Evidence map›Paper›PMID 27060628›Full record

ArticleDevelopmental biology2016

An Fgf-Shh signaling hierarchy regulates early specification of the zebrafish skull.

Neil McCarthy, Alfire Sidik, Julien Y Bertrand, Johann K Eberhart

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Mesenchymal-derived neural progenitors underlie localbioRxiv : the preprint server for biology · 2026
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  17. Frontiers in physiology · 2021
    Article
  18. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
  19. Review
  20. 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

4 authors at 3 institutions in 3 countries.

Neil McCarthyDepartment of Molecular Biosciences; Institute of Cell and Molecular Biology, Waggoner Center for Alcohol and Alcohol Addiction Research, University of Texas, Austin, TX, United States.
Alfire SidikDepartment of Molecular Biosciences; Institute of Cell and Molecular Biology, Waggoner Center for Alcohol and Alcohol Addiction Research, University of Texas, Austin, TX, United States.
Julien Y BertrandDepartment of Pathology and Immunology, University of Geneva Medical School, Geneva, Switzerland.
Johann K EberhartDepartment of Molecular Biosciences; Institute of Cell and Molecular Biology, Waggoner Center for Alcohol and Alcohol Addiction Research, University of Texas, Austin, TX, United States; Department of Molecular Biosciences; Institute of Neurobiology, University of Texas, Austin, TX, United States. Electronic address: eberhart@austin.utexas.edu.
Institute of Alcohol Studies · GBThe University of Texas at Austin · USUniversity of Geneva · CH

Funding

Cross-Cultural Assessment of FASDU24AA014811 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI EDWARD P RILEY · 2003 to 2026
$13.1M
Causes of Variability in Craniofacial DiseaseR01DE020884 · NIDCR · UNIVERSITY OF TEXAS AT AUSTIN · PI EBERHART, JOHANN K · 2010 to 2019
$3.4M
Gene/environment interactions underlying Fetal Alcohol Spectrum Disorder.F31AA020731 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI MCCARTHY, NEIL · 2011 to 2012
$63k
NIAAA NIH HHS F31 AA020731NIAAA NIH HHS U24 AA014811NIDCR NIH HHS R01 DE020884
6 · The paper itself

Abstract

The neurocranium generates most of the craniofacial skeleton and consists of prechordal and postchordal regions. Although development of the prechordal is well studied, little is known of the postchordal region. Here we characterize a signaling hierarchy necessary for postchordal neurocranial development involving Fibroblast growth factor (Fgf) signaling for early specification of mesodermally-derived progenitor cells. The expression of hyaluron synthetase 2 (has2) in the cephalic mesoderm requires Fgf signaling and Has2 function, in turn, is required for postchordal neurocranial development. While Hedgehog (Hh)-deficient embryos also lack a postchordal neurocranium, this appears primarily due to a later defect in chondrocyte differentiation. Inhibitor studies demonstrate that postchordal neurocranial development requires early Fgf and later Hh signaling. Collectively, our results provide a mechanistic understanding of early postchordal neurocranial development and demonstrate a hierarchy of signaling between Fgf and Hh in the development of this structure.

Indexed as

Signal TransductionAnimalsCell DifferentiationFibroblast Growth Factor 3Fibroblast Growth FactorsGene Expression Regulation, DevelopmentalGlucuronosyltransferaseHedgehog ProteinsHyaluronan SynthasesMesodermSkullZebrafishZebrafish Proteinsfgf3 protein, zebrafishfgf8a protein, zebrafishFibroblast Growth Factor 3Fibroblast Growth FactorsGlucuronosyltransferasehas2 protein, zebrafishHedgehog ProteinsHyaluronan SynthasesShha protein, zebrafishZebrafish ProteinsCraniofacial developmentFgfHead mesodermShhZebrafish

Identifiers

PMID27060628
PMCPMC4967541
OpenAlexW2330073603

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.