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
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism in males and premature… (More)
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2010
2010
FMR1 and FXR1 are RNA binding proteins interacting with the miRNA-induced silencing complex, RISC. Here we describe for the first… (More)
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Highly Cited
2009
Highly Cited
2009
The loss of Fragile X mental retardation protein (FMRP) causes Fragile X syndrome, the most common inherited mental retardation… (More)
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Highly Cited
2004
Highly Cited
2004
FXR1 is one of the two known homologues of FMR1. FXR1 shares a high degree of sequence homology with FMR1 and also encodes two KH… (More)
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2001
2001
Mutations in the X-linked gene FMR1 cause fragile X syndrome, the leading cause of inherited mental retardation. Two autosomal… (More)
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Review
2001
Review
2001
The clinical features of the Fragile X mental retardation syndrome are linked to the absence of the set of protein isoforms… (More)
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Highly Cited
2000
Highly Cited
2000
Fragile X syndrome is the most common inherited form of mental retardation. It is caused by loss of FMR1 gene activity due to… (More)
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1999
1999
Fragile X syndrome results from mutations in the X-linked FMR1 gene. The most common mutation is expansion and hypermethylation… (More)
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Highly Cited
1995
Highly Cited
1995
Fragile X mental retardation syndrome, the most common cause of hereditary mental retardation, is directly associated with the… (More)
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Highly Cited
1995
Highly Cited
1995
Fragile X Mental Retardation Syndrome is the most common form of hereditary mental retardation, and is caused by defects in the… (More)
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