Evidence map›Paper›PMID 20338175›Full record

ReviewGeneral and comparative endocrinology2011

Mechanisms and significance of nuclear receptor auto- and cross-regulation.

Pia Bagamasbad, Robert J Denver

Abstract readReview
In one paragraph

Review in General and comparative endocrinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Review
  10. YAP inhibits ERα and ERNature communications · 2022
    Article
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  12. Review
  13. Review
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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

2 authors at 1 institution in 1 country.

Pia BagamasbadDepartment of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor, MI 48109-1048, USA.
Robert J Denver
University of Michigan–Ann Arbor · US

Funding

Hormone and Activity-Dependent Neural Gene ExpressionR01NS046690 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DENVER, ROBERT J · 2004 to 2007
$815k
NINDS NIH HHS 1 R01 NS046690NINDS NIH HHS R01 NS046690
6 · The paper itself

Abstract

The number of functional hormone receptors expressed by a cell in large part determines its responsiveness to the hormonal signal. The regulation of hormone receptor gene expression is therefore a central component of hormone action. Vertebrate steroid and thyroid hormones act by binding to nuclear receptors (NR) that function as ligand-activated transcription factors. Nuclear receptor genes are regulated by diverse and interacting intracellular signaling pathways. Nuclear receptor ligands can regulate the expression of the gene for the NR that mediates the hormone's action (autoregulation), thus influencing how a cell responds to the hormone. Autoregulation can be either positive or negative, the hormone increasing or decreasing, respectively, the expression of its own NR. Positive autoregulation (autoinduction) is often observed during postembryonic development, and during the ovarian cycle, where it enhances cellular sensitivity to the hormonal signal to drive the developmental process. By contrast, negative autoregulation (autorepression) may become important in the juvenile and adult for homeostatic negative feedback responses. In addition to autoregulation, a NR can influence the expression other types of NRs (cross-regulation), thus modifying how a cell responds to a different hormone. Cross-regulation by NRs is an important means to temporally coordinate cell responses to a subsequent (different) hormonal signal, or to allow for crosstalk between hormone signaling pathways.

Indexed as

AnimalsHumansReceptors, AndrogenReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, EstrogenReceptors, ProgesteroneReceptors, Retinoic AcidReceptors, SteroidReceptors, Thyroid HormoneReceptors, AndrogenReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, EstrogenReceptors, ProgesteroneReceptors, Retinoic AcidReceptors, SteroidReceptors, Thyroid Hormone

Identifiers

PMID20338175
PMCPMC2911511
OpenAlexW2054206401

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.