Disruption of the foxe1 gene in zebrafish reveals conserved functions in development of the craniofacial skeleton and the thyroid

Introduction: Mutations in the FOXE1 gene are implicated in cleft palate and thyroid dysgenesis in humans. Methods: To investigate whether zebrafish could provide meaningful insights into the etiology of developmental defects in humans related to FOXE1, we generated a zebrafish mutant that has a dis...

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Detalles Bibliográficos
Autores principales: Raterman, Sophie T., Von Den Hoff, Johannes W., Dijkstra, Sietske, De Vriend, Cheyenne, Te Morsche, Tim, Broekman, Sanne, Zethof, Jan, De Vrieze, Erik, Wagener, Frank A. D. T. G., Metz, Juriaan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040582/
https://www.ncbi.nlm.nih.gov/pubmed/36994096
http://dx.doi.org/10.3389/fcell.2023.1143844

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