Evidence map›Paper›PMID 33741714›Full record

ArticleDevelopment (Cambridge, England)2021

The alx3 gene shapes the zebrafish neurocranium by regulating frontonasal neural crest cell differentiation timing.

Jennyfer M Mitchell, Juliana Sucharov, Anthony T Pulvino, Elliott P Brooks, Austin E Gillen, James T Nichols

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Craniofacial developmental biology in the single-cell era.Development (Cambridge, England) · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Distinct and redundant roles for zebrafishFrontiers in endocrinology · 2022
    Article
  18. Frontiers in cell and developmental biology · 2022
    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

6 authors at 1 institution in 1 country.

Jennyfer M MitchellDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Juliana SucharovDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Anthony T PulvinoDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Elliott P BrooksDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Austin E GillenRNA Bioscience Initiative, Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
James T NicholsDepartment of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
University of Colorado Anschutz Medical Campus · US

Funding

Cell Fate Choices in the SkeletonR00DE024190 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI NICHOLS, JAMES TUCKER · 2017 to 2019
$887k
Mechanisms underlying the incomplete penetrance of craniofacial anomaliesR56DE027955 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI NICHOLS, JAMES TUCKER · 2019 to 2019
$363k
Using Zebrafish as an in vivo Model for Frontonasal Development and DiseaseF32DE029995 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI MITCHELL, JENNYFER MORA · 2020 to 2022
$227k
NIDCR NIH HHS F32 DE029995NIDCR NIH HHS R00 DE024190NIDCR NIH HHS R56 DE027955
6 · The paper itself

Abstract

During craniofacial development, different populations of cartilage- and bone-forming cells develop in precise locations in the head. Most of these cells are derived from pluripotent cranial neural crest cells and differentiate with distinct developmental timing and cellular morphologies. The mechanisms that divide neural crest cells into discrete populations are not fully understood. Here, we use single-cell RNA sequencing to transcriptomically define different populations of cranial neural crest cells. We discovered that the gene family encoding the Alx transcription factors is enriched in the frontonasal population of neural crest cells. Genetic mutant analyses indicate that alx3 functions to regulate the distinct differentiation timing and cellular morphologies among frontonasal neural crest cell subpopulations. This study furthers our understanding of how genes controlling developmental timing shape craniofacial skeletal elements.

Indexed as

AnimalsCartilageCell DifferentiationGene Expression Regulation, DevelopmentalHeadHomeodomain ProteinsMice, TransgenicMorphogenesisNeural CrestOrganogenesisSkullTranscription FactorsTranscriptomeZebrafishZebrafish ProteinsHomeodomain ProteinsTranscription FactorsZebrafish ProteinsAlxBoneCartilageCraniofacial skeletonDifferentiationNeural crest cellsNeurocraniumscRNA-seqZebrafish

Identifiers

PMID33741714
PMCPMC8077506
OpenAlexW3137345948

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.