Detalhe da pesquisa
1.
Aberrant MNX1 expression associated with t(7;12)(q36;p13) pediatric acute myeloid leukemia induces the disease through altering histone methylation.
Haematologica
; 109(3): 725-739, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37317878
2.
An induced pluripotent stem cell t(7;12)(q36;p13) acute myeloid leukemia model shows high expression of MNX1 and a block in differentiation of the erythroid and megakaryocytic lineages.
Int J Cancer
; 151(5): 770-782, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35583991
3.
ASXL1 mutations, previous vascular complications and age at diagnosis predict survival in 85 WHO-defined polycythaemia vera patients.
Br J Haematol
; 189(5): 913-919, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32066200
4.
International external quality assurance of JAK2 V617F quantification.
Ann Hematol
; 98(5): 1111-1118, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30535576
5.
Acute myeloid leukemia (AML) with t(7;12)(q36;p13) is associated with infancy and trisomy 19: Data from Nordic Society for Pediatric Hematology and Oncology (NOPHO-AML) and review of the literature.
Genes Chromosomes Cancer
; 57(7): 359-365, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29569294
6.
Micro-ribonucleic acid-155 is a direct target of Meis1, but not a driver in acute myeloid leukemia.
Haematologica
; 103(2): 246-255, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29217774
7.
The aldehyde dehydrogenase cord blood potency assay excludes early apoptotic cells.
Transfusion
; 58(6): 1452-1457, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29516519
8.
Patient-tailored analysis of minimal residual disease in acute myeloid leukemia using next-generation sequencing.
Eur J Haematol
; 98(1): 26-37, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27197529
9.
Exploring the heterogeneity of the hematopoietic stem and progenitor cell pool in cord blood: simultaneous staining for side population, aldehyde dehydrogenase activity, and CD34 expression.
Transfusion
; 55(6): 1283-9, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25647229
10.
Molecular diagnostics of myeloproliferative neoplasms.
Eur J Haematol
; 95(4): 270-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25951317
11.
Impact of ABCB1 single nucleotide polymorphisms 1236C>T and 2677G>T on overall survival in FLT3 wild-type de novo AML patients with normal karyotype.
Br J Haematol
; 167(5): 671-80, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25155901
12.
Monocytic AML cells inactivate antileukemic lymphocytes: role of NADPH oxidase/gp91(phox) expression and the PARP-1/PAR pathway of apoptosis.
Blood
; 119(24): 5832-7, 2012 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22550344
13.
Prognostic implications of mutations in NOTCH1 and FBXW7 in childhood T-ALL treated according to the NOPHO ALL-1992 and ALL-2000 protocols.
Pediatr Blood Cancer
; 61(3): 424-30, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24424791
14.
Role of NOX2 for leukaemic expansion in a murine model of BCR-ABL1+ leukaemia.
Br J Haematol
; 182(2): 290-294, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28542840
15.
Reduced expression of NLRP3 and MEFV in human ischemic heart tissue.
Biochem Biophys Res Commun
; 430(1): 425-8, 2013 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23206693
16.
Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemia.
Blood
; 118(22): 5905-13, 2011 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21967978
17.
Comprehensive analysis of mammalian miRNA* species and their role in myeloid cells.
Blood
; 118(12): 3350-8, 2011 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-21628414
18.
High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols.
Haematologica
; 98(9): 1424-32, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23645689
19.
Decreased survival in normal karyotype AML with single-nucleotide polymorphisms in genes encoding the AraC metabolizing enzymes cytidine deaminase and 5'-nucleotidase.
Am J Hematol
; 88(12): 1001-6, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23873772
20.
High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
Genes Chromosomes Cancer
; 51(2): 196-206, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22072402