Evidence map›Paper›PMID 7892230›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

OR-1, a member of the nuclear receptor superfamily that interacts with the 9-cis-retinoic acid receptor.

M Teboul, E Enmark, Q Li, A C Wikström, M Pelto-Huikko, J A Gustafsson

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.8field-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

63 citing papers in PubMed, 234 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Nuclear Receptors in Energy Metabolism.Advances in experimental medicine and biology · 2022
    Article
  8. Liver X receptorAmerican journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  9. Review
  10. Review
  11. Retinal and optic nerve degeneration in liver X receptor β knockout mice.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. Liver X receptor-α activation enhances cholesterol secretion in lactating mammary epithelium.American journal of physiology. Endocrinology and metabolism · 2019
    Article
  13. Article
  14. Beyond the Foam Cell: The Role of LXRs in Preventing Atherogenesis.International journal of molecular sciences · 2018
    Review
  15. Disrupting LXRα phosphorylation promotes FoxM1 expression and modulates atherosclerosis by inducing macrophage proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

M TeboulCenter for Biotechnology, Karolinska Institute, NOVUM, Huddinge, Sweden.
E Enmark
Q Li
A C Wikström
M Pelto-Huikko
J A Gustafsson
Karolinska Institutet · SEHouston Methodist · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have cloned a member of the nuclear receptor superfamily. The cDNA was isolated from a rat liver library and encodes a protein of 446 aa with a predicted mass of 50 kDa. This clone (OR-1) shows no striking homology to any known member of the steroid/thyroid hormone receptor superfamily. The most related receptor is the ecdysone receptor and the highest homologies represent < 10% in the amino-terminal domain, between 15-37% in the carboxyl-terminal domain and 50-62% in the DNA binding domain. The expression of OR-1 appears to be widespread in both fetal and adult rat tissues. Potential DNA response elements composed of a direct repeat of the hexameric motif AGGTCA spaced by 0-6 nt were tested in gel shift experiments. OR-1 was shown to interact with the 9-cis-retinoic acid receptor (retinoid X receptor, RXR) and the OR-1/RXR complex to bind to a direct repeat spaced by 4 nt (DR4). In transfection experiments, OR-1 appears to activate RXR-mediated function through the DR4. Therefore OR-1 might modulate 9-cis-retinoic acid signaling by interacting with RXR.

Indexed as

Amino Acid SequenceAnimalsBase SequenceCHO CellsCloning, MolecularCricetinaeDNA-Binding ProteinsDNA, ComplementaryFetusGene LibraryIn Situ HybridizationIsomerismLiverLiver X ReceptorsMolecular Sequence DataOligonucleotide ProbesDNA-Binding ProteinsDNA, ComplementaryLiver X ReceptorsNr1h2 protein, ratOligonucleotide ProbesOrphan Nuclear ReceptorsReceptors, Cytoplasmic and NuclearReceptors, Retinoic AcidRNA, MessengerTretinoin

Identifiers

PMID7892230
PMCPMC42430
OpenAlexW2081732968

What OpenQuestion holds

Textmetadata
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.