Increased IGF-II protein affects p57(kip2) expression in vivo and in vitro: Implications for Beckwith–Wiedemann syndrome

Gelijkaardige items

• Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
  door: Lee, M P, et al.
  Gepubliceerd in: (1997)
• Oppositely imprinted genes p57(Kip2) and Igf2 interact in a mouse model for Beckwith–Wiedemann syndrome
  door: Caspary, Tamara, et al.
  Gepubliceerd in: (1999)
• Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?
  door: Okamoto, K, et al.
  Gepubliceerd in: (1998)
• Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.
  door: O'Keefe, D, et al.
  Gepubliceerd in: (1997)
• Silencing of CDKN1C (p57(KIP2)) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome
  door: Diaz-Meyer, N, et al.
  Gepubliceerd in: (2003)