Evidence map›Paper›PMID 24095857›Full record

ReviewJournal of molecular biology2013

The antiviral activities of ISG15.

David J Morales, Deborah J Lenschow

Abstract readReview
In one paragraph

Review in Journal of molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

156 citing papers in PubMed, 257 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. From bats to humans: uncoveringbioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. ISGylation of NF-κBp65 by SCFArteriosclerosis, thrombosis, and vascular biology · 2023
    Article
  20. Review

96 more citing papers are in PubMed but not listed here.

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.

David J MoralesDepartment of Medicine and Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Deborah J Lenschow
Washington University in St. Louis · US

Funding

TRAINING PROGRAM IN CELLULAR AND MOLECULAR BIOLOGYT32GM007067 · NIGMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L · 1985 to 2020
$20.4M
TRAINING IN THE IMMUNOLOGY OF RHEUMATIC DISEASEST32AR007279 · NIAMS · WASHINGTON UNIVERSITY · PI Megan Anne Cooper, Deborah J Lenschow · 1986 to 2026
$6.0M
REGULATION OF INFLUENZA VIRUS INFECTION BY ISG15R01AI080672 · NIAID · WASHINGTON UNIVERSITY · PI LENSCHOW, DEBORAH J · 2009 to 2021
$2.9M
NIAID NIH HHS R01 AI080672NIAMS NIH HHS T32 AR007279NIGMS NIH HHS T32 GM007067
6 · The paper itself

Abstract

Post-translational protein modification is an important strategy for the regulation of the cell proteome independent of the need for new gene expression. Ubiquitin and ubiquitin-like modifiers mediate the regulation of protein levels, signaling pathways, vesicular trafficking, and many other cellular processes through their covalent conjugation to proteins. Interferon stimulated gene 15 (ISG15) is a ubiquitin-like modifier induced by type I interferon. In addition to conjugating to potentially hundreds of target proteins, ISG15 can be found in an unconjugated form both inside of the cell and released from interferon stimulated cells into the extracellular environment. Due to its robust expression after type I interferon stimulation and the broad panel of proteins that it targets, ISG15 has drawn much attention as a potential regulator of the immune response and has been shown to mediate protection in a number of different viral infection models. Here we will review the current state of the field of ISG15, the viruses against which ISG15 mediates protection, and the mechanisms by which ISG15 exerts antiviral activity.

Indexed as

Immunity, InnateProtein Processing, Post-TranslationalAntiviral AgentsCytokinesGene Expression RegulationHumansInterferon Type IUbiquitinsVirus ReleaseVirus ReplicationAntiviral AgentsCytokinesInterferon Type IISG15 protein, humanUbiquitinsASLVavian sarcoma leukosis virusChikungunya virusCHIKVendosomal sorting complexes required for transportESCRTherpes simplex virus 1HIV-1HPVHSV-1human immunodeficiency virus 1human papilloma virusinnate immunityinterferon regulatory factor 3interferonsinterferon stimulated gene 15IRF3ISG15JNKJun N-terminal kinaseLCMVlymphocytic choriomeningitis virusMEFmouse embryonic fibroblastnatural killerNDVNewcastle disease virusNKPKRprotein kinase Rretinoic acid inducible gene 1RIG-ISendai virusSeVshort interfering RNAsiRNAubiquitin-like proteinvesicular stomatitis virusvirusesvirus-like particleVLPVSVWest Nile viruswild typeWNVWT

Identifiers

PMID24095857
PMCPMC4090058
OpenAlexW2051227636

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.