Molecular interactions in macrophage activation

Molecules, membranes and macrophage activation

Adams, D. O. (1982) · Immunology Today · doi:10.1016/0167-5699(82)90026-3 · Cited by 20

Interferon-γ: an overview of signals, mechanisms and functions

Schroder, K., Hertzog, P. J., Ravasi, T., & Hume, D. A. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.0603252 · Cited by 4,120

Macrophage activation and polarization

Martinez, F. O. (2008) · Frontiers in Bioscience · doi:10.2741/2692 · Cited by 3,160

T lymphocytes from human atherosclerotic plaques recognize oxidized low density lipoprotein.

Stemme, S., Faber, B., Holm, J., Wiklund, O., Witztum, J. L., & Hansson, G. K. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.9.3893 · Cited by 943

Immunology of Wound Healing

Ellis, S., Lin, E. J., & Tartar, D. (2018) · Current Dermatology Reports · doi:10.1007/s13671-018-0234-9 · Cited by 625

Monocyte-mediated Tumoricidal Activity via the Tumor Necrosis Factor–related Cytokine, TRAIL

Griffith, T. S., Wiley, S. R., Kubin, M. Z., Sedger, L. M., Maliszewski, C. R., & Fanger, N. A. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.8.1343 · Cited by 477

Macrophage-derived angiogenesis factors

Sunderkötter, C. H., Goebeler, M., Schulze-Osthoff, K., Bhardwaj, R. S., & Sorg, C. (1991) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(91)90077-y · Cited by 328

A macrophage mRNA selectively induced by gamma-interferon encodes a member of the platelet factor 4 family of cytokines.

Farber, J. M. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.14.5238 · Cited by 299

Interferon-gamma inhibits scavenger receptor expression and foam cell formation in human monocyte-derived macrophages.

Geng, Y., & Hansson, G. K. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115718 · Cited by 263

Aging and cancer: The role of macrophages and neutrophils

Jackaman, C., Tomay, F., Duong, L., Abdol Razak, N. B., Pixley, F. J., Metharom, P., & Nelson, D. J. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.03.008 · Cited by 251

Radiobiological mechanisms in inflammatory diseases of low-dose radiation therapy

Rödel, F., Keilholz, L., i, M. H., Sauer, R., & Hildebrandt, G. (2007) · International Journal of Radiation Biology · doi:10.1080/09553000701317358 · Cited by 210

Modulation of Inflammatory Immune Reactions by Low-Dose Ionizing Radiation: Molecular Mechanisms and Clinical Application

Rödel, F., Frey, B., Gaipl, U. S., Keilholz, L., Fournier, C., Manda, K., Schöllnberger, H., Hildebrandt, G., & Rödel, C. M. (2012) · Current Medicinal Chemistry · doi:10.2174/092986712800099866 · Cited by 195

Fas–Fas Ligand: Checkpoint of T Cell Functions in Multiple Sclerosis

Volpe, E., Sambucci, M., Battistini, L., & Borsellino, G. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00382 · Cited by 197

The Signalling Pathways of Interleukin-6 and Gamma Interferon Converge by the Activation of Different Transcription Factors Which Bind to Common Responsive DNA Elements

Yuan, J., Wegenka, U. M., Lütticken, C., Buschmann, J., Decker, T., Schindler, C., Heinrich, P. C., & Horn, F. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.3.1657 · Cited by 179

Interferon gamma-induced transcription of the high-affinity Fc receptor for IgG requires assembly of a complex that includes the 91-kDa subunit of transcription factor ISGF3.

Pearse, R. N., Feinman, R., Shuai, K., Darnell, J. E., Jr., & Ravetch, J. V. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.9.4314 · Cited by 179

The Pathology of Mycobacterium tuberculosis Infection

Sakamoto, K. (2012) · Veterinary Pathology · doi:10.1177/0300985811429313 · Cited by 167

Advancing islet transplantation: from engraftment to the immune response

Gibly, R. F., Graham, J. G., Luo, X., Lowe, W. L., Hering, B. J., & Shea, L. D. (2011) · Diabetologia · doi:10.1007/s00125-011-2243-0 · Cited by 143

Outflow Obstruction in Pigmentary and Primary Open Angle Glaucoma

Alvarado, J. A. (1992) · Archives of Ophthalmology · doi:10.1001/archopht.1992.01080240109042 · Cited by 140

Monocyte deactivation by interleukin 10 via inhibition of tyrosine kinase activity and the Ras signaling pathway.

Geng, Y., Gulbins, E., Altman, A., & Lotz, M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8602 · Cited by 139

Immunomodulatory Properties and Molecular Effects in Inflammatory Diseases of Low-Dose X-Irradiation

Rödel, F., Frey, B., Manda, K., Hildebrandt, G., Hehlgans, S., Keilholz, L., Seegenschmiedt, M. H., Gaipl, U. S., & Rödel, C. M. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00120 · Cited by 124

Molecular Changes Underlying Hypertrophic Scarring Following Burns Involve Specific Deregulations at All Wound Healing Stages (Inflammation, Proliferation and Maturation)

Čoma, M., Fröhlichová, L., Urban, L., Zajíček, R., Urban, T., Szabó, P., Novak, S., Fetissov, V., Dvořánková, B., Smetana, K., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020897 · Cited by 124

Stimulation of the human intercellular adhesion molecule-1 promoter by interleukin-6 and interferon-gamma involves binding of distinct factors to a palindromic response element.

Caldenhoven, E., Coffer, P. J., Yuan, J., van de Stolpe, A., Horn, F., Kruijer, W., & van der Saag, P. T. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)31942-7 · Cited by 117

Role of endogenous interferon-beta in lipopolysaccharide-triggered activation of the inducible nitric-oxide synthase gene in a mouse macrophage cell line, J774.

Fujihara, M., Ito, N., Pace, J. L., Watanabe, Y., Russell, S. W., & Suzuki, T. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99942-4 · Cited by 106

Langerhans' cell histiocytosis pathobiology and pathogenesis.

Favara, B. E. (1991) · PubMed · Cited by 110

Corticosteroid receptors, macrophages and cardiovascular disease

Rickard, A. J., & Young, M. J. (2009) · Journal of Molecular Endocrinology · doi:10.1677/jme-08-0144 · Cited by 105

Differentiation-regulated serine phosphorylation of STAT1 promotes GAF activation in macrophages

Eilers, A., Georgellis, D., Klose, B., Schindler, C., Ziemiecki, A., Harpur, A., Wilks, A., & Decker, T. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.7.3579 · Cited by 114

Therapeutic Ultrasound: Its Effects on the Cellular and Molecular Mechanisms of Inflammation and Repair

Maxwell, L. (1992) · Physiotherapy · doi:10.1016/s0031-9406(10)61528-3 · Cited by 98

Precise immunomodulation of the M1 to M2 macrophage transition enhances mesenchymal stem cell osteogenesis and differs by sex

Nathan, K., Lu, L. Y., Lin, T., Pajarinen, J., Jämsen, E., Huang, J., Romero-López, M., Maruyama, M., Kohno, Y., Yao, Z., et al. (2019) · Bone and Joint Research · doi:10.1302/2046-3758.810.bjr-2018-0231.r2 · Cited by 90

Role of the macrophage in angiogenesis-dependent diseases

Polverini, P. J. (1997) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-0348-9006-9_2 · Cited by 88

Microglial polarization in TBI: Signaling pathways and influencing pharmaceuticals

Li, Y., Ren, X., Zhang, L., Wang, Y., & Chen, T. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.901117 · Cited by 77

Plasmacytoid Dendritic Cell-Derived IFN-α Induces TNF-Related Apoptosis-Inducing Ligand/Apo-2L-Mediated Antitumor Activity by Human Monocytes Following CpG Oligodeoxynucleotide Stimulation

Kemp, T. J., Elzey, B. D., & Griffith, T. S. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.1.212 · Cited by 66

PI3K/Akt Signaling Pathway Modulates Influenza Virus Induced Mouse Alveolar Macrophage Polarization to M1/M2b

Zhao, X., Dai, J., Xiao, X., Wu, L., Zeng, J., Sheng, J., Su, J., Chen, X., Wang, G., & Li, K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104506 · Cited by 63

Advances in T Helper 17 Cell Biology: Pathogenic Role and Potential Therapy in Multiple Sclerosis

Volpe, E., Battistini, L., & Borsellino, G. (2015) · Mediators of Inflammation · doi:10.1155/2015/475158 · Cited by 64

Protein kinase C in tumoricidal activation of mouse macrophage cell lines

Novotney, M., Chang, Z. L., Uchiyama, H., & Suzuki, T. (1991) · Biochemistry · doi:10.1021/bi00236a037 · Cited by 55

The Response of Gamma Interferon Activation Factor is Under Developmental Control in Cells of the Macrophage Lineage

Eilers, A., Seegert, D., Schindler, C., Baccarini, M., & Decker, T. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.6.3245 · Cited by 52

DEGRO practical guidelines for radiotherapy of non-malignant disorders

the German Cooperative Group on Radiotherapy for Benign Diseases (GCG-BD), Reichl, B., Block, A., Schäfer, U., Bert, C., Müller, R. G., Jung, H., & Rödel, F. (2015) · Strahlentherapie und Onkologie · doi:10.1007/s00066-015-0865-8 · Cited by 42

Irradiated tumor cells adenovirally engineered to secrete granulocyte/macrophage-colony-stimulating factor establish antitumor immunity and eliminate pre-existing tumors in syngeneic mice

Nagai, E., Ogawa, T., Kielian, T., Ikubo, A., & Suzuki, T. (1998) · Cancer Immunology Immunotherapy · doi:10.1007/s002620050506 · Cited by 39

Macrophage Polarization in the Skin Lesion Caused by Neotropical Species of Leishmania sp

Pacheco, C. M. S., Flores, G. V. A., González, K., Gomes, C. M. D. C., Passero, L., Tomokane, T. Y., Sosa-Ochoa, W. H., Zúniga, C., Calzada, J., Saldaña, A., et al. (2021) · Journal of Immunological Research · doi:10.1155/2021/5596876 · Cited by 28

Mitigation of radiation-induced hematopoietic injury by the polyphenolic acetate 7, 8-diacetoxy-4-methylthiocoumarin in mice

Venkateswaran, K., Shrivastava, A., Agrawala, P. K., Prasad, A. K., Kalra, N., Pandey, P. R., Manda, K., Raj, H. G., Parmar, V. S., & Dwarakanath, B. S. R. (2016) · Scientific Reports · doi:10.1038/srep37305 · Cited by 38

Transcriptional regulation of LDL receptor-related protein by IFN-γ and the antagonistic activity of TGF-β1 in the RAW 264.7 macrophage-like cell line

Hussaini, I. M., LaMarre, J., Lysiak, J. J., Karns, L. R., VandenBerg, S. R., & Gonias, S. L. (1996) · Journal of Leukocyte Biology · doi:10.1002/jlb.59.5.733 · Cited by 37

Enhanced killing capacity of human Kupffer cells after activation with human granulocyte/macrophage-colony- stimulating factor and interferon ?

Schuurman, B., Heuff, G., Beelen, R. H. J., & Meyer, S. (1994) · Cancer Immunology Immunotherapy · doi:10.1007/bf01533384 · Cited by 34

Non-invasive classification of macrophage polarisation by 2P-FLIM and machine learning

Neto, N. G. B., O’Rourke, S. A., Zhang, M., Fitzgerald, H. K., Dunne, A., & Monaghan, M. G. (2022) · eLife · doi:10.7554/elife.77373 · Cited by 33

Nuclear Receptors Are Involved in the Enhanced IL-6 Production by Melatonin in U937 Cells

Guerrero, J. M., Pozo, D., García‐Mauriño, S., Carrillo‐Vico, A., Osuna, C., Molinero, P., & Calvo, J. R. (2000) · Neurosignals · doi:10.1159/000014639 · Cited by 31

High-density lipoproteins reduce the effect of endotoxin on cytokine production and systemic hemodynamics in cirrhotic rats with ascites

Ramírez‐Lázaro, M. J., Ibáñez, Á., Navasa, M., Casals, E., Morales‐Ruiz, M., Jiménez, W., Arroyo, V., & Rodés, J. (2003) · Journal of Hepatology · doi:10.1016/j.jhep.2003.11.017 · Cited by 30

Differential regulation of the expression of transporters associated with antigen processing, TAP1 and TAP2, by cytokines and lipopolysaccharide in primary human macrophages

Schiffer, R., Baron, J. M., Dagtekin, G., Jahnen‐Dechent, W., & Zwadlo‐Klarwasser, G. (2002) · Inflammation Research · doi:10.1007/pl00000321 · Cited by 29

Shift Toward an Alternatively Activated Macrophage Response in Lungs of NO2-Exposed Rats

Garn, H., Siese, A., Stumpf, S., Barth, P. J., Müller, B., & Gemsa, D. (2003) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.4888 · Cited by 28

Characterization of Murine Grancalcin Specifically Expressed in Leukocytes and Its Possible Role in Host Defense against Bacterial Infection

Liu, F., Shinomiya, H., Kirikae, T., Hirata, H., & Asano, Y. (2004) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.68.894 · Cited by 22

2,4-diamino-6-hydroxypyrimidine, an inhibitor of GTP cyclohydrolase I, suppresses nitric oxide production by chicken macrophages

Sung, Y., Hotchkiss, J. H., & Dieteri, R. R. (1994) · International Journal of Immunopharmacology · doi:10.1016/0192-0561(94)90065-5 · Cited by 22

Progress in Tumor‐Associated Macrophages: From Bench to Bedside

Wang, Y., Lin, Y., Qiao, S., Wang, J., & Wang, H. (2018) · Advanced Biosystems · doi:10.1002/adbi.201800232 · Cited by 20

Effects of cytokines on β-adrenoceptor function of human peripheral blood mononuclear cells and guinea pig trachea

van Oosterhout, A. J. M., Stam, W. B., Vanderschueren, R. G. J. R. A., & Nijkamp, F. P. (1992) · Journal of Allergy and Clinical Immunology · doi:10.1016/s0091-6749(05)80013-2 · Cited by 19

Mycobacterium tuberculosis: Macrophage Takeover and Modulation of Innate Effector Responses

Bhat, K. H., & Yaseen, I. (2018) · InTech eBooks · doi:10.5772/intechopen.75003 · Cited by 18

Effects of Oxysterols Upon Macrophage and Lymphocyte Functions In Vitro

Dushkin, M. I., Schwartz, Y. S., Volsky, N. N., Musatov, M. I., Vereschagin, E., Ragino, Y. I., Perminova, O. M., & Va, K. (1998) · Prostaglandins & Other Lipid Mediators · doi:10.1016/s0090-6980(98)00024-0 · Cited by 18

A chelate theory for the mechanism of action of aspirin-like drugs

Wang, X. (1998) · Medical Hypotheses · doi:10.1016/s0306-9877(98)90024-x · Cited by 17

Granulocyte–macrophage colony-stimulating factor and interleukin-3 potentiate interferon-γ-mediated endothelin production by human monocytes: role of protein kinase C

Salh, B. (1998) · Immunology · doi:10.1046/j.1365-2567.1998.00614.x · Cited by 15

SENSITIVITY OF ACTIVATED MURINE PERITONEAL MACROPHAGES TO PHOTODYNAMIC KILLING WITH BENZOPORPHYRIN DERIVATIVE

Hunt, D. W. C., Jiang, H., Levy, J. G., & Chan, A. H. (1995) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1995.tb08633.x · Cited by 14

The Cytokines: Physiological and Pathophysiological Aspects

Evans, S. W., & Whicher, J. T. (1993) · Advances in clinical chemistry · doi:10.1016/s0065-2423(08)60194-8 · Cited by 14

Cocaine modulation in vitro of tumor necrosis factor production by macrophages from retrovirally infected mice

Chen, G.-J., Tachibana, K., Huang, D. S., & WATSON, R. R. (1993) · Life Sciences · doi:10.1016/0024-3205(93)90046-6 · Cited by 13

Macrophage and Preeclampsia: Macrophage Polarization Imbalance at the Maternal‐Fetal Interface

Wei, Y., Su, Y., Liu, C., Ma, X., Ling, Z., Wang, Y., & Qiao, R. (2025) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.70046 · Cited by 12

Impaired function of Fanconi anemia type C-deficient macrophages

Liu, Y., Ballman, K. K., Li, D., Khan, S., Derr-Yellin, E. C., Shou, W., & Haneline, L. S. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.0811418 · Cited by 12

Role of HSP70i in regulation of biomaterial-induced activation of human monocytes-derived macrophages in culture

Bhardwaj, R. S., Eblenkamp, M., Berndt, T., Tietze, L., & Klosterhalfen, B. (2001) · Journal of Materials Science Materials in Medicine · doi:10.1023/a:1008974524580 · Cited by 12

Immunotoxicity screening in vitro using an economical multiple endpoint approach

Fautz, R., & Miltenburger, H. G. (1993) · Toxicology in Vitro · doi:10.1016/0887-2333(93)90019-2 · Cited by 12

The plasma-membrane internalization and recycling is enhanced in macrophages upon activation with gamma-interferon and lipopolysaccharide; a study using the fluorescent probe trimethylaminodiphenylhexatriene

Illinger, D., Poindron, P., Glasser, N., Modolell, M., & Kuhry, J. (1990) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(90)90241-f · Cited by 12

Supplementation of vitamin E and omega-3 fatty acids during the early posthatch period on intestinal morphology and gene expression differentiation in broilers

Wang, J., Clark, D. L., Jacobi, S. K., & Velleman, S. G. (2020) · Poultry Science · doi:10.1016/j.psj.2020.12.051 · Cited by 10

Heritability of cervical tumours

Magnusson, P. K. E., Lichtenstein, P., & Gyllensten, U. B. (2000) · International Journal of Cancer · doi:10.1002/1097-0215(20001201)88:5 · Cited by 179

Activation of murine macrophages by tumor necrosis factor, interleukin-1, interferon-γ and cisplatin

Sodhi, A., Singh, R. K., & Pai, K. R. (1990) · Immunology Letters · doi:10.1016/0165-2478(90)90174-o · Cited by 10

Cloning and Expression of Bovine Interleukin-15: Analysis and Modulation of Transcription by Exogenous Stimulation

Canals, A., Gasbarre, L. C., Boyd, P. C., Almería, S., & Zarlenga, D. S. (1997) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.1997.17.473 · Cited by 9

Effects of protease inhibitors on LPS-mediated activation of a mouse macrophage cell line (J774)

Muroi, M., Muroi, Y., Ito, N., Rice, N. R., & Suzuki, T. (1995) · Journal of Endotoxin Research · doi:10.1177/096805199500200504 · Cited by 8

Long Term iNOS Expression in Thoracic Lymph Nodes of Silicotic Rats

Friedetzky, A. (2002) · Immunobiology · doi:10.1078/0171-2985-00127 · Cited by 6

Alteration of Platelet Activating Factor-Induced Macrophage Tumoricidal Response, IA Expression, and Signal Transduction by N-3 Fatty Acids

Erickson, K. L., Howard, A. D., Chakrabarti, R., & Hubbard, N. E. (1997) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-1813-0_55 · Cited by 6

Interleukin-33 Ameliorates Murine Systemic Lupus Erythematosus and Is Associated with Induction of M2 Macrophage Polarisation and Regulatory T Cells

Mok, M. Y., Law, K. S., Kong, W. Y., Luo, C. Y., Asfaw, E. T., Chan, K. W., Huang, F. P., Lau, C. S., & Chan, G. (2023) · Journal of Innate Immunity · doi:10.1159/000529931 · Cited by 5

LPS–induced activation of phospholipase A2 phospholipase C and protein kinase C of murine macrophage–like cell lines (J774 and P388D1)

Chang, Z., Novotney, M., & Suzuki, T. (1992) · Cell Research · doi:10.1038/cr.1992.6 · Cited by 5

IFN-γ-independent intraocular tumor rejection is mediated by a macrophage-dependent process that leaves the eye intact

Coursey, T. G., Chen, P. W., & Niederkorn, J. Y. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0312122 · Cited by 5

The RNA binding protein Sam68 controls T helper 1 differentiation and anti-mycobacterial response through modulation of miR-29

Volpe, E., Cesari, E., Mercatelli, N., Cicconi, R., Bardi, M. D., Capone, A., Bonvissuto, D., Fraziano, M., Mattei, M., Battistini, L., et al. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0201-9 · Cited by 7

EFFICIENCY AND PERFORMANCE OF THE USE OF RECOMBINANT INTERFERON GAMMA IN COMPLEX THERAPY OF INFLUENZA A(H1N1)PDM09 PATIENTS

Tv, S., Сергеевич, М. А., Agafonov, V. N., Suzdalcev, A. A., & Цветков, В. В. (2017) · Epidemiology and Infectious Diseases · doi:10.17816/eid42628 · Cited by 5

Proteinase-activated receptors induce nonoxidative, antimicrobial peptides and increased antimicrobial activity in human mononuclear phagocytes

Lippuner, N., Morell, B. K., Schaffner, A., & Schaer, D. J. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.1105634 · Cited by 5

Augmentation of recombinant interleukin‐2‐dependent murine macrophage‐mediated tumour cytotoxicity by recombinant tumour necrosis factor‐α

Kos, F. J. (1989) · Immunology and Cell Biology · doi:10.1038/icb.1989.61 · Cited by 5

Bacterial endotoxin lipopolysaccharide modulates synthesis of the 70 kDa heat stress protein family

Tomasovic, S. P., & Klostergaard, J. (1991) · International Journal of Hyperthermia · doi:10.3109/02656739109034976 · Cited by 5

Leishmaniavirus Type 1 Enhances In Vitro Infectivity and Modulates the Immune Response to Leishmania (Viannia) Isolates

Fong, A. A. B., Pineda, V. J., Calzada, J. E., Laurenti, M. D., Passero, L. F. D., Beltrán, D., Chaves, L. F., Saldaña, A., & González, K. A. (2025) · Pathogens · doi:10.3390/pathogens14121263 · Cited by 4

Enhancement of in vitro nonspecific immune functions by African plant extracts

Ottendorfer, D., Frevert, J., Kaufmann, R., Beuscher, N., Bodinet, C., Msonthi, J. D., Marston, A., & Hostettmann, K. (1994) · Phytotherapy Research · doi:10.1002/ptr.2650080702 · Cited by 4

IFNγ and TNFα cause an increased release of C3 by murine macrophages

Renzo, L. D., Cristofaro, M. R. D., Zicari, A., Viola, R., Pontieri, G. M., & Lipari, M. (1994) · Immunology Letters · doi:10.1016/0165-2478(94)90081-7 · Cited by 4

Proliferation of Glomerular Cells

Rees, A. J. (1990) · Springer eBooks · doi:10.1007/978-94-009-2225-9_6 · Cited by 4

The Mononuclear Phagocyte and Rheumatoid Arthritis

Highton, J., & Palmer, D. G. (1994) · Springer eBooks · doi:10.1007/978-94-011-1432-5_3 · Cited by 4

Phenotype modulation of human adult fibroblasts by oncogenes

Kopelovich, L., & Demian, S. E. (1996) · Molecular Carcinogenesis · doi:10.1002/(sici)1098-2744(199603)15:3 · Cited by 3

Regulation of cytokine release from peritoneal macrophages of patients on continuous ambulatory peritoneal dialysis

Fieren, M. W. J. A. (1992) · RePub (Erasmus University Rotterdam) · Cited by 3

Immune-modulation by 7, 8-diacetoxy-4-methylthiocoumarin in total body-irradiated mice: Implications for the mitigation of radiation-induced hematopoietic injury

Venkateswaran, K., Shrivastava, A., Agrawala, P. K., Prasad, A. K., Manda, K., Parmar, V. S., & Dwarakanath, B. S. R. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121140 · Cited by 2

The possibility of the use of interferon-gamma in Influenza infection

Никифоров, В. В., Tv, S., Tokin, I. I., Цветков, В. В., Ерофеева, М. К., & Zarubaev, V. V. (2015) · Epidemiology and Infectious Diseases · doi:10.17816/eid40849 · Cited by 2

Avian cytokines

Siatskas, C., Lowenthal, J. W., Obranovich, T. D., & Boyd, R. L. (1996) · Elsevier eBooks · doi:10.1016/b978-012442710-5.50255-0 · Cited by 2

Role of Acetylsalicylic Acid in Cytokine Stimulation of Macrophagesin Antibody‐Dependent Cellular Cytotoxicity (ADCC)

Jäpel, M., Lötzerich, H., & Rogalla, K. (1994) · Mediators of Inflammation · doi:10.1155/s0962935194000591 · Cited by 2

Effects of human cytomegalovirus challenge on monocyte function

Moses, A. V. (1990) · Research Online (University of Wollongong) · Cited by 1

Cellular and molecular aspects of the anti-inflammatory effects of low-dose radiation therapy

Large, M. (2015) · Technischen Universität Darmstadt · doi:10.26083/tuprints-00004977 · Cited by 1

MOLECULAR REGULATION OF THE TUMOR KILLING ACTIVITY OF DENDRITIC CELLS

Hanke, N. T. (2012) · UA Campus Repository (The University of Arizona) · Cited by 1

Contribuição farmacológica à gênese da inflamação neurogênica em vias aéreas de ratos frente a dois poluentes: Partículas eliminadas na exaustão do diesel (PED) e 1,2-naftoquinona (1,2-NQ).

Teles, A. M. (2007) · doi:10.11606/t.42.2007.tde-24092007-094137

Differentiation by LPS and IFN-γ of expression of adenosine receptors in macrophage cell lines RAW264 and J774

Watanabe, K. (2005) · Pediatric Dental Journal · doi:10.1016/s0917-2394(05)70028-8

Stimulation of bactericidal activity of human neutrophils by interleukin-2-activated lymphoid cells: Effect of proinflammatory cytokines

Потапнев, М. П., & Dv, P. (1992) · Bulletin of Experimental Biology and Medicine · doi:10.1007/bf00840483

P48-Triggered transmembrane signaling transduction of human monocytes: mobilization of calcium ion and activation of protein kinase C (PKC)

Chang, Z., & Hall, R. (1995) · Cell Research · doi:10.1038/cr.1995.10

The biocompatibility of novel phosphorylcholine based biomaterials

Barraud, J. E. (2001) · University of Brighton Repository (University of Brighton)

UNIVERSITÁ DEGLI STUDI DI MILANO FACOLTÁ DI MEDICINA E CHIRURGIA

Ricerca, D. D. (2010)

Differentiation of the expression of A2a adenosine receptor in macrophage cell lines RAW264

Watanabe, K., Shirasu, S., Daito, K., Motoyama, M., Ogawa, Y., Nakai, K., Ohura, K., & Daito, M. (2006) · 歯科薬物療法 · doi:10.11263/jsotp1982.25.8

Paclitaxel-induced macrophage activities in the tumor-bearing host: immunologic implications and therapeutic applications

Mullins, D. W. (1998) · VTechWorks (Virginia Tech)

Macrophage activation by interleukin 4

Whittall, T. (1992) · UCL Discovery (University College London)

Gene Expression in Early Stages of Low-Intensity Pulsed Ultrasound Exposure on Bone Marrow Cells

Yamaguchi, D., Takeuchi, K., Ueno, A., Yamaguchi, M., Murakami, H., & Kimoto, S. (2022) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.31.23

Molecular bases of macrophage activation: regulation of class II MHC genes in tissue macrophages

Adams, D. O., & Johnson, S. P. (1992) · Springer eBooks · doi:10.1007/978-94-015-8070-0_56 · Cited by 5

The molecular biology of macrophage activation.

Paulnock, D. M. (1994) · PubMed · Cited by 18

Molecular features of macrophage activation

Schultze, J. L., & Schmidt, S. V. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2016.03.009 · Cited by 97

Macrophage activation

Poinsot, B., Yip, D., Trouvd, V. A., & Samaniego, M. (1977)

Macrophage activation by T cells

Paulnock, D. M. (1992) · Current Opinion in Immunology · doi:10.1016/0952-7915(92)90087-u · Cited by 69