Mouse Dspp frameshift model of human dentinogenesis imperfecta

Non-syndromic inherited defects of tooth dentin are caused by two classes of dominant negative/gain-of-function mutations in dentin sialophosphoprotein (DSPP): 5′ mutations affecting an N-terminal targeting sequence and 3′ mutations that shift translation into the − 1 reading frame. DSPP defects cau...

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Detalles Bibliográficos
Autores principales: Liang, Tian, Hu, Yuanyuan, Zhang, Hong, Xu, Qian, Smith, Charles E., Zhang, Chuhua, Kim, Jung-Wook, Wang, Shih-Kai, Saunders, Thomas L., Lu, Yongbo, Hu, Jan C.-C., Simmer, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526674/
https://www.ncbi.nlm.nih.gov/pubmed/34667213
http://dx.doi.org/10.1038/s41598-021-00219-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526674/
https://www.ncbi.nlm.nih.gov/pubmed/34667213
http://dx.doi.org/10.1038/s41598-021-00219-4

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