Src Homology 2 Domain-Containing, Transforming Protein 1
                             
                            
                            
                                
                            
                            
                                
                            
                            
                            
                                
                                    
                                            
	"Src Homology 2 Domain-Containing, Transforming Protein 1" 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.
	
	
		
			
			
				An SHC-signaling adaptor protein that transduces PHOSPHOTYROSINE-dependent signals downstream of RECEPTOR PROTEIN-TYROSINE KINASES and non-receptor tyrosine kinases. It is required for TGF-BETA-induced CELL MIGRATION; NEOLPASM INVASION; and METASTASIS of BREAST NEOPLASMS; its SH2 DOMAIN is essential for tumor survival. It also functions in signaling downstream of  ANGIOPOIETIN RECEPTOR TIE-2, regulating the migration of ENDOTHELIAL CELLS; and PHYSIOLOGIC NEOVASCULARIZATION.
    
			
			
				
				
					
						| Descriptor ID | D000071425 | 
					
						| MeSH Number(s) | D12.644.360.024.330.500 D12.776.157.057.162.500 D12.776.476.024.424.500 | 
					
						| Concept/Terms | Src Homology 2 Domain-Containing, Transforming Protein 1Src Homology 2 Domain-Containing, Transforming Protein 1Src Homology 2 Domain Containing, Transforming Protein 1ShcA ProteinSHC1 (Src Homology 2 Domain-Containing) ProteinSrc Homology 2 Domain-Containing-Transforming Protein C1Src Homology 2 Domain Containing Transforming Protein C1SHC (Src Homology 2 Domain-Containing) Transforming Protein 1SHC1 ProteinSHC-Transforming Protein 1SHC Transforming Protein 1
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				Below are MeSH descriptors whose meaning is more general than "Src Homology 2 Domain-Containing, Transforming Protein 1".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Src Homology 2 Domain-Containing, Transforming Protein 1".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Src Homology 2 Domain-Containing, Transforming Protein 1" by people in this website by year, and whether "Src Homology 2 Domain-Containing, Transforming Protein 1" was a major or minor topic of these publications. 
				
					 
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 1997 | 0 | 2 | 2 | 
| 1999 | 0 | 1 | 1 | 
| 2013 | 0 | 1 | 1 | 
| 2015 | 0 | 1 | 1 | 
| 2022 | 0 | 1 | 1 | 
| 2024 | 0 | 1 | 1 | 
| 2025 | 1 | 0 | 1 | 
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				Below are the most recent publications written about "Src Homology 2 Domain-Containing, Transforming Protein 1" by people in Profiles.
						
					
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								Prevention of hypertension-induced renal vascular dysfunction through a p66Shc-targeted mechanism. Am J Physiol Renal Physiol. 2025 May 01; 328(5):F693-F701. 
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								Exploring the Gut-Mitochondrial Axis: p66Shc Adapter Protein and Its Implications for Metabolic Disorders. Int J Mol Sci. 2024 Mar 25; 25(7). 
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								p66Shc in Cardiovascular Pathology. Cells. 2022 06 06; 11(11). 
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								Conformation-Dependent Human p52Shc Phosphorylation by Human c-Src. Biochemistry. 2015 Jun 09; 54(22):3469-82. 
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								SHetA2 interference with mortalin binding to p66shc and p53 identified using drug-conjugated magnetic microspheres. Invest New Drugs. 2014 Jun; 32(3):412-23. 
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								Protein interactions of Src homology 2 (SH2) domain-containing inositol phosphatase (SHIP): association with Shc displaces SHIP from FcgammaRIIb in B cells. J Immunol. 1999 Feb 01; 162(3):1408-14. 
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								Modulation of insulin-like growth factor actions in L6A1 myoblasts by insulin-like growth factor binding protein (IGFBP)-4 and IGFBP-5: a dual role for IGFBP-5. J Cell Physiol. 1998 Oct; 177(1):47-57. 
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								Evidence for a direct interaction between insulin receptor substrate-1 and Shc. J Biol Chem. 1997 Jul 04; 272(27):17166-70. 
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								Negative signaling in B cells causes reduced Ras activity by reducing Shc-Grb2 interactions. J Immunol. 1997 Feb 01; 158(3):1125-32.