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Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1996 The human skeletal muscle glycogenin gene: cDNA, tissue expression, and chromosomal localization Barbetti, F; Rocchi, M; Bossolasco, M; Cordera, R; Sbraccia, P; Finelli, P; Consalez, Gg Articolo su rivista
1-gen-1998 Increased OB gene expression leads to elevated plasma leptin concetrations in patients with chronic primary hyperinsulinemia D'Adamo, M; Buongiorno, A; Maroccia, E; Leonetti, F; Barbetti, F; Giaccari, A; Zorretta, D; Tamburrano, G; Sbraccia, P Articolo su rivista
1-gen-1998 Expression of insulin/IGF-I hybrid receptors is increased in skeletal muscle of patients with chronic primary hyperinsulinemia Federici, M; Lauro, D; D'Adamo, M; Giovannone, B; Porzio, O; Mellozzi, M; Tamburrano, G; Sbraccia, P; Sesti, G Articolo su rivista
1-gen-2000 High insulin levels do not influence PC-1 gene expression and protein content in human muscle tissue and hepatoma cells Frittitta, L; Sbraccia, P; Costanzo, B; Tassi, V; D'Adamo, M; Spampinato, D; Ercolino, T; Purrello, F; Tamburrano, G; Vigneri, R; Trischitta, V Articolo su rivista
1-gen-2000 Insulin receptor substrate (IRS) transduction system: Distinct and overlapping signaling potential Giovannone, B; Scaldaferri, M; Federici, M; Porzio, O; Lauro, D; Fusco, A; Sbraccia, P; Borboni, P; Lauro, R; Sesti, G Articolo su rivista
1-gen-2001 Defects of the insulin receptor substrate (IRS) system in human metabolic disorders Sesti, G; Federici, M; Hribal, Ml; Lauro, D; Sbraccia, P; Lauro, R Articolo su rivista
1-ott-2001 Defects of the insulin receptor substrate (IRS) system in human metabolic disorders Sesti, G; Federici, M; Hribal, M; Lauro, D; Sbraccia, P; Lauro, R Articolo su rivista
1-gen-2002 Hyperglycemia induces pro-atherosclerotic events through O-linked-glycosylation modification of insulin signaling proteins Menghini, R; Hribal, M; Mauriello, A; Ferrelli, F; Lauro, D; Sbraccia, P; Spagnoli, Lg; Sesti, G; Lauro, R; Federici, M Articolo su rivista
1-gen-2002 Relationship between plasma free fatty acids and uncoupling protein-3 gene expression in skeletal muscle of obese subjects: in vitro evidence of a causal link Sbraccia, P; D'Adamo, M; Leonetti, F; Buongiorno, A; Silecchia, G; Basso, Ms; Tamburrano, G; Lauro, D; Federici, M; Di Daniele, N; Lauro, R Articolo su rivista
1-gen-2002 Insulin-dependent activation of endothelial nitric oxide synthase is impaired by O-linked glycosylation modification of signaling proteins in human coronary endothelial cells Federici, M; Menghini, R; Mauriello, A; Hribal, M; Ferrelli, F; Lauro, D; Sbraccia, P; Spagnoli, L; Sesti, G; Lauro, R Articolo su rivista
23-lug-2002 Insulin-dependent activation of endothelial nitric oxide synthase is impaired by O-linked glycosylation modification of signaling proteins in human coronary endothelial cells Federici, M; Menghini, R; Mauriello, A; Hribal, M; Ferrelli, F; Lauro, D; Sbraccia, P; Spagnoli, L; Sesti, G; Lauro, R Articolo su rivista
1-ago-2002 Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C Novelli, G; Muchir, A; Sangiuolo, Fc; Helbling Leclerc, A; D'Apice, Mr; Massart, C; Capon, F; Sbraccia, P; Federici, M; Lauro, R; Tudisco, C; Pallotta, R; Scarano, G; Dallapiccola, B; Merlini, L; Bonne, G Articolo su rivista
1-gen-2003 A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects Sesti, G; Cardellini, M; Marini, Ma; Frontoni, S; D'Adamo, M; Del Guerra, S; Lauro, D; De Nicolais, P; Sbraccia, P; Del Prato, S; Gambardella, S; Federici, M; Marchetti, P; Lauro, R Articolo su rivista
1-mag-2003 A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects Sesti, G; Cardellini, M; Marini, Ma; Frontoni, S; D'Adamo, M; Del Guerra, S; Lauro, D; De Nicolais, P; Sbraccia, P; Del Prato, S; Gambardella, S; Federici, M; Marchetti, P; Lauro, R Articolo su rivista
1-mag-2003 A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects Sesti, G; Cardellini, M; Marini, Ma; Frontoni, S; D'Adamo, M; Del Guerra, S; Lauro, D; De Nicolais, P; Sbraccia, P; Del Prato, S; Gambardella, S; Federici, M; Marchetti, P; Lauro, R Articolo su rivista
1-mag-2003 A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects Sesti, G; Cardellini, M; Marini, Ma; Frontoni, S; D'Adamo, M; Del Guerra, S; Lauro, D; De Nicolais, P; Sbraccia, P; Del Prato, S; Gambardella, S; Federici, M; Marchetti, P; Lauro, R Articolo su rivista
1-gen-2004 Gene expression profiling of fibroblasts from a human progeroid disease mandibuloacral dysplasia, MAD #248370 through cDNA microarrays Amati, F; Biancolella, M; D'Apice, Mr; Gambardella, S; Mango, R; Sbraccia, P; D'Adamo, M; Margiotti, K; Nardone, A; Lewis, M; Novelli, G Articolo su rivista
1-lug-2004 The -866A/A genotype in the promoter of the human uncoupling protein 2 gene is associated with insulin resistance and increased risk of type 2 diabetes D'Adamo, M; Perego, L; Cardellini, M; Marini, Ma; Frontoni, S; Andreozzi, F; Sciacqua, A; Lauro, D; Sbraccia, P; Federici, M; Paganelli, M; Pontiroli, A; Lauro, R; Perticone, F; Folli, F; Sesti, G Articolo su rivista
1-lug-2004 Obesity and anorexia as neuroendocrine disorders. Sbraccia, P; D'Adamo, M; Lauro, R Contributo in libro
1-gen-2005 Timp3 deficiency in insulin receptor-haploinsufficient mice promotes diabetes and vascular inflammation via increased TNF-alpha Federici, M; Hribal, Ml; Menghini, R; Kanno, H; Marchetti, V; Porzio, O; Sunnarborg, Sw; Rizza, S; Serino, M; Cunsolo, V; Lauro, D; Mauriello, A; Smookler, Ds; Sbraccia, P; Sesti, G; Lee, Dc; Khokha, R; Accili, ; Lauro, R Articolo su rivista
Mostrati risultati da 1 a 20 di 120
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