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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...
Uloženo v:
| Vydáno v: | J Dent Res |
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| Hlavní autoři: | , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2018
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| Témata: | |
| On-line přístup: | 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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