Evidence map›Paper›PMID 28406481›Full record

ArticleCell death & disease2017

Liver receptor homolog-1 (NR5a2) regulates CD95/Fas ligand transcription and associated T-cell effector functions.

Juliane Schwaderer, Ann-Kathrin Gaiser, Truong San Phan, M Eugenia Delgado, Thomas Brunner

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
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.

Juliane SchwadererBiochemical Pharmacology, Department of Biology, University of Konstanz, Konstanz, Germany.
Ann-Kathrin GaiserBiochemical Pharmacology, Department of Biology, University of Konstanz, Konstanz, Germany.
Truong San PhanBiochemical Pharmacology, Department of Biology, University of Konstanz, Konstanz, Germany.
M Eugenia DelgadoBiochemical Pharmacology, Department of Biology, University of Konstanz, Konstanz, Germany.
Thomas BrunnerBiochemical Pharmacology, Department of Biology, University of Konstanz, Konstanz, Germany.
University of Konstanz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD95/Fas ligand (FasL) is a cell death-promoting member of the tumor necrosis factor family with important functions in the regulation of T-cell homeostasis and cytotoxicity. In T cells, FasL expression is tightly regulated on a transcriptional level involving a complex set of different transcription factors. The orphan nuclear receptor liver receptor homolog-1 (LRH-1/NR5a2) is involved in the regulation of development, lipid metabolism and proliferation and is predominantly expressed in epithelial tissues. However, its expression in T lymphocytes has never been reported so far. Based on in silico analysis, we identified potential LRH-1 binding sites within the FASLG promoter. Here, we report that LRH-1 is expressed in primary and secondary lymphatic tissues, as well as in CD4

Indexed as

Gene Expression RegulationResponse ElementsTranscription, GeneticAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChemical and Drug Induced Liver InjuryConcanavalin ADisease Models, AnimalFas Ligand ProteinLiverMiceMice, Mutant StrainsReceptors, Cytoplasmic and NuclearConcanavalin AFas Ligand ProteinFasl protein, mouseNr5a2 protein, mouseReceptors, Cytoplasmic and Nuclear

Identifiers

PMID28406481
PMCPMC5477591
OpenAlexW2607237702

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.