TGFα expression in myeloid malignancies

Por Kavanagh, Simon, Mirzai, Bob, Fuller, Kathy, Erber, Wendy N
Publicado no J Clin Pathol (2016)

Somatic mutations in glioblastoma are associated with methylguanine-DNA methyltransferase methylation

Por MCDONALD, KERRIE L., TABONE, TANIA, NOWAK, ANNA K., ERBER, WENDY N.
Publicado no Oncol Lett (2015)

How I treat essential thrombocythemia

Por Beer, Philip A., Erber, Wendy N., Campbell, Peter J., Green, Anthony R.
Publicado em 2010

Reticulin Accumulation in Essential Thrombocythemia: Prognostic Significance and Relationship to Therapy

Por Campbell, Peter J., Bareford, David, Erber, Wendy N., Wilkins, Bridget S., Wright, Penny, Buck, Georgina, Wheatley, Keith, Harrison, Claire N., Green, Anthony R.
Publicado em 2009

Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms

Por Malherbe, Jacques A J, Fuller, Kathryn A, Mirzai, Bob, Kavanagh, Simon, So, Chi-Chiu, Ip, Ho-Wan, Guo, Belinda B, Forsyth, Cecily, Howman, Rebecca, Erber, Wendy N
Publicado no J Clin Pathol (2016)

Megakaryocytes in Myeloproliferative Neoplasms Have Unique Somatic Mutations

Por Guo, Belinda B., Allcock, Richard J., Mirzai, Bob, Malherbe, Jacques A., Choudry, Fizzah A., Frontini, Mattia, Chuah, Hun, Liang, James, Kavanagh, Simon E., Howman, Rebecca, Ouwehand, Willem H., Fuller, Kathryn A., Erber, Wendy N.
Publicado no Am J Pathol (2017)

Can cytoplasmic nucleophosmin be detected by immunocytochemical staining of cell smears in acute myeloid leukemia?

Por Mattsson, Göran, Turner, Susan H., Cordell, Jacqueline, Ferguson, David J.P., Schuh, Anna, Grimwade, Lizz F., Bench, Anthony J., Weinberg, Olga K., Marafioti, Teresa, George, Tracy I., Arber, Daniel A., Erber, Wendy N., Mason, David Y.
Publicado em 2010

The scl +18/19 Stem Cell Enhancer Is Not Required for Hematopoiesis: Identification of a 5′ Bifunctional Hematopoietic-Endothelial Enhancer Bound by Fli-1 and Elf-1

Por Göttgens, Berthold, Broccardo, Cyril, Sanchez, Maria-Jose, Deveaux, Sophie, Murphy, George, Göthert, Joachim R., Kotsopoulou, Ekaterini, Kinston, Sarah, Delaney, Liz, Piltz, Sandie, Barton, Linda M., Knezevic, Kathy, Erber, Wendy N., Begley, C. Glenn, Frampton, Jonathan, Green, Anthony R.
Publicado em 2004

JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis

Por Scott, Linda M., Tong, Wei, Levine, Ross L., Scott, Mike A., Beer, Philip A., Stratton, Michael R., Futreal, P. Andrew, Erber, Wendy N., McMullin, Mary Frances, Harrison, Claire N., Warren, Alan J., Gilliland, D. Gary, Lodish, Harvey F., Green, Anthony R.
Publicado em 2007

JAK2 V617F impairs hematopoietic stem cell function in a conditional knock-in mouse model of JAK2 V617F–positive essential thrombocythemia

Por Li, Juan, Spensberger, Dominik, Ahn, Jong Sook, Anand, Shubha, Beer, Philip A., Ghevaert, Cedric, Chen, Edwin, Forrai, Ariel, Scott, Linda M., Ferreira, Rita, Campbell, Peter J., Watson, Steve P., Liu, Pentao, Erber, Wendy N., Huntly, Brian J. P., Ottersbach, Katrin, Green, Anthony R.
Publicado em 2010

Disruption of IKAROS activity in primitive chronic-phase CML cells mimics myeloid disease progression

Por Beer, Philip A., Knapp, David J. H. F., Miller, Paul H., Kannan, Nagarajan, Sloma, Ivan, Heel, Kathy, Babovic, Sonja, Bulaeva, Elizabeth, Rabu, Gabrielle, Terry, Jefferson, Druker, Brian J., Loriaux, Marc M., Loeb, Keith R., Radich, Jerald P., Erber, Wendy N., Eaves, Connie J.
Publicado no Blood (2015)

Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease

Por Royo, Cristina, Navarro, Alba, Clot, Guillem, Salaverria, Itziar, Giné, Eva, Jares, Pedro, Colomer, Dolors, Wiestner, Adrian, Wilson, Wyndham H., Vegliante, Maria Carmela, Fernandez, Veronica, Hartmann, Elena M., Trim, Nicola, Erber, Wendy N., Swerdlow, Steven H., Klapper, Wolfram, Dyer, Martin J.S., Vargas-Pabón, Manuel, Ott, German, Rosenwald, Andreas, Siebert, Reiner, López-Guillermo, Armando, Campo, Elías, Beà, Sílvia
Publicado em 2012

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

Por Westbury, Sarah K, Turro, Ernest, Greene, Daniel, Lentaigne, Claire, Kelly, Anne M, Bariana, Tadbir K, Simeoni, Ilenia, Pillois, Xavier, Attwood, Antony, Austin, Steve, Jansen, Sjoert BG, Bakchoul, Tamam, Crisp-Hihn, Abi, Erber, Wendy N, Favier, Rémi, Foad, Nicola, Gattens, Michael, Jolley, Jennifer D, Liesner, Ri, Meacham, Stuart, Millar, Carolyn M, Nurden, Alan T, Peerlinck, Kathelijne, Perry, David J, Poudel, Pawan, Schulman, Sol, Schulze, Harald, Stephens, Jonathan C, Furie, Bruce, Robinson, Peter N, van Geet, Chris, Rendon, Augusto, Gomez, Keith, Laffan, Michael A, Lambert, Michele P, Nurden, Paquita, Ouwehand, Willem H, Richardson, Sylvia, Mumford, Andrew D, Freson, Kathleen
Publicado no Genome Med (2015)

Transcriptional diversity during lineage commitment of human blood progenitors

Por Chen, Lu, Kostadima, Myrto, Martens, Joost H.A., Canu, Giovanni, Garcia, Sara P., Turro, Ernest, Downes, Kate, Macaulay, Iain C., Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert B.G., Astle, William J., Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C., Consortium, BRIDGE, Choudry, Fizzah A., Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N., Jansen, Joop H., Favier, Rémi, Fenech, Matthew E., Foad, Nicola, Freson, Kathleen, van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M., Kerstens, Hindrik H.D., Kooner, Jaspal S., Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A., Richardson, David, Sammut, Stephen J., Slodkowicz, Greg, Tamuri, Asif U., Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J., Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H., Stunnenberg, Hendrik G., Frontini, Mattia, Rendon, Augusto
Publicado no Science (2014)