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A RING-type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity
Abstract
Despite the sequencing of the human and mouse genomes, few genetic mechanisms for protecting against autoimmune disease are currently known. Here we systematically screen the mouse genome for autoimmune regulators to isolate a mouse strain, sanroque, with severe autoimmune disease resulting from a single recessive defect in a previously unknown mechanism for repressing antibody responses to self. The sanroque mutation acts within mature T cells to cause formation of excessive numbers of follicular helper T cells and germinal centres. The mutation disrupts a repressor of ICOS, an essential co-stimulatory receptor for follicular T cells, and results in excessive production of the cytokine interleukin-21. sanroque mice fail to repress diabetes-causing T cells, and develop high titres of autoantibodies and a pattern of pathology consistent with lupus. The causative mutation is in a gene of previously unknown function, roquin (Rc3h1), which encodes a highly conserved member of the RING-type ubiquitin ligase protein family. The Roquin protein is distinguished by the presence of a CCCH zinc-finger found in RNA-binding proteins, and localization to cytosolic RNA granules implicated in regulating messenger RNA translation and stability.
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“Interestingly, RC3H1 also encodes a protein that has an amino-terminal RING-1 zinc-finger, which is characteristic to that of the E3 ubiquitin ligase family.50”
From APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease (2016) · cites this paper as [50]
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Cites
Foxp3 programs the development and function of CD4+CD25+ regulatory T cells
Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745
An essential role for Scurfin in CD4+CD25+ T regulatory cells
Khattri, R., Cox, T., Yasayko, S.-A., & Ramsdell, F. (2003) · Nature Immunology · doi:10.1038/ni909 · Cited by 2,860
MacLennan, I. C. M. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.001001 · Cited by 1,795
Structure of the Cul1–Rbx1–Skp1–F boxSkp2 SCF ubiquitin ligase complex
Zheng, N., Schulman, B. A., Song, L., Miller, J. J., Jeffrey, P. D., Wang, P., Chu, C., Koepp, D. M., Elledge, S. J., Pagano, M., et al. (2002) · Nature · doi:10.1038/416703a · Cited by 1,507
ICOS is an inducible T-cell co-stimulator structurally and functionally related to CD28
Hutloff, A., Dittrich, A. M., Beier, K. C., Eljaschewitsch, B., Kraft, R., Anagnostopoulos, I., & Kroczek, R. A. (1999) · Nature · doi:10.1038/16717 · Cited by 1,482
Parrish-Novak, J. E., Dillon, S. R., Nelson, A., Hammond, A., Sprecher, C. A., Gross, J. A., Johnston, J. V., Madden, K., Xu, W., West, J., et al. (2000) · Nature · doi:10.1038/35040504 · Cited by 1,222
Visualization of peptide-specific T cell immunity and peripheral tolerance induction in vivo.
Kearney, E. R., Pape, K., Loh, D., & Jenkins, M. (1994) · Immunity · doi:10.1016/1074-7613(94)90084-1 · Cited by 1,126
A Critical Role for IL-21 in Regulating Immunoglobulin Production
Ozaki, K., Spolski, R., Feng, C. G., Qi, C.-F., Cheng, J., Sher, A., Morse, H. C., Liu, C., Schwartzberg, P. L., & Leonard, W. J. (2002) · Science · doi:10.1126/science.1077002 · Cited by 978
ICOS co-stimulatory receptor is essential for T-cell activation and function
Dong, C., Juedes, A. E., Temann, U.-A., Shresta, S., Allison, J. P., Ruddle, N. H., & Flavell, R. A. (2001) · Nature · doi:10.1038/35051100 · Cited by 929
Structure of a c-Cbl–UbcH7 Complex
Zheng, N., Wang, P., Jeffrey, P. D., & Pavletich, N. P. (2000) · Cell · doi:10.1016/s0092-8674(00)00057-x · Cited by 839
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WEISENBURGER, T. H., von Neubeck, B., Schneider, A. M., Ebert, N., Schreyer, D., Acs, A., & Winkler, T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01551 · Cited by 42
New preclinical models for angioimmunoblastic T-cell lymphoma: filling the GAP
Mhaidly, R., Krug, A., Gaulard, P., Lemonnier, F., Ricci, J., & Verhoeyen, E. (2020) · Oncogenesis · doi:10.1038/s41389-020-00259-x · Cited by 39
How do SAP family deficiencies compromise immunity?
Dong, Z., & Veillette, A. (2010) · Trends in Immunology · doi:10.1016/j.it.2010.05.008 · Cited by 37
Understanding the genetic regulation of IgE production
Altin, J. A., Shen, C., & Liston, A. (2010) · Blood Reviews · doi:10.1016/j.blre.2010.06.002 · Cited by 37
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McKinney, E. F., & Smith, K. G. (2016) · Immunology & Cell Biology · doi:10.1038/icb.2016.81 · Cited by 36
Aberrant B Cell Selection and Activation in Systemic Lupus Erythematosus
Kil, L. P., & Hendriks, R. W. (2013) · International Reviews of Immunology · doi:10.3109/08830185.2013.786712 · Cited by 38
Posttranscriptional regulation of cytokine expression
Kovarik, P., Ebner, F., & Sedlyarov, V. (2015) · Cytokine · doi:10.1016/j.cyto.2015.11.007 · Cited by 37
Binding of NUFIP2 to Roquin promotes recognition and regulation of ICOS mRNA
Rehage, N., Davydova, E., Conrad, C., Behrens, G., Maiser, A., Stehklein, J. E., Brenner, S., Klein, J., Jeridi, A., Hoffmann, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02582-1 · Cited by 36
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Ujiie, H. (2018) · Experimental Dermatology · doi:10.1111/exd.13535 · Cited by 36
RNA binding proteins in the control of autoimmune diseases
Yoshinaga, M., & Takeuchi, O. (2019) · Immunological Medicine · doi:10.1080/25785826.2019.1655192 · Cited by 36
Kumar, D., Prince, C. Z., Bennett, C. M., Briones, M. A., Lucas, L., Russell, A. L., Patel, K. P., Chonat, S., Graciaa, S. H., Edington, H. J., et al. (2021) · Blood · doi:10.1182/blood.2021012924 · Cited by 36
TRAF6 prevents fatal inflammation by homeostatic suppression of MALT1 protease
O’Neill, T. J., Seeholzer, T., Gewies, A., Gehring, T., Giesert, F., Hamp, I., Graß, C., Schmidt, H., Kriegsmann, K., Tofaute, M. J., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abh2095 · Cited by 36
Xiao, F., Zhang, H.-Y., Liu, Y., Zhao, D., Shan, Y., & Jiang, Y. (2013) · The Journal of Rheumatology · doi:10.3899/jrheum.130125 · Cited by 36
Chakera, A., Bennett, S. C., Morteau, O., Bowness, P., Luqmani, R. A., & Cornall, R. J. (2012) · Clinical and Developmental Immunology · doi:10.1155/2012/948218 · Cited by 35
Self-citationImmunological function of Blimp-1 in dendritic cells and relevance to autoimmune diseases
Kim, S. J. (2015) · Immunologic Research · doi:10.1007/s12026-015-8694-5 · Cited by 35
Interleukin-21: A New Mediator of Inflammation in Systemic Lupus Erythematosus
Sarra, M., & Monteleone, G. (2010) · BioMed Research International · doi:10.1155/2010/294582 · Cited by 35
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Li, W., Sivakumar, R., Titov, A. A., Choi, S., & Morel, L. M. (2016) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2016017164 · Cited by 35
IL-21 shapes germinal center polarization via light zone B cell selection and cyclin D3 upregulation
Petersone, L., Wang, C. J., Edner, N. M., Fabri, A., Nikou, S.-A., Hinze, C., Ross, E. M., Ntavli, E., Elfaki, Y., Heuts, F. W. H., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221653 · Cited by 34
Takeuchi, O. (2017) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1449 · Cited by 34
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Shao, F., Zheng, P., Yu, D., Zhou, Z., & Jia, L. (2019) · The FASEB Journal · doi:10.1096/fj.201901637r · Cited by 36
Self-citationBhlhe40 function in activated B and TFH cells restrains the GC reaction and prevents lymphomagenesis
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The darker side of follicular helper T cells: from autoimmunity to immunodeficiency
Shekhar, S., & Yang, X. (2012) · Cellular and Molecular Immunology · doi:10.1038/cmi.2012.26 · Cited by 37
Zhang, H., Wu, C., Matesic, L. E., Li, X., Wang, Z., Boyce, B. F., & Xing, L. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.442459 · Cited by 33
MCP-1-induced protein-1, an immune regulator
Xu, J.-W., Fu, S., Peng, W., & Rao, Z. (2012) · Protein & Cell · doi:10.1007/s13238-012-2075-9 · Cited by 34
Bautista-Caro, M.-B., Arroyo-Villa, I., Castillo-Gallego, C., de Miguel, E., Peiteado, D., Plasencia‐Rodríguez, C., Villalba, A., Sánchez‐Mateos, P., Puig‐Kröger, A., Martín-Mola, E., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107086 · Cited by 33
Dhamija, S., Doerrie, A., Winzen, R., Dittrich‐Breiholz, O., Taghipour, A., Kühne, N., Kracht, M., & Holtmann, H. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.146365 · Cited by 33
Comparative Genomics and Protein Domain Graph Analyses Link Ubiquitination and RNA Metabolism
Lucas‐Lledó, J. I., Arnau, V., & Marı́n, I. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2005.12.068 · Cited by 33
Ogbe, A., Miao, T., Symonds, A. L. J., Omodho, B., Singh, R. K., Bhullar, P., Li, S., & Wang, P. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.634816 · Cited by 35
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Olson, W. J., Jakic, B., Labi, V., Schoeler, K., Kind, M., Klepsch, V., Baier, G., & Hermann‐Kleiter, N. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.024 · Cited by 33
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Hamel, K. M., Cao, Y., Olalekan, S. A., & Finnegan, A. (2013) · Arthritis & Rheumatology · doi:10.1002/art.38207 · Cited by 32
Blankenhorn, E. P., Butterfield, R. J., Case, L. K., Wall, E. H., del Río, R., Diehl, S. A., Krementsov, D. N., Saligrama, N., & Teuscher, C. (2011) · Annals of Neurology · doi:10.1002/ana.22642 · Cited by 32
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Crickx, É., Poullot, E., Moulis, G., Goulabchand, R., Fieschi, C., Galicier, L., Meignin, V., Coppo, P., Delarue, R., Casasnovas, O., et al. (2019) · European Journal Of Haematology · doi:10.1111/ejh.13239 · Cited by 31
Shilling, R. A., Bandukwala, H. S., & Sperling, A. I. (2006) · Clinical Immunology · doi:10.1016/j.clim.2006.04.574 · Cited by 31
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Xie, W. Q., & Denman, R. B. (2011) · Molecular Biology International · doi:10.4061/2011/137459 · Cited by 32
Abe, J., Ueha, S., Suzuki, J., Tokano, Y., Matsushima, K., & Ishikawa, S. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080314 · Cited by 31
RNA regulation of the immune system
Ansel, K. M. (2013) · Immunological Reviews · doi:10.1111/imr.12062 · Cited by 30
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Vijayan, D., Redzwan, N. M., Avery, D. T., Wirasinha, R. C., Brink, R. A., Walters, G. D., Adelstein, S., Kobayashi, M., Gray, P. E., Elliott, M., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600652 · Cited by 30
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Yang, Y., Zhang, M., Ye, Y., Ma, S., Fan, L., & Li, Z. (2017) · Neurological Sciences · doi:10.1007/s10072-017-3009-3 · Cited by 30
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Iborra-Pernichi, M., García, J. R., de la Esperanza, M. V., Estrada, B. S., Bovolenta, E. R., Cifuentes, C., Carro, C., Martínez, T. G., García-Consuegra, J., Rey-Stolle, F., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46763-1 · Cited by 35
Tfh Cells in Health and Immunity: Potential Targets for Systems Biology Approaches to Vaccination
Law, H. L., Venturi, V., Kelleher, A. D., & Munier, C. M. L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228524 · Cited by 30
Vincent, F. B., Bourke, P., Morand, E. F., Mackay, F., & Bossingham, D. (2012) · Internal Medicine Journal · doi:10.1111/imj.12039 · Cited by 29
Serum IL-21 levels decrease with glucocorticoid treatment in myasthenia gravis
Li, Y., Rauniyar, V. K., Yin, W., Hu, B., Ouyang, S., Xiao, B., & Yang, H. (2013) · Neurological Sciences · doi:10.1007/s10072-013-1460-3 · Cited by 29
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Cassar, P. A., Carpenedo, R. L., Samavarchi‐Tehrani, P., Olsen, J. B., Park, C. J., Chang, W. Y., Chen, Z., Choey, C., Delaney, S. P., Guo, H., et al. (2015) · EMBO Reports · doi:10.15252/embr.201540974 · Cited by 29
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Hoefig, K. P., & Heissmeyer, V. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201708075 · Cited by 31
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Fairfax, K. A., Tsantikos, E., Figgett, W. A., Vincent, F. B., Quah, P. S., LePage, M., Hibbs, M. L., & Mackay, F. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2015.06.001 · Cited by 29
A cell autonomous role for the Notch ligand Delta‐like 3 in αβ T‐cell development
Hoyne, G. F., Chapman, G., Sontani, Y., Pursglove, S. E., & Dunwoodie, S. L. (2010) · Immunology and Cell Biology · doi:10.1038/icb.2010.154 · Cited by 29
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Li, J., Pan, H., Cen, H., Tian, J., Ma, Y., Tao, J., & Ye, D. (2010) · Molecular Biology Reports · doi:10.1007/s11033-010-0527-y · Cited by 28
Jain, S., Chen, J., Nicolae, A., Wang, H., Shin, D., Adkins, E. B., Sproule, T. J., Leeth, C. M., Sakai, T., Kovalchuk, A. L., et al. (2015) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.07.021 · Cited by 30
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Gómez‐Martín, D., Díaz‐Zamudio, M., Romo‐Tena, J., Ibarra-Sánchez, M. D. J., & Alcocer-Varela, J. C. (2010) · Autoimmunity Reviews · doi:10.1016/j.autrev.2010.11.007 · Cited by 29
Sawaf, M., Dumortier, H., & Monneaux, F. (2016) · Journal of Immunology Research · doi:10.1155/2016/5767106 · Cited by 28
Regnase‐1–related endoribonucleases in health and immunological diseases
Mino, T., & Takeuchi, O. (2021) · Immunological Reviews · doi:10.1111/imr.13023 · Cited by 29
Chevalier, N., Macia, L., Tan, J. K., Mason, L. J., Robert, R., Thorburn, A. N., Wong, C. H. Y., Tsai, L. M., Bourne, K., Brink, R. A., et al. (2015) · Arthritis & Rheumatology · doi:10.1002/art.39481 · Cited by 28
Self-citationDysregulation of circulating CD 4+ CXCR 5+ T cells in type 2 diabetes mellitus
Wang, Q., Zhai, X., Chen, X., Lu, J., Zhang, Y., & Huang, Q. (2014) · Apmis · doi:10.1111/apm.12330 · Cited by 28
Gutierrez, T., Halcomb, K. E., Coughran, A. J., Li, Q., & Satterthwaite, A. B. (2010) · European Journal of Immunology · doi:10.1002/eji.200940043 · Cited by 28
Deng, X., Yan, S., & Wei, W. (2014) · Cellular and Molecular Immunology · doi:10.1038/cmi.2014.58 · Cited by 29
Development of autoimmune nephritis in genetically asplenic and splenectomized BAFF transgenic mice
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Nakatsuka, Y., Vandenbon, A., Mino, T., Yoshinaga, M., Uehata, T., Cui, X., Sato, A., Tsujimura, T., Suzuki, Y., Sato, A., et al. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0024-5 · Cited by 30
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Braun, J., Fischer, S. E., Xu, Z. Z., Sun, H., Ghoneim, D. H., Gimbel, A. T., Plessmann, U., Urlaub, H., Mathews, D. H., & Weigand, J. E. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky908 · Cited by 28
Uncovering the uncharacterized and unexpected: Unbiased phenotype‐driven screens in the mouse
Caspary, T., & Anderson, K. V. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20853 · Cited by 28
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Luo, R., Chang, D., Zhang, N., Cheng, Y., Ge, S., & Xu, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612535 · Cited by 27
Roquin—a multifunctional regulator of immune homeostasis
Schaefer, J. S., & Klein, J. R. (2015) · Genes and Immunity · doi:10.1038/gene.2015.58 · Cited by 27
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Pelletier, M., & Girard, D. (2007) · The Scientific World JOURNAL · doi:10.1100/tsw.2007.275 · Cited by 28
Ferry, H., Leung, J. C. H., Lewis, G., Nijnik, A., Silver, K., Lambe, T., & Cornall, R. J. (2006) · Transplantation · doi:10.1097/01.tp.0000203830.79357.39 · Cited by 27
Self-citationAn update on pathogenesis of systemic lupus erythematosus.
Ahmadpoor, P., Dalili, N., & Rostami, M. (2014) · Iranian Journal of Kidney Diseases · Cited by 26
Leonardo, S. M., Santis, J. L. D., Gehrand, A. L., Malherbe, L. P., & Gauld, S. B. (2012) · European Journal of Immunology · doi:10.1002/eji.201242616 · Cited by 26
Loss of Immune Tolerance Is Controlled by ICOS in Sle1 Mice
Mittereder, N., Kuta, E. G., Bhat, G., Dacosta, K., Cheng, L., Herbst, R., & Carlesso, G. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502241 · Cited by 26
Genes and power athlete status
Maciejewska, A., Sawczuk, M., Cięszczyk, P., & Ahmetov, I. I. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816193-7.00003-8 · Cited by 26
Small Intestine Inflammation in Roquin-Mutant and Roquin-Deficient Mice
Schaefer, J. S., Montufar‐Solis, D., Nakra, N., Vigneswaran, N., & Klein, J. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056436 · Cited by 25
Afridi, S., Hoessli, D. C., & Hameed, M. W. (2016) · Immunological Reviews · doi:10.1111/imr.12435 · Cited by 25
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Yang, G., Yang, X., Zhang, J., Li, G., Zheng, D., Peng, A., Hu, J., Xu, L., Yang, B., Yang, H., et al. (2017) · Immunology · doi:10.1111/imm.12815 · Cited by 27
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Misawa, T., SoRelle, J. A., Choi, J. H., Yue, T., Wang, K.-W., McAlpine, W., Wang, J., Liu, A., Tabeta, K., Turer, E. E., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.aaz0085 · Cited by 25
Eri, T., Kawahata, K., Kanzaki, T., Imamura, M., Michishita, K., Akahira, L., Bannai, E., Yoshikawa, N., Kimura, Y., Satoh, T., et al. (2017) · Scientific Reports · doi:10.1038/srep46037 · Cited by 25
Li, X., Sun, W., Huang, M., Gong, L., Zhang, X., Li, Z., Calderon, V., Bian, Z., He, Y., Suh, W., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.04.023 · Cited by 24
The role of interleukin-21 in HIV infection
Pallikkuth, S., Parmigiani, A., & Pahwa, S. G. (2012) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2012.05.004 · Cited by 24
IL-17–producing follicular Th cells enhance plasma cell differentiation in lupus-prone mice
Kim, V., Lee, K., Tian, H. W., Jang, S. H., Diamond, B., & Kim, S. J. (2022) · JCI Insight · doi:10.1172/jci.insight.157332 · Cited by 24
Contribution of Dysregulated B-Cells and IgE Antibody Responses to Multiple Sclerosis
Seals, M. R., Moran, M. M., Leavenworth, J. D., & Leavenworth, J. W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900117 · Cited by 25
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Metadata
- Authors
- Vinuesa, C. G., Cook, M. C., Angelucci, C., Athanasopoulos, V., Rui, L., Hill, K. M., Yu, D., Domaschenz, H., Whittle, B., Lambe, T., Roberts, I. S., Copley, R. R., Bell, J. I., Cornall, R. J., & Goodnow, C. C.
- Affiliations
- Australian National University (AU)
- University of Oxford (GB)
- John Radcliffe Hospital (GB)
- Centre for Human Genetics (GB)
- Corresponding author
- Vinuesa, Carola G.
- Goodnow, Christopher C.
- ORCID
- Venue
- Nature
- Published
- 2005-05
- Volume
- 435
- Issue
- 7041
- Pages
- 452-458
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2031622194
- Cited by
- 862
- References
- 50
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 28 · 2023: 21 · 2022: 24 · 2021: 46 · 2020: 33 · 2019: 50 · 2018: 43 · 2017: 34 · 2016: 61 · 2015: 54 · 2014: 60 · 2013: 64 · 2012: 50
- FWCI
- 14.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- ANU Open Research (Australian National University) (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Keywords
- Roquin, T follicular helper cells, germinal center, ICOS, IL-21, autoimmunity, lupus, diabetes mellitus, autoantibodies, self-tolerance, RNA granules, CCCH zinc finger, RNA-binding proteins, mRNA stability, T cell costimulation
- MeSH terms
- Amino Acid Sequence, Animals, Autoantibodies, Disease Models, Animal, Female, T-Lymphocytes, Helper-Inducer, Humans, Lupus Erythematosus, Systemic, Male, Molecular Sequence Data, Receptors, Antigen, T-Cell, Autoimmunity, Mutation, Missense, Ubiquitin-Protein Ligases, Cell Line, Tumor, Mice
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