Transcription, translation and fragile X syndrome

This publication has 65 references indexed in Scilit:

• X-linked premature ovarian failure: a complex disease
  Current Opinion in Genetics & Development, 2006
• Fragile X syndrome
  American Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2005
• Postadolescent Changes in Regional Cerebral Protein Synthesis: AnIn VivoStudy in theFmr1Null Mouse
  Journal of Neuroscience, 2005
• The Fragile-X Premutation: A Maturing Perspective
  American Journal of Human Genetics, 2004
• RNA-Mediated Neurodegeneration Caused by the Fragile X Premutation rCGG Repeats in Drosophila
  Neuron, 2003
• The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
  Human Molecular Genetics, 2003
• Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome
  Cell, 2001
• The fragile X mental retardation protein inhibits translation via interacting with mRNA
  Nucleic Acids Research, 2001
• Evidence that fragile X mental retardation protein is a negative regulator of translation
  Human Molecular Genetics, 2001
• FMRP Associates with Polyribosomes as an mRNP, and the I304N Mutation of Severe Fragile X Syndrome Abolishes This Association
  Molecular Cell, 1997