Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

This publication has 30 references indexed in Scilit:

• Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation
  Experimental Cell Research, 2006
• Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)
  Brain, 2005
• Long CGG‐repeat tracts are toxic to human cells: Implications for carriers of Fragile X premutation alleles
  FEBS Letters, 2005
• Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome
  Journal of Medical Genetics, 2004
• Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome
  Cell, 2001
• Epigenetic and Genotype-specific Effects on the Stability ofde Novo Imposed Methylation Patterns in Transgenic Mice
  Journal of Biological Chemistry, 2000
• Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome
  American Journal of Human Genetics, 2000
• Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice
  Genomics, 1998
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991