Cellular drug resistance in childhood acute myeloid leukemia is related to chromosomal abnormalities von Zwaan, Christian M., Kaspers, Gertjan J.L., Pieters, Rob, Hählen, Karel, Huismans, Dieuwke R., Zimmermann, Martin, Harbott, Jochen, Slater, Rosalyn M., Creutzig, Ursala, Veerman, Anjo J.P.

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Detection of Genetic Prognostic Markers in Uveal Melanoma Biopsies Using Fluorescence in Situ Hybridization von NAUS, Nicole C, VERHOEVEN, Anette C. A, VAN DRUNEN, Ellen, SLATER, Rosalyn, MOOY, Cornelia M, PARIDAENS, Dion A, LUYTEN, Grégorius P. M, DE KLEIN, Annelies

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LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia von von Bergh, Anne R.M., Beverloo, H. Berna, Rombout, Paul, van Wering, Elisabeth R., van Weel, Margreet H., Beverstock, Geoffrey C., Kluin, Philip M., Slater, Rosalyn M., Schuuring, Ed

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Carcinogen-Induced Loss of Heterozygosity at the Aprt Locus in Somatic Cells of the Mouse von Susan W. P. Wijnhoven, Petra P. H. Van Sloun, Hanneke J. M. Kool, Weeda, Geert, Slater, Rosalyn, Paul H. M. Lohman, Van Zeeland, Albert A., Vrieling, Harry

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High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients von Barjesteh van Waalwijk van Doorn-Khosrovani, Sahar, Erpelinck, Claudia, van Putten, WimL.J., Valk, PeterJ.M., van der Poel-van de Luytgaarde, Sonja, Hack, Ronald, Slater, Rosalyn, Smit, ElisabethM.E., Beverloo, H. Berna, Verhoef, Gregor, Verdonck, Leo F., Ossenkoppele, Gert J., Sonneveld, Pieter, de Greef, Georgine E., Löwenberg, Bob, Delwel, Ruud

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Sensitivity to L-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+ pediatric ALL von STAMS, Wendy A. G, DEN BOER, Monique L, BEVERLOO, H. Berna, MEIJERINK, Jules P. P, STIGTER, Rolinda L, VAN WERING, Elisabeth R, JANKA-SCHAUB, Gritta E, SLATER, Rosalyn, PIETERS, Rob

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Overall and event-free survival are not improved by the use of myeloablative therapy following intensified chemotherapy in previously untreated patients with multiple myeloma: a pr... von Segeren, Christine M., Sonneveld, Pieter, van der Holt, Bronno, Vellenga, Edo, Croockewit, Alexandra J., Verhoef, Gregor E.G., Cornelissen, Jan J., Schaafsma, Martijn R., van Oers, Marinus H.J., Wijermans, Pierre W., Fibbe, Wim E., Wittebol, Shulamit, Schouten, Harry C., Kooy, Marinus van Marwijk, Biesma, Douwe H., Baars, Joke W., Slater, Rosalyn, Steijaert, Monique M.C., Buijt, Ivon, Lokhorst, Henk M.

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Allelic Loss of Chromosome 1p as a Predictor of Unfavorable Outcome in Patients with Neuroblastoma von Caron, Huib, van Sluis, Peter, de Kraker, Jan, Bökkerink, Jos, Egeler, Maarten, Laureys, Geneviève, Slater, Rosalyn, Westerveld, Andries, Voûte, P.A, Versteeg, Rogier

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Molecular cytogenetic and clinical findings inETV6/ABL1-positive leukemia von Van Limbergen, Heidi, Beverloo, H. Berna, van Drunen, Ellen, Janssens, Ann, H hlen, Karel, Poppe, Bruce, Van Roy, Nadine, Marynen, Peter, De Paepe, Anne, Slater, Rosalyn, Speleman, Frank

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21q22 balanced chromosome aberrations in therapy-related hematopoietic disorders: Report from an International Workshop von Slovak, Marilyn L., Bedell, Victoria, Popplewell, Leslie, Arber, Daniel A., Schoch, Claudia, Slater, Rosalyn

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Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13) von BEVERLOO, H. Berna, PANAGOPOULOS, Loannis, ISAKSSON, Magareth, VAN WERING, Elisabeth, VAN DRUNEN, Ellen, DE KLEIN, Annelies, JOHANSSON, Bertil, SLATER, Rosalyn

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Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization von Naus, Nicole C., van Drunen, Ellen, de Klein, Annelies, Luyten, Gregorius P.M., Paridaens, Dion A., Alers, Janneke C., Ksander, Bruce R., Beverloo, H. Berna, Slater, Rosalyn M.

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Evidence for two tumour suppressor loci on chromosomal bands 1p35–36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification von Caron, Huib, Peter, Martine, van Sluis, Peter, Speleman, Frank, de Kraker, Jan, Laureys, Geneviève, Michon, Jean, Brugières, Laurence, Voûte, P.A., Westerveld, Andries, Slater, Rosalyn, Delattre, Olivier, Versteeg, Rogier

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Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous mice von Van Sloun, Petra P. H., Wijnhoven, Susan W. P., Kool, Hanneke J. M., Slater, Rosalyn, Weeda, Geert, van Zeeland, Albert A., Lohman, Paul H. M., Vrieling, Harry

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Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification von Caron, Huib, van Sluis, Peter, van Hoeve, Melanie, de Kraker, Jan, Bras, Johannes, Slater, Rosalyn, Mannens, Marcel, Voûte, P.A, Westerveld, Andries, Versteeg, Rogier

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DMBA-induced toxic and mutagenic responses vary dramatically between NER-deficient Xpa, Xpc and Csb mice von Wijnhoven, Susan W.P., Kool, Hanneke J.M., Mullenders, Leon H.F., Slater, Rosalyn, van Zeeland, Albert A., Vrieling, Harry

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Mutation analysis of the PTEN gene in uveal melanoma cell lines von Naus, Nicole C., Zuidervaart, Wieke, Rayman, Nazik, Slater, Rosalyn, van Drunen, Ellen, Ksander, Bruce, Luyten, Gregorius P.M., Klein, Annelies

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Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma von Hermsen, Mario A. J. A., Joenje, Hans, Arwert, Fré, Welters, Marij J. P., Braakhuis, Boudewijn J. M., Bagnay, Marjan, Westerveld, Andries, Slater, Rosalyn

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Maintenance of Vascular Endothelial Cell-Specific Properties after Immortalization with an Amphotrophic Replication-Deficient Retrovirus Containing Human Papilloma Virus 16 E6/E7 D... von Fontijn, Ruud, Hop, Caroline, Brinkman, Herm-Jan, Slater, Rosalyn, Westerveld, Andries, van Mourik, Jan A., Pannekoek, Hans

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Characterization of mRAD18Sc, a Mouse Homolog of the Yeast Postreplication Repair Gene RAD18 von van der Laan, Roald, Roest, Henk P., Hoogerbrugge, Jos W., Smit, Elisabeth M.E., Slater, Rosalyn, Baarends, Willy M., Hoeijmakers, Jan H.J., Grootegoed, J.Anton

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