Gene-Expression Analysis Identifies IGFBP2 Dysregulation in Dental Pulp Cells From Human Cleidocranial Dysplasia

Cleidocranial dysplasia (CCD) is an autosomal dominant disorder affecting osteoblast differentiation, chondrocyte maturation, skeletal morphogenesis, and tooth formation. Dental phenotype in CCD include over-retained primary teeth, failed eruption of permanent teeth, and supernumerary teeth. The und...

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Detalles Bibliográficos
Autores principales: Greene, Stephen L., Mamaeva, Olga, Crossman, David K., Lu, Changming, MacDougall, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974155/
https://www.ncbi.nlm.nih.gov/pubmed/29875795
http://dx.doi.org/10.3389/fgene.2018.00178

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974155/
https://www.ncbi.nlm.nih.gov/pubmed/29875795
http://dx.doi.org/10.3389/fgene.2018.00178

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