Cited by 985Estrogen and related hormone effectsReceptor Mechanisms and SignalingAdrenal Hormones and Disorders

The DOI matches its Crossref record; 124 of the 124 references it cites were found in a registry or an index.

Nongenomic actions of steroid hormones

Lösel, Ralf, Wehling, Martin·2003·Nature Reviews Molecular Cell Biology

Open this paper in CoChat — free account

Abstract

Steroid hormones modulate many physiological processes. The effects of steroids that are mediated by the modulation of gene expression are known to occur with a time lag of hours or even days. Research that has been carried out mainly in the past decade has identified other responses to steroids that are much more rapid and take place in seconds or minutes. These responses follow nongenomic pathways, and they are not rare.

Integrity signals

Registry

Crossref · 10.1038/nrm1009

Cites

124 of 124 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Gene regulation by steroid hormones
Beato, M. (1989) · Cell · doi:10.1016/0092-8674(89)90237-7 · Cited by 3,383
Steroid hormone metabolites are barbiturate-like modulators of the GABA receptor
Majewska, M. D., Harrison, N. L., Schwartz, R. D., Barker, J. L., & Paul, S. M. (1986) · Science · doi:10.1126/science.2422758 · Cited by 2,225
Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes
Masui, Y., & Markert, C. L. (1971) · Journal of Experimental Zoology · doi:10.1002/jez.1401770202 · Cited by 1,559
Estrogen receptor α mediates the nongenomic activation of endothelial nitric oxide synthase by estrogen
Chen, Z., Yuhanna, I. S., Galcheva-Gargova, Z., Karas, R. H., Mendelsohn, M. E., & Shaul, P. W. (1999) · Journal of Clinical Investigation · doi:10.1172/jci5347 · Cited by 924
Specific binding sites for oestrogen at the outer surfaces of isolated endometrial cells
Pietras, R. J., & Szego, C. M. (1977) · Nature · doi:10.1038/265069a0 · Cited by 697
SPECIFIC, NONGENOMIC ACTIONS OF STEROID HORMONES
Wehling, M. (1997) · Annual Review of Physiology · doi:10.1146/annurev.physiol.59.1.365 · Cited by 663
Self-citation
Acute cardiovascular protective effects of corticosteroids are mediated by non-transcriptional activation of endothelial nitric oxide synthase
Hafezi‐Moghadam, A., Simoncini, T., Yang, Z., Limbourg, F. P., Plumier, J.-C., Rebsamen, M. C., Hsieh, C.-M., Chui, D.-S., Thomas, K. L., Prorock, A. J., et al. (2002) · Nature Medicine · doi:10.1038/nm0502-473 · Cited by 596
Progesterone Receptor Contains a Proline-Rich Motif that Directly Interacts with SH3 Domains and Activates c-Src Family Tyrosine Kinases
Boonyaratanakornkit, V., Scott, M. P., Ribon, V., Sherman, L., Anderson, S. M., Maller, J. L., Miller, W. T., & Edwards, D. P. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00304-5 · Cited by 590
Membrane Estrogen Receptor Engagement Activates Endothelial Nitric Oxide Synthase via the PI3-Kinase–Akt Pathway in Human Endothelial Cells
Haynes, M. P., Sinha, D., Russell, K. S., Collinge, M., Fulton, D. J., Morales‐Ruiz, M., Sessa, W. C., & Bender, J. R. (2000) · Circulation Research · doi:10.1161/01.res.87.8.677 · Cited by 576
Nongenomic steroid action: controversies, questions, and answers
LÖSEL, R. M., FALKENSTEIN, E., FEURING, M., SCHULTZ, A., TILLMANN, H.-C., ROSSOL-HASEROTH, K., & WEHLING, M. (2003) · Physiological Reviews · doi:10.1152/physrev.00003.2003 · Cited by 561
Self-citation

Flagged first, then by citations

Show all 124 references

Research works printed but not linked: 1

Klein, K. & Henk, W. Klinisch-experimentelle Untersuchungen über den Einfluβ von Aldosteron auf Hämodynamik und Gerinnung. Z. Kreisl. Forsch. 52, 40–53 (1963).

Sorted by citations

Items 401–500 of 985

Hormonal therapy in traumatic spinal cord injury.
Ludwig, P. E., Patil, A. A., Chamczuk, A. J., & Agrawal, D. K. (2017) · Europe PMC (PubMed Central) · Cited by 35
Therapeutic Potential of Brassinosteroids in Biomedical and Clinical Research
Kohli, S. K., Bhardwaj, A., Bhardwaj, V., Sharma, A., Kalia, N., Landi, M., & Bhardwaj, R. (2020) · Biomolecules · doi:10.3390/biom10040572 · Cited by 35
Expression of progesterone and oestrogen receptors by early intrauterine equine conceptuses
Rambags, B. P. B., van Tol, H. T. A., van den Eng, M. M., Colenbrander, B., & Stout, T. A. E. (2007) · Theriogenology · doi:10.1016/j.theriogenology.2007.10.011 · Cited by 35
PELP1: A novel therapeutic target for hormonal cancers
Chakravarty, D., TEKMAL, R. R., & Vadlamudi, R. K. (2009) · IUBMB Life · doi:10.1002/iub.287 · Cited by 35
Suppression of progesterone-enhanced hyperactivation in hamster spermatozoa by estrogen
Fujinoki, M. (2010) · Reproduction · doi:10.1530/rep-10-0168 · Cited by 35
Examining the spatio-temporal expression of mRNA encoding the membrane-bound progesterone receptor-alpha isoform in human cervix and myometrium during pregnancy and labour
Chapman, N., Kennelly, M., Harper, K., Europe‐Finner, G. N., & Robson, S. C. (2006) · Molecular Human Reproduction · doi:10.1093/molehr/gah248 · Cited by 35
Growth Factor Regulation of Estrogen Receptor Coregulator PELP1 Functions via Protein Kinase A Pathway
Nagpal, J. K., Nair, S. S., Chakravarty, D., Rajhans, R., Saikumar, P., Brann, D. W., TEKMAL, R. R., & Vadlamudi, R. K. (2008) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-07-2030 · Cited by 35
A novel gene family in Arabidopsis encoding putative heptahelical transmembrane proteins homologous to human adiponectin receptors and progestin receptors
Hsieh, M., & Goodman, H. M. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri311 · Cited by 35
3-Tesla High-Field Magnetic Resonance Neurography for Guiding Nerve Blocks and Its Role in Pain Management
Fritz, J. M., Dellon, A. L., Williams, E. H., Belzberg, A. J., & Carrino, J. A. (2015) · Magnetic Resonance Imaging Clinics of North America · doi:10.1016/j.mric.2015.05.010 · Cited by 34
Nuclear and Extra-Nuclear Effects of Retinoid Acid Receptors: How They Are Interconnected
Piskunov, A., Tanoury, Z. A., & Rochette‐Egly, C. (2014) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-017-9050-5_6 · Cited by 38
Sexual Dimorphism in Drug Metabolism and Pharmacokinetics
Valodara, A. M., & Johar, K. (2019) · Current Drug Metabolism · doi:10.2174/1389200220666191021094906 · Cited by 37
Effects of low dose treatment of tributyltin on the regulation of estrogen receptor functions in MCF-7 cells
Sharan, S., Nikhil, K., & Roy, P. (2013) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2013.03.009 · Cited by 34
Lipid Raft- and Protein Kinase C-mediated Synergism between Glucocorticoid- and Gonadotropin-releasing Hormone Signaling Results in Decreased Cell Proliferation
Wehmeyer, L., Toit, A. D., Lang, D. M., & Hapgood, J. P. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.544742 · Cited by 34
Mechanisms of Hormonal Regulation of Sertoli Cell Development and Proliferation: A Key Process for Spermatogenesis
Escott, G. M., da Rosa, L., & Loss, E. D. S. (2015) · Current Molecular Pharmacology · doi:10.2174/1874467208666150126155032 · Cited by 35
Testosterone inhibits bradykinin-induced intracellular calcium kinetics in rat aortic endothelial cells in culture
Rubio‐Gayosso, I., Garcia-Ramirez, O., Gutiérrez-Serdán, R., Guevara‐Balcázar, G., Muñoz-Garcı́a, O., Cartagena, T. M., Zamora-Garza, M., & Ceballos, G. M. (2002) · Steroids · doi:10.1016/s0039-128x(01)00192-1 · Cited by 34
Estrogen and Progestogen Correlates of the Structure of Female Copulation Calls in Semi-Free-Ranging Barbary Macaques (Macaca sylvanus)
Pfefferle, D., Heistermann, M., Pirow, R., Hodges, J. K., & Fischer, J. (2011) · International Journal of Primatology · doi:10.1007/s10764-011-9517-8 · Cited by 33
Non-genomic regulation and disruption of spermatozoal in vitro hyperactivation by oviductal hormones
Fujinoki, M., Takei, G. L., & Kon, H. (2015) · The Journal of Physiological Sciences · doi:10.1007/s12576-015-0419-y · Cited by 33
Innate Immune Modulation in Chronic Obstructive Pulmonary Disease: Moving Closer toward Vitamin D Therapy
Heulens, N., Korf, H., & Janssens, W. (2015) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.223032 · Cited by 33
Early Effects of Intravitreal Triamcinolone on Macular Edema
Miyamoto, N., Iossifov, D., Metge, F., & Béhar‐Cohen, F. (2006) · Ophthalmology · doi:10.1016/j.ophtha.2006.05.037 · Cited by 33
Retinoic Acid Stimulation of the Sodium/Iodide Symporter in MCF-7 Breast Cancer Cells Is Meditated by the Insulin Growth Factor-I/Phosphatidylinositol 3-Kinase and p38 Mitogen-Activated Protein Kinase Signaling Pathways
Kogai, T., Ohashi, E., Jacobs, M. S., Sajid-Crockett, S., Fisher, M., Kanamoto, Y., & Brent, G. A. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2007-1627 · Cited by 33
Differential expression and comparative subcellular localization of estrogen receptor beta isoforms in virally transformed and normal cultured human lens epithelial cells
Cammarata, P. R., Flynn, J. M., Gottipati, S., Chu, S., Dimitrijevich, S., Younes, M., Skliris, G. P., & Murphy, L. C. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2005.01.019 · Cited by 33
Ontogenic variations in the content and distribution of progesterone receptor isoforms in the reproductive tract and brain of chicks
Camacho‐Arroyo, I., González‐Arenas, A., & González‐Morán, M. G. (2006) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2006.04.023 · Cited by 33
Changes in Energy Metabolism Trigger Pupal Diapause Transition of Bactrocera minax After 20-Hydroxyecdysone Application
Dong, Y., Chen, Z.-Z., Clarke, A. R., & Niu, C.-Y. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01288 · Cited by 32
Role of estrogen receptor coregulators in endocrine resistant breast cancer
Altwegg, K. A., & Vadlamudi, R. K. (2021) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2021.00052 · Cited by 32
Testosterone treatment diminishes sickness behavior in male songbirds
Ashley, N. T., Hays, Q. R., Bentley, G. E., & Wingfield, J. C. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.04.003 · Cited by 32
Glucocorticoids in the treatment of neonatal meconium aspiration syndrome
Mokrá, D., & Mokrý, J. (2011) · European Journal of Pediatrics · doi:10.1007/s00431-011-1453-2 · Cited by 32
Regulation of leptin expression by 17beta-estradiol in human placental cells involves membrane associated estrogen receptor alpha
Gambino, Y. P., Pérez‐Pérez, A., Dueñas, J. L., Calvo, J. C., Sánchez‐Margalet, V., & Varone, C. L. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.01.015 · Cited by 32
Obesity and Postmenopausal Hormone Receptor-positive Breast Cancer: Epidemiology and Mechanisms
Zuo, Q., Band, S., Kesavadas, M. P., & Madak‐Erdogan, Z. (2021) · Endocrinology · doi:10.1210/endocr/bqab195 · Cited by 32
Membrane Progesterone Receptor Alpha as a Potential Prognostic Biomarker for Breast Cancer Survival: A Retrospective Study
Xie, M., Zhu, X., Liu, Z., Shrubsole, M. J., Varma, V. A., Mayer, I. A., Dai, Q., Chen, Q., & You, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035198 · Cited by 31
Genomic and non-genomic effects of dexamethasone on equine peripheral blood neutrophils
Lecoq, L., Vincent, P., Lavoie‐Lamoureux, A., & Lavoie, J. (2008) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2008.10.303 · Cited by 32
Glucocorticoids increase NPY gene expression in the arcuate nucleus by inhibiting mTOR signaling in rat hypothalamic organotypic cultures
Shimizu, H., Arima, H., Ozawa, Y., Watanabe, M., Banno, R., Sugimura, Y., Ozaki, N., Nagasaki, H., & Oiso, Y. (2009) · Peptides · doi:10.1016/j.peptides.2009.09.036 · Cited by 36
Comparing Expression of Progesterone and Estrogen Receptors in Testicular Tissue From Men With Obstructive and Nonobstructive Azoospermia
Han, Y., Feng, H. L., Sandlow, J. I., & Haines, C. J. (2009) · Journal of Andrology · doi:10.2164/jandrol.108.005157 · Cited by 32
Vitamin D in Chronic Kidney Disease: New Potential for Intervention
Mirković, K., van den Born, J., Navis, G. J., & de Borst, M. H. (2010) · Current Drug Targets · doi:10.2174/138945011793591572 · Cited by 32
Discovery of novel nuclear receptor modulating ligands: an integral role for peptide interaction profiling
Pearce, K. H., Iannone, M. A., Simmons, C. A., & Gray, J. G. (2004) · Drug Discovery Today · doi:10.1016/s1359-6446(04)03201-5 · Cited by 32
Mineralocorticoid receptor inhibits CREB signaling by calcineurin activation
Großmann, C., Wuttke, M., Ruhs, S., Seiferth, A., Mildenberger, S., Rabe, S., Schwerdt, G., & Gekle, M. (2010) · The FASEB Journal · doi:10.1096/fj.09-146985 · Cited by 31
The Unique Dopamine/Ecdysteroid Receptor Modulates Ethanol-Induced Sedation inDrosophila
Petruccelli, E., Li, Q., Rao, Y., & Kitamoto, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3774-15.2016 · Cited by 31
Estrogens and Androgens in Plants: The Last 20 Years of Studies
Janeczko, A. (2021) · Plants · doi:10.3390/plants10122783 · Cited by 31
17β-Estradiol rapidly mobilizes intracellular calcium from ryanodine-receptor-gated stores via a PKC–PKA–Erk-dependent pathway in the human eccrine sweat gland cell line NCL-SG3
Muchekehu, R. W., & Harvey, B. J. (2008) · Cell Calcium · doi:10.1016/j.ceca.2007.12.001 · Cited by 31
Transcriptional Analysis of Novel Hormone Receptors PGRMC1 and PGRMC2 as Potential Biomarkers of Breast Adenocarcinoma Staging
Causey, M. W., Huston, L. J., Harold, D. M., Charaba, C. J., Ippolito, D. L., Hoffer, Z. S., Brown, T. A., & Stallings, J. D. (2010) · Journal of Surgical Research · doi:10.1016/j.jss.2010.04.034 · Cited by 31
Mechanism of inhibition of mitochondrial ATP synthase by 17β−Estradiol
Moreno, A. J., Moreira, P. I., Custódio, J. B. A., & Santos, M. S. (2012) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-012-9497-1 · Cited by 31
Differential distribution of glucocorticoid and estrogen receptor isoforms: localization of GRbeta and ERalpha in nucleoli and GRalpha and ERbeta in the mitochondria of human osteosarcoma SaOS-2 and hepatocarcinoma HepG2 cell lines.
Solakidi, S., Psarra, A. G., & Sekeris, C. E. (2007) · PubMed · Cited by 31
Immune Cells, Gut Microbiota, and Vaccines: A Gender Perspective
Rio, P., Caldarelli, M., Chiantore, M., Ocarino, F., Candelli, M., Gasbarrini, A., Gambassi, G., & Cianci, R. (2024) · Cells · doi:10.3390/cells13060526 · Cited by 31
Potential Dissociative Glucocorticoid Receptor Activity for Protopanaxadiol and Protopanaxatriol
Karra, A. G., Konstantinou, M., Tzortziou, M., Tsialtas, I., Kalousi, F. D., Garagounis, C., Hayes, J. M., & Psarra, A. G. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms20010094 · Cited by 30
Association of vitamin D 3 and its metabolites in patients with and without type 2 diabetes and their relationship to diabetes complications
Butler, A. E., Dargham, S. R., Latif, A., Mokhtar, H. R. B., Robay, A., Chidiac, O. M., Jayyousi, A., Suwaidi, J. M. S. A., Crystal, R. G., Khalil, C. A., et al. (2020) · Therapeutic Advances in Chronic Disease · doi:10.1177/2040622320924159 · Cited by 30
Anabolic Steroids in Fattening Food-Producing Animals—A Review
Skoupá, K., Šťastný, K., & Sládek, Z. (2022) · Animals · doi:10.3390/ani12162115 · Cited by 31
Rapid responses to thyroxine in the testis: Active protein synthesis-independent pathway
Menegaz, D., Zamoner, A., Royer, C., Leite, L. D., Bortolotto, Z. A., & Silva, F. R. M. B. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.11.019 · Cited by 30
Preoperative steroids for hearing preservation cochlear implantation: A review
Kuthubutheen, J., Smith, L., Hwang, E., & Lin, V. (2016) · Cochlear Implants International · doi:10.1080/14670100.2016.1148319 · Cited by 30
Membrane 5α-pregnane-3,20-dione (5αP) receptors in MCF-7 and MCF-10A breast cancer cells are up-regulated by estradiol and 5αP and down-regulated by the progesterone metabolites, 3α-dihydroprogesterone and 20α-dihydroprogesterone, with associated changes in cell proliferation and detachment
Pawlak, K. J., Zhang, G., & Wiebe, J. P. (2005) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2005.05.014 · Cited by 30
Membrane testosterone binding sites in prostate carcinoma as a potential new marker and therapeutic target: Study in paraffin tissue sections
Dambaki, C., Kogia, C., Kampa, M., Darivianaki, K., Nomikos, M. S., Anezinis, P., Theodoropoulos, P. A., Castanas, E., & Stathopoulos, E. N. (2005) · BMC Cancer · doi:10.1186/1471-2407-5-148 · Cited by 30
The opioid agonist ethylketocyclazocine reverts the rapid, non-genomic effects of membrane testosterone receptors in the human prostate LNCaP cell line
Kampa, M., Papakonstanti, E. A., Alexaki, V. I., Hatzoglou, A., Stournaras, C., & Castanas, E. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2003.11.027 · Cited by 30
Brassinosteroid Signal Transduction: A Mix of Conservation and Novelty
Peng, P., & Li, J. (2003) · Journal of Plant Growth Regulation · doi:10.1007/s00344-003-0059-y · Cited by 30
Rapid signaling of steroid hormones in the vertebrate nervous system
Sakamoto, H. (2011) · Frontiers in bioscience · doi:10.2741/3970 · Cited by 30
Retinoic acid-induced nNOS expression depends on a novel PI3K/Akt/DAX1 pathway in human TGW-nu-I neuroblastoma cells
Nagl, F., Schönhofer, K., Seidler, B., Mages, J., Allescher, H., Schmid, R. M., Schneider, G., & Saur, D. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00034.2009 · Cited by 29
Eosinophilia in cancer and its regulation by sex hormones
Artham, S., Chang, C., & McDonnell, D. P. (2022) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2022.11.002 · Cited by 29
Progesterone‐enhanced sperm hyperactivation through IP3–PKC and PKA signals
Fujinoki, M. (2012) · Reproductive Medicine and Biology · doi:10.1007/s12522-012-0137-6 · Cited by 29
Ionic involvement and kinase activity on the mechanism of nongenomic action of thyroid hormones on 45Ca2+ uptake in cerebral cortex from young rats
Zamoner, A., Royer, C., Barreto, K. P., Pessoa‐Pureur, R., & Silva, F. R. M. B. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.09.012 · Cited by 29
Stimulation of catecholamine synthesis through unique estrogen receptors in the bovine adrenomedullary plasma membrane by 17β-estradiol
Yanagihara, N., Liu, M., Toyohira, Y., Tsutsui, M., Ueno, S., Shinohara, Y., TAKAHASHI, K., & Tanaka, K. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.11.047 · Cited by 29
Oestrogen-mediated tyrosine phosphorylation of caveolin-1 and its effect on the oestrogen receptor localisation: An in vivo study
Kiss, A. L., Turi, Á., Müllner, N., Kovács, E., Botos, E., & Greger, A. (2005) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.11.005 · Cited by 29
Functional interactions between calmodulin and estrogen receptor-α
Li, L., & Sacks, D. B. (2006) · Cellular Signalling · doi:10.1016/j.cellsig.2006.08.018 · Cited by 28
Time course of behavioral, physiological, and morphological changes after estradiol treatment of ovariectomized rats
Graves, N. S., Hayes, H., Fan, L., & Curtis, K. S. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.02.017 · Cited by 28
PPARγ agonists negatively regulate αIIbβ3 integrin outside‐in signaling and platelet function through up‐regulation of protein kinase A activity
Unsworth, A. J., Kriek, N., Bye, A. P., Naran, K., Sage, T., Flora, G. D., & Gibbins, J. M. (2016) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.13578 · Cited by 28
Modeling Sex Differences in Anti-inflammatory Effects of Dexamethasone in Arthritic Rats
Song, D., DuBois, D. C., Almon, R. R., & Jusko, W. J. (2018) · Pharmaceutical Research · doi:10.1007/s11095-018-2483-5 · Cited by 28
Sweroside promotes osteoblastic differentiation and mineralization via interaction of membrane estrogen receptor-α and GPR30 mediated p38 signalling pathway on MC3T3-E1 cells
Wu, Q.-C., Tang, X., Dai, Z.-Q., Dai, Y., Xiao, H.-H., & Yao, X. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.153146 · Cited by 28
Androgen Receptor Function in Motor Neuron Survival and Degeneration
Cary, G. A., & Spada, A. R. L. (2008) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2008.03.002 · Cited by 28
Effect of formoterol/budesonide combination on arterial blood gases in patients with acute exacerbation of COPD
Cazzola, M., Noschese, P., Michele, F. D., D’Amato, M., & Matera, M. G. (2005) · Respiratory Medicine · doi:10.1016/j.rmed.2005.04.024 · Cited by 28
N‐terminal region of progesterone receptor B isoform in human spermatozoa
Shah, C., Modi, D. N., Sachdeva, G., Gadkar, S., D'Souza, S. J., & Puri, C. P. (2005) · International Journal of Andrology · doi:10.1111/j.1365-2605.2005.00566.x · Cited by 28
Rapid effects of 17β-estradiol on aggressive behavior in songbirds: Environmental and genetic influences
Heimovics, S. A., Merritt, J. R., Jalabert, C., Ma, C., Maney, D. L., & Soma, K. K. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.03.010 · Cited by 29
Mini-review: estrogen action in the uterus and insulin-like growth factor-I.
Moyano, P., & Rotwein, P. (2004) · Growth Hormone & IGF Research · doi:10.1016/j.ghir.2004.09.001 · Cited by 29
An Aryl Hydrocarbon Receptor Agonist Amplifies the Mitogenic Actions of Estradiol in Granulosa Cells: Evidence of Involvement of the Cognate Receptors1
Bussmann, U. A., Bussmann, L. E., & Barañao, J. L. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.043901 · Cited by 28
Reflections on the Diseases Linked to Mutations of the Androgen Receptor
Poletti, A., Negri‐Cesi, P., & Martini, L. (2005) · Endocrine · doi:10.1385/endo:28:3:243 · Cited by 28
Non‐genomic effects of androgens on isolated human vascular and nonvascular penile erectile tissue
Waldkirch, E., Ückert, S., Schultheiss, D., Geismar, U., Bruns, C., Scheller, F., Jonas, U., Becker, A. J., Stief, C. G., & Hedlund, P. (2008) · BJU International · doi:10.1111/j.1464-410x.2007.07182.x · Cited by 27
Hypovitaminosis D and frailty: Epiphenomenon or causal?
Wong, Y. Y., & Flicker, L. A. (2015) · Maturitas · doi:10.1016/j.maturitas.2015.07.027 · Cited by 27
Image-guided Sports Medicine and Musculoskeletal Tumor Interventions: A Patient-Centered Model
Dalili, D., Isaac, A., Rashidi, A., Åström, G., & Fritz, J. M. (2020) · Seminars in Musculoskeletal Radiology · doi:10.1055/s-0040-1710065 · Cited by 27
Crosstalk between the muscular estrogen receptor α and BDNF/TrkB signaling alleviates metabolic syndrome via 7,8-dihydroxyflavone in female mice
Zhao, Z., Fan, X., Gu, Y., Han, J., Jia, Y., Ye, K., & Zhang, Y. Q. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.101149 · Cited by 27
A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism
Wittkowski, K. M., Sonakya, V., Bigio, B., Tonn, M. K., Shic, F., Ascano, M., Nasca, C., & Simson, G. G. (2014) · Translational Psychiatry · doi:10.1038/tp.2013.124 · Cited by 26
Molecular Field Analysis and 3D-Quantitative Structure−Activity Relationship Study (MFA 3D-QSAR) Unveil Novel Features of Bile Acid Recognition at TGR5
Macchiarulo, A., Gioiello, A., Thomas, C., Massarotti, A., Nuti, R., Rosatelli, E., Sabbatini, P., Schoonjans, K., Auwerx, J. H., & Pellicciari, R. (2008) · Journal of Chemical Information and Modeling · doi:10.1021/ci800196h · Cited by 28
The mitogenic effect of testosterone and 17β-estradiol on airway smooth muscle cells
Stamatiou, R., Paraskeva, E., Papagianni, M., Molyvdas, P. A., & Hatziefthimiou, A. A. (2010) · Steroids · doi:10.1016/j.steroids.2010.12.010 · Cited by 27
Inositol triphosphate participates in an oestradiol nongenomic signalling pathway involved in accelerated oviductal transport in cycling rats
Orihuela, P. A., Parada‐Bustamante, A., Zúñiga, L. M., & Croxatto, H. B. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06448 · Cited by 27
Sex-Specific and Estrous Cycle-Dependent Antidepressant-Like Effects and Hippocampal Akt Signaling of Leptin
Carrier, N., Wang, X., Sun, L., & Lu, X. (2015) · Endocrinology · doi:10.1210/en.2015-1029 · Cited by 26
Four New Sulfated Polar Steroids from the Far Eastern Starfish Leptasterias ochotensis: Structures and Activities
Malyarenko, T. V., Malyarenko, O. S., Ivanchina, N. V., Kalinovsky, A. L., Popov, R. S., & Kicha, A. A. (2015) · Marine Drugs · doi:10.3390/md13074418 · Cited by 26
Voltage‐dependent K+ channel acts as sex steroid sensor in endocrine cells of the human ovary
Kunz, L., Rämsch, R., Krieger, A., Young, K. A., Dissen, G. A., Stouffer, R. L., Ojeda, S. R., & Mayerhofer, A. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20453 · Cited by 26
Testosterone and dihydrotestosterone inhibit gallbladder motility through multiple signalling pathways
Kline, L., & Karpinski, E. (2008) · Steroids · doi:10.1016/j.steroids.2008.05.006 · Cited by 25
Estrogen receptor beta interacts and colocalizes with HADHB in mitochondria
Zhou, Z., Zhou, J., & Du, Y. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.09.047 · Cited by 26
Increased expression of integrin-linked kinase during decidualization regulates the morphological transformation of endometrial stromal cells
Yen, C., Kim, S. H., Liao, S., Atabekoğlu, C. S., Erdin, S. U., Arici, A. M., Arlıer, S., Lee, C., Wang, H., & Kayisli, U. A. (2017) · Fertility and Sterility · doi:10.1016/j.fertnstert.2016.11.025 · Cited by 26
Emerging significance of ER-coregulator PELP1/MNAR in cancer.
Nair, S. S., & Vadlamudi, R. K. (2007) · PubMed · doi:10.14670/hh-22.91 · Cited by 26
p28, a truncated form of TRα1 regulates mitochondrial physiology
Pessemesse, L., Lepourry, L., Bouton, K., Levin, J. M., Cabello, G., Wrutniak‐Cabello, C., & Casas, F. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.09.026 · Cited by 23
Inhibition of ERα/ERK/P62 cascades induces “autophagic switch” in the estrogen receptor-positive breast cancer cells exposed to gemcitabine
Shen, P., Chen, M., He, M., Chen, L., Song, Y., Xiao, P., Wan, X., Dai, F., Pan, T. S., & Wang, Q. (2016) · Oncotarget · doi:10.18632/oncotarget.10363 · Cited by 25
Roles of Estrogens in the Healthy and Diseased Oviparous Vertebrate Liver
Tramunt, B., Montagner, A., Tan, N. S., Gourdy, P., Rémignon, H., & Wahli, W. (2021) · Metabolites · doi:10.3390/metabo11080502 · Cited by 27
Acute glucocorticoid effects on the multicomponent model of working memory
Vaz, L. J., Pradella‐Hallinan, M., Bueno, O. F. A., & Pompéia, S. (2011) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/hup.1230 · Cited by 25
ASAS Centennial Paper: Lactation biology for the twenty-first century
Loor, J. J., & Cohick, W. S. (2008) · Journal of Animal Science · doi:10.2527/jas.2008-1375 · Cited by 25
Rapid Inhibitory Effect of Corticosterone on Histamine Release from Rat Peritoneal Mast Cells
Liu, C., Zhou, J., Zhang, L.-D., Wang, Y.-X., Kang, Z.-M., Chen, Y.-Z., & Jiang, C. (2007) · Hormone and Metabolic Research · doi:10.1055/s-2007-973809 · Cited by 25
Amplification of neuromuscular transmission by methylprednisolone involves activation of presynaptic facilitatory adenosine A2A receptors and redistribution of synaptic vesicles
Oliveira, L., Costa, A., Noronha‐Matos, J. B., da Silva, I. C. B., Cavalcante, W. L. G., Timóteo, M. A., Corrado, A. P., Belo, C. A. D., Ambiel, C. R., Alves‐Do‐Prado, W., et al. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.004 · Cited by 25
Commitment of human pluripotent stem cells to a neural lineage is induced by the pro-estrogenic flavonoid apigenin
Souza, C. D. S., Paulsen, B. S., Devalle, S., Costa, S. L., Borges, H. L., & Rehen, S. K. (2015) · Advances in Regenerative Biology · doi:10.3402/arb.v2.29244 · Cited by 25
The Nuclear Receptor DHR3 Modulates dS6 Kinase–Dependent Growth in Drosophila
Montagne, J., Lecerf, C., Parvy, J.-P., Callister, J. B., Radimerski, T., Ruhf, M.-L., Zilbermann, F., Vouilloz, N., Stocker, H., Hafen, E., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000937 · Cited by 27
Dexamethasone stimulates store-operated calcium entry and protein degradation in cultured L6 myotubes through a phospholipase A2-dependent mechanism
Itagaki, K., Menconi, M. J., Antoniu, B. A., Zhang, Q., GONNELLA, P. A., Soybel, D. I., Hauser, C. J., & Hasselgren, P. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00309.2009 · Cited by 24
Nongenomic effects of progesterone on the contraction of muscle cells from the guinea pig colon
Xiao, Z.-L., Cao, W., Biancani, P., & Behar, J. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00382.2005 · Cited by 25
Noradrenergic–glucocorticoid mechanisms in emotion-induced amnesia: from adaptation to disease
Hurlemann, R. (2007) · Psychopharmacology · doi:10.1007/s00213-007-1002-x · Cited by 26
Ca2+ but not H2O2 modulates GRE-element activation by the human mineralocorticoid receptor in HEK cells
Pfau, A. C., Großmann, C., Freudinger, R., Mildenberger, S., Benesic, A., & Gekle, M. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2006.10.002 · Cited by 24
Steroid hormones of the octopus self-destruct system
Wang, Z. Y., Pergande, M. R., Ragsdale, C. W., & Cologna, S. M. (2022) · Current Biology · doi:10.1016/j.cub.2022.04.043 · Cited by 24
Role of Estrogen Receptor-α in the Regulation of Claudin-6 Expression in Breast Cancer Cells
Liu, Y., Wu, Q., Ren, Y., Xu, X., Lina, Y., Zhang, M., Ting, Z., Yu-lin, L., & Quan, C. (2011) · Journal of Breast Cancer · doi:10.4048/jbc.2011.14.1.20 · Cited by 24

Authors: Lösel, R., & Wehling, M.
Affiliations: Heidelberg University (DE)
Corresponding author: Wehling, Martin
ORCID: Lösel, Ralf
Venue: Nature Reviews Molecular Cell Biology
Publisher: Springer Science and Business Media LLC
Published: 2003-01
Volume: 4
Issue: 1
Pages: 46-55
ISSN: 1471-0072 (ISSN-L)
1471-0080
DOI: 10.1038/nrm1009
OpenAlex: W2029032935
Cited by: 980
References: 124
Citations by year: 2026: 21 · 2025: 17 · 2024: 28 · 2023: 31 · 2022: 36 · 2021: 35 · 2020: 26 · 2019: 32 · 2018: 24 · 2017: 39 · 2016: 34 · 2015: 45 · 2014: 42 · 2013: 36 · 2012: 37
FWCI: 6.04
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature Reviews Molecular Cell Biology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Keywords: non-genomic steroid action, steroid hormones, steroid receptor signaling
MeSH terms: Animals, Cell Communication, Gene Expression Regulation, Humans, Receptors, Steroid, Steroids, Signal Transduction

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Nongenomic actions of steroid hormones

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks