Evidence map›Paper›PMID 27391798›Full record

ArticleCell death and differentiation2016

Expression of Twist2 is controlled by T-cell receptor signaling and determines the survival and death of thymocytes.

S Oh, J Oh, C Lee, S Oh, S Jeon, J Choi, S Hwang, Y Lee, H Lee, R H Seong

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

7 citing papers in PubMed, 10 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

10 authors at 2 institutions in 1 country.

S OhSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
J OhSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
C LeeSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
S OhSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
S JeonSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
J ChoiSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
S HwangSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
Y LeeSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
H LeeGraduate School of Cancer Science and Policy, National Cancer Center, Gyeonggi 10408, Republic of Korea.
R H SeongSchool of Biological Sciences and Institute for Molecular Biology and Genetics, Seoul National University, Seoul 151-742, Republic of Korea.
Seoul National University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Self-reactive thymocytes are eliminated by negative selection, whereas competent thymocytes survive by positive selection. The strength of the T-cell receptor (TCR) signal determines the fate of thymocytes undergoing either positive or negative selection. The TCR signal strength is relatively higher in negative selection than in positive selection and induces pro-apoptotic molecules such as Nur77 and Nor-1, which are members of the orphan nuclear receptor family, that then cause TCR-mediated apoptosis. However, at the molecular level, it remains unclear how positive or negative selection is distinguished based on the TCR signal. We found that the expression of Twist2 is differentially regulated in positively and negatively selected thymocytes. In particular, TCR signal strength that elicits positive selection induces Twist2 expression via the Ca

Indexed as

ApoptosisSignal TransductionAnimalsCalcineurinCell SurvivalDNA-Binding ProteinsHistone DeacetylasesJNK Mitogen-Activated Protein KinasesMEF2 Transcription FactorsMice, Inbred C57BLNerve Tissue ProteinsNFATC Transcription FactorsNuclear Receptor Subfamily 4, Group A, Member 1Protein BindingReceptors, Antigen, T-CellReceptors, SteroidCalcineurinDNA-Binding ProteinsHdac7 protein, mouseHistone DeacetylasesJNK Mitogen-Activated Protein KinasesMef2d protein, mouseMEF2 Transcription FactorsNerve Tissue ProteinsNFATC Transcription FactorsNr4a3 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 1Receptors, Antigen, T-CellReceptors, SteroidReceptors, Thyroid HormoneRepressor ProteinsTwist2 protein, mouseTwist-Related Protein 1

Identifiers

PMID27391798
PMCPMC5071571
OpenAlexW2474411298

What OpenQuestion holds

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Registered trials

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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.