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Cited by 548

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

A20: linking a complex regulator of ubiquitylation to immunity and human disease

Open access
Ma, Averil, Malynn, Barbara A.·2012·Nature Reviews Immunology

Abstract

A20 (also known as TNFAIP3) is a potent anti-inflammatory signalling molecule that restricts multiple intracellular signalling cascades. Recent studies in three general areas have converged to highlight the clinical and biological importance of A20. First, human genetic studies have strongly linked polymorphisms and mutations in the gene encoding A20 to inflammatory, autoimmune and malignant diseases. Second, studies in gene-targeted mice have revealed that A20 regulates multiple immune cell functions and prevents experimental diseases that closely mimic human conditions. Third, biochemical studies have unveiled complex mechanisms by which A20 regulates ubiquitin-dependent nuclear factor-κB and cell-survival signals. Taken together, these studies are revealing the importance of A20-mediated regulation of ubiquitin-dependent signalling in human disease.

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Metadata

Authors
Ma, A., & Malynn, B. A.
Venue
Nature Reviews Immunology
Published
2012-10-12
Volume
12
Issue
11
Pages
774-785
ISSN
  • 1474-1733 (ISSN-L)
  • 1474-1741
OpenAlex
W2020781390
Cited by
548
References
9
FWCI
2.12
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: A20: linking a complex regulator of ubiquitylation to immunity and human disease. https://app.cochat.ai/papers/10.1038/nri3313
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Ma, A., & Malynn, B. A. (2012). A20: linking a complex regulator of ubiquitylation to immunity and human disease. Nature Reviews Immunology. https://doi.org/10.1038/nri3313

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.