Detalhe da pesquisa
1.
Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms.
Blood
; 119(5): 1208-13, 2012 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22053108
2.
Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes.
Blood
; 119(14): 3211-8, 2012 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-22343920
3.
EZH2 mutational status predicts poor survival in myelofibrosis.
Blood
; 118(19): 5227-34, 2011 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21921040
4.
Identification of FOXP1 and SNX2 as novel ABL1 fusion partners in acute lymphoblastic leukaemia.
Br J Haematol
; 153(1): 43-6, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21391972
5.
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms.
Blood
; 113(24): 6182-92, 2009 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-19387008
6.
Fusion of PDGFRB to two distinct loci at 3p21 and a third at 12q13 in imatinib-responsive myeloproliferative neoplasms.
Br J Haematol
; 148(2): 268-73, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20085582
7.
Transcription factor mutations in myelodysplastic/myeloproliferative neoplasms.
Haematologica
; 95(9): 1473-80, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20421268
8.
The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre-mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1.
Genes Chromosomes Cancer
; 47(5): 379-85, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18205209
9.
Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations.
PLoS One
; 9(1): e86940, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24497998
10.
Recurrent CEP85L-PDGFRB fusion in patient with t(5;6) and imatinib-responsive myeloproliferative neoplasm with eosinophilia.
Leuk Lymphoma
; 54(7): 1527-31, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23186533
11.
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Nat Genet
; 42(8): 722-6, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20601953