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Mostrati risultati da 61.221 a 61.240 di 101.314
Data di pubblicazione Titolo Autore(i) Tipo File
1-mag-1993 Mutations in the 3A genomic region of two cytopathic strains of hepatitis A virus isolated in Italy Morace, G; Pisani, G; Beneduce, F; Divizia, M; Pana', A Articolo su rivista
1-gen-2017 Mutations in the 3′ untranslated region of NOTCH1 are associated with low CD20 expression levels in chronic lymphocytic leukemia Bittolo, T; Pozzo, F; Bomben, R; D'Agaro, T; Bravin, V; Bulian, P; Rossi, Fm; Zucchetto, A; Degan, M; Macor, P; D'Arena, G; Chiarenza, A; Zaja, F; Pozzato, G; Di Raimondo, F; Rossi, D; Gaidano, G; Del Poeta, G; Gattei, V; Dal Bo, M 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-gen-1992 Mutations in the insulin receptor gene in patients with genetic syndromes of insulin resistance and acanthosis nigricans Accili, D; Barbetti, F; Cama, A; Kadowaki, H; Kadowaki, T; Imano, E; Levy-Toledano, R; Taylor, Si Articolo su rivista
1-gen-1992 MUTATIONS IN THE INSULIN-RECEPTOR GENE Taylor, S; Cama, A; Accili, D; Barbetti, F; Quon, M; Sierra, M; Suzuki, Y; Koller, E; Levytoledano, R; Wertheimer, E; Moncada, V; Kadowaki, H; Kadowaki, T 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 in ZBTB20 cause Primrose syndrome Cordeddu, V; Redeker, B; Stellacci, E; Jongejan, A; Fragale, A; Bradley, T; Anselmi, M; Ciolfi, A; Cecchetti, S; Muto, V; Bernardini, L; Azage, M; Carvalho, D; Espay, A; Male, A; Molin, A; Posmyk, R; Battisti, C; Casertano, A; Melis, D; Van Kampen, A; Baas, F; Mannens, M; Bocchinfuso, G; Stella, L; Tartaglia, M; Hennekam, R Articolo su rivista
1-apr-2013 Mutations of epigenetic regulators and of the spliceosome machinery in therapy-related myeloid neoplasms and in acute leukemias evolved from chronic myeloproliferative diseases Voso, Mt; Fabiani, E; Fianchi, L; Falconi, G; Criscuolo, M; Santangelo, R; Chiusolo, P; Betti, S; D'Alo', F; Hohaus, S; De Stefano, V; Leone, G Articolo su rivista
18-dic-1998 Mutations of Gly to Ala in human glutathione transferase P1-1 affect helix 2 (G-site) and induce positive cooperativity in the binding of glutathione LO BELLO, M; Nuccetelli, M; Chiessi, E; Lahm, A; Mazzetti, A; Battistoni, A; Caccuri, Am; Oakley, A; Parker, M; Tramontano, A; Federici, G; Ricci, G 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-1999 Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] Wadey, R; Mckie, J; Papapetrou, C; Sutherland, H; Lohman, F; Osinga, J; Frohn, I; Hofstra, R; Meijers, C; Amati, F; Conti, E; Pizzuti, A; Dallapiccola, B; Novelli, G; Scambler, P Articolo su rivista
1-gen-2003 Mutations of ZFPM2/FOG2 gene in sporadic cases of Tetralogy of Fallot Pizzuti, A; Sarkozy, A; Newton, A; Conti, E; Flex, E; Digilio, M; Amati, F; Gianni, D; Tandoi, C; Marino, B; Crossley, M; Dallapiccola, B Articolo su rivista
15-nov-2006 Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages. Liebe, B; Petukhova, G; Barchi, M; Bellani, M; Braselmann, H; Nakano, T; Pandita, T; Jasin, M; Fornace, A; Meistrich, M; Baarends, W; Schimenti, J; de Lange, T; Keeney, S; Camerini Otero, R; Scherthan, H 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
25-mar-2010 Mutazioni del gene INS come causa di diabete neonatale permanente/dell’infanzia Colombo, Carlo Tesi di dottorato
1-gen-2009 Mutazioni funzionali e ibridazioni formali: un eco dall’antico Cinque, Ge; Lazzeri, E Intervento a convegno
1-mag-2018 Mutual coupling reduction using metamaterial supersubstrate for high performance & densely packed planar phased arrays Alibakhshikenari, M; Salvucci, A; Polli, G; Virdee, Bs; See, Ch; Abd-Alhameed, R; Falcone, F; Andujar, A; Anguera, J; Limiti, E Intervento a convegno
Mostrati risultati da 61.221 a 61.240 di 101.314
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