Myeloid antigens in childhood lymphoblastic leukemia:clinical data point to regulation of CD66c distinct from other myeloid antigens

Por Kalina, Tomas, Vaskova, Martina, Mejstrikova, Ester, Madzo, Jozef, Trka, Jan, Stary, Jan, Hrusak, Ondrej
Publicado em 2005

Intragenic ERG Deletions Do Not Explain the Biology of ERG-Related Acute Lymphoblastic Leukemia

Por Potuckova, Eliska, Zuna, Jan, Hovorkova, Lenka, Starkova, Julia, Stary, Jan, Trka, Jan, Zaliova, Marketa
Publicado no PLoS One (2016)

Reprogramming of B cell acute lymphoblastic leukemia cells: Do we need to shoot a moving target?

Por Fišer, Karel, Slámová, Lucie, Bourquin, Jean-Pierre, Trka, Jan, Starý, Jan, Hrušák, Ondřej, Mejstříková, Ester
Publicado no Proc Natl Acad Sci U S A (2015)

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1

Por Steinemann, Doris, Arning, Larissa, Praulich, Inka, Stuhrmann, Manfred, Hasle, Henrik, Starý, Jan, Schlegelberger, Brigitte, Niemeyer, Charlotte M., Flotho, Christian
Publicado em 2010

Prenatal origin of childhood AML occurs less frequently than in childhood ALL

Por Burjanivova, Tatiana, Madzo, Jozef, Muzikova, Katerina, Meyer, Claus, Schneider, Bjoern, Votava, Felix, Marschalek, Rolf, Stary, Jan, Trka, Jan, Zuna, Jan
Publicado em 2006

MB-80 OUTCOME OF CHILDREN WITH POSTERIOR FOSSA MEDULLOBLASTOMA

Por Sumerauer, David, Zapotocky, Michal, Cyprova, Sona, Zamecnik, Josef, Malinova, Bela, Vicha, Ales, Pernikova, Ivana, Ondrova, Barbora, Kyncl, Martin, Tichy, Michal, Stary, Jan
Publicado no Neuro Oncol (2016)

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

Por Lizcova, Libuse, Zemanova, Zuzana, Lhotska, Halka, Zuna, Jan, Hovorkova, Lenka, Mejstrikova, Ester, Malinova, Eva, Rabasova, Jana, Raska, Ivan, Sramkova, Lucie, Stary, Jan, Michalova, Kyra
Publicado em 2014

Homeobox gene expression in acute myeloid leukemia is linked to typical underlying molecular aberrations

Por Skvarova Kramarzova, Karolina, Fiser, Karel, Mejstrikova, Ester, Rejlova, Katerina, Zaliova, Marketa, Fornerod, Maarten, Drabkin, Harry A, van den Heuvel-Eibrink, Marry M, Stary, Jan, Trka, Jan, Starkova, Julia
Publicado no J Hematol Oncol (2014)

Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood

Por Svobodova, Tamara, Mejstrikova, Ester, Salzer, Ulrich, Sukova, Martina, Hubacek, Petr, Matej, Radoslav, Vasakova, Martina, Hornofova, Ludmila, Dvorakova, Marcela, Fronkova, Eva, Votava, Felix, Freiberger, Tomas, Pohunek, Petr, Stary, Jan, Janda, Ales
Publicado no BMC Pulm Med (2015)

The predictive strength of next-generation sequencing MRD detection for relapse compared with current methods in childhood ALL

Por Kotrova, Michaela, Muzikova, Katerina, Mejstrikova, Ester, Novakova, Michaela, Bakardjieva-Mihaylova, Violeta, Fiser, Karel, Stuchly, Jan, Giraud, Mathieu, Salson, Mikaël, Pott, Christiane, Brüggemann, Monika, Füllgrabe, Marc, Stary, Jan, Trka, Jan, Fronkova, Eva
Publicado no Blood (2015)

Minimal residual disease in peripheral blood at day 15 identifies a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with superior prognosis

Por Volejnikova, Jana, Mejstrikova, Ester, Valova, Tatana, Reznickova, Leona, Hodonska, Ladislava, Mihal, Vladimir, Sterba, Jaroslav, Jabali, Yahia, Prochazkova, Daniela, Blazek, Bohumir, Hak, Jiri, Cerna, Zdenka, Hrusak, Ondrej, Stary, Jan, Trka, Jan, Fronkova, Eva
Publicado em 2011

Imatinib after induction for treatment of children and adolescents with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (EsPhALL): a randomised, open-label, intergro...

Por Biondi, Andrea, Schrappe, Martin, De Lorenzo, Paola, Castor, Anders, Lucchini, Giovanna, Gandemer, Virginie, Pieters, Rob, Stary, Jan, Escherich, Gabriele, Campbell, Myriam, Li, Chi-Kong, Vora, Ajay, Aricò, Maurizio, Röttgers, Silja, Saha, Vaskar, Valsecchi, Maria Grazia
Publicado em 2012

Mapping epigenetic regulator gene mutations in cytogenetically normal pediatric acute myeloid leukemia

Por Valerio, Daria G., Katsman-Kuipers, Jenny E., Jansen, Joop H., Verboon, Lonneke J., de Haas, Valerie, Stary, Jan, Baruchel, André, Zimmermann, Martin, Pieters, Rob, Reinhardt, Dirk, van den Heuvel-Eibrink, Marry M., Zwaan, C. Michel
Publicado em 2014

The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease

Por Kratz, Christian P., Niemeyer, Charlotte M., Castleberry, Robert P., Cetin, Mualla, Bergsträsser, Eva, Emanuel, Peter D., Hasle, Henrik, Kardos, Gabriela, Klein, Cornelia, Kojima, Seiji, Stary, Jan, Trebo, Monika, Zecca, Marco, Gelb, Bruce D., Tartaglia, Marco, Loh, Mignon L.
Publicado em 2005

BCOR and BCORL1 mutations in pediatric acute myeloid leukemia

Por de Rooij, Jasmijn D.E., van den Heuvel-Eibrink, Marry M., Hermkens, Malou C.H., Verboon, Lonneke J., Arentsen-Peters, Susan T.C.J.M., Fornerod, Maarten, Baruchel, Andre, Stary, Jan, Reinhardt, Dirk, de Haas, Valerie, Pieters, Rob, Zwaan, C. Michel
Publicado no Haematologica (2015)

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

Por 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
Publicado em 2010

RASA4 undergoes DNA hypermethylation in resistant juvenile myelomonocytic leukemia

Por Poetsch, Anna R, Lipka, Daniel B, Witte, Tania, Claus, Rainer, Nöllke, Peter, Zucknick, Manuela, Olk-Batz, Christiane, Fluhr, Silvia, Dworzak, Michael, De Moerloose, Barbara, Starý, Jan, Zecca, Marco, Hasle, Henrik, Schmugge, Markus, van den Heuvel-Eibrink, Marry M, Locatelli, Franco, Niemeyer, Charlotte M, Flotho, Christian, Plass, Christoph
Publicado em 2014

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

Por 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
Publicado no Haematologica (2016)

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

Por Loh, Mignon L., Sakai, Debbie S., Flotho, Christian, Kang, Michelle, Fliegauf, Manfred, Archambeault, Sophie, Mullighan, Charles G., Chen, Leslie, Bergstraesser, Eva, Bueso-Ramos, Carlos E., Emanuel, Peter D., Hasle, Henrik, Issa, Jean-Pierre, van den Heuvel-Eibrink, Marry M., Locatelli, Franco, Starý, Jan, Trebo, Monica, Wlodarski, Marcin, Zecca, Marco, Shannon, Kevin M., Niemeyer, Charlotte M.
Publicado em 2009

LIN28B is over-expressed in specific subtypes of pediatric leukemia and regulates lncRNA H19

Por Helsmoortel, Hetty H., De Moerloose, Barbara, Pieters, Tim, Ghazavi, Farzaneh, Bresolin, Silvia, Cavé, Hélène, de Vries, Andrica, de Haas, Valerie, Flotho, Christian, Labarque, Veerle, Niemeyer, Charlotte, De Paepe, Pascale, Van Roy, Nadine, Stary, Jan, van den Heuvel-Eibrink, Marry M., Benoit, Yves, Schulte, Johannes, Goossens, Steven, Berx, Geert, Haigh, Jody J., Speleman, Frank, Van Vlierberghe, Pieter, Lammens, Tim
Publicado no Haematologica (2016)