FMR1 protein, human

Known as: Fragile X Mental Retardation 1 Protein, Fragile X Mental Retardation Protein 1, Protein FMR-1 
Fragile X mental retardation protein 1 (632 aa, ~71 kDa) is encoded by the human FMR1 gene. This protein plays a role in both translational… (More)
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Within the past few years, there has been a significant change in identifying and characterizing the FMR1 premutation associated… (More)
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Highly Cited
2009
Highly Cited
2009
Fragile X syndrome, a common form of inherited mental retardation, is caused by the loss of fragile X mental retardation protein… (More)
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Review
2008
Review
2008
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans and perhaps the best-understood single… (More)
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Highly Cited
2006
Highly Cited
2006
Fragile X syndrome (FXS) is a common form of mental retardation caused by the absence of functional fragile X mental retardation… (More)
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Review
2006
Review
2006
Local or dendritic protein synthesis is required for long-term functional synaptic change, such as long-term potentiation (LTP… (More)
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Highly Cited
2003
Highly Cited
2003
The Fragile X syndrome, which results from the absence of functional FMRP protein, is the most common heritable form of mental… (More)
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Highly Cited
2002
Highly Cited
2002
Lack of expression of the fragile X mental retardation protein (FMRP), due to silencing of the FMR1 gene, causes the Fragile X… (More)
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Highly Cited
2001
Highly Cited
2001
Loss of fragile X mental retardation protein (FMRP) function causes the fragile X mental retardation syndrome. FMRP harbors three… (More)
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Highly Cited
2001
Highly Cited
2001
Fragile X syndrome results from the absence of the RNA binding FMR protein. Here, mRNA was coimmunoprecipitated with the FMRP… (More)
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Highly Cited
1997
Highly Cited
1997
The fragile X syndrome results from a transcriptional silencing of the FMR1 gene and the absence of its encoded protein. FMRP is… (More)
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