Evidence map›Paper›PMID 35859176›Full record

ArticleNature2022

ADAR1 averts fatal type I interferon induction by ZBP1.

Huipeng Jiao, Laurens Wachsmuth, Simone Wolf, Juliane Lohmann, Masahiro Nagata, Göksu Gökberk Kaya, Nikos Oikonomou, Vangelis Kondylis, Manuel Rogg, Martin Diebold and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
15.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

146 citing papers in PubMed, 191 citations in OpenAlex.

  1. Review
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  4. Mechanisms, regulation and clinical relevance of necroptosis.Nature reviews. Molecular cell biology · 2026
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86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Huipeng Jiao *Institute for Genetics, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0001-9632-6176
Laurens Wachsmuth *Institute for Genetics, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0003-1701-9384
Simone WolfInstitute for Genetics, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0003-2073-8312
Juliane LohmannInstitute for Genetics, University of Cologne, Cologne, Germany.
Masahiro NagataInstitute for Genetics, University of Cologne, Cologne, Germany.
Göksu Gökberk KayaInstitute for Genetics, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0003-2976-9318
Nikos OikonomouInstitute for Genetics, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0002-4383-9741
Vangelis KondylisInstitute for Pathology, Medical Faculty and University Hospital of Cologne, University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0002-6970-8731
Manuel RoggInstitute of Surgical Pathology, Faculty of Medicine, Medical Center-University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-6658-9159
Martin DieboldInstitute of Neuropathology, Medical Faculty, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0001-9636-6936
Simon E TröderCologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0003-1156-2976
Branko ZevnikCologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0001-7845-9522
Marco PrinzInstitute of Neuropathology, Medical Faculty, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-0349-1955
Christoph SchellInstitute of Surgical Pathology, Faculty of Medicine, Medical Center-University of Freiburg, Freiburg, Germany.
George R YoungBioinformatics and Biostatistics STP, London, UK.ORCID http://orcid.org/0000-0002-1203-588X
George KassiotisRetroviral Immunology, The Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0002-8457-2633
Manolis PasparakisInstitute for Genetics, University of Cologne, Cologne, Germany. pasparakis@uni-koeln.de.ORCID http://orcid.org/0000-0002-9870-0966
University of Cologne · DEUniversity of Freiburg · DEMRC Biostatistics Unit · GBThe Francis Crick Institute · GB

Funding

European Research Council 787826Wellcome Trust FC001099
6 · The paper itself

Abstract

Mutations of the ADAR1 gene encoding an RNA deaminase cause severe diseases associated with chronic activation of type I interferon (IFN) responses, including Aicardi-Goutières syndrome and bilateral striatal necrosis

Indexed as

Adenosine DeaminaseInterferon Type IRNA-Binding ProteinsAnimalsApoptosisCaspase 8MiceMutationNecroptosisRNA, Double-StrandedADAR1 protein, mouseAdenosine DeaminaseCaspase 8Interferon Type IRNA-Binding ProteinsRNA, Double-StrandedZbp1 protein, mouse

Identifiers

PMID35859176
PMCPMC9329096
OpenAlexW4286007813

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.