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25. Induction of tumor formation and cell transformation by polyoma middle T antigen in the absence of Src. Thomas JE; Aguzzi A; Soriano P; Wagner EF; Brugge JS Oncogene; 1993 Sep; 8(9):2521-9. PubMed ID: 7689725 [TBL] [Abstract][Full Text] [Related]
26. Shc and a novel 89-kDa component couple to the Grb2-Sos complex in fibroblast growth factor-2-stimulated cells. Klint P; Kanda S; Claesson-Welsh L J Biol Chem; 1995 Oct; 270(40):23337-44. PubMed ID: 7559490 [TBL] [Abstract][Full Text] [Related]
27. Biphasic activation of p21ras by endothelin-1 sequentially activates the ERK cascade and phosphatidylinositol 3-kinase. Foschi M; Chari S; Dunn MJ; Sorokin A EMBO J; 1997 Nov; 16(21):6439-51. PubMed ID: 9351826 [TBL] [Abstract][Full Text] [Related]
28. Direct interaction between Shc and the platelet-derived growth factor beta-receptor. Yokote K; Mori S; Hansen K; McGlade J; Pawson T; Heldin CH; Claesson-Welsh L J Biol Chem; 1994 May; 269(21):15337-43. PubMed ID: 8195171 [TBL] [Abstract][Full Text] [Related]
30. A Drosophila shc gene product is implicated in signaling by the DER receptor tyrosine kinase. Lai KM; Olivier JP; Gish GD; Henkemeyer M; McGlade J; Pawson T Mol Cell Biol; 1995 Sep; 15(9):4810-8. PubMed ID: 7651398 [TBL] [Abstract][Full Text] [Related]
31. Gi-mediated activation of the Ras/MAP kinase pathway involves a 100 kDa tyrosine-phosphorylated Grb2 SH3 binding protein, but not Src nor Shc. Kranenburg O; Verlaan I; Hordijk PL; Moolenaar WH EMBO J; 1997 Jun; 16(11):3097-105. PubMed ID: 9214627 [TBL] [Abstract][Full Text] [Related]
32. The catalytic subunit of phosphatidylinositol 3-kinase is a substrate for the activated platelet-derived growth factor receptor, but not for middle-T antigen-pp60c-src complexes. Roche S; Dhand R; Waterfield MD; Courtneidge SA Biochem J; 1994 Aug; 301 ( Pt 3)(Pt 3):703-11. PubMed ID: 7519847 [TBL] [Abstract][Full Text] [Related]
33. At the onset of transformation polyomavirus middle-T recruits shc and src to a perinuclear compartment coincident with condensation of endosomes. Zhu W; Eicher A; Leber B; Andrews DW Oncogene; 1998 Aug; 17(5):565-76. PubMed ID: 9704922 [TBL] [Abstract][Full Text] [Related]
34. Activation of the JNK pathway is essential for transformation by the Met oncogene. Rodrigues GA; Park M; Schlessinger J EMBO J; 1997 May; 16(10):2634-45. PubMed ID: 9184210 [TBL] [Abstract][Full Text] [Related]
35. Analysis of protein-protein interactions involved in the activation of the Shc/Grb-2 pathway by the ErbB-2 kinase. Ricci A; Lanfrancone L; Chiari R; Belardo G; Pertica C; Natali PG; Pelicci PG; Segatto O Oncogene; 1995 Oct; 11(8):1519-29. PubMed ID: 7478576 [TBL] [Abstract][Full Text] [Related]
36. ShcA tyrosine phosphorylation sites can replace ShcA binding in signalling by middle T-antigen. Nicholson PR; Empereur S; Glover HR; Dilworth SM EMBO J; 2001 Nov; 20(22):6337-46. PubMed ID: 11707405 [TBL] [Abstract][Full Text] [Related]
37. Tyrosine residues 239 and 240 of Shc are phosphatidylinositol 4,5-bisphosphate-dependent phosphorylation sites by c-Src. Sato K; Gotoh N; Otsuki T; Kakumoto M; Aoto M; Tokmakov AA; Shibuya M; Fukami Y Biochem Biophys Res Commun; 1997 Nov; 240(2):399-404. PubMed ID: 9388490 [TBL] [Abstract][Full Text] [Related]
38. Dynamin associates with Src-Homology Collagen (Shc) and becomes tyrosine phosphorylated in response to insulin. Baron V; Alengrin F; Van Obberghen E Endocrinology; 1998 Jun; 139(6):3034-7. PubMed ID: 9607818 [TBL] [Abstract][Full Text] [Related]
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