نتائج البحث - Sanders, Mathijs A

Mutant allelic burden in acute myeloid leukaemia: Why bother? حسب Touw, Ivo P., Sanders, Mathijs A.

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The Landscape of KMT2A-PTD AML: Concurrent Mutations, Gene Expression Signatures, and Clinical Outcome حسب Hinai, Adil S.A. Al, Pratcorona, Marta, Grob, Tim, Kavelaars, François G., Bussaglia, Elena, Sanders, Mathijs A., Nomdedeu, Josep, Valk, Peter J.M.

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SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels حسب Sanders, Mathijs A, Verhaak, Roel GW, Geertsma-Kleinekoort, Wendy MC, Abbas, Saman, Horsman, Sebastiaan, van der Spek, Peter J, Löwenberg, Bob, Valk, Peter JM

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RNA sequencing reveals a unique fusion of the lysine (K)-specific methyltransferase 2A and smooth muscle myosin heavy chain 11 in myelodysplastic syndrome and acute myeloid leukemi... حسب Sanders, Mathijs A., Kavelaars, François G., Zeilemaker, Annelieke, Al Hinai, Adil S.A., Abbas, Saman, Beverloo, H. Berna, van Lom, Kirsten, Valk, Peter J.M.

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HeatMapper: powerful combined visualization of gene expression profile correlations, genotypes, phenotypes and sample characteristics حسب Verhaak, Roel GW, Sanders, Mathijs A, Bijl, Maarten A, Delwel, Ruud, Horsman, Sebastiaan, Moorhouse, Michael J, van der Spek, Peter J, Löwenberg, Bob, Valk, Peter JM

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Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value حسب Pratcorona, Marta, Abbas, Saman, Sanders, Mathijs A., Koenders, Jasper E., Kavelaars, François G., Erpelinck-Verschueren, Claudia A.J., Zeilemakers, Annelieke, Löwenberg, Bob, Valk, Peter J.M.

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Expression profiling of adult acute lymphoblastic leukemia identifies a BCR-ABL1-like subgroup characterized by high non-response and relapse rates حسب Boer, Judith M., Koenders, Jasper E., van der Holt, Bronno, Exalto, Carla, Sanders, Mathijs A., Cornelissen, Jan J., Valk, Peter J.M., den Boer, Monique L., Rijneveld, Anita W.

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Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3′ MECOM حسب van der Veken, Lars T., Maiburg, Merel C., Groenendaal, Floris, van Gijn, Mariëlle E., Bloem, Andries C., Erpelinck, Claudia, Gröschel, Stefan, Sanders, Mathijs A., Delwel, Ruud, Bierings, Marc B., Buijs, Arjan

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Mutational spectrum of myeloid malignancies with inv(3)/t(3;3) reveals a predominant involvement of RAS/RTK signaling pathways حسب Gröschel, Stefan, Sanders, Mathijs A., Hoogenboezem, Remco, Zeilemaker, Annelieke, Havermans, Marije, Erpelinck, Claudia, Bindels, Eric M. J., Beverloo, H. Berna, Döhner, Hartmut, Löwenberg, Bob, Döhner, Konstanze, Delwel, Ruud, Valk, Peter J. M.

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Autophagy inhibition as a potential future targeted therapy for ETV6-RUNX1-driven B-cell precursor acute lymphoblastic leukemia حسب Polak, Roel, Bierings, Marc B., van der Leije, Cindy S., Sanders, Mathijs A., Roovers, Onno, Marchante, João R. M., Boer, Judith M., Cornelissen, Jan J., Pieters, Rob, den Boer, Monique L., Buitenhuis, Miranda

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Allele-specific expression of GATA2 due to epigenetic dysregulation in CEBPA double-mutant AML حسب Mulet-Lazaro, Roger, van Herk, Stanley, Erpelinck, Claudia, Bindels, Eric, Sanders, Mathijs A., Vermeulen, Carlo, Renkens, Ivo, Valk, Peter, Melnick, Ari M., de Ridder, Jeroen, Rehli, Michael, Gebhard, Claudia, Delwel, Ruud, Wouters, Bas J.

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Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes حسب Zambetti, Noemi A., Bindels, Eric M. J., Van Strien, Paulina M. H., Valkhof, Marijke G., Adisty, Maria N., Hoogenboezem, Remco M., Sanders, Mathijs A., Rommens, Johanna M., Touw, Ivo P., Raaijmakers, Marc H. G. P.

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Somatic mutations and clonal dynamics in healthy and cirrhotic human liver حسب Brunner, Simon F, Roberts, Nicola D, Wylie, Luke A, Moore, Luiza, Aitken, Sarah J, Davies, Susan E, Sanders, Mathijs A, Ellis, Pete, Alder, Chris, Hooks, Yvette, Abascal, Federico, Stratton, Michael R, Martincorena, Inigo, Hoare, Matthew, Campbell, Peter J

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Lack of splice factor and cohesin complex mutations in pediatric myelodysplastic syndrome حسب Obenauer, Julia C., Kavelaars, François G., Sanders, Mathijs A., Hoogenboezem, Remco M., de Vries, Andrica C. H., van Strien, Paulina M. H., de Haas, Valerie, Locatelli, Franco, Hasle, Henrik, Valk, Peter J. M., Touw, Ivo P., van den Heuvel-Eibrink, Marry M.

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Clonal evolution after treatment pressure in multiple myeloma: heterogenous genomic aberrations and transcriptomic convergence حسب Misund, Kristine, Hofste op Bruinink, Davine, Coward, Eivind, Hoogenboezem, Remco M., Rustad, Even Holth, Sanders, Mathijs A., Rye, Morten, Sponaas, Anne-Marit, van der Holt, Bronno, Zweegman, Sonja, Hovig, Eivind, Meza-Zepeda, Leonardo A., Sundan, Anders, Myklebost, Ola, Sonneveld, Pieter, Waage, Anders

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Altered NFE2 activity predisposes to leukemic transformation and myelosarcoma with AML-specific aberrations حسب Jutzi, Jonas Samuel, Basu, Titiksha, Pellmann, Maximilian, Kaiser, Sandra, Steinemann, Doris, Sanders, Mathijs A., Hinai, Adil S. A., Zeilemaker, Annelieke, Bojtine Kovacs, Sarolta, Koellerer, Christoph, Ostendorp, Jenny, Aumann, Konrad, Wang, Wei, Raffoux, Emmanuel, Cassinat, Bruno, Bullinger, Lars, Schlegelberger, Brigitte, Valk, Peter J. M., Pahl, Heike Luise

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Somatic Evolution in Non-neoplastic IBD-Affected Colon حسب Olafsson, Sigurgeir, McIntyre, Rebecca E., Coorens, Tim, Butler, Timothy, Jung, Hyunchul, Robinson, Philip S., Lee-Six, Henry, Sanders, Mathijs A., Arestang, Kenneth, Dawson, Claire, Tripathi, Monika, Strongili, Konstantina, Hooks, Yvette, Stratton, Michael R., Parkes, Miles, Martincorena, Inigo, Raine, Tim, Campbell, Peter J., Anderson, Carl A.

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Integrated genome-wide genotyping and gene expression profiling reveals BCL11B as a putative oncogene in acute myeloid leukemia with 14q32 aberrations حسب Abbas, Saman, Sanders, Mathijs A., Zeilemaker, Annelieke, Geertsma-Kleinekoort, Wendy M.C., Koenders, Jasper E., Kavelaars, Francois G., Abbas, Zabiollah G., Mahamoud, Souad, Chu, Isabel W.T., Hoogenboezem, Remco, Peeters, Justine K., van Drunen, Ellen, van Galen, Janneke, Beverloo, H. Berna, Löwenberg, Bob, Valk, Peter J.M.

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An autonomous CEBPA enhancer specific for myeloid-lineage priming and neutrophilic differentiation حسب Avellino, Roberto, Havermans, Marije, Erpelinck, Claudia, Sanders, Mathijs A., Hoogenboezem, Remco, van de Werken, Harmen J. G., Rombouts, Elwin, van Lom, Kirsten, van Strien, Paulina M. H., Gebhard, Claudia, Rehli, Michael, Pimanda, John, Beck, Dominik, Erkeland, Stefan, Kuiken, Thijs, de Looper, Hans, Gröschel, Stefan, Touw, Ivo, Bindels, Eric, Delwel, Ruud

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MBD4 guards against methylation damage and germ line deficiency predisposes to clonal hematopoiesis and early-onset AML حسب Sanders, Mathijs A., Chew, Edward, Flensburg, Christoffer, Zeilemaker, Annelieke, Miller, Sarah E., al Hinai, Adil S., Bajel, Ashish, Luiken, Bram, Rijken, Melissa, Mclennan, Tamara, Hoogenboezem, Remco M., Kavelaars, François G., Fröhling, Stefan, Blewitt, Marnie E., Bindels, Eric M., Alexander, Warren S., Löwenberg, Bob, Roberts, Andrew W., Valk, Peter J. M., Majewski, Ian J.

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