FIGURE
            Fig. S10
- ID
 - ZDB-FIG-080922-16
 - Publication
 - Tobin et al., 2008 - Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome
 - Other Figures
 - All Figure Page
 - Back to All Figure Page
 
                
                    
                        Fig. S10
                    
                    
                
                
            
        
        
    
        
            
            
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 Effect of cyclopamine treatment on early NCC migration. (A) Adding cyclopamine at 4 hpf causes no defect in CNCC migration at 19 hpf shown by Sox10:eGFP expression. (B) At 30 hpf, the embryos show morphological signs of Shh pathway inhibition, but CNCCs have still migrated into the head, showing that Shh signaling is not important for initial migration of cells but is critical for patterning.  | 
    
                
                    
                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
    | Gene: | |
|---|---|
| Fish: | |
| Condition: | |
| Anatomical Term: | |
| Stage: | 20-25 somites | 
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ Proc. Natl. Acad. Sci. USA