The DOI matches its Crossref record; 146 of the 148 references it cites were found in a registry or an index.
Genomic views of STAT function in CD4+ T helper cell differentiation
Open accessAbstract
Signal transducer and activator of transcription (STAT) proteins are well known for their essential roles in transmitting cytokine-mediated signals and specifying T helper (T(H)) cell differentiation. Recent technological advances have revealed that STAT proteins have broad and complex roles in gene regulation and epigenetic control, including important roles as functional repressors. However, the challenge of how to link signal transduction, nucleosome biology and gene regulation remains. The relevance of tackling this problem is highlighted by genome-wide association studies that link cytokine signalling and STATs to various autoimmune or immune deficiency disorders. Defining exactly how extrinsic signals control the specification and plasticity of T(H) cells will provide important insights and perhaps therapeutic opportunities in these diseases.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The cited source says what the claim attributes to it.
In the citing paper
“The appropriate differentiation of these CD4+ T-cell subsets requires activation of transcription factors, including signal transducers and activators of transcription (STATs) [11].”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
MicroRNAs: Target Recognition and Regulatory Functions
Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068
Chromatin modifications and their function
Kouzarides, T. (2007) · Cell · doi:10.1016/j.cell.2007.02.005 · Cited by 10,883
Jenuwein, T., & Allis, C. D. (2001) · Science · doi:10.1126/science.1063127 · Cited by 9,756
Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145
Korn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873
Next-generation DNA sequencing
Shendure, J., & Ji, H. (2008) · Nature Biotechnology · doi:10.1038/nbt1486 · Cited by 4,509
Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
Guttman, M., Amit, I., Garber, M., French, C., Lin, M. F., Feldser, D., Huarte, M., Zuk, O., Carey, B. W., Cassady, J. P., et al. (2009) · Nature · doi:10.1038/nature07672 · Cited by 4,098
Veldhoen, M., Hocking, R. J., Atkins, C. J., Locksley, R. M., & Stockinger, B. (2006) · Immunity · doi:10.1016/j.immuni.2006.01.001 · Cited by 3,605
Flagged first, then by citations
2 of the 148 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Danoy, P. et al. Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease. PLoS Genet. 6, e1001195 (2010). · DOI
Cited by
Sorted by citations
Items 201–295 of 295
Lamprianidou, E., Daniilidis, M., Kordella, C., Zoulia, E., Nakou, E., Gerofotis, A., Vasilaki, A., Pantos, G., & Kotsianidis, Ι. (2019) · Clinical Immunology · doi:10.1016/j.clim.2019.108261 · Cited by 8
Biological and clinical significance of T helper 17 cell deficiency: insight into monogenic defects
Anka, A. U., Abdullahi, I. N., Umar, K., Bello, Z. M., Mohammed, M., Sarkhiz, S. G., Kaoje, N. A., Alsabbagh, M. Y., Kamali, A. N., & Azizi (2020) · European Annals of Allergy and Clinical Immunology · doi:10.23822/eurannaci.1764-1489.160 · Cited by 8
A population of naive‐like CD4 + T cells stably polarized to the T H 1 lineage
Lo, J. W., de Mucha, M. V., Henderson, S. R., Roberts, L. B., Constable, L. E., Garrido‐Mesa, N., Hertweck, A., Stolarczyk, É., Houlder, E. L., Jackson, I., et al. (2022) · European Journal of Immunology · doi:10.1002/eji.202149228 · Cited by 7
Subedi, P., Huber, K., Sterr, C., Dietz, A., Strasser, L., Kaestle, F., Hauck, S. M., Duchrow, L., Aldrian, C. J., Ordonez, E. B. M., et al. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1180642 · Cited by 8
Superantigens induce IL-17 production from polarized Th1 clones
Yomogida, K., Chou, Y. K., & Chu, C. (2013) · Cytokine · doi:10.1016/j.cyto.2013.04.015 · Cited by 7
Janus kinase inhibitor ruxolitinib blocks thymic regeneration after acute thymus injury
Li, L., Shang, L., Gao, J., Liu, C., Xia, F., Xu, M., Qi, K., Zeng, L., Pan, B., & Xu, K. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.113712 · Cited by 7
Maródi, L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00040-6 · Cited by 7
RUNX1 gene expression changes in the placentas of women smokers
Bermúdez, L. G., Madariaga, I., Zuñiga, M., Olaya, M., Cañas, A., Rodríguez, L., Moreno, O. M., & Rojas, A. P. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10334 · Cited by 7
The miR-141/200c-STAT4 Axis Contributes to Leukemogenesis by Enhancing Cell Proliferation in T-PLL
Otte, M., Stachelscheid, J., Glaß, M., Wahnschaffe, L., Jiang, Q., Lone, W., Ianevski, A., Aittokallio, T. A., Iqbal, J., Hallek, M. J., et al. (2023) · Cancers · doi:10.3390/cancers15092527 · Cited by 7
Pathogenic Th cell subsets in chronic inflammatory diseases
KUMAGAI, J., Hirahara, K., & Nakayama, T. (2016) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.39.114 · Cited by 7
Th9 Cells: New Member of T Helper Cell Family
Goswami, R. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6877-0_1 · Cited by 7
Nagy, Z. S., Ross, J. A., Rodriguez, G., Bálint, B. L., Széles, L., Nagy, L., & Kirken, R. A. (2013) · PLoS ONE · doi:10.1371/annotation/cb55d096-61f8-46de-b58f-81a872be6dd3 · Cited by 7
Bi, Z., Zhang, Q., Gao, H., Ge, H., Zhan, J., 桂梦翠, Lin, J., Li, Y., 季素琼, Yang, M., et al. (2025) · Muscle & Nerve · doi:10.1002/mus.28348 · Cited by 6
Su, Q. Y., Zhang, S., Yang, L., Luo, J., Li, X., Zhang, J., Zhang, Y., Liu, J., & Shi, L. G. (2022) · Advances in Therapy · doi:10.1007/s12325-022-02337-5 · Cited by 6
Lung cancer treatment potential and limits associated with the STAT family of transcription factors
Faida, P., Attiogbe, M. K. I., Majeed, U., Zhao, J., Qu, L., & Fan, D. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110797 · Cited by 6
Johnson, H. M. (2011) · Journal of Clinical & Cellular Immunology · doi:10.4172/2155-9899.1000112 · Cited by 7
Molecular Diagnostics of T-Cell Lymphoproliferative Disorders
Bailey, N. G., & Elenitoba‐Johnson, K. S. J. (2014) · The Cancer Journal · doi:10.1097/ppo.0000000000000016 · Cited by 6
Yang, X., Zhao, H., Li, Y., & Zhang, P. (2020) · Preprints.org · doi:10.20944/preprints202004.0466.v1 · Cited by 5
The distinctive signature of regulatory CD4 T cells committed in the human thymus
Raposo, A. A. S. F., Paço, S., Ângelo‐Dias, M., Rosmaninho, P., Almeida, A. R. M., & Sousa, A. E. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1553554 · Cited by 5
Interferon-γ activated T-cell IRGM–autophagy axis in oral lichen planus
Tan, Y., Wang, F., Ma, R.-J., Zhang, J., & Zhou, G. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.107478 · Cited by 5
Li, S., Zhang, P., Li, A., Bao, J., Pan, Z., & Jie, Y. (2024) · Experimental Eye Research · doi:10.1016/j.exer.2024.109857 · Cited by 5
Wu, W., Zuo, L., Dine, K. E., & Shindler, K. S. (2013) · Immunology Innovation · doi:10.7243/2053-213x-1-3 · Cited by 5
Short Communication: Nuclear JAK3 and Its Involvement in CD4 Activation in HIV-Infected Patients
Landires, I., Núñez-Samudio, V., & Thèze, J. (2013) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2012.0249 · Cited by 5
Fukuda, K., Miura, Y., Maeda, T., Hayashi, S., & Kuroda, R. (2019) · Biomedical Reports · doi:10.3892/br.2019.1216 · Cited by 5
An immunomodulating peptide with potential to suppress tumour growth and autoimmunity
Agrez, M., Chandler, C., Thurecht, K. J., Fletcher, N. L., Liu, F., Subramaniam, G., Howard, C. B., Blyth, B. J., Parker, S., Turner, D. G., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-47229-y · Cited by 4
Gene function revealed at the moment of stochastic gene silencing
Gupta, S., & Cai, J. J. (2025) · Communications Biology · doi:10.1038/s42003-025-07530-0 · Cited by 4
Groner, B., & Vafaizadeh, V. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.08.019 · Cited by 4
Negative regulators take center stage
Monticelli, S., & Sallusto, F. (2012) · Nature Immunology · doi:10.1038/ni.2377 · Cited by 4
Gaafar, N. A. G., Aslani, M., Aghazadeh, Z., Mortazavi‐Jahromi, S. S., Razavi, A., & Mirshafiey, A. (2020) · Reumatismo · doi:10.4081/reumatismo.2020.1235 · Cited by 4
IL-23 enhances the malignant properties of hepatoma cells by attenuation of HNF4α
Jiang, Q., Sun, Y., Guo, Z., Chen, R., Ma, S., Fu, M., Zhu, H., Ning, Q., Lei, P., & Shen, G. (2018) · Oncotarget · doi:10.18632/oncotarget.24875 · Cited by 4
Adoue, V., & Joffre, O. P. (2020) · médecine/sciences · doi:10.1051/medsci/2020022 · Cited by 4
Wang, Z., Lai, L., Ran, S., Li, Y., Zhao, J., Wu, J., Guo, C., Cui, J., & Xia, J. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-07383-5 · Cited by 4
Zhao, M., Zhang, C., Zhang, X., Mu, Q., Li, Q., & Liu, Y. (2026) · Nature Communications · doi:10.1038/s41467-025-67665-w · Cited by 3
Raykhel, I. B., Ronkainen, V., Myllyharju, J., & Manninen, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-62955-7 · Cited by 3
Role of SOCS proteins in inflammation and autoimmune diseases
Fukaya, T., Suzuki, M., Sakaguchi, R., Yasukawa, H., & Yoshimura, A. (2011) · Inflammation and Regeneration · doi:10.2492/inflammregen.31.382 · Cited by 3
Seo, J. M., Lee, J., Ji, G. E., & You, J. C. (2011) · Experimental & Molecular Medicine · doi:10.3858/emm.2011.43.9.058 · Cited by 3
A survey of disease connections for CD4+ T cell master genes and their directly linked genes
Li, W., Enríquez, J. E., Simpfendorfer, K. R., & Lemus, E. H. (2015) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2015.08.009 · Cited by 3
How Stats Interact with the Molecular Machinery of Transcriptional Activation
Jamieson, A. M., Farlik, M., & Decker, T. (2012) · Springer eBooks · doi:10.1007/978-3-7091-0891-8_5 · Cited by 3
Fowler, D. H. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812630-1.00012-8 · Cited by 3
Hai, L., Shi, X., & Wang, Q. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.642585 · Cited by 3
González‐Serna, D., Shi, C., Kerick, M., Hankinson, J., Ding, J., McGovern, A., Tutino, M., Martin, G. V., Ortego‐Centeno, N., Callejas-Rubio, J. L., et al. (2022) · medRxiv · doi:10.1101/2022.05.08.22274711 · Cited by 3
Transcriptomic Analysis of CRISPR/Cas9-Mediated TDP1-Knockout HEK293A CellsPreprint
Dyrkheeva, N. S., Zakharenko, A. L., Malakhova, A. A., Okorokova, L. S., Shtokalo, D. N., Medvedev, S. P., Tupikin, A. A., Kabilov, M. R., & Lavrik, O. I. (2023) · Preprints.org · doi:10.20944/preprints202312.0002.v1 · Cited by 3
Wüthrich, M., Okaa, U. J., Taira, C. L., Dias, L. D. S., & Klein, B. S. (2026) · mBio · doi:10.1128/mbio.00505-26 · Cited by 2
Yang, L., Liu, X., Lin, S., Chen, P., Chen, L., & Zhao, G. (2022) · Scandinavian Journal of Immunology · doi:10.1111/sji.13226 · Cited by 2
The Role of Human IL-17 Immunity in Fungal Disease
Maródi, L., Cypowyj, S., Casanova, J., & Puel, A. (2013) · Current Fungal Infection Reports · doi:10.1007/s12281-013-0131-4 · Cited by 2
Sardarmelli, Z., Sheikh, V., Solgi, G., & Behzad, M. (2023) · Human Immunology · doi:10.1016/j.humimm.2023.01.002 · Cited by 2
Kostrzewa‐Nowak, D., & Nowak, R. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.823469 · Cited by 2
Dreisinger, M., Roškar, Z., Goropevšek, A., Zakelšek, A., Čurič, S., Živko, N., Bevc, S., & Homšak, E. (2025) · Biomedicines · doi:10.3390/biomedicines13051204 · Cited by 2
Inflammatory Bowel Disease: Pathobiology
Connelly, T. M., & Koltun, W. A. (2016) · Springer eBooks · doi:10.1007/978-3-319-25970-3_44 · Cited by 1
The Interplay between Transcription Factors and Epigenetic Modifications in Th2 Cells
Onodera, A., Kokubo, K., & Nakayama, T. (2018) · InTech eBooks · doi:10.5772/intechopen.73027 · Cited by 1
Fowler, D. H. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-416004-0.00011-2 · Cited by 2
Zhuang, M., Le, J., Zhu, B., Zhang, W., Yan, H., Zhang, P., Wang, T., & Sun, Y. J. (2020) · Letters in Drug Design & Discovery · doi:10.2174/1570180817666200204104420 · Cited by 1
STAT3 Signaling Heterogeneity Underlies Cytokine-Expressing Fate in Th17 Cultures
Niese, M., Glosson, N. L., Serezani, A. P. M., Alakhras, N. S., & Kaplan, M. H. (2023) · ImmunoHorizons · doi:10.4049/immunohorizons.2300072 · Cited by 1
Molecular and Genetic Factors in Crohn’s Disease
Connelly, T. M., & Koltun, W. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-14181-7_2 · Cited by 1
Epigenetics and the Regulation of Inflammation
Hedrich, C. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800957-4.00006-0 · Cited by 1
Activation-induced re-organization of chromatin in human T cellsPreprint
Bediaga, N. G., Coughlan, H. D., Johanson, T. M., Garnham, A. L., Naselli, G., Schröder, J., Fearnley, L. G., Bandala‐Sanchez, E., Allan, R. S., Smyth, G. K., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.08.135020 · Cited by 1
Overview of Hematopoietic Cell Transplantation Immunology
Martin, P. J., & Shlomchik, W. D. (2015) · Wiley eBooks · doi:10.1002/9781118416426.ch9 · Cited by 1
Autoimmune Regulator (AIRE) in the Maintenance of Immunological Tolerance
Kekäläinen, E. (2011) · Työväentutkimus Vuosikirja
The effects of host response and vaccine design on early signaling profiles of MUC1-specific T cells
Reichenbach, D. K. (2013) · D-Scholarship@Pitt (University of Pittsburgh)
Development and stability of IL-17-secreting T cells
Glosson, N. L. (2014) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1736
Debuisson, D., Mari, N., Denanglaire, S., Léo, O., & Andris, F. (2014) · PLoS ONE · doi:10.1371/annotation/b0c3d5f5-5778-48af-85ed-abf1b9113a48
Function of JAKs and STATs in Lymphocytes: Bench to Bedside
Villarino, A. V., Yang, X., Hirahara, K., Kanno, Y., Shea, J. J. O., & Laurence, A. D. J. (2012) · Springer eBooks · doi:10.1007/978-3-7091-0891-8_13
Self-citationGwack, Y., Ribalet, B., Jew, M., Damoiseaux, R. D., Jung, M. E., Kim, K., & Srikanth, S. (2014)
Immunity and Disease Mechanisms of Jak/STAT Signaling in
O’Shea, J. J., Villarino, A. V., Kanno, Y., & Ferdinand, J. R. (2015)
Self-citationThe Secrets of T Cell Polarization
Vargas, T. R., & Apétoh, L. (2017) · Springer eBooks · doi:10.1007/978-3-319-62431-0_5
Chen, S., van Tok, M. N., Pots, D., Taurog, J. D., van de Sande, M. G. H., Baeten, D., & van Duivenvoorde, L. M. (2018) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2018-eular.3475
Locus specific DNA methylation in human immunological responses
Bergman, E. A. (2018) · Figshare
Liu, H., Li, X., & Wang, J. (2018) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2018-eular.2570
Ciccia, F., Rizzo, A., Guggino, G., Alessandro, R., Raimondo, S., Macaluso, F., Peralta, S., Milling, S. W. F., & Elewaut, D. S. (2018) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2018-eular.4535
Insights Into the Regulatory Requirements for T Follicular Helper Cell Development
Powell, M. D. (2019) · VTechWorks (Virginia Tech)
Dynamic regulation of DNA methylation in human T-cell biology
Lentini, A. (2019) · Linköping University medical dissertations · doi:10.3384/diss.diva-155116
Ghadiri, N., Hoseini, A., Ghaedi, K., Emamnia, N., Ganjalıkhani-Hakemi, M., Navabi, P., Shirzad, H., & Nasr‐Esfahani, M. H. (2018) · Journal of Shahrekord University of Medical Sciences · doi:10.34172/jsums.2019.48
A population of CD4 + T cells with a naïve phenotype stably polarized to the T H 1 lineagePreprint
Lo, J. W., de Mucha, M. V., Roberts, L. B., Garrido‐Mesa, N., Hertweck, A., Neves, J. F., Stolarczyk, É., Henderson, S. R., Jackson, I., Howard, J. K., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.14.202168
Sugiyama, G., Ohyama, Y., Yamada, T., Ishii, K., Kumamaru, W., Sumimoto, Y., Kiyoshima, T., Niiro, H., & Mori, Y. (2021) · Journal of Oral and Maxillofacial Surgery Medicine and Pathology · doi:10.1016/j.ajoms.2020.12.002
Multi-Level Chromosome Remodeling Underlying Activation of Human T CellsPreprint
Bediaga, N. G., Coughlan, H. D., Johanson, T. M., Garnham, A. L., Naselli, G., Schröder, J., Fearnley, L. G., anon, E., Smyth, G. K., Allan, R. S., et al. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3329249
Shumanska, M. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9677
Transcriptomic analysis of HEK293A cells with a CRISPR/Cas9-mediated TDP1 knockout
Dyrkheeva, N. S., Zakharenko, A. L., Malakhova, A. A., Okorokova, L. S., Shtokalo, D. N., Medvedev, S. P., Tupikin, A. A., Kabilov, M. R., & Lavrik, O. I. (2024) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2024.130616 · Cited by 3
Giraud, L., Guillou, C., Level, T., Durand, A., Charvet, C., Auffray, C., Martin, B., & Lucas, B. (2025) · Research Square · doi:10.21203/rs.3.rs-8403997/v1
Brunialti, E., Panzeri, A., Rizzi, N., Villa, A. M., Meda, C., Sfogliarini, C., Persano, S., Arlati, F., Lopez, M. L. G., Martelli, C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.29.702227
Tong, Y. E., Triana, S., Russo, D. D., Reiné, J., Rylance, J., Jochems, S. P., Akeju, O., Sabeti, P. C., Shalek, A. K., Ferreira, D. M., et al. (2026) · medRxiv · doi:10.64898/2026.02.05.26345662
Kroemer, M. (2018) · theses.fr (ABES) · doi:10.70675/f4ebb828z8a7ez47e9zbb78z4453ed026df3
Contrôle épigénétique de la biologie des lymphocytes T CD4
Malbec, A. (2018) · theses.fr (ABES) · doi:10.70675/6286d187zb91fz4014z9075z77e8f3c56b09
Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1
Binet, B. (2017) · theses.fr (ABES) · doi:10.70675/6d41174dz3861z4135za1c1zca48e1f1c237
Michieletto, M. F. (2018) · theses.fr (ABES) · doi:10.70675/08ff4eefze6baz4742zb02ez0942397f8c5a
Brunialti, E., Panzeri, A., Rizzi, N., Villa, A. M., Meda, C., Sfogliarini, C., Persano, S., Arlati, F., Lopez, M. L. G., Martelli, C., et al. (2026) · Molecular Therapy · doi:10.1016/j.ymthe.2026.05.028
Yi, F., Xiao, T., Jin, R., Zhou, J., Li, Y., Liao, H., Xu, W., Yuan, Y., Wu, M., Bi, P., et al. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1854754
Gao, F., Fung, A. A., Zhang, D., Lou, X., Nam, J., Yang, M., Tian, X., Farzad, N., Wang, D., Li, G., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.18.732453
Transcription factors in the development of Th9 cells
Goswami, R. (2013) · ProQuest Demo Repository · doi:10.7912/c2/1714
Metadata
- Authors
- O'Shea, J. J., Lahesmaa, R., Vahedi, G., Laurence, A., & Kanno, Y.
- Affiliations
- Åbo Akademi University (FI)
- National Institutes of Health (US)
- Venue
- Nature Reviews Immunology
- Published
- 2011-03-25
- Volume
- 11
- Issue
- 4
- Pages
- 239-250
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC3070307
- OpenAlex
- W2055082742
- Cited by
- 295
- References
- 148
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 11 · 2023: 9 · 2022: 16 · 2021: 17 · 2020: 15 · 2019: 24 · 2018: 27 · 2017: 15 · 2016: 19 · 2015: 25 · 2014: 27 · 2013: 36 · 2012: 26
- FWCI
- 2.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (ZIAAR041159)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- STAT proteins, cytokine signaling, epigenetic regulation, gene expression regulation, transcriptional repression, autoimmune disease, genome-wide association study
- MeSH terms
- Animals, Autoimmune Diseases, Gene Expression Regulation, T-Lymphocytes, Helper-Inducer, Humans, Immunologic Deficiency Syndromes, Lymphocyte Activation, Nucleosomes, Signal Transduction, Cytokines, Sequence Analysis, DNA, Genomics, STAT Transcription Factors, Mice, Genome-Wide Association Study
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