemicals and the Brain

Walker, D. M., & Gore, A. C. (2007) · Humana Press eBooks · doi:10.1007/1-59745-107-x_4 · Cited by 9

Fresh approaches to antidepressant drug discovery

Anacker, C. (2014) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2014.892071 · Cited by 9

The neurobiology of life course socioeconomic conditions and associated cognitive performance in middle to late adulthood

Schrempft, S., Trofimova, O., Künzi, M., Ramponi, C., Lutti, A., Kherif, F., Latypova, A., Vollenweider, P., Marques-Vidal, P. M., Preisig, M., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1231-23.2024 · Cited by 8

Coffee polyphenols ameliorate early-life stress-induced cognitive deficits in male mice

Geertsema, J., Kratochvil, M., González‐Domínguez, R., Lefèvre‐Arbogast, S., Low, D. Y., Preez, A. D., Lee, H., Urpí-Sardà, M., Sánchez‐Pla, Á., Aigner, L., et al. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100641 · Cited by 8

Bi-Parental Care Contributes to Sexually Dimorphic Neural Cell Genesis in the Adult Mammalian Brain

Mak, G. K., Antle, M. C., Dyck, R. H., & Weiss, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062701 · Cited by 8

Taking neurogenesis out of the lab and into the world with MAP Train My Brain™

Millon, E. M., & Shors, T. J. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112154 · Cited by 8

Resistance of Postnatal Hippocampal Neurogenesis to Alcohol Toxicity in a Third Trimester‐Equivalent Mouse Model of Gestational Alcohol Exposure

Gustus, K., Lozano, E., Newville, J., Li, L., Valenzuela, C. F., & Cunningham, L. A. (2019) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14207 · Cited by 8

Social isolation improves the performance of rodents in a novel cognitive flexibility task

Fei, X.-Y., Liu, S., Sun, Y., & Cheng, L. (2019) · Frontiers in Zoology · doi:10.1186/s12983-019-0339-4 · Cited by 10

Noli Timere: The Role of Reassuring Adults in Dealing with COVID-19 Anxiety in Pediatric Age

Smirni, D. (2021) · Pediatric Reports · doi:10.3390/pediatric13010003 · Cited by 8

Inhibition of adult neurogenesis reduces avoidance behavior in male, but not female, mice subjected to early life adversity

Waters, R. C., Worth, H. M., Vasquez, B., & Gould, E. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100436 · Cited by 8

Definicja i cele poznawcze neurosocjobiologii

Godzińska, E. J. (2006) · Cited by 8

The Contribution of Adult Hippocampal Neurogenesis to the Progression of Psychiatric Disorders

Kohman, R. A., & Rhodes, J. S. (2017) · Modern trends in psychiatry · doi:10.1159/000470812 · Cited by 8

Female rats are resilient to the behavioral effects of maternal separation stress and exhibit stress-induced neurogenesis

Lee, Y. J., Koe, A. S., Ashokan, A., & Mitra, R. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e04753 · Cited by 8

Melatonin administration modifies circadian motor activity under constant light depending on the lighting conditions during suckling.

Carpentieri, A. R., Oliva, C., Dı́ez-Noguera, A., & Cambras, T. (2015) · PubMed · doi:10.3109/07420528.2015.1060243 · Cited by 7

Impact of Maternal Separation on Dopamine System and its Association with Parkinson's Disease

He, K.-J., Zhang, Y., Wei, S., Jiang, S., Xu, L., Ren, C., & Wang, F. (2020) · NeuroMolecular Medicine · doi:10.1007/s12017-019-08587-x · Cited by 7

Evolutionary Biology of Hormonal Responses to Social Challenges in the Human Child

Flinn, M. V. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781193.030 · Cited by 7

Hormone Regulation of Adult Hippocampal Neurogenesis in the Mammalian Brain

Barha, C. K., Barker, J. M., Brummelte, S., Epp, J. R., & Galea, L. A. M. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00067-x · Cited by 7

The developmental environment: influences on subsequent cognitive function and behaviour

Landon, J., Davison, M., & Breier, B. H. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544699.028 · Cited by 7

Lipopolysaccharide differentially alters systemic and brain glucocorticoid levels in neonatal and adult mice

Hamden, J. E., Salehzadeh, M., Bajaj, H., Li, M. X., & Soma, K. K. (2024) · Journal of Neuroendocrinology · doi:10.1111/jne.13481 · Cited by 6

Examining the relationship between anxiety and regional brain volumes in the National Alzheimer's Coordinating Center uniform, imaging, and biomarker datasets

Burke, S. L., Grudzien, A., Li, T., Abril, M., Yin, W., Tyrell, T. A., Barnes, C. P., Hanson, K., & DeKosky, S. T. (2024) · Cerebral Circulation - Cognition and Behavior · doi:10.1016/j.cccb.2024.100201 · Cited by 7

Comprehensive analysis of genetic risk loci uncovers novel candidate genes and pathways in the comorbidity between depression and Alzheimer’s disease

Hofstra, B., Kas, M. J., & Verbeek, D. S. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02968-y · Cited by 7

Effects of Total Light Deprivation on Hippocampal Neurogenesis and Memory of Adult Rats: A Sexual Dimorphic Study

Jameie, S. B., Mousavi, M., Farhadi, M., Mehraein, F., Ababzadeh, S., Soleimani, M., Kerdari, M., & Jalilpouraghdam, M. (2015) · Thrita · doi:10.5812/thrita.36420 · Cited by 6

Endocrine response and perceived stress test during an experimental challenge task in adult survivors of a childhood cancer

Laufer, D., Ansermet, F., von der Weid, N., Popovic, M. B., Torrisi, R., & Pierrehumbert, B. (2011) · Pediatric Blood & Cancer · doi:10.1002/pbc.24044 · Cited by 6

Correlazione fra misure di stress, indicatori di natura bioumorale e considerazioni medico-legali

Ricci, S., Massoni, F., Meo, M. D., Petrone, L., Canitano, N., Ippoliti, F., & Cinti, M. E. (2013) · Rivista di psichiatria · doi:10.1708/1272.14035 · Cited by 6

Handling-induced tonic/clonic seizures in captive born bank voles (Clethrionomys glareolus)

Schønecker, B. (2009) · Applied Animal Behaviour Science · doi:10.1016/j.applanim.2009.02.024 · Cited by 6

The Mediating Effects of Chronic Diseases in the Relationship Between Adverse Childhood Experiences and Trajectories of Depressive Symptoms in Later Life: A Nationwide Longitudinal Study

Dai, Q., Li, M., Wang, Z., Xu, Q., Zhang, X., & Tao, L. (2024) · Healthcare · doi:10.3390/healthcare12242539 · Cited by 5

Melatonin treatment during early life interacts with restraint to alter neuronal morphology and provoke depressive-like responses

Aubrecht, T. G., Weil, Z. M., & Nelson, R. J. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.01.025 · Cited by 5

In Vivo Structural and Functional Abnormalities of the Striatums Is Related to Decreased Astrocytic BDNF in Itpr2-/- Mice Exhibiting Depressive-Like Behavior

Zeng, S., Liu, K., Zhang, J., Chen, C., Xu, Y., Wu, Y., Deng, Y., Sun, X., Wen, G., & Jing, L. (2020) · Neural Plasticity · doi:10.1155/2020/8830670 · Cited by 5

No Evidence for Long-Term Carryover Effects in a Wild Salmonid Fish

Birnie‐Gauvin, K., Larsen, M. H., Peiman, K. S., Midwood, J. D., Wilson, A. D. M., Cooke, S. J., & Aarestrup, K. (2021) · Physiological and Biochemical Zoology · doi:10.1086/716000 · Cited by 5

Analysis of hippocampal synaptic function in a rodent model of early life stress

Wilkinson, M. P., Robinson, E. S. J., & Mellor, J. R. (2024) · Wellcome Open Research · doi:10.12688/wellcomeopenres.22276.1 · Cited by 5

Impacts of maternal separation stress on ethanol intake and endocannabinoid system in adolescent mice

Favoretto, C. A., Bertagna, N. B., Anjos-Santos, A., Loss, C. M., Rodolpho, B. T., Righi, T., Bezerra, F. R., Bianchi, P., & Cruz, F. C. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.11.037 · Cited by 5

Main Biological Models of Resilience.

Marazziti, D., Fantasia, S., Palermo, S., Arone, A., Massa, L., Gambini, M., & Carmassi, C. (2024) · PubMed Central · doi:10.36131/cnfioritieditore20240201 · Cited by 6

Stress périnatal et développement neuropsychologique

Cambonie, G., Novais, A. R. B., Bienfait, M., Pidoux, O., Toubin, R.-M., Picaud, J., & Barbanel, G. (2010) · Revue de médecine périnatale · doi:10.1007/s12611-010-0072-x · Cited by 5

Social Cues of Future Sperm Competition Received during Development Affect Learning in Adult Male Fruit Flies, Drosophila melanogaster

McDowall, L., Rouse, J. L., Sait, S. M., & Bretman, A. J. (2019) · Journal of Insect Behavior · doi:10.1007/s10905-019-09712-1 · Cited by 5

EARLY PREWEANING METHAMPHETAMINE AND POSTWEANING REARING CONDITIONS INTERFERE WITH THE DEVELOPMENT OF PERIPHERAL STRESS PARAMETERS AND NEURAL GROWTH FACTORS IN GERBILS

Lehmann, K., Garea‐Rodríguez, E., Kratz, O., Moll, G. H., Dawirs, R. R., & Teuchert, G. (2007) · International Journal of Neuroscience · doi:10.1080/00207450600934937 · Cited by 5

From neurotoxin to neurotrophin

Mirescu, C., & Gould, E. (2004) · Nature Neuroscience · doi:10.1038/nn0904-899 · Cited by 5

Acute Stress and Anxiety

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