Colony-stimulating factors in inflammation and autoimmunity

Obesity is associated with macrophage accumulation in adipose tissue

Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041

Inflammation and metabolic disorders

Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199

Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes

MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528

Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor.

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Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties

Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,504

Tumour-educated macrophages promote tumour progression and metastasis

Pollard, J. W. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1256 · Cited by 3,413

Macrophages: Obligate Partners for Tumor Cell Migration, Invasion, and Metastasis

Condeelis, J. S., & Pollard, J. W. (2006) · Cell · doi:10.1016/j.cell.2006.01.007 · Cited by 2,677

Cytokines in the pathogenesis of rheumatoid arthritis

McInnes, I. B., & Schett, G. A. (2007) · Nature reviews. Immunology · doi:10.1038/nri2094 · Cited by 2,575

Ischemia- and cytokine-induced mobilization of bone marrow-derived endothelial progenitor cells for neovascularization

Takahashi, T., Kalka, C., Masuda, H., Chen, D., Silver, M., Kearney, M., Magner, M., Isner, J. M., & Asahara, T. (1999) · Nature Medicine · doi:10.1038/7434 · Cited by 2,421

The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF 1

Sherr, C. J., Rettenmier, C. W., Sacca, R. E., Roussel, M. F., Look, A. T., & Stanley, E. R. (1985) · Cell · doi:10.1016/s0092-8674(85)80047-7 · Cited by 1,539

Culture and Differentiation of Monocyte Derived Macrophages Using Human Serum: An Optimized Method

Jazi, M. S., Mohammadi, S., & Sedighi, S. (2016) · Zahedan Journal of Research in Medical Sciences · doi:10.17795/zjrms-7362 · Cited by 10

Pulmonary pharmacodynamics of an anti-GM-CSFRα antibody enables therapeutic dosing that limits exposure in the lung

Campbell, J., Nys, J. A., Eghobamien, L., Cohen, E. S., Robinson, M. J., & Sleeman, M. A. (2016) · mAbs · doi:10.1080/19420862.2016.1215790 · Cited by 10

M-MDSC in vitro generation from mouse bone marrow with IL-3 reveals high expression and functional activity of arginase 1

Aintablian, A., Strozniak, S., Heuer, M., & Lutz, M. B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1130600 · Cited by 9

Amniotic suspension allograft improves pain and function in a rat meniscal tear-induced osteoarthritis model

Kimmerling, K. A., Gomoll, A. H., Farr, J., & Mowry, K. C. (2022) · Arthritis Research & Therapy · doi:10.1186/s13075-022-02750-9 · Cited by 9

Identification and characterization of three Siglec15-related immune and prognostic subtypes of breast-invasive cancer

Cao, X., Zhou, Y., Mao, F., Lin, Y., Zhou, X., & Sun, Q. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108561 · Cited by 9

Innate immune cellular therapeutics in transplantation

Ott, L. C., & Cuenca, A. G. (2023) · Frontiers in Transplantation · doi:10.3389/frtra.2023.1067512 · Cited by 10

Shooting the messenger: Targeting signal transduction pathways in leukemia and related disorders

Noor, S. M., Bell, R., & Ward, A. C. (2010) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2010.05.002 · Cited by 9

Serum vitamin C levels modulate the lifespan and endoplasmic reticulum stress response pathways in mice synthesizing a nonfunctional mutant WRN protein

Aumailley, L., Dubois, M. J., Brennan, T. A., Garand, C., Paquet, É. R., Pignolo, R. J., Marette, A., & Lebel, M. (2018) · The FASEB Journal · doi:10.1096/fj.201701176r · Cited by 9

Presymptomatic change in microRNAs modulates Tau pathology

Sharma, S., Khadimallah, I., Corya, A. W., Ali, Y., Rao, X., Liu, Y., & Lu, H. (2018) · Scientific Reports · doi:10.1038/s41598-018-27527-6 · Cited by 9

Severe Acute Respiratory Syndrome coronavirus-2 (SARS-CoV-2) Infection: Let the Virus Be Its Own Demise

Nemunaitis, J. J., Stanbery, L., & Senzer, N. N. (2020) · Future Virology · doi:10.2217/fvl-2020-0068 · Cited by 9

M2 Monocyte Polarization in Dialyzed Patients Is Associated with Increased Levels of M-CSF and Myeloperoxidase-Associated Oxidative Stress: Preliminary Results

Pireaux, V., Delporte, C., Rousseau, A., Desmet, J.-M., Antwerpen, P. V., Raes, M. J., & Boudjeltia, K. Z. (2021) · Biomedicines · doi:10.3390/biomedicines9010084 · Cited by 9

Diagnostic Value of Interleukin-34 as a Novel Biomarker for Severity of Knee Osteoarthritis

Udomsinprasert, W., Panon, K., Preechanukul, S., Jittikoon, J., Jinawath, A., & Honsawek, S. (2021) · Cartilage · doi:10.1177/1947603521990866 · Cited by 9

Shikonin alleviates collagen-induced arthritis mice by inhibiting M1 macrophage polarization.

He, L., Luan, H., Qin, Q., Juan, H. E., Chen, J., Yiping, H. U., Yueming, C., Sun, D., Yu, S., & Wang, Q. (2022) · PubMed Central · doi:10.19852/j.cnki.jtcm.20220815.004 · Cited by 9

Tryptase and Exogenous Trypsin: Mechanisms and Ophthalmic Applications

Ma, C., Li, H., Lü, S., Li, X., Wang, S., & Wang, W. (2023) · Journal of Inflammation Research · doi:10.2147/jir.s402900 · Cited by 9

Aciculatin Inhibits Granulocyte Colony-Stimulating Factor Production by Human Interleukin 1β-Stimulated Fibroblast-Like Synoviocytes

Shih, K., Wang, J., Wu, Y.-W., Teng, C., Chen, C., & Yang, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042389 · Cited by 9

The Effects of Hypoxia on U937 Cell Line in Mesenchymal Stem Cells Co-Culture System

Ejtehadifar, M., Shamsasenjan, K., Akbarzadehlaleh, P., Zahedi, S., & Kazemi, N. (2016) · Advanced Pharmaceutical Bulletin · doi:10.15171/apb.2016.079 · Cited by 9

Role of GM-CSF in a mouse model of experimental autoimmune prostatitis

Liu, Y., Li, Y., Liu, Q., Wu, Z., Cui, J., Zhu, K., Zhao, H., Zhou, C., & Shi, B. (2019) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00013.2018 · Cited by 9

Tetramerization of STAT5 regulates monocyte differentiation and the dextran sulfate sodium-induced colitis in mice

Monaghan, K. L., Zheng, W., Akhter, H., Wang, L., Ammer, A. G., Li, P., Lin, J., Hu, G., Leonard, W. J., & Wan, E. C. K. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1117828 · Cited by 8

Serum GM-CSF level is a predictor of treatment response to tocilizumab in rheumatoid arthritis patients: a prospective observational cohort study

Su, J., Hu, W., Ding, Y., Zhang, P., Li, T.-F., Liu, S., & Xing, L. (2024) · Arthritis Research & Therapy · doi:10.1186/s13075-024-03373-y · Cited by 8

Novel insights into the ROCK-JAK-STAT signaling pathway in upper respiratory tract infections and neurodegenerative diseases

Li, J., Mao, N., Wang, Y., Deng, S., & Chen, K. (2024) · Molecular Therapy · doi:10.1016/j.ymthe.2024.11.011 · Cited by 9

Granulocyte macrophage colony stimulating factor in virus-host interactions and its implication for immunotherapy

Bouzeineddine, N. Z., Philippi, A., Gee, K., & Basta, S. (2024) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2024.12.002 · Cited by 8

Harnessing Microbiome-Mediated and Macrophage-Driven Mechanisms for Oral Wound Healing

Sekar, K., Schmiliver, B., Pieterick, P. E., Cha, T., Patel, H. A., Robinson, H., Kumar, P., Wu, D. T., Jones, R. M., & Goudy, S. L. (2026) · Microorganisms · doi:10.3390/microorganisms14020330 · Cited by 8

Mimicking Behçet's disease: GM-CSF gain of function mutation in a family suffering from a Behçet's disease-like disorder marked by extreme pathergy

Rösler, B., Heinhuis, B., Wang, X., Silvestre, R., Joosten, L. A. B., Netea, M. G., Arts, P., Mantere, T., Lefeber, D. J., Hoischen, A., et al. (2020) · Clinical & Experimental Immunology · doi:10.1111/cei.13568 · Cited by 8

Adenine is an anti-inflammatory metabolite found to be more abundant in M-CSF over GM-CSF-differentiated human macrophages

Harber, K. J., Nguyen, T.-A., Schomakers, B. V., Heister, D., de Vries, H. E., van Weeghel, M., den Bossche, J. V., & de Winther, M. P. J. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.12.003 · Cited by 8

Inflammatory and Innate Immune Cells in Cancer Microenvironment and Progression

Brennecke, P., Allavena, P., Laface, I., Mantovani, A., & Bottazzi, B. (2014) · Springer eBooks · doi:10.1007/978-3-662-44006-3_2 · Cited by 8

Molecular and Clinical Oncology

Vahedi, A., Fazeli, S. A., Hashemi, S. M., Arabpour-Dahouei, F., Davarian, A., & Golabchifard, R. (2015) · Cited by 8

Small Molecular Immune Modulators as Anticancer Agents

Han, Y., Zhu, L., Wu, W., Zhang, H., Hu, W., Dai, L., & Yang, Y. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-3266-5_22 · Cited by 8

Different Roles of Beclin1 in the Interaction Between Glia and Neurons after Exposure to Morphine and the HIV- Trans-Activator of Transcription (Tat) Protein

Lapierre, J., Karuppan, M. K. M., Pokharel, M. D., Rodriguez, M., & El‐Hage, N. (2021) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-021-10017-4 · Cited by 9

Ureaplasma-Driven Neonatal Neuroinflammation: Novel Insights from an Ovine Model

Silwedel, C., Hütten, M. C., Speer, C. P., Härtel, C., Haarmann, A., Henrich, B., Tijssen, M. P. M., Alnakhli, A. A., Spiller, O. B., Schlegel, N., et al. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-022-01213-8 · Cited by 8

Isosteviol Sodium (STVNA) Reduces Pro-Inflammatory Cytokine IL-6 and GM-CSF in an In Vitro Murine Stroke Model of the Blood–Brain Barrier (BBB)

Reschke, M., Salvador, E., Schlegel, N., Burek, M., Karnati, S., Wunder, C., & Förster, C. Y. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14091753 · Cited by 9

T Cell-Derived GM-CSF, Regulation of Expression and Function

Sheng, W. (2015) · Immunome Research · doi:10.4172/1745-7580.1000098 · Cited by 8

Myocyte TLR4 enhances enteric and systemic inflammation driving late murine endotoxic ileus

Buchholz, B. M., Shapiro, R. A., Yoram Vodovotz, B., Billiar, T. R., Sodhi, C. P., Hackam, D. J., & Bauer, A. J. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00211.2014 · Cited by 8

Application of SILAC Labeling to Primary Bone Marrow-Derived Dendritic Cells Reveals Extensive GM-CSF-Dependent Arginine Metabolism

Fabrik, I., Link, M., Härtlová, A., Daňková, V., Řehulka, P., & Stulík, J. (2013) · Journal of Proteome Research · doi:10.1021/pr4007798 · Cited by 8

Pleomorphic carcinoma of the lung producing granulocyte colony-stimulating factor: Report of a case

Wada, H., Yoshida, S., Ishibashi, F., Mizobuchi, T., Moriya, Y., Hoshino, H., Okamoto, T., Suzuki, M., Shibuya, K., & Yoshino, I. (2011) · Surgery Today · doi:10.1007/s00595-010-4426-6 · Cited by 8

Recent advances on cellular therapies and immune modulators for graft-versus-host disease

Filippini, P., & Rutella, S. (2014) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2014.955475 · Cited by 8

Deficiency of IL-1 receptor antagonist suppresses IL-10-producing B cells in autoimmune arthritis in an IL-17/Th17-dependent manner

Park, J., Kim, N., Lim, M., Kim, S., Hwang, S., Jung, K., Choi, J., Park, S., & Cho, M. (2018) · Immunology Letters · doi:10.1016/j.imlet.2018.05.003 · Cited by 8

A systematic investigation on animal models of cyclosporine A combined with Escherichia coli to simulate the immunosuppressive status of sepsis patients before onset

Kong, X., Zhang, J., Huo, J., Wang, L., Guo, L., Liu, Y., He, T., Sun, Z., Chen, X., Hou, Z.-J., et al. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.05.031 · Cited by 8

Immunomodulatory activity in tumor-bearing mice treated with Withania somnifera extract

de Melo, A., de Melo, A. L., Marcucci, M. C., de Carvalho, C., & Gonçalves, C. P. (2021) · Journal of Analytical & Pharmaceutical Research · doi:10.15406/japlr.2021.10.00369 · Cited by 8

PKCα and PKCϵ differentially regulateLegionella pneumophila-induced GM-CSF

Vardarova, K., Scharf, S., Lang, F., Schmeck, B., Opitz, B., Eitel, J., Hocke, A. C., Slevogt, H., Flieger, A., Hippenstiel, S., et al. (2009) · European Respiratory Journal · doi:10.1183/09031936.00171908 · Cited by 8

Trans‐System Mechanisms Against Ischemic Myocardial Injury

Liu, S. Q., Ma, X., Qin, G., Liu, Q., Li, Y., & Wu, Y. H. (2014) · Comprehensive physiology · doi:10.1002/cphy.c140026 · Cited by 8

Cytokines

Benveniste, E. N. (2014) · Encyclopedia of the Neurological Sciences · doi:10.1016/b978-0-12-385157-4.00175-5 · Cited by 8

HCST Expression Distinguishes Immune-hot and Immune-cold Subtypes in Pancreatic Ductal Adenocarcinoma

Ma, B., Zhang, D.-J., Hu, Y., Chen, X., Gong, R., Lei, K., Yu, Q., & Ren, H. (2023) · Current Gene Therapy · doi:10.2174/1566523223666230720101531 · Cited by 7

Apoptosis of Dendritic Cells and Autoimmune Disease

Sun, L. Y., Ding, F., Zhou, L., Wang, J., Li, M., Zhou, P., Li, J., Ding, C., Wang, H., & Xu, Y. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2904157 · Cited by 7

Endogenous and exogenous cytokines: An overview and introduction

Spitzer, T. R., & Lazarus, H. M. (2025) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2025.101615 · Cited by 8

Targeting hypercoagulability in ischemic stroke modulates fibrin-driven microglial polarization via JAK-STAT pathway

Guan, S., Lu, T., Li, L., Zhang, Y., Huang, C., Li, C., Li, B., Hu, J., & Wan, C. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03582-5 · Cited by 7

Fibroblasts as Immunological Sentinels in Cutaneous Inflammation: A Review

Quan, T. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15020556 · Cited by 7

Irilin D suppresses RANKL-induced osteoclastogenesis and prevents inflammation-induced bone loss by disrupting the NF-κB and MAPK signaling pathways

Gal, M., Hà, M. T., Park, J., Park, K.-H., Kim, O., Min, B.-S., & Lee, J. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176956 · Cited by 7

Granulocyte-Macrophage Colony Stimulating Factor and Inflammatory Bowel Disease: Establishing a Connection

Dranoff, G. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.05.023 · Cited by 7

p53 Mutation: Critical Mediator of Therapy Resistance against Tumor Microenvironment

Arbab, A. S., & Jain, M. (2016) · Biochemistry & Physiology Open Access · doi:10.4172/2168-9652.1000e153 · Cited by 7

Antitumor Macrophage Response to Bacillus pumilus Ribonuclease (Binase)

Владимировна, М. А., Rodriguez-Montesinos, J., Zelenikhin, P., Nesmelov, A. A., Preissner, K. T., Cabrera-Fuentes, H. A., & Ilinskaya, O. N. (2017) · Mediators of Inflammation · doi:10.1155/2017/4029641 · Cited by 7

Urokinase-type plasminogen activator protects human umbilical vein endothelial cells from apoptosis in sepsis.

Long, D., Yang, J., Wu, X., Gui, Y., & Yu, L. (2019) · Europe PMC (PubMed Central) · Cited by 7

Comments on the ambiguity of selected surface markers, signaling pathways and omics profiles hampering the identification of myeloid-derived suppressor cells

Lutz, M. B., & Eckert, I. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2021.104347 · Cited by 7

Novel brain PET imaging agents: Strategies for imaging neuroinflammation in Alzheimer’s disease and mild cognitive impairment

Huang, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1010946 · Cited by 7

New Insights into Risk Genes and Their Candidates in Multiple Sclerosis

Shirai, R., & Yamauchi, J. (2022) · Neurology International · doi:10.3390/neurolint15010003 · Cited by 7

Development of Membrane-Bound GM-CSF and IL-18 as an Effective Tumor Vaccine

Huang, C.-C., Kuo, K., Cheng, T.-C., Chuang, C., Kao, C.-H., Hsieh, Y.-C., Cheng, K., Wang, J.-Y., Cheng, C., Chen, C., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133470 · Cited by 7

Granulocyte–Colony‐Stimulating Factor Treatment Enhances Foxp3+ T Lymphocytes and Modifies the Proinflammatory Response in Experimental Autoimmune Neuritis

Pradella, F. M., Moraes, A. S., Santos, M. P. A., DePaula, R. F. O., Degaki, K., Longhini, A. L. F., Silva, V. D. R., dos Santos, L. M. B., & Farias, A. S. (2013) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12112 · Cited by 7

Golgi GRASPs: moonlighting membrane tethers

Linstedt, A. D., & Jarvela (2012) · Cell Health and Cytoskeleton · doi:10.2147/chc.s21849 · Cited by 7

Regulation of Lymphatic GM-CSF Expression by the E3 Ubiquitin Ligase Cbl-b

Peer, S., Cappellano, G., Hermann‐Kleiter, N., Albrecht-Schgoer, K., Hinterleitner, R., Baier, G., & Gruber, T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02311 · Cited by 7

Expression of granulocyte macrophage-colony stimulating factor and its receptor in the synovium of osteoarthritis patients is negatively correlated with pain

van Helvoort, E. M., Eijkelkamp, N., Lafeber, F. P. J. G., & Mastbergen, S. C. (2020) · Lara D. Veeken · doi:10.1093/rheumatology/keaa199 · Cited by 7

Combination of Methotrexate and Resveratrol Reduces Pro-Inflammatory Chemokines in Human THP-1 Cells

Alnasser, M. M., Al-Saeedi, M., Alhowaiti, S. A., Shinwari, Z., Alhamlan, F. S., Alothaid, H., Alkahtani, S. H., & Al-Qahtani, A. A. (2024) · Journal of Inflammation Research · doi:10.2147/jir.s482503 · Cited by 6

Evaluating the evidence for GM-CSF as a host-directed therapy in respiratory infections

David, C., Verney, C., Si‐Tahar, M., & Guillon, A. (2025) · Cytokine · doi:10.1016/j.cyto.2025.156902 · Cited by 7

CSF3 enhances the innate immune responses to ALV-J infections via NF-κB and interferon pathways

Xia, J., Chen, W., Xu, C., Wang, M., Mo, G., & Zhang, X. (2025) · Poultry Science · doi:10.1016/j.psj.2025.105648 · Cited by 6

T cell–macrophage interactions in tuberculosis: What we've got here is failure to communicate

Mortensen, R. J., Arlehamn, C. S. L., Coler, R. N., Gerner, M. Y., Goletti, D., Lewinsohn, D. A., Modlin, R. L., Musvosvi, M., Rengarajan, J., Urdahl, K. B., et al. (2025) · Journal of Internal Medicine · doi:10.1111/joim.70028 · Cited by 9

Microglia in Gliomas: Friend or Foe?

Kaminska, B. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1431-5_9 · Cited by 6

Necrotizing Gingivitis: Microbial Diversity and Quantification of Protein Secretion in Necrotizing Gingivitis

Gerhard, N., Thurnheer, T., Kreutzer, S., Gmür, R., Attin, T., Russo, G., & Karygianni, L. (2021) · Antibiotics · doi:10.3390/antibiotics10101197 · Cited by 6

A GITRL‐mTORC1‐GM‐CSF Positive Loop Promotes Pathogenic Th17 Response in Primary Sjögren Syndrome

Gan, Y., Zhou, H., Guo, Y., Huang, B., Liu, H., Wang, Z., Li, Z., Zhao, X., Zhu, H., Han, Q., et al. (2024) · Arthritis & Rheumatology · doi:10.1002/art.42859 · Cited by 6

Causal roles of circulating cytokines in sarcopenia-related traits: a Mendelian randomization study

Chen, Z., Sun, J., Shi, T., Song, C., Wu, C., Wu, Z., & Lin, J. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1370985 · Cited by 6

The influence of macrophage growth factors on Theiler’s Murine Encephalomyelitis Virus (TMEV) infection and activation of macrophages

Schneider, K. M., Watson, N. B., Minchenberg, S. B., & Massa, P. T. (2017) · Cytokine · doi:10.1016/j.cyto.2017.07.015 · Cited by 6

Asymptomatic cerebral cavernous angiomas associated with plasma marker signature

Bicalho, V. C., Galvão, G. D. F., Fontes-Dantas, F. L., Gonçalves, J. P. D. C., de Araújo, A. D., França, L. C., Leite, P. E. C., Vidal, D. C., Filho, R. C. D. O., Alves‐Leon, S. V., et al. (2021) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2021.04.024 · Cited by 5

High Granulocyte-Macrophage Colony Stimulating Factor to Interleukin 10 Ratio and Marked Antioxidant Enzyme Activities Predominate in Symptomatic Cattle Naturally Infected with Candidatus Mycoplasma haemobos, Theileria orientalis, Theileria sinensis and Trypanosoma evansi

Agina, O. A., Cheah, K. T., Sayuti, N. S. A., Shaari, M. R., Isa, N. M. M., Ajat, M., Saad, M. Z., Mazlan, M., & Hamzah, H. B. (2021) · Animals · doi:10.3390/ani11082235 · Cited by 6

Concurrent stimulation of monocytes with CSF1 and polarizing cytokines reveals phenotypic and functional differences with classical polarized macrophages

An, L., Michaeli, J. C., Pallavi, P., Breedijk, A., Xu, X., Dietrich, N., Sigl, M., Keese, M., Nitschke, K., Jarczyk, J., et al. (2022) · Journal of Leukocyte Biology · doi:10.1002/jlb.3a0721-383r · Cited by 6

ATP citrate lyase links increases in glycolysis to diminished release of vesicular suppressor of cytokine signaling 3 by alveolar macrophages

Haggadone, M. D., Speth, J. M., Hong, H. S., Penke, L. R. K., Zhang, E., Lyssiotis, C. A., & Peters-Golden, M. L. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2022.166458 · Cited by 6

Identification, molecular characterization, and pathological features of orf virus in sheep and goats in Punjab province, Pakistan

Hussain, I., Khan, M. U. R., Aslam, A., Rabbani, M., Masood, S., & Anjum, A. A. (2022) · Tropical Animal Health and Production · doi:10.1007/s11250-022-03432-z · Cited by 6

Endothelial Glycocalyx Injury in SARS-CoV-2 Infection: Molecular Mechanisms and Potential Targeted Therapy

Lv, B., Huang, S., Hong, H., Niu, N., & Liu, J. (2023) · Mediators of Inflammation · doi:10.1155/2023/6685251 · Cited by 6

Noncanonical Nuclear Factor Kappa B (NF-κB) Signaling and Potential for Therapeutics in Sepsis

Thair, S. A., & Russell, J. A. (2013) · Current Infectious Disease Reports · doi:10.1007/s11908-013-0362-0 · Cited by 6

GM-CSF is not essential for optimal fertility or for weight control

Hamilton, J. A., Davis, J., Pobjoy, J., & Cook, A. D. (2011) · Cytokine · doi:10.1016/j.cyto.2011.10.021 · Cited by 6

αB‐Crystallin regulates expansion of CD11b + Gr‐1 + immature myeloid cells during tumor progression

Dieterich, L. C., Schiller, P., Huang, H., Wawrousek, E. F., Loskog, A., Wanders, A., Moons, L., & Dimberg, A. (2012) · The FASEB Journal · doi:10.1096/fj.12-213017 · Cited by 6

Engineered cell migration to lesions linked to autoimmune disease

Mosabbir, A. A., Qudrat, A., & Truong, K. (2017) · Biotechnology and Bioengineering · doi:10.1002/bit.26523 · Cited by 6

Anticitrullinated Protein Antibodies Induce Inflammatory Gene Expression Profile in Peripheral Blood Cells from CCP–positive Patients with RA

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MicroRNA-21 Mediates the Inhibiting Effect of Praziquantel on NLRP3 Inflammasome in Schistosoma japonicum Infection

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