Evidence map›Paper›PMID 28637900›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Activation of Mouse

Jiang-Yang Zhao, Oleg Osipovich, Olivia I Koues, Kinjal Majumder, Eugene M Oltz

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Transcriptional network dynamics in early T cell development.The Journal of experimental medicine · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Specific subfamilies of transposable elements contribute to different domains of T lymphocyte enhancers.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. 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

5 authors at 1 institution in 1 country.

Jiang-Yang ZhaoDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0001-5484-3845
Oleg OsipovichDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
Olivia I KouesDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
Kinjal MajumderDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
Eugene M OltzDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110 eoltz@pathology.wustl.edu.
Washington University in St. Louis · US

Funding

TOPOLOGICAL MECHANISMS OF DNA BREAK REPAIR IN LYMPHOCYTESR37AI118852 · NIAID · OHIO STATE UNIVERSITY · PI Eugene M Oltz · 2021 to 2026
$2.8M
TOPOLOGICAL MECHANISMS OF DNA BREAK REPAIR IN LYMPHOCYTESR01AI118852 · NIAID · WASHINGTON UNIVERSITY · PI OLTZ, EUGENE M · 2015 to 2019
$1.9M
SEQUENCE-SPECIFIC CHROMATIN MODIFIERS; NOVEL PROTEIN THERAPEUTICS FOR B CELL LYMPHOMAR01CA188286 · NCI · WASHINGTON UNIVERSITY · PI OLTZ, EUGENE M, PAYTON, JACQUELINE E. · 2015 to 2019
$1.7M
CHROMATIN-BASED DISCOVERY AND FUNCTION OF NOVEL TCR REGULATORY ELEMENTSR21AI115734 · NIAID · WASHINGTON UNIVERSITY · PI ARTOMOV, MAKSYM, OLTZ, EUGENE M · 2015 to 2016
$419k
REGULATION OF OF GENOME ARCHITECTURE IN LYMPHOCYTES: OPPOSING TETHER AND BOUNDARY FUNCTIONSR21AI122726 · NIAID · WASHINGTON UNIVERSITY · PI OLTZ, EUGENE M · 2016 to 2017
$419k
NCI NIH HHS R01 CA188286NIAID NIH HHS R01 AI118852NIAID NIH HHS R21 AI115734NIAID NIH HHS R21 AI122726NIAID NIH HHS R37 AI118852
6 · The paper itself

Abstract

T lineage commitment requires the coordination of key transcription factors (TFs) in multipotent progenitors that transition them away from other lineages and cement T cell identity. Two important TFs for the multipotent progenitors to T lineage transition are RUNX1 and ETS1, which bind cooperatively to composite sites throughout the genome, especially in regulatory elements for genes involved in T lymphopoiesis. Activation of the TCR β (

Indexed as

AnimalsBinding SitesChromatinCore Binding Factor Alpha 2 SubunitGenomeMicePromoter Regions, GeneticProtein BindingProto-Oncogene Protein c-ets-1Receptors, Antigen, T-Cell, alpha-betaRecombination, GeneticThymocytesChromatinCore Binding Factor Alpha 2 SubunitEts1 protein, mouseProto-Oncogene Protein c-ets-1Receptors, Antigen, T-Cell, alpha-betaRunx1 protein, mouse

Identifiers

PMID28637900
PMCPMC5526733
OpenAlexW2701061630

What Socratic 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 Socratic graph.