Výsledky vyhledávání - Sanders, Mathijs A

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

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The Landscape of KMT2A-PTD AML: Concurrent Mutations, Gene Expression Signatures, and Clinical Outcome Autor 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 Autor 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... Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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