^“A novel 160-kDa phosphotyrosine protein in insulin-treated embryonic kidney cells is a new member of the insulin receptor substrate family”. J Biol Chem272 (34): 21403–7. (Sep 1997). doi:10.1074/jbc.272.34.21403. PMID (9261155).
^“Characterization of insulin receptor substrate 4 in human embryonic kidney 293 cells”. J Biol Chem273 (17): 10726–32. (May 1998). doi:10.1074/jbc.273.17.10726. PMID (9553137).
^Karas, M; Koval A P; Zick Y; LeRoith D (May 2001). “The insulin-like growth factor I receptor-induced interaction of insulin receptor substrate-4 and Crk-II”. Endocrinology (United States) 142 (5): 1835–40. doi:10.1210/en.142.5.1835. ISSN 0013-7227. PMID (11316748).
^Koval, A P; Karas M; Zick Y; LeRoith D (Jun 1998). “Interplay of the proto-oncogene proteins CrkL and CrkII in insulin-like growth factor-I receptor-mediated signal transduction”. J. Biol. Chem. (UNITED STATES) 273 (24): 14780–7. doi:10.1074/jbc.273.24.14780. ISSN 0021-9258. PMID (9614078).
^Sano, Hiroyuki; Liu Simon C H; Lane William S; Piletz John E; Lienhard Gustav E (May 2002). “Insulin receptor substrate 4 associates with the protein IRAS”. J. Biol. Chem. (United States) 277 (22): 19439–47. doi:10.1074/jbc.M111838200. ISSN 0021-9258. PMID (11912194).
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White MF (1999). “The IRS-signalling system: a network of docking proteins that mediate insulin action.”. Mol. Cell. Biochem.182 (1–2): 3–11. doi:10.1023/A:1006806722619. PMID (9609109).
“Interplay of the proto-oncogene proteins CrkL and CrkII in insulin-like growth factor-I receptor-mediated signal transduction.”. J. Biol. Chem.273 (24): 14780–7. (1998). doi:10.1074/jbc.273.24.14780. PMID (9614078).
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“Insulin receptor substrate 4 associates with the protein IRAS.”. J. Biol. Chem.277 (22): 19439–47. (2002). doi:10.1074/jbc.M111838200. PMID (11912194).
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“Insulin receptor substrate-4 signaling in quiescent rat hepatocytes and in regenerating rat liver.”. Hepatology37 (6): 1461–9. (2003). doi:10.1053/jhep.2003.50245. PMID (12774026).
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“Tyrosine phosphoproteomics of fibroblast growth factor signaling: a role for insulin receptor substrate-4.”. J. Biol. Chem.279 (45): 46438–47. (2004). doi:10.1074/jbc.M404537200. PMID (15316024).
“Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization.”. Curr. Biol.14 (16): 1436–50. (2004). doi:10.1016/j.cub.2004.07.051. PMID (15324660).
“Protein phosphatase 4 interacts with and down-regulates insulin receptor substrate 4 following tumor necrosis factor-alpha stimulation.”. J. Biol. Chem.279 (45): 46588–94. (2004). doi:10.1074/jbc.M408067200. PMID (15331607).
“Interaction between Brk kinase and insulin receptor substrate-4.”. Oncogene24 (36): 5656–64. (2005). doi:10.1038/sj.onc.1208721. PMID (15870689).
“Role of insulin receptor substrate-4 in IGF-I-stimulated HEPG2 proliferation.”. J. Hepatol.46 (6): 1089–98. (2007). doi:10.1016/j.jhep.2007.01.031. PMID (17408801).