Výsledky vyhledávání - Nebral, Karin
- Zobrazuji výsledky 1 - 14 z 14
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Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor Autor Poyer, Fiona, Jimenez Heredia, Raúl, Novak, Wolfgang, Zeitlhofer, Petra, Nebral, Karin, Dworzak, Michael N., Haas, Oskar A., Boztug, Kaan, Kager, Leo
Vydáno 2022Text -
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Single nucleotide polymorphism array‐based signature of low hypodiploidy in acute lymphoblastic leukemia Autor Creasey, Thomas, Enshaei, Amir, Nebral, Karin, Schwab, Claire, Watts, Kathryn, Cuthbert, Gavin, Vora, Ajay, Moppett, John, Harrison, Christine J., Fielding, Adele K., Haas, Oskar A., Moorman, Anthony V.
Vydáno 2021Text -
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Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia Autor Abbasi, M. Reza, Nebral, Karin, Haslinger, Sabrina, Inthal, Andrea, Zeitlhofer, Petra, König, Margit, Schinnerl, Dagmar, Köhrer, Stefan, Strehl, Sabine, Panzer-Grümayer, Renate, Mann, Georg, Attarbaschi, Andishe, Haas, Oskar A.
Vydáno 2021Text -
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JAK2 p.G571S in B-cell precursor acute lymphoblastic leukemia: a synergizing germline susceptibility Autor Lin, Minhui, Nebral, Karin, Gertzen, Christoph G. W., Ganmore, Ithamar, Haas, Oskar A., Bhatia, Sanil, Fischer, Ute, Kuhlen, Michaela, Gohlke, Holger, Izraeli, Shai, Trka, Jan, Hu, Jianda, Borkhardt, Arndt, Hauer, Julia, Auer, Franziska
Vydáno 2019Text -
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Phospho-Profiling Linking Biology and Clinics in Pediatric Acute Myeloid Leukemia Autor Schumich, Angela, Prchal-Murphy, Michaela, Maurer-Granofszky, Margarita, Hoelbl-Kovacic, Andrea, Mühlegger, Nora, Pötschger, Ulrike, Fajmann, Sabine, Haas, Oskar A., Nebral, Karin, von Neuhoff, Nils, Zimmermann, Martin, Boztug, Heidrun, Rasche, Mareike, Dolezal, Marlies, Walter, Christiane, Reinhardt, Dirk, Sexl, Veronika, Dworzak, Michael N.
Vydáno 2019Text -
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Surface expression of Cytokine Receptor-Like Factor 2 increases risk of relapse in pediatric acute lymphoblastic leukemia patients harboring IKZF1 deletions Autor Pastorczak, Agata, Sedek, Lukasz, Braun, Marcin, Madzio, Joanna, Sonsala, Alicja, Twardoch, Magdalena, Fendler, Wojciech, Nebral, Karin, Taha, Joanna, Bielska, Marta, Gorniak, Patryk, Romiszewska, Magdalena, Matysiak, Michal, Derwich, Katarzyna, Lejman, Monika, Kowalczyk, Jerzy, Badowska, Wanda, Niedzwiecki, Maciej, Kazanowska, Bernarda, Muszynska-Roslan, Katarzyna, Sobol-Milejska, Grazyna, Karolczyk, Grazyna, Koltan, Andrzej, Ociepa, Tomasz, Szczepanski, Tomasz, Młynarski, Wojciech
Vydáno 2018Text -
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CD371 cell surface expression: a unique feature of DUX4-rearranged acute lymphoblastic leukemia Autor Schumich, Angela, Zaliova, Marketa, Fortschegger, Klaus, Nebral, Karin, Attarbaschi, Andishe, Fiser, Karel, Kauer, Maximilian O., Popitsch, Niko, Haslinger, Sabrina, Inthal, Andrea, Buldini, Barbara, Basso, Giuseppe, Bourquin, Jean-Pierre, Gaipa, Giuseppe, Brüggemann, Monika, Feuerstein, Tamar, Maurer-Granofszky, Margarita, Panzer-Grümayer, Renate, Trka, Jan, Mann, Georg, Haas, Oskar A., Hrusak, Ondrej, Dworzak, Michael N., Strehl, Sabine
Vydáno 2019Text -
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Expression Patterns of Coagulation Factor XIII Subunit A on Leukemic Lymphoblasts Correlate with Clinical Outcome and Genetic Subtypes in Childhood B-cell Progenitor Acute Lymphobl... Autor Kárai, Bettina, Gyurina, Katalin, Ujfalusi, Anikó, Sędek, Łukasz, Barna, Gábor, Jáksó, Pál, Svec, Peter, Szánthó, Eszter, Nagy, Attila Csaba, Müller, Judit, Simon, Réka, Vojczek, Ágnes, Szegedi, István, Tiszlavicz, Lilla Györgyi, Kowalczyk, Jerzy R., Kolenova, Alexandra, Kovács, Gábor T., Szczepański, Tomasz, Dworzak, Michael, Schumich, Angela, Attarbaschi, Andishe, Nebral, Karin, Haas, Oskar A., Kappelmayer, János, Hevessy, Zsuzsanna, Kiss, Csongor
Vydáno 2020Text -
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B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH-Rearranged B-ALL Autor Fournier, Benjamin, Balducci, Estelle, Duployez, Nicolas, Clappier, Emmanuelle, Cuccuini, Wendy, Arfeuille, Chloé, Caye-Eude, Aurélie, Delabesse, Eric, Bottollier-Lemallaz Colomb, Elodie, Nebral, Karin, Chrétien, Marie-Lorraine, Derrieux, Coralie, Cabannes-Hamy, Aurélie, Dumezy, Florent, Etancelin, Pascaline, Fenneteau, Odile, Frayfer, Jamile, Gourmel, Antoine, Loosveld, Marie, Michel, Gérard, Nadal, Nathalie, Penther, Dominique, Tigaud, Isabelle, Fournier, Elise, Reismüller, Bettina, Attarbaschi, Andishe, Lafage-Pochitaloff, Marina, Baruchel, André
Vydáno 2019Text -
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Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia? Autor Schwab, Claire, Nebral, Karin, Chilton, Lucy, Leschi, Cristina, Waanders, Esmé, Boer, Judith M., Žaliová, Markéta, Sutton, Rosemary, Öfverholm, Ingegerd Ivanov, Ohki, Kentaro, Yamashita, Yuka, Groeneveld-Krentz, Stefanie, Froňková, Eva, Bakkus, Marleen, Tchinda, Joelle, Barbosa, Thayana da Conceição, Fazio, Grazia, Mlynarski, Wojciech, Pastorczak, Agata, Cazzaniga, Giovanni, Pombo-de-Oliveira, Maria S., Trka, Jan, Kirschner-Schwabe, Renate, Imamura, Toshihiko, Barbany, Gisela, Stanulla, Martin, Attarbaschi, Andishe, Panzer-Grümayer, Renate, Kuiper, Roland P., den Boer, Monique L., Cavé, Hélène, Moorman, Anthony V., Harrison, Christine J., Strehl, Sabine
Vydáno 2017Text -
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Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL Autor Hamadeh, Lina, Enshaei, Amir, Schwab, Claire, Alonso, Cristina N., Attarbaschi, Andishe, Barbany, Gisela, den Boer, Monique L., Boer, Judith M., Braun, Marcin, Dalla Pozza, Luciano, Elitzur, Sarah, Emerenciano, Mariana, Fechina, Larisa, Felice, Maria Sara, Fronkova, Eva, Haltrich, Irén, Heyman, Mats M., Horibe, Keizo, Imamura, Toshihiko, Jeison, Marta, Kovács, Gábor, Kuiper, Roland P., Mlynarski, Wojciech, Nebral, Karin, Ivanov Öfverholm, Ingegerd, Pastorczak, Agata, Pieters, Rob, Piko, Henriett, Pombo-de-Oliveira, Maria S., Rubio, Patricia, Strehl, Sabine, Stary, Jan, Sutton, Rosemary, Trka, Jan, Tsaur, Grigory, Venn, Nicola, Vora, Ajay, Yano, Mio, Harrison, Christine J., Moorman, Anthony V.
Vydáno 2019Text -
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Association of unbalanced translocation der(1;7) with germline GATA2 mutations Autor Kozyra, Emilia J., Göhring, Gudrun, Hickstein, Dennis D., Calvo, Katherine R., DiNardo, Courtney D., Dworzak, Michael, de Haas, Valerie, Starý, Jan, Hasle, Henrik, Shimamura, Akiko, Fleming, Mark D., Inaba, Hiroto, Lewis, Sara, Hsu, Amy P., Holland, Steven M., Arnold, Danielle E., Mecucci, Cristina, Keel, Siobán B., Bertuch, Alison A., Tawana, Kiran, Barzilai, Shlomit, Hirabayashi, Shinsuke, Onozawa, Masahiro, Lei, Shaohua, Alaiz, Helena, Andrikovics, Hajnalka, Betts, David, Beverloo, Berna H., Buechner, Jochen, Čermák, Martin, Cervera, José, Haus, Olga, Jahnukainen, Kirsi, Manola, Kalliopi N., Nebral, Karin, Pasquali, Francesco, Tchinda, Joelle, Turkiewicz, Dominik, Van Roy, Nadine, Zemanova, Zuzana, Pastor, Victor B., Strahm, Brigitte, Noellke, Peter, Niemeyer, Charlotte M., Schlegelberger, Brigitte, Yoshimi, Ayami, Wlodarski, Marcin W.
Vydáno 2021Text