STAT3 positively regulates an early step in B-cell development

Stat3 as an Oncogene

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Identification of Clonogenic Common Lymphoid Progenitors in Mouse Bone Marrow

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Inducible Gene Targeting in Mice

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Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine

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Resolution and characterization of pro-B and pre-pro-B cell stages in normal mouse bone marrow.

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

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Roles of STAT3 in mediating the cell growth, differentiation and survival signals relayed through the IL-6 family of cytokine receptors

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What does Stat3 do?

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Development and maintenance of B and T lymphocytes requires antiapoptotic MCL-1

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The role of shared receptor motifs and common Stat proteins in the generation of cytokine pleiotropy and redundancy by IL-2, IL-4, IL-7, IL-13, and IL-15

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What does Stat3 do?

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B lymphocyte-specific, Cre-mediated mutagenesis in mice

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Targeted disruption of the flk2/flt3 gene leads to deficiencies in primitive hematopoietic progenitors

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Keratinocyte-specific ablation of Stat3 exhibits impaired skin remodeling, but does not affect skin morphogenesis

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Transcriptional Control of Early B Cell Development

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Expression and function of the interleukin 7 receptor in murine lymphocytes.

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Stat3 is required for ALK-mediated lymphomagenesis and provides a possible therapeutic target

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Distinctive and indispensable roles of PU.1 in maintenance of hematopoietic stem cells and their differentiation

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Hes binding to STAT3 mediates crosstalk between Notch and JAK–STAT signalling

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Essential role of STAT3 for embryonic stem cell pluripotency

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Stat5a/b are essential for normal lymphoid development and differentiation

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Notch signaling controls the generation and differentiation of early T lineage progenitors

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STAT3 is required for Flt3L-dependent dendritic cell differentiation

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Resistance to chemotherapy via Stat3-dependent overexpression of Bcl-2 in metastatic breast cancer cells

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PU.1 Regulates Expression of the Interleukin-7 Receptor in Lymphoid Progenitors

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Key Role of flt3 Ligand in Regulation of the Common Lymphoid Progenitor but Not in Maintenance of the Hematopoietic Stem Cell Pool

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Arrested B Lymphopoiesis and Persistence of Activated B Cells in Adult Interleukin 7−/− Mice

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STAT3 is a negative regulator of granulopoiesis but is not required for G-CSF-dependent differentiation

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Assembling a Gene Regulatory Network for Specification of the B Cell Fate

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Transcriptional networks in developing and mature B cells

Matthias, P., & Rolink, A. G. (2005) · Nature reviews. Immunology · doi:10.1038/nri1633 · Cited by 238 · see citing works

Stat5a/b contribute to interleukin 7–induced B-cell precursor expansion, but abl- andbcr/abl-induced transformation are independent of Stat5

Sexl, V., Piekorz, R. P., Moriggl, R., Rohrer, J., Brown, M. P., Bunting, K. D., Rothammer, K., Roussel, M. F., & Ihle, J. N. (2000) · Blood · doi:10.1182/blood.v96.6.2277 · Cited by 198 · see citing works

Contingent gene regulatory networks and B cell fate specification

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Complementary Signaling through flt3 and Interleukin-7 Receptor α Is Indispensable for Fetal and Adult B Cell Genesis

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Signal Transducer and Activator of Transcription-3 (STAT3) Is Constitutively Activated in Normal, Self-renewing B-1 Cells but Only Inducibly Expressed in Conventional B Lymphocytes

Karras, J., Wang, Z.-H., Huo, L., Howard, R., Frank, D., & Rothstein, T. (1997) · Journal of Experimental Medicine · doi:10.1084/jem.185.6.1035 · Cited by 160 · see citing works

Regulation of interleukin 7–dependent immunoglobulin heavy-chain variable gene rearrangements by transcription factor STAT5

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Critical role for Stat3 in T-dependent terminal differentiation of IgG B cells

Fornek, J. L., Tygrett, L. T., Waldschmidt, T. J., Poli, V., Rickert, R. C., & Kansas, G. S. (2006) · Blood · doi:10.1182/blood-2005-07-2871 · Cited by 148 · see citing works

Role of STAT3 and PI 3-Kinase/Akt in Mediating the Survival Actions of Cytokines on Sensory Neurons

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STAT1 Affects Lymphocyte Survival and Proliferation Partially Independent of Its Role Downstream of IFN-γ

Lee, C., Smith, E., Gimeno, R., Gertner, R., & Levy, D. E. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.3.1286 · Cited by 145 · see citing works

STAT5 Activation Underlies IL7 Receptor-Dependent B Cell Development

Goetz, C. A., Harmon, I., O’Neil, J. J., Burchill, M. A., & Farrar, M. A. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.8.4770 · Cited by 144 · see citing works

Serine phosphorylation of STAT3 is essential for Mcl-1 expression and macrophage survival

Liu, H., Ma, Y., Cole, S. M., Zander, C., Chen, K.-H., Karras, J., & Pope, R. M. (2003) · Blood · doi:10.1182/blood-2002-11-3396 · Cited by 136 · see citing works

Density of the Notch ligand Delta1 determines generation of B and T cell precursors from hematopoietic stem cells

Dallas, M. H., Varnum‐Finney, B., Delaney, C. S., Kato, K., & Bernstein, I. D. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20042450 · Cited by 112 · see citing works

Stat3 in Thymic Epithelial Cells Is Essential for Postnatal Maintenance of Thymic Architecture and Thymocyte Survival

Sano, S., Takahama, Y., Sugawara, T., Kosaka, H., Itami, S., Yoshikawa, K., Miyazaki, J., van Ewijk, W., & Takeda, J. (2001) · Immunity · doi:10.1016/s1074-7613(01)00180-7 · Cited by 111 · see citing works

PU.1 is not strictly required for B cell development and its absence induces a B-2 to B-1 cell switch

Ye, M., Ermakova, O. V., & Graf, T. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051089 · Cited by 90 · see citing works

CD19 Function in Central and Peripheral B-Cell Development

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The development of functional B lymphocytes in conditional PU.1 knock-out mice

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Differential Regulation of Constitutive Major Histocompatibility Complex Class I Expression in T and B Lymphocytes

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Overexpression of Bcl-2 does not rescue impaired B lymphopoiesis in IL- 7 receptor-deficient mice but can enhance survival of mature B cells

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STAT3 signaling in immunity

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Orchestrating B cell lymphopoiesis through interplay of IL-7 receptor and pre-B cell receptor signalling

Clark, M. R., Mandal, M., Ochiai, K., & Singh, H. (2013) · Nature reviews. Immunology · doi:10.1038/nri3570 · Cited by 337 · see citing works

Targeting Janus Kinases and Signal Transducer and Activator of Transcription 3 To Treat Inflammation, Fibrosis, and Cancer: Rationale, Progress, and Caution

Bharadwaj, U., Kasembeli, M. M., Robinson, P., & Tweardy, D. J. (2020) · Pharmacological Reviews · doi:10.1124/pr.119.018440 · Cited by 314 · see citing works

The many roles of IL-7 in B cell development; Mediator of survival, proliferation and differentiation

Corfe, S. A., & Paige, C. J. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.02.001 · Cited by 211 · see citing works

Small Molecule Inhibitors of Signal Transducer and Activator of Transcription 3 (Stat3) Protein

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Survival of Long-Lived Plasma Cells (LLPC): Piecing Together the Puzzle

Lightman, S. M., Utley, A. T., & Lee, K. P. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00965 · Cited by 198 · see citing works

Clinical Manifestations, Etiology, and Pathogenesis of the Hyper-IgE Syndromes

Freeman, A. F., & Holland, S. M. (2009) · Pediatric Research · doi:10.1203/pdr.0b013e31819dc8c5 · Cited by 193 · see citing works

STAT3 Negatively Regulates Type I IFN-Mediated Antiviral Response

Wang, W., Levy, D. E., & Lee, C. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004128 · Cited by 178 · see citing works

Mechanisms regulating dendritic cell specification and development

Watowich, S. S., & Liu, Y. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00949.x · Cited by 148 · see citing works

Fine-Tuning of Type I Interferon Response by STAT3

Tsai, M.-H., Pai, L., & Lee, C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01448 · Cited by 119 · see citing works

The Role of IL-7 and IL-7R in Cancer Pathophysiology and Immunotherapy

Wang, C., Kong, L.-Z., Kim, S., Lee, S., Oh, S., Jo, S., Jang, I.-H., & Kim, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810412 · Cited by 112 · see citing works

Leptin signaling maintains B-cell homeostasis via induction of Bcl-2 and Cyclin D1

Lam, Q. L. K., Wang, S., Ko, O. K. H., Kincade, P. W., & Lu, L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004185107 · Cited by 106 · see citing works

Interleukin-27 directly induces differentiation in hematopoietic stem cells.

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Reduced memory B cells in patients with hyper IgE syndrome

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Reduction of Stat3 Activity Attenuates HIV-Induced Kidney Injury

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STAT transcription factors in hematopoiesis and leukemogenesis: opportunities for therapeutic intervention

Dorritie, K., McCubrey, J. A., & Johnson, D. E. (2014) · Leukemia · doi:10.1038/leu.2013.192 · Cited by 72 · see citing works

Multicellular Effects of STAT3 in Non-small Cell Lung Cancer: Mechanistic Insights and Therapeutic Opportunities

Parakh, S., Ernst, M., & Poh, A. R. (2021) · Cancers · doi:10.3390/cancers13246228 · Cited by 76 · see citing works

The Mouse Immunoglobulin Heavy Chain V-D Intergenic Sequence Contains Insulators That May Regulate Ordered V(D)J Recombination

Featherstone, K., Wood, A. L., Bowen, A. J., & Corcoran, A. E. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.098251 · Cited by 75 · see citing works

Human hyper-IgE syndrome: singular or plural?

Zhang, Q., Boisson, B., Béziat, V., Puel, A., & Casanova, J.-L. (2018) · Mammalian Genome · doi:10.1007/s00335-018-9767-2 · Cited by 67 · see citing works

Lymphocyte Development: Integration of DNA Damage Response Signaling

Bednarski, J. J., & Sleckman, B. P. (2012) · Advances in immunology · doi:10.1016/b978-0-12-394300-2.00006-5 · Cited by 61 · see citing works

Role of STAT3 in Transformation and Drug Resistance in CML

Nair, R. R., Tolentino, J. H. G., & Hazlehurst, L. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00030 · Cited by 56 · see citing works

The dark and the bright side of Stat3: proto-oncogene and tumor-suppressor

Ecker, A. (2009) · Frontiers in bioscience · doi:10.2741/3425 · Cited by 48 · see citing works

STAT3 mediates oncogenic addiction to TEL-AML1 in t(12;21) acute lymphoblastic leukemia

Mangolini, M., de Boer, J., Walf-Vorderwülbecke, V., Pieters, R., den Boer, M. L., & Williams, O. (2013) · Blood · doi:10.1182/blood-2012-11-465252 · Cited by 47 · see citing works

STAT3 Role in T-Cell Memory Formation

Kaminskiy, Y., & Melenhorst, J. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052878 · Cited by 44 · see citing works

Isoform-specific targeting of ROCK proteins in immune cells

Zanin‐Zhorov, A., Flynn, R. P., Waksal, S. D., & Blazar, B. R. (2016) · Small GTPases · doi:10.1080/21541248.2016.1181698 · Cited by 44 · see citing works

Regulation of hematopoietic cell development and function by Stat3

Pamela, A. H. (2009) · Frontiers in bioscience · doi:10.2741/3597 · Cited by 36 · see citing works

GRiNCH: simultaneous smoothing and detection of topological units of genome organization from sparse chromatin contact count matrices with matrix factorization

Lee, D.-I., & Roy, S. (2021) · Genome biology · doi:10.1186/s13059-021-02378-z · Cited by 34 · see citing works

STAT transcription factors in normal and cancer stem cells.

Dorritie, K., Redner, R., & Johnson, D. E. (2014) · Advances in Biological Regulation · doi:10.1016/j.jbior.2014.05.004 · Cited by 34 · see citing works

BATF regulates innate lymphoid cell hematopoiesis and homeostasis

Liu, Q., Kim, M. H., Friesen, L., & Kim, C. H. (2020) · Science Immunology · doi:10.1126/sciimmunol.aaz8154 · Cited by 31 · see citing works

TGF-βR inhibitor SB431542 restores immune suppression induced by regulatory B–T cell axis and decreases tumour burden in murine fibrosarcoma

Premkumar, K., & Shankar, B. S. (2020) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-020-02666-w · Cited by 29 · see citing works

STAT3 deficiency in B cells exacerbates uveitis by promoting expansion of pathogenic lymphocytes and suppressing regulatory B cells (Bregs) and Tregs

Oladipupo, F. O., Yu, C., Olumuyide, E., Jittaysothorn, Y., Choi, J. K., & Egwuagu, C. E. (2020) · Scientific Reports · doi:10.1038/s41598-020-73093-1 · Cited by 28 · see citing works

Interleukin-7, a New Cytokine Targeting the Mouse Hypothalamic Arcuate Nucleus: Role in Body Weight and Food Intake Regulation

Macia, L., Viltart, O., Delacre, M., Sachot, C., Héliot, L., Santo, J. P. D., & Wolowczuk, I. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009953 · Cited by 26 · see citing works

Molecular characterization of acute myeloid leukemia and its impact on treatment

Frankfurt, O., Licht, J. D., & Tallman, M. S. (2007) · Current Opinion in Oncology · doi:10.1097/cco.0b013e3282f10e55 · Cited by 26 · see citing works

Combining STAT3-Targeting Agents with Immune Checkpoint Inhibitors in NSCLC

Papavassiliou, K. A., Marinos, G., & Papavassiliou, A. G. (2023) · Cancers · doi:10.3390/cancers15020386 · Cited by 26 · see citing works

Advances in IL-7 Research on Tumour Therapy

Fu, C., Zhang, X., Zhang, X., Wang, D., Han, S., & Ma, Z. (2024) · Pharmaceuticals · doi:10.3390/ph17040415 · Cited by 25 · see citing works

STAT2 hypomorphic mutant mice display impaired dendritic cell development and antiviral response

Chen, L., Wei, P., Liu, T., Kao, C.-H., Pai, L., & Lee, C. (2009) · Journal of Biomedical Science · doi:10.1186/1423-0127-16-22 · Cited by 25 · see citing works

Meta-Analysis of Two Human RNA-seq Datasets to Determine Periodontitis Diagnostic Biomarkers and Drug Target Candidates

Moreno, C. M., Bybee, E., Freitas, C. M. T., Pickett, B. E., & Weber, K. S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105580 · Cited by 23 · see citing works

Human and mouse early B cell development: So similar but so different

Korzhenevich, J., Janowska, I., van der Burg, M., & Rizzi, M. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.07.004 · Cited by 23 · see citing works

A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis

Kasap, N., Çelik, V., Işık, S., Cennetoğlu, P., Kıykım, A. A., Eltan, S. B., Nain, E., Öğülür, İ., Başer, D., Akkelle, E., et al. (2020) · Clinical Immunology · doi:10.1016/j.clim.2020.108645 · Cited by 22 · see citing works

Cell atlas of the Atlantic salmon spleen reveals immune cell heterogeneity and cell-specific responses to bacterial infection

Sun, J., Daniels, R. R., Balic, A., Andresen, A. M. S., Bjørgen, H., Dobie, R., Henderson, N. C., Koppang, E. O., Martín, S., Fosse, J. H., et al. (2024) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2024.109358 · Cited by 21 · see citing works

SOCS3 Deletion in B Cells Alters Cytokine Responses and Germinal Center Output

Jones, S. A., White, C. A., Robb, L. G., Alexander, W. S., & Tarlinton, D. M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1102057 · Cited by 20 · see citing works

Circular RNA Circ_0000677 promotes cell proliferation by regulating microRNA-106b-5p/CCND1 in non-small cell lung cancer

Hu, X. T., Wang, P., Qu, C., Zhang, H., & Li, L. (2021) · Bioengineered · doi:10.1080/21655979.2021.1965697 · Cited by 19 · see citing works

Oncogenic STAT Transcription Factors as Targets for Cancer Therapy: Innovative Strategies and Clinical Translation

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Treatment of IL-21R-Fc control autoimmune arthritis via suppression of STAT3 signal pathway mediated regulation of the Th17/Treg balance and plasma B cells

Ryu, J., Lee, J. J., Kim, E., Seo, H.-B., Park, J., Lee, S.-Y., Moon, Y., Yoo, S., Park, Y.-W., Park, S., et al. (2014) · Immunology Letters · doi:10.1016/j.imlet.2014.09.007 · Cited by 19 · see citing works

Signal transducer and activator of transcription 3 regulation by novel binding partners

Matsuda, T. (2015) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v6.i4.324 · Cited by 19 · see citing works

Improvement of Sclerodermatous Graft-Versus-Host Disease in Mice by Niclosamide

Morin, F., Kavian, N., Nicco, C., Cerles, O., Chéreau, C., & Batteux, F. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.06.624 · Cited by 19 · see citing works

PIAS3 suppresses acute graft- versus -host disease by modulating effector T and B cell subsets through inhibition of STAT3 activation

Lee, S., Moon, S.-J., Park, M.-J., Kim, E., Moon, Y., & Cho, M. (2014) · Immunology Letters · doi:10.1016/j.imlet.2014.03.014 · Cited by 18 · see citing works

Deletion of Stat3 enhances myeloid cell expansion and increases the severity of myeloproliferative neoplasms in Jak2V617F knock-in mice

Yan, D., Jobe, F., Hutchison, R. E., & Mohi, G. (2015) · Leukemia · doi:10.1038/leu.2015.116 · Cited by 17 · see citing works

The research development of STAT3 in hepatic ischemia-reperfusion injury

Yang, H., Zhang, P., Wang, Q., Cheng, K., & Zhao, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1066222 · Cited by 16 · see citing works

A Hematopoietic Perspective on the Promiscuity and Specificity of Gα16 Signaling

Su, Y. L., Ho, M. K. C., & Wong, Y. H. (2009) · Neurosignals · doi:10.1159/000186691 · Cited by 16 · see citing works

Interleukin (IL)-7 Signaling in the Tumor Microenvironment

Bednarz-Misa, I. S., Bromke, M. A., & Krzystek‐Korpacka, M. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-55617-4_2 · Cited by 15 · see citing works

The Role of the JAK–STAT Pathway in Childhood B-Cell Acute Lymphoblastic Leukemia

Ziętara, K. J., Wróblewska, K., Zajączkowska, M., Taczała, J., & Lejman, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136844 · Cited by 14 · see citing works

Impaired B-Cell Differentiation in a Patient With STAT1 Gain-of-Function Mutation

Nemoto, K., Kawanami, T., Hoshina, T., Ishimura, M., Yamasaki, K., Okada, S., Kanegane, H., Yatera, K., & Kusuhara, K. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.557521 · Cited by 14 · see citing works

Epigenomic profiling of isolated blood cell types reveals highly specific B cell smoking signatures and links to disease risk

Wang, X., Campbell, M. R., Cho, H., Pittman, G. S., Martos, S. N., & Bell, D. A. (2023) · Clinical Epigenetics · doi:10.1186/s13148-023-01507-8 · Cited by 14 · see citing works

STAT3 couples with 14-3-3σ to regulate BCR signaling, B-cell differentiation, and IgE production

Du, Z., Chen, A., Huang, L., Dai, X., Chen, Q., Yang, D., Li, L., Miller, H. E., Westerberg, L. S., Ding, Y., et al. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.09.033 · Cited by 13 · see citing works

TCDD-mediated suppression of naïve human B cell IgM secretion involves aryl hydrocarbon receptor-mediated reduction in STAT3 serine 727 phosphorylation and is restored by interferon-γ

Blevins, L. K., Zhou, J., Crawford, R. B., & Kaminski, N. E. (2019) · Cellular Signalling · doi:10.1016/j.cellsig.2019.109447 · Cited by 13 · see citing works

Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells

Bekiaris, V., Šedý, J. R., & Ware, C. F. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00654 · Cited by 12 · see citing works

Prolactin Rescues Immature B Cells from Apoptosis-Induced BCR-Aggregation through STAT3, Bcl2a1a, Bcl2l2, and Birc5 in Lupus-Prone MRL/lpr Mice

Flores-Fernández, R., Aponte-López, A., Suárez-Arriaga, M. C., Gorocica-Rosete, P., Pizaña-Venegas, A., Chávez-Sanchéz, L., Blanco-Favela, F., Fuentes‐Pananá, E. M., & Chávez-Rueda, A. K. (2021) · Cells · doi:10.3390/cells10020316 · Cited by 12 · see citing works

Natural pseurotins and analogs thereof inhibit activation of B-cells and differentiation into the plasma cells

Vašíček, O., Fedr, R., Skoroplyas, S., Chalupa, D., Sklenář, M., Tharra, P. R., Švenda, J., & Kubala, L. (2020) · Phytomedicine · doi:10.1016/j.phymed.2020.153194 · Cited by 11 · see citing works

Functional involvement of Daxx in gp130‐mediated cell growth and survival in BaF3 cells

Muromoto, R., Kuroda, M., Togi, S., Sekine, Y., Nanbo, A., Shimoda, K., Oritani, K., & Matsuda, T. (2010) · European Journal of Immunology · doi:10.1002/eji.201040688 · Cited by 10 · see citing works

Apigenin ameliorates lupus nephritis by inhibiting SAT3 signaling in CD8 + T cells

Liu, J., Wang, N.-Z., Wu, Z., Gan, Y.-H., Ji, J., Huang, Z., Du, Y., Wen, C., Tian, F.-Y., Fan, Y., et al. (2024) · Food & Function · doi:10.1039/d4fo02773f · Cited by 9 · see citing works

Single-cell transcriptomic profiling reveals dysregulation of B-cell subset function in patients with chronic hepatitis B

Li, J., Chen, S., Zhen, C., Fan, P., Tang, L., Zhang, Y., Wang, F., & Zhang, C. (2025) · Hepatology International · doi:10.1007/s12072-025-10846-y · Cited by 7 · see citing works

Signal-transducing adaptor protein-1 and protein-2 in hematopoiesis and diseases

Ichii, M., Oritani, K., Toda, J., Hosen, N., Matsuda, T., & Kanakura, Y. (2021) · Experimental Hematology · doi:10.1016/j.exphem.2021.11.002 · Cited by 7 · see citing works

Replenishment of the B cell compartment after doxorubicin-induced hematopoietic toxicity is facilitated by STAT1

Datta, S., Parajuli, N., Tymoszuk, P., Ottina, E., Parson, W., Sgonc, R., Villunger, A., & Doppler, W. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0113053 · Cited by 6 · see citing works

Molecular mechanisms of versatile biological activity of interleukin-7

Slyvka, A., & Okunev, O. V. (2014) · Biopolymers and Cell · doi:10.7124/bc.0008b1 · Cited by 6 · see citing works

Dichotomy in redundant enhancers points to presence of initiators of gene regulation

Song, W., & Ovcharenko, I. (2018) · BMC Genomics · doi:10.1186/s12864-018-5335-0 · Cited by 6 · see citing works

Enhancer jungles establish robust tissue-specific regulatory control in the human genome

Li, S., & Ovcharenko, I. (2019) · Genomics · doi:10.1016/j.ygeno.2019.12.022 · Cited by 5 · see citing works

Stat3 Regulates Developmental Hematopoiesis and Impacts Myeloid Cell Function via Canonical and Non-Canonical Modalities

Sobah, M. L., Liongue, C., & Ward, A. C. (2024) · Journal of Innate Immunity · doi:10.1159/000538364 · Cited by 5 · see citing works

Hepatitis C virus modified sE2 F442NYT as an antigen in candidate vaccine facilitates human immune cell activation

Haga, Y., Meyer, K., Sung, M. M. H., Reagan, E. K., Weissman, D., & Ray, R. (2023) · Journal of Virology · doi:10.1128/jvi.01809-23 · Cited by 5 · see citing works

Efficient Generation of Plasmacytoid Dendritic Cell from Common Lymphoid Progenitors by Flt3 Ligand

Chen, Y., Chang, S., Chen, T., & Lee, C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135217 · Cited by 5 · see citing works

Targeting the Bone Marrow with Activin A-Overexpressing Embryonic Multipotent Stromal Cells Specifically Modifies B Lymphopoiesis

Parameswaran, R., Morad, V., Laronne, A., Rousso-Noori, L., Shani, N., Amara, S. N.-A., & Zipori, D. (2008) · Stem Cells and Development · doi:10.1089/scd.2007.0099 · Cited by 5 · see citing works

A novel immunological perspective on female-specific cancers: Exploring the signaling pathways of tertiary lymphoid structures and their clinical applications

Li, S., Zhu, X., Liu, Y.-Y., & Chen, M. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123800 · Cited by 4 · see citing works

Susceptibility of pediatric acute lymphoblastic leukemia to STAT3 inhibition depends on p53 induction

Gasparoli, L., Virely, C., Tsakaneli, A., Che, N., Edwards, D., Bartram, J. L., Hubank, M. J. F., Pal, D., Heidenreich, O. T., Martens, J. H. A., et al. (2023) · Haematologica · doi:10.3324/haematol.2023.283613 · Cited by 4 · see citing works

The roles of BST‐2 in murine B cell development and on virus propagation

Urata, S., Yamaguchi, S., Nambu, A., Sudo, K., Nakae, S., & Yasuda, J. (2023) · Microbiology and Immunology · doi:10.1111/1348-0421.13049 · Cited by 4 · see citing works

<i>PELI2</i> regulates early B-cell progenitor differentiation and related leukemia via the IL-7R expression

Xu, Y., Zhou, Q., Wang, X., Zhang, A., Qi, W., Li, Y., Zheng, C., Guan, J., Sun, T., Li, J., et al. (2023) · Haematologica · doi:10.3324/haematol.2023.284041 · Cited by 3 · see citing works

Development of B Lymphocytes

Corfe, S. A., & Paige, C. (2009) · Springer eBooks · doi:10.1007/978-0-387-85816-6_8 · Cited by 8 · see citing works

Expression of biologically active bovine interleukin 7 and evaluating the activity in vitro

Lijo, J., Nagaraj, V. K., Dechamma, H. J., & Reddy, G. R. (2016) · Veterinary World · doi:10.14202/vetworld.2016.160-165 · Cited by 3 · see citing works

A CD4-lineage erythro–myeloid progenitor within the adult bone marrow defines an alternative pathway for macrophage generation

Tikoo, S., Rohit, J., Martinez, B., Song, R., Wielscher, M., Márquez-Burgoa, C., Hladik, A., Rizzetto, S., Shaw, L. E., Ghannadan, M., et al. (2026) · Nature Immunology · doi:10.1038/s41590-026-02686-1 · Cited by 2 · see citing works

Death Domain-associated Protein (DAXX)-mediated Regulation of Transcription and Cell Death

Muromoto, R. (2012) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.132.979 · Cited by 2 · see citing works

Proliferation and Differentiation Programs of Developing B Cells

Werner, M., & Jumaa, H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397933-9.00006-0 · Cited by 2 · see citing works

A distinct CD115 - erythro-myeloid precursor present at the maternal-embryonic interface and in the bone marrow of adult micePreprint

Tikoo, S., Jain, R., Martinez, B., Song, R., Wielscher, M., Rizzetto, S., Shaw, L. E., Mitchell, A. J., Torres-Pacheco, M. E., Luciani, F., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.24.453629 · Cited by 2 · see citing works

Insights Into the Susceptibility of Fungal Infection and STAT3 Genetic Mutations

Li, F., Liu, X., Li, Y., Wu, J., Dang, N., & Guo, J. (2026) · Mycoses · doi:10.1111/myc.70200 · Cited by 1 · see citing works

New Insights in the Development of Human B Lymphocytes

Blom, B. (2012) · Springer eBooks · doi:10.1007/978-1-4471-4174-7_1 · Cited by 1 · see citing works

SUMO-SPECIFIC PROTEASE 1 CONTROLS LYMPHOID DEVELOPMENT THROUGH REGULATION OF SUMOYLATION/ ACETYLATION SWITCH IN STAT5

Nguyen, T. V. (2011)

Regulación de la linfopoyesis B por la cisteín proteasa catepsina-L

Badano, M. N. (2012) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)

Regulation of B Lymphopoiesis: The Role of IL-7, SOCS-1, Heparan Sulfate and CD19 in Mediating B Cell Development

Corfe, S. A. (2012) · TSpace (University of Toronto)

Role of STAT3 N-terminal domain and GAS-site recognition in signaling and crosstalk with STAT1 and NF-κB

Martincuks, A., Müller-Newen, G., Lüscher, B., & Zenke, M. (2017) · RWTH Publications (RWTH Aachen) · doi:10.18154/rwth-2017-01944

Defining the Requirement for ShcA IN Murine B Cell Development

Giles, A. J. (2009) · doi:10.18130/v3rz7f

Xist-Dependent Impaired Lymphopoiesis in Male Offspring is a Unique Hallmark of Xchromosome Imprinting During Maternal SchistosomiasisPreprint

Gibbs, L. C., Oviedo, J. M., Ondigo, B. N., & Fairfax, K. C. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4135720

Additional file 2 of GRiNCH: simultaneous smoothing and detection of topological units of genome organization from sparse chromatin contact count matrices with matrix factorization

Lee, D.-I., & Roy, S. (2021) · Figshare · doi:10.6084/m9.figshare.14676791

Additional file 1 of GRiNCH: simultaneous smoothing and detection of topological units of genome organization from sparse chromatin contact count matrices with matrix factorization

Lee, D.-I., & Roy, S. (2021) · Figshare · doi:10.6084/m9.figshare.14676788

Additional file 4 of GRiNCH: simultaneous smoothing and detection of topological units of genome organization from sparse chromatin contact count matrices with matrix factorization

Lee, D.-I., & Roy, S. (2021) · Figshare · doi:10.6084/m9.figshare.14676797

Caractérisation et modélisation des pathologies lymphoïdes présentant des gains du chromosome 21

Laurent, A. P. (2019) · doi:10.70675/ed87382fza9bcz45fdz8589zd8c7fb99d3a9

Régulation de la prolifération des leucémies aiguës lymphocytaires de type B (LAL-B) par le microenvironnement de la moëlle osseuse

Pelletier, J. (2019) · doi:10.70675/4adb151dzc474z4467z8a3ez0e929ea88d07

BindingDB Entry 50040568: Small molecule inhibitors of signal transducer and activator of transcription 3 (Stat3) protein.

BindingDB (2013) · UC San Diego · doi:10.7270/q2cj8fkk

From bloodjournal.hematologylibrary.org at PENN STATE UNIVERSITY on February 21, 2013. For personal use only.

Chou, W.-C., Levy, D. E., Lee, C.-K., & Levy, W.-C. C. D. E. (2006)

The Tetraspanin CD53 Regulates Early B Cell Development by Promoting IL-7R Signaling

Greenberg, Z. J., Monlish, D. A., Bartnett, R. L., Yang, Y., Shen, G., Li, W., Bednarski, J. J., & Schuettpelz, L. G. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900539 · Cited by 27 · see citing works

Intrinsic function of STAT3 in B cells is to promote B cell proliferation and maturation

Oladipupo, F. O., Egwuagu, C. E., Yu, C., & Choi, J. K. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.202.supp.123.10 · Cited by 3 · see citing works

Non-cirrhotic portal hypertension with hypoxaemia.

Cadranel, J., Cadranel, J. L., Buffet, C., Fabrè, M., Pelletier, G., Ink, O., Milleron, B. J., & Etienne, J. P. (1988) · Gut · doi:10.1136/gut.29.6.876 · Cited by 1 · see citing works

Stat5 Is Essential for Early B Cell Development but Not for B Cell Maturation and Function

Dai, X., Chen, Y., Di, L., Podd, A., Li, G., Bunting, K. D., Hennighausen, L. G., Wen, R., & Wang, D. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.2.1068 · Cited by 65 · see citing works