MicroRNA-193b-3p acts as a tumor suppressor by targeting the MYB oncogene in T-cell acute lymphoblastic leukemia von Mets, E, Van der Meulen, J, Van Peer, G, Boice, M, Mestdagh, P, Van de Walle, I, Lammens, T, Goossens, S, De Moerloose, B, Benoit, Y, Van Roy, N, Clappier, E, Poppe, B, Vandesompele, J, Wendel, H-G, Taghon, T, Rondou, P, Soulier, J, Van Vlierberghe, P, Speleman, F

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Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food aller... von Asai, Yuka, Eslami, Aida, van Ginkel, C. Dorien, Akhabir, Loubna, Wan, Ming, Ellis, George, Ben-Shoshan, Moshe, Martino, David, Ferreira, Manuel A., Allen, Katrina, Mazer, Bruce, de Groot, Hans, de Jong, Nicolette W., Gerth van Wijk, Roy N., Dubois, Anthony E.J., Chin, Rick, Cheuk, Stephen, Hoffman, Joshua, Jorgensen, Eric, Witte, John S., Melles, Ronald B., Hong, Xiumei, Wang, Xiaobin, Hui, Jennie, Musk, Arthur W. (Bill), Hunter, Michael, James, Alan L., Koppelman, Gerard H., Sandford, Andrew J., Clarke, Ann E., Daley, Denise

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Characterization of the genome-wide TLX1 binding profile in T-cell acute lymphoblastic leukemia von Durinck, K, Van Loocke, W, Van der Meulen, J, Van de Walle, I, Ongenaert, M, Rondou, P, Wallaert, A, de Bock, C E, Van Roy, N, Poppe, B, Cools, J, Soulier, J, Taghon, T, Speleman, F, Van Vlierberghe, P

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A Water Soluble Pd2L4 Cage for Selective Binding of Neu5Ac von Schaapkens, Xander, Sluis, Roy N., Bobylev, Eduard O., Reek, Joost N. H., Mooibroek, Tiddo J.

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MYCN c-MYC-induced microRNAs repress coding gene networks associated with poor outcome in MYCN c-MYC-activated tumors von Mestdagh, P, Fredlund, E, Pattyn, F, Schulte, J H, Muth, D, Vermeulen, J, Kumps, C, Schlierf, S, De Preter, K, Van Roy, N, Noguera, R, Laureys, G, Schramm, A, Eggert, A, Westermann, F, Speleman, F, Vandesompele, J

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Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas von Fieuw, Annelies, Kumps, Candy, Schramm, Alexander, Pattyn, Filip, Menten, Björn, Antonacci, Francesca, Sudmant, Peter, Schulte, Johannes H., Van Roy, N, Vergult, Sarah, Buckley, Patrick G., De Paepe, A, Noguera, Rosa, Versteeg, Rogier, Stallings, Raymond, Eggert, Angelika, Vandesompele, Jo, De Preter, K, Speleman, Frank

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A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias von SPELEMAN, F, CAUWELIER, B, BOOGAERTS, M, DE MOERLOOSE, B, BENOIT, Y, SELLESLAG, D, BILLIET, J, ROBERT, A, HUGUET, F, VANDENBERGHE, P, DE PAEPE, A, MARYNEN, P, DASTUGUE, N, HAGEMEIJER, A, COOLS, J, VERHASSELT, B, POPPE, B, VAN ROY, N, VANDESOMPELE, J, GRAUX, C, UYTTEBROECK, A

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Mutation analysis of P73 and TP53 in Merkel cell carcinoma von Gele, M Van, Kaghad, M, Leonard, J H, Roy, N Van, Naeyaert, J M, Geerts, M L, Belle, S Van, Cocquyt, V, Bridge, J, Sciot, R, Wolf-Peeters, C De, Paepe, A De, Caput, D, Speleman, F

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Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis von Vandesompele, Jo, Verschueren, Kristin, Savarirayan, Ravi, Costa, Teresa, Huylebroeck, Danny, Mortier, Geert R, Willaert, Andy, Preobrazhenska, Olena, Janssens, Katrien, Vermeulen, Stefan J T, Naeyaert, Jean-Marie, Hul, Wim Van, Coucke, Paul J, Paepe, Anne De, Menten, Bjorn, Hellemans, Jan, Debeer, Philippe, Verdonk, Peter C M, Vanhoenacker, Filip, Speleman, Frank, Roy, Nadine Van

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Differential impact of drugs on the outcome of ETV6-RUNX1 positive childhood B-cell precursor acute lymphoblastic leukaemia: results of the EORTC CLG 58881 and 58951 trials von Piette, C, Suciu, S, Clappier, E, Bertrand, Y, Drunat, S, Girard, S, Yakouben, K, Plat, G, Dastugue, N, Mazingue, F, Grardel, N, van Roy, N, Uyttebroeck, A, Costa, V, Minckes, O, Sirvent, N, Simon, P, Lutz, P, Ferster, A, Pluchart, C, Poirée, M, Freycon, C, Dresse, M-F, Millot, F, Chantrain, C, van der Werff ten Bosch, J, Norga, K, Gilotay, C, Rohrlich, P-S, Benoit, Y, Cavé, H

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Influence of segmental chromosome abnormalities on survival in children over the age of 12 months with unresectable localised peripheral neuroblastic tumours without MYCN amplifica... von Defferrari, R, Mazzocco, K, Ambros, I M, Ambros, P F, Bedwell, C, Beiske, K, Bénard, J, Berbegall, A P, Bown, N, Combaret, V, Couturier, J, Erminio, G, Gambini, C, Garaventa, A, Gross, N, Haupt, R, Kohler, J, Jeison, M, Lunec, J, Marques, B, Martinsson, T, Noguera, R, Parodi, S, Schleiermacher, G, Tweddle, D A, Valent, A, Van Roy, N, Vicha, A, Villamon, E, Tonini, G P

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Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/disseminated neuroblastoma (a SIOPEN collaborative stud... von Schleiermacher, G, Michon, J, Ribeiro, A, Pierron, G, Mosseri, V, Rubie, H, Munzer, C, Bénard, J, Auger, N, Combaret, V, Janoueix-Lerosey, I, Pearson, A, Tweddle, D A, Bown, N, Gerrard, M, Wheeler, K, Noguera, R, Villamon, E, Cañete, A, Castel, V, Marques, B, de Lacerda, A, Tonini, G P, Mazzocco, K, Defferrari, R, de Bernardi, B, di Cataldo, A, van Roy, N, Brichard, B, Ladenstein, R, Ambros, I, Ambros, P, Beiske, K, Delattre, O, Couturier, J

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A Water Soluble Pd 2 L 4 Cage for Selective Binding of Neu5Ac von Schaapkens, Xander, van Sluis, Roy N, Bobylev, Eduard O, Reek, Joost N H, Mooibroek, Tiddo J

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A JAK3/STAT3 passenger activation in a lapatinib-acquired resistance model of HER2-amplified breast cancer von Van Bockstal, M, Van Roy, N, Vergauwen, G, Lambein, K, Cocquyt, V, Libbrecht, L, Denys, H, Bracke, M, De Wever, O

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Demonstration of Microchimerism in pregnant sows and fetuses and putative Microchimerism involvement in the pathogenesis of congenital PRRSV infection von Karniychuk, U, Van Breedam, W, Van Roy, N, Rogel-Gaillard, C, Nauwynck, H

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Quality Assessment of Genetic Markers Used for Therapy Stratification von Ambros, I.M., Benard, J., Boavida, M., Bown, N., Caron, H., Combaret, V., Couturier, J., Darnfors, C., Delattre, O., Freeman-Edward, J., Gambini, C., Gross, N., Hattinger, C.M., Luegmayr, A., Lunec, J., Martinsson, T., Mazzocco, K., Navarro, S., Noguera, R., O’Neill, S., Pötschger, U., Rumpler, S., Speleman, F., Tonini, G.P., Valent, A., Van Roy, N., Amann, G., De Bernardi, B., Kogner, P., Ladenstein, R., Michon, J., Pearson, A.D.J., Ambros, P.F.

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Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity von CARON, H, VAN SLUIS, P, VAN ROY, N, DE KRAKER, J, SPELEMAN, F, VOUTE, P. A, WESTERVELD, A, SLATER, R, VERSTEEG, R

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Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification von Plantaz, D., Vandesompele, J., Van Roy, N., Łastowska, M., Bown, N., Combaret, V., Favrot, M.C., Delattre, O., Michon, J., Bénard, J., Hartmann, O., Nicholson, J.C., Ross, F.M., Brinkschmidt, C., Laureys, G., Caron, H., Matthay, K.K., Feuerstein, B.G., Speleman, F.

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Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRβ-HOXA rearrangement : a study of the Groupe Francophone de Cytogénétique Hématologique von CAUWELIER, B, CAVE, H, GRAGOIRE, M.-J, JONVEAUX, P, LAFAGE-POCHITALOFF, M, MOZZICCONACCI, M. J, TERRE, C, LUQUET, I, CORNILLET-LEFEBVRE, P, LAURENCE, B, PLESSIS, G, LEFEBVRE, C, GERVAIS, C, LEROUX, D, ANTOINE, H, GRAUX, C, MAUVIEUX, L, HEIMANN, P, CHALAS, C, CLAPPIER, E, VERHASSELT, B, BENOIT, Y, MOERLOOSE, B. D, LESSARD, M, POPPE, B, VAN ROY, N, KEERSMAECKER, K. D, COOLS, J, SIGAUX, F, SOULIER, J, HAGEMEIJER, A, PAEPE, A. D, DASTUGUE, N, BERGER, R, BARIN, C, SPELEMAN, F, PEROT, C, VAN DEN AKKER, J, MUGNERET, F, CHARRIN, C, PAGES, M. P

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Refined physical mapping and genomic structure of the EXTL1 gene von Wuyts, W., Spieker, N., van Roy, N., De Boulle, K., De Paepe, A., Willems, P.J., van Hul, W., Versteeg, R., Speleman, F.

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