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Mostrati risultati da 21 a 40 di 1.506
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1991 A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among caucasoids: The quantitative isoelectrophoretic variation of the Gd+ allele Modiano, G; Ciminelli, Bm; Malaspina, P; Santolamazza, P; Sedran, L; Meloni, T; Forteleoni, G; Mela, G Articolo su rivista
1-gen-2009 A gene conversion hotspot in the human growth hormone (GH1) gene promoter Wolf, A; Millar, D; Caliebe, A; Horan, M; Newsway, V; Kumpf, D; Steinmann, K; Chee, I; Lee, Y; Mutirangura, A; Pepe, G; Rickards, O; Schmidtke, J; Schempp, W; Chuzhanova, N; Kehrer Sawatzki, H; Krawczak, M; Cooper, D Articolo su rivista
1-gen-2000 A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus Terrinoni, A; Candi, E; Oddi, S; Gobello, T; Camaione, Db; Mazzanti, C; Zambruno, G; Knight, R; Melino, G Articolo su rivista
1-gen-1998 A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B Articolo su rivista
1-dic-2005 A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome Cassidy, A; van Steensel, M; Steijlen, P; van Geel, M; van der Velden, J; Morley, S; Terrinoni, A; Melino, G; Candi, E; Mclean, W Articolo su rivista
1-gen-2006 A human derived SSADH coding variant is replacing the ancestral allele shared with primates. Leone, O; Blasi, P; Palmerio, F; Kozlov, A; Malaspina, P; Novelletto, A Articolo su rivista
1-gen-2005 A large-scale study of the random variability of a coding sequence: a study on the CFTR gene Modiano, G; Bombieri, C; Ciminelli, Bm; Belpinati, F; Giorgi, S; De_georges, M; Scotet, V; Pompei, F; Ciccacci, C; Guittard, C; Audrezet, Mp; Begnini, A; Toepfer, ; M., Mmjr; Ferec, C; Claustres, M; Pignatti, Pf Articolo su rivista
1-gen-2000 A molecular approach to the study of the ancient populations of southern Italy Rickards, O; MARTINEZ-LABARGA, Mc; Castellana, G; Mallegni, F Articolo su rivista
1-gen-1998 A molecular approach to the study of the ancient populations of southern Italy Rickards, O; MARTINEZ-LABARGA, Mc; Bianco, S; Scano, G; Doro Garetto, G; Masali, M; Biondi, G Intervento a convegno
1-gen-2005 A most welcome new edition in a fast advancing field. Iodice, C Articolo su rivista
2-set-2011 A multicancer-like syndrome in a dog characterized by p53 and cell cycle-checkpoint kinase 2 (CHK2) mutations and Sirtuin gene (SIRT1) down-regulation Marfe, G; De Martino, L; Tafani, M; Irno Consalvo, M; Pasolini, M; Navas, L; Papparella, S; Gambacurta, A; P. a. c. i. e. l. l. o., O Articolo su rivista
1-gen-2001 A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area Malaspina, P; Tsopanomichalou, M; Duman, T; Stefan, M; Silvestri, A; Rinaldi, B; Garcia, O; Giparaki, M; Plata, E; Kozlov, A; Barbujani, G; Vernesi, C; Papola, F; Ciavarella, G; Kovatchev, D; Kerimova, M; Anagnou, N; Gavrila, L; Veneziano, L; Akar, N; Loutradis, A; Michalodimitrakis, E; Terrenato, L; Novelletto, A Articolo su rivista
1-gen-2000 A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus Terrinoni, A; Puddu, P; Didona, B; De Laurenzi, V; Candi, E; Smith, Fjd; Mclean, Whi; Melino, G Articolo su rivista
1-dic-2005 A neural strategy for the inference of SH3 domain-peptide interaction specificity Ferraro, E; Via, A; Ausiello, G; HELMER CITTERICH, M Articolo su rivista
1-gen-2000 A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals Bombieri, C; Giorgi, S; Carles, S; De Cid, R; Belpinati, F; Tandoi, C; Pallares Ruiz, N; Lazaro, C; Ciminelli, Bm; Romey, M; Casals, T; Pompei, F; Gandini, G; Claustres, M; Estivill, X; Pignatti, P; Modiano, G Articolo su rivista
1-gen-2012 A new clinical approach: Use of blood-derived stem cells (BDSCs) for superficial digital flexor tendon injuries in horses Marfe, G; Rotta, G; De Martino, L; Tafani, M; Fiorito, F; Di Stefano, C; Polettini, M; Ranalli, M; Russo, M; Gambacurta, A Articolo su rivista
1-gen-2008 A new T677C mutation of the aspartoacylase gene encodes for a protein with no enzymatic activity Di Pietro, V; Gambacurta, A; Amorini, A; Finocchiaro, A; D'Urso, S; Ceccarelli, L; Tavazzi, B; Giardina, B; Lazzarino, G Articolo su rivista
1-gen-1995 A novel approach to protein-protein interaction: Complex formation between the p53 tumor suppressor and the HIV Tat proteins Longo, F; Marchetti, Ma; Castagnoli, L; Battaglia, Pa; Gigliani, F Articolo su rivista
1-gen-2004 A novel recessive connexin 31 (GJB3) mutation in a case of erythrokeratodermia variabilis [2] Terrinoni, A; Leta, A; Pedicelli, C; Candi, E; Ranalli, M; Puddu, P; Paradisi, M; Angelo, C; Baggetta, G; Melino, G Articolo su rivista
1-ott-2006 A novel structure-based encoding for machine-learning applied to the inference of SH3 domain specificity Ferraro, E; Via, A; Ausiello, G; HELMER CITTERICH, M Articolo su rivista
Mostrati risultati da 21 a 40 di 1.506
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