Immune regulation by glucocorticoids

How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions

Sapolsky, R. M., Romero, L. M., & Munck, A. U. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.1.0389 · Cited by 7,541

Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin

Aziz, J., Shezali, H., Radzi, Z., Yahya, N. A., Abu Kassim, N. H., Czernuszka, J., & Rahman, M. T. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000447017 · Cited by 7,323

Factors affecting wound healing

Guo, S., & DiPietro, L. A. (2010) · Journal of Dental Research · doi:10.1177/0022034509359125 · Cited by 5,792

Neutrophil recruitment and function in health and inflammation

Kolaczkowska, E., & Kubes, P. (2013) · Nature Reviews Immunology · doi:10.1038/nri3399 · Cited by 5,472

Cytokine-mediated regulation of CXCR4 expression in human neutrophils

Nagase, H., Miyamasu, M., Yamaguchi, M., Imanishi, M., Tsuno, N. H., Matsushima, K., Yamamoto, K., Morita, Y., & Hirai, K. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.711 · Cited by 4,713

Macrophage activation and polarization

Martinez, F. O. (2008) · Frontiers in Bioscience · doi:10.2741/2692 · Cited by 3,160

Resolution of inflammation: the beginning programs the end

Serhan, C. N., & Savill, J. (2005) · Nature Immunology · doi:10.1038/ni1276 · Cited by 2,552

The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

Miller, W. L., & Auchus, R. J. (2011) · Endocrine Reviews · doi:10.1210/er.2010-0013 · Cited by 2,458

The anti-inflammatory and immunosuppressive effects of glucocorticoids, recent developments and mechanistic insights

Coutinho, A. E., & Chapman, K. E. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.04.005 · Cited by 1,815

Inhibition of osteoblastogenesis and promotion of apoptosis of osteoblasts and osteocytes by glucocorticoids. Potential mechanisms of their deleterious effects on bone.

Weinstein, R. S., Jilka, R. L., Parfitt, A. M., & Manolagas, S. C. (1998) · Journal of Clinical Investigation · doi:10.1172/jci2799 · Cited by 1,753

Development of a Molecular Signature to Monitor Pharmacodynamic Responses Mediated by In Vivo Administration of Glucocorticoids

Hu, Y., Carman, J., Holloway, D. A., Kansal, S., Li, F., Goldstine, C. B., Lee, D., Somerville, J. E., Latek, R. R., Townsend, R. C., et al. (2018) · Arthritis & Rheumatology · doi:10.1002/art.40476 · Cited by 28

Role of Endogenous Glucocorticoids in Cancer in the Elderly

Ayroldi, E., Cannarile, L., Adorisio, S., Delfino, D. V., & Riccardi, C. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123774 · Cited by 27

Molecular mechanisms contributing to glucocorticoid resistance in lymphoid malignancies

Scheijen, B. (2019) · Cancer Drug Resistance · doi:10.20517/cdr.2019.29 · Cited by 29

Systemic lupus erythematosus: new horizons for diagnosis and therapy

Solovyev, S. K., Aseeva, E. A., Попкова, Т. В., Lila, A. M., Vi, M., & Nasonov, E. L. (2020) · Rheumatology Science and Practice · doi:10.14412/1995-4484-2020-5-14 · Cited by 29

Bacterial and Viral Infection and Sepsis in Kidney Transplanted Patients

Mella, A., Mariano, F., Dolla, C., Gallo, E., Manzione, A. M., Vico, M. C. D., Cavallo, R., Rosa, F. G. D., Costa, C. S., & Biancone, L. (2022) · Biomedicines · doi:10.3390/biomedicines10030701 · Cited by 28

Cell Senescence and Central Regulators of Immune Response

Lunin, S. M., Novoselova, E. G., Glushkova, O. V., Parfenyuk, S. B., Novoselova, T. V., & Khrenov, M. O. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084109 · Cited by 28

Dexamethasone attenuates interferon-related cytokine hyperresponsiveness in COVID-19 patients

Engel, J. J., van der Made, C. I., Keur, N., Setiabudiawan, T. P., Röring, R. J., Damoraki, G., Dijkstra, H., Lemmers, H., Ioannou, S., Poulakou, G., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1233318 · Cited by 33

Mechanisms of action and historical facts on the use of intravenous immunoglobulins in systemic lupus erythematosus

Martínez, T. M., García-Robledo, J. E., Plata, I., Urbano, M.-A., Posso‐Osorio, I., Ríos-Serna, L. J., Barrera, M. C., & Tobón, G. J. (2019) · Autoimmunity Reviews · doi:10.1016/j.autrev.2018.10.002 · Cited by 29

Regulation of tissue immune responses by local glucocorticoids at epithelial barriers and their impact on interorgan crosstalk

Merk, V. M., Phan, T. S., & Brunner, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.672808 · Cited by 27

Glucocorticoids regulate thrombopoiesis by remodeling the megakaryocyte transcriptome

Grodzielski, M., & Cidlowski, J. A. (2023) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2023.06.012 · Cited by 27

GDF15/MIC-1: a stress-induced immunosuppressive factor which promotes the aging process

Salminen, A. (2024) · Biogerontology · doi:10.1007/s10522-024-10164-0 · Cited by 30

Overcoming Oncogenic Mediated Tumor Immunity in Prostate Cancer

Bryant, G., Wang, L., & Mulholland, D. J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071542 · Cited by 30

The effect of beta-adrenergic blockade on inflammatory and cardiovascular responses to acute mental stress

Steptoe, A., Ronaldson, A., Kostich, K., Lazzarino, A. I., Urbanova, L., & de Carvalho, L. A. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.03.027 · Cited by 27

1,25(OH)2D3 and dexamethasone additively suppress synovial fibroblast activation by CCR6+ T helper memory cells and enhance the effect of tumor necrosis factor alpha blockade

Dankers, W., González-Leal, C., Davelaar, N., Asmawidjaja, P. S., Mus, A. M. C., Hazes, J. M. W., Colin, E. M., & Lubberts, E. (2018) · Arthritis Research & Therapy · doi:10.1186/s13075-018-1706-9 · Cited by 28

Modulation of Inflammation-Related Genes in the Cornea of a Mouse Model of Dry Eye upon Treatment with Cyclosporine Eye Drops

Daull, P., Barabino, S., Feraille, L., Kessal, K., Docquier, M., Parsadaniantz, S. M., Baudouin, C., & Garrigue, J. (2019) · Current Eye Research · doi:10.1080/02713683.2018.1563197 · Cited by 27

Glucocorticoids mediate stress induction of the alarmin HMGB1 and reduction of the microglia checkpoint receptor CD200R1 in limbic brain structures

Frank, M. G., Annis, J. L., Watkins, L. R., & Maier, S. F. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.05.014 · Cited by 28

Stress and immunity: Field comparisons among populations of invasive cane toads in Florida

Assis, V. R., Gardner, S. T., Smith, K. M., Gomes, F. R., & Mendonça, M. T. (2020) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2389 · Cited by 27

KLF15 cistromes reveal a hepatocyte pathway governing plasma corticosteroid transport and systemic inflammation

Jiang, Z., Elsarrag, S. Z., Duan, Q., LaGory, E. L., Wang, Z., Alexanian, M., McMahon, S., Rulifson, I. C., Winchester, S. A. B., Wang, Y., et al. (2022) · Science Advances · doi:10.1126/sciadv.abj2917 · Cited by 26

Nutritional recommendations for patients undergoing prolonged glucocorticoid therapy

Esteves, G. P., Mazzolani, B. C., Smaira, F. I., Mendes, E. S., Oliveira, G. G., Roschel, H., Gualano, B., Pereira, R. M. R., & Dolan, E. (2022) · Rheumatology Advances in Practice · doi:10.1093/rap/rkac029 · Cited by 28

Mesoporous Materials as Elements of Modern Drug Delivery Systems for Anti-Inflammatory Agents: A Review of Recent Achievements

Moritz, M., & Geszke-Moritz, M. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14081542 · Cited by 27

Induction of natural IgE by glucocorticoids

Lim, J., Lin, E. V., Hong, J. Y., Vaidyanathan, B., Erickson, S. A., Annicelli, C., & Medzhitov, R. M. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20220903 · Cited by 27

Drug‐resistant seizures associated with hyperinflammatory monocytes in FIRES

Howe, C. L., Johnson, R. K., Overlee, B. L., Sagen, J. A., Mehta, N., & Farias‐Moeller, R. (2023) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.51755 · Cited by 27

The clinical recovery of tuberculosis patients undergoing specific treatment is associated with changes in the immune and neuroendocrine responses

Díaz, A., Bongiovanni, B., D’Attilio, L., Santucci, N. E., Dídoli, G., Fernández, R. D. V., Kovalevski, L., Lioi, S., Gardeñez, W., Brandan, N., et al. (2017) · Pathogens and Disease · doi:10.1093/femspd/ftx087 · Cited by 27

Neutrophils in critical illness

McDonald, B. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2752-3 · Cited by 28

DHEA Inhibits Leukocyte Recruitment through Regulation of the Integrin Antagonist DEL-1

Ziogas, A., Maekawa, T., Wiessner, J. R., Le, T. T., Sprott, D., Troullinaki, M., Neuwirth, A., Anastasopoulou, V., Großklaus, S., Chung, K., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1900746 · Cited by 27

LC-APCI+-MS/MS method for the analysis of ten hormones and two endocannabinoids in plasma and hair from the mice with different gut microbiota

Chu, L., Li, N., Deng, J. H., Wu, Y., Yang, H., Wang, W., Zhou, D., & Deng, H. (2020) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2020.113223 · Cited by 27

Chronic Corticosterone Administration-Induced Mood Disorders in Laboratory Rodents: Features, Mechanisms, and Research Perspectives

Wang, H., Wang, X., Wang, H., Shao, S.-J., & Zhu, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011245 · Cited by 28

A high fat diet with a high C18:0/C16:0 ratio induced worse metabolic and transcriptomic profiles in C57BL/6 mice

Wang, L., Xu, F., Song, Z., Han, D., Zhang, J., Chen, L., & Na, L. (2020) · Lipids in Health and Disease · doi:10.1186/s12944-020-01346-z · Cited by 26

Dexamethasone Promotes Aspergillus fumigatus Growth in Macrophages by Triggering M2 Repolarization via Targeting PKM2

Luvanda, M. K., Posch, W., Vosper, J., Zaderer, V., Noureen, A., Lass‐Flörl, C., & Wilflingseder, D. (2021) · Journal of Fungi · doi:10.3390/jof7020070 · Cited by 27

Short-term stressors and corticosterone effects on immunity in male toads (Rhinella icterica): A neuroimmune-endocrine approach

Titon, S. C. M., Titon, B., Gomes, F. R., & Assis, V. R. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100230 · Cited by 26

The emergence of post-COVID-19 mucormycosis in India: Can we prevent it?

Gupta, A., Sharma, A., & Chakrabarti, A. (2021) · Indian Journal of Ophthalmology · doi:10.4103/ijo.ijo_1392_21 · Cited by 26

Double-Layer Nucleoside-Microneedles Co-Delivering Dexamethasone Vesicles and Adenosine Overcome Pseudomembrane Barriers for the Treatment of Oral Ulcer

Zhang, B., Qian, Y., Li, J., Fan, Y., Mingyuan, G., Wu, Q., Li, Z., Hu, Y. M., & Du, J. (2025) · ACS Nano · doi:10.1021/acsnano.5c05542 · Cited by 27

Design and development of glucocorticoid receptor modulators

Buttgereit, F., Elling, C., & Jakob, F. (2025) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2025.06.005 · Cited by 28

Understanding regulatory B cells in autoimmune diseases: the case of multiple sclerosis

Cuc, B. T., Pohar, J., & Fillatreau, S. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.07.007 · Cited by 25

Hormonal daily variation co-varies with immunity in captive male bullfrogs (Lithobates catesbeianus)

Titon, S. C. M., Titon, B., Assis, V. R., Vasconcelos‐Teixeira, R., Neto, P. G. G., Lima, A. S., Ferreira, L. D. F., Fernandes, P. A. C. M., Gomes, F. R., & Markus, R. P. (2020) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2020.113702 · Cited by 25

A chicken and egg scenario in psychoneuroimmunology: Bidirectional mechanisms linking cytokines and depression

Rengasamy, M. L., Marsland, A. L., Spada, M. L., Hsiung, K. S., Kovats, T., & Price, R. B. (2021) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2021.100177 · Cited by 29

Immunomodulatory functions of TRPM7 and its implications in autoimmune diseases

Liang, H., Chen, Y., Wei, X., Ma, G., Ding, J., Lu, C., Zhou, R., & Hu, W. M. (2021) · Immunology · doi:10.1111/imm.13420 · Cited by 27

Dyslipidemia in Transplant Patients: Which Therapy?

Iannuzzo, G., Cuomo, G., Lorenzo, A. D., Tripaldella, M., Mallardo, V., Idelson, P. I., Sagnelli, C., Sica, A., Creta, M., Baltar, J., et al. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11144080 · Cited by 31

Glucocorticoids for IgA nephropathy—pro

Zhang, Y., Lv, J., Wong, M. G., Zhang, H., & Perkovic, V. (2023) · Kidney International · doi:10.1016/j.kint.2023.01.018 · Cited by 26

Increased Risk of Multimorbidity in Patients With Sarcoidosis: A Population-Based Cohort Study 1976 to 2013

Ungprasert, P., Matteson, E. L., & Crowson, C. S. (2017) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2017.09.015 · Cited by 25

Immune Relevant and Immune Deficient Mice: Options and Opportunities in Translational Research

Radaelli, E., Santagostino, S. F., Sellers, R. S., & Brayton, C. F. (2018) · ILAR Journal · doi:10.1093/ilar/ily026 · Cited by 27

Methylprednisolone Decreases Mitochondria-Mediated Apoptosis and Autophagy Dysfunction in Hepatocytes of Experimental Autoimmune Hepatitis Model via the Akt/mTOR Signaling

Fan, X., Men, R., Wang, H., Shen, M., Wang, T., Ye, T., Luo, X., & Yang, L. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01189 · Cited by 25

Neuronal regulation of B-cell immunity: Anticipatory immune posturing?

You, Z., Liu, B., & Qi, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.014 · Cited by 25

The glucocorticoid dexamethasone inhibits HIF-1α stabilization and metabolic reprogramming in lipopolysaccharide-stimulated primary macrophages

Clayton, S. A., Lockwood, C., O’Neil, J. D., Daley, K. K., Hain, S., Abdelmottaleb, D. I., Bolimowska, O. O., Tennant, D. A., & Clark, A. R. (2023) · Discovery Immunology · doi:10.1093/discim/kyad027 · Cited by 23

Cochlear implantation with a dexamethasone-eluting electrode array: First-in-human safety and performance results

Prenzler, N., Salcher, R. B., Büchner, A., Warnecke, A., Kley, D., Batsoulis, C., Vormelcher, S., Mitterberger-Vogt, M., Morettini, S., Schilp, S., et al. (2025) · Hearing Research · doi:10.1016/j.heares.2025.109255 · Cited by 24

GLCCI1 is a novel protector against glucocorticoid‐induced apoptosis in T cells

Kiuchi, Z., Nishibori, Y., Kutsuna, S., Kotani, M., Hada, I., Kimura, T., Fukutomi, T., Fukuhara, D., Ito‐Nitta, N., Kudo, A., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201800344rr · Cited by 26

NADPH oxidases and HIF1 promote cardiac dysfunction and pulmonary hypertension in response to glucocorticoid excess

Kračun, D., Klop, M., Knirsch, A., Petry, A., Kanchev, I., Chalupský, K., Wolf, C. M., & Görlach, A. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101536 · Cited by 23

Early-Life Stress Regulates Cardiac Development through an IL-4-Glucocorticoid Signaling Balance

Apaydin, D. C., Jaramillo, P. A. M., Corradi, L., Cosco, F., Rathjen, F. G., Kammertoens, T., Filosa, A., & Sawamiphak, S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108404 · Cited by 24

Systemic hormonal and immune regulation induced by intraperitoneal LPS injection in bullfrogs (Lithobates catesbeianus)

de Figueiredo, A. C., Titon, S. C. M., Titon, B., Vasconcelos‐Teixeira, R., Barsotti, A. M. G., & Gomes, F. R. (2020) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2020.110872 · Cited by 24

Clinical course and outcome of patients with ACTH-dependent Cushing’s syndrome infected with novel coronavirus disease-19 (COVID-19): case presentations

Belaya, Z. E., Golounina, O. O., Mel'nichenko, G. A., Tarbaeva, N. V., Pashkova, E., Gorokhov, M., Kalashnikov, V., Dzeranova, L. K., Fadeev, V. V., Volchkov, P., et al. (2021) · Endocrine · doi:10.1007/s12020-021-02674-5 · Cited by 24

Is stress related to the presence and persistence of oncogenic human papillomavirus infection in young women?

Kuebler, U., Fischer, S., Mernone, L., Breymann, C., Abbruzzese, E., & Ehlert, U. (2021) · BMC Cancer · doi:10.1186/s12885-021-08010-4 · Cited by 28

Immunomodulation and mechanisms of fucoidan from Cladosiphon okamuranus ameliorates atopic dermatitis symptoms

Chen, B.-R., Hsu, K.-T., Hsu, W.-H., Lee, B., Li, T., Chan, Y.-L., & Wu, C. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.08.001 · Cited by 24

Overexpression of SIRT1 Inhibits Corticosterone-Induced Autophagy

Jiang, Y., Botchway, B. O. A., Hu, Z., & Fang, M. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.035 · Cited by 26

Divergent Effects of a Transient Corticosteroid Therapy on Virus-Specific Quiescent and Effector CD8+ T Cells

Kumar, D., & Sehrawat, S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01521 · Cited by 24

Multi-Systemic Biological Risk and Cancer Mortality: The NHANES III Study

Acheampong, T., Jiang, L., Ziogas, A., & Odegaard, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-61945-9 · Cited by 28

Intravenous Infusion of Cortisol, Adrenaline, or Noradrenaline Alters Porcine Immune Cell Numbers and Promotes Innate over Adaptive Immune Functionality

Reiske, L., Schmucker, S. S., Pfaffinger, B., Weiler, U., Steuber, J., & Stefanski, V. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000269 · Cited by 26

LPS‐induced immunomodulation and hormonal variation over time in toads

Titon, B., Titon, S. C. M., Assis, V. R., Barsotti, A. M. G., Vasconcelos‐Teixeira, R., Fernandes, P. A. C. M., & Gomes, F. R. (2021) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2474 · Cited by 24

Physiological plasticity in elephants: highly dynamic glucocorticoids in African and Asian elephants

Pokharel, S. S., & Brown, J. L. (2023) · Conservation Physiology · doi:10.1093/conphys/coad088 · Cited by 23

Micro- and Macrovascular Effects of Inflammation in Peripheral Artery Disease—Pathophysiology and Translational Therapeutic Approaches

Poledniczek, M., Neumayer, C., Kopp, C. W., Schlager, O., Gremmel, T., Józkowicz, A., Gschwandtner, M. E., Koppensteiner, R., & Wadowski, P. P. (2023) · Biomedicines · doi:10.3390/biomedicines11082284 · Cited by 26

Stress-induced red nucleus attenuation induces anxiety-like behavior and lymph node CCL5 secretion

Shi, D., Zhang, Y.-D., Zhang, S., Liao, B.-B., Chu, M., Su, S., Zhuo, K., Hu, H., Zhang, C., & Wang, Z. (2023) · Nature Communications · doi:10.1038/s41467-023-42814-1 · Cited by 22

Paraventricular nucleus CRH neurons regulate acute lung injury via sympathetic nerve–neutrophil axis

Li, H., Liu, T., Wang, Y., Miao, X.-M., Xiong, Y.-Y., Zhao, Q., Shen, W., Su, F., Chen, K., & Dai, R. (2025) · Nature Communications · doi:10.1038/s41467-025-63953-7 · Cited by 23

Tuberculosis and systemic lupus erythematosus: a case-control study in Mexico City

Torres‐González, P., Romero‐Díaz, J., Cervera-Hernandez, M. E., Ocampo-Torres, M. C., Chaires-Garza, L. G., Lastiri-González, E. A., Atisha‐Fregoso, Y., Bobadilla-del-Valle, M., Ponce‐de‐León, A., & Sifuentes‐Osornio, J. (2018) · Clinical Rheumatology · doi:10.1007/s10067-018-4109-z · Cited by 23

The Effect of Immunosuppressive Drugs on MDSCs in Transplantation

Yang, F., Li, Y., Zhang, Q., Tan, L., Peng, L., & Zhao, Y. X. (2018) · Journal of Immunology Research · doi:10.1155/2018/5414808 · Cited by 24

Unbiased Screening Identifies Functional Differences in NK Cells After Early Life Psychosocial Stress

Fernandes, S. B., Patil, N. D., Mériaux, S. B., Thérésine, M., Muller, C. P., Leenen, F. A. D., Elwenspoek, M. M. C., Zimmer, J., & Turner, J. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.674532 · Cited by 23

Pulmonate slug evolution is reflected in the de novo genome of Arion vulgaris Moquin-Tandon, 1855

Chen, Z., Doğan, Ö., Guiglielmoni, N., Guichard, A., & Schrödl, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-18099-7 · Cited by 31

Innovative Strategies for Hair Regrowth and Skin Visualization

Mai, Q., Han, Y., Cheng, G., Ma, R., Zhao, Y., Chen, X., Yu, G., Chen, T., & Zhang, S. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15041201 · Cited by 23

Graves’ disease as a driver of depression: a mechanistic insight

Song, Y., Wang, X., Ma, W., Yang, Y., Yan, S., Sun, J., Zhu, X., & Tang, Y. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1162445 · Cited by 26

Synephrine and Its Derivative Compound A: Common and Specific Biological Effects

Dodonova, S. A., Михайловна, Ж. Е., Kryukov, A. A., Valiev, T. T., Игоревич, К. К., Kulikov, E. P., Budunova, I. V., Геннадиевна, Я. М., & Lesovaya, E. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242417537 · Cited by 23

Chromatin reprogramming in breast cancer

Swinstead, E. E., Paakinaho, V., & Hager, G. L. (2018) · Endocrine Related Cancer · doi:10.1530/erc-18-0033 · Cited by 24

Identification of amniotic fluid metabolomic and placental transcriptomic changes associated with abnormal development of cloned pig fetuses

Ao, Z., Li, Z., Wang, X., Zhao, C., Gan, Y., Wu, X. F., Zeng, F., Shi, J., Gu, T., Hong, L., et al. (2019) · Molecular Reproduction and Development · doi:10.1002/mrd.23102 · Cited by 23

Exogenous glucocorticoids amplify the costs of infection by reducing resistance and tolerance, but effects are mitigated by co-infection

Schoenle, L. A., Moore, I. T., Dudek, A. M., Garcia, E. B., Mays, M., Haussmann, M. F., Cimini, D., & Bonier, F. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.2913 · Cited by 23

Factors associated with active tuberculosis in Colombian patients with systemic lupus erythematosus: a case-control study

González, L. A., Coral-Enríquez, J. A., Restrepo‐Escobar, M., Muñoz‐Vahos, C. H., Jaramillo-Arroyave, D., Vanegas-García, A. L., Eraso, R., Vásquez, G. M., & Jaimes, F. A. (2020) · Clinical Rheumatology · doi:10.1007/s10067-020-05225-x · Cited by 23

HIF1α is a direct regulator of steroidogenesis in the adrenal gland

Watts, D., Stein, J., Meneses, A., Bechmann, N., Neuwirth, A., Kaden, D., Krüger, A., Sinha, A. N., Alexaki, V. I., Perez‐Rivas, L. G., et al. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03750-1 · Cited by 24

Astragaloside IV ameliorates peripheral immunosuppression induced by cerebral ischemia through inhibiting HPA axis

Zou, Y., Li, S., Chen, T., Li, Z., Gao, X., & Wang, Z. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108569 · Cited by 22

Cell-Specific Immune Regulation by Glucocorticoids in Murine Models of Infection and Inflammation

Rocamora‐Reverte, L., Villunger, A., & Wiegers, G. J. (2022) · Cells · doi:10.3390/cells11142126 · Cited by 22

Chronic stress induced duration dependent alterations in immune system and their reversibility in rats

Sarjan, H. N., & Yajurvedi, H. N. (2018) · Immunology Letters · doi:10.1016/j.imlet.2018.02.008 · Cited by 22

Evidence for a More Disrupted Immune-Endocrine Relation and Cortisol Immunologic Influences in the Context of Tuberculosis and Type 2 Diabetes Comorbidity

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