"Neural Crest" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The two longitudinal ridges along the PRIMITIVE STREAK appearing near the end of GASTRULATION during development of nervous system (NEURULATION). The ridges are formed by folding of NEURAL PLATE. Between the ridges is a neural groove which deepens as the fold become elevated. When the folds meet at midline, the groove becomes a closed tube, the NEURAL TUBE.
Descriptor ID |
D009432
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MeSH Number(s) |
A16.627
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Concept/Terms |
Neural Crest- Neural Crest
- Crest, Neural
- Crests, Neural
- Neural Crests
Neural Fold- Neural Fold
- Fold, Neural
- Folds, Neural
- Neural Folds
Neural Groove- Neural Groove
- Groove, Neural
- Grooves, Neural
- Neural Grooves
Neural Crest Cells- Neural Crest Cells
- Cell, Neural Crest
- Cells, Neural Crest
- Neural Crest Cell
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Below are MeSH descriptors whose meaning is more general than "Neural Crest".
Below are MeSH descriptors whose meaning is more specific than "Neural Crest".
This graph shows the total number of publications written about "Neural Crest" by people in this website by year, and whether "Neural Crest" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2011 | 1 | 0 | 1 |
2015 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neural Crest" by people in Profiles.
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MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration. J Dent Res. 2022 03; 101(3):323-330.
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POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4. Genet Med. 2020 03; 22(3):547-556.
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Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction. Am J Hum Genet. 2015 May 07; 96(5):765-74.
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FAF1, a gene that is disrupted in cleft palate and has conserved function in zebrafish. Am J Hum Genet. 2011 Feb 11; 88(2):150-61.