Evidence map›Paper›PMID 28652368›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Antagonistic BMP-cWNT signaling in the cnidarian

Naveen Wijesena, David K Simmons, Mark Q Martindale

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.6field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

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  13. The developmental biology ofScience advances · 2021
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  20. Germ-layer commitment and axis formation in sea anemone embryonic cell aggregates.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

3 authors at 1 institution in 1 country.

Naveen WijesenaWhitney Laboratory for Marine Bioscience, University of Florida, Saint Augustine, FL 32080.
David K SimmonsWhitney Laboratory for Marine Bioscience, University of Florida, Saint Augustine, FL 32080.
Mark Q MartindaleWhitney Laboratory for Marine Bioscience, University of Florida, Saint Augustine, FL 32080 mqmartin@whitney.ufl.edu.ORCID 0000-0002-5805-5640
Whitney Museum of American Art · US

Funding

Gene regulatory network evolution and the origin of biological noveltiesR01GM093116 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI MARTINDALE, MARK Q · 2010 to 2013
$1.1M
NIGMS NIH HHS R01 GM093116
6 · The paper itself

Abstract

Gastrulation was arguably the key evolutionary innovation that enabled metazoan diversification, leading to the formation of distinct germ layers and specialized tissues. Differential gene expression specifying cell fate is governed by the inputs of intracellular and/or extracellular signals. Beta-catenin/Tcf and the TGF-beta bone morphogenetic protein (BMP) provide critical molecular signaling inputs during germ layer specification in bilaterian metazoans, but there has been no direct experimental evidence for a specific role for BMP signaling during endomesoderm specification in the early branching metazoan

Indexed as

Signal TransductionActinsAnimalsBone Morphogenetic ProteinsCell LineageCnidariaCRISPR-Cas SystemsEndodermFemaleGene Expression Regulation, DevelopmentalGene Regulatory NetworksMaleMesodermOligonucleotides, AntisenseWnt ProteinsActinsBone Morphogenetic ProteinsOligonucleotides, AntisenseWnt Proteinscell fatecell signalingevodevogene regulatory networkheart kernel

Identifiers

PMID28652368
PMCPMC5514723
OpenAlexW2688192192

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.