Loading...
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...
Na minha lista:
| Udgivet i: | J Dent Res |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2020
|
| Fag: | |
| Online adgang: | 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|