Evidence map›Paper›PMID 31610145›Full record

ArticleDevelopmental biology2020

Blastula stage specification of avian neural crest.

Maneeshi S Prasad, Eileen Uribe-Querol, Jonathan Marquez, Stephanie Vadasz, Nathan Yardley, Patrick B Shelar, Rebekah M Charney, Martín I García-Castro

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. A dual role for GLI3 signaling in neural crest development.Development (Cambridge, England) · 2026
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  7. Post-transcriptional regulation in cranial neural crest cells expands developmental potential.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

8 authors at 2 institutions in 1 country.

Maneeshi S PrasadDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
Eileen Uribe-QuerolYale University, New Haven, CT, USA.
Jonathan MarquezYale University, New Haven, CT, USA.
Stephanie VadaszYale University, New Haven, CT, USA.
Nathan YardleyYale University, New Haven, CT, USA.
Patrick B ShelarDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
Rebekah M CharneyDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, USA.
Martín I García-CastroDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, USA. Electronic address: martin.garcia-castro@ucr.edu.
University of California, Riverside · USYale University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007205 · NIGMS · YALE UNIVERSITY · PI KAZMIERCZAK, BARBARA I · 1985 to 2019
$42.9M
Molecular Interactions During Neural Crest FormationR01DE017914 · NIDCR · YALE UNIVERSITY · PI GARCIA-CASTRO, MARTIN I. · 2007 to 2025
$6.3M
Specification, induction and development of the neural crest in rabbit embryosR21DE028112 · NIDCR · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI GARCIA-CASTRO, MARTIN I. · 2018 to 2019
$409k
Molecular Interactions During Neural Crest FormationR56DE017914 · NIDCR · YALE UNIVERSITY · PI GARCIA-CASTRO, MARTIN I. · 2013 to 2013
$333k
Identification of a novel regulatory program underlying the early specification of Neural Crest cellsF32DE027862 · NIDCR · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI CHARNEY, REBEKAH · 2018 to 2020
$133k
NIDCR NIH HHS F32 DE027862NIDCR NIH HHS R01 DE017914NIDCR NIH HHS R56 DE017914NIGMS NIH HHS T32 GM007205
6 · The paper itself

Abstract

Cell fate specification defines the earliest steps towards a distinct cell lineage. Neural crest, a multipotent stem cell population, is thought to be specified from the ectoderm, but its varied contributions defy canons of segregation potential and challenges its embryonic origin. Aiming to resolve this conflict, we have assayed the earliest specification of neural crest using blastula stage chick embryos. Specification assays on isolated chick epiblast explants identify an intermediate region specified towards the neural crest cell fate. Furthermore, low density culture suggests that the specification of intermediate cells towards the neural crest lineage is independent of contact mediated induction and Wnt-ligand induced signaling, but is, however, dependent on transcriptional activity of β-catenin. Finally, we have validated the regional identity of the intermediate region towards the neural crest cell fate using fate map studies. Our results suggest a model of neural crest specification within a restricted epiblast region in blastula stage chick embryos.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsbeta CateninBiomarkersBlastulaCell CommunicationCell LineageCells, CulturedChick EmbryoGerm LayersModels, BiologicalMultipotent Stem CellsNeural CrestPAX7 Transcription FactorSignal TransductionSOX9 Transcription Factorbeta CateninBiomarkersPAX7 Transcription FactorSOX9 Transcription Factor

Identifiers

PMID31610145
PMCPMC7050198
OpenAlexW2980180190

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.