Fragile X Syndrome Research Today is a free monthly online journal that collates and summarizes the latest research about Fragile X Syndrome, including details on symptoms, treatment, heritability, diagnosis.

Volume 3 (2007), Issue 1 (January)

1. An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene.
   Mol Cell Biol, 27(2): 426-37. [Abstract] [Full-text]
2. Attentional dysfunction, impulsivity, and resistance to change in a mouse model of fragile x syndrome.
   Behav Neurosci, 120(6): 1367-79. [Abstract] [Full-text]
3. A multidisciplinary approach to the management of individuals with fragile X syndrome.
   J Intellect Disabil Res, 51: 151-61. [Abstract] [Full-text]
4. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation.
   Exp Cell Res, 313(2): 244-53. [Abstract] [Full-text]
5. Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure.
   Nucleic Acids Res, 35(1): 299-306. [Abstract] [Full-text]
6. 3D pattern of brain abnormalities in Fragile X syndrome visualized using tensor-based morphometry.
   Neuroimage, 34(3): 924-38. [Abstract] [Full-text]
7. Molecular testing for Fragile X Syndrome: Lessons learned from 119,232 tests performed in a clinical laboratory.
   Genet Med, 9(1): 46-51. [Abstract] [Full-text]
8. Amygdala dysfunction in men with the fragile X premutation.
   Brain, 130: 404-16. [Abstract] [Full-text]
9. Major defects in neocortical GABAergic inhibitory circuits in mice lacking the fragile X mental retardation protein.
   Neurosci Lett, 412(3): 227-32. [Abstract] [Full-text]

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