FMRP Associates with Polyribosomes as an mRNP, and the I304N Mutation of Severe Fragile X Syndrome Abolishes This Association

This publication has 43 references indexed in Scilit:

• The fragile X mental retardation protein is associated with ribosomes
  Nature Genetics, 1996
• Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome
  Nature Genetics, 1995
• The KH module has an αβ fold
  FEBS Letters, 1995
• Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat
  Nature Genetics, 1993
• Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
  Nature Genetics, 1993
• A point mutation in the FMR-1 gene associated with fragile X mental retardation
  Nature Genetics, 1993
• 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
• Reversal of Creatine Kinase Translational Repression by 3′ Untranslated Sequences
  Science, 1990
• Importance of polysomal mRNA‐associated polypeptides for protein synthesis initiation in yeast
  European Journal of Biochemistry, 1988