Evidence map›Paper›PMID 24495544›Full record

ReviewJournal of inorganic biochemistry2014

Modulation of nuclear receptor function by cellular redox poise.

Eric L Carter, Stephen W Ragsdale

Abstract readReview
In one paragraph

Review in Journal of inorganic biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Fundamentals of redox regulation in biology.Nature reviews. Molecular cell biology · 2024
    Review
  3. Review
  4. Review
  5. Regulation of protein function and degradation by heme, heme responsive motifs, and CO.Critical reviews in biochemistry and molecular biology · 2022
    Review
  6. Review
  7. Ferric heme as a CO/NO sensor in the nuclear receptor Rev-Erbß by coupling gas binding to electron transfer.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Article
  9. Review
  10. Cellular Timekeeping: It's Redox o'Clock.Cold Spring Harbor perspectives in biology · 2018
    Review
  11. Article
  12. Article
  13. Circadian redox oscillations and metabolism.Trends in endocrinology and metabolism: TEM · 2015
    Review
  14. 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

2 authors at 1 institution in 1 country.

Eric L CarterDepartment of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Stephen W RagsdaleDepartment of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA. Electronic address: sragsdal@umich.edu.
University of Michigan · US

Funding

Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Dana Dolinoy · 2011 to 2026
$21.3M
ENVIRONMENTAL TOXICOLOGY PRE/POST DOCTORAL RES.TRAININGT32ES007062 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Justin Adam Colacino · 1985 to 2026
$10.5M
Thiol/Disulfide Redox Regulation of Heme Oxygenase-2R01HL102662 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAGSDALE, STEPHEN WILEY · 2010 to 2013
$2.2M
NHLBI NIH HHS R01 HL102662NHLBI NIH HHS R01HL 102662NIEHS NIH HHS P30 ES017885NIEHS NIH HHS T32 ES007062NIEHS NIH HHS T32ES007062
6 · The paper itself

Abstract

Nuclear receptors (NRs) are ligand-responsive transcription factors involved in diverse cellular processes ranging from metabolism to circadian rhythms. This review focuses on NRs that contain redox-active thiol groups, a common feature within the superfamily. We will begin by describing NRs, how they regulate various cellular processes and how binding ligands, corepressors and/or coactivators modulate their activity. We will then describe the general area of redox regulation, especially as it pertains to thiol-disulfide interconversion and the cellular systems that respond to and govern this redox equilibrium. Lastly, we will discuss specific examples of NRs whose activities are regulated by redox-active thiols. Glucocorticoid, estrogen, and the heme-responsive receptor, Rev-erb, will be described in the most detail as they exhibit archetypal redox regulatory mechanisms.

Indexed as

Nuclear ReactorsOxidation-ReductionTranscription, GeneticDisulfidesHemeHumansLigandsProtein BindingSulfhydryl CompoundsTranscription FactorsDisulfidesHemeLigandsSulfhydryl CompoundsTranscription FactorsHormoneNuclear receptorOxidative stressRedoxThiol–disulfideTranscription

Identifiers

PMID24495544
PMCPMC3986263
OpenAlexW1994689790

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.