Detalhe da pesquisa
1.
Critical evaluation of molecular tumour board outcomes following 2 years of clinical practice in a Comprehensive Cancer Centre.
Br J Cancer
; 128(6): 1134-1147, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36572733
2.
Acute megakaryoblastic leukaemia shows high frequency of chromosome 1q aberrations and dismal outcome.
Br J Haematol
; 202(6): 1165-1177, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37455345
3.
Targeting intracellular WT1 in AML with a novel RMF-peptide-MHC-specific T-cell bispecific antibody.
Blood
; 138(25): 2655-2669, 2021 12 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34280257
4.
Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia.
Blood
; 128(5): 686-98, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27288520
5.
Genetics of acute myeloid leukemia in the elderly: mutation spectrum and clinical impact in intensively treated patients aged 75 years or older.
Haematologica
; 103(11): 1853-1861, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29903761
6.
A 29-gene and cytogenetic score for the prediction of resistance to induction treatment in acute myeloid leukemia.
Haematologica
; 103(3): 456-465, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29242298
7.
Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Genes Chromosomes Cancer
; 56(1): 75-86, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636548
8.
Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis.
Haematologica
; 102(1): 130-138, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27561722
9.
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations.
Blood
; 121(23): 4749-52, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23603912
10.
Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia.
Blood
; 122(10): 1761-9, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23878140
11.
GATA2 zinc finger 1 mutations associated with biallelic CEBPA mutations define a unique genetic entity of acute myeloid leukemia.
Blood
; 120(2): 395-403, 2012 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-22649106
12.
Relapse of acute myeloid leukemia after allogeneic stem cell transplantation is associated with gain of WT1 alterations and high mutation load.
Haematologica
; 103(12): e581-e584, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29954937
13.
RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes.
Haematologica
; 97(12): 1909-15, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22689681
14.
Clinical presentation and differential splicing of SRSF2, U2AF1 and SF3B1 mutations in patients with acute myeloid leukemia.
Leukemia
; 34(10): 2621-2634, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32358566
15.
Toll-like receptor 7/8-matured RNA-transduced dendritic cells as post-remission therapy in acute myeloid leukaemia: results of a phase I trial.
Clin Transl Immunology
; 9(3): e1117, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32153780
16.
Validation and refinement of the revised 2017 European LeukemiaNet genetic risk stratification of acute myeloid leukemia.
Leukemia
; 34(12): 3161-3172, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32231256
17.
The clinical mutatome of core binding factor leukemia.
Leukemia
; 34(6): 1553-1562, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31896782
18.
Allelic Imbalance of Recurrently Mutated Genes in Acute Myeloid Leukaemia.
Sci Rep
; 9(1): 11796, 2019 08 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31409822
19.
Genetic heterogeneity of cytogenetically normal AML with mutations of CEBPA.
Blood Adv
; 2(20): 2724-2731, 2018 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30337300
20.
Persistence of pre-leukemic clones during first remission and risk of relapse in acute myeloid leukemia.
Leukemia
; 32(7): 1598-1608, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29472724