Specific Pathogen-Free Organisms
                             
                            
                            
                                
                            
                            
                                
                            
                            
                            
                                
                                    
                                            
	"Specific Pathogen-Free Organisms" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
	
	
		
			
			
				Animals or humans raised in the absence of a particular disease-causing virus or other microorganism. Less frequently plants are cultivated pathogen-free.
    
			
			
				
				
					
						| Descriptor ID | 
										
							D013047
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						| MeSH Number(s) | 
						
							 G06.320.676 
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						| Concept/Terms | 
						
							Specific Pathogen-Free Organisms- Specific Pathogen-Free Organisms
 - Organism, Specific Pathogen-Free
 - Organisms, Specific Pathogen-Free
 - Pathogen-Free Organism, Specific
 - Pathogen-Free Organisms, Specific
 - Specific Pathogen Free Organisms
 - Specific Pathogen-Free Organism
 - Pathogen-Free Organisms
 - Organism, Pathogen-Free
 - Organisms, Pathogen-Free
 - Pathogen Free Organisms
 - Pathogen-Free Organism
 
  
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				Below are MeSH descriptors whose meaning is more general than "Specific Pathogen-Free Organisms".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Specific Pathogen-Free Organisms".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Specific Pathogen-Free Organisms" by people in this website by year, and whether "Specific Pathogen-Free Organisms" was a major or minor topic of these publications. 
				
					
                    To see the data from this visualization as text, 
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 1996 | 0 | 1 | 1 | 
| 2001 | 0 | 1 | 1 | 
| 2004 | 0 | 2 | 2 | 
| 2007 | 0 | 2 | 2 | 
| 2011 | 0 | 1 | 1 | 
| 2013 | 0 | 2 | 2 | 
| 2019 | 0 | 1 | 1 | 
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				Below are the most recent publications written about "Specific Pathogen-Free Organisms" by people in Profiles.
						
					
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Secretory Microneme Proteins Induce T-Cell Recall Responses in Mice Chronically Infected with Toxoplasma gondii. mSphere. 2019 02 27; 4(1).
															
								 
							
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An epigenetically distinct breast cancer cell subpopulation promotes collective invasion. J Clin Invest. 2015 May; 125(5):1927-43.
															
								 
							
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Immunization with 60 kD Ro peptide produces different stages of preclinical autoimmunity in a Sjögren's syndrome model among multiple strains of inbred mice. Clin Exp Immunol. 2013 Jul; 173(1):67-75.
															
								 
							
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Evaluation of reproduction and raising offspring in a nursery-reared SPF baboon (Papio hamadryas anubis) colony. Am J Primatol. 2013 Aug; 75(8):798-806.
															
								 
							
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Efficacy of vitrectomy in improving the outcome of Bacillus cereus endophthalmitis. Retina. 2011 Sep; 31(8):1518-24.
															
								 
							
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Proteinuria of nonautoimmune origin in wild-type FVB/NJ mice. Comp Med. 2007 Jun; 57(3):255-66.
															
								 
							
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Lipoprotein e (P4) of Haemophilus influenzae: role in heme utilization and pathogenesis. Microbes Infect. 2007 Jul; 9(8):932-9.
															
								 
							
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Surface fucosylation of human cord blood cells augments binding to P-selectin and E-selectin and enhances engraftment in bone marrow. Blood. 2004 Nov 15; 104(10):3091-6.
															
								 
							
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Bacteria-induced intestinal cancer in mice with disrupted Gpx1 and Gpx2 genes. Cancer Res. 2004 Feb 01; 64(3):962-8.
															
								 
							
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Relatively normal human lymphopoiesis but rapid turnover of newly formed B cells in transplanted nonobese diabetic/SCID mice. J Immunol. 2001 Sep 15; 167(6):3033-42.