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Cited by 490

The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.

ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling

Open access
Hartner, Jochen C, Walkley, Carl R, Lu, Jun, Orkin, Stuart H·2009·Nature Immunology

Abstract

The deaminase ADAR1 edits adenosines in nuclear transcripts of nervous tissue and is required in the fetal liver of the developing mouse embryo. Here we show by inducible gene disruption in mice that ADAR1 is essential for maintenance of both fetal and adult hematopoietic stem cells. Loss of ADAR1 in hematopoietic stem cells led to global upregulation of type I and II interferon–inducible transcripts and rapid apoptosis. Our findings identify ADAR1 as an essential regulator of hematopoietic stem cell maintenance and suppressor of interferon signaling that may protect organisms from the deleterious effects of interferon activation associated with many pathological processes, including chronic inflammation, autoimmune disorders and cancer.

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Crossref · 10.1038/ni.1680

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Metadata

Authors
Hartner, J. C., Walkley, C. R., Lu, J., & Orkin, S. H.
Venue
Nature Immunology
Published
2008-12-07
Volume
10
Issue
1
Pages
109-115
ISSN
  • 1529-2908 (ISSN-L)
  • 1529-2916
OpenAlex
W2059439438
Cited by
490
References
44
FWCI
7.32
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling. https://app.cochat.ai/papers/10.1038/ni.1680
The paper
Hartner, J. C., Walkley, C. R., Lu, J., & Orkin, S. H. (2009). ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling. Nature Immunology. https://doi.org/10.1038/ni.1680

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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.