Imprinted Expression of SNRPN in Human Preimplantation Embryos

This publication has 15 references indexed in Scilit:

• IGF2 is parentally imprinted in human preimplantation embryos
  Nature Genetics, 1997
• Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo
  Mechanisms of Development, 1997
• Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
  Nature Genetics, 1996
• Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms.
  Genes & Development, 1995
• Stage-Specific Induction and Regulation by Genomic Imprinting of the Mouse U2afbp-rs Gene during Preimplantation Development
  Developmental Biology, 1995
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
  Nature Genetics, 1995
• Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndrome
  Nature Genetics, 1994
• A candidate mouse model for Prader–Willi syndrome which shows an absence of Snrpn expression
  Nature Genetics, 1992
• Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
  Nature Genetics, 1992
• Tissue-specific expression and cDNA cloning of small nuclear ribonucleoprotein-associated polypeptide N.
  Proceedings of the National Academy of Sciences, 1988