All Stories

  1. FXTAS: regional decrease of mitochondrial DNA copy number relates to clinical manifestations
  2. Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology
  3. An Integrative Study of Protein-RNA Condensates Identifies Scaffolding RNAs and Reveals Players in Fragile X-Associated Tremor/Ataxia Syndrome
  4. Paradoxical effect of baclofen on social behavior in the fragile X syndrome mouse model
  5. BC RNA mislocalization in the fragile X premutation
  6. An Integrative Study of Ribonucleoprotein Condensates Reveals a Biomarker for Fragile X-Associated Tremor/Ataxia Syndrome
  7. Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?
  8. Combination Therapy in Fragile X Syndrome; Possibilities and Pitfalls Illustrated by Targeting the mGluR5 and GABA Pathway Simultaneously
  9. Selective rescue of heightened anxiety but not gait ataxia in a premutation 90CGG mouse model of Fragile X-associated tremor/ataxia syndrome
  10. Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome
  11. Model Systems for Understanding FXPOI
  12. Mouse Models for FXTAS and the Fragile X Premutation
  13. Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency
  14. Corrigendum
  15. The quest for targeted therapy in fragile X syndrome
  16. Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS
  17. Corrigendum
  18. A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTD
  19. FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
  20. Cerebral Protein Synthesis in a Knockin Mouse Model of the Fragile X Premutation
  21. Induced expression of expanded CGG RNA causes mitochondrial dysfunctionin vivo
  22. Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome
  23. PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology
  24. Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)
  25. FBXO7 Immunoreactivity in α-Synuclein—Containing Inclusions in Parkinson Disease and Multiple System Atrophy
  26. The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapse
  27. The CGG Repeat and the FMR1 Gene
  28. The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
  29. Mouse Models of the Fragile X Premutation and the Fragile X Associated Tremor/Ataxia Syndrome
  30. Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice
  31. Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients
  32. Erratum for Ann. N. Y. Acad. Sci. 1170: 682-687
  33. Signaling Proteins that Regulate NaCL Chemotaxis Responses Modulate Longevity in C. elegans
  34. CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome
  35. Gustatory plasticity in C. elegans involves integration of negative cues and NaCl taste mediated by serotonin, dopamine, and glutamate
  36. Antagonistic sensory cues generate gustatory plasticity in Caenorhabditis elegans