EZH2 in Myeloid Malignancies

por Rinke, Jenny, Chase, Andrew, Cross, Nicholas C. P., Hochhaus, Andreas, Ernst, Thomas
Publicado 2020

Mutational mechanisms of EZH2 inactivation in myeloid neoplasms

por Chase, Andrew, Score, Joannah, Lin, Feng, Bryant, Catherine, Waghorn, Katherine, Yapp, Sarah, Carreno-Tarragona, Gonzalo, Aranaz, Paula, Villasante, Aranzazu, Ernst, Thomas, Cross, Nicholas C. P.
Publicado 2020

Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activity

por Blakes, Alexander J. M., Gaul, Emily, Lam, Wayne, Shannon, Nora, Knapp, Karen M., Bicknell, Louise S., Jackson, Meremaihi R., Wade, Emma M., Robertson, Stephen, White, Susan M., Heller, Raoul, Chase, Andrew, Baralle, Diana, Douglas, Andrew G. L.
Publicado 2020

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age related clonal hematopoiesis and myeloid neoplasia

por Chase, Andrew, Pellagatti, Andrea, Singh, Shalini, Score, Joannah, Tapper, William J., Lin, Feng, Hoade, Yvette, Bryant, Catherine, Trim, Nicola, Yip, Bon Ham, Zoi, Katerina, Rasi, Chiara, Forsberg, Lars A., Dumanski, Jan P., Boultwood, Jacqueline, Cross, Nicholas C. P.
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

Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia

por Cross, Nicholas C. P., Hoade, Yvette, Tapper, William J., Carreno-Tarragona, Gonzalo, Fanelli, Tiziana, Jawhar, Mohamad, Naumann, Nicole, Pieniak, Iwo, Lübke, Johannes, Ali, Sahra, Bhuller, Kaljit, Burgstaller, Sonja, Cargo, Catherine, Cavenagh, Jamie, Duncombe, Andrew S., Das-Gupta, Emma, Evans, Paul, Forsyth, Peter, George, Philip, Grimley, Charlotte, Jack, Fergus, Munro, Laura, Mehra, Varun, Patel, Kavita, Rismani, Ali, Sciuccati, Gabriela, Thomas-Dewing, Rowena, Thornton, Patrick, Virchis, Andres, Watt, Simon, Wallis, Louise, Whiteway, Alastair, Zegocki, Kris, Bain, Barbara J., Reiter, Andreas, Chase, Andrew
Publicado 2018

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