Detalhe da pesquisa
1.
p53 activation during ribosome biogenesis regulates normal erythroid differentiation.
Blood
; 137(1): 89-102, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32818241
2.
Deciphering Potential Molecular Signatures to Differentiate Acute Myeloid Leukemia (AML) with BCR::ABL1 from Chronic Myeloid Leukemia (CML) in Blast Crisis.
Int J Mol Sci
; 24(20)2023 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37895120
3.
Germline DDX41 mutations define a significant entity within adult MDS/AML patients.
Blood
; 134(17): 1441-1444, 2019 10 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31484648
4.
Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells.
Haematologica
; 106(3): 746-758, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32327500
5.
De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia.
Clin Genet
; 98(4): 374-378, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32627184
6.
A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.
Blood
; 131(7): 717-732, 2018 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29146883
7.
A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis.
Genes Chromosomes Cancer
; 58(8): 595-601, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30779244
8.
CD13 expression in B cell malignancies is a hallmark of plasmacytic differentiation.
Br J Haematol
; 184(4): 625-633, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30198568
9.
Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.
Haematologica
; 104(6): 1244-1255, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30545930
10.
Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion.
Blood
; 127(6): 749-60, 2016 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26626993
11.
Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.
Blood
; 133(25): 2718-2724, 2019 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30914417
12.
Holding on to the Matutes score while dropping FMC7: new opportunity from standardised approaches in multiparameter flow cytometry.
Br J Haematol
; 190(4): e255-e258, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32557566
13.
Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression.
Blood
; 120(13): 2708-18, 2012 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22898599
14.
Flow cytometry thresholds of myeloperoxidase detection to discriminate between acute lymphoblastic or myeloblastic leukaemia.
Br J Haematol
; 161(4): 551-5, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23432206
15.
Plasma cell leukemia revealing a G6PD deficiency.
Blood
; 128(26): 3178, 2016 12 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-28034875
16.
Hairy cell leukemia with isolated bone lesions.
Clin Case Rep
; 11(5): e7343, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37207087
17.
Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.
Cell Stem Cell
; 30(2): 153-170.e9, 2023 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36736290
18.
Clonal dominance is an adverse prognostic factor in acute myeloid leukemia treated with intensive chemotherapy.
Leukemia
; 35(3): 712-723, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32581253
19.
Phenotypic landscape of granulocytes and monocytes by multiparametric flow cytometry: A prospective study of a 1-tube panel strategy for diagnosis and prognosis of patients with MDS.
Cytometry B Clin Cytom
; 98(3): 226-237, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31498561
20.
Emergence of secondary fusions in chronic myeloid leukemia as a driver of tyrosine kinase inhibitor resistance and blast crisis transformation.
Leuk Res
; 137: 107439, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38281466