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Results: 1-9 |
Results: 9

Authors: De Vita, G
Citation: G. De Vita, Learning styles, culture and inclusive instruction in the multicultural classroom: A business and management perspective, INNOV EDUC, 38(2), 2001, pp. 165-174

Authors: Melillo, RM Carlomagno, F De Vita, G Formisano, P Vecchio, G Fusco, A Billaud, M Santoro, M
Citation: Rm. Melillo et al., The insulin receptor substrate (IRS)-1 recruits phosphatidylinositol 3-kinase to Ret: evidence for a competition between Shc and IRS-1 for the binding to Ret, ONCOGENE, 20(2), 2001, pp. 209-218

Authors: Villone, G De Vita, G Chieffi, P Picascia, A Stanzione, R Santoro, M Fusco, A Tramontano, D
Citation: G. Villone et al., Association between the expression of E1A oncogene and increased sensitivity to growth inhibition induced by sustained levels of cAMP in rat thyroid cells, EUR J ENDOC, 142(3), 2000, pp. 286-293

Authors: De Vita, G Melillo, RM Carlomagno, F Visconti, R Castellone, MD Bellacosa, A Billaud, M Fusco, A Tsichlis, PN Santoro, M
Citation: G. De Vita et al., Tyrosine 1062 of RET-MEN2A mediates activation of Akt (protein kinase B) and mitogen-activated protein kinase pathways leading to PC12 cell survival, CANCER RES, 60(14), 2000, pp. 3727-3731

Authors: De Vita, G Berlingieri, MT Visconti, R Castellone, MD Viglietto, G Baldassarre, G Zannini, M Bellacosa, A Tsichlis, PN Fusco, A Santoro, M
Citation: G. De Vita et al., Akt/protein kinase B promotes survival and hormone-independent proliferation of thyroid cells in the absence of dedifferentiating and transforming effects, CANCER RES, 60(14), 2000, pp. 3916-3920

Authors: Geneste, O Bidaud, C De Vita, G Hofstra, RMW Tartare-Deckert, S Buys, CHCM Lenoir, GM Santoro, M Billaud, M
Citation: O. Geneste et al., Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effecters to a multifunctional docking site, HUM MOL GEN, 8(11), 1999, pp. 1989-1999

Authors: Santoro, M Melillo, RM Carlomagno, F Visconti, R De Vita, G Salvatore, G Fusco, A Vecchio, G
Citation: M. Santoro et al., Different mutations of the RET gene cause different human tumoral diseases, BIOCHIMIE, 81(4), 1999, pp. 397-402

Authors: Chappuis-Flament, S Pasini, A De Vita, G Segouffin-Cariou, C Fusco, A Attie, T Lenoir, GM Santoro, M Billaud, M
Citation: S. Chappuis-flament et al., Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines, ONCOGENE, 17(22), 1998, pp. 2851-2861

Authors: Pasini, A Chappuis-Flament, S Geneste, O Fournier, L Schuffenecker, I Michiels, FM Feunteun, J Pelet, A Lyonnet, S De Vita, G Santoro, M Lenoir, GM Giraud, S Billaud, M
Citation: A. Pasini et al., RET, hereditary cancers and congenital malformation: A deregulation model of a tyrosine kinase receptor in human pathology, EUROCANCER 98, 1998, pp. 95-96
Risultati: 1-9 |