Immunoglobulin V(H) Gene Mutational Analysis Suggests that Primary Effusion Lymphomas Derive from Different Stages of B Cell Maturation

Por Matolcsy, András, Nádor, Roland G., Cesarman, Ethel, Knowles, Daniel M.
Publicado em 1998

Shifting gears higher - digital slides in graduate education - 4 years experience at Semmelweis University

Por Fónyad, László, Gerely, László, Cserneky, Mária, Molnár, Béla, Matolcsy, András
Publicado em 2010

Clonal evolution of B cells in transformation from low- to high-grade lymphoma

Por Matolcsy, András, Schattner, Elaine J., Knowles, Daniel M., Casali, Paolo
Publicado no Eur J Immunol (1999)

Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia

Por Gadó Klára, Matolcsy András, Csomor Judit, Kicsi Dóra, Bödör Csaba, Domján Gyula
Publicado em 2012-07-01

Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia

Por Gadó, Klára, Matolcsy, András, Csomor, Judit, Kicsi, Dóra, Bödör, Csaba, Domján, Gyula
Publicado em 2012

Somatic Mutation of the 5′ Noncoding Region of the BCL-6 Gene Is Associated with Intraclonal Diversity and Clonal Selection in Histological Transformation of Follicular Lymphoma

Por Szereday, Zoltán, Csernus, Balázs, Nagy, Monika, László, Terézia, Warnke, Roger A., Matolcsy, András
Publicado em 2000

Molecular Characterization of IgA- and/or IgG-Switched Chronic Lymphocytic Leukemia B Cells

Por Matolcsy, András, Casali, Paolo, Nádor, Roland G., Liu, Yi-Fang, Knowles, Daniel M.
Publicado no Blood (1997)

Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure

Por Beke, Artur, Piko, Henriett, Haltrich, Iren, Csomor, Judit, Matolcsy, Andras, Fekete, György, Rigo, Janos, Karcagi, Veronika
Publicado em 2013

Selenite promotes all-trans retinoic acid-induced maturation of acute promyelocytic leukemia cells

Por Misra, Sougat, Selvam, Arun Kumar, Wallenberg, Marita, Ambati, Aditya, Matolcsy, András, Magalhaes, Isabelle, Lauter, Gilbert, Björnstedt, Mikael
Publicado no Oncotarget (2016)

Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas

Por Rajnai, Hajnalka, Teleki, Ivett, Kiszner, Gergo, Meggyesházi, Nora, Balla, Peter, Vancsik, Tamas, Muzes, Gyorgyi, Csomor, Judit, Matolcsy, Andras, Krenacs, Tibor
Publicado no J Immunol Res (2015)

Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival

Por Bödör, Csaba, Renneville, Aline, Smith, Matthew, Charazac, Aurélie, Iqbal, Sameena, Étancelin, Pascaline, Cavenagh, Jamie, Barnett, Michael J, Kramarzová, Karolina, Krishnan, Biju, Matolcsy, András, Preudhomme, Claude, Fitzgibbon, Jude, Owen, Carolyn
Publicado em 2012

Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree

Por Tawana, Kiran, Wang, Jun, Király, Péter A, Kállay, Krisztián, Benyó, Gábor, Zombori, Marianna, Csomor, Judit, Al Seraihi, Ahad, Rio-Machin, Ana, Matolcsy, András, Chelala, Claude, Cavenagh, Jamie, Fitzgibbon, Jude, Bödör, Csaba
Publicado no Eur J Hum Genet (2017)

p53 protein expression independently predicts outcome in patients with lower-risk myelodysplastic syndromes with del(5q)

Por Saft, Leonie, Karimi, Mohsen, Ghaderi, Mehran, Matolcsy, András, Mufti, Ghulam J., Kulasekararaj, Austin, Göhring, Gudrun, Giagounidis, Aristoteles, Selleslag, Dominik, Muus, Petra, Sanz, Guillermo, Mittelman, Moshe, Bowen, David, Porwit, Anna, Fu, Tommy, Backstrom, Jay, Fenaux, Pierre, MacBeth, Kyle J., Hellström-Lindberg, Eva
Publicado em 2014

Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma

Por Okosun, Jessica, Bödör, Csaba, Wang, Jun, Araf, Shamzah, Yang, Cheng-Yuan, Pan, Chenyi, Boller, Sören, Cittaro, Davide, Bozek, Monika, Iqbal, Sameena, Matthews, Janet, Wrench, David, Marzec, Jacek, Tawana, Kiran, Popov, Nikolay, O’Riain, Ciaran, O’Shea, Derville, Carlotti, Emanuela, Davies, Andrew, Lawrie, Charles H., Matolcsy, Andras, Calaminici, Maria, Norton, Andrew, Byers, Richard J., Mein, Charles, Stupka, Elia, Lister, T. Andrew, Lenz, Georg, Montoto, Silvia, Gribben, John G., Fan, Yuhong, Grosschedl, Rudolf, Chelala, Claude, Fitzgibbon, Jude
Publicado em 2013

EZH2 mutations are frequent and represent an early event in follicular lymphoma

Por Bödör, Csaba, Grossmann, Vera, Popov, Nikolay, Okosun, Jessica, O’Riain, Ciarán, Tan, King, Marzec, Jacek, Araf, Shamzah, Wang, Jun, Lee, Abigail M., Clear, Andrew, Montoto, Silvia, Matthews, Janet, Iqbal, Sameena, Rajnai, Hajnalka, Rosenwald, Andreas, Ott, German, Campo, Elias, Rimsza, Lisa M., Smeland, Erlend B., Chan, Wing C., Braziel, Rita M., Staudt, Louis M., Wright, George, Lister, T. Andrew, Elemento, Olivier, Hills, Robert, Gribben, John G., Chelala, Claude, Matolcsy, András, Kohlmann, Alexander, Haferlach, Torsten, Gascoyne, Randy D., Fitzgibbon, Jude
Publicado em 2013