Evidence map›Paper›PMID 36724256›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Post-transcriptional regulation in cranial neural crest cells expands developmental potential.

Rachel A Keuls, Young Sun Oh, Ivanshi Patel, Ronald J Parchem

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Role of non-coding RNAs in OOncology letters · 2026
    Review
  4. Article
  5. Ectomesenchymal identity emerges via relief ofbioRxiv : the preprint server for biology · 2025
    Article
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  9. 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

4 authors at 1 institution in 1 country.

Rachel A KeulsDevelopment, Disease Models & Therapeutics Graduate Program, Baylor College of Medicine, Houston, TX 77030.
Young Sun OhStem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX 77030.
Ivanshi PatelStem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX 77030.
Ronald J ParchemDevelopment, Disease Models & Therapeutics Graduate Program, Baylor College of Medicine, Houston, TX 77030.ORCID 0000-0003-0038-2806
Baylor College of Medicine · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Suzanne AW Fuqua · 2007 to 2026
$73.9M
Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
MicroRNA regulation of neural tube closureR01HD098131 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI FINNELL, RICHARD H., PARCHEM, RONALD J · 2020 to 2024
$2.8M
Training in Precision Environmental Health SciencesT32ES027801 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI Cheryl L. Walker · 2018 to 2026
$2.8M
MicroRNA regulation of neural crest differentiationR01HD099252 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI PARCHEM, RONALD J · 2019 to 2023
$2.8M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
NCI NIH HHS P30 CA125123NCRR NIH HHS S10 RR024574NHLBI NIH HHS T32 HL092332NICHD NIH HHS R01 HD098131NICHD NIH HHS R01 HD099252NIEHS NIH HHS T32 ES027801
6 · The paper itself

Abstract

Developmental potential is progressively restricted after germ layer specification during gastrulation. However, cranial neural crest cells challenge this paradigm, as they develop from anterior ectoderm, yet give rise to both ectodermal derivatives of the peripheral nervous system and ectomesenchymal bone and cartilage. How cranial neural crest cells differentiate into multiple lineages is poorly understood. Here, we demonstrate that cranial neural crest cells possess a transient state of increased chromatin accessibility. We profile the spatiotemporal emergence of premigratory neural crest and find evidence of lineage bias toward either a neuronal or ectomesenchymal fate, with each expressing distinct factors from earlier stages of development. We identify the miR-302 miRNA family to be highly expressed in cranial neural crest cells and genetic deletion leads to precocious specification of the ectomesenchymal lineage. Loss of

Indexed as

MicroRNAsNeural CrestCell DifferentiationChromatinGene Expression Regulation, DevelopmentalRNA Processing, Post-TranscriptionalChromatinMicroRNAschromatin accessibilitymicroRNAsmultipotencypluripotencysingle-cell

Identifiers

PMID36724256
PMCPMC9963983
OpenAlexW4318765072

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.