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 4 (April)

1. A girl with fragile X premutation from sperm donation.
   Am J Med Genet A, 146(7): 888-92. [Abstract] [Full-text]
2. MeCP2-dependent repression of an imprinted miR-184 released by depolarization.
   Hum Mol Genet, 17(8): 1192-9. [Abstract] [Full-text]
3. A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys.
   Am J Med Genet A, 146(7): 803-12. [Abstract] [Full-text]
4. Expanded clinical phenotype of women with the FMR1 premutation.
   Am J Med Genet A, 146(8): 1009-16. [Abstract] [Full-text]
5. Mechanistic relationships between Drosophila fragile X mental retardation protein and metabotropic glutamate receptor A signaling.
   Mol Cell Neurosci, 37(4): 747-60. [Abstract] [Full-text]
6. Signaling noncomprehension of language: a comparison of fragile X syndrome and Down syndrome.
   Am J Ment Retard, 113(3): 214-30. [Abstract] [Full-text]
7. Perceived quality of life in mothers of children with fragile X syndrome.
   Am J Ment Retard, 113(3): 159-77. [Abstract] [Full-text]
8. Social behavior phenotypes in fragile X syndrome, autism, and the Fmr1 knockout mouse: Theoretical comment on McNaughton et al. (2008).
   Behav Neurosci, 122(2): 483-9. [Abstract] [Full-text]
9. Evidence for social anxiety and impaired social cognition in a mouse model of fragile X syndrome.
   Behav Neurosci, 122(2): 293-300. [Abstract] [Full-text]
10. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
    Neurology, 70(16): 1397-402. [Abstract] [Full-text]
11. The Fragile X Prevalence Paradox.
    J Med Genet. [Abstract] [Full-text]
12. Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara.
    Am J Hum Biol, 20(3): 259-63. [Abstract] [Full-text]
13. Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.
    Menopause. [Abstract] [Full-text]
14. Roles of calcium-stimulated adenylyl cyclase and calmodulin-dependent protein kinase IV in the regulation of FMRP by group I metabotropic glutamate receptors.
    J Neurosci, 28(17): 4385-97. [Abstract] [Full-text]
15. The substrates of memory: defects, treatments, and enhancement.
    Eur J Pharmacol, 585(1): 2-13. [Abstract] [Full-text]
16. A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotype.
    J Mol Diagn, 10(3): 272-5. [Abstract] [Full-text]
17. Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery.
    J Med Genet, 45(5): 290-7. [Abstract] [Full-text]
18. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.
    Am J Med Genet A, 146(10): 1358-67. [Abstract] [Full-text]

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