Evidence map›Paper›PMID 27721430›Full record

ArticleNature immunology2017

USP15 regulates type I interferon response and is required for pathogenesis of neuroinflammation.

Sabrina Torre, Maria J Polyak, David Langlais, Nassima Fodil, James M Kennedy, Irena Radovanovic, Joanne Berghout, Gabriel A Leiva-Torres, Connie M Krawczyk, Subburaj Ilangumaran and 11 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
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  7. The roles of ubiquitination in AML.Annals of hematology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 6 institutions in 1 country.

Sabrina TorreDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Maria J PolyakMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.ORCID 0000-0003-3762-9278
David LanglaisMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.
Nassima FodilMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.
James M KennedyMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.
Irena RadovanovicMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.ORCID 0000-0002-3823-3729
Joanne BerghoutMcGill Center for Complex Traits, McGill University, Montreal, Quebec, Canada.
Gabriel A Leiva-TorresDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Connie M KrawczykDepartment of Microbiology, and Immunology, McGill University, Montreal, Quebec, Canada.
Subburaj IlangumaranDepartment of Pediatrics, Faculty of Medicine, University of Sherbrooke, Sherbrooke, Quebec, Canada.
Karen MossmanDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Chen LiangDepartment of Medicine, Lady Davis Institute for Medical Research, Montreal, Quebec, Canada.
Klaus-Peter KnobelochInstitute for Neuropathology, University Clinic Freiburg, Freiburg, Germany.
Luke M HealyDepartment of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
Jack AntelDepartment of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
Nathalie ArbourDepartment of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Alexandre PratDepartment of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Jacek MajewskiDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.ORCID 0000-0003-3572-9558
Mark LathropDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Silvia M VidalDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Philippe GrosDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
McGill University · CAMcGill University and Génome Québec Innovation Centre · CAUniversité de Montréal · CAJewish General Hospital · CAMcMaster University · CAUniversité de Sherbrooke · CA

Funding

CIHR MOP119342CIHR MOP133487
6 · The paper itself

Abstract

Genes and pathways in which inactivation dampens tissue inflammation present new opportunities for understanding the pathogenesis of common human inflammatory diseases, including inflammatory bowel disease, rheumatoid arthritis and multiple sclerosis. We identified a mutation in the gene encoding the deubiquitination enzyme USP15 (Usp15

Indexed as

AnimalsDNA-Binding ProteinsEncephalomyelitis, Autoimmune, ExperimentalHEK293 CellsHumansImmunity, InnateInterferon Type IMalaria, CerebralMiceMice, 129 StrainMice, Inbred C57BLMice, TransgenicMolecular Targeted TherapyMyelin-Oligodendrocyte GlycoproteinNeurogenic InflammationPeptide FragmentsDNA-Binding ProteinsInterferon Type IMyelin-Oligodendrocyte Glycoproteinmyelin oligodendrocyte glycoprotein (35-55)Peptide FragmentsTranscription FactorsTrim25 protein, mouseUbiquitin-Specific ProteasesUsp15 protein, mouse

Identifiers

PMID27721430
OpenAlexW2530312898

What OpenQuestion holds

Textmetadata
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.