Evidence map›Paper›PMID 23998733›Full record

ReviewImmunotherapy2013

Histone methyltransferase and histone methylation in inflammatory T-cell responses.

Shan He, Qing Tong, Dennis Keith Bishop, Yi Zhang

Open access · greenAbstract readReview
In one paragraph

Review in Immunotherapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 43 citations in OpenAlex.

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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

4 authors at 1 institution in 2 countries.

Shan HeDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI 48109-5942, USA.
Qing Tong
Dennis Keith Bishop
Yi Zhang
University of Michigan–Ann Arbor · US

Funding

Delta-like ligand 4+ dendritic cells and induction of alloimmunityR01CA172106 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHANG, YI · 2013 to 2017
$1.6M
NCI NIH HHS R01 CA172106NCI NIH HHS R01-CA-172106-01
6 · The paper itself

Abstract

During immune responses, T cells require tightly controlled expression of transcriptional programs to regulate the balance between beneficial and harmful immunity. These transcriptional programs are critical for the lineage specification of effector T cells, the production of effector cytokines and molecules, and the development and maintenance of memory T cells. An emerging theme is that post-translational modification of histones by methylation plays an important role in orchestrating the expression of transcriptional programs in T cells. In this article, we provide a broad overview of histone methylation signatures for effector molecules and transcription factors in T cells, and the functional importance of histone methyltransferases in regulating T-cell immune responses.

Indexed as

Histone-Lysine N-MethyltransferaseT-LymphocytesAnimalsGene Expression Regulation, EnzymologicHistone MethyltransferasesHumansImmunity, CellularImmunologic MemoryTranscription, GeneticHistone-Lysine N-MethyltransferaseHistone Methyltransferases

Identifiers

PMID23998733
PMCPMC3879725
OpenAlexW2065934375

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.