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 6 (2010), Issue 3 (March)

1. A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.
   Clin Chem, 56(3): 399-408. [Abstract] [Full-text]
2. Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.
   PLoS One, 5(3): e9476. [Abstract] [Full-text]
3. Dynamic Object Representations in Infants with and without Fragile X Syndrome.
   Front Hum Neurosci, 4: 12. [Abstract] [Full-text]
4. Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA.
   Hum Mol Genet, 19(7): 1314-23. [Abstract] [Full-text]
5. GSK3 influences social preference and anxiety-related behaviors during social interaction in a mouse model of fragile X syndrome and autism.
   PLoS One, 5(3): e9706. [Abstract] [Full-text]
6. The developmental roles of FMRP.
   Biochem Soc Trans, 38(2): 507-10. [Abstract] [Full-text]
7. Astrocytes prevent abnormal neuronal development in the fragile x mouse.
   J Neurosci, 30(12): 4508-14. [Abstract] [Full-text]
8. Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.
   Hum Mol Genet, 19(8): 1618-32. [Abstract] [Full-text]

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