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Fragile X Mental Retardation Protein

Known as: Fragile X Mental Retardation 1 Protein, FMRP Protein, Fragile X Mental Retardation-1 Protein 
A RNA-binding protein that is found predominately in the CYTOPLASM. It helps regulate GENETIC TRANSLATION in NEURONS and is absent or under-expressed… Expand
National Institutes of Health

Papers overview

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Review
2018
Review
2018
Fragile X syndrome (FXS) is caused by the full mutation (>200 CGG repeats) in the Fragile X Mental Retardation 1 (FMR1) gene. It… Expand
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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… Expand
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Highly Cited
2006
Highly Cited
2006
Genetic deletion of fragile X mental retardation protein (FMRP) has been shown to enhance mGluR-dependent long-term depression… Expand
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Highly Cited
2004
Highly Cited
2004
Fragile X syndrome is caused by a loss of expression of the fragile X mental retardation protein (FMRP). FMRP is a selective RNA… Expand
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Highly Cited
2001
Highly Cited
2001
Fragile X syndrome is a common form of inherited mental retardation. Most fragile X patients exhibit mutations in the fragile X… Expand
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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… Expand
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Highly Cited
2001
Highly Cited
2001
Fragile X syndrome is caused by the absence of protein FMRP, the function of which is still poorly understood. Previous studies… Expand
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Highly Cited
2001
Highly Cited
2001
Fragile X syndrome is a frequent form of inherited mental retardation caused by functional loss of the fragile X mental… Expand
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Review
2000
Review
2000
Fragile-X syndrome is the most common single-gene inherited form of mental retardation. Morphological studies suggest a possible… Expand
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Highly Cited
1997
Highly Cited
1997
Local translation of proteins in distal dendrites is thought to support synaptic structural plasticity. We have previously shown… Expand
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