MN1 overexpression is an important step in the development of inv(16) AML von CARELLA, C, BONTEN, J, GROSVELD, G. C, SIRMA, S, KRANENBURG, T. A, TERRANOVA, S, KLEIN-GELTINK, R, SHURTLEFF, S, DOWNING, J. R, ZWARTHOFF, E. C, LIU, P. P

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FGFR3 and PIK3CA mutations are involved in the molecular pathogenesis of solar lentigo von Hafner, C., Stoehr, R., Van Oers, J.M.M., Zwarthoff, E.C., Hofstaedter, F., Landthaler, M., Hartmann, A., Vogt, T.

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Absence of TERT promoter mutations in esophageal adenocarcinoma von Nistelrooij, A.M.J., Zwarthoff, E.C., Post, E., Lurkin, I., Marion, R., Kopershoek, E., Biermann, K., Wijnhoven, B.P.L., Dinjens, W.N.M.

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Absence of BRAF and HRAS mutations in eruptive Spitz naevi von Gantner, S., Wiesner, T., Cerroni, L., Lurkin, I., Zwarthoff, E.C., Landthaler, M., Hafner, C.

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Analysis of molecular intra-patient variation and delineation of a prognostic 12-gene signature in non-muscle invasive bladder cancer; technology transfer from microarrays to PCR von Dyrskjøt, L, Reinert, T, Novoradovsky, A, Zuiverloon, T C M, Beukers, W, Zwarthoff, E, Malats, N, Real, F X, Segersten, U, Malmström, P-U, Knowles, M, Hurst, C, Sorge, J, Borre, M, Ørntoft, T F

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FGFR3 and P53 characterize alternative genetic pathways in the pathogenesis of urothelial cell carcinoma von VAN RHIJN, Bas W. G, VAN DER KWAST, Theo H, VIS, André N, KIRKELS, Wim J, BOEVE, Egbert R, JÖBSIS, Adriaan C, ZWARTHOFF, Ellen C

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The fibroblast growth factor receptor 3 (FGFR3) mutation is a strong indicator of superficial bladder cancer with low recurrence rate von VAN RHIJN, Bas W. G, LURKIN, Irene, RADVANYI, Francois, KIRKELS, Wim J, VAN DER KWAST, Theodorus H, ZWARTHOFF, Ellen C

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The MN1-TEL myeloid leukemia-associated fusion protein has a dominant-negative effect on RAR-RXR-mediated transcription von van Wely, K H M, Meester-Smoor, M A, Janssen, M J F W, Aarnoudse, A-J, Grosveld, G C, Zwarthoff, E C

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Genomic aberrations are rare in urothelial neoplasms of patients 19 years or younger von Wild, PJ, Giedl, J, Stoehr, R, Junker, K, Boehm, S, van Oers, JMM, Zwarthoff, EC, Blaszyk, H, Fine, SW, Humphrey, PA, Dehner, LP, Amin, MB, Epstein, JI, Hartmann, A

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Frequent FGFR3 mutations in urothelial papilloma von van Rhijn, Bas W. G., Montironi, Rodolfo, Zwarthoff, Ellen C., Jöbsis, Adriaan C., van der Kwast, Theo H.

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Molecular evolution of multiple recurrent cancers of the bladder von VAN TILBORG, Angela A. G, DE VRIES, Annie, DE BONT, Maarten, GROENFELD, Lilian E, VAN DER KWAST, Theo H, ZWARTHOFF, Ellen C

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The MN1-TEL Fusion Protein, Encoded by the Translocation (12;22)(p13;q11) in Myeloid Leukemia, Is a Transcription Factor with Transforming Activity von Buijs, Arjan, van Rompaey, Luc, Molijn, Anco C., Davis, J. Nathan, Vertegaal, Alfred C. O., Potter, Mark D., Adams, Constantin, van Baal, Sjozèf, Zwarthoff, Ellen C., Roussel, Martine F., Grosveld, Gerard C.

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A new system for substaging pT1 papillary bladder cancer: a prognostic evaluation von van der Aa, Madelon N.M., van Leenders, Geert J.L.H., Steyerberg, Ewout W., van Rhijn, Bas W., Jöbsis, Adriaan C., Zwarthoff, Ellen C., van der Kwast, Theodorus H.

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The MN1 oncoprotein synergizes with coactivators RAC3 and p300 in RAR-RXR-mediated transcription von van Wely, Karel H M, Molijn, Anco C, Buijs, Arjan, Meester-Smoor, Magda A, Aarnoudse, Albert Jan, Hellemons, Anita, den Besten, Pim, Grosveld, Gerard C, Zwarthoff, Ellen C

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Efficient Rescue of Integrated Shuttle Vectors from Transgenic Mice: A Model for Studying Mutations in vivo von Gossen, Jan A., Wiljo J. F. De Leeuw, Cecilia H. T. Tan, Zwarthoff, Ellen C., Berends, Frits, Paul H. M. Lohman, Knook, Dick L., Vijg, Jan

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MP-2.17: Feasibility Study of Population-Based Screening for Bladder Cancer with Urinary Molecular Markers (BLUP): (www.blu-project.org) von Roobol, M, Zuiverloon, T, Zwarthoff, E, Busstra, M, Franken-Raab, C, Bangma, C

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Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas von DEPREZ, R. H. L, BIANCHI, A. B, ZWARTHOFF, E. C, GROEN, N. A, SEIZINGER, B. R, HAGEMEIJER, A, VAN DRUNEN, E, BOOTSMA, D, KOPER, J. W, AVEZAAT, C. J. J, KLEY, N

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Expression of the MN1–TEL fusion protein in the human UCSD/AML1 leukemic cell line von Valle, V Della, Guglielmi, L, Busson, M, Zwarthoff, E C, Berger, R, Bernard, O A

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Cytogenetic, Molecular Genetic and Pathological Analyses in 126 Meningiomas von Lekanne Deprez, Ronald H, Riegman, Peter H, van Drunen, Ellen, Warringa, Ursula L, Groen, Nicole A, Stefanko, Stanislaw Z, Koper, Jan W, Avezaat, Cees J. J, Zwarthoff, Ellen C, Hagemeizer, Anne

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A G→A Transition Creates a Branch Point Sequence and Activation of a Cryptic Exon, Resulting in the Hereditary Disorder Neurofibromatosis 2 von De Klein, Annelies, Riegman, Peter H.J., Bijlsma, Emilia K., Heldoorn, Anneliek, Muijtjens, Manja, den Bakker, Michael A., Avezaat, Cees J.J., Zwarthoff, Ellen C.

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