Cited by 1,902Immune cells in cancerImmune Response and InflammationPhagocytosis and Immune Regulation

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The many faces of macrophage activation

Mosser, David M·2003·Journal of Leukocyte Biology

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Journal of Leukocyte Biology considers manuscripts of original investigations focusing on the origins, developmental biology, biochemistry and functions of granulocytes, lymphocytes, mononuclear phagocytes, and other cells involved in host defense. These include full-length papers on original research, rapid communications of new discoveries, letters, commentaries, and invited reviews.

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NITRIC OXIDE AND MACROPHAGE FUNCTION
MacMicking, J. D., Xie, Q. W., & Nathan, C. (1997) · Annual Review of Immunology · doi:10.1146/annurev.immunol.15.1.323 · Cited by 4,245
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Interleukin 4 potently enhances murine macrophage mannose receptor activity: A marker of alternative immunologic macrophage activation
Stein, M., Keshav, S., Harris, N., & Gordon, S. (1992) · The Journal of experimental medicine · doi:10.1084/jem.176.1.287 · Cited by 1,960
Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-beta1 secretion and the resolution of inflammation.
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Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-β1 secretion and the resolution of inflammation
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Differential Regulation of Nitric Oxide Synthase-2 and Arginase-1 by Type 1/Type 2 Cytokines In Vivo: Granulomatous Pathology Is Shaped by the Pattern of l -Arginine Metabolism
Hesse, M., Modolell, M., Flamme, A. C. L., Schito, M. L., Fuentes, J. M., Cheever, A. W., Pearce, E. J., & Wynn, T. A. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.11.6533 · Cited by 723
Other Functions, Other Genes
Goerdt, S., & Orfanos, C. E. (1999) · Immunity · doi:10.1016/s1074-7613(00)80014-x · Cited by 678
Reciprocal regulation of the nitric oxide synthase/arginase balance in mouse bone marrow‐derived macrophages by TH 1 and TH 2 cytokines
Modolell, M., Corraliza, I. M., Link, F., Soler, G., & Eichmann, K. (1995) · European Journal of Immunology · doi:10.1002/eji.1830250436 · Cited by 554
Reprogramming of the Macrophage Transcriptome in Response to Interferon-γ and Mycobacterium tuberculosis
Ehrt, S., Schnappinger, D., Bekiranov, S., Drenkow, J., Shi, S., Gingeras, T., Gaasterland, T., Schoolnik, G. K., & Nathan, C. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.8.1123 · Cited by 467
Influence of alternatively and classically activated macrophages on fibrogenic activities of human fibroblasts
Song, E., Ouyang, N., Hörbelt, M., Antus, B., Wang, M., & Exton, M. S. (2000) · Cellular Immunology · doi:10.1006/cimm.2000.1687 · Cited by 447

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Authors: Mosser, D. M.
Affiliations: University of Maryland, College Park (US)
Corresponding author: Mosser, David M
ORCID: Mosser, David M
Venue: Journal of Leukocyte Biology
Publisher: Oxford University Press (OUP)
Published: 2003-02-01
Volume: 73
Issue: 2
Pages: 209-212
ISSN: 0741-5400 (ISSN-L)
1938-3673
DOI: 10.1189/jlb.0602325
OpenAlex: W2016293419
Cited by: 1,902
References: 38
Citations by year: 2026: 16 · 2025: 30 · 2024: 57 · 2023: 42 · 2022: 67 · 2021: 76 · 2020: 68 · 2019: 81 · 2018: 65 · 2017: 92 · 2016: 115 · 2015: 111 · 2014: 139 · 2013: 129 · 2012: 133
FWCI: 5.27
Type: journal article
Language: en
Open access: closed
Licence: academic.oup.com/pages/standard-publication-reuse-rights (vor)
Locations: Journal of Leukocyte Biology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
Keywords: macrophage activation, macrophages, mononuclear phagocytes, host defense, granulocytes, lymphocytes, cell development
MeSH terms: Animals, Humans, Interferon-gamma, Macrophage Activation, Macrophages, Interleukin-4, Interleukin-10

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