Showing 1 - 5 results of 5 for search 'Winkelmann, N', query time: 0.64s
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Recurrent SETBP1 mutations in atypical chronic myeloid leukemia by 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
Published 2013Journal article -
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Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J
Published 2013Journal article -
3
Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J
Published 2013Journal article -
4
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. by 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
Published 2013Journal article -
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Recurrent SETBP1 Mutations in Atypical Chronic Myeloid Leukemia Abrogate an Ubiquitination Site and Dysregulate SETBP1 Protein Levels by 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
Published 2012Conference item