The features of the follicular thyroid cancer genetic determination
          
      
    
      
    
                        
          
    
  
      
  
    
                
            Abstract
            The complex analysis of the follicular thyroid cancer (FTC) hereditary predisposition with using of genealogical, molecular methods and selection indexes is shown the FTC genetic independence; the distribution in the population and families may well be described by means of a variants polygene model with the importance role of genetic factors in determination of disease (88,8 %) and have allowed to assume the presence of interloci interactions in system of its genetic control; positive selection (Δs =0,041) of FTC and association of mutations Р12А and H449H in 2 and 6 exons of gene PPARγ with follicular structure of neoplasias.
         
              
        
                        		
                     
    
      
                  About the Authors
              
               
             S. A. Shtandel
         
        
                        V.Danilevsky Institute for Endocrine Pathology Problems National Academy of Medical Sciences of Ukraine
        
Russian Federation
    
				    
    
    
             
             V. V. Khaziev
         
        
                        V.Danilevsky Institute for Endocrine Pathology Problems National Academy of Medical Sciences of Ukraine
        
Russian Federation
    
				    
    
    
             
             M. E. Sazonov
         
        
                        V.Danilevsky Institute for Endocrine Pathology Problems National Academy of Medical Sciences of Ukraine
        
Russian Federation
    
				    
    
    
          
     
        
    
    
    
 
    
      For citations:
                                    Shtandel S.A., 
                                Khaziev V.V., 
                                Sazonov M.E.
                                              The features of the follicular thyroid cancer genetic determination.      Medical Genetics.            2020;19(6):100-102.  
                                                                                                      (In Russ.)
                                          
                                                          
    
  
  
  
  
    
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