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Genes, Chromosomes & Cancer|November 27, 2015
Recurrent translocation t(10;17)(p15;q21) in minimally differentiated acute myeloid leukemia results in ZMYND11/MBTD1 fusionJasmijn D E de Rooij, Marry M van den Heuvel-Eibrink, Wouter J W Kollen, et al.
Molecular and Cellular Biology|June 17, 2004
The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaksLaura J Niedernhofer, Hanny Odijk, Magda Budzowska, et al.
Blood|August 30, 2003
Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignanciesBruce Poppe, Jo Vandesompele, Claudia Schoch, et al.
Journal of Neuropathology and Experimental Neurology|April 20, 2005
Chromosomal instability in meningiomasAngela A G van Tilborg, Bushra Al Allak, Sandra C J M Velthuizen, et al.
Blood|November 9, 2014
Mutational spectrum of myeloid malignancies with inv(3)/t(3;3) reveals a predominant involvement of RAS/RTK signaling pathwaysStefan Gröschel, Mathijs A Sanders, Remco Hoogenboezem, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|April 15, 2003
Biallelic mutations in the CEBPA gene and low CEBPA expression levels as prognostic markers in intermediate-risk AMLSahar Barjesteh van Waalwijk van Doorn-Khosrovani, Claudia Erpelinck, Joost Meijer, et al.
Haematologica|June 15, 2004
Two dual-color split signal fluorescence in situ hybridization assays to detect t(5;14) involving HOX11L2 or CSX in T-cell acute lymphoblastic leukemiaLaura J C M van Zutven, Sandra C J M Velthuizen, Ingrid L M Wolvers-Tettero, et al.
Blood|June 16, 2005
Targeting FLT3 in primary MLL-gene-rearranged infant acute lymphoblastic leukemiaRonald W Stam, Monique L den Boer, Pauline Schneider, et al.
Genes, Chromosomes & Cancer|July 11, 2007
Gene expression profiling and gene copy-number changes in malignant mesothelioma cell linesClaudia Zanazzi, Remko Hersmus, Imke M Veltman, et al.
Investigative Ophthalmology & Visual Science|June 28, 2005
Concurrent loss of chromosome arm 1p and chromosome 3 predicts a decreased disease-free survival in uveal melanoma patientsEmine Kilic, Nicole C Naus, Walter van Gils, et al.
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