p66shc Negatively Regulates Insulin-Like Growth Factor I Signal Transduction via Inhibition of p52shc Binding to Src Homology 2 Domain-Containing Protein Tyrosine Phosphatase Substrate-1 Leading to Impaired Growth Factor Receptor-Bound Protein-2 Membrane Recruitment

Samankaltaisia teoksia

• p66(shc) Inhibits Insulin-like Growth Factor-I Signaling via Direct Binding to Src through Its Polyproline and Src Homology 2 Domains, Resulting in Impairment of Src Kinase Activation
  Tekijä: Xi, Gang, et al.
  Julkaistu: (2010)
• p66Shc Aging Protein in Control of Fibroblasts Cell Fate
  Tekijä: Mariusz R. Wieckowski, et al.
  Julkaistu: (2011-08-01)
• Hyperglycemia-Induced p66shc Inhibits Insulin-Like Growth Factor I-Dependent Cell Survival via Impairment of Src Kinase-Mediated Phosphoinositide-3 Kinase/AKT Activation in Vascular Smooth Muscle Cells
  Tekijä: Xi, Gang, et al.
  Julkaistu: (2010)
• Epidermal Growth Factor Receptor and the Adaptor Protein p52(Shc) Are Specific Substrates of T-Cell Protein Tyrosine Phosphatase
  Tekijä: Tiganis, Tony, et al.
  Julkaistu: (1998)
• Opposite effects of the p52shc/p46shc and p66shc splicing isoforms on the EGF receptor-MAP kinase-fos signalling pathway.
  Tekijä: Migliaccio, E, et al.
  Julkaistu: (1997)