Cranial neural crest and the building of the vertebrate head

A gene complex controlling segmentation in Drosophila

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Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis

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Patterning the Vertebrate Neuraxis

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Does Exposure to Simulated Microgravity Affect Cranial Neural Crest-Derived Tissues in Danio rerio?

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Neural Crest Contributions to Dental Pulp Stem/Progenitor Cells and Craniofacial Structures: Alveolar Processes, Tongue and Temporomandibular Joint

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The glycine cleavage system in embryonic brain development

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Hedgehog Signaling in Palatal and Facial Development

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A pluri- és multipotencia határán: a ganglionléc őssejtjei

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From stem cells to Schwann cells

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Identificação de novas variantes causativas e investigação da heterogeneidade clínica da Síndrome aurículo-condilar

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Mapping the Shh regulatory landscape

Anderson, E. S. (2015) · ERA

Identificação de novas variantes causativas e investigação da heterogeneidade clínica da Síndrome Aurículo-Condilar Identification of novel causative variants and investigation of clinical heterogeneity of Auriculocondylar Syndrome

Luiza, V., & Tavares, R. (2016)

Characterization of SPECC1L function in cell adhesion and migration in craniofacial morphogenesis

Wilson, N. R. (2017) · KU ScholarWorks (The University of Kansas)

exploring patterns of morphological integration in the crania of papio hamadryas ursinus and homo sapiens

Hemingway, J. (2017)

Developmental abnormalities of the otic capsule and inner ear following application of prolyl‐hydroxylase inhibitors in chick embryos

Kumar, A., Davies, T. G., & Itasaki, N. (2018) · Birth Defects Research · doi:10.1002/bdr2.1375

Early Skeletal Morphogenesis in Embryonic Development

Yang, Y. (2018) · Primer on the metabolic bone diseases and disorders of mineral metabolism · doi:10.1002/9781119266594.ch1

The regulatory network of PITX1 during mouse limb and craniofacial development

Wang, J. (2017)

Retinoic acid regulates the cell migration and proliferation for facial patterning

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The Development of the Chicken Skull and the Histology of Some of its Sutures

Arnaout, B. (2020) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2020-13990

Investigação funcional do novo locus candidato, HDAC9, causativo da síndrome aurículo-condilar

Ramos, S. L. G. (2021) · doi:10.11606/d.41.2021.tde-25052021-091729

A Label-free Xenograft Model for Investigating the Behavior of Human Stem Cell Spheroids in Chick Embryos

Cordeiro, I. R., & Brito, J. M. (2021) · Journal of Visualized Experiments · doi:10.3791/63067

Kulturrelativismus und Menschenrechte

Kühne, D. (2008) · Dialnet (Universidad de la Rioja)

The Head

Morriss‐Kay, G. M. (2008) · Wiley eBooks · doi:10.1002/9780470090121.ch12

Etiology and Anatomical Variation in Treacher Collins Syndrome

Smith, F. J. (2022) · Springer eBooks · doi:10.1007/978-3-030-84733-3_13

Editorial: The Long Road to Building a Head: Smooth Travels and Accidents on the Journey From Patterning via Morphogenesis to Phenotype

Feistel, K., Hammes, A., & Sela‐Donenfeld, D. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.895497

Biological Aspects of Bone Growth and Metabolism in Orthodontics

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Development of specific phenotypes and genetic consequences in Down syndrome

Ganguly, B. B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90456-8.00002-8 · Cited by 1

Adaptive Divergence and Radiations: Insights From Evo-Devo

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Tying the knot between morphology and development: Using enamel-knot determined dental morphology to study the evolution of molarization in hoofed mammalsPreprint

Ashbaugh, A. J., Jamniczky, H. A., & Theodor, J. M. (2024) · Research Square · doi:10.21203/rs.3.rs-4504565/v1

Peripheral neuroprotective potential and toxicological profile of fascaplysin in zebrafish models

Park, K.-H., Huh, Y., Chung, H.-J., Konishi, H., Jung, J., & Jeong, N. Y. (2025) · Anatomy & Cell Biology · doi:10.5115/acb.24.290

Bones, brains, and bias—neural crest cell contribution to craniofacial structure

Carmichael, J. S., Darland, D. C., Pedersen, D. E., & Simmons, R. B. (2025) · Developmental Biology · doi:10.1016/j.ydbio.2025.05.008

Developmental Anatomy and Histology of the Scalp and Calvarium

Kılıç, K. D., Orif, S. E., Turgut, A. Ç., Çelik, S., & Uyanıkgil, Y. (2025) · Springer eBooks · doi:10.1007/978-3-031-88244-9_3 · Cited by 1

Getting a head start: Craniofacial heterochrony in marsupials involves dynamic changes to molecular and cellular mechanisms underlying neural crest developmentPreprint

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Skull Development: Normal Findings and Craniosynostosis

Tonni, G., Rosignoli, L., Grisolia, G., Peixoto, A. B., JÚNIOR, E. A., Rolo, L. C., & Sepúlveda, W. (2025) · Springer eBooks · doi:10.1007/978-3-031-96947-8_13

The E3 Ubiquitin Ligase DCAF13 Is Essential for Craniofacial Development

Liu, L., Xu, X., Huang, P., Wang, W., Lin, Y., Song, P., Cui, X., Lv, J., Wang, F., Yuman, L., et al. (2026) · genesis · doi:10.1002/dvg.70039

The Use of Organoids in Dentistry: An Overview of New Research Approaches

Wadan, A. S., El‑Sadek, M. Z., Shaaban, A. H., Abdeldayem, K. N. E., Ahmed, A. H., Ahmed, M. A., Elsonpaty, H. S. A., Tawfik, A., Nabih, M. T., Elmesalamy, N., et al. (2026) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-025-00541-7

Rôle du facteur de transcription Meis2 dans les dérivés de la crête neurale par l'étude des souris Wnt1crecKOMeis2-/- et Islet1cre/+cKOMeis2-/-

Birchenall, A. (2012) · theses.fr (ABES) · doi:10.70675/7153ac68z613fz4fc3z9a6dz8c5a651c9033

Mesenchymal potentials of the trunk neural crest cells

Aguiar, J. D. M. C. (2012) · theses.fr (ABES) · doi:10.70675/e7671849zef3bz4115zb6f4ze3803844e2a1

Rôle du Rho-GEF Trio dans la division cellulaire

Cannet, A. (2014) · theses.fr (ABES) · doi:10.70675/30d6056bz3ae0z421cz9d73z509e0090a426

Bases moléculaires et cellulaires du syndrome de Waardenburg : de la génétique à la fonction de SOX10

Chaoui, A. (2013) · theses.fr (ABES) · doi:10.70675/53d367d0z8524z49f0zb693z431c6d0f4e94

Study of Pax3 and Pax7 functions during the development of the mouse embryo

Zalc, A. (2014) · theses.fr (ABES) · doi:10.70675/1b3f0375zc09bz4e45z8c85z1e0f6985f9f2

Caractérisation phénotypique des anomalies de développement et d'homéostasie du lignage mélanocytaire de deux lignées de souris transgéniques

Reyes‐Gomez, E. (2014) · theses.fr (ABES) · doi:10.70675/80f3f21fz7fadz4cc9z9a7bz62880412d893

Rôle des cellules orales dérivées des crêtes neurales dans la morphogenèse craniofaciale

Nassif, A. (2016) · doi:10.70675/0ca05675z0116z412eza374z03e98aefb9ce

Caractérisation des nouveaux mécanismes au cour du développement normal et pathologique de la Crête Neurale : interaction entre SOX10 et p54NRB et rôle d'editing

Kavo, A. (2015) · theses.fr (ABES) · doi:10.70675/f3a38a35zd096z421ez9381z8083e0d73df9

Regulation of Mesenchymal Differentiation Potentials in the avian Neural Crest

Fonseca, B. F. (2017) · theses.fr (ABES) · doi:10.70675/5816101azc0fbz4824za8b5zf99a32792cc7

Sources alternatives de cellules souches pour la bio-ingénierie de la dent

Acuna‐Mendoza, S. (2015) · theses.fr (ABES) · doi:10.70675/f9cbcaafzdd96z4c70z9746z530850532d17

De novo myogenesis and neurogenesis during budding of the colonial ascidian, Botryllus schlosseri

Prünster, M. M. (2018) · doi:10.70675/02a6aa79z3c43z4f51z9498z306596326f97

Regulatory roots of cranial muscle diversity : developmental origins of muscular resilience

Grimaldi, A. (2020) · theses.fr (ABES) · doi:10.70675/d30bcd75z2b3dz47b1za355zb03cfbe26c48

Caractérisation d'un défaut cutanéo-muqueux et osseux chez le minipig et mise au point d'un protocole de thérapie cellulaire

Duong, L. T. (2023) · theses.fr (ABES) · doi:10.70675/5a282c32z0ad0z46e9z843dz815369bf0766

Origines développementale et évolutive de la région cervicale des tétrapodes

Sánchez-Garrido, F. (2025) · theses.fr (ABES) · doi:10.70675/afc713dczee64z48b8za364zcddc2beb5f83

Engineering craniofacial skeletal organoids from human pluripotent stem cells via neural crest cells

Motoike, S., & Ikeya, M. (2026) · Cell Biomaterials · doi:10.1016/j.celbio.2026.100442

Quantitative imaging of corneal endothelial development reveals dynamic but resilient monolayerPreprint

Ramarapu, R., Stoehr, W. R., Miesen, M., Amro, N. J., Thomasy, S. M., & Rogers, C. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.01.722310

Polycomb chromatin topology enables long-range enhancer recruitment during craniofacial development

Zouari, Y. B., Joshi, O., Salvi, A., Kessler, S., Ducret, S., Ross, F., Holwerda, S. J. B., Vilain, N., Mamilla-Sanivaram, S., Smallwood, S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73065-5

Epigenetic Remodeling of Pharyngeal Arch Derivatives: Analyzing the Impact of Maternal Microplastic Exposure on Craniofacial Morphogenesis

R, D. J. B. (2026) · International Journal for Clinical Anatomy and Research · doi:10.66715/ijcar/2026v2.i1.7686

A Modified Subcondylar Endaural Approach for Proportional Condylectomy in Condylar Hyperplasia: Clinical Report

Contreras, P. T., Barrientos-Morales, C., Steffens, E., Flores-Mancilla, M. J., & Niklander, S. E. (2026) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000012932

Trends in craniofacial organ development and regeneration: From the single-cell and spatial transcriptomics perspective

Wang, D., Zhu, X., Hu, N., Wu, B., Dong, Y., Song, Y., Li, X., Wang, Z., Huang, Z., Li, Y., et al. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102272

Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiology

Petrin, A. L., Machado‐Paula, L. A., Romanowska, J., Lie, R., Hovey, L., Doolittle, B., Awotoye, W. A., Dunlay, L., Xie, X., Zeng, E., et al. (2026) · Molecular Genetics and Genomics · doi:10.1007/s00438-026-02474-4

Co-option and innovation in neural crest evolution

Adameyko, I. I. (2026) · Science Advances · doi:10.1126/sciadv.aed9037

Embryonic and postnatal macrophages are necessary for proper tooth development and homeostasis

Lopez, M. G., Katsura, K. A., Neves, V. C. M., Soldatov, R., Lavický, J., Azam, M., Kavková, M., Cigosova, K., Temsamrit, B., Bonnardel, J., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75576-7

Tooth development, replacement and regeneration

Shan, C., Zhang, Z., Du, L., Xu, Z., & Li, Z. (2026) · Development · doi:10.1242/dev.205531

Membrane lipid metabolism as a regulatory frontier in neural crest biology: Roles for sphingolipids, cholesterol, and lipid rafts

Mancini, A. E., Jenne, M. P., & Piacentino, M. L. (2026) · Developmental Dynamics · doi:10.1002/dvdy.70182

PDGF Signaling Modulates Autophagy Following Cellular Stress in Cranial Neural Crest Cells Across Vertebrate SpeciesPreprint

Eberhart, J. K., Sun, S., Walsh, L., Ghosal, R., Tucker, S., & Zoldan, J. (2026) · Research Square · doi:10.21203/rs.3.rs-10923857/v1

Counting Your Chickens Before They Hatch: A Framework for Responsible AI Consciousness Development

Robichaud, C. (2026) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.19152942

Induction and Patterning of Neural Crest Cells in the Developing Mouse Embryo: Roles for Gcnf and Hhat

Dennis, J. F. (2008)

Molecular mechanisms of cranial neural crest cell migration and patterning in craniofacial development

Minoux, M., & Rijli, F. M. (2010) · Development · doi:10.1242/dev.040048 · Cited by 507

Neural crest: facing the facts of head development

Chambers, D. J., & McGonnell, I. M. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02733-6 · Cited by 24

Neural crest‐dependent interactions that regulate pattern and growth

Schneider, R. A. (2011) · The FASEB Journal · doi:10.1096/fasebj.25.1_supplement.299.4

Making Headway: The Roles of Hox Genes and Neural Crest Cells in Craniofacial Development

Trainor, P. A. (2003) · The Scientific World JOURNAL · doi:10.1100/tsw.2003.11 · Cited by 21

Summary

(2016)