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    Induction of cALL antigen and terminal deoxynucleotidyltransferase in normal peripheral lymphocyte during PHA stimulation.
        
        Leuk. Res. 6, 421-423 (1982)
    
    
    
				In PHA cultures of peripheral lymphocytes from three healthy donors the extent and time sequence of cALL and TdT positivity was followed over a period of seven days. In all cases significant percentages of cALL + and TdT + cells were observed. However, the period of positivity for both these markers tended to be short. In contrast to previous results with the diffusion chamber system which yielded a comparatively uniform pattern of positivity, PHA cultures of the present cases revealed a more heterogeneous pattern concerning the extent as well as the time sequence of positivity. These experiments provide a broader basis for the notion that those markers are expressed during blastogenesis of normal lymphocytes which are generally regarded as indicative of early lymphatic differentiation and of the stage of developmental arrest of acute lymphatic leukemias.
			
			
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
     
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        1982
    
 
     
    
        HGF-Berichtsjahr
        0
    
 
    
    
        ISSN (print) / ISBN
        0145-2126
    
 
    
        e-ISSN
        1873-5835
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Leukemia Research
    
 
		
    
        Quellenangaben
        
	    Band: 6,  
	    Heft: 3,  
	    Seiten: 421-423 
	    
	    
	
    
 
  
         
        
            Verlag
            Elsevier
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institut für Hämatologie
    
 
     
     
     
     
     	
    
    
        Scopus ID
        0019982278
    
    
        Erfassungsdatum
        1982-12-31