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FXR2 gene

Known as: FXR2, FRAGILE X MENTAL RETARDATION, AUTOSOMAL HOMOLOG 2, FRAGILE X-RELATED PROTEIN 2 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Comparative Behavioral Phenotypes of Fmr1 KO, Fxr2 Het, and Fmr1 KO/Fxr2 Het Mice
Fragile X syndrome (FXS) is caused by silencing of the FMR1 gene leading to loss of the protein product fragile X mental… 
Review
2018
Review
2018
Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins
The fragile X mental retardation protein (FMRP) has an important role in neural development. Functional loss of FMRP in humans… 
2009
2009
Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons
2009
2009
Delayed Development of Dendritic Spines in Fxr2 Knockout Mouse
Fragile X syndrome, the most common form of inherited mental retardation is caused by silencing of the Fmr1 (fragile x mental… 
2007
2007
Zebrafish as a Model to study Human Disease: Functional Studies of the FXR Proteins
textabstractThe FMR1 protein, FMRP, has been extensively studied due to its involvement in the fragile X syndrome, which is… 
2006
2006
NF-Y, AP2, Nrf1 and Sp1 regulate the fragile X-related gene 2 (FXR2).
Fragile X syndrome, the most common heritable form of mental retardation, is caused by silencing of the FMR1 (fragile X mental… 
2005
2005
Construction and Transformation of Yeast Two-hybrid System “Bait” of FXR2
Objective Fragile X syndrome is a form of hereditary mental retardation, usually results from lack of expression of the FMR1 gene… 
Review
2002
Review
2002
Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets
Fragile X syndrome (FraX) is one of the most prevalent genetic causes of mental retardation. FraX is associated with an unstable… 
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