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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...
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| Publicado no: | J Dent Res |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2020
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| Assuntos: | |
| Acesso em linha: | 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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