Resultats de la cerca - Sanders, Mathijs

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

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Derepression of retroelements in acute myeloid leukemia with 3q aberrations per Mika, Jagoda, Ottema, Sophie, Kiehlmeier, Sandra, Kruse, Sabrina, Smeenk, Leonie, Müller, Judith, Schweiggert, Sabrina, Herrmann, Carl, Sanders, Mathijs, Delwel, Ruud, Gröschel, Stefan

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The Landscape of KMT2A-PTD AML: Concurrent Mutations, Gene Expression Signatures, and Clinical Outcome per 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 per 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... per 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 per 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 per 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 per 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 per 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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Classification of pediatric acute myeloid leukemia based on miRNA expression profiles per Obulkasim, Askar, Katsman-Kuipers, Jenny E., Verboon, Lonneke, Sanders, Mathijs, Touw, Ivo, Jongen-Lavrencic, Mojca, Pieters, Rob, Klusmann, Jan-Henning, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M., Fornerod, Maarten

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Mutational spectrum of myeloid malignancies with inv(3)/t(3;3) reveals a predominant involvement of RAS/RTK signaling pathways per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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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