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Genome-wide Identification of Foxf2 Target Genes in Palate Development
Cleft palate is among the most common structural birth defects in humans. Previous studies have shown that mutations in FOXF2 are associated with cleft palate in humans and mice and that Foxf2 acts in a Shh-Foxf-Fgf18-Shh molecular network controlling palatal shelf growth. In this study, we combined...
Gespeichert in:
| Veröffentlicht in: | J Dent Res |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
SAGE Publications
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7088206/ https://ncbi.nlm.nih.gov/pubmed/32040930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034520904018 |
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