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Cited by 1,324

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

MACROPHAGE RECEPTORS AND IMMUNE RECOGNITION

Taylor, P.R., Martinez-Pomares, L., Stacey, M., Lin, H-H., Brown, G.D., Gordon, S.·2005·Annual Review of Immunology

Abstract

▪ Abstract Macrophages express a broad range of plasma membrane receptors that mediate their interactions with natural and altered-self components of the host as well as a range of microorganisms. Recognition is followed by surface changes, uptake, signaling, and altered gene expression, contributing to homeostasis, host defense, innate effector mechanisms, and the induction of acquired immunity. This review covers recent studies of selected families of structurally defined molecules, studies that have improved understanding of ligand discrimination in the absence of opsonins and differential responses by macrophages and related myeloid cells.

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Crossref · 10.1146/annurev.immunol.23.021704.115816

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Metadata

Authors
Taylor, P. R., Martinez-Pomares, L., Stacey, M., Lin, H.-H., Brown, G. D., & Gordon, S.
Venue
Annual Review of Immunology
Published
2005-04-01
Volume
23
Issue
1
Pages
901-944
ISSN
  • 0732-0582 (ISSN-L)
  • 1545-3278
OpenAlex
W2104460754
Cited by
1,324
References
7
FWCI
3.59
Type
journal article
Language
en
Open access
closed

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This page
CoChat. (2026). Citation check: MACROPHAGE RECEPTORS AND IMMUNE RECOGNITION. https://app.cochat.ai/papers/10.1146/annurev.immunol.23.021704.115816
The paper
Taylor, P. R., Martinez-Pomares, L., Stacey, M., Lin, H.-H., Brown, G. D., & Gordon, S. (2005). MACROPHAGE RECEPTORS AND IMMUNE RECOGNITION. Annual Review of Immunology. https://doi.org/10.1146/annurev.immunol.23.021704.115816

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.