FIGURE
            Fig. 1
- ID
- ZDB-FIG-090224-46
- Publication
- Dowling et al., 2009 - Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy
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                        Fig. 1
                    
                    
                
                
            
        
        
    
        
            
            
| Abnormal morphology in myotubularin morphant embryos. (A) Live embryos at 24 hpf injected with either control (CTL) or myotubularin (MTM) morpholinos. MTM morphants are of equivalent size, but are bent or U-shaped in appearance. (B) Live embryos at 72 hpf injected with control (CTL MO) or myotubularin (MTM MO) morpholinos. MTM morphants are mildly dysmorphic in appearance, and display selective thinning of the muscle compartment (brackets) as well as foreshortening of their tails. | 
                
                    
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                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
  
    | Fish: | |
|---|---|
| Knockdown Reagent: | |
| Observed In: | |
| Stage Range: | Prim-5 to Protruding-mouth | 
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ PLoS Genet.
                
                
            
        
        
    
    
     
        