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Mostrati risultati da 8.209 a 8.228 di 13.257
Data di pubblicazione Titolo Autore(i) Tipo File
1-ott-1998 Mutation of the mismatch repair gene hMSH2 and hMSH6 in a human T-cell leukemia line tolerant to methylating agents Levati, L; Marra, G; Lettieri, T; D'Atri, S; Vernole, P; Tentori, L; Lacal, P; Pagani, E; Bonmassar, E; Jiricny, J; Graziani, G Articolo su rivista
1-mag-2013 Mutational analysis of gastrointestinal stromal tumors (GISTs): procedural approach for diagnostic purposes Palmirotta, R; De Marchis, M; Ludovici, G; Leone, B; Covello, R; Conti, S; Costarelli, L; DELLA MORTE, D; Ferroni, P; Roselli, M; Guadagni, F Articolo su rivista
1-gen-2010 Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome Woellner, C; Gertz, E; Schäffer, A; Lagos, M; Perro, M; Glocker, E; Pietrogrande, M; Cossu, F; Franco, J; Matamoros, N; Pietrucha, B; Heropolitańska-Pliszka, E; Yeganeh, M; Moin, M; Español, T; Ehl, S; Gennery, A; Abinun, M; Breborowicz, A; Niehues, T; Kilic, S; Junker, A; Turvey, S; Plebani, A; Sánchez, B; Garty, B; Pignata, C; Cancrini, C; Litzman, J; Sanal, O; Baumann, U; Bacchetta, R; Hsu, A; Davis, J; Hammarström, L; Davies, E; Eren, E; Arkwright, P; Moilanen, J; Viemann, D; Khan, S; Maródi, L; Cant, A; Freeman, A; Puck, J; Holland, S; Grimbacher, B Articolo su rivista
1-feb-2012 Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 Montenegro, G; Rebelo, A; Connell, J; Allison, R; Babalini, C; D'Aloia, M; Montieri, P; Schüle, R; Ishiura, H; Price, J; Strickland, A; Gonzalez, M; Baumbach Reardon, L; Deconinck, T; Huang, J; Bernardi, G; Vance, J; Rogers, M; Tsuji, S; De Jonghe, P; Pericak Vance, M; Schöls, L; Orlacchio, A; Reid, E; Züchner, S Articolo su rivista
1-ott-2001 Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease Nicolaou, M; Song, Y; Sato, C; Orlacchio, A; Kawarai, T; Medeiros, H; Liang, Y; Sorbi, S; Richard, E; Rogaev, E; Moliaka, Y; Bruni, A; Jorge, R; Percy, M; Duara, R; Farrer, L; St Georg Hyslop, P; Rogaeva, E Articolo su rivista
1-gen-2014 Mutations of human DNA topoisomerase I at poly(ADP-ribose) binding sites: modulation of camptothecin activity by ADP-ribose polymers. Tesauro, C; Graziani, G; Arnò, B; Zuccaro, L; Muzi, A; D'Annessa, I; Santori, E; Tentori, L; Leonetti, C; Fiorani, P; Desideri, A Articolo su rivista
1-gen-2014 Mutations of human DNA topoisomerase I at poly(ADP-ribose) binding sites: modulation of camptothecin activity by ADP-ribose polymers. Tesauro, C; Graziani, G; Arnò, B; Zuccaro, L; Muzi, A; D'Annessa, I; Santori, E; Tentori, L; Leonetti, C; Fiorani, P; Desideri, A Articolo su rivista
1-gen-2001 Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancer Lucci-Cordisco, E; Rovella, V; Carrara, S; Percesepe, A; Pedroni, M; Bellacosa, A; Caluseriu, O; Forasarig, M; Anti, M; Neri, G; Ponz de Leon, M; Viel, A; Genuardi, M Articolo su rivista
1-dic-2004 Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia Sinibaldi, L; De Luca, A; Bellacchio, E; Conti, E; Pasini, A; Paloscia, C; Spalletta, G; Caltagirone, C; Pizzuti, A; Dallapiccola, B Articolo su rivista
1-gen-2006 Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamopituitary-gonadal axis in mice and humans Kelberman, D; Rizzoti, K; Avilion, A; Bitner Glindzicz, M; Cianfarani, S; Collins, J; Kling Chong, W; Kirk, J; Achermann, J; Ross, R; Carmignac, D; Lovell, B; R. Robinson I. C. A., F; Dattani, Mt Articolo su rivista
1-gen-2014 La mutualità nel caregiving: una revisione della letteratura Simeone, S; Savini, S; Torino, F; Vellone, E; Alvaro, R Articolo su rivista
1-gen-2020 Myasthenia Gravis Associated With SARS-CoV-2 Infection Restivo, D; Centonze, D; Alesina, A; Marchese-Ragona, R Articolo su rivista
1-gen-2012 Mycobacterium avium subsp. paratuberculosis in an Italian cohort of type 1 diabetes pediatric patients MANCA BITTI, Ml; Masala, S; Capasso, F; Rapini, N; Piccinini, S; Angelini, F; Pierantozzi, A; Lidano, R; Pietrosanti, S; Paccagnini, D; Sechi, L Articolo su rivista
1-gen-2019 Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters Iannetta, M; Savinelli, S; Rossi, R; Mascia, C; Marocco, R; Vita, S; Zuccala, P; Zingaropoli, Ma; Mengoni, F; Massetti, Ap; Falciano, M; D'Ettorre, G; Ciardi, Mr; Mastroianni, Cm; Vullo, V; Lichtner, M Articolo su rivista
1-gen-2016 Myeloid dendritic cells are decreased in peripheral blood of Alzheimer's disease patients in association with disease progression and severity of depressive symptoms Ciaramella, A; Salani, F; Bizzoni, F; Orfei, M; Caltagirone, C; Spalletta, G; Bossu, P Articolo su rivista
1-gen-2015 Myeloid dendritic cells are potential players in human neurodegenerative diseases Bossu, P; Spalletta, G; Caltagirone, C; Ciaramella, A Articolo su rivista
1-gen-2016 MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients Fiorillo, C; Astrea, G; Savarese, M; Cassandrini, D; Brisca, G; Trucco, F; Pedemonte, M; Trovato, R; Ruggiero, L; Vercelli, L; D'Amico, A; Tasca, G; Pane, M; Fanin, M; Bello, L; Broda, P; Musumeci, O; Rodolico, C; Messina, S; Vita, Gl; Sframeli, M; Gibertini, S; Morandi, L; Mora, M; Maggi, L; Petrucci, A; Massa, R; Grandis, M; Toscano, A; Pegoraro, E; Mercuri, E; Bertini, E; Mongini, T; Santoro, L; Nigro, V; Minetti, C; Santorelli, Fm; Bruno, C Articolo su rivista
1-gen-2021 Myocardial metastasis of tongue cancer: a rare localization Carbonaro, M; Russo, G; Mezi, S; Mancuso, G; Paravati, V; Barilla', F; Gaudio, C; Pannarale, G; Torromeo, C Articolo su rivista
1-gen-2021 Myocardial perfusion imaging in patients with unprotected left main disease Nudi, F; Nudi, A; Neri, G; Procaccini, E; Schillaci, O; Versaci, F; Frati, G; Biondi-Zoccai, G Articolo su rivista
1-gen-2013 Myocardial revascularization with drug-eluting coronary artery stents: the clinical impact of technological progress - Tesi di dottorato
Mostrati risultati da 8.209 a 8.228 di 13.257
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