Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis

著者: Pavlistova, Lenka, Izakova, Silvia, Zemanova, Zuzana, Bartuskova, Lucie, Langova, Martina, Malikova, Pavlina, Michalova, Kyra
出版年 Mol Cytogenet (2016)

Primary and recurrent diffuse astrocytomas: genomic profile comparison reveals acquisition of biologically relevant aberrations

著者: Lhotska, Halka, Zemanova, Zuzana, Cechova, Hana, Ransdorfova, Sarka, Svobodova, Karla, Kramar, Filip, Krejcik, Zdenek, Michalova, Kyra
出版年 Mol Cytogenet (2016)

Somatic mutation dynamics in MDS patients treated with azacitidine indicate clonal selection in patients-responders

著者: Polgarova, Kamila, Vargova, Karina, Kulvait, Vojtech, Dusilkova, Nina, Minarik, Lubomir, Zemanova, Zuzana, Pesta, Michal, Jonasova, Anna, Stopka, Tomas
出版年 Oncotarget (2017)

An unusual case of high hyperdiploid childhood ALL with cryptic BCR/ABL1 rearrangement

著者: Lizcova, Libuse, Zemanova, Zuzana, Lhotska, Halka, Zuna, Jan, Hovorkova, Lenka, Mejstrikova, Ester, Malinova, Eva, Rabasova, Jana, Raska, Ivan, Sramkova, Lucie, Stary, Jan, Michalova, Kyra
出版事項 2014

Acute lymphoblastic leukemia with aleukemic prodrome: preleukemic dynamics and possible mechanisms of immunosurveillance

著者: Zimmermannova, Olga, Zaliova, Marketa, Moorman, Anthony V., Al-Shehhi, Halima, Fronkova, Eva, Zemanova, Zuzana, Kalina, Tomas, Vora, Ajay, Stary, Jan, Trka, Jan, Hrusak, Ondrej, Zuna, Jan
出版年 Haematologica (2017)

Concurrent TP53 and CDKN2A Gene Aberrations in Newly Diagnosed Mantle Cell Lymphoma Correlate with Chemoresistance and Call for Innovative Upfront Therapy

著者: Malarikova, Diana, Berkova, Adela, Obr, Ales, Blahovcova, Petra, Svaton, Michael, Forsterova, Kristina, Kriegova, Eva, Prihodova, Eva, Pavlistova, Lenka, Petrackova, Anna, Zemanova, Zuzana, Trneny, Marek, Klener, Pavel
出版年 Cancers (Basel) (2020)

Fibroblast Activation Protein Expressing Mesenchymal Cells Promote Glioblastoma Angiogenesis

著者: Balaziova, Eva, Vymola, Petr, Hrabal, Petr, Mateu, Rosana, Zubal, Michal, Tomas, Robert, Netuka, David, Kramar, Filip, Zemanova, Zuzana, Svobodova, Karla, Brabec, Marek, Sedo, Aleksi, Busek, Petr
出版年 Cancers (Basel) (2021)

TP53 mutation variant allele frequency is a potential predictor for clinical outcome of patients with lower-risk myelodysplastic syndromes

著者: Belickova, Monika, Vesela, Jitka, Jonasova, Anna, Pejsova, Barbora, Votavova, Hana, Merkerova, Michaela Dostalova, Zemanova, Zuzana, Brezinova, Jana, Mikulenkova, Dana, Lauermannova, Marie, Valka, Jan, Michalova, Kyra, Neuwirtova, Radana, Cermak, Jaroslav
出版年 Oncotarget (2016)

Prognosis of children with mixed phenotype acute leukemia treated on the basis of consistent immunophenotypic criteria

著者: Mejstrikova, Ester, Volejnikova, Jana, Fronkova, Eva, Zdrahalova, Katerina, Kalina, Tomas, Sterba, Jaroslav, Jabali, Yahia, Mihal, Vladimir, Blazek, Bohumir, Cerna, Zdena, Prochazkova, Daniela, Hak, Jiri, Zemanova, Zuzana, Jarosova, Marie, Oltova, Alexandra, Sedlacek, Petr, Schwarz, Jiri, Zuna, Jan, Trka, Jan, Stary, Jan, Hrusak, Ondrej
出版事項 2010

Guidelines for cytogenetic investigations in tumours

著者: Hastings, Rosalind J, Bown, Nick, Tibiletti, Maria G, Debiec-Rychter, Maria, Vanni, Roberta, Espinet, Blanca, van Roy, Nadine, Roberts, Paul, van den Berg-de-Ruiter, Eva, Bernheim, Alain, Schoumans, Jacqueline, Chatters, Steve, Zemanova, Zuzana, Stevens-Kroef, Marian, Simons, Annet, Heim, Sverre, Salido, Marta, Ylstra, Bauke, Betts, David R
出版年 Eur J Hum Genet (2016)

Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome

著者: Nováková, Michaela, Žaliová, Markéta, Suková, Martina, Wlodarski, Marcin, Janda, Aleš, Froňková, Eva, Campr, Vít, Lejhancová, Kateřina, Zapletal, Ondřej, Pospíšilová, Dagmar, Černá, Zdeňka, Kuhn, Tomáš, Švec, Peter, Pelková, Vendula, Zemanová, Zuzana, Kerndrup, Gitte, van den Heuvel-Eibrink, Marry, van der Velden, Vincent, Niemeyer, Charlotte, Kalina, Tomáš, Trka, Jan, Starý, Jan, Hrušák, Ondřej, Mejstříková, Ester
出版年 Haematologica (2016)

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

著者: Formankova, Renata, Kanderova, Veronika, Rackova, Marketa, Svaton, Michael, Brdicka, Tomas, Riha, Petr, Keslova, Petra, Mejstrikova, Ester, Zaliova, Marketa, Freiberger, Tomas, Grombirikova, Hana, Zemanova, Zuzana, Vlkova, Marcela, Fencl, Filip, Copova, Ivana, Bronsky, Jiri, Jabandziev, Petr, Sedlacek, Petr, Soukalova, Jana, Zapletal, Ondrej, Stary, Jan, Trka, Jan, Kalina, Tomas, Skvarova Kramarzova, Karolina, Hlavackova, Eva, Litzman, Jiri, Fronkova, Eva
出版年 Front Immunol (2019)

Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

著者: Balgobind, Brian V., Hollink, Iris H.I.M., Arentsen-Peters, Susan T.C.J.M., Zimmermann, Martin, Harbott, Jochen, Beverloo, H. Berna, von Bergh, Anne R.M., Cloos, Jacqueline, Kaspers, Gertjan J.L., de Haas, Valerie, Zemanova, Zuzana, Stary, Jan, Cayuela, Jean-Michel, Baruchel, Andre, Creutzig, Ursula, Reinhardt, Dirk, Pieters, Rob, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M.
出版事項 2011

Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders

著者: Ross, Fiona M., Avet-Loiseau, Hervé, Ameye, Geneviève, Gutiérrez, Norma C., Liebisch, Peter, O’Connor, Sheila, Dalva, Klara, Fabris, Sonia, Testi, Adele M., Jarosova, Marie, Hodkinson, Clare, Collin, Anna, Kerndrup, Gitte, Kuglik, Petr, Ladon, Dariusz, Bernasconi, Paolo, Maes, Brigitte, Zemanova, Zuzana, Michalova, Kyra, Michau, Lucienne, Neben, Kai, Hermansen, N. Emil U., Rack, Katrina, Rocci, Alberto, Protheroe, Rebecca, Chiecchio, Laura, Poirel, Hélène A, Sonneveld, Pieter, Nyegaard, Mette, Johnsen, Hans E.
出版事項 2012

Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study

著者: Balgobind, Brian V., Raimondi, Susana C., Harbott, Jochen, Zimmermann, Martin, Alonzo, Todd A., Auvrignon, Anne, Beverloo, H. Berna, Chang, Myron, Creutzig, Ursula, Dworzak, Michael N., Forestier, Erik, Gibson, Brenda, Hasle, Henrik, Harrison, Christine J., Heerema, Nyla A., Kaspers, Gertjan J. L., Leszl, Anna, Litvinko, Nathalia, Nigro, Luca Lo, Morimoto, Akira, Perot, Christine, Pieters, Rob, Reinhardt, Dirk, Rubnitz, Jeffrey E., Smith, Franklin O., Stary, Jan, Stasevich, Irina, Strehl, Sabine, Taga, Takashi, Tomizawa, Daisuke, Webb, David, Zemanova, Zuzana, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M.
出版事項 2009

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study

著者: Coenen, Eva A., Raimondi, Susana C., Harbott, Jochen, Zimmermann, Martin, Alonzo, Todd A., Auvrignon, Anne, Beverloo, H. Berna, Chang, Myron, Creutzig, Ursula, Dworzak, Michael N., Forestier, Erik, Gibson, Brenda, Hasle, Henrik, Harrison, Christine J., Heerema, Nyla A., Kaspers, Gertjan J. L., Leszl, Anna, Litvinko, Nathalia, Lo Nigro, Luca, Morimoto, Akira, Perot, Christine, Reinhardt, Dirk, Rubnitz, Jeffrey E., Smith, Franklin O., Stary, Jan, Stasevich, Irina, Strehl, Sabine, Taga, Takashi, Tomizawa, Daisuke, Webb, David, Zemanova, Zuzana, Pieters, Rob, Zwaan, C. Michel, van den Heuvel-Eibrink, Marry M.
出版事項 2011