Histone modification defects in developmental disorders and cancer

por Cross, Nicholas CP
Publicado 2012

Antisense Oligonucleotides Modulating Activation of a Nonsense-Mediated RNA Decay Switch Exon in the ATM Gene

por Kralovicova, Jana, Moreno, Pedro M.D., Cross, Nicholas C.P., Pêgo, Ana Paula, Vorechovsky, Igor
Publicado 2016

The clinical and molecular diversity of mast cell leukemia with or without associated hematologic neoplasm

por Jawhar, Mohamad, Schwaab, Juliana, Meggendorfer, Manja, Naumann, Nicole, Horny, Hans-Peter, Sotlar, Karl, Haferlach, Torsten, Schmitt, Karla, Fabarius, Alice, Valent, Peter, Hofmann, Wolf-Karsten, Cross, Nicholas C.P., Metzgeroth, Georgia, Reiter, Andreas
Publicado 2017

Diagnosis and Treatment of Chronic Myelomonocytic Leukemias in Adults: Recommendations From the European Hematology Association and the European LeukemiaNet

por Itzykson, Raphael, Fenaux, Pierre, Bowen, David, Cross, Nicholas C.P., Cortes, Jorge, De Witte, Theo, Germing, Ulrich, Onida, Francesco, Padron, Eric, Platzbecker, Uwe, Santini, Valeria, Sanz, Guillermo F., Solary, Eric, Van de Loosdrecht, Arjan, Malcovati, Luca
Publicado 2018

Cytogenetically cryptic ZMYM2-FLT3 and DIAPH1-PDGFRB gene fusions in myeloid neoplasms with eosinophilia

por Jawhar, Mohamad, Naumann, Nicole, Knut, Marcin, Score, Joannah, Ghazzawi, Muna, Schneider, Brigitte, Kreuzer, Karl-Anton, Hallek, Michael, Drexler, Hans G, Chacko, Joseph, Wallis, Louise, Fabarius, Alice, Metzgeroth, Georgia, Hofmann, Wolf-Karsten, Chase, Andrew, Tapper, Will, Reiter, Andreas, Cross, Nicholas C.P.
Publicado 2017

The U2AF1(S34F) mutation induces lineage-specific splicing alterations in myelodysplastic syndromes

por Yip, Bon Ham, Steeples, Violetta, Repapi, Emmanouela, Armstrong, Richard N., Llorian, Miriam, Roy, Swagata, Shaw, Jacqueline, Dolatshad, Hamid, Taylor, Stephen, Verma, Amit, Bartenstein, Matthias, Vyas, Paresh, Cross, Nicholas C.P., Malcovati, Luca, Cazzola, Mario, Hellström-Lindberg, Eva, Ogawa, Seishi, Smith, Christopher W.J., Pellagatti, Andrea, Boultwood, Jacqueline
Publicado 2017

Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer

por Forsberg, Lars A., Rasi, Chiara, Malmqvist, Niklas, Davies, Hanna, Pasupulati, Saichand, Pakalapati, Geeta, Sandgren, Johanna, de Ståhl, Teresita Diaz, Zaghlool, Ammar, Giedraitis, Vilmantas, Lannfelt, Lars, Score, Joannah, Cross, Nicholas C.P., Absher, Devin, Janson, Eva Tiensuu, Lindgren, Cecilia M., Morris, Andrew P., Ingelsson, Erik, Lind, Lars, Dumanski, Jan P.
Publicado 2014

MARS: Mutation-Adjusted Risk Score for Advanced Systemic Mastocytosis

por Jawhar, Mohamad, Schwaab, Juliana, Álvarez-Twose, Iván, Shoumariyeh, Khalid, Naumann, Nicole, Lübke, Johannes, Perkins, Cecelia, Muñoz-González, Javier I., Meggendorfer, Manja, Kennedy, Vanessa, Metzgeroth, Georgia, Fabarius, Alice, Pfeifer, Dietmar, Sotlar, Karl, Horny, Hans-Peter, von Bubnoff, Nikolas, Haferlach, Torsten, Cross, Nicholas C.P., Hofmann, Wolf-Karsten, Sperr, Wolfgang R., García-Montero, Andrés C., Valent, Peter, Gotlib, Jason, Orfao, Alberto, Reiter, Andreas
Publicado 2019

Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms

por Tapper, William, Jones, Amy V., Kralovics, Robert, Harutyunyan, Ashot S., Zoi, Katerina, Leung, William, Godfrey, Anna L., Guglielmelli, Paola, Callaway, Alison, Ward, Daniel, Aranaz, Paula, White, Helen E., Waghorn, Katherine, Lin, Feng, Chase, Andrew, Joanna Baxter, E., Maclean, Cathy, Nangalia, Jyoti, Chen, Edwin, Evans, Paul, Short, Michael, Jack, Andrew, Wallis, Louise, Oscier, David, Duncombe, Andrew S., Schuh, Anna, Mead, Adam J., Griffiths, Michael, Ewing, Joanne, Gale, Rosemary E., Schnittger, Susanne, Haferlach, Torsten, Stegelmann, Frank, Döhner, Konstanze, Grallert, Harald, Strauch, Konstantin, Tanaka, Toshiko, Bandinelli, Stefania, Giannopoulos, Andreas, Pieri, Lisa, Mannarelli, Carmela, Gisslinger, Heinz, Barosi, Giovanni, Cazzola, Mario, Reiter, Andreas, Harrison, Claire, Campbell, Peter, Green, Anthony R., Vannucchi, Alessandro, Cross, Nicholas C.P.
Publicado 2015