Evidence map›Paper›PMID 31030956›Full record

ReviewCellular immunology2019

A20: A multifunctional tool for regulating immunity and preventing disease.

Barbara A Malynn, Averil Ma

Open access · greenAbstract readReview
In one paragraph

Review in Cellular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

57 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. MALT1 substrate cleavage: what is it good for?Frontiers in immunology · 2024
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Barbara A MalynnDepartment of Medicine, University of California, San Francisco, San Francisco, CA 94143, United States.
Averil MaDepartment of Medicine, University of California, San Francisco, San Francisco, CA 94143, United States. Electronic address: averil.ma@ucsf.edu.
University of California, San Francisco · US

Funding

TRAINING PROGRAM IN DISGESTIVE DISEASES AND NUTRITIONT32DK007007 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AVERIL I MA · 1986 to 2026
$6.4M
A20 Mediated Regulation of Colitis and SpondyloarthritisR01DK095693 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, AVERIL I · 2012 to 2021
$3.1M
Regulation of Ubiquitination and ArthritisR01AI135198 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, AVERIL I · 2018 to 2022
$2.0M
Ubiquitin and PsoriasisR01AI117908 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, AVERIL I · 2015 to 2019
$2.0M
NIAID NIH HHS R01 AI117908NIAID NIH HHS R01 AI135198NIDDK NIH HHS R01 DK095693NIDDK NIH HHS T32 DK007007
6 · The paper itself

Abstract

A20, also known as TNFAIP3, is a potent regulator of ubiquitin (Ub) dependent signals. A20 prevents multiple human diseases, indicating that the critical functions of this protein are clinically as well as biologically impactful. As revealed by mouse models, cell specific functions of A20 are linked to its ability to regulate diverse signaling pathways. Aberrant expression or functions of A20 in specific cell types underlie divergent disease outcomes. Discernment of A20's biochemical functions and their phenotypic outcomes will contribute to our understanding of how ubiquitination is regulated, how Ub mediated functions can prevent disease, and will pave the way for future therapeutic interventions.

Indexed as

Protein Processing, Post-TranslationalAnimalsArthritis, RheumatoidAsthmaB-LymphocytesDisease Models, AnimalHumansImmunity, InnateImmunologic FactorsLupus Erythematosus, SystemicMolecular Targeted TherapyNF-kappa BSignal TransductionT-LymphocytesTumor Necrosis Factor alpha-Induced Protein 3UbiquitinationImmunologic FactorsNF-kappa BTNFAIP3 protein, humanTumor Necrosis Factor alpha-Induced Protein 3A20AutoimmunityInflammationInnate immunityTNFAIP3Ubiquitin

Identifiers

PMID31030956
PMCPMC6584049
OpenAlexW2933917059

What OpenQuestion holds

Textmetadata
LicenceTDM
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.