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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
BAXTER, E, SCOTT, L, CAMPBELL, P, EAST, C, FOUROUCLAS, N, SWANTON, S, VASSILIOU, G, BENCH, A, BOYD, E, CURTIN, N
Published in The Lancet (British edition) (25.03.2005)
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Lung cancer Intragenic ERBB2 kinase mutations in tumours
Futreal, P. Andrew, Stephens, Philip, Hunter, Chris, Bignell, Graham, Edkins, Sarah, Davies, Helen, Teague, Jon, Stevens, Claire, O'Meara, Sarah, Smith, Raffaella, Parker, Adrian, Barthorpe, Andy, Blow, Matthew, Brackenbury, Lisa, Butler, Adam, Clarke, Oliver, Cole, Jennifer, Dicks, Ed, Dike, Angus, Drozd, Anja, Edwards, Ken, Forbes, Simon, Foster, Rebecca, Gray, Kristian, Greenman, Chris, Halliday, Kelly, Hills, Katy, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andy, Perry, Janet, Petty, Robert, Raine, Keiran, Ratford, Lewis, Shepherd, Rebecca, Small, Alexandra, Stephens, Yvonne, Tofts, Calli, Varian, Jennifer, West, Sofie, Widaa, Sara, Yates, Andrew, Brasseur, Francis, Cooper, Colin S, Flanagan, Adrienne M, Knowles, Margaret, Leung, Suet Y, Louis, David N, Looijenga, Leendert H. J, Malkowicz, Bruce, Pierotti, Marco A, Teh, Bin, Chenevix-Trench, Georgia, Weber, Barbara L, Yuen, Siu T, Harris, Grace, Goldstraw, Peter, Nicholson, Andrew G, Wooster, Richard, Stratton, Michael R
Published in Nature (30.09.2004)
Published in Nature (30.09.2004)
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Intragenic ERBB2 kinase mutations in tumours
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Published in Nature (London) (30.09.2004)
Published in Nature (London) (30.09.2004)
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Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor
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Published in American journal of human genetics (01.02.2007)
Published in American journal of human genetics (01.02.2007)
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Haploinsufficiency of RPS14 in 5q− syndrome is associated with deregulation of ribosomal‐ and translation‐related genes
Pellagatti, Andrea, Hellström‐Lindberg, Eva, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Della Porta, Matteo G., Jädersten, Martin, Killick, Sally, Fidler, Carrie, Cazzola, Mario, Wainscoat, James S., Boultwood, Jacqueline
Published in British journal of haematology (01.07.2008)
Published in British journal of haematology (01.07.2008)
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Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus
Raymond, F. Lucy, Tarpey, Patrick S., Edkins, Sarah, Tofts, Calli, O’Meara, Sarah, Teague, Jon, Butler, Adam, Stevens, Claire, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Dicks, Ed, Gray, Kristian, Halliday, Kelly, Hills, Katy, Hinton, Jonathon, Jones, David, Menzies, Andrew, Perry, Janet, Raine, Keiran, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, Widaa, Sara, Mallya, Uma, Moon, Jenny, Luo, Ying, Shaw, Marie, Boyle, Jackie, Kerr, Bronwyn, Turner, Gillian, Quarrell, Oliver, Cole, Trevor, Easton, Douglas F., Wooster, Richard, Bobrow, Martin, Schwartz, Charles E., Gecz, Jozef, Stratton, Michael R., Futreal, P. Andrew
Published in American journal of human genetics (01.05.2007)
Published in American journal of human genetics (01.05.2007)
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Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly
Field, Michael, Tarpey, Patrick S., Smith, Raffaella, Edkins, Sarah, O’Meara, Sarah, Stevens, Claire, Tofts, Calli, Teague, Jon, Butler, Adam, Dicks, Ed, Barthorpe, Syd, Buck, Gemma, Cole, Jennifer, Gray, Kristian, Halliday, Kelly, Hills, Katy, Jenkinson, Andrew, Jones, David, Menzies, Andrew, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alexandra, Varian, Jennifer, West, Sofie, Widaa, Sara, Mallya, Uma, Wooster, Richard, Moon, Jenny, Luo, Ying, Hughes, Helen, Shaw, Marie, Friend, Kathryn L., Corbett, Mark, Turner, Gillian, Partington, Michael, Mulley, John, Bobrow, Martin, Schwartz, Charles, Stevenson, Roger, Gecz, Jozef, Stratton, Michael R., Andrew Futreal, P., Lucy Raymond, F.
Published in American journal of human genetics (01.08.2007)
Published in American journal of human genetics (01.08.2007)
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Identification of Gene Expression Based Prognostic Markers in the Hematopoietic Stem Cells of Patients with Myelodysplastic Syndromes
Pellagatti, Andrea, Benner, Axel, Mills, Ken I, Cazzola, Mario, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Della Porta, Matteo G, Jadersten, Martin, Verma, Amit, McDonald, Emma-Jane, Killick, Sally, Hellstrom-Lindberg, Eva, Bullinger, Lars, Wainscoat, James S, Boultwood, Jacqueline
Published in Blood (16.11.2012)
Published in Blood (16.11.2012)
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Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
Fernandez-Mercado, Marta, Pellagatti, Andrea, Perry, Janet, Fernandez-Santamaria, Cristina, Calasanz, Maria J., Larrayoz, Maria J., Odero, Maria D., Killick, Sally, Wainscoat, James S., Boultwood, Jacqueline
Published in Blood (19.11.2010)
Published in Blood (19.11.2010)
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Marked down‐regulation of nucleophosmin‐1 is associated with advanced del(5q) myelodysplastic syndrome
Pellagatti, Andrea, Cazzola, Mario, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Della Porta, Matteo G., Jädersten, Martin, Killick, Sally, Vyas, Paresh, Hellström‐Lindberg, Eva, Wainscoat, James S., Boultwood, Jacqueline
Published in British journal of haematology (01.10.2011)
Published in British journal of haematology (01.10.2011)
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Journal Article
Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
Pellagatti, Andrea, Cazzola, Mario, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Porta, Matteo G. Della, Jädersten, Martin, Killick, Sally, Vyas, Paresh, Hellström-Lindberg, Eva, Boultwood, Jacqueline, Wainscoat, James S.
Published in Blood (19.11.2010)
Published in Blood (19.11.2010)
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Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
Pellagatti, Andrea, Cazzola, Mario, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Porta, Matteo G Della, Jädersten, Martin, Killick, Sally, Verma, Amit, Hellström-Lindberg, Eva, Wainscoat, James S, Boultwood, Jacqueline
Published in Blood (20.11.2009)
Published in Blood (20.11.2009)
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Journal Article
Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
Boultwood, Jacqueline, Perry, Janet, Pellagatti, Andrea, Giagounidis, Aristoteles, Malcovati, Luca, Porta, Matteo G Della, Jädersten, Martin, Killick, Sally, Hellström-Lindberg, Eva, Cazzola, Mario, Wainscoat, James S
Published in Blood (20.11.2009)
Published in Blood (20.11.2009)
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Journal Article
Haploinsufficiency of RPS14 and Deregulation of Ribosomal- and Translation-Related Genes in MDS Patients with Del(5q)
Pellagatti, Andrea, Hellström-Lindberg, Eva, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Porta, Matteo Della, Jädersten, Martin, Killick, Sally, Sohal, Davendra P., Verma, Amit, Cazzola, Mario, Wainscoat, James S., Boultwood, Jacqueline
Published in Blood (16.11.2008)
Published in Blood (16.11.2008)
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Journal Article
Gene Expression Profiling of CD34+ Cells in Patients with Myelodysplastic Syndromes
Pellagatti, Andrea, Cazzola, Mario, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Porta, Matteo Della, Jädersten, Martin, Killick, Sally, Hellström-Lindberg, Eva, Wainscoat, James S., Boultwood, Jacqueline
Published in Blood (16.11.2008)
Published in Blood (16.11.2008)
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