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FXR1 gene

Known as: FRAGILE X-RELATED PROTEIN 1, FXR1, FMR1 autosomal homolog 1 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
FMR1 targets distinct mRNA sequence elements to regulate protein expression
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism in males and premature… Expand
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Highly Cited
2009
Highly Cited
2009
The FXG: A Presynaptic Fragile X Granule Expressed in a Subset of Developing Brain Circuits
The loss of Fragile X mental retardation protein (FMRP) causes Fragile X syndrome, the most common inherited mental retardation… Expand
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Highly Cited
2005
Highly Cited
2005
Fragile X-related Protein FXR1P Regulates Proinflammatory Cytokine Tumor Necrosis Factor Expression at the Post-transcriptional Level*
Tumor necrosis factor (TNF) is regulated post-transcriptionally by the AU-rich element (ARE) within the 3′-untranslated region of… Expand
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Highly Cited
2001
Highly Cited
2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
The absence of the fragile X mental retardation protein (FMRP), encoded by the FMR1 gene, is responsible for pathologic… Expand
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Review
2001
Review
2001
The Fragile X mental retardation protein
The clinical features of the Fragile X mental retardation syndrome are linked to the absence of the set of protein isoforms… Expand
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Highly Cited
1999
Highly Cited
1999
Isolation of an FMRP-Associated Messenger Ribonucleoprotein Particle and Identification of Nucleolin and the Fragile X-Related Proteins as Components of the Complex
ABSTRACT The loss of FMR1 expression due to trinucleotide repeat expansion leads to fragile X syndrome, a cause of mental… Expand
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Highly Cited
1999
Highly Cited
1999
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.
Fragile X syndrome is caused by the absence of the fragile X mental retardation protein (FMRP). FMRP and its structural… Expand
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Highly Cited
1997
Highly Cited
1997
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis.
Lack of expression of the fragile X mental retardation protein (FMRP) results in mental retardation and macroorchidism, seen as… Expand
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Highly Cited
1995
Highly Cited
1995
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.
Fragile X Mental Retardation Syndrome is the most common form of hereditary mental retardation, and is caused by defects in the… Expand
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Highly Cited
1995
Highly Cited
1995
FXR1, an autosomal homolog of the fragile X mental retardation gene.
Fragile X mental retardation syndrome, the most common cause of hereditary mental retardation, is directly associated with the… Expand
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