Fragile X Mental Retardation Protein
                             
                            
                            
                                
                            
                            
                                
                            
                            
                            
                                
                                    
                                            
	"Fragile X Mental Retardation Protein" 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.
	
	
		
			
			
				A RNA-binding protein that is found predominately in the CYTOPLASM. It helps regulate GENETIC TRANSLATION in NEURONS and is absent or under-expressed in FRAGILE X SYNDROME.
    
			
			
				
				
					
						| Descriptor ID | 
										
							D051860
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						| MeSH Number(s) | 
						
							 D12.776.157.725.061 D12.776.631.299 D12.776.664.962.124 
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						| Concept/Terms | 
						
							
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				Below are MeSH descriptors whose meaning is more general than "Fragile X Mental Retardation Protein".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Fragile X Mental Retardation Protein".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Fragile X Mental Retardation Protein" by people in this website by year, and whether "Fragile X Mental Retardation Protein" was a major or minor topic of these publications. 
				
					
                    To see the data from this visualization as text, 
click here. 
				 
                
		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 1995 | 0 | 1 | 1 | 
| 1997 | 0 | 1 | 1 | 
| 2002 | 0 | 2 | 2 | 
| 2003 | 0 | 1 | 1 | 
| 2004 | 0 | 2 | 2 | 
| 2005 | 1 | 1 | 2 | 
| 2006 | 1 | 0 | 1 | 
| 2007 | 2 | 2 | 4 | 
| 2008 | 2 | 2 | 4 | 
| 2009 | 3 | 0 | 3 | 
| 2010 | 2 | 3 | 5 | 
| 2011 | 5 | 2 | 7 | 
| 2012 | 0 | 3 | 3 | 
| 2013 | 0 | 3 | 3 | 
| 2014 | 1 | 1 | 2 | 
| 2015 | 2 | 2 | 4 | 
| 2016 | 3 | 2 | 5 | 
| 2017 | 0 | 3 | 3 | 
| 2018 | 1 | 0 | 1 | 
| 2019 | 4 | 0 | 4 | 
| 2020 | 0 | 1 | 1 | 
| 2021 | 5 | 5 | 10 | 
| 2022 | 2 | 5 | 7 | 
| 2023 | 3 | 3 | 6 | 
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				Below are the most recent publications written about "Fragile X Mental Retardation Protein" by people in Profiles.
						
					
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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation. Cells. 2023 09 21; 12(18).
															
								 
							
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Mortality in Women across the FMR1 CGG Repeat Range: The Neuroprotective Effect of Higher Education. Cells. 2023 08 24; 12(17).
															
								 
							
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Antisense oligonucleotide rescue of CGG expansion-dependent FMR1 mis-splicing in fragile X syndrome restores FMRP. Proc Natl Acad Sci U S A. 2023 07 04; 120(27):e2302534120.
															
								 
							
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Atypical vocal quality in women with the FMR1 premutation: an indicator of impaired sensorimotor control. Exp Brain Res. 2023 Aug; 241(8):1975-1987.
															
								 
							
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Health Effects of Sleep Quality in Premutation Carrier Mothers of Individuals With Fragile X Syndrome. Am J Intellect Dev Disabil. 2023 05 01; 128(3):254-268.
															
								 
							
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FMR1 CGG Repeats and Stress Influence Self-Reported Cognitive Functioning in Mothers. Am J Intellect Dev Disabil. 2023 01 01; 128(1):1-20.
															
								 
							
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A randomized, controlled trial of ZYN002 cannabidiol transdermal gel in children and adolescents with fragile X syndrome (CONNECT-FX). J Neurodev Disord. 2022 11 25; 14(1):56.
															
								 
							
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Mechanistic convergence across initiation sites for RAN translation in fragile X associated tremor ataxia syndrome. Hum Mol Genet. 2022 07 21; 31(14):2317-2332.
															
								 
							
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Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Mol Genet Genomic Med. 2022 08; 10(8):e2001.
															
								 
							
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Disease-Targeted Treatment Translation in Fragile X Syndrome as a Model for Neurodevelopmental Disorders. J Child Neurol. 2022 10; 37(10-11):797-812.