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 7 (2011), Issue 4 (April)

1. Negotiating desires and options: How mothers who carry the fragile X gene experience reproductive decisions.
   Soc Sci Med, 72(6): 992-8. [Abstract] [Full-text]
2. The neurochemical basis for the treatment of autism spectrum disorders and Fragile X Syndrome.
   Biochem Pharmacol, 81(9): 1078-86. [Abstract] [Full-text]
3. Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles.
   Nucleic Acids Res. [Abstract] [Full-text]
4. Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.
   Clin Genet. [Abstract] [Full-text]
5. Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles.
   Nucleic Acids Res. [Abstract] [Full-text]
6. Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.
   Clin Genet. [Abstract] [Full-text]
7. Autism, Alzheimer disease, and fragile X: APP, FMRP, and mGluR5 are molecular links.
   Neurology, 76(15): 1344-52. [Abstract] [Full-text]
8. Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.
   J Neurodev Disord, 3(1): 57-67. [Abstract] [Full-text]
9. Autism, Alzheimer disease, and fragile X: APP, FMRP, and mGluR5 are molecular links.
   Neurology, 76(15): 1344-52. [Abstract] [Full-text]
10. Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome.
    Psychopharmacology (Berl). [Abstract] [Full-text]
11. Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome.
    Psychopharmacology (Berl). [Abstract] [Full-text]
12. Phenotypic changes in calbindin D28K immunoreactivity in the hippocampus of Fmr1 knockout mice.
    J Comp Neurol. [Abstract] [Full-text]
13. Fragile x mental retardation protein regulates protein expression and mRNA translation of the potassium channel kv4.2.
    J Neurosci, 31(15): 5693-8. [Abstract] [Full-text]
14. Phenotypic changes in calbindin D28K immunoreactivity in the hippocampus of Fmr1 knockout mice.
    J Comp Neurol. [Abstract] [Full-text]
15. Fragile x mental retardation protein regulates protein expression and mRNA translation of the potassium channel kv4.2.
    J Neurosci, 31(15): 5693-8. [Abstract] [Full-text]
16. Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.
    Chromosome Res. [Abstract] [Full-text]
17. Behavioral phenotypes of genetic syndromes with Intellectual Disability: Comparison of adaptive profiles.
    Psychiatry Res. [Abstract] [Full-text]
18. Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning.
    Nat Med. [Abstract] [Full-text]
19. Discrimination learning and attentional set formation in a mouse model of Fragile X.
    Behav Neurosci. [Abstract] [Full-text]
20. White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonism.
    Am J Med Genet B Neuropsychiatr Genet, 156(4): 502-6. [Abstract] [Full-text]
21. Memory Profiles of Down, Williams, and Fragile X Syndromes: Implications for Reading Development.
    J Dev Behav Pediatr. [Abstract] [Full-text]
22. Diagnostic Yield of Genetic Testing in Children Diagnosed With Autism Spectrum Disorders at a Regional Referral Center.
    Clin Pediatr (Phila). [Abstract] [Full-text]
23. Early continuous inhibition of group 1 mGlu signaling partially rescues dendritic spine abnormalities in the Fmr1 knockout mouse model for fragile X syndrome.
    Psychopharmacology (Berl), 215(2): 291-300. [Abstract] [Full-text]
24. Psychiatric and Autistic Comorbidity in Fragile X Syndrome Across Ages.
    J Child Neurol. [Abstract] [Full-text]

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