A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. door Hemminki, A, Markie, D, Tomlinson, I, Avizienyte, E, Roth, S, Loukola, A, Bignell, G, Warren, W, Aminoff, M, Höglund, P, Järvinen, H, Kristo, P, Pelin, K, Ridanpää, M, Salovaara, R, Toro, T, Bodmer, W, Olschwang, S, Olsen, A, Stratton, MR, de la Chapelle, A, Aaltonen, L

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia door Piazza, R, Valletta, S, Winkelmann, N, Winkelmann, N, Redaelli, S, Spinelli, R, Pirola, A, Antolini, L, Mologni, L, Donadoni, C, Papaemmanuil, E, Schnittger, S, Kim, D, Boultwood, J, Rossi, F, Gaipa, G, De Martini, G, Di Celle, P, Jang, H, Jang, H, Fantin, V, Fantin, V, Bignell, G, Magistroni, V, Haferlach, T

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. door Piazza, R, Valletta, S, Winkelmann, N, Redaelli, S, Spinelli, R, Pirola, A, Antolini, L, Mologni, L, Donadoni, C, Papaemmanuil, E, Schnittger, S, Kim, D, Boultwood, J, Rossi, F, Gaipa, G, De Martini, G, di Celle, P, Jang, H, Fantin, V, Bignell, G, Magistroni, V, Haferlach, T, Pogliani, E, Campbell, P, Chase, A

Recurrent SETBP1 Mutations in Atypical Chronic Myeloid Leukemia Abrogate an Ubiquitination Site and Dysregulate SETBP1 Protein Levels door Gambacorti-Passerini, C, Valletta, S, Winkelmann, N, Redaelli, S, Spinelli, R, Pirola, A, Antolini, L, Mologni, L, Donadoni, C, Papaemmanuil, E, Schnittger, S, Dong-Wook, K, Boultwood, J, Rossi, F, Gaipa, G, De Martini, G, di Celle, P, Jang, H, Fantin, V, Bignell, G, Magistroni, V, Haferlach, T, Pogliani, E, Campbell, P, Chase, A