Abstract Fragile X Mental Retardation Protein (FMRP) regulates activity‐dependent RNA
localization and local translation to modulate synaptic plasticity throughout the central …

Fragile X mental retardation is caused by silencing of the gene (FMR1) that encodes the
RNA-binding protein (FMRP) that influences translation in neurons. A prominent feature of …

The purpose of this chapter is to discuss the role of the fragile X mental retardation protein
(FMRP) in the spinal sensory system and the potential for use of the mouse model of fragile …

Loss of Fragile X mental retardation protein (FMRP) leads to Fragile X syndrome (FXS), the
most common form of inherited intellectual disability and autism. Although the functions of …

Alterations in sensory processing constitute prominent symptoms of fragile X syndrome;
however, little is known about how disrupted synaptic and circuit development in sensory …

Fragile X syndrome is caused by the absence of the mRNA-binding protein Fragile X mental
retardation protein (FMRP), which may play a role in activity-regulated localization and …

Studies have verified that Fragile X mental retardation protein (FMRP), an RNA‐binding
protein, plays a potential role in the pathogenesis of formalin‐and (RS)‐3, 5 …

Fragile X syndrome is the most common inherited form of cognitive deficiency in humans
and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion …

Fragile X syndrome, as well as other forms of mental retardation and autism, is associated
with altered dendritic spine number and structure. Fragile X syndrome is caused by loss-of …

Fragile X syndrome (FXS) is the most common genetic form of intellectual disability caused
by a CGG repeat expansion in the 5′‐UTR of the Fragile X mental retardation gene FMR1 …