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1 dapters linker for activation of T cells and growth factor receptor-bound protein 2.
2 ated whether Grb3-3, an isoform of the Grb2 (growth factor receptor-bound protein-2) adaptor molecule
4 oduct failed to bind adaptor molecules Grb2 (growth factor receptor-bound protein 2) and Crk (CT10 re
5 binding of the isolated SH2 domain of Grb2 (growth factor receptor-bound protein 2) and the isolated
6 self, insulin-like growth factor receptor 1, growth factor receptor-bound protein 2, and kinase suppr
7 eceptor type 11 and its association with the growth factor receptor-bound protein 2, as well as activ
9 as a model system, we found that endogenous growth factor receptor-bound protein 2-associated binder
11 ce of canonical protein-RTK complexes (e.g., growth factor receptor bound protein 2-ErbB1 and Src hom
14 it their oncogenic signals by binding to the growth factor receptor bound protein-2 (Grb2), which in
15 demonstrate that NS5A specifically bound to growth factor receptor-bound protein 2 (Grb2) adaptor pr
16 which paralleled the lesser association with growth factor receptor-bound protein 2 (Grb2) and phosph
17 a 1.5-Mb zero recombination interval between growth factor receptor-bound protein 2 (GRB2) and SEC14-
18 t time that phospholipase D2 (PLD2) binds to growth factor receptor-bound protein 2 (Grb2) and to the
20 we show that THEMIS and the adapter molecule growth factor receptor-bound protein 2 (GRB2) associate
21 nositol 3'-kinase activity and reduced IRS-1/growth factor receptor-bound protein 2 (GRB2) binding.
23 r (EGFR) and the cytoplasmic adaptor protein growth factor receptor-bound protein 2 (Grb2) in a cellu
30 containing peptides in extended fashion, the growth factor receptor-bound protein 2 (Grb2) SH2 domain
31 A family of NMR solution structures of the growth factor receptor-bound protein 2 (Grb2) SH2 domain
32 iously that a potent synthetic antagonist of growth factor receptor-bound protein 2 (Grb2) Src homolo
33 analyses indicate that the adaptor molecule, growth factor receptor-bound protein 2 (Grb2) that is bo
34 ond is evidenced by PLD association with the growth factor receptor-bound protein 2 (Grb2) through re
35 ment from the disordered protein Gab2 by the growth factor receptor-bound protein 2 (Grb2), a key int
37 ins including phosphatidylinositol 3-kinase, growth factor receptor-bound protein 2 (Grb2), and ITK.
38 tein downstream of kinase 1 (p62(dok); Dok), growth factor receptor-bound protein 2 (Grb2), and SH2 d
39 described here in which the adaptor protein, growth factor receptor-bound protein 2 (Grb2), controls
41 r adaptors comprised one major set including growth factor receptor-bound protein 2 (GRB2)-associated
42 d linker for the activation of T cells (LAT):growth factor receptor-bound protein 2 (Grb2):Son of Sev
43 y the recruitment by IL-4Ralpha(R576) of the growth-factor-receptor-bound protein 2 (GRB2) adaptor pr
45 ons of both IL-2-inducible T cell kinase and growth factor receptor-bound protein 2-related adaptor d
46 athway upstream small adaptor protein, Grb2 (growth factor receptor-bound protein 2), were also enric
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