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Cited by 356

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

D rosophila : The Genetics of Innate Immune Recognition and Response

Brennan, Catherine A., Anderson, Kathryn V.·2004·Annual Review of Immunology

Abstract

▪ Abstract Because of the evolutionary conservation of innate mechanisms of host defense, Drosophila has emerged as an ideal animal in which to study the genetic control of immune recognition and responses. The discovery that the Toll pathway is required for defense against fungal infection in Drosophila was pivotal in studies of both mammalian and Drosophila immunity. Subsequent genetic screens in Drosophila to isolate additional mutants unable to induce humoral responses to infection have identified and ordered the function of components of two signaling cascades, the Toll and Imd pathways, that activate responses to infection. Drosophila blood cells also contribute to host defense through phagocytosis and signaling, and may carry out a form of self-nonself recognition that is independent of microbial pattern recognition. Recent work suggests that Drosophila will be a useful model for dissecting virulence mechanisms of several medically important pathogens.

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Crossref · 10.1146/annurev.immunol.22.012703.104626

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Metadata

Authors
Brennan, C. A., & Anderson, K. V.
Venue
Annual Review of Immunology
Published
2004-04-01
Volume
22
Issue
1
Pages
457-483
ISSN
  • 0732-0582 (ISSN-L)
  • 1545-3278
OpenAlex
W2156739718
Cited by
356
References
4
FWCI
1.78
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: D rosophila : The Genetics of Innate Immune Recognition and Response. https://app.cochat.ai/papers/10.1146/annurev.immunol.22.012703.104626
The paper
Brennan, C. A., & Anderson, K. V. (2004). D rosophila : The Genetics of Innate Immune Recognition and Response. Annual Review of Immunology. https://doi.org/10.1146/annurev.immunol.22.012703.104626

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.