Protein Arginine Methyltransferase PRMT1 Is Essential for Palatogenesis

Cleft palate is among the most common birth defects. Currently, only 30% of cases have identified genetic causes, whereas the etiology of the majority remains to be discovered. We identified a new regulator of palate development, protein arginine methyltransferase 1 (PRMT1), and demonstrated that di...

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Detalhes bibliográficos
Publicado no:J Dent Res
Main Authors: Gou, Y., Li, J., Jackson-Weaver, O., Wu, J., Zhang, T., Gupta, R., Cho, I., Ho, T.V., Chen, Y., Li, M., Richard, S., Wang, J., Chai, Y., Xu, J.
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2018
Assuntos:
Research Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6728548/
https://ncbi.nlm.nih.gov/pubmed/29986157
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034518785164
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