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Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP
Fragile X mGluR MPEP audiogenic seizures open field fmr1
2015/8/3
Fragile X Syndrome is the most common form of inherited mental retardation worldwide. A Fragile X mouse model, fmr1, with a disruption in the X-linked Fmr1 gene, has three substantial deficits observe...
Multiple, short learning sessions strengthen memory formation in fragile X syndrome
Multiple short learning sessions strengthen memory formation fragile X syndrome
2014/12/30
Christine Gall, Gary Lynch and colleagues found that fragile X model mice trained in three short, repetitious episodes spaced one hour apart performed as well on memory tests as normal mice. These sam...
Establishment of a Nonradioactive Molecular Diagnosis of Fragile-X Syndrome
Lp(a) coronary artery disease dot blot analysis DIG-labeling apo(a) gene
2009/6/30
Fragile-X syndrome is a hereditary dynamic mutation disorder, predominantly caused by a large expansion of CGG trinucleotide repeats in the FMR 1 gene leading to methylation and down regulation of tra...
Measurement of Cerebral and Cerebellar Volumes in Children with Fragile X Syndrome
Brain volume Cavalieri method fragile X syndrome magnetic resonance imaging mental retardation
2009/6/19
Background and Aim: Fragile X syndrome (FXS) is a genetic disease associated with mental retardation, speech and memory deficits, developmental/learning disabilities, and, frequently, also with neurop...