Sun et al., 2020
- Fgfr3 mutation disrupts chondrogenesis and bone ossification in zebrafish model mimicking CATSHL syndrome partially via enhanced Wnt/β-catenin signaling.
Theranostics
10:7111-7130
Full text @ Theranostics
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | axin2 | axin 2 (conductin, axil) |
| Gene | fgfr3 | fibroblast growth factor receptor 3 |
| Gene | letm1 | leucine zipper-EF-hand containing transmembrane protein 1 |
| Gene | nsd2 | nuclear receptor binding SET domain protein 2 |
| Gene | tacc3 | transforming, acidic coiled-coil containing protein 3 |