Evidence map›Paper›PMID 30576078›Full record

ReviewGenesis (New York, N.Y. : 2000)2019

Specification and formation of the neural crest: Perspectives on lineage segregation.

Maneeshi S Prasad, Rebekah M Charney, Martín I García-Castro

Abstract readReview
In one paragraph

Review in Genesis (New York, N.Y. : 2000), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
–field-weighted citation impact
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

58 citing papers in PubMed.

  1. Article
  2. The lipid raft-linker gene Raftlin-2 is expressed in migrating neural crest cells.Differentiation; research in biological diversity · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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
  10. Article
  11. Article
  12. Modeling of skeletal development and diseases using human pluripotent stem cells.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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.

Maneeshi S PrasadDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, California.ORCID 0000-0003-0813-4153
Rebekah M CharneyDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, California.ORCID 0000-0002-1198-8865
Martín I García-CastroDivision of Biomedical Sciences, School of Medicine, University of California, Riverside, California.ORCID 0000-0001-5128-0004

Funding

Molecular Interactions During Neural Crest FormationR01DE017914 · NIDCR · YALE UNIVERSITY · PI GARCIA-CASTRO, MARTIN I. · 2007 to 2025
$6.3M
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 F32DE027862NIDCR NIH HHS R01 DE017914NIDCR NIH HHS R01DE017914
6 · The paper itself

Abstract

The neural crest is a fascinating embryonic population unique to vertebrates that is endowed with remarkable differentiation capacity. Thought to originate from ectodermal tissue, neural crest cells generate neurons and glia of the peripheral nervous system, and melanocytes throughout the body. However, the neural crest also generates many ectomesenchymal derivatives in the cranial region, including cell types considered to be of mesodermal origin such as cartilage, bone, and adipose tissue. These ectomesenchymal derivatives play a critical role in the formation of the vertebrate head, and are thought to be a key attribute at the center of vertebrate evolution and diversity. Further, aberrant neural crest cell development and differentiation is the root cause of many human pathologies, including cancers, rare syndromes, and birth malformations. In this review, we discuss the current findings of neural crest cell ontogeny, and consider tissue, cell, and molecular contributions toward neural crest formation. We further provide current perspectives into the molecular network involved during the segregation of the neural crest lineage.

Indexed as

Cell LineageGene Expression Regulation, DevelopmentalAnimalsEpigenesis, GeneticHumansNeural CrestNeurogenesisBMPcraniofacial developmentembryonic stem cellsepigeneticFGFgene regulatory networkinductionmultipotentneural crest cellsneural plate borderspecificationWnt

Identifiers

PMID30576078
PMCPMC6570420

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.