Hypothalamic–pituitary–adrenal function

Maternal Care, Hippocampal Glucocorticoid Receptors, and Hypothalamic-Pituitary-Adrenal Responses to Stress

Liu, D., Diorio, J., Tannenbaum, B., Caldji, C., Francis, D., Freedman, A., Sharma, S., Pearson, D., Plotsky, P. M., & Meaney, M. J. (1997) · Science · doi:10.1126/science.277.5332.1659 · Cited by 3,170 · see citing works

Do early‐life events permanently alter behavioral and hormonal responses to stressors?

Anisman, H., Zaharia, M. D., Meaney, M. J., & Merali, Z. (1998) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(98)00025-2 · Cited by 654 · see citing works

Early-life exposure to endotoxin alters hypothalamic-pituitary-adrenal function and predisposition to inflammation

Shanks, N., Windle, R. J., Perks, P. A., Harbuz, M. S., Jessop, D. S., Ingram, C. D., & Lightman, S. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.090571897 · Cited by 374 · see citing works

Ultradian rhythm of basal corticosterone release in the female rat: dynamic interaction with the response to acute stress

Windle, R. J., Wood, S. A., Shanks, N., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/en.139.2.443 · Cited by 276 · see citing works

Endocrine and Behavioural Responses to Noise Stress:Comparison of Virgin and Lactating Female Ratsduring Non‐Disrupted Maternal Activity

Windle, R. J., Wood, S. A., Shanks, N. M., Perks, P., Condé, G. L., Costa, A. P. C., Ingram, C. D., & Lightman, S. L. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.00587.x · Cited by 226 · see citing works

Paradoxical responses of hypothalamic corticotropin-releasing factor (CRF) messenger ribonucleic acid (mRNA) and CRF-41 peptide and adenohypophysial proopiomelanocortin mRNA during chronic inflammatory stress

Harbuz, M. S., Rees, R. G., Eckland, D. J. A., Jessop, D. S., Brewerton, D. A., & Lightman, S. L. (1992) · Endocrinology · doi:10.1210/endo.130.3.1537299 · Cited by 206 · see citing works

The Pulsatile Characteristics of Hypothalamo-Pituitary-Adrenal Activity in Female Lewis and Fischer 344 Rats and Its Relationship to Differential Stress Responses*

Windle, R. J., Wood, S. A., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/endo.139.10.6238 · Cited by 201 · cited 5× · see citing works

Vasopressin and Corticotropin-Releasing Hormone Gene Responses to Novel Stress in Rats Adapted to Repeated Restraint

Ma, X., Lightman, S. L., & Aguilera, G. (1999) · Endocrinology · doi:10.1210/endo.140.8.6943 · Cited by 182 · see citing works

The hypothalamic-pituitary-adrenal axis in rat pregnancy and lactation: circadian variation and interrelationship of plasma adrenocorticotropin and corticosterone.

Atkinson, H. C., & Waddell, B. J. (1995) · Endocrinology · doi:10.1210/endo.136.2.7835284 · Cited by 167 · see citing works

Suckling is a persistent stimulus to the adrenocortical system of the rat

Walker, C. D., Lightman, S. L., Steele, M. K., & Dallman, M. F. (1992) · Endocrinology · doi:10.1210/endo.130.1.1309321 · Cited by 162 · see citing works

Postnatal maternal separation during the stress hyporesponsive period enhances the adrenocortical response to novelty in adult rats by affecting feedback regulation in the CA1 hippocampal field

Biagini, G., Pich, E. M., Carani, C., Marrama, P., & Agnati, L. F. (1998) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(98)00019-7 · Cited by 149 · see citing works

Evidence for arginine vasopressin as the primary activator of the HPA axis during adjuvant‐induced arthritis

Chowdrey, H. S., Larsen, P. J., Harbuz, M. S., Jessop, D. S., Aguilera, G., Eckland, D. J. A., & Lightman, S. L. (1995) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1995.tb15089.x · Cited by 118 · see citing works

Sex and strain differences in the circadian rhythm fluctuation of endocrine and immune function in the rat: implications for rodent models of autoimmune disease

Griffin, A. C., & Whitacre, C. C. (1991) · Journal of Neuroimmunology · doi:10.1016/0165-5728(91)90161-y · Cited by 109 · see citing works

Long-term effects of maternal deprivation on the corticosterone response to stress in rats

Suchecki, D., & Tufik, S. (1997) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1997.273.4.r1332 · Cited by 75 · see citing works

Changes in hypothalamic corticotrophin-releasing factor and anterior pituitary pro-opiomelanocortin mRNA during the course of experimental allergic encephalomyelitis

Harbuz, M. S., Leonard, J. P., Lightman, S. L., & Cuzner, M. L. (1993) · Journal of Neuroimmunology · doi:10.1016/0165-5728(93)90172-u · Cited by 47 · see citing works

Alterations in Hypothalamic–Pituitary–Adrenal Function Correlated with the Onset of Murine SLE in MRL +/+ and lpr/lpr Mice

Shanks, N. M., Moore, P. M., Perks, P., & Lightman, S. L. (1999) · Brain Behavior and Immunity · doi:10.1006/brbi.1998.0535 · Cited by 41 · see citing works

Lactation: a physiological model of stress hyporesponsiveness of the neuroendocrine system

Lightman, S. L., Windle, R., Costa, A. D., Shanks, N., & Ingram, C. D. (1998) · Explore Bristol Research · Cited by 10 · see citing works

Ultradian hormone stimulation induces glucocorticoid receptor-mediated pulses of gene transcription

Stavreva, D. A., Wiench, M., John, S., Conway-Campbell, B. L., McKenna, M. A., Pooley, J. R., Johnson, T. A., Voss, T. C., Lightman, S. L., & Hager, G. L. (2009) · Nature Cell Biology · doi:10.1038/ncb1922 · Cited by 375 · see citing works

Interpreting Stress Responses during Routine Toxicity Studies

Everds, N. E., Snyder, P. W., Bailey, K. L., Bolon, B. N., Creasy, D. M., Foley, G. L., Rosol, T. J., & Sellers, T. S. (2013) · Toxicologic Pathology · doi:10.1177/0192623312466452 · Cited by 338 · see citing works

Role of neuropeptides in anxiety, stress, and depression: From animals to humans

Kormos, V., & Gaszner, B. (2013) · Neuropeptides · doi:10.1016/j.npep.2013.10.014 · Cited by 327 · see citing works

Molecular mechanisms in the regulation of adult neurogenesis during stress

Egeland, M., Zunszain, P. A., & Pariante, C. M. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3855 · Cited by 203 · see citing works

Neural immune pathways and their connection to inflammatory diseases.

Eskandari, F., Webster, J. I., & Sternberg, E. M. (2003) · Arthritis Research · doi:10.1186/ar1002 · Cited by 201 · see citing works

Cellular and Molecular Specificity of Pituitary Gland Physiology

Perez-Castro, C., Renner, U., Haedo, M. R., Stalla, G. K., & ARZT, E. S. (2012) · Physiological Reviews · doi:10.1152/physrev.00003.2011 · Cited by 115 · see citing works

Glucocorticoid interaction with aggression in non-mammalian vertebrates: Reciprocal action

Summers, C. H., Watt, M. J., Ling, T. J., Forster, G. L., Carpenter, R. E., Korzan, W. J., Lukkes, J. L., & Øverli, Ø. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.09.059 · Cited by 106 · see citing works

Dynamics of chromatin accessibility and long-range interactions in response to glucocorticoid pulsingPreprint

Stavreva, D. A., Coulon, A., Baek, S., Sung, M., John, S., Stixová, L., Tesikova, M., Hakim, O., Miranda, T. B., Hawkins, M. E., et al. (2015) · Genome Research · doi:10.1101/gr.184168.114 · Cited by 93 · see citing works

Substance P at the nexus of mind and body in chronic inflammation and affective disorders.

Rosenkranz, M. A. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.6.1007 · Cited by 81 · see citing works

Neuroendocrine function following traumatic brain injury and subsequent intensive care treatment: a prospective longitudinal evaluation

Kleindienst, A., Brabant, G., Bock, C., Maser-Gluth, C., & Buchfelder, M. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2008.0601 · Cited by 76 · see citing works

Physiological Significance of the Rhythmic Secretion of Hypothalamic and Pituitary Hormones

Gan, E. H., & Quinton, R. (2010) · Progress in brain research · doi:10.1016/s0079-6123(08)81007-2 · Cited by 71 · see citing works

Disrupted brain–immune system–joint communication during experimental arthritis

del Rey, A., Wolff, C., Wildmann, J., Randolf, A., Hahnel, A., Besedovsky, H. O., & Straub, R. H. (2008) · Arthritis & Rheumatism · doi:10.1002/art.23869 · Cited by 68 · see citing works

Female specific risk factors for the development of Alzheimer’s disease neuropathology and cognitive impairment: Call for a precision medicine approach

Udeh-Momoh, C., & Watermeyer, T. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101459 · Cited by 67 · see citing works

Complex genomic interactions in the dynamic regulation of transcription by the glucocorticoid receptor

Miranda, T. B., Morris, S. A., & Hager, G. L. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.03.002 · Cited by 66 · see citing works

Rapid Effects of Corticosterone in the Mouse Dentate Gyrus Via a Nongenomic Pathway

Pasricha, N., Joëls, M., & Karst, H. (2010) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2010.02091.x · Cited by 58 · see citing works

Increased HPA axis response to psychosocial stress in remitted depression: the influence of coping style

Höhne, N., Poidinger, M., Merz, F., Pfister, H., Brückl, T. M., Zimmermann, P., Uhr, M., Holsboer, F., & Ising, M. (2014) · Biological Psychology · doi:10.1016/j.biopsycho.2014.09.008 · Cited by 56 · see citing works

The stimuli-specific role of vasopressin in the hypothalamus–pituitary–adrenal axis response to stress

Zelena, D., Domokos, Á., Jain, S. K., Jankord, R., & Filaretova, L. P. (2009) · Journal of Endocrinology · doi:10.1677/joe-09-0096 · Cited by 56 · see citing works

Predictive modeling of the hypothalamic-pituitary-adrenal (HPA) axis response to acute and chronic stress

Markovic, V. M., Cupic, Z., Vukojevic, V., & Kolar-Anic, L. (2011) · Endocrine Journal · doi:10.1507/endocrj.ej11-0037 · Cited by 54 · see citing works

Effects of Chronic Alcoholic Disease on Magnocellular and Parvocellular Hypothalamic Neurons in Men

Sivukhina, E. V., Dolzhikov, A. A., Morozov, I. E., Jirikowski, G. F., & Grinevich, V. (2006) · Hormone and Metabolic Research · doi:10.1055/s-2006-944522 · Cited by 54 · see citing works

Effects of repeated restraint stress on hypothalamo-pituitary-adrenocortical function in vasopressin deficient Brattleboro rats

Zelena, D., Földes, A., Mergl, Z., Barna, I., Kovács, K., & Makara, G. B. (2004) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.04.007 · Cited by 53 · see citing works

Ultradian Cortisol Pulsatility Encodes a Distinct, Biologically Important Signal

McMaster, A., Jangani, M., Sommer, P., Han, N., Brass, A., Beesley, S., Lu, W., Berry, A. A., Loudon, A. S. I., Donn, R. P., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015766 · Cited by 48 · see citing works

Family history, early adversity and the hypothalamic-pituitary-adrenal (HPA) axis: Mediation of the vulnerability to mood disorders

Watson, S., Owen, B. M., Gallagher, P., Hearn, A. J., Young, A. H., & Ferrier, I. N. (2007) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.a939 · Cited by 42 · see citing works

Dissociation between Rat Hippocampal CA1 and Dentate Gyrus Cells in Their Response to Corticosterone: Effects on Calcium Channel Protein and Current

van Gemert, N. G., Carvalho, D. M., Karst, H., van der Laan, S., Zhang, M., Meijer, O. C., Hell, J. W., & Joëls, M. (2009) · Endocrinology · doi:10.1210/en.2009-0525 · Cited by 43 · see citing works

Temporal control of glucocorticoid neurodynamics and its relevance for brain homeostasis, neuropathology and glucocorticoid-based therapeutics

Kalafatakis, K., Russell, G. M., Ζάρρος, Α., & Lightman, S. L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.11.009 · Cited by 39 · see citing works

Neonatal dexamethasone and chronic tianeptine treatment inhibit ligature‐induced periodontitis in adult rats

Breivik, T. J., Gundersen, Y., Osmundsen, H., Fonnum, F., & Opstad, P. K. (2005) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.2005.00833.x · Cited by 38 · see citing works

Hypothalamic paraventricular nucleus, but not vasopressin, participates in chronic hyperactivity of the HPA axis in diabetic rats

Zelena, D., Filaretova, L. P., Mergl, Z., Barna, I., Tóth, Z., & Makara, G. B. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00118.2005 · Cited by 36 · see citing works

Association between infection early in life and mental disorders among youth in the community: a cross-sectional study

Goodwin, R. D. (2011) · BMC Public Health · doi:10.1186/1471-2458-11-878 · Cited by 34 · see citing works

Critical Illness-Related Corticosteroid Insufficiency in Children

Levy‐Shraga, Y., & Pinhas‐Hamiel, O. (2013) · Hormone Research in Paediatrics · doi:10.1159/000354759 · Cited by 33 · see citing works

Stress and Reproduction in Reptiles

Tokarz, R. R., & Summers, C. H. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-374930-7.10007-x · Cited by 33 · see citing works

Modelling cholesterol effects on the dynamics of the hypothalamic–pituitary–adrenal (HPA) axis

Marković, V. M., Čupić, Ž., Maćešić, S., Stanojević, A., Vukojević, V., & Kolar-Anić, L. (2016) · Mathematical Medicine and Biology · doi:10.1093/imammb/dqu020 · Cited by 31 · see citing works

The use of saliva for assessment of cortisol pulsatile secretion by deconvolution analysis

Trifonova, S. T., Gantenbein, M., Turner, J. D., & Muller, C. P. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.10.016 · Cited by 29 · see citing works

Magnocellular hypothalamic system and its interaction with the hypothalamo-pituitary-adrenal axis

Sivukhina, E. V., & Jirikowski, G. F. (2016) · Steroids · doi:10.1016/j.steroids.2016.01.008 · Cited by 29 · see citing works

MECHANISMS IN ENDOCRINOLOGY: Does circadian and ultradian glucocorticoid exposure affect the brain?

Kalafatakis, K., Russell, G. M., & Lightman, S. L. (2018) · European Journal of Endocrinology · doi:10.1530/eje-18-0853 · Cited by 29 · see citing works

Evolution of stress responses refine mechanisms of social rank

Korzan, W. J., & Summers, C. H. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100328 · Cited by 30 · see citing works

Cohabitation with a sick partner increases allergic lung inflammatory response in mice

Hamasato, E. K., Lima, A. P., de Oliveira, A. P. L., Lino‐dos‐Santos‐Franco, A., de Lima, W. T., & Palermo‐Neto, J. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.06.001 · Cited by 27 · see citing works

How to tame your genes: mechanisms of inflammatory gene repression by glucocorticoids

Strickland, B. A., Ansari, S. A., Dantoft, W., & Uhlenhaut, N. H. (2022) · FEBS Letters · doi:10.1002/1873-3468.14409 · Cited by 21 · see citing works

The Vasopressin-Deficient Brattleboro Rat: Lessons for the Hypothalamo–Pituitary–Adrenal Axis Regulation

Makara, G. B., Varga, J. M., Barna, I., Pintér, O., Klausz, B., & Zelena, D. (2012) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-012-9842-2 · Cited by 20 · see citing works

The role of vasopressin in diabetes mellitus-induced hypothalamo-pituitary-adrenal axis activation: Studies in Brattleboro rats

Zelena, D., Mergl, Z., & Makara, G. B. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2005.10.009 · Cited by 20 · see citing works

Hypothalamic-Pituitary-Adrenal Axis in Rheumatoid Arthritis

Imrich, R., & Rovenský, J. (2010) · Rheumatic Disease Clinics of North America · doi:10.1016/j.rdc.2010.09.003 · Cited by 19 · see citing works

Scientific and Regulatory Policy Committee Review

Fikes, J. D., Patrick, D. J., Francke, S., Frazier, K. S., Reindel, J. F., Romeike, A., Spaet, R. H., Tomlinson, L., & Schafer, K. A. (2015) · Toxicologic Pathology · doi:10.1177/0192623315596382 · Cited by 19 · see citing works

Advances in mathematical modelling of the hypothalamic–pituitary–adrenal (HPA) axis dynamics and the neuroendocrine response to stress

Stanojević, A., Marković, V., Čupić, Ž., Kolar-Anic, L. Z., & Vukojević, V. B. (2018) · Current Opinion in Chemical Engineering · doi:10.1016/j.coche.2018.04.003 · Cited by 19 · see citing works

Sex‐Specific Effects of Stress on Respiratory Control: Plasticity, Adaptation, and Dysfunction

Lopes, L. T., & Kinkead, R. (2021) · Comprehensive physiology · doi:10.1002/cphy.c200022 · Cited by 27 · see citing works

Predictive Modeling of the Hypothalamic-Pituitary-Adrenal (ΗΡΑ) Function. Dynamic Systems Theory Approach by Stoichiometric Network Analysis and Quenching Small Amplitude Oscillations

S. Jelić, Čupić, Ž., Kolar-Anic, L. Z., & Vukojević, V. B. (2009) · International Journal of Nonlinear Sciences and Numerical Simulation · doi:10.1515/ijnsns.2009.10.11-12.1451 · Cited by 18 · see citing works

Altered Hypothalamic-Pituitary-Adrenal Axis Activity in Patients with Chronic Heart Failure

Sivukhina, E. V., Поскребышева, А. С., Смурова, Ю. В., Должиков, А. А., Morozov, I. E., Jirikowski, G. F., & Grinevich, V. (2009) · Hormone and Metabolic Research · doi:10.1055/s-0029-1224182 · Cited by 17 · see citing works

Therapeutic implications of hypothalamic-pituitaryadrenal-axis modulation in Alzheimer’s disease: A narrative review of pharmacological and lifestyle interventions

Watermeyer, T., Robb, C. E., Gregory, S., & Udeh‐Momoh, C. T. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100877 · Cited by 15 · see citing works

Endocrine rhythms in the brown bear (Ursus arctos): Evidence supporting selection for decreased pineal gland size

Ware, J. V., Nelson, O. L., Robbins, C. T., Carter, P. A., Sarver, B. A. J., & Jansen, H. T. (2013) · Physiological Reports · doi:10.1002/phy2.48 · Cited by 14 · see citing works

Gene therapy in rodent amygdala against fear disorders

Mitra, R., & Sapolsky, R. M. (2010) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2010.509341 · Cited by 14 · see citing works

Increased exposure to sodium during pregnancy and lactation changes basal and induced behavioral and neuroendocrine responses in adult male offspring

Silva, M. S., Lucio-Oliveira, F., Mecawi, A. S., de Almeida, L. F., Ruginsk, S. G., Greenwood, M. P., Greenwood, M., Vivas, L., Elias, L. L. K., Murphy, D., et al. (2017) · Physiological Reports · doi:10.14814/phy2.13210 · Cited by 12 · see citing works

Chronic treatment with the glutamate receptor antagonist MK‐801 alters periodontal disease susceptibility

Breivik, T. J., Gundersen, Y., Osmundsen, H., Opstad, P. K., & Fonnum, F. (2004) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.2004.00765.x · Cited by 13 · see citing works

The stability of the extended model of hypothalamic-pituitary-adrenal axis examined by stoichiometric network analysis

Marković, V. M., Čupić, Ž., Ivanović, A., & Kolar-Anić, L. (2011) · Russian Journal of Physical Chemistry A · doi:10.1134/s0036024411130115 · Cited by 12 · see citing works

Tail docking in horses: a review of the issues

Lefebvre, D., Lips, D., Ödberg, F. O., & Giffroy, J.-M. (2007) · animal · doi:10.1017/s1751731107000420 · Cited by 12 · see citing works

Glucocorticoids and Aggression: A Tripartite Interaction

Haller, J. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_307 · Cited by 11 · see citing works

Anxiety and the brain: Neuropeptides as emerging factors

Satao, K. S., & Doshi, G. (2024) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2024.173878 · Cited by 12 · see citing works

Chronic treatment with the glucocorticoid receptor antagonist RU 486 inhibits diabetes‐induced enhancement of experimental periodontitis

Breivik, T. J., Gundersen, Y., Gjermo, P. E., & Opstad, P. K. (2013) · Journal of Periodontal Research · doi:10.1111/jre.12076 · Cited by 11 · see citing works

Phenotypic alterations of neuropeptide Y and calcitonin gene-related peptide-containing neurons innervating the rat temporomandibular joint during carrageenan-induced arthritis

Damico, J. P., Ervolino, E., Torres, K. R., Battagello, D. S., Cruz-Rizzolo, R. J., Casatti, C. A., & Bauer, J. A. (2012) · European Journal of Histochemistry · doi:10.4081/ejh.2012.e31 · Cited by 11 · see citing works

Sex and gender differences in genetic and lifestyle risk and protective factors for dementia

Sindi, S., Toopchiani, S. T., Barbera, M., Håkansson, K., Lehtisalo, J., Rosenberg, A., Stephen, R., Udeh‐Momoh, C. T., & Kivipelto, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819344-0.00013-2 · Cited by 10 · see citing works

Budesonide + formoterol fumarate dihydrate for the treatment of asthma

Wolthers, O. D. (2016) · Expert Opinion on Pharmacotherapy · doi:10.1517/14656566.2016.1165207 · Cited by 10 · see citing works

Influence of arginine vasopressin on the ultradian dynamics of Hypothalamic-Pituitary-Adrenal axis

Stojiljković, A. S., Čupić, Ž., Maćešić, S., Ivanović-Šašić, A., & Kolar-Anić, L. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.976323 · Cited by 9 · see citing works

Sex‐Specific Effects of Stress on Respiratory Control: Plasticity, Adaptation, and Dysfunction

Lopes, L. T., & Kinkead, R. (2021) · Comprehensive physiology · doi:10.1002/j.2040-4603.2021.tb00175.x · Cited by 9 · see citing works

The HPA axis and ethanol: a synthesis of mathematical modelling and experimental observations

Čupić, Ž., Stanojević, A., Marković, V., Kolar-Anic, L. Z., Terenius, L. Y., & Vukojević, V. B. (2016) · Addiction Biology · doi:10.1111/adb.12409 · Cited by 8 · see citing works

Stress and Reproduction in Reptiles

Tokarz, R. R., & Summers, C. H. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-374932-1.00031-7 · Cited by 9 · see citing works

A role for the Cockayne Syndrome B (CSB)-Elongin ubiquitin ligase complex in signal-dependent RNA polymerase II transcription

Weems, J. C., Slaughter, B. D., Unruh, J. R., Weaver, K. J., Miller, B. D., Delventhal, K. M., Conaway, J. W., & Conaway, R. C. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100862 · Cited by 7 · see citing works

Organization of the Mammalian Hypothalamus–Pituitary Axes

Norris, D. O., & Carr, J. A. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-394815-1.00004-5 · Cited by 7 · see citing works

Corticosterone oscillations during mania induction in the lateral hypothalamic kindled rat—Experimental observations and mathematical modeling

Abulseoud, O. A., Ho, A. M., Choi, D., Stanojević, A., Čupić, Ž., Kolar-Anic, L. Z., & Vukojević, V. B. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177551 · Cited by 5 · see citing works

The Hypothalamic–Pituitary–Adrenal Axis and Serotonin Metabolism in Individual Brain Nuclei of Mice with Genetic Disruption of the NK1 Receptor Exposed to Acute Stress

Čulman, J., Mühlenhoff, S., Blume, A., Hedderich, J., Lützen, U., Hunt, S. P., Rupniak, N. M. J., & Zhao, Y. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0594-5 · Cited by 5 · see citing works

Dexamethasone Modulates Nonvisual Opsins, Glucocorticoid Receptor, and Clock Genes inDanio rerioZEM-2S Cells

de Sousa, J. C., Magalhães-Marques, K. K., Cruz‐Machado, S. D. S., Moraes, M. N., & Castrucci, A. M. D. L. (2017) · BioMed Research International · doi:10.1155/2017/8459385 · Cited by 5 · see citing works

Influence of a New Backpack Design on Kinematics and Dynamics of Walking

Gillet, C., Foissac, M., Leteneur, S., Freychat, P., & Barbier, F. (2006) · Springer eBooks · doi:10.1007/978-0-387-45951-6_66 · Cited by 4 · see citing works

Unlocking ferulic acid for neurological diseases and tailoring of nanoformulations to advance its brain delivery

de Andrade, P. R. A., Motta, R. C., & Fonseca‐Santos, B. (2025) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2025.126173 · Cited by 3 · see citing works

Untargeted metabolomics revealed that quercetin improved adrenal gland metabolism disorders and modulated the HPA axis in perimenopausal depression model rats

Yu, Z., Feng, C., Chen, Y., Wang, W., & Zhao, X. (2025) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2025.106696 · Cited by 3 · see citing works

Arthritis Accompanying Endocrine and Metabolic Disorders

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