Evidence map›Paper›PMID 36918845›Full record

ArticleJournal of biomedical science2023

Attenuation of IFN signaling due to m

Dipayan Bose, Xiang Lin, Le Gao, Zhi Wei, Yonggang Pei, Erle S Robertson

Open access · diamondFull text read
In one paragraph

Article in Journal of biomedical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
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  4. The role of NJournal of virology · 2025
    Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. mViruses · 2023
    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

6 authors at 3 institutions in 2 countries.

Dipayan BoseDepartment of Otorhinolaryngology-Head and Neck Surgery, and Tumor Virology Program, Perelman School of Medicine, University of Pennsylvania, 19104, Philadelphia, PA, USA.
Xiang LinDepartment of Computer Science, New Jersey Institute of Technology, 07102, New Jersey, United States of America.
Le GaoDepartment of Computer Science, New Jersey Institute of Technology, 07102, New Jersey, United States of America.
Zhi WeiDepartment of Computer Science, New Jersey Institute of Technology, 07102, New Jersey, United States of America.
Yonggang PeiSchool of Public Health and Emergency Management, Southern University of Science and Technology, 518055, Shenzhen, Guangdong, China.
Erle S RobertsonDepartment of Otorhinolaryngology-Head and Neck Surgery, and Tumor Virology Program, Perelman School of Medicine, University of Pennsylvania, 19104, Philadelphia, PA, USA. erle@pennmedicine.upenn.edu.
New Jersey Institute of Technology · USUniversity of Pennsylvania · USSouthern University of Science and Technology · CN

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Robert H. Vonderheide · 1985 to 2026
$222.3M
Role of LANA-RBP-jk During Early KSHV InfectionP01CA174439 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2013 to 2018
$8.7M
Shared Resources CoreU54CA190158 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2014 to 2023
$4.2M
Tumor suppressor reprogramming by EBV through post-translational modificationR01CA268998 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2022 to 2025
$2.6M
Epigenetic Regulation of KSHV Genome ReplicationR01CA244074 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2019 to 2023
$2.5M
Genome Persistence of KSHVR01CA171979 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2013 to 2017
$1.5M
NCI NIH HHS P01 CA174439NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA171979NCI NIH HHS R01 CA244074NCI NIH HHS R01 CA268998NCI NIH HHS U54 CA190158
6 · The paper itself

Abstract

backgroundReactivation of Epstein Barr virus (EBV) leads to modulation of the viral and cellular epitranscriptome. N6-methyladenosine (m

methodsMethylated RNA immunoprecipitation sequencing (MeRIP-seq), transcriptomic RNA sequencing (RNA-seq) and RNA pull-down PCR were used to screen and validate differentially methylated targets. Western blotting, quantitative real-time PCR (RT-qPCR) and immunocytochemistry were used to investigate the expression and localization of different proteins. RNA stability and polysome analysis assays were used to detect the half-lives and translation efficiencies of downstream genes. Insertion of point mutation to disrupt the m

resultsWe report that during EBV reactivation the m

conclusionOur findings illuminate the significance of m

Indexed as

Epstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansRNAVirus ActivationVirus ReplicationRNAEpitranscriptomeInnate Immune responseLytic reactivationN6-methyladenosineRNA immunoprecipitation

Identifiers

PMID36918845
PMCPMC10012557
OpenAlexW4324144704

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read129
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.