Proto-Oncogene Proteins c-akt
                             
                            
                            
                                
                                    
                                            
	"Proto-Oncogene Proteins c-akt" 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.
	
	
		
			
			
				Protein-serine-threonine kinases that contain PLECKSTRIN HOMOLOGY DOMAINS and are activated by PHOSPHORYLATION in response to GROWTH FACTORS or INSULIN. They play a major role in cell metabolism, growth, and survival as a core component of SIGNAL TRANSDUCTION. Three isoforms have been described in mammalian cells.
    
			
			
				
				
					
						| Descriptor ID | 
										
							D051057
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						| MeSH Number(s) | 
						
							 D08.811.913.696.620.682.700.755 D12.776.476.565 D12.776.624.664.700.168 
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						| Concept/Terms | 
						
							Proto-Oncogene Proteins c-akt- Proto-Oncogene Proteins c-akt
 - Proto Oncogene Proteins c akt
 - c-akt, Proto-Oncogene Proteins
 - Protein Kinase B
 - Proto-Oncogene Protein RAC
 - Proto Oncogene Protein RAC
 - RAC, Proto-Oncogene Protein
 - Proto-Oncogene Protein Akt
 - Akt, Proto-Oncogene Protein
 - Proto Oncogene Protein Akt
 - Rac Protein Kinase
 - akt Proto-Oncogene Protein
 - Protein, akt Proto-Oncogene
 - Proto-Oncogene Protein, akt
 - akt Proto Oncogene Protein
 - RAC-PK Protein
 - RAC PK Protein
 - Related to A and C-Protein
 - Related to A and C Protein
 - c-akt Proto-Oncogene Protein
 - Protein, c-akt Proto-Oncogene
 - Proto-Oncogene Protein, c-akt
 - c akt Proto Oncogene Protein
 - c-akt Protein
 - Protein-Serine-Threonine Kinase (Rac)
 
  Proto-Oncogene Proteins c-akt1- Proto-Oncogene Proteins c-akt1
 - Proteins c-akt1, Proto-Oncogene
 - Proto Oncogene Proteins c akt1
 - c-akt1, Proto-Oncogene Proteins
 - AKT1 Protein Kinase
 - Rac-PK alpha Protein
 - Rac PK alpha Protein
 - alpha Protein, Rac-PK
 - Protein Kinase B alpha
 - Akt-alpha Protein
 - Akt alpha Protein
 
  Proto-Oncogene Proteins c-akt2- Proto-Oncogene Proteins c-akt2
 - Proteins c-akt2, Proto-Oncogene
 - Proto Oncogene Proteins c akt2
 - c-akt2, Proto-Oncogene Proteins
 - Protein Kinase B beta
 - Rac-PK beta Protein
 - Rac PK beta Protein
 - AKT2 Protein Kinase
 - Akt-beta Protein
 - Akt beta Protein
 
  Proto-Oncogene Proteins c-akt3- Proto-Oncogene Proteins c-akt3
 - Proteins c-akt3, Proto-Oncogene
 - Proto Oncogene Proteins c akt3
 - c-akt3, Proto-Oncogene Proteins
 - Akt-gamma Protein
 - Akt gamma Protein
 - AKT3 Protein Kinase
 - Protein Kinase B gamma
 
  
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				Below are MeSH descriptors whose meaning is more general than "Proto-Oncogene Proteins c-akt".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Proto-Oncogene Proteins c-akt".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Proto-Oncogene Proteins c-akt" by people in this website by year, and whether "Proto-Oncogene Proteins c-akt" was a major or minor topic of these publications. 
				
					
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 2011 | 0 | 1 | 1 | 
| 2017 | 1 | 0 | 1 | 
| 2021 | 1 | 0 | 1 | 
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				Below are the most recent publications written about "Proto-Oncogene Proteins c-akt" by people in Profiles.
						
					
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Hypoxia-induced CNPY2 upregulation promotes glycolysis in cervical cancer through activation of AKT pathway. Biochem Biophys Res Commun. 2021 04 30; 551:63-70.
															
								 
							
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The PI3K/AKT signaling pathway: Associations of miRNAs with dysregulated gene expression in colorectal cancer. Mol Carcinog. 2018 02; 57(2):243-261.
															
								 
							
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Diet and colorectal cancer: analysis of a candidate pathway using SNPS, haplotypes, and multi-gene assessment. Nutr Cancer. 2011 Nov; 63(8):1226-34.
															
								 
							
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Interactions between genetic polymorphisms in the apoptotic pathway and environmental factors on esophageal adenocarcinoma risk. Carcinogenesis. 2011 Apr; 32(4):502-6.