The NR4A subfamily of nuclear receptors: Potential new therapeutic targets for the treatment of inflammatory diseases
Open accessAbstract
INTRODUCTION: Prolonged inflammatory response contributes to the pathogenesis of chronic disease-related disturbances. Among nuclear receptors (NRs), the orphan NR4A subfamily, which includes Nur77 (NR4A1), Nurr1 (NR4A2) and NOR1 (NR4A3), has recently emerged as a therapeutic target for the treatment of inflammation. Areas covered: This review focuses on the capacity of NR4A receptors to counter-regulate the development of the inflammatory response, with a special focus on the molecular transrepression mechanisms. Expert opinion: Recent studies have highlighted the role of NR4A receptors as significant regulators of the inflammatory response. NR4A receptors are rapidly induced by inflammatory stimuli, thus suggesting that they are required for the initiation of inflammation. Nevertheless, NR4A anti-inflammatory properties indicate that this acute regulation could be a protective reaction aimed at resolving inflammation in the later stages. Therefore, NR4A receptors are involved in a negative feedback mechanism to maintain the inflammatory balance. However, the underlying mechanisms are not entirely clear. Only a small number of NR4A-target genes have been identified, and the transcriptional repression mechanisms are only beginning to emerge. Despite further research is needed to fully understand the role of NR4A receptors in inflammation, these NRs should be considered as targets for new therapeutic approaches to inflammatory diseases.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
Transcriptome revealed decreased expression of NR4A nuclear receptors (NR4A1, NR4A2, NR4A3) in hEDS/HSD cells.
“As further evidence of unbalanced inflammatory responses in patients’ cells, transcriptome revealed a decreased expression of the NR4A nuclear receptors (NR4A1, NR4A2, NR4A3), which act as transcriptional regulators of inflammatory responses mediated by NF-kB signaling [159,160,161].”
From Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes (2019) · cites this paper as [159]
NR4A nuclear receptors attenuate inflammatory events through inhibition of NF-kB nuclear translocation and induction of NFKBIA expression.
“These receptors attenuate inflammatory events through inhibition of the NF-kB nuclear translocation and induction of the expression of its inhibitor NFKBIA, which, in turn, blocks the NF-kB nuclear localizing sequence [159].”
From Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes (2019) · cites this paper as [159]
Cites
The nuclear receptor superfamily: the second decade
Mangelsdorf, D. J., Thummel, C., Beato, M., Herrlich, P., Schütz, G., Umesono, K., Blumberg, B., Kastner, P., Mark, M., Chambon, P., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90199-x · Cited by 6,964 · see citing works
Shared Principles in NF-κB Signaling
Hayden, M. S., & Ghosh, S. (2008) · Cell · doi:10.1016/j.cell.2008.01.020 · Cited by 4,814 · see citing works
Hayden, M. S., & Ghosh, S. (2004) · Genes & Development · doi:10.1101/gad.1228704 · Cited by 3,842 · see citing works
Missing Pieces in the NF-κB Puzzle
Ghosh, S., & Karin, M. (2002) · Cell · doi:10.1016/s0092-8674(02)00703-1 · Cited by 3,638 · see citing works
AP-1 as a regulator of cell life and death
Shaulian, E., & Karin, M. (2002) · Nature Cell Biology · doi:10.1038/ncb0502-e131 · Cited by 2,961 · see citing works
The NF- B Family of Transcription Factors and Its RegulationPreprint
Oeckinghaus, A., & Ghosh, S. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000034 · Cited by 2,850 · see citing works
A cytokine-responsive IκB kinase that activates the transcription factor NF-κB
DiDonato, J. A., Hayakawa, M., Rothwarf, D. M., Zandi, E., & Karin, M. (1997) · Nature · doi:10.1038/41493 · Cited by 2,125 · see citing works
Nuclear Receptors and Lipid Physiology: Opening the X-Files
Chawla, A., Repa, J. J., Evans, R. M., & Mangelsdorf, D. J. (2001) · Science · doi:10.1126/science.294.5548.1866 · Cited by 2,085 · see citing works
IKK-1 and IKK-2: Cytokine-Activated IκB Kinases Essential for NF-κB Activation
Mercurio, F., Zhu, H., Murray, B. W., Shevchenko, A., Bennett, B. L., Li, J. W., Young, D. B., Barbosa, M. S., Mann, M., Manning, A. M., et al. (1997) · Science · doi:10.1126/science.278.5339.860 · Cited by 2,042 · see citing works
Zandi, E., Rothwarf, D. M., Delhase, M., Hayakawa, M., & Karin, M. (1997) · Cell · doi:10.1016/s0092-8674(00)80406-7 · Cited by 1,814 · see citing works
Nuclear Hormone Receptors and Gene Expression
Aranda, A., & Pascual, A. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.3.1269 · Cited by 1,562 · see citing works
AP-1 subunits: quarrel and harmony among siblings
Heß, J., Angel, P. E., & Schorpp‐Kistner, M. (2004) · Journal of Cell Science · doi:10.1242/jcs.01589 · Cited by 1,305 · see citing works
Involvement of linear polyubiquitylation of NEMO in NF-κB activation
Tokunaga, F., Sakata, S., Saeki, Y., Satomi, Y., Kirisako, T., Kamei, K., Nakagawa, T., Kato, M., Murata, S., Yamaoka, S., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1821 · Cited by 943 · see citing works
How NF-κB is activated: the role of the IκB kinase (IKK) complex
Karin, M. (1999) · Oncogene · doi:10.1038/sj.onc.1203219 · Cited by 935 · see citing works
Saijo, K., Winner, B., Carson, C. T., Collier, J. G., Boyer, L., Rosenfeld, M. G., Gage, F. H., & Glass, C. K. (2009) · Cell · doi:10.1016/j.cell.2009.01.038 · Cited by 859 · see citing works
Orphan Nuclear Receptors: From Gene to Function
Giguère, V. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.5.0378 · Cited by 848 · see citing works
Acetylation of RelA at discrete sites regulates distinct nuclear functions of NF‐κB
Chen, L., Mu, Y., & Greene, W. C. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf660 · Cited by 827 · see citing works
Mapping of the Inducible IκB Phosphorylation Sites That Signal Its Ubiquitination and Degradation†
Didonato, J., Mercurio, F., Rosette, C., Wu-Li, J., Suyang, H., Ghosh, S., & Karin, M. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.4.1295 · Cited by 707 · see citing works
Standiford, T. J., Kunkel, S. L., Aseem Basha, M., Chensue, S. W., Lynch, J. P., Toews, G. B., Westwick, J. K., & Strieter, R. M. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114928 · Cited by 687 · see citing works
Perkins, N. D. (2006) · Oncogene · doi:10.1038/sj.onc.1209937 · Cited by 674 · see citing works
Nerve growth factor induces a gene homologous to the glucocorticoid receptor gene
Milbrandt, J. (1988) · Neuron · doi:10.1016/0896-6273(88)90138-9 · Cited by 661 · see citing works
Hanna, R. N., Carlin, L. M., Hubbeling, H. G., Nackiewicz, D., Green, A. M., Punt, J. A., Geissmann, F., & Hedrick, C. C. (2011) · Nature Immunology · doi:10.1038/ni.2063 · Cited by 639 · see citing works
Nuclear receptor transrepression pathways that regulate inflammation in macrophages and T cells
Glass, C. K., & Saijo, K. (2010) · Nature Reviews Immunology · doi:10.1038/nri2748 · Cited by 619 · see citing works
The interleukin‐1 receptor/Toll‐like receptor superfamily: 10 years of progress
O'Neill, L. A. J. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00701.x · Cited by 612 · see citing works
Structure and function of Nurr1 identifies a class of ligand-independent nuclear receptors
Wang, Z., Benoit, G., Liu, J., Prasad, S., Aarnisalo, P., Liu, X., Xu, H., Walker, N. P. C., & Perlmann, T. (2003) · Nature · doi:10.1038/nature01645 · Cited by 583 · see citing works
Identification of the DNA Binding Site for NGFI-B by Genetic Selection in Yeast
Wilson, T. E., Fahrner, T. J., Johnston, M., & Milbrandt, J. (1991) · Science · doi:10.1126/science.1925541 · Cited by 557 · see citing works
Hilgendorf, I., Gerhardt, L. M. S., Tan, T. C., Winter, C., Holderried, T. A. W., Chousterman, B. G., Iwamoto, Y., Liao, R., Zirlik, A., Scherrer‐Crosbie, M., et al. (2014) · Circulation Research · doi:10.1161/circresaha.114.303204 · Cited by 549 · see citing works
A novel pathway for vitamin A signaling mediated by RXR heterodimerization with NGFI-B and NURR1.Preprint
Perlmann, T., & Jansson, L. E. (1995) · Genes & Development · doi:10.1101/gad.9.7.769 · Cited by 548 · see citing works
Fos/AP‐1 proteins in bone and the immune system
Wagner, E. F., & Eferl, R. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00332.x · Cited by 537 · see citing works
Post-activation Turn-off of NF-κB-dependent Transcription Is Regulated by Acetylation of p65
Kiernan, R. E., Brès, V., Ng, R. W. M., Coudart, M.-P., Messaoudi, S. E., Sardet, C., Jin, D., Emiliani, S., & Benkirane, M. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209572200 · Cited by 536 · see citing works
Distinct roles of Jun : Fos and Jun : ATF dimers in oncogenesis
van Dam, H., & Castellazzi, M. (2001) · Oncogene · doi:10.1038/sj.onc.1204239 · Cited by 462 · see citing works
Hanna, R. N., Shaked, I., Hubbeling, H., Punt, J. A., Wu, R., Herrley, E., Zaugg, C., Pei, H., Geissmann, F., Ley, K. F., et al. (2011) · Circulation Research · doi:10.1161/circresaha.111.253377 · Cited by 449 · see citing works
The NR4A Subgroup: Immediate Early Response Genes with Pleiotropic Physiological Roles
Maxwell, M., & Muscat, G. E. O. (2006) · Nuclear Receptor Signaling · doi:10.1621/nrs.04002 · Cited by 447 · see citing works
TLR-4, IL-1R and TNF-R signaling to NF-κB: variations on a common theme
Verstrepen, L., Bekaert, T., Chau, T., Tavernier, J. H., Chariot, A., & Beyaert, R. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8064-8 · Cited by 440 · see citing works
NF-κB RelA Phosphorylation Regulates RelA Acetylation
Chen, L.-F., Williams, S. A., Mu, Y., Nakano, H., Duerr, J. M., Buckbinder, L., & Greene, W. C. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.18.7966-7975.2005 · Cited by 438 · see citing works
Identification of a new brain-specific transcription factor, NURR1
Law, S. W. T., Conneely, O. M., DeMayo, F. J., & O’Malley, B. W. (1992) · Molecular Endocrinology · doi:10.1210/mend.6.12.1491694 · Cited by 399 · see citing works
Novel Dimeric Nur77 Signaling Mechanism in Endocrine and Lymphoid Cells
Philips, A., Lesage, S., Gingras, R., Maira, M., Gauthier, Y., Hugo, P., & Drouin, J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.10.5946 · Cited by 369 · see citing works
Cytosporone B is an agonist for nuclear orphan receptor Nur77
Zhan, Y.-Y., Du, X., Chen, H., Liu, J., Zhao, B., Huang, D., Li, G., Xu, Q., Zhang, M., Weimer, B. C., et al. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.106 · Cited by 361 · see citing works
Activator protein 1 (Fos/Jun) functions in inflammatory bone and skin disease
Zenz, R., Eferl, R., Scheinecker, C., Redlich, K., Smolen, J. S., Schönthaler, H. B., Kenner, L., Tschachler, E., & Wagner, E. F. (2007) · Arthritis Research & Therapy · doi:10.1186/ar2338 · Cited by 353 · see citing works
Hong, C. Y., Park, J. H., Ahn, R. S., Im, S., Choi, H., Soh, J., Mellon, S. H., & Lee, K. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.7.2593-2604.2004 · Cited by 322 · see citing works
NR4A orphan nuclear receptors are transcriptional regulators of hepatic glucose metabolism
Pei, L., Waki, H., Vaitheesvaran, B., Wilpitz, D. C., Kurland, I. J., & Tontonoz, P. (2006) · Nature Medicine · doi:10.1038/nm1471 · Cited by 319 · see citing works
Nr4a receptors are essential for thymic regulatory T cell development and immune homeostasis
Sekiya, T., Kashiwagi, I., Yoshida, R., Fukaya, T., Morita, R., Kimura, A., Ichinose, H., METZGER, D., Chambon, P., & Yoshimura, A. (2013) · Nature Immunology · doi:10.1038/ni.2520 · Cited by 314 · see citing works
Minireview: Nuclear Hormone Receptor 4A Signaling: Implications for Metabolic Disease
Pearen, M. A., & Muscat, G. E. O. (2010) · Molecular Endocrinology · doi:10.1210/me.2010-0015 · Cited by 308 · see citing works
Beck, I. M. E., Vanden Berghe, W., Vermeulen, L., Yamamoto, K. R., Haegeman, G., & De Bosscher, K. (2009) · Endocrine Reviews · doi:10.1210/er.2009-0013 · Cited by 298 · see citing works
Pei, L., Castrillo, A., Chen, M., Hoffmann, A., & Tontonoz, P. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502606200 · Cited by 282 · see citing works
Beyond IκBs: alternative regulation of NF‐KB activity
Neumann, M., & Naumann, M. (2007) · The FASEB Journal · doi:10.1096/fj.06-7615rev · Cited by 267 · see citing works
Bonta, P. I., van Tiel, C. M., Vos, M., Pols, T. W. H., van Thienen, J. V., Ferreira, V., Arkenbout, E. K., Seppen, J., Spek, C. A., van der Poll, T., et al. (2006) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000238346.84458.5d · Cited by 248 · see citing works
Zetterström, R. H., Solomin, L., Mitsiadis, T. A., Olson, L., & Perlmann, T. (1996) · Molecular Endocrinology · doi:10.1210/mend.10.12.8961274 · Cited by 246 · see citing works
Orphan nuclear receptor TR3 acts in autophagic cell death via mitochondrial signaling pathway
Wang, W.-J., Wang, Y., Chen, H., Xing, Y.-Z., Li, F.-W., Zhang, Q., Zhou, B., Zhang, H., Zhang, J., Bian, X., et al. (2013) · Nature Chemical Biology · doi:10.1038/nchembio.1406 · Cited by 245 · see citing works
The Drosophila Orphan Nuclear Receptor DHR38 Mediates an Atypical Ecdysteroid Signaling Pathway
Baker, K. D., Shewchuk, L. M., Kozlova, T., Makishima, M., Hassell, A. M., Wisely, B., Caravella, J. A., Lambert, M. H., Reinking, J. L., Krause, H. M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00420-3 · Cited by 238 · see citing works
Epithelial cells as regulators of airway inflammation
Polito, A. J., & Proud, D. M. (1998) · Journal of Allergy and Clinical Immunology · doi:10.1016/s0091-6749(98)70008-9 · Cited by 236 · see citing works
Nuclear receptors versus inflammation: mechanisms of transrepression
Pascual, G., & Glass, C. K. (2006) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2006.08.005 · Cited by 225 · see citing works
A Short Nur77-Derived Peptide Converts Bcl-2 from a Protector to a Killer
Kolluri, S. K., Zhu, X., Zhou, X., Lin, B., Chen, Y., Sun, K., Tian, X., Town, J. A., Cao, X., Lin, F., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.09.002 · Cited by 217 · see citing works
Role of I Bα Ubiquitination in Signal-induced Activation of NF- B in Vivo
Roff, M. A., Thompson, J., Rodríguez, M. S., Jacqué, J.-M., Baleux, F., Arenzana‐Seisdedos, F., & Hay, R. T. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.13.7844 · Cited by 215 · see citing works
Eychène, A., Rocques, N., & Pouponnot, C. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2460 · Cited by 214 · see citing works
Regulation of Macrophage Inflammatory Gene Expression by the Orphan Nuclear Receptor Nur77
Pei, L., Castrillo, A., & Tontonoz, P. (2005) · Molecular Endocrinology · doi:10.1210/me.2005-0331 · Cited by 207 · see citing works
Ohkura, N., Hijikuro, M., Yamamoto, A., & Miki, K. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.2900 · Cited by 186 · see citing works
Bone Marrow–Specific Deficiency of Nuclear Receptor Nur77 Enhances Atherosclerosis
Hamers, A. A. J., Vos, M., Rassam, F., Marinković, G., Kurakula, K., van Gorp, P. J., de Winther, M. P. J., Gijbels, M. J., de Waard, V., & de Vries, C. J. M. (2011) · Circulation Research · doi:10.1161/circresaha.111.260760 · Cited by 180 · see citing works
The orphan nuclear receptor Nur77 regulates LKB1 localization and activates AMPK
Zhan, Y.-Y., Chen, Y., Zhang, Q., Zhuang, J.-J., Tian, M., Chen, H.-Z., Zhang, L.-R., Zhang, H.-K., He, J.-P., Wang, W.-J., et al. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.1069 · Cited by 180 · see citing works
Akt phosphorylates and regulates the orphan nuclear receptor Nur77
Pekarsky, Y., Hallas, C., Palamarchuk, A., Koval, A. P., Bullrich, F., Hirata, Y., Bichi, R., Letofsky, J., & Croce, C. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051003198 · Cited by 177 · see citing works
Impeding the interaction between Nur77 and p38 reduces LPS-induced inflammation
Li, L., Liu, Y., Chen, H., Li, F.-W., Wu, J., Zhang, H.-K., He, J., Xing, Y.-Z., Chen, Y., Wang, W.-J., et al. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1788 · Cited by 176 · see citing works
Lee, S., Abdelrahim, M., Yoon, K., Chintharlapalli, S. R., Papineni, S., Kim, K., Wang, H., & Safe, S. H. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-1992 · Cited by 171 · see citing works
NR4A orphan nuclear receptors as mediators of CREB-dependent neuroprotection
Volakakis, N., Kadkhodaei, B., Joodmardi, E., Wallis, K., Panman, L., Silvaggi, J., Spiegelman, B. M., & Perlmann, T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007088107 · Cited by 167 · see citing works
Vascular Endothelial Growth Factor–Regulated Gene Expression in Endothelial Cells
Liu, D., Jia, H., Holmes, D. I. R., Stannard, A. K., & Zachary, I. C. (2003) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000098644.03153.6f · Cited by 167 · see citing works
Martínez‐González, J., & Badimón, L. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.10.002 · Cited by 167 · see citing works
Paclitaxel Directly Binds to Bcl-2 and Functionally Mimics Activity of Nur77
Ferlini, C., Cicchillitti, L., Raspaglio, G., Bartollino, S., Cimitan, S., Bertucci, C., Mozzetti, S., Gallo, D., Persico, M., Fattorusso, C., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0540 · Cited by 166 · see citing works
Zeng, H., Qin, L., Zhao, D., Tan, X., Manseau, E. J., Hoang, M. V., Senger, D. R., Brown, L. F., Nagy, J. A., & Dvorak, H. F. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20051523 · Cited by 163 · see citing works
Fibroblast biology. Effector signals released by the synovial fibroblast in arthritis.
Ritchlin, C. T. (2000) · Arthritis Research · doi:10.1186/ar112 · Cited by 158 · see citing works
Wansa, K. D. S. A., Harris, J. M., Yan, G., Ordentlich, P., & Muscat, G. E. O. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300088200 · Cited by 155 · see citing works
Insulin resistance and altered systemic glucose metabolism in mice lacking Nur77
Chao, L. C., Wroblewski, K., Zhang, Z., Pei, L., Vergnes, L., Ilkayeva, O. R., Ding, S. Y., Reue, K., Watt, M. J., Newgard, C. B., et al. (2009) · Diabetes · doi:10.2337/db09-0763 · Cited by 154 · see citing works
NR4A nuclear receptors are orphans but not lonesome
Kurakula, K., Koenis, D. S., van Tiel, C. M., & de Vries, C. J. M. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2014.06.010 · Cited by 153 · see citing works
Minireview: Role Of Orphan Nuclear Receptors in Cancer and Potential as Drug Targets
Safe, S. H., Jin, U.-H., Hedrick, E., Reeder, A., & Lee, S. (2013) · Molecular Endocrinology · doi:10.1210/me.2013-1291 · Cited by 153 · see citing works
Akt Inhibits the Orphan Nuclear Receptor Nur77 and T-cell Apoptosis
Masuyama, N., Oishi, K., Mori, Y., Ueno, T., Takahama, Y., & Gotoh, Y. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105431200 · Cited by 151 · see citing works
Protective Function of Transcription Factor TR3 Orphan Receptor in Atherogenesis
Arkenbout, E. K., de Waard, V., van Bragt, M. P. A., van Achterberg, T. A. E., Grimbergen, J. M., Pichon, B., Pannekoek, H., & de Vries, C. J. M. (2002) · Circulation · doi:10.1161/01.cir.0000028811.03056.bf · Cited by 148 · see citing works
NR4A nuclear receptors support memory enhancement by histone deacetylase inhibitors
Hawk, J. D., Bookout, A. L., Poplawski, S. G., Bridi, M. S., Rao, A. J., Sulewski, M. E., Kroener, B., Manglesdorf, D. J., & Abel, T. G. (2012) · Journal of Clinical Investigation · doi:10.1172/jci64145 · Cited by 147 · see citing works
Wansa, K. D. S. A., Harris, J. M., & Muscat, G. E. O. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203572200 · Cited by 146 · see citing works
The NGFI-B subfamily of the nuclear receptor superfamily (review).
Maruyama, K., Tsukada, T., Ohkura, N., Bandoh, S., Hosono, T., & Yamaguchi, K. (1998) · International Journal of Oncology · doi:10.3892/ijo.12.6.1237 · Cited by 144 · see citing works
Nuclear Factor-κB Induction by Visfatin in Human Vascular Endothelial Cells
Adya, R., Tan, B. K., Chen, J., & Randeva, H. S. (2008) · Diabetes Care · doi:10.2337/dc07-1544 · Cited by 135 · see citing works
The role of NR4A transcription factors in memory formation
Hawk, J. D., & Abel, T. G. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.02.001 · Cited by 128 · see citing works
Neuron-Derived Orphan Receptor-1 (NOR-1) Modulates Vascular Smooth Muscle Cell Proliferation
Martínez‐González, J., Rius, J., Castelló, A., Cases-Langhoff, C., & Badimón, L. (2003) · Circulation Research · doi:10.1161/01.res.0000050921.53008.47 · Cited by 127 · see citing works
Nuclear receptor Nr4a1 modulates both regulatory T-cell (Treg) differentiation and clonal deletion
Fassett, M. S., Jiang, W., D'Alise, A. M., Mathis, D., & Benoist, C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200090109 · Cited by 126 · see citing works
You, B., Jiang, Y., Chen, S., Yan, G., & Sun, J. (2009) · Circulation Research · doi:10.1161/circresaha.108.192286 · Cited by 124 · see citing works
The nuclear receptor TR3 regulates mTORC1 signaling in lung cancer cells expressing wild-type p53
Lee, S.-O., Andey, T. A., Jin, U.-H., Kim, K., Sachdeva, M. S., & Safe, S. H. (2011) · Oncogene · doi:10.1038/onc.2011.504 · Cited by 122 · see citing works
Ms, R., Wright, J., Thompson, J., Thomas, D., Baleux, F., Virelizier, J. L., Hay, R. T., & Arenzana‐Seisdedos, F. (1996) · PubMed · Cited by 121 · see citing works
Ordentlich, P., Yan, Y. G., Zhou, S., & Heyman, R. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302167200 · Cited by 119 · see citing works
Prostaglandin E2 Regulates the Nuclear Receptor NR4A2 in Colorectal Cancer
Holla, V. R., Mann, J. R., Shi, Q., & DuBois, R. N. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507752200 · Cited by 118 · see citing works
McNulty, S. E., Barrett, R. M., Vogel-Ciernia, A., Malvaez, M., Hernandez, N., Davatolhagh, M. F., Matheos, D. P., Schiffman, A., & Wood, M. A. (2012) · Learning & Memory · doi:10.1101/lm.026385.112 · Cited by 117 · see citing works
Lee, S., Jin, U.-H., Kang, J. H., Kim, S. B., Guthrie, A. S., Sreevalsan, S., Lee, J., & Safe, S. H. (2014) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0567 · Cited by 109 · see citing works
A Unique Pharmacophore for Activation of the Nuclear Orphan Receptor Nur77 In vivo and In vitro
Liu, J., Zeng, H.-N., Zhang, L., Zhan, Y.-Y., Chen, Y., Wang, Y., Wang, J., Xiang, S., Liu, W.-J., Wang, W.-J., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-3160 · Cited by 105 · see citing works
Inamoto, T., Papineni, S., Chintharlapalli, S. R., Cho, S. D., Safe, S. H., & Kamat, A. M. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-08-0730 · Cited by 102 · see citing works
Mabb, A. M., & Miyamoto, S. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7005-2 · Cited by 100 · see citing works
Diindolylmethane Analogs Bind NR4A1 and Are NR4A1 Antagonists in Colon Cancer Cells
Lee, S., Li, X., Hedrick, E., Jin, U.-H., Tjalkens, R. B., Backos, D. S., Li, L., Zhang, Y., Wu, Q., & Safe, S. H. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1102 · Cited by 99 · see citing works
Nur77 and retinoid X receptors: crucial factors in dopamine-related neuroadaptation
Lévesque, D., & Rouillard, C. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.11.006 · Cited by 98 · see citing works
Грубер, Ф., Hufnagl, P., Hofer-Warbinek, R., Schmid, J. A., Breuss, J. M., Huber-Beckmann, R., Lucerna, M., Papac-Miličević, N., Harant, H., Lindley, I. J. D., et al. (2003) · Blood · doi:10.1182/blood-2002-07-2331 · Cited by 93 · see citing works
Doi, Y., Oki, S., Ozawa, T., Hohjoh, H., Miyake, S., & Yamamura, T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803454105 · Cited by 91 · see citing works
Mahajan, S., Saini, A., Chandra, V., Nanduri, R., Kalra, R., Bhagyaraj, E., Khatri, N., & Gupta, P. K. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.638064 · Cited by 90 · see citing works
Control of IκBα proteolysis by the ubiquitin-proteasome pathway
Tanaka, K., Kawakami, T., Tateishi, K., Yashiroda, H., & Chiba, T. (2001) · Biochimie · doi:10.1016/s0300-9084(01)01237-8 · Cited by 90 · see citing works
Deficiency of the NR4A Orphan Nuclear Receptor NOR1 Decreases Monocyte Adhesion and Atherosclerosis
Zhao, Y., Howatt, D. A., Gizard, F., Nomiyama, T., Findeisen, H. M., Heywood, E. B., Jones, K. L., Conneely, O. M., Daugherty, A., & Bruemmer, D. (2010) · Circulation Research · doi:10.1161/circresaha.110.222083 · Cited by 89 · see citing works
Nuclear Receptor NR4A2 Orchestrates Th17 Cell-Mediated Autoimmune Inflammation via IL-21 Signalling
Raveney, B. J. E., Oki, S., & Yamamura, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056595 · Cited by 88 · see citing works
The Nuclear Receptor Nr4a1 Mediates Anti-Inflammatory Effects of Apoptotic Cells
Ipseiz, N., Uderhardt, S., Scholtysek, C., Steffen, M., Schabbauer, G., Bözec, A., Schett, G. A., & Krönke, G. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303377 · Cited by 87 · see citing works
Colón, W. I., Martínez, M., Morales, S., Félix, J., Cruz, J., Adorno, M., Pereira, L., Colón, N., Maldonado-Vlaar, C. S., & de Ortı́z, S. P. (2006) · Learning & Memory · doi:10.1101/lm.407706 · Cited by 81 · see citing works
Activation of Nuclear Receptor Nur77 by 6-Mercaptopurine Protects Against Neointima Formation
Pires, N. M., Pols, T. W. H., de Vries, M. R., van Tiel, C. M., Bonta, P. I., Vos, M., Arkenbout, E. K., Pannekoek, H., Jukema, J. W., Quax, P. H. A., et al. (2007) · Circulation · doi:10.1161/circulationaha.106.626838 · Cited by 79 · see citing works
Prostaglandin A2 Acts as a Transactivator for NOR1 (NR4A3) within the Nuclear Receptor Superfamily
Kagaya, S., Ohkura, N., Tsukada, T., Miyagawa, M., Sugita, Y., Tsujimoto, G., Matsumoto, K., Saito, H., & Hashida, R. (2005) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.28.1603 · Cited by 78 · see citing works
Nomiyama, T., Zhao, Y., Gizard, F., Findeisen, H. M., Heywood, E. B., Jones, K. L., Conneely, O. M., & Bruemmer, D. (2009) · Circulation · doi:10.1161/circulationaha.108.822056 · Cited by 77 · see citing works
Miranda, B. R. D., Popichak, K. A., Hammond, S. L., Jorgensen, B. A., Phillips, A. T., Safe, S. H., & Tjalkens, R. B. (2015) · Molecular Pharmacology · doi:10.1124/mol.114.095398 · Cited by 76 · see citing works
Regulation of the Osteopontin Gene by the Orphan Nuclear Receptor NURR1 in Osteoblasts
Lammi, J., Huppunen, J., & Aarnisalo, P. (2004) · Molecular Endocrinology · doi:10.1210/me.2003-0247 · Cited by 76 · see citing works
Mix, K. S., Attur, M. G., Al-Mussawir, H., Abramson, S. B., Brinckerhoff, C., & Murphy, E. P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608327200 · Cited by 73 · see citing works
NR4A nuclear receptors in immunity and atherosclerosis
Hamers, A. A. J., Hanna, R. N., Nowyhed, H. N., Hedrick, C. C., & de Vries, C. J. M. (2013) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e3283643eac · Cited by 73 · see citing works
The NR4A orphan nuclear receptors: mediators in metabolism and diseases
Ranhotra, H. S. (2014) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2014.948555 · Cited by 71 · see citing works
NR4A nuclear orphan receptors: protective in vascular disease?
Pols, T. W. H., Bonta, P. I., & de Vries, C. J. M. (2007) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e3282ef77d1 · Cited by 70 · see citing works
Negative cross-talk between the human orphan nuclear receptor Nur77/NAK-1/TR3 and nuclear factor- B
Harant, H. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh856 · Cited by 69 · see citing works
PIASγ Represses the Transcriptional Activation Induced by the Nuclear Receptor Nurr1
Galleguillos, D., Vecchiola, A., Fuentealba, J. A., Ojeda, V., Álvarez, K., Gómez, A. V., & Andrés, M. E. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m308113200 · Cited by 68 · see citing works
NR4A1 Antagonists Inhibit β1-Integrin-Dependent Breast Cancer Cell Migration
Hedrick, E., Lee, S., Doddapaneni, R., Singh, M. S., & Safe, S. H. (2016) · Molecular and Cellular Biology · doi:10.1128/mcb.00912-15 · Cited by 67 · see citing works
de Waard, V., Arkenbout, E. K., Vos, M., Mocking, A. I. M., Niessen, H. W. M., Stooker, W., de Mol, B. A. J. M., Quax, P. H. A., Bakker, E. N. T. P., VanBavel, E., et al. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050932 · Cited by 63 · see citing works
Codina, A., Benoit, G., Gooch, J. T., Neuhaus, D., Perlmann, T., & Schwabe, J. W. R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409096200 · Cited by 63 · see citing works
NOR-1 is involved in VEGF-induced endothelial cell growth
Rius, J., Martínez‐González, J., Crespo, J., & Badimón, L. (2005) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2005.04.008 · Cited by 62 · see citing works
Aherne, C. M., McMorrow, J. P., Kane, D. J., FitzGerald, O., Mix, K. S., & Murphy, E. P. (2009) · Molecular Immunology · doi:10.1016/j.molimm.2009.07.019 · Cited by 60 · see citing works
NR4A Nuclear Receptors in Atherosclerosis and Vein-Graft Disease
Bonta, P. I., Pols, T. W. H., & de Vries, C. J. M. (2007) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2007.02.001 · Cited by 55 · see citing works
Wu, Y., Ghosh, S., Nishi, Y., Yanase, T., Nawata, H., & Hu, Y. (2004) · Endocrinology · doi:10.1210/en.2004-0889 · Cited by 54 · see citing works
Watanabe, T., Sekine, S., Naguro, I., Sekine, Y., & Ichijo, H. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.623280 · Cited by 53 · see citing works
Bonta, P. I., Pols, T. W. H., van Tiel, C. M., Vos, M., Arkenbout, E. K., Rohlena, J., Koch, K. T., de Maat, M. P. M., Tanck, M. W. T., de Winter, R. J., et al. (2010) · Circulation · doi:10.1161/circulationaha.109.885673 · Cited by 53 · see citing works
Crean, D., Cummins, E. P., Bahar, B., Mohan, H. M., McMorrow, J. P., & Murphy, E. P. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402039 · Cited by 52 · see citing works
Calvayrac, O., Rodríguez‐Calvo, R., Martí-Pàmies, Í., Alonso, J., Ferrán, B., Aguiló, S., Crespo, J., Rodríguez‐Sinovas, A., Rodrı́guez, C., & Martínez‐González, J. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.12.015 · Cited by 51 · see citing works
Self-citationHammond, S. L., Safe, S. H., & Tjalkens, R. B. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.09.015 · Cited by 51 · see citing works
Miranda, B. R. D., Popichak, K. A., Hammond, S. L., Miller, J. A., Safe, S. H., & Tjalkens, R. B. (2014) · Toxicological Sciences · doi:10.1093/toxsci/kfu236 · Cited by 50 · see citing works
Nur77 Decreases Atherosclerosis Progression in apoE−/− Mice Fed a High-Fat/High-Cholesterol Diet
Hu, Y., Zhang, P., Yang, J., Huang, J.-L., Ma, X., Li, S., Zhao, J., Hu, Y.-R., Wang, Y., Gao, J.-J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087313 · Cited by 50 · see citing works
Diatchenko, L. B., Romanov, S., Malinina, I. V., Clarke, J., Tchivilev, I., Li, X., & Makarov, S. S. (2005) · Journal of Leukocyte Biology · doi:10.1189/jlb.0405211 · Cited by 48 · see citing works
Shao, Q., Shen, L., Hu, L., Pu, J., Qi, M., Li, W.-Q., Tian, F., Jing, Q., & He, B. (2010) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2010.03.023 · Cited by 48 · see citing works
Rodríguez‐Calvo, R., Ferrán, B., Alonso, J., Martí-Pàmies, Í., Aguiló, S., Calvayrac, O., Rodrı́guez, C., & Martínez‐González, J. (2015) · Thrombosis and Haemostasis · doi:10.1160/th14-07-0645 · Cited by 47 · see citing works
Self-citationRodríguez‐Calvo, R., Guadall, A., Calvayrac, O., Navarro, M. A., Alonso, J., Ferrán, B., de Diego, A., Muniesa, P., Osada, J., Rodrı́guez, C., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt042 · Cited by 47 · see citing works
Self-citationOrphan Nuclear Receptor Nur77 Inhibits Cardiac Hypertrophic Response to Beta-Adrenergic Stimulation
Yan, G., Zhu, N., Huang, S., Yi, B., Shang, X., Chen, M., Wang, N., Zhang, G., Talarico, J. A., Tilley, D. G., et al. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00229-15 · Cited by 46 · see citing works
Kim, H., Kim, J., Lee, S. J., Kim, H.-J., Oh, C. J., Choi, Y., Lee, H., Do, J.-Y., Kim, S.-Y., Kwon, T., et al. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.212308 · Cited by 46 · see citing works
Mix, K. S., McMahon, K., McMorrow, J. P., Walkenhorst, D. E., Smyth, A. M., Petrella, B. L., Gogarty, M., Fearon, U., Veale, D. J., Attur, M. G., et al. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34399 · Cited by 44 · see citing works
Bonta, P. I., Matlung, H. L., Vos, M., Peters, S. L. M., Pannekoek, H., Bakker, E. N. T. P., & de Vries, C. J. M. (2010) · Cardiovascular Research · doi:10.1093/cvr/cvq064 · Cited by 44 · see citing works
Nowyhed, H. N., Huynh, T. R., Blatchley, A., Wu, R., Thomas, G. D., & Hedrick, C. C. (2015) · Scientific Reports · doi:10.1038/srep09059 · Cited by 42 · see citing works
O’Kane, M., Markham, T., McEvoy, A. N., Fearon, U., Veale, D. J., FitzGerald, O., Kirby, B., & Murphy, E. P. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701023 · Cited by 38 · see citing works
Nur77 mRNA levels and L-Dopa-induced dyskinesias in MPTP monkeys treated with docosahexaenoic acid
Mahmoudi, S., Samadi, P., Gilbert, F., Ouattara, B., Morissette, M., Grégoire, L., Rouillard, C., Paolo, T. D., & Lévesque, D. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.07.017 · Cited by 37 · see citing works
Eells, J. B., Wilcots, J., Sisk, S., & Guo‐Ross, S. X. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9642-z · Cited by 36 · see citing works
Mount, M. P., Zhang, Y., Amini, M., Callaghan, S. M., Kulczycki, J., Mao, Z., Slack, R. S., Anisman, H., & Park, D. S. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.439216 · Cited by 36 · see citing works
Carbone, D. L., Popichak, K. A., Moreno, J. A., Safe, S. H., & Tjalkens, R. B. (2008) · Molecular Pharmacology · doi:10.1124/mol.108.050781 · Cited by 36 · see citing works
NR4A orphan nuclear receptors in cardiovascular biology
Zhao, Y., & Bruemmer, D. (2009) · Drug Discovery Today Disease Mechanisms · doi:10.1016/j.ddmec.2009.06.001 · Cited by 33 · see citing works
McCoy, J. M., Walkenhorst, D. E., McCauley, K. S., Elaasar, H., Everett, J. R., & Mix, K. S. (2015) · Journal of Inflammation · doi:10.1186/s12950-015-0059-2 · Cited by 32 · see citing works
Oita, R. C., Mazzatti, D. J., Lim, F.-L., Powell, J. R., & Merry, B. J. (2008) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2008.12.004 · Cited by 30 · see citing works
Kim, Y. D., Kim, S., Hwang, S., Choi, H.-S., Bae, J., Song, D., & Im, S. (2014) · Diabetes · doi:10.2337/db13-1368 · Cited by 30 · see citing works
Chen, P., Li, J., Huo, Y., Lu, J., Wan, L., Li, B., Gan, R., & Guo, C. (2015) · PeerJ · doi:10.7717/peerj.1518 · Cited by 30 · see citing works
Nur77-mediated TRAF6 signalling protects against LPS-induced sepsis in mice
Li, X., Zhang, S., He, X., Guo, P.-D., Lu, X.-X., Wang, J., Li, J., & Wu, H. (2016) · Journal of Inflammation · doi:10.1186/s12950-016-0112-9 · Cited by 30 · see citing works
Alpha 1‐antichymotrypsin/SerpinA3 is a novel target of orphan nuclear receptor Nur77
Zhao, Y. J., Liu, Y., & Zheng, D. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06269.x · Cited by 25 · see citing works
NR4A1 enhances neural survival following oxygen and glucose deprivation: An in vitro study
Xiao, G., Sun, T., Songming, C., & Cao, Y. (2013) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2013.04.010 · Cited by 25 · see citing works
Schaffer, D. J., Tunc‐Ozcan, E., Shukla, P. K., Volenec, A., & Redei, E. E. (2010) · Brain Research · doi:10.1016/j.brainres.2010.09.041 · Cited by 24 · see citing works
St‐Hilaire, M., Bourhis, E., Lévesque, D., & Rouillard, C. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04954.x · Cited by 24 · see citing works
Zhang, X., Yan, G., Diao, Z., Sun, H., & Hu, Y. (2012) · Placenta · doi:10.1016/j.placenta.2012.04.005 · Cited by 24 · see citing works
Novak, G., Zai, C. C., Mirkhani, M., Shaikh, S., Vincent, J. B., Meltzer, H., Lieberman, J. A., Strauss, J., Lévesque, D., Kennedy, J. L., et al. (2010) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2010.00631.x · Cited by 23 · see citing works
Tjalkens, R. B., Liu, X., Mohl, B., Wright, T. T., Moreno, J. A., Carbone, D. L., & Safe, S. H. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21524 · Cited by 22 · see citing works
Xiang, B., Wang, W., Li, W., Li, X., Li, X., & Li, G. (2011) · Gene · doi:10.1016/j.gene.2011.11.039 · Cited by 20 · see citing works
Haloperidol-induced striatalNur77expression in a non-human primate model of tardive dyskinesia
Mahmoudi, S., Blanchet, P. J., & Lévesque, D. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12198 · Cited by 15 · see citing works
Rodríguez‐Calvo, R., Guadall, A., Calvayrac, O., Alonso, J., Ferrán, B., Martí-Pàmies, Í., Navarro, M. Á. M., de Diego, A., Osada, J., Rodrı́guez, C., et al. (2014) · Clínica e Investigación en Arteriosclerosis · doi:10.1016/j.arteri.2013.11.001 · Cited by 5 · see citing works
Self-citationExpression of host defense scavenger receptors in spondylarthropathy
McBeth (2001) · Pure Amsterdam UMC · doi:10.1002/1529-0131(200104)44:4 · Cited by 1 · see citing works
Straub, R. H., & Cutolo, M. (2001) · Arthritis & Rheumatism · doi:10.1002/1529-0131(200103)44:3
Flagged first, then by citations
Cited by
Sorted by citations
Toll-like receptors in immunity and inflammatory diseases: Past, present, and future
Kumar, V. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.03.002 · Cited by 649 · see citing works
Hepler, C., Shan, B., Zhang, Q., Henry, G. H., Shao, M., Vishvanath, L., Ghaben, A. L., Mobley, A. B., Strand, D., Hon, G. C., et al. (2018) · eLife · doi:10.7554/elife.39636 · Cited by 346 · see citing works
Kumar, V. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107087 · Cited by 276 · see citing works
Inducing Different Neuronal Subtypes from Astrocytes in the Injured Mouse Cerebral Cortex
Mattugini, N., Bocchi, R., Scheuss, V., Russo, G. L., Torper, O., Lao, C. L., & Götz, M. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.009 · Cited by 159 · see citing works
Radical-Scavenging and Subchondral Bone-Regenerating Nanomedicine for Osteoarthritis Treatment
Lu, H., Wei, J., Liu, K., Li, Z., Xu, T., Yang, D., Gao, Q., Xiang, H., Li, G., & Chen, Y. (2023) · ACS Nano · doi:10.1021/acsnano.3c01789 · Cited by 148 · see citing works
Li, S., Cai, Y., Guan, T., Zhang, Y., Huang, K., Zhang, Z., Cao, W., & Guan, X. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2374608 · Cited by 103 · see citing works
Peng, S., Chen, X.-H., Chen, S., Zhang, J., Wang, C.-Y., Liu, W.-R., Zhang, D., Su, Y., & Zhang, X.-K. (2021) · Nature Communications · doi:10.1038/s41467-021-26295-8 · Cited by 96 · see citing works
Chiarelli, N., Ritelli, M., Zoppi, N., & Colombi, M. (2019) · Genes · doi:10.3390/genes10080609 · Cited by 82 · see citing works
Therapeutic RNA Strategies for Chronic Obstructive Pulmonary Disease
Mei, D. F., Tan, W. S. D., Tay, Y., Mukhopadhyay, A., & Wong, W. S. F. (2020) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2020.04.007 · Cited by 59 · see citing works
The Orphan Nuclear Receptor 4A1: A Potential New Therapeutic Target for Metabolic Diseases
Zhang, L., Wang, Q., Liu, W., Liu, F., Ji, A., & Li, Y. (2018) · Journal of Diabetes Research · doi:10.1155/2018/9363461 · Cited by 54 · see citing works
Key Functions and Therapeutic Prospects of Nur77 in Inflammation Related Lung Diseases
Banno, A., Lakshmi, S. P., Reddy, A. T., Kim, S. C., & Reddy, R. C. (2019) · The American Journal of Pathology · doi:10.1016/j.ajpath.2018.10.002 · Cited by 53 · see citing works
Jeon, S. G., Yoo, A., Chun, D. W., Hong, S. B., Chung, H., Kim, J.-I., & Moon, M. (2020) · Aging and Disease · doi:10.14336/ad.2019.0718 · Cited by 55 · see citing works
Reactivation of NR4A1 Restrains Chondrocyte Inflammation and Ameliorates Osteoarthritis in Rats
Xiong, Y., Ran, J., Xu, L., Tong, Z., Moqbel, S. A. A., Ma, C., Xu, K., He, Y., Wu, Z., Chen, Z., et al. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00158 · Cited by 44 · see citing works
Age-associated changes in microglia and astrocytes ameliorate blood-brain barrier dysfunction
Pan, J., Ma, N., Zhong, J., Yu, B., Wan, J., & Zhang, W. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.08.030 · Cited by 42 · see citing works
Rauch, F., Geng, Y., Lamplugh, L., Hekmatnejad, B., Gaumond, M.-H., Penney, J. E., Yamanaka, Y., & Moffatt, P. (2017) · Bone · doi:10.1016/j.bone.2017.11.013 · Cited by 43 · see citing works
Wang, H., Yao, H., Yi, B., Kazama, K., Liu, Y., Deshpande, D. A., Zhang, J., & Sun, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26930 · Cited by 43 · see citing works
Jiang, Y. D., Feng, Y., Tang, L., Yan, Y.-L., & Bai, J. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.07.116 · Cited by 42 · see citing works
Chen, J., Jia, J., Ma, L., Li, B., Qin, Q., Qian, J., & Ge, J. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29877 · Cited by 40 · see citing works
Gao, Y., Zou, Y., Sokolowskei, D., Xing, X., Tower, R. J., Lai, Z., Shi, J., Zhu, L., Zheng, Q., James, A. W., et al. (2024) · Molecular Therapy · doi:10.1016/j.ymthe.2024.02.034 · Cited by 36 · see citing works
Chiu, H., Chu, C.-W., Huang, C., Chia, Z., Wang, Y.-L., & Lee, Y. (2025) · Environmental Pollution · doi:10.1016/j.envpol.2025.125850 · Cited by 37 · see citing works
Nuclear Receptors in Cancer Inflammation and Immunity
Zhao, L., Hu, H., Gustafsson, J.-Α., & Zhou, S. (2020) · Trends in Immunology · doi:10.1016/j.it.2019.12.006 · Cited by 36 · see citing works
Lakshmi, S. P., Reddy, A. T., Banno, A., & Reddy, R. C. (2019) · Biochemical Journal · doi:10.1042/bcj20190253 · Cited by 36 · see citing works
Song, H., Wu, H., Dong, J., Huang, S., Ye, J., & Liu, R. (2021) · Mediators of Inflammation · doi:10.1155/2021/6359652 · Cited by 33 · see citing works
Xu, S., Wei, W., Zhang, F., Chen, T., Dong, L., Shi, J., Wu, X., Zhang, T., Li, Z., Zhang, J., et al. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.881954 · Cited by 33 · see citing works
Targeting Orphan Nuclear Receptors NR4As for Energy Homeostasis and Diabetes
Zhang, C., Zhang, B., Zhang, X., Sun, G., & Sun, X. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.587457 · Cited by 32 · see citing works
The E3 ubiquitin ligase Trim13 regulates Nur77 stability via casein kinase 2α
Huang, B., Pei, H. Z., Chang, H., & Baek, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-32391-5 · Cited by 32 · see citing works
Tissue-Specific Control of Tissue-Resident Memory T Cells
Liu, Y., Ma, C., & Zhang, N. (2018) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2018025653 · Cited by 29 · see citing works
Yao, P., Parmar, V. M., Choudhary, M., & Malek, G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2202256119 · Cited by 31 · see citing works
Wang, W.-L., Kasamatsu, J., Joshita, S., Gilfillan, S., Luccia, B. D., Panda, S. K., Kim, D., Desai, P., Bando, J. K., Huang, S. C., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2204557119 · Cited by 29 · see citing works
Geng, N., Chen, T., Chen, L., Zhang, H., Sun, L., Lyu, Y., Che, X., Xiao, Q., Tao, Z., & Shao, Q. (2022) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2022.05.007 · Cited by 27 · see citing works
The effect of NR4A1 on APP metabolism and tau phosphorylation
Zhao, L., Tang, Y., Tan, J.-Z., Wang, J., Chen, G., & Zhu, B. (2018) · Genes & Diseases · doi:10.1016/j.gendis.2018.04.008 · Cited by 24 · see citing works
Phelan, D. E., Shigemura, M., Aldhafiri, S., Mota, C., Hall, T. J., Sznajder, J. I., Murphy, E. P., Crean, D., & Cummins, E. P. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.676644 · Cited by 24 · see citing works
Liu, T., Wen, H., Li, H., Xu, H., Xiao, N., Liu, R., Chen, L., Sun, Y., Song, L., Bai, C., et al. (2020) · Hypertension · doi:10.1161/hypertensionaha.119.14167 · Cited by 24 · see citing works
Yuan, R., Zhang, W., Nie, P., Lan, K., Yang, X., Yin, A., Xiao, Q., Shen, Y., Xu, K., Wang, X., et al. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/2017815 · Cited by 23 · see citing works
Minireview: What is Known about SUMOylation Among NR4A Family Members?
Dodat, F., Mader, S., & Lévesque, D. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167212 · Cited by 22 · see citing works
Jin, F., Li, X., Deng, Y., Timilshina, M., Huang, B., Kim, D. Y., Chang, J., Ichinose, H., Baek, S., Murakami, M., et al. (2018) · Allergy · doi:10.1111/all.13702 · Cited by 21 · see citing works
Fang, H., Zhang, J., Ao, M., He, F., Chen, W., Qian, Y., Zhang, Y., Xu, Y., & Fang, M. (2020) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2020.104456 · Cited by 20 · see citing works
Bladder Exposure to Gardnerella Activates Host Pathways Necessary for Escherichia coli Recurrent UTI
O'Brien, V. P., Lewis, A., & Gilbert, N. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.788229 · Cited by 20 · see citing works
Valsecchi, V., Boido, M., Montarolo, F., Guglielmotto, M., Perga, S., Martire, S., Cutrupi, S., Iannello, A., Gionchiglia, N., Signorino, E., et al. (2020) · Disease Models & Mechanisms · doi:10.1242/dmm.043513 · Cited by 19 · see citing works
Ma, Y., Chen, S., Jiang, F., Ma, R., & Wang, H. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16523 · Cited by 19 · see citing works
Yan, D., Hamed, O., Joshi, T., Mostafa, M., Jamieson, K. C., Joshi, R., Newton, R. C., & Giembycz, M. A. (2018) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.118.249292 · Cited by 19 · see citing works
NR4A1-3 nuclear receptor activity and immune cell dysregulation in rheumatic diseases
Murphy, E. P., & Crean, D. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.874182 · Cited by 18 · see citing works
Anti-inflammatory Effects of Siponimod in a Mouse Model of Excitotoxicity-Induced Retinal Injury
Basavarajappa, D. K., Gupta, V., Chitranshi, N., Viswanathan, D., Gupta, V., Wall, R. V., Palanivel, V., Mirzaei, M., You, Y., Klistorner, A. I., et al. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03535-0 · Cited by 18 · see citing works
Ao, M., Zhang, J., Qian, Y., Li, B., Wang, X., Chen, J., Zhang, Y., Cao, Y., Qiu, Y., Xu, Y., et al. (2022) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2022.105645 · Cited by 18 · see citing works
Li, X., Chen, Q., Liu, J., Lai, S., Zhang, M., Zhen, T., Hu, H., Gao, X., Wong, A. S. T., & Zeng, J.-Z. (2022) · Cells · doi:10.3390/cells11233870 · Cited by 17 · see citing works
Potential Roles of Nr4a3-Mediated Inflammation in Immunological and Neurological Diseases
He, S., Jiang, W., Jiang, B., Yu, C., Zhao, G., Li, Y., Qi, L., Zhang, J., & Wang, D. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-03945-8 · Cited by 17 · see citing works
Optimization of novel oxidative DIMs as Nur77 modulators of the Nur77-Bcl-2 apoptotic pathway
Tu, X., Chen, X., Zhang, D., Gao, M., Liang, J., Bao, G., Zhang, J., Peng, S., Zhang, X.-K., Zeng, Z., et al. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.113020 · Cited by 17 · see citing works
Mey, J. T., Solomon, T. P. J., Kirwan, J. P., & Haus, J. M. (2019) · Physiological Reports · doi:10.14814/phy2.14042 · Cited by 17 · see citing works
The Roles of White Adipose Tissue and Liver NADPH in Dietary Restriction-Induced Longevity
Jamerson, L. E., & Bradshaw, P. C. (2024) · Antioxidants · doi:10.3390/antiox13070820 · Cited by 18 · see citing works
Pei, H. Z., Huang, B., Chang, H., & Baek, S. (2019) · Cellular Signalling · doi:10.1016/j.cellsig.2019.03.018 · Cited by 16 · see citing works
Men, L., Hui, W., Guan, X., Song, T., Wang, X., Zhang, S., & Chen, X. (2020) · Genes · doi:10.3390/genes11070720 · Cited by 16 · see citing works
Knockout of Nur77 Leads to Amino Acid, Lipid, and Glucose Metabolism Disorders in Zebrafish
Xu, Y. Y., Tian, J., Kang, Q., Yuan, H., Liu, C., Li, Z., Liu, J., & Li, M. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.864631 · Cited by 15 · see citing works
Yuan, R., Xin, Q., Ma, X., Yu, M., Miao, Y., Chen, K., & Cong, W. (2023) · Molecules · doi:10.3390/molecules28031271 · Cited by 15 · see citing works
Hong, H., Su, J., Huang, C., Xu, L., & Cui, Z. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.981490 · Cited by 14 · see citing works
Patiño-Martínez, E., Solís-Barbosa, M. A., Santana, E., González-Domínguez, É., Segovia-gamboa, N., Meraz-Ríos, M., Córdova, E., Valdés, J., Corbí, Á., & Sánchez-Torres, C. (2022) · Immunobiology · doi:10.1016/j.imbio.2022.152299 · Cited by 12 · see citing works
Cui, P., Wu, S., Xu, X., Ye, H., Hou, J., Liu, X., Wang, H., & Fang, X. (2018) · Shock · doi:10.1097/shk.0000000000001184 · Cited by 14 · see citing works
Reddy, A. T., Lakshmi, S. P., Banno, A., Jadhav, S. K., Kadamberi, I. P., Kim, S. C., & Reddy, R. C. (2020) · PLoS ONE · doi:10.1371/journal.pone.0229256 · Cited by 14 · see citing works
Microbiota Ecosystem in Recurrent Cystitis and the Immunological Microenvironment of Urothelium
Dominoni, M., Scatigno, A. L., La Verde, M., Bogliolo, S., Melito, C., Gritti, A., Pasquali, M. F., Torella, M., & Gardella, B. (2023) · Healthcare · doi:10.3390/healthcare11040525 · Cited by 13 · see citing works
Structural insights into ligand-binding pocket formation in Nurr1 by molecular dynamics simulations
Windshügel, B. (2018) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2018.1559099 · Cited by 12 · see citing works
Lin, H.-Y., Ko, C., Lo, T.-Y., Wu, S., Lan, S.-W., Huang, C.-A., Lin, Y., Lin, H.-H., Tu, H.-F., Lee, C., et al. (2022) · Oncogene · doi:10.1038/s41388-022-02303-z · Cited by 12 · see citing works
Teichmann, T., Pflüger‐Müller, B., Giménez, V. M. M., Sailer, F. K., Dirks, H., Zehr, S., Warwick, T., Brettner, F. E. B., Munoz‐Tello, P., Zimmer, A., et al. (2024) · British Journal of Pharmacology · doi:10.1111/bph.17366 · Cited by 11 · see citing works
Store‐operated calcium entry mediates hyperalgesic responses during neuropathy
Wang, W., Wang, Q., Huang, J., Li, H., Li, F., Li, X., Liu, R., Xu, M., Chen, J., Mao, Y., et al. (2023) · FEBS Open Bio · doi:10.1002/2211-5463.13699 · Cited by 12 · see citing works
Xue, J., Wu, S., Zhu, Q., Liu, X., He, Z., Ye, W., Wang, P., & Wu, F. (2024) · Industrial Crops and Products · doi:10.1016/j.indcrop.2024.118445 · Cited by 10 · see citing works
DNA-PKcs participated in hypoxic pulmonary hypertension
Liu, Y., Zhang, W., Zhang, M., Wang, Y.-J., Ma, X.-Y., Jiang, J.-H., Wang, R., & Zeng, D. (2022) · Respiratory Research · doi:10.1186/s12931-022-02171-x · Cited by 10 · see citing works
Mimouna, S., Rollins, D. A., Shibu, G., Tharmalingam, B., Deochand, D. K., Chen, X., Oliver, D., Chinenov, Y. V., & Rogatsky, I. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20192386 · Cited by 10 · see citing works
Regulation of NR4A2 Gene Expression and Its Importance in Neurodegenerative and Psychiatric Diseases
Ruiz-Sánchez, E., Rojas, C., Gómez, P. Y., Martínez‐Rodríguez, N., Ruíz-Chow, Á. A., Nava-Ruíz, C., Ibáñez-Cervantes, G., Arciniega-Martínez, I. M., Reséndiz‐Albor, A. A., & Rojas, P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26189162 · Cited by 9 · see citing works
Ruiz-Sánchez, E., López-Ramírez, A. M., Ruíz-Chow, Á. A., Calvillo, M., Reséndiz‐Albor, A. A., Anguiano, B., & Rojas, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222312700 · Cited by 9 · see citing works
Maranda, V., Gaumond, M.-H., & Moffatt, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042148 · Cited by 10 · see citing works
Huang, B., Li, Y., Yao, Y., Shu, W., & Chen, M. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.09.002 · Cited by 9 · see citing works
Nuclear receptors in abdominal aortic aneurysms
Neels, J. G., Hassen‐Khodja, R., & Chinetti, G. (2020) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2020.02.009 · Cited by 9 · see citing works
Yuan, L. X., Yang, B., Fung, T. S., Chen, R., & Liu, D. X. (2022) · Virology · doi:10.1016/j.virol.2022.08.001 · Cited by 8 · see citing works
The role of nuclear receptor 4A1 (NR4A1) in drug‐induced gingival overgrowth
Hatano, S., Matsuda, S., Okanobu, A., Furutama, D., Memida, T., Kajiya, M., Ouhara, K., Fujita, T., Mizuno, N., & Kurihara, H. (2021) · The FASEB Journal · doi:10.1096/fj.202100032r · Cited by 8 · see citing works
Yuan, R., Xin, Q., Shi, W., Yu, M., Zhu, Z., Yuan, Y., Chen, Y., Chen, X., Leng, S. X., Chen, K., et al. (2023) · Food Science and Human Wellness · doi:10.26599/fshw.2022.9250212 · Cited by 7 · see citing works
Nur77 promotes embryo adhesion by transcriptionally regulating HOXA10 expression
Shen, J., Zhu, X., Zhang, M., Jiang, Y., Yan, G., Wang, Z., Sun, L., & Zhang, Q. (2019) · Systems Biology in Reproductive Medicine · doi:10.1080/19396368.2019.1671536 · Cited by 7 · see citing works
Decreased Steroid Hormone Receptor NR4A2 Expression in Kawasaki Disease Before IVIG Treatment
Huang, Y., Chen, K., Lo, M., Cai, X.-Y., & Kuo, H. (2019) · Frontiers in Pediatrics · doi:10.3389/fped.2019.00007 · Cited by 7 · see citing works
Joshi, R., Hamed, O., Yan, D., Michi, A. N., Mostafa, M., Wiehler, S., Newton, R. C., & Giembycz, M. A. (2020) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.000196 · Cited by 7 · see citing works
Natalia, P., Zwirchmayr, J., Rudžionytė, I., Pulsinger, A., Breuss, J. M., Uhrín, P., Rollinger, J. M., & de Martin, R. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.802153 · Cited by 6 · see citing works
Li, R., Chen, S., Gu, X., An, S., & Wang, Z. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.02.017 · Cited by 6 · see citing works
A Novel Mechanism of Coactivator Recruitment by the Nurr1 Nuclear Receptor
Daffern, N., & Radhakrishnan, I. (2022) · Journal of Molecular Biology · doi:10.1016/j.jmb.2022.167718 · Cited by 6 · see citing works
Phelan, D. E., Reddan, B., Shigemura, M., Sznajder, J. I., Crean, D., & Cummins, E. P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25052852 · Cited by 6 · see citing works
MSCs Contribute to the Conversion of Ly6Chigh Monocytes into Ly6Clow Subsets under AMI
Lu, W., Ma, G., Sheng, Z., Wang, Q., Chen, L., Qi, J., Shi, R. H., Ji, J., Ji, Z., & Dai, Q. (2020) · Stem Cells International · doi:10.1155/2020/2460158 · Cited by 6 · see citing works
Joshi, R., Yan, D., Hamed, O., Mostafa, M., Joshi, T., Newton, R. C., & Giembycz, M. A. (2019) · Molecular Pharmacology · doi:10.1124/mol.118.115311 · Cited by 6 · see citing works
Atri, C., Mkannez, G., Attia, H., Sghaier, R. M., Bali, A., Ben-Cheikh, A., Rabhi, I., Regnault, B., Piquemal, D., Ghedira, K., et al. (2025) · Microbes and Infection · doi:10.1016/j.micinf.2025.105502 · Cited by 5 · see citing works
Yehuda, H., Madrer, N., Goldberg, D., Soreq, H., & Meerson, A. (2023) · Cells · doi:10.3390/cells12131794 · Cited by 5 · see citing works
Guo, Y., Lu, Q., Yang, X.-J., He, Y., Wu, Y., Qin, B., Li, T., Duan, M., Liu, N., Wu, X., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0299376 · Cited by 4 · see citing works
Hu, H., Li, R., He, K., Wu, L., Li, R., Lu, J., Tian, R., Zhang, C., He, J., Chen, Y., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02495-2 · Cited by 4 · see citing works
Reddy, A. T., Lakshmi, S. P., Nyunoya, T., & Reddy, R. C. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176945 · Cited by 4 · see citing works
Identification of novel anti-inflammatory Nur77 modulators by virtual screening
Ding, X., Zhao, Z., Wu, Y., Zhang, H., Chen, K., Luo, C., Luo, X., & Xu, H. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.104912 · Cited by 4 · see citing works
Smyth, A. M., Gogarty, M., Crean, D., & Murphy, E. P. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9195-2_3 · Cited by 4 · see citing works
Alsharif, O., & Rombouts, K. (2025) · npj Gut and Liver · doi:10.1038/s44355-025-00037-9 · Cited by 3 · see citing works
γδ T cells in diabetes mellitus: dual roles and therapeutic implications
Wang, B., Li, Q., & Wang, Q. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1693466 · Cited by 3 · see citing works
Akbulut, S., Küçükakçalı, Z., & Çolak, C. (2022) · Çukurova medical journal (Online)/Çukurova medical journal · doi:10.17826/cumj.1128653 · Cited by 3 · see citing works
Chen, L., Shi, Y., Xiao, D., Huang, Y., Jiang, Y., Liang, M., Liang, F., Xue, J., Chen, H., Liu, Z., et al. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05602-2 · Cited by 3 · see citing works
Li, Y., Hu, Q., Luoreng, Z., Yang, J., Wang, X., Ma, Y., & Wei, D. (2022) · Animals · doi:10.3390/ani12111431 · Cited by 3 · see citing works
Santucci, N. E., Stampone, R., da Silva, E. B. F., Villar, S. R., Spinelli, S. V., Linhares‐Lacerda, L., Alves, M. R., Bay, M. L., & Bottasso, O. A. (2020) · NeuroImmunoModulation · doi:10.1159/000512325 · Cited by 3 · see citing works
Kiprina, A., Teichmann, T., Giménez, V. M. M., Wen-qing, X., Sailer, F. K., Windbergs, M., Manucha, W. A., Weigert, A., & Brandes, R. P. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1528759 · Cited by 2 · see citing works
Wang, K., Wang, M., Shang, Y., He, Y., Li, Q., Gao, W., & Yin, H. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4565246 · Cited by 2 · see citing works
Mimouna, S., Rollins, D. A., Shibu, G., Tharmalingam, B., Deochand, D. K., Chen, X., Oliver, D., Chinenov, Y. V., & Rogatsky, I. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.2019238611162020c · Cited by 3 · see citing works
da Bandeira, D. S., Nevitt, C. D., Dezem, F. S., Marção, M., Liu, Y., Kelley, Z., DuBose, H., Chabot, A., Hall, T., Caprio, C., et al. (2024) · Development · doi:10.1242/dev.201957 · Cited by 1 · see citing works
Nuclear receptors as therapeutic targets in metabolic and cardiovascular disorders
Li, F., Chen, Q., Dai, Y., & Lu, L. (2025) · iScience · doi:10.1016/j.isci.2025.114042 · Cited by 1 · see citing works
- Authors
- Rodríguez-Calvo, R., Tajes, M., & Vázquez-Carrera, M.
- Affiliations
- Vascular Medicine and Metabolism Unit, Research Unit on Lipids and Atherosclerosis, Sant Joan University Hospital, Pere Virgili Health Research Institute (IISPV) and Spanish Biomedical Research Centre in Diabetes and Associated Metabolic Disorders (CIBERDEM)-Instituto de Salud Carlos III, Faculty of Medicine and Health Sciences, Rovira i Virgili University, Reus, Spain
- Hospital Del Mar (ES)
- Department of Pharmacology, Toxicology and Therapeutic Chemistry, Institut de Biomedicina de la Universitat de Barcelona (IBUB), Institut de Recerca Pediàtrica-Hospital Sant Joan de Déu, and Spanish Biomedical Research Centre in Diabetes and Associated Metabolic Disorders (CIBERDEM)-Instituto de Salud Carlos III, Faculty of Pharmacy, Diagonal 643, University of Barcelona, Barcelona, Spain
- Venue
- Expert Opinion on Therapeutic Targets
- Publisher
- Informa UK Limited
- Published
- 2017-01-12
- Volume
- 21
- Issue
- 3
- Pages
- 291-304
- ISSN
- 1472-8222 (ISSN-L)
- 1744-7631
- OpenAlex
- W2569529038
- Cited by
- 117
- References
- 158
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 12 · 2023: 9 · 2022: 20 · 2021: 11 · 2020: 21 · 2019: 10 · 2018: 14 · 2017: 1
- FWCI
- 1.55
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- cc-by
- Locations
- Expert Opinion on Therapeutic Targets (publishedVersion)
- PubMed (publishedVersion)
- Rovira & Virgili repository (submittedVersion, cc-by)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nuclear Receptors and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- NR4A nuclear receptors, Nur77, Nurr1, NOR-1, inflammatory diseases, inflammation, transrepression, transcriptional repression, negative feedback regulation, anti-inflammatory mechanism, therapeutic target
- MeSH terms
- Animals, DNA-Binding Proteins, Humans, Inflammation, Receptors, Steroid, Receptors, Thyroid Hormone, Drug Design, Nuclear Receptor Subfamily 4, Group A, Member 1, Nuclear Receptor Subfamily 4, Group A, Member 2, Molecular Targeted Therapy
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