Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes

SHOX deficiency causes a spectrum of clinical phenotypes related to skeletal dysplasia and short stature, including Léri-Weill dyschondrosteosis, Langer mesomelic dysplasia, Turner syndrome, and idiopathic short stature. SHOX controls chondrocyte proliferation and differentiation, bone maturation, a...

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Detalles Bibliográficos
Autores principales: Hoffmann, Sandra, Roeth, Ralph, Diebold, Sabrina, Gogel, Jasmin, Hassel, David, Just, Steffen, Rappold, Gudrun A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191631/
https://www.ncbi.nlm.nih.gov/pubmed/34122528
http://dx.doi.org/10.3389/fgene.2021.688808

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191631/
https://www.ncbi.nlm.nih.gov/pubmed/34122528
http://dx.doi.org/10.3389/fgene.2021.688808

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