Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation

This publication has 42 references indexed in Scilit:

• DNA Methylation and Replication: Implications for the “Deletion Hotspot” Region of FMR1
  Human Genetics, 2005
• Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability
  Trends in Genetics, 2005
• A study of the distributional characteristics of FMR1 transcript levels in 238 individuals
  Human Genetics, 2004
• Premature Ovarian Failure among Fragile X Premutation Carriers: Parent-of-Origin Effect?
  The American Journal of Human Genetics, 2000
• Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome
  The American Journal of Human Genetics, 2000
• Strong similarities of theFMR1 mutation in multiple tissues: Postmortem studies of a male with a full mutation and a male carrier of a premutation
  American Journal of Medical Genetics, 1999
• Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice
  Genomics, 1998
• Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation
  Biochemistry, 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
  Cell, 1991