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 4 (2008), Issue 6 (June)

1. Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene.
   Behav Neurosci, 122(3): 710-5. [Abstract] [Full-text]
2. Proteomics- and transcriptomics-based screening of differentially expressed proteins and genes in brain of Wig rat: a model for attention deficit hyperactivity disorder (ADHD) research.
   J Proteome Res, 7(6): 2471-89. [Abstract] [Full-text]
3. A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.
   Dev Cell, 14(6): 926-39. [Abstract] [Full-text]
4. Genetic aspects of female reproduction.
   Hum Reprod Update, 14(4): 293-307. [Abstract] [Full-text]
5. Contrast detection in infants with fragile X syndrome.
   Vision Res, 48(13): 1471-8. [Abstract] [Full-text]
6. Deletion 22q13.3 syndrome.
   Orphanet J Rare Dis, 3: 14. [Abstract] [Full-text]
7. The Italian External Quality Assessment scheme for fragile x syndrome: the results of a 5-year survey.
   Genet Test, 12(2): 279-88. [Abstract] [Full-text]
8. Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability.
   DNA Repair (Amst), 7(7): 1135-54. [Abstract] [Full-text]
9. A mouse model of fragile X syndrome exhibits heightened arousal and/or emotion following errors or reversal of contingencies.
   Dev Psychobiol, 50(5): 473-85. [Abstract] [Full-text]
10. Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice.
    Neurobiol Dis, 31(1): 127-32. [Abstract] [Full-text]
11. Reproductive Health of Adolescent Girls Who Carry the FMR1 Premutation: Expected Phenotype Based on Current Knowledge of Fragile X-Associated Primary Ovarian Insufficiency.
    Ann N Y Acad Sci, 1135: 99-111. [Abstract] [Full-text]
12. Role of DNA dynamics in Alzheimer's disease.
    Brain Res Rev, 58(1): 136-48. [Abstract] [Full-text]
13. Heterogeneous dysregulation of microRNAs across the autism spectrum.
    Neurogenetics, 9(3): 153-61. [Abstract] [Full-text]
14. Fragile x syndrome in Korea: a case series and a review of the literature.
    J Korean Med Sci, 23(3): 470-6. [Abstract] [Full-text]
15. S6K1 phosphorylates and regulates fragile X mental retardation protein (FMRP) with the neuronal protein synthesis-dependent mammalian target of rapamycin (mTOR) signaling cascade.
    J Biol Chem, 283(27): 18478-82. [Abstract] [Full-text]

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