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Mostrati risultati da 195 a 214 di 587
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2004 Evidence for a Modifier of Onset Age in Huntington’s Disease Linked to the HD Gene in 4p16. Djoussé, L; Knowlton, B; Hayden, M; Almqvist, E; Brinkman, R; Ross, C; Margolis, R; Rosenblatt, A; Durr, A; Dode, C; Morrison, P; Novelletto, A; Frontali, M; Trent, R; Mccusker, E; Gómez Tortosa, E; Cabrero, D; Jones, R; Zanko, A; Nance, M; Abramson, R; Suchowersky, O; Paulsen, J; Harrison, M; Yang, Q; Cupples, L; Gusella, J; Macdonald, M; Myers, R Articolo su rivista
1-gen-2021 Evidence of another anthropic impact on iguana delicatissima from the lesser Antilles: the presence of antibiotic resistant enterobacteria Di Lallo, G; D’Andrea, Mm; Sennati, S; Thaller, Mc; Migliore, L; Gentile, G Articolo su rivista
1-gen-2005 Evolution of human IgH3 ' EC duplicated structures: both enhancers HS1,2 are polymorphic with variation of transcription factor's consensus sites Giambra, V; Fruscalzo, A; Giufrea, M; MARTINEZ-LABARGA, Mc; Favaro, M; Rocchi, M; Frezza, D Articolo su rivista
1-gen-2022 The evolutionary history of the polyQ tract in huntingtin sheds light on its functional pro-neural activities Iennaco, R; Formenti, G; Trovesi, C; Rossi, Rl; Zuccato, C; Lischetti, T; Bocchi, Vd; Scolz, A; Martinez-Labarga, C; Rickards, O; Pacifico, M; Crottini, A; Moller, Ap; Chen, Rz; Vogt, Tf; Pavesi, G; Horner, Ds; Saino, N; Cattaneo, E Articolo su rivista
1-gen-1998 Evoluzione genetica dell’uomo Rickards, O; Biondi, G; Modiano, G Contributo in libro
1-gen-2013 Exploring the diversity of SPRY/B30.2-mediated interactions Perfetto, L; Gherardini, P; Davey, N; Diella, F; HELMER CITTERICH, M; Cesareni, G Articolo su rivista
1-mar-2016 Exposure to 915 MHz radiation induces micronuclei in Vicia faba root tips. Gustavino, B; Carboni, G; Petrillo, R; Paoluzzi, G; Santovetti, E; Rizzoni, M Articolo su rivista
1-gen-2015 FAS-ligand regulates differential activation-induced cell death of human T-helper 1 and 17 cells in healthy donors and multiple sclerosis patients Cencioni, Mt; Santini, S; Ruocco, G; Borsellino, G; De Bardi, M; Grasso, M; Ruggieri, S; Gasperini, C; Centonze, D; Barila', D; Battistini, L; Volpe, E Articolo su rivista
1-giu-2019 Fibro-adipogenic progenitors of dystrophic mice are insensitive to NOTCH regulation of adipogenesis Marinkovic, M; Fuoco, C; Sacco, F; Cerquone Perpetuini, A; Giuliani, G; Micarelli, E; Pavlidou, T; Petrilli, Ll; Reggio, A; Riccio, F; Spada, F; Vumbaca, S; Zuccotti, A; Castagnoli, L; Mann, M; Gargioli, C; Cesareni, G Articolo su rivista
25-giu-2019 Fibro-adipogenic progenitors of dystrophic mice are insensitive to NOTCH regulation of adipogenesis Marinkovic, M; Fuoco, C; Sacco, F; Perpetuini, Ac; Giuliani, G; Micarelli, E; Pavlidou, T; Petrilli, Ll; Reggio, A; Riccio, F; Spada, F; Vumbaca, S; Zuccotti, A; Castagnoli, L; Mann, M; Gargioli, C; Cesareni, G Articolo su rivista
1-gen-2008 Finally: The digital, democratic age of scientific abstracts Superti_furga, G; Wieland, F; Cesareni, G Articolo su rivista
1-gen-2010 Finding and sharing: new approaches to registries of databases and services for the biomedical sciences Smedley, D; Schofield, P; Chen, C; Aidinis, V; Ainali, C; Bard, J; Balling, R; Birney, E; Blake, A; Bongcam Rudloff, E; Brookes, A; Cesareni, G; Chandras, C; Eppig, J; Flicek, P; Gkoutos, G; Greenaway, S; Gruenberger, M; Hériché, J; Lyall, A; Mallon, A; Muddyman, D; Reisinger, F; Ringwald, M; Rosenthal, N; Schughart, K; Swertz, M; Thorisson, G; Zouberakis, M; Hancock, J Articolo su rivista
1-gen-2018 A finely resolved phylogeny of y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean Finocchio, A; Trombetta, B; Messina, F; D'Atanasio, E; Akar, N; Loutradis, A; Michalodimitrakis, Ei; Cruciani, F; Novelletto, A Articolo su rivista
1-gen-2013 Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes. Polimanti, R; Di Girolamo, M; Manfellotto, D; Fuciarelli, Mf Articolo su rivista
1-gen-1981 Further genetic heterogeneity of red cell phosphoglucomutase-1: a non electrophoretic polymorphism. Scozzari, R; Trippa, G; SANTACHIARA BENERECETTI, S; Terrenato, L; Iodice, C; Benincasa, A Articolo su rivista
1-gen-2018 GABA catabolism involvement in Alzheimer’s disease: a case-control study of SNPs in ALDH5A1 gene. Menduti, G; Benussi, L; Ghidoni, R; Squitti, R; Siotto, M; Binetti, G; Capo, C; Ciminelli, B; Malaspina, P; Rossi, L Intervento a convegno
1-gen-2022 The gene regulation knowledge commons: the action area of GREEKC Kuiper, M; Bonello, J; Fernández-Breis, Jt; Bucher, P; Futschik, Me; Gaudet, P; Kulakovskiy, Iv; Licata, L; Logie, C; Lovering, Rc; Makeev, Vj; Orchard, S; Panni, S; Perfetto, L; Sant, D; Schulz, S; Vercruysse, S; Zerbino, Dr; Lægreid, A Articolo su rivista
1-gen-2007 Genetic analysis of early holocene skeletal remains from Alaska and its implications for the settlement of the Americas Kemp, B; Malhi, R; Mcdonough, J; Bolnick, D; Eshleman, J; Rickards, O; Martinez-Labarga, C; Johnson, J; Lorenz, J; Dixon, E; Fifield, T; Heaton, T; Worl, R; Smith, D Articolo su rivista
25-set-2014 Genetic analysis of the 16 STR loci for human identification in Native Amazonian populations from Perù. Messina, F; DI CORCIA, T; Ragazzo, M; SANCHEZ MELLADO, C; Malaspina, P; Ciminelli, B; Rickards, O; Iodice, C Intervento a convegno
1-set-2023 Genetic aspects underlying the Normocalcemic and Hypercalcemic phenotypes of Primary Hyperparathyroidism Viviani, A; Colangelo, L; Ciminelli, B; Iodice, C; Novelletto, A; Sonato, C; Occhiuto, M; Cipriani, C; Diacinti, D; DE MARTINO, V; Gianni, W; Pepe, J; Minisola, S; Malaspina, P Intervento a convegno
Mostrati risultati da 195 a 214 di 587
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