The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL–BFM 2000 protocol can be separated from FBXW7 loss of functio...

por Kox, C, Zimmermann, M, Stanulla, M, Leible, S, Schrappe, M, Ludwig, W-D, Koehler, R, Tolle, G, Bandapalli, O R, Breit, S, Muckenthaler, M U, Kulozik, A E
Publicado 2010

P08-03. Genetic complexity of TRIM5 and APOBEC in East Africa

por Walsh, AM, Perret, K, Koehler, R, Moqueet, N, Bautista, C, Eller, L, Eller, M, Kibuuka, H, Hoelscher, M, Maboko, L, Wabwire-Mangen, F, Robb, ML, Michael, NL, McCutchan, F, Kim, J, Kijak, GH
Publicado 2009

Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients

por Wesołowska-Andersen, A, Borst, L, Dalgaard, M D, Yadav, R, Rasmussen, K K, Wehner, P S, Rasmussen, M, Ørntoft, T F, Nordentoft, I, Koehler, R, Bartram, C R, Schrappe, M, Sicheritz-Ponten, T, Gautier, L, Marquart, H, Madsen, H O, Brunak, S, Stanulla, M, Gupta, R, Schmiegelow, K
Publicado 2015

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1

por Vijayakrishnan, J, Kumar, R, Henrion, M Y R, Moorman, A V, Rachakonda, P S, Hosen, I, da Silva Filho, M I, Holroyd, A, Dobbins, S E, Koehler, R, Thomsen, H, Irving, J A, Allan, J M, Lightfoot, T, Roman, E, Kinsey, S E, Sheridan, E, Thompson, P D, Hoffmann, P, Nöthen, M M, Heilmann-Heimbach, S, Jöckel, K H, Greaves, M, Harrison, C J, Bartram, C R, Schrappe, M, Stanulla, M, Hemminki, K, Houlston, R S
Publicado 2017