Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta

Amelogenesis imperfecta is a congenital form of enamel hypoplasia. Although a number of genetic mutations have been reported in humans, the regulatory network of these genes remains mostly unclear. To identify signatures of biological pathways in amelogenesis imperfecta, we conducted bioinformatic a...

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Detalles Bibliográficos
Autores principales: Yoshioka, Hiroki, Wang, Yin-Ying, Suzuki, Akiko, Shayegh, Meysam, Gajera, Mona V., Zhao, Zhongming, Iwata, Junichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926528/
https://www.ncbi.nlm.nih.gov/pubmed/33672174
http://dx.doi.org/10.3390/ijms22042202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926528/
https://www.ncbi.nlm.nih.gov/pubmed/33672174
http://dx.doi.org/10.3390/ijms22042202

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