Paternal Expression of a Novel Imprinted Gene, Peg12/Frat3, in the Mouse 7C Region Homologous to the Prader–Willi Syndrome Region

This publication has 24 references indexed in Scilit:

• Molecular Cloning and Characterization of FRAT2, Encoding a Positive Regulator of the WNT Signaling Pathway
  Biochemical and Biophysical Research Communications, 2001
• A GSK3‐binding peptide from FRAT1 selectively inhibits the GSK3‐catalysed phosphorylation of Axin and β‐catenin
  FEBS Letters, 1999
• MECHANISMS OF WNT SIGNALING IN DEVELOPMENT
  Annual Review of Cell and Developmental Biology, 1998
• A mouse model for Prader-Willi syndrome imprinting-centre mutations
  Nature Genetics, 1998
• Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse
  Nucleic Acids Research, 1997
• Social Interaction and Sensorimotor Gating Abnormalities in Mice Lacking Dvl1
  Cell, 1997
• Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
  Nature Genetics, 1996
• Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
  Nature Genetics, 1995
• A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression
  Nature Genetics, 1992
• Completion of mouse embryogenesis requires both the maternal and paternal genomes
  Cell, 1984