Evidence map›Paper›PMID 8265655›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Transcriptional regulatory elements downstream of the JunB gene.

E D Perez-Albuerne, G Schatteman, L K Sanders, D Nathans

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 50 citations in OpenAlex.

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  14. Multivalent DNA-binding properties of the HMG-1 proteins.Proceedings of the National Academy of Sciences of the United States of America · 1996
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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

4 authors at 2 institutions in 1 country.

E D Perez-AlbuerneHoward Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185.
G Schatteman
L K Sanders
D Nathans
Johns Hopkins University · USHoward Hughes Medical Institute · US

Funding

TRANSPOSITION OF TN7P01CA016519 · NCI · JOHNS HOPKINS UNIVERSITY · PI BOEKE, JEF D · 1985 to 2010
$21.4M
NCI NIH HHS P01 CA16519NIGMS NIH HHS GM-07309
6 · The paper itself

Abstract

JunB is an immediate early transcription factor that is induced by a variety of extracellular signaling agents, including growth factors, phorbol esters, and agents that elevate cyclic AMP. The mechanism of activation of the gene encoding JunB by these agents is not well understood. By using the JunB gene together with flanking DNA in transfection experiments, we show that a serum response element (SRE) and/or a cAMP response element (CRE) downstream of the gene mediate the response of the gene in mouse NIH 3T3 cells to serum, platelet-derived growth factor, basic fibroblast growth factor, phorbol ester, and forskolin. In addition, a segment of DNA just upstream of the TATA box is required for optimal activation of the gene.

Indexed as

Gene Expression RegulationGenes, fosGenes, junRegulatory Sequences, Nucleic AcidTATA BoxTranscription, Genetic3T3 CellsAnimalsBase SequenceBinding SitesCyclic AMPGene LibraryKineticsMiceMice, Inbred BALB CMolecular Sequence DataCyclic AMPOligodeoxyribonucleotidesProto-Oncogene Proteins c-jun

Identifiers

PMID8265655
PMCPMC48105
OpenAlexW1979315750

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.