Evidence map›Paper›PMID 31702881›Full record

ReviewWiley interdisciplinary reviews. Systems biology and medicine2020

Network architecture and regulatory logic in neural crest development.

Austin S Hovland, Megan Rothstein, Marcos Simoes-Costa

Open access · greenAbstract readReview
In one paragraph

Review in Wiley interdisciplinary reviews. Systems biology and medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Core microRNAs regulate neural crest delamination and condensation in the developing trigeminal ganglion.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
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  9. The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Article
  10. Article
  11. Influencers in the Somatosensory System: Extrinsic Control of Sensory Neuron Phenotypes.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2023
    Review
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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.

Austin S HovlandDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York.ORCID 0000-0002-7590-734X
Megan RothsteinDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York.
Marcos Simoes-CostaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York.ORCID 0000-0003-1452-7068
Cornell University · US

Funding

Genomic control of neural crest identity by signaling systemsR01DE028576 · NIDCR · CORNELL UNIVERSITY · PI SIMOES-COSTA, MARCOS · 2019 to 2023
$1.9M
Research and Career Training in Vertebrate Developmental GenomicsT32HD057854 · NICHD · CORNELL UNIVERSITY · PI SCHIMENTI, JOHN C · 2010 to 2020
$1.3M
Integrating signaling and transcriptional control in neural crest specificationR00DE024232 · NIDCR · CORNELL UNIVERSITY · PI SIMOES-COSTA, MARCOS · 2017 to 2019
$747k
NICHD NIH HHS T32 HD057854NIDCR NIH HHS R00 DE024232NIDCR NIH HHS R01 DE028576
6 · The paper itself

Abstract

The neural crest is an ectodermal cell population that gives rise to over 30 cell types during vertebrate embryogenesis. These stem cells are formed at the border of the developing central nervous system and undergo extensive migration before differentiating into components of multiple tissues and organs. Neural crest formation and differentiation is a multistep process, as these cells transition through sequential regulatory states before adopting their adult phenotype. Such changes are governed by a complex gene regulatory network (GRN) that integrates environmental and cell-intrinsic inputs to regulate cell identity. Studies of neural crest cells in a variety of vertebrate models have elucidated the function and regulation of dozens of the molecular players that are part of this network. The neural crest GRN has served as a platform to explore the molecular control of multipotency, cell differentiation, and the evolution of vertebrates. In this review, we employ this genetic program as a stepping-stone to explore the architecture and the regulatory principles of developmental GRNs. We also discuss how modern genomic approaches can further expand our understanding of genetic networks in this system and others. This article is categorized under: Physiology > Mammalian Physiology in Health and Disease Biological Mechanisms > Cell Fates Developmental Biology > Lineages Models of Systems Properties and Processes > Cellular Models.

Indexed as

Gene Regulatory NetworksAnimalsBiological EvolutionCell DifferentiationCell MovementEpithelial-Mesenchymal TransitionGene Expression Regulation, DevelopmentalNeural CrestSignal Transductioncell differentiationcircuitsgene regulatory networkneural crest cellsstem cells

Identifiers

PMID31702881
PMCPMC7236752
OpenAlexW2983007830

What OpenQuestion holds

Textmetadata
LicenceTDM
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.