PUBLICATION
            Short body length phenotype is compensated by the upregulation of nidogen family members in a deleterious nid1a mutation of zebrafish
- Authors
- Zhu, P., Ma, Z., Guo, L., Zhang, W., Zhang, Q., Zhao, T., Jiang, K., Peng, J., Chen, J.
- ID
- ZDB-PUB-171126-1
- Date
- 2017
- Source
- Journal of genetics and genomics = Yi chuan xue bao 44(11): 553-556 (Journal)
- Registered Authors
- Chen, Jun, Peng, Jinrong, Zhao, Ting
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Zebrafish Proteins/deficiency*
- Zebrafish Proteins/genetics
- Phenotype*
- Up-Regulation*
- Sequence Deletion*
- Zebrafish/anatomy & histology*
- Zebrafish/genetics
- Animals
- Membrane Glycoproteins/deficiency*
- Membrane Glycoproteins/genetics
- Calcium-Binding Proteins/deficiency*
- Calcium-Binding Proteins/genetics
- Body Size/genetics*
 
- PubMed
- 29169924 Full text @ J. Genet. Genomics
            Citation
        
        
            Zhu, P., Ma, Z., Guo, L., Zhang, W., Zhang, Q., Zhao, T., Jiang, K., Peng, J., Chen, J. (2017) Short body length phenotype is compensated by the upregulation of nidogen family members in a deleterious nid1a mutation of zebrafish. Journal of genetics and genomics = Yi chuan xue bao. 44(11):553-556.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    