Evidence map›Paper›PMID 19043594›Full record

ReviewNuclear receptor signaling2008

Atrophin proteins: an overview of a new class of nuclear receptor corepressors.

Lei Wang, Chih-Cheng Tsai

Open access · hybridAbstract readReview
In one paragraph

Review in Nuclear receptor signaling, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

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  17. Deciphering GRINA/Lifeguard1: Nuclear Location, CaInternational journal of molecular sciences · 2019
    Review
  18. Article
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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.

Lei WangDepartment of Physiology and Biophysics, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey, USA.
Chih-Cheng Tsai
Johnson University · US

Funding

Molecular Mechanisms of Ataxin-1 ActionR01NS050365 · NINDS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI TSAI, CHIH-CHENG · 2007 to 2010
$1.1M
NINDS NIH HHS 5R01NS050365NINDS NIH HHS R01 NS050365
6 · The paper itself

Abstract

The normal development and physiological functions of multicellular organisms are regulated by complex gene transcriptional networks that include myriad transcription factors, their associating coregulators, and multiple chromatin-modifying factors. Aberrant gene transcriptional regulation resulting from mutations among these elements often leads to developmental defects and diseases. This review article concentrates on the Atrophin family proteins, including vertebrate Atrophin-1 (ATN1), vertebrate arginine-glutamic acid dipeptide repeats protein (RERE), and Drosophila Atrophin (Atro), which we recently identified as nuclear receptor corepressors. Disruption of Atrophin-mediated pathways causes multiple developmental defects in mouse, zebrafish, and Drosophila, while an aberrant form of ATN1 and altered expression levels of RERE are associated with neurodegenerative disease and cancer in humans, respectively. We here provide an overview of current knowledge about these Atrophin proteins. We hope that this information on Atrophin proteins may help stimulate fresh ideas about how this newly identified class of nuclear receptor corepressors aids specific nuclear receptors and other transcriptional factors in regulating gene transcription, manifesting physiological effects, and causing diseases.

Indexed as

AnimalsCarrier ProteinsDrosophilaDrosophila ProteinsGene Expression RegulationHumansNerve Tissue ProteinsReceptors, Cytoplasmic and NuclearRepressor ProteinsTranscription Factorsatrophin-1Carrier ProteinsDrosophila Proteinsgug protein, DrosophilaNerve Tissue ProteinsReceptors, Cytoplasmic and NuclearRepressor ProteinsRERE protein, humanTranscription Factors

Identifiers

PMID19043594
PMCPMC2586093
OpenAlexW2084230759

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.