Extra-adrenal glucocorticoid synthesis: immune regulation and aspects on local organ homeostasis

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 · see citing works

How Do Glucocorticoids Influence Stress Responses? Integrating Permissive, Suppressive, Stimulatory, and Preparative Actions

Sapolsky, R. M. (2000) · Endocrine Reviews · doi:10.1210/er.21.1.55 · Cited by 7,533 · see citing works

Stress and the brain: from adaptation to disease

de Kloet, E. R., Joëls, M., & Holsboer, F. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1683 · Cited by 4,621 · see citing works

Brain corticosteroid receptor balance in health and disease

de Kloet, E. R., Vreugdenhil, E., Oitzl, M. S., & Joëls, M. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.3.0331 · Cited by 2,614 · see citing works

Brain corticosteroid receptor balance in health and disease

de Kloet, E. R. (1998) · Endocrine Reviews · doi:10.1210/er.19.3.269 · Cited by 2,614 · see citing works

Mechanisms involved in the side effects of glucocorticoids

SCHACKE, H. (2002) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(02)00297-8 · Cited by 1,847 · see citing works

Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones

Payne, A. H., & Hales, D. B. (2004) · Endocrine Reviews · doi:10.1210/er.2003-0030 · Cited by 1,766 · see citing works

Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice.

Peschon, J. J., Morrissey, P., Grabstein, K. H., Ramsdell, F. J., Maraskovsky, E., Gliniak, B., Park, L. S., Ziegler, S. F., Williams, D. E., Ware, C. B., et al. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.180.5.1955 · Cited by 1,553 · see citing works

Molecular and Cellular Endocrinology

Rainey, W. E., & Rodgers, R. J. (2004) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2004.10.007 · Cited by 1,309 · see citing works

The Interplay between the Glucocorticoid Receptor and Nuclear Factor-κB or Activator Protein-1: Molecular Mechanisms for Gene Repression

De Bosscher, K., Vanden Berghe, W., & Haegeman, G. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0006 · Cited by 898 · see citing works

Glucocorticoids in T Cell Development and Function

Ashwell, J. D., Lu, F. W. M., & Vacchio, M. S. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.309 · Cited by 777 · see citing works

Journey through the thymus: stromal guides for T-cell development and selection

Takahama, Y. (2006) · Nature reviews. Immunology · doi:10.1038/nri1781 · Cited by 730 · see citing works

Neuroendocrinology of the Skin1

Slominski, A., & Wortsman, J. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.5.0410 · Cited by 727 · see citing works

Antigen presentation in the thymus for positive selection and central tolerance induction

Klein, L., Hinterberger, M., Wirnsberger, G., & Kyewski, B. (2009) · Nature reviews. Immunology · doi:10.1038/nri2669 · Cited by 588 · see citing works

Thymic involution and immune reconstitution.

Lynch, H. E., Goldberg, G. L., Chidgey, A., Van den Brink, M. R. M., Boyd, R., & Sempowski, G. D. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.04.003 · Cited by 522 · see citing works

Foxp3+ regulatory T cells: differentiation, specification, subphenotypes

Feuerer, M., Hill, J. A., Mathis, D. J., & Benoist, C. O. (2009) · Nature Immunology · doi:10.1038/ni.1760 · Cited by 507 · see citing works

Neuroendocrinology of the Skin

Slominski, A. T. (2000) · Endocrine Reviews · doi:10.1210/er.21.5.457 · Cited by 503 · see citing works

Human hair follicles display a functional equivalent of the hypothalamic‐pituitary‐adrenal (HPA) axis and synthesize cortisol

Ito, N., Ito, T., Kromminga, A., Bettermann, A., Takigawa, M., Kees, F., Straub, R. H., & Paus, R. (2005) · The FASEB Journal · doi:10.1096/fj.04-1968fje · Cited by 498 · see citing works

Myocardial Production of Aldosterone and Corticosterone in the Rat

Silvestre, J., Robert, V., Heymes, C., Aupetit, B., Mouas, C., Moalic, J., Bernard Swynghedauw, A., & Delcayre, C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.9.4883 · Cited by 446 · see citing works

The role of astroglia in neuroprotection

Bélanger, M., & Magistretti, P. J. (2009) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2009.11.3/mbelanger · Cited by 396 · see citing works

Circadian rhythms in the hypothalamo-pituitary-adrenal (HPA) axis

Kalsbeek, A., van der Spek, R., Lei, J., Endert, E., Buijs, R. M., & Fliers, E. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.06.042 · Cited by 380 · see citing works

Thymic epithelial cells: working class heroes for T cell development and repertoire selection

Anderson, G., & Takahama, Y. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.03.005 · Cited by 360 · see citing works

Steroid production in the thymus: implications for thymocyte selection.

Vacchio, M. S., Papadopoulos, V. D., & Ashwell, J. D. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.6.1835 · Cited by 355 · see citing works

Cytokine activation of the HPA axis

DUNN, A. J. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05426.x · Cited by 352 · see citing works

Neurosteroids: Beginning of the story

Baulieu, E. E., Röbel, P., & Schumacher, M. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)46057-0 · Cited by 351 · see citing works

The five rs of glucocorticoid action during inflammation: Ready, reinforce, repress, resolve, and restore

Busillo, J. M., & Cidlowski, J. A. (2013) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2012.11.005 · Cited by 339 · see citing works

Selection of Self-Reactive T Cells in the Thymus

Stritesky, G. L., Jameson, S. C., & Hogquist, K. A. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-020711-075035 · Cited by 329 · see citing works

Extra-adrenal glucocorticoids and mineralocorticoids: evidence for local synthesis, regulation, and function

Taves, M. D., Gomez-Sanchez, C. E., & Soma, K. K. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00100.2011 · Cited by 293 · see citing works

Prevention and treatment of systemic glucocorticoid side effects

Moghadam‐Kia, S., & Werth, V. P. (2010) · International Journal of Dermatology · doi:10.1111/j.1365-4632.2009.04322.x · Cited by 285 · see citing works

Checkpoints in lymphocyte development and autoimmune disease

von Boehmer, H., & Melchers, F. (2009) · Nature Immunology · doi:10.1038/ni.1794 · Cited by 282 · see citing works

Acute and Chronic Inflammation

Klatt, E. C., & Kumar, V. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4160-4930-2.00002-5 · Cited by 253 · see citing works

MLN64 contains a domain with homology to the steroidogenic acute regulatory protein (StAR) that stimulates steroidogenesis

Watari, H., Arakane, F., Moog-Lutz, C., Kallen, C. B., Tomasetto, C., Gerton, G. L., Rio, M.-C., Baker, M. E., & Strauss, J. F. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.16.8462 · Cited by 247 · see citing works

A novel pathway for sequential transformation of 7-dehydrocholesterol and expression of the P450scc system in mammalian skin

Slominski, A., Zjawiony, J., Wortsman, J., Semak, I., Stewart, J., Pisarchik, A., Sweatman, T., Marcos, J., Dunbar, C., & C. Tuckey, R. (2004) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.2004.04356.x · Cited by 243 · see citing works

The significance of glucocorticoid pulsatility

Lightman, S. L., Wiles, C. C., Atkinson, H. C., Henley, D. E., Russell, G. M., Leendertz, J. A., McKenna, M. A., Spiga, F., Wood, S. A., & Conway-Campbell, B. L. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.073 · Cited by 241 · see citing works

Neuroactive steroids: State of the art and new perspectives

Melcangi, R. C., García‐Segura, L. M., & Mensah‐Nyagan, A. G. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7403-5 · Cited by 232 · see citing works

CRH stimulation of corticosteroids production in melanocytes is mediated by ACTH

Slominski, A., Zbytek, B., Szczesniewski, A., Semak, I., Kaminski, J., Sweatman, T., & Wortsman, J. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00519.2004 · Cited by 211 · see citing works

Intestinal Epithelial Cells Synthesize Glucocorticoids and Regulate T Cell Activation

Cima, I., Corazza, N., Dick, B., Fuhrer, A. C., Herren, S., Jakob, S., Ayuni, E., Mueller, C., & Brunner, T. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031958 · Cited by 200 · see citing works

Corticosteroid Actions in the Hippocampus

Joëls, M. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00688.x · Cited by 196 · see citing works

Both age and gender affect thymic output: more recent thymic migrants in females than males as they age

Pido-Lopez, J., Imami, N., & Aspinall, R. (2001) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.2001.01640.x · Cited by 195 · see citing works

Cortisol synthesis in epidermis is induced by IL-1 and tissue injury

Vukelic, S., Stojadinovic, O., Pastar, I., Rabach, M., Krzyzanowska, A., Lebrun, E., Davis, S. C., Resnik, S., Brem, H., & Tomic-Canic, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.188268 · Cited by 193 · cited 9× · see citing works

Minireview: Neuro-Immuno-Endocrine Modulation of the Hypothalamic-Pituitary-Adrenal (HPA) Axis by gp130 Signaling Molecules

Chesnokova, V., & Melmed, S. K. (2002) · Endocrinology · doi:10.1210/endo.143.5.8861 · Cited by 188 · see citing works

Rapid immunosuppressive effects of glucocorticoids mediated through Lck and Fyn

Löwenberg, M., Tuynman, J. B., Bilderbeek, J., Gaber, T., Buttgereit, F., van Deventer, S. J. H., Peppelenbosch, M. P., & Hommes, D. W. (2005) · Blood · doi:10.1182/blood-2004-12-4790 · Cited by 170 · see citing works

TNF suppresses acute intestinal inflammation by inducing local glucocorticoid synthesis

Noti, M., Corazza, N., Mueller, C., Berger, B., & Brunner, T. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20090849 · Cited by 170 · see citing works

Messenger RNAs encoding steroidogenic enzymes are expressed in rodent brain

Strömstedt, M., & Waterman, M. R. (1995) · Molecular Brain Research · doi:10.1016/0169-328x(95)00140-n · Cited by 164 · see citing works

LRH-1-mediated glucocorticoid synthesis in enterocytes protects against inflammatory bowel disease

Coste, A., Dubuquoy, L., Barnouin, R., Annicotte, J., Magnier, B. C., Noti, M., Corazza, N., Antal, M. C., METZGER, D., Desreumaux, P., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702440104 · Cited by 160 · see citing works

Glucocorticoids cause rapid dissociation of a T‐cell‐receptor‐associated protein complex containing LCK and FYN

Löwenberg, M., Verhaar, A. P., Bilderbeek, J., van Marle, J., Buttgereit, F., Peppelenbosch, M. P., van Deventer, S. J. H., & Hommes, D. W. (2006) · EMBO Reports · doi:10.1038/sj.embor.7400775 · Cited by 157 · see citing works

Expression and costimulatory effects of the TNF receptor superfamily members CD134 (OX40) and CD137 (4-1BB), and their role in the generation of anti-tumor immune responses

Taraban, V. Y., Rowley, T. F., O'Brien, L., Chan, H. T. C., Haswell, L. E., Green, M. H. A., Tutt, A. L., Glennie, M. J., & Al‐Shamkhani, A. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200212)32:12 · Cited by 149 · see citing works

T-cell glucocorticoid receptor is required to suppress COX-2-mediated lethal immune activation

Brewer, J. A., Khor, B., Vogt, S. K., Muglia, L. M., Fujiwara, H., Haegele, K. E., Sleckman, B. P., & Muglia, L. J. (2003) · Nature Medicine · doi:10.1038/nm895 · Cited by 149 · see citing works

Neurosteroids, immunosteroids, and the Balkanization of endocrinology

Schmidt, K. L., Pradhan, D. S., Shah, A. H., Charlier, T. D., Chin, E. H., & Soma, K. K. (2008) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2008.03.025 · Cited by 147 · see citing works

CRH stimulates POMC activity and corticosterone production in dermal fibroblasts

Slominski, A., Zbytek, B., Semak, I., Sweatman, T., & Wortsman, J. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.01.014 · Cited by 143 · see citing works

Thymus-derived Glucocorticoids Regulate Antigen-specific Positive Selection

Vacchio, M. S., & Ashwell, J. D. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.11.2033 · Cited by 137 · see citing works

Thymocyte Apoptosis Induced by T Cell Activation Is Mediated by Glucocorticoids In Vivo

Brewer, J. A., Kanagawa, O., Sleckman, B. P., & Muglia, L. J. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.4.1837 · Cited by 133 · see citing works

Origin of Aldosterone in the Rat Heart

Gómez-Sánchez, E. P., Ahmad, N., Romero, D. G., & Gómez-Sánchez, C. E. (2004) · Endocrinology · doi:10.1210/en.2004-0295 · Cited by 133 · see citing works

Cardiac Steroidogenesis in the Normal and Failing Heart

Young, M. J., Clyne, C. D., Cole, T. J., & Funder, J. W. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.11.7925 · Cited by 132 · see citing works

Is aldosterone synthesized within the rat brain?

Gómez-Sánchez, E. P., Ahmad, N., Romero, D. G., & Gómez-Sánchez, C. E. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00355.2004 · Cited by 131 · see citing works

Analysis of steroids in songbird plasma and brain by coupling solid phase extraction to radioimmunoassay

Newman, A. E. M., Chin, E. H., Schmidt, K. L., Bond, L., Wynne‐Edwards, K. E., & Soma, K. K. (2007) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2007.08.007 · Cited by 128 · see citing works

Thymocyte responsiveness to endogenous glucocorticoids is required for immunological fitness

Mittelstadt, P. R., Monteiro, J. P., & Ashwell, J. D. (2012) · Journal of Clinical Investigation · doi:10.1172/jci63067 · Cited by 128 · see citing works

Paracrine glucocorticoid activity produced by mouse thymic epithelial cells

Pazirandeh, A., Xue, Y., Rafter, I., Sjövall, J., Jondal, M., & Okret, S. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.8.893 · Cited by 125 · see citing works

Expression of 11beta-hydroxylase and aldosterone synthase genes in the rat brain

MacKenzie, S. M., CLARK, C. J., Fräser, R., Gómez-Sánchez, C. E., Connell, J. M. C., & Davies, E. (2000) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0240321 · Cited by 124 · see citing works

Extraadrenal steroid 21-hydroxylation is not mediated by P450c21.

Mellon, S. H., & Miller, W. L. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114325 · Cited by 121 · see citing works

The nuclear receptor LRH-1 critically regulates extra-adrenal glucocorticoid synthesis in the intestine

Mueller, M., Cima, I., Noti, M., Fuhrer, A. C., Jakob, S., Dubuquoy, L., Schoonjans, K., & Brunner, T. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060357 · Cited by 121 · see citing works

Keratinocytes synthesize and activate cortisol

Cirillo, N., & Prime, S. S. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23081 · Cited by 118 · see citing works

Changing glucocorticoid action: 11β-Hydroxysteroid dehydrogenase type 1 in acute and chronic inflammation

Chapman, K. E., Coutinho, A. E., Zhang, Z., Kipari, T. M. J., Savill, J., & Seckl, J. R. (2013) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2013.02.002 · Cited by 118 · see citing works

Intrathymic T Cell Development and Selection Proceeds Normally in the Absence of Glucocorticoid Receptor Signaling

Purton, J. F., Boyd, R. L., Cole, T. J., & Godfrey, D. I. (2000) · Immunity · doi:10.1016/s1074-7613(00)00018-2 · Cited by 115 · see citing works

Colon cancer cells produce immunoregulatory glucocorticoids

Sidler, D., Renzulli, P., Schnoz, C., Berger, B., Schneider-Jakob, S., Flück, C., Inderbitzin, D., Corazza, N., Candinas, D., & Brunner, T. (2011) · Oncogene · doi:10.1038/onc.2010.629 · Cited by 107 · see citing works

Thymus-Derived Glucocorticoids Set the Thresholds for Thymocyte Selection by Inhibiting TCR-Mediated Thymocyte Activation

Vacchio, M. S., Lee, J. Y. M., & Ashwell, J. D. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.3.1327 · Cited by 106 · see citing works

Elevated cardiac tissue level of aldosterone and mineralocorticoid receptor in diastolic heart failure: beneficial effects of mineralocorticoid receptor blocker

Ohtani, T., Ohta, M., Yamamoto, K., Mano, T., Sakata, Y., Nishio, M., Takeda, Y., Yoshida, J., Miwa, T., Okamoto, M., et al. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00402.2006 · Cited by 104 · see citing works

Ablation and Regeneration of Tolerance-Inducing Medullary Thymic Epithelial Cells after Cyclosporine, Cyclophosphamide, and Dexamethasone Treatment

Fletcher, A. L., Lowen, T. E., Sakkal, S., Reiseger, J. J., Hammett, M. V., Seach, N., Scott, H. S., Boyd, R. L., & Chidgey, A. P. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900225 · Cited by 97 · see citing works

Steroid synthesis by primary human keratinocytes; implications for skin disease

Hannen, R. F., Michael, A. E., Jaulim, A., Bhogal, R., Burrin, J. M., & Philpott, M. P. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.11.059 · Cited by 96 · see citing works

Cytochrome P450 2D catalyze steroid 21-hydroxylation in the brain

Kishimoto, W., Hiroi, T., Shiraishi, M., Osada, M., Imaoka, S., Kominami, S., Igarashi, T., & Funae, Y. (2004) · Endocrinology · doi:10.1210/en.2003-1109 · Cited by 90 · see citing works

Aldosterone synthesis in the brain contributes to Dahl salt‐sensitive rat hypertension

Gómez-Sánchez, E. P., Gomez‐Sanchez, C. M., Plonczynski, M. W., & Gómez-Sánchez, C. E. (2009) · Experimental Physiology · doi:10.1113/expphysiol.2009.048900 · Cited by 84 · see citing works

Aldosterone Is Produced From Ventricles in Patients With Essential Hypertension

Yamamoto, N., Yasue, H., Mizuno, Y., Yoshimura, M., Fujii, H., Nakayama, M., Harada, E., Nakamura, S., Ito, T., & Ogawa, H. (2002) · Hypertension · doi:10.1161/01.hyp.0000015905.27598.e9 · Cited by 81 · see citing works

Cortisol and corticosterone in the songbird immune and nervous systems: local vs. systemic levels during development

Schmidt, K. L., & Soma, K. K. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00002.2008 · Cited by 81 · see citing works

Glucocorticoid (GC) sensitivity and GC receptor expression differ in thymocyte subpopulations

Berki, T., Pàlinkàs, L., Boldizsár, F., & Németh, P. (2002) · International Immunology · doi:10.1093/intimm/14.5.463 · Cited by 80 · see citing works

Aldosterone biosynthesis and action in vascular cells

Takeda, R., Hatakeyama, H., Takeda, Y., Iki, K., Miyamori, I., Sheng, W. P., Yamamoto, H., & Blair, I. A. (1995) · Steroids · doi:10.1016/0039-128x(94)00026-9 · Cited by 79 · see citing works

Different roles for glucocorticoids in thymocyte homeostasis?

Jondal, M., Pazirandeh, A., & Okret, S. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.003 · Cited by 79 · see citing works

Origin and functional activity of the membrane-bound glucocorticoid receptor

Strehl, C., Gaber, T., Löwenberg, M., Hommes, D. W., Verhaar, A. P., Schellmann, S., Hahne, M., Fangradt, M., Wagegg, M., Hoff, P., et al. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30637 · Cited by 79 · see citing works

Glucocorticoid production in the chicken bursa and thymus

Lechner, O., Dietrich, H., Wiegers, G. J., Vacchio, M. S., & Wick, G. (2001) · International Immunology · doi:10.1093/intimm/13.6.769 · Cited by 77 · see citing works

The why and how of thymocyte negative selection

Siggs, O. M., Makaroff, L., & Liston, A. (2006) · Current Opinion in Immunology · doi:10.1016/j.coi.2006.01.001 · Cited by 74 · see citing works

Selective increases in regional brain glucocorticoid: A novel effect of chronic alcohol

Little, H. J., Croft, A. P., O’Callaghan, M. J., Brooks, S. P., Wang, G., & Shaw, S. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.08.029 · Cited by 74 · see citing works

Neuroendocrinology of the skin

Zmijewski, M. A., & Slominski, A. T. (2011) · Dermato-Endocrinology · doi:10.4161/derm.3.1.14617 · Cited by 73 · see citing works

Regulation of Proopiomelanocortin Gene Expression

Jenks, B. G. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2008.03620.x · Cited by 70 · see citing works

Transcription factor‐mediated molecular mechanisms involved in the functional cross‐talk between cytokines and glucocorticoids

Refojo, D., Liberman, A., Holsboer, F., & ARZT, E. S. (2001) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2001.01023.x · Cited by 68 · see citing works

A role for endogenous glucocorticoids in wound repair

Grose, R., Werner, S., Kessler, D., Tuckermann, J., Huggel, K., Durka, S., Reichardt, H. M., & Werner, S. (2002) · The EMBO Reports · doi:10.1093/embo-reports/kvf119 · Cited by 66 · see citing works

Synthesis of corticosterone in the vascular wall

Takeda, Y., Miyamori, I., Yoneda, T., Iki, K., Hatakeyama, H., Blair, I. A., Hsieh, F.-Y., & Takeda, R. (1994) · Endocrinology · doi:10.1210/endo.135.5.7956952 · Cited by 65 · see citing works

Thymic epithelial cells: the multi-tasking framework of the T cell “cradle”

Alves, N. L., Huntington, N. D., Rodewald, H.-R., & Santo, J. P. D. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.07.010 · Cited by 65 · see citing works

Local glucocorticoid production in the mouse lung is induced by immune cell stimulation

Hostettler, N., Bianchi, P., Gennari‐Moser, C., Kassahn, D., Schoonjans, K., Corazza, N., & Brunner, T. (2011) · Allergy · doi:10.1111/j.1398-9995.2011.02749.x · Cited by 65 · see citing works

Corticosteroid synthesis in the central nervous system

Gómez-Sánchez, C. E., Zhou, M. Y., Cozza, E. N., Morita, H., Eddleman, F. C., & Gómez-Sánchez, E. P. (1996) · Endocrine Research · doi:10.1080/07435809609043732 · Cited by 64 · see citing works

Mutagenesis of the glucocorticoid receptor in mice

Kellendonk, C., Tronche, F., Reichardt, H. M., & Schütz, G. (1999) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(99)00041-2 · Cited by 62 · see citing works

Effects of minor laboratory procedures, adrenalectomy, social defeat or acute alcohol on regional brain concentrations of corticosterone

Croft, A. P., O’Callaghan, M. J., Shaw, S., Connolly, G., Jacquot, C., & Little, H. J. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.009 · Cited by 62 · see citing works

Differential Regulation of Glucocorticoid Synthesis in Murine Intestinal EpithelialVersusAdrenocortical Cell Lines

Müeller, M., Atanasov, A. G., Cima, I., Corazza, N., Schoonjans, K., & Brunner, T. (2006) · Endocrinology · doi:10.1210/en.2006-0591 · Cited by 59 · see citing works

Steroid Concentrations in Plasma, Whole Blood and Brain: Effects of Saline Perfusion to Remove Blood Contamination from Brain

Taves, M. D., Schmidt, K. L., Ruhr, I. M., Kapusta, K., Prior, N. H., & Soma, K. K. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015727 · Cited by 53 · see citing works

Wnt-4 Protects Thymic Epithelial Cells Against Dexamethasone-Induced Senescence

Talabér, G., Kvell, K., Varecza, Z., Boldizsár, F., Parnell, S. M., Jenkinson, E. J., Anderson, G., Berki, T., & Pongracz, J. E. (2011) · Rejuvenation Research · doi:10.1089/rej.2010.1110 · Cited by 50 · see citing works

Age-related synthesis of glucocorticoids in thymocytes

Qiao, S., Chen, L., Okret, S., & Jondal, M. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.06.014 · Cited by 50 · see citing works

Do Human Vascular Endothelial Cells Produce Aldosterone?

Ahmad, N., Romero, D. G., Gómez-Sánchez, E. P., & Gómez-Sánchez, C. E. (2004) · Endocrinology · doi:10.1210/en.2004-0081 · Cited by 50 · see citing works

Glucocorticoid Regulation of Astrocytic Fate and Function

Yu, S., Yang, S., Holsboer, F., Sousa, N., & Almeida, O. F. X. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022419 · Cited by 49 · see citing works

Thymus-derived glucocorticoids mediate androgen effects on thymocyte homeostasis

Chen, Y., Qiao, S., Tuckermann, J. P., Okret, S., & Jondal, M. (2010) · The FASEB Journal · doi:10.1096/fj.10-168724 · Cited by 49 · see citing works

Presence of glucocorticoid receptors in cultured thymic epithelial cells

Dardenne, M., Itoh, T., & Homo-Delarche, F. (1986) · Cellular Immunology · doi:10.1016/0008-8749(86)90011-0 · Cited by 47 · see citing works

Lipopolysaccharide induces intestinal glucocorticoid synthesis in a TNFα‐dependent manner

Noti, M., Corazza, N., Tuffin, G., Schoonjans, K., & Brunner, T. (2010) · The FASEB Journal · doi:10.1096/fj.09-140913 · Cited by 46 · see citing works

Thymocyte-Synthesized Glucocorticoids Play a Role in Thymocyte Homeostasis and Are Down-Regulated by Adrenocorticotropic Hormone

Qiao, S., Okret, S., & Jondal, M. (2009) · Endocrinology · doi:10.1210/en.2009-0195 · Cited by 43 · see citing works

Conditional Expression of a Glucocorticoid Receptor Transgene in Thymocytes Reveals a Role for Thymic-Derived Glucocorticoids in Thymopoiesis in Vivo

Pazirandeh, A., Jondal, M., & Okret, S. (2005) · Endocrinology · doi:10.1210/en.2004-0943 · Cited by 42 · see citing works

Cell cycle‐dependent regulation of extra‐adrenal glucocorticoid synthesis in murine intestinal epithelial cells

Atanasov, A. G., Leiser, D., Urwyler-Rösselet, C., Noti, M., Corazza, N., Schoonjans, K., & Brunner, T. (2008) · The FASEB Journal · doi:10.1096/fj.08-114157 · Cited by 38 · see citing works

Shaping the T‐cell repertoire: a matter of life and death

Wiegers, G. J., Kaufmann, M., Tischner, D., & Villunger, A. (2010) · Immunology and Cell Biology · doi:10.1038/icb.2010.127 · Cited by 35 · see citing works

Keratinocyte-Targeted Overexpression of the Glucocorticoid Receptor Delays Cutaneous Wound Healing

Sanchis, A., Alba, L., Latorre, V., Sevilla, L. M., & Pérez, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029701 · Cited by 35 · see citing works

FOXP3~+ regulatory T cells

Li, B. (2010) · Shengming kexue · Cited by 35 · see citing works

Genes Involved in the Adrenal Pathway of Glucocorticoid Synthesis Are Transiently Expressed in the Developing Lung

Provost, P. R., & Tremblay, Y. (2005) · Endocrinology · doi:10.1210/en.2005-0077 · Cited by 32 · see citing works

Low glucocorticoid receptor (GR), high Dig2 and low Bcl-2 expression in double positive thymocytes of BALB/c mice indicates their endogenous glucocorticoid hormone exposure

Boldizsár, F., Pàlinkàs, L., Czömpöly, T., Bartis, D., Németh, P., & Berki, T. (2006) · Immunobiology · doi:10.1016/j.imbio.2006.06.005 · Cited by 31 · see citing works

Characterization of a Novel Oral Glucocorticoid System and Its Possible Role in Disease

Cirillo, N., Hassona, Y. M., Pignatelli, M. N., Gasparoto, T. H., Morgan, D. J. W., & Prime, S. S. (2011) · Journal of Dental Research · doi:10.1177/0022034511427909 · Cited by 31 · see citing works

Glucocorticoid Production and Regulation in Thymus: Of Mice and Birds

Gómez-Sánchez, C. E. (2009) · Endocrinology · doi:10.1210/en.2009-0615 · Cited by 24 · see citing works

Developmental shift in TcR-mediated rescue of thymocytes from glucocorticoid-induced apoptosis

Pàlinkàs, L., Talabér, G., Boldizsár, F., Bartis, D., Németh, P., & Berki, T. (2007) · Immunobiology · doi:10.1016/j.imbio.2007.06.004 · Cited by 22 · see citing works

Antigen and glucocorticoid hormone (GC) induce positive selection of DP thymocytes in a TcR transgenic mouse model

Boldizsár, F., Pàlinkàs, L., Bartis, D., Németh, P., & Berki, T. (2003) · Immunology Letters · doi:10.1016/j.imlet.2003.08.001 · Cited by 8 · see citing works

Post-transcriptional regulation of E2A proteins via lipopolysaccharide and CD40 signaling

Meyer, K. B., & Mufti, D. A. H. (2000) · European Journal of Immunology · doi:10.1002/1521-4141(200002)30:2 · Cited by 8 · see citing works

Untitled work

(2001) · doi:10.1002/1521-4141(200108)31:8

Immune regulation by glucocorticoids

Cain, D. W., & Cidlowski, J. A. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.1 · Cited by 1,846 · see citing works

Neuroimmune Interactions: From the Brain to the Immune System and Vice Versa

Dantzer, R. (2018) · Physiological Reviews · doi:10.1152/physrev.00039.2016 · Cited by 1,073 · see citing works

Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis

Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415 · see citing works

Extra-adrenal glucocorticoid biosynthesis: implications for autoimmune and inflammatory disorders

Slominski, R. M., Tuckey, R. C., Manna, P. R., Jetten, A. M., Postlethwaite, A., Raman, C., & Slominski, A. T. (2020) · Genes & Immunity · doi:10.1038/s41435-020-0096-6 · Cited by 155 · see citing works

Inflammation and immunity in organ regeneration

Mescher, A. L., Neff, A. W., & King, M. W. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.02.015 · Cited by 145 · see citing works

Cutaneous glucocorticosteroidogenesis: securing local homeostasis and the skin integrity

Slominski, A. T., Manna, P. R., & Tuckey, R. C. (2014) · Experimental Dermatology · doi:10.1111/exd.12376 · Cited by 79 · see citing works

The regulation of the mitochondrial apoptotic pathway by glucocorticoid receptor in collaboration with Bcl-2 family proteins in developing T cells

Prenek, L., Boldizsár, F., Kugyelka, R., Ugor, E., Berta, G., Németh, P., & Berki, T. (2016) · APOPTOSIS · doi:10.1007/s10495-016-1320-8 · Cited by 75 · see citing works

Glucocorticoid Resistance: Interference between the Glucocorticoid Receptor and the MAPK Signalling Pathways

Sevilla, L. M., Jiménez‐Panizo, A., Alegre‐Martí, A., Estébanez‐Perpiñá, E., Caelles, C., & Pérez, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810049 · Cited by 72 · see citing works

Microenvironmental signals govern the cellular identity of testicular macrophages

Meinhardt, A., Wang, M., Schulz, C., & Bhushan, S. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0318-086rr · Cited by 68 · see citing works

Extra-Adrenal Glucocorticoid Synthesis in the Intestinal Mucosa: Between Immune Homeostasis and Immune Escape

Ahmed, A. S., Schmidt, C., & Brunner, T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01438 · Cited by 66 · see citing works

Glucocorticoid hormone treatment enhances the cytokine production of regulatory T cells by upregulation of Foxp3 expression

Ugor, E., Prenek, L., Pap, R., Berta, G., Ernszt, D., Najbauer, J., Németh, P., Boldizsár, F., & Berki, T. (2017) · Immunobiology · doi:10.1016/j.imbio.2017.10.010 · Cited by 58 · see citing works

Mechanisms of Action of Dehydroepiandrosterone

Clark, B. J., Prough, R. A., & Klinge, C. M. (2018) · Vitamins and hormones · doi:10.1016/bs.vh.2018.02.003 · Cited by 56 · see citing works

Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes

Nicolaides, N. C., & Charmandari, E. (2017) · Hormones · doi:10.14310/horm.2002.1728 · Cited by 52 · see citing works

Gallbladder-derived surfactant protein D regulates gut commensal bacteria for maintaining intestinal homeostasis

Sarashina-Kida, H., Negishi, H., Nishio, J., Suda, W., Nakajima, Y., Yasui-Kato, M., Iwaisako, K., Kang, S., Endo, N., Yanai, H., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712837114 · Cited by 50 · see citing works

The Immunoendocrine Thymus as a Pacemaker of Lifespan

Csaba, G. (2016) · Acta Microbiologica et Immunologica Hungarica · doi:10.1556/030.63.2016.2.1 · Cited by 49 · see citing works

Chronic Stress Suppresses the Expression of Cutaneous Hypothalamic–Pituitary–Adrenocortical Axis Elements and Melanogenesis

Pang, S., Wu, H., Wang, Q., Cai, M., Shi, W., & Shang, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098283 · Cited by 46 · see citing works

Gut feelings about bacterial steroid-17,20-desmolase

Ly, L. K., Doden, H. L., & Ridlon, J. M. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111174 · Cited by 43 · see citing works

Bioactive forms of vitamin D selectively stimulate the skin analog of the hypothalamus-pituitary-adrenal axis in human epidermal keratinocytes

Wierzbicka, J., Zmijewski, M. A., Piotrowska, A., Nedoszytko, B., Lange, M., Tuckey, R. C., & Slominski, A. T. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.08.006 · Cited by 34 · see citing works

Novel candidate genes for ECT response prediction—a pilot study analyzing the DNA methylome of depressed patients receiving electroconvulsive therapy

Moschny, N., Zindler, T., Jahn, K., Dorda, M., Davenport, C., Wiehlmann, L., Maier, H. B., Eberle, F. C., Bleich, S., Neyazi, A., et al. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00891-9 · Cited by 33 · see citing works

ACTH controls thymocyte homeostasis independent of glucocorticoids

Talabér, G., Tuckermann, J. P., & Okret, S. (2015) · The FASEB Journal · doi:10.1096/fj.14-268508 · Cited by 30 · see citing works

Steroid profiling of glucocorticoids in microdissected mouse brain across development

Hamden, J. E., Gray, K. M., Salehzadeh, M., Kachkovski, G. V., Forys, B. J., Ma, C., Austin, S. H., & Soma, K. K. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22808 · Cited by 30 · see citing works

Extra-adrenal glucocorticoid synthesis at epithelial barriers

Phan, T. S., Merk, V. M., & Brunner, T. (2019) · Genes and Immunity · doi:10.1038/s41435-019-0058-z · Cited by 28 · see citing works

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 · see citing works

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 · see citing works

Local glucocorticoid production in the thymus

Talabér, G., Jondal, M., & Okret, S. (2015) · Steroids · doi:10.1016/j.steroids.2015.06.010 · Cited by 26 · see citing works

Intestinal epithelial deletion of the glucocorticoid receptor NR3C1 alters expression of inflammatory mediators and barrier function

Aranda, C. J., Arredondo‐Amador, M., Ocón, B., Lavín, J. L., Aransay, A. M., Martínez‐Augustin, O., & de Medina, F. S. (2019) · The FASEB Journal · doi:10.1096/fj.201900404rr · Cited by 25 · see citing works

Steroid Hormone Receptors and Signal Transduction Processes

Klinge, C. M. (2018) · Endocrinology · doi:10.1007/978-3-319-44675-2_9 · Cited by 24 · see citing works

An Overview of the Glucocorticoids’ Pathways in the Environment and Their Removal Using Conventional Wastewater Treatment Systems

Yazdan, M. M. S., Ahad, M. T., Mallick, Z., Mallick, S. P., Jahan, I., & Mazumder, M. (2021) · Pollutants · doi:10.3390/pollutants1030012 · Cited by 22 · see citing works

Analysis of Corticosterone and Testosterone Synthesis in Rat Salivary Gland Homogenates

Ieko, T., Sasaki, H., Maeda, N., Fujiki, J., Iwano, H., & Yokota, H. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00479 · Cited by 21 · see citing works

T-cell autonomous death induced by regeneration of inert glucocorticoid metabolites

Rocamora‐Reverte, L., Reichardt, H. M., Villunger, A., & Wiegers, G. J. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.344 · Cited by 19 · see citing works

16α-Bromoepiandrosterone as a new candidate for experimental diabetes–tuberculosis co-morbidity treatment

López-Torres, M. O., Marquina‐Castillo, B., Ramos‐Espinosa, O., Mata‐Espinosa, D., Barrios‐Payán, J., Baay-Guzman, G. J., Huerta‐Yépez, S., Bini, E. I., Torre-Villalvazo, I., Torres, N., et al. (2021) · Clinical & Experimental Immunology · doi:10.1111/cei.13603 · Cited by 16 · see citing works

Epithelial deletion of the glucocorticoid receptor (Nr3c1) protects the mouse intestine against experimental inflammation

Arredondo‐Amador, M., Aranda, C. J., Ocón, B., González, R., Martínez‐Augustin, O., & de Medina, F. S. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15434 · Cited by 15 · see citing works

Altered lipid partitioning and glucocorticoid availability in CBG‐deficient male mice with diet‐induced obesity

Gulfo, J., Ledda, A., Serra, E., Cabot, C., Esteve, M., & Grasa, M. (2016) · Obesity · doi:10.1002/oby.21543 · Cited by 14 · see citing works

Modulation of 11β-hydroxysteroid dehydrogenase functions by the cloud of endogenous metabolites in a local microenvironment: The glycyrrhetinic acid-like factor (GALF) hypothesis

Morris, D. J., Brem, A. S., & Odermatt, A. (2021) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2021.105988 · Cited by 13 · see citing works

In obese mice, exercise training increases 11β-HSD1 expression, contributing to glucocorticoid activation and suppression of pulmonary inflammation

Du, S., Yu, Q., Chuan, K., Ye, C., He, Z., Liu, S., Zhu, X., & Liu, Y. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00652.2016 · Cited by 12 · see citing works

Critical Roles of Endogenous Glucocorticoids for Disease Tolerance in Malaria

Vandermosten, L., Vanhorebeek, I., Bosscher, K. D., Opdenakker, G., & den Steen, P. E. V. (2019) · Trends in Parasitology · doi:10.1016/j.pt.2019.08.007 · Cited by 12 · see citing works

Pharmacology of drugs used in autoimmune dermatopathies in cats and dogs: A narrative review

Tham, H. L., & Davis, J. L. (2024) · Veterinary Dermatology · doi:10.1111/vde.13253 · Cited by 11 · see citing works

Effect of acute restraint stress in a polytrauma rat model

Arnaud, F. G., Pappas, G., Chen, Y., Maudlin-Jeronimo, E., & McCarron, R. M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.07.006 · Cited by 10 · see citing works

Local biosynthesis of corticosterone in rat skeletal muscle

Sato, M., Sugiyama, K., Maeda, N., Fujiki, J., Ieko, T., Kawamura, Y., Iwano, H., Mukai, K., & Yokota, H. (2020) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2020.105693 · Cited by 10 · see citing works

MANAGEMENT OF ENDOCRINE DISEASE: Residual adrenal function in Addison’s disease

Pearce, S. H. S., Gan, E. H., & Napier, C. (2020) · European Journal of Endocrinology · doi:10.1530/eje-20-0894 · Cited by 10 · see citing works

Early Life Stress in Mice Leads to Impaired Colonic Corticosterone Production and Prolonged Inflammation Following Induction of Colitis

Muir, R. Q., Klocke, B. J., Jennings, M. S., Molina, P. A., Hsu, J.-S., Kellum, C. E., Alexander, K. L., Lee, G., Foote, J. B., Lorenz, R. G., et al. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izac280 · Cited by 9 · see citing works

Glucocorticoids are differentially synthesized along the murine and human respiratory tree

Merk, V. M., Renzulli, P., Vrugt, B., Fleischmann, A., & Brunner, T. (2023) · Allergy · doi:10.1111/all.15765 · Cited by 8 · see citing works

“Neuroimmunoendocrinology” in Children with Rheumatic Diseases: How Glucocorticoids Are the Orchestra Director

Maggio, M. C., Miniaci, A., Gallizzi, R., & Civino, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713192 · Cited by 7 · see citing works

Hormone (ACTH, T3) content of immunophenotyped lymphocyte subpopulations

Pállinger, É., Kiss, G. A., & Csaba, G. (2016) · Acta Microbiologica et Immunologica Hungarica · doi:10.1556/030.63.2016.016 · Cited by 7 · see citing works

High-throughput sequencing analysis of differences in intestinal microflora between ulcerative colitis patients with different glucocorticoid response types

Zhu, Y., Luo, J., Yang, Z., & Miao, Y. (2020) · Genes & Genomics · doi:10.1007/s13258-020-00986-w · Cited by 7 · see citing works

Dexamethasone Reduces Cell Adhesion and Migration of T47D Breast Cancer Cell Line

Mohammadi, L., Mosayyebi, B., Imani, M., & Rahmati, M. (2020) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520621666201214150427 · Cited by 6 · see citing works

Therapeutic Agents Rounding Up the Immunopathology of COVID-19

Li, H. P., He, X., Zhang, L., Li, C. X., Li, S. Q., & Li, Q. Y. (2021) · Therapeutics and Clinical Risk Management · doi:10.2147/tcrm.s313003 · Cited by 5 · see citing works

Repository corticotropin injection reverses critical elements of the TLR9/B cell receptor activation response in human B cells in vitro

Olsen, N. J., Benko, A. L., McAloose, C. A., Becker, P. M., Wright, D., Sunyer, T., Kawasawa, Y. I., & Kovacs, W. J. (2019) · Clinical Immunology · doi:10.1016/j.clim.2019.02.009 · Cited by 5 · see citing works

Cancer Neuroscience: Innovative Conception and Emerging Strategy of Therapy

Wang, T., Dong, Z., Wang, Y., An, Z., Wang, S., & Jin, W. (2026) · MedComm · doi:10.1002/mco2.70708 · Cited by 4 · see citing works

A primer Sjögren-szindróma pszichológiai vonatkozásai

Módis, L., Szántó, A., & Bugán, A. (2021) · Orvosi Hetilap · doi:10.1556/650.2021.32234 · Cited by 4 · see citing works

Part III: Steroid Hormone Receptors and Signal Transduction Processes

Klinge, C. M. (2016) · Endocrinology · doi:10.1007/978-3-319-27318-1_9-1 · Cited by 5 · see citing works

Day Versus Night Melatonin and Corticosterone Modulation by LPS in Distinct Tissues of Toads ( Rhinella Icterica )

Cyrino, J. C., de Figueiredo, A. C., Córdoba-Moreno, M. O., Gomes, F. R., & Titon, S. C. M. (2022) · Integrative and Comparative Biology · doi:10.1093/icb/icac028 · Cited by 4 · see citing works

Cortisol

Tobias Stalder, A., & Kirschbaum, C. (2020) · Springer eBooks · doi:10.1007/978-3-030-39903-0_171 · Cited by 4 · see citing works

Diagnostic value of cortisol identification in biological body fluid in case of infectious diseases (literature review)

Alekseeva, L. A., Makarenkova, E. V., Скрипченко, Н. В., Бессонова, Т. В., Zhirkov, A. A., & Евгеньевна, М. Н. (2021) · Pediatrician (St Petersburg) · doi:10.17816/ped12559-69 · Cited by 3 · see citing works

Primary Adrenal Lymphomas with Cushing’s Syndrome: Two Cases with Evidence of Endogeneous Cortisol Production by the Neoplastic Lymphoid Cells

Papageorgiou, S. G., Mavroeidi, I., Kostakis, M. G., Spathis, A., Leventakou, D., Kritikou, E., Oikonomopoulos, N., Kourkouti, C., Krania, M., Bouchla, A., et al. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12155032 · Cited by 3 · see citing works

Pathogenetic Mechanisms of Burn Pathology Associated with Oxidative Membrane Damage and Methods of their Correction

Vilyanen, D. V., Pashkevich, N. I., Borisova‐Mubarakshina, M. M., & Стефанович, О. С. (2023) · BIOPHYSICS · doi:10.1134/s0006350923010190 · Cited by 2 · see citing works

Der weitreichende Einfluss der Hormone

Krause, W. K. H. (2015) · hautnah dermatologie · doi:10.1007/s15012-015-1729-8 · Cited by 1 · see citing works

Glucocorticoids Immunotropic Effects Realization: the Role of Glucocorticoid Receptors, Transport and Regulatory Systems. The Literature Review

Голюченко, О. А., & Стефанович, О. С. (2022) · Рецепт · doi:10.34883/pi.2022.25.3.006 · Cited by 1 · see citing works

Pathogenetic mechanisms of burn disease associated with oxidative membrane damage and ways of their correction

Vilyanen, D. V., Pashkevich, N. I., Borisova‐Mubarakshina, M. M., & Стефанович, О. С. (2023) · Биофизика · doi:10.31857/s0006302923010180 · Cited by 1 · see citing works

Mechanism of glucocorticoid action in immunology—Basic concepts

Wood, M., & Whirledge, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818508-7.00020-8 · Cited by 1 · see citing works

Immunosuppressive glucocorticoids at epithelial barriers in the regulation of anti-viral immune response

Merk, V. M., & Brunner, T. (2021) · Vitamins and hormones · doi:10.1016/bs.vh.2021.06.002 · Cited by 1 · see citing works

Gut Microbiota and the Gut–Brain Axis in Neonatal Calves: Implications for Psychobiotic Usage for Stress Regulation

Pratt, J., Hromádková, J., Malmuthuge, N., & Guan, L. L. (2022) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-030-90303-9_15 · Cited by 1 · see citing works

Roles of GR Isoforms and Hsp90-binding Immunophilins in the Modulation of Glucocorticoid Biological Responses

Galigniana, M. D., Ciucci, S. M., & Mazaira, G. I. (2022) · Current Clinical Pharmacology · doi:10.2174/2772432817666220428135138 · Cited by 1 · see citing works

[Glucagon-based cleansing enemas prior to a double-contrast barium enema].

Ja, P. (1992) · PubMed · Cited by 1 · see citing works

Physiological functions of the adrenocortical circadian clock

Leliavski, A. (2014) · doi:10.53846/goediss-4675

Ultramicroscopic changes of rat parathyroid glands after immunosuppression

Ерохина, В. В., & Avilova, O. (2017) · Morphologia · doi:10.26641/1997-9665.2017.4.35-39

Extraadrenalis glükokortikoidszintézis

Szappanos, Á., Mészáros, K. V., Nagy, Z., Kövesdi, A., Likó, I., Kiss, E. V., Tóth, M., & Patócs, A. (2018) · Orvosi Hetilap · doi:10.1556/650.2018.31019

16a-Bromoepiandrosterone as a new candidate for diabetes-tuberculosis comorbidity treatmentPreprint

López-Torres, M. O., Marquina, B., Ramos‐Espinosa, O., Mata, D., Barrios‐Payán, J., Baay, G., Huerta‐Yépez, S., Segura-Cerda, C. A., Bini, E. I., Torre-Villalvazo, I., et al. (2020) · doi:10.22541/au.160381984.46208315/v1

Contribuciones relativas de los receptores de glucocorticoides y mineralocorticoides en la biología cutánea

Corominas, J. B. (2020) · doi:10.4995/thesis/10251/156214

Habitat y Territorio

Kanashiro, M. C., Roitman, S., Becerra, A. M. Q., Anton, C. S., Jofré, C., Videla, D., & Liceda, S. N. (2012)

Treatment of acute Graft-versus-Host Disease using inorganic-organic hybrid nanoparticles

Kaiser, T. K. (2019) · doi:10.53846/goediss-7756

Cortisol

Tobias Stalder, A., & Kirschbaum, C. (2017) · Springer eBooks · doi:10.1007/978-1-4614-6439-6_171-2

Chemopreventative potential of Salsola tuberculatiformis Botch and Compound A in the differential regulation of IL-1Ra:IL-1α in UVB exposed skin keratinocytes

Magcwebeba, T., McEvoy, L., Hayward, S., Tait, T., Quanson, J. L., Kelbe, L., Gelderblom, W., Lilly, M., Swart, A. C., & Swart, P. (2024) · Phytomedicine Plus · doi:10.1016/j.phyplu.2024.100688

Aging and Thymosin Alpha-1

Simonova, M. A., Ivanov, I., Shoshina, N. S., Komyakova, A. M., Makarov, D. A., Baranovskii, D., Klabukov, I., Telepenina, K. P., Atiakshin, D., Shegay, P., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311470

Additional file 1 of Novel candidate genes for ECT response prediction—a pilot study analyzing the DNA methylome of depressed patients receiving electroconvulsive therapy

Moschny, N., Zindler, T., Jahn, K., Dorda, M., Davenport, C., Wiehlmann, L., Maier, H. B., Eberle, F., Bleich, S., Neyazi, A., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12737559

Étude de l’implication de la protéine immunorégulatrice GILZ dans la régulation de la phagocytose et de l’opsonophagocytose de bactéries à gram négatif et positif

Vigouroux, L. (2019) · doi:10.70675/7fb0ead0z8533z4a86z8b0fzf0ef4bc25323

Glucocorticoid receptor activity in triple negative breast cancer

Noureddine, L. M. (2022) · doi:10.70675/13ab50cfz7edbz4a44z918aza657b9614a4d

Effect of glucocorticoid production by the enteric nervous system on neuronal connectivity is blocked during inflammation in a GR-dependent pathway

Blin, J., Moullé, V. S., Garel, Z., Bertholon, U., Oullier, T., Durand, T., Berre‐Scoul, C. L., Masson, D., Bach‐Ngohou, K., & Neunlist, M. (2026) · iScience · doi:10.1016/j.isci.2026.116993

Steroid Hormone Receptors and Signal Transduction Processes

Klinge, C. M. (2026) · Endocrinology · doi:10.1007/978-3-319-27318-1_9-2

The inhibitory effect of rooibos on cytochromes P450 and downstream in vitro modulation of steroid hormones

Mugari, M. (2015) · SUNScholar (Stellenbosch University)

Extraadrenalis glükokortikoidszintézis

Szappanos, Á., Mészáros, K. V., Nagy, Z., Kövesdi, A., Likó, I., Kiss, E. V., Tóth, M., & Patócs, A. (2018) · Orvosi Hetilap · doi:10.1556/650.2018.31019

Local glucocorticoid production in the thymus

Talabér, G., Jondal, M., & Okret, S. (2015) · Steroids · doi:10.1016/j.steroids.2015.06.010 · Cited by 26 · see citing works

Extra-adrenal glucocorticoids and mineralocorticoids: evidence for local synthesis, regulation, and function

Taves, M. D., Gomez-Sanchez, C. E., & Soma, K. K. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00100.2011 · Cited by 293 · see citing works

Cutting Edge: De Novo Glucocorticoid Synthesis by Thymic Epithelial Cells Regulates Antigen-Specific Thymocyte Selection

Mittelstadt, P. R., Taves, M. D., & Ashwell, J. D. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701328 · Cited by 31 · see citing works

Lymphoid organs of neonatal and adult mice preferentially produce active glucocorticoids from metabolites, not precursors

Taves, M. D., Plumb, A. W., Korol, A. M., van der Gugten, J. G., Holmes, D. T., Abraham, N. B., & Soma, K. K. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.05.003 · Cited by 27 · see citing works