Detalhe da pesquisa
1.
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotype.
Genes Chromosomes Cancer
; 60(6): 452-457, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486841
2.
Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol.
Genes Chromosomes Cancer
; 59(11): 667-671, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32592278
3.
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants.
Int J Cancer
; 144(11): 2683-2694, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30426508
4.
Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.
Br J Haematol
; 155(2): 209-17, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21848520
5.
Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Genes Chromosomes Cancer
; 49(10): 885-900, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20589934
6.
BCR-ABL1 positive AML or CML in blast crisis? A pediatric case report with inv(3) and t(9;22) in the initial clone.
Cancer Genet
; 254-255: 70-74, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33647814
7.
Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease.
Genes Chromosomes Cancer
; 47(6): 471-80, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18311775
8.
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas.
Haematologica
; 92(4): 460-8, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17488656
9.
GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families.
Genes Cancer
; 8(1-2): 472-483, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28435519
10.
Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency.
Haematologica
; 96(12): 1892-4, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21880633
11.
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase.
Sci Rep
; 6: 38198, 2016 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27910942
12.
Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?
Haematologica
; 95(9): 1616, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20460640
13.
Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia.
Haematologica
; 90(11): 1484-92, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16266895
14.
Array-CGH in childhood MDS.
Methods Mol Biol
; 973: 267-78, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23412796
15.
Induced G1 phase arrest of fast-dividing cells improves the quality of genomic profiles generated by array-CGH.
Biotechniques
; 53(4): 245-8, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23046508
16.
Analysis of array-CGH data using the R and Bioconductor software suite.
Comp Funct Genomics
; : 201325, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19696946
17.
Replication timing influences DNA copy number determination by array-CGH.
Biotechniques
; 55(5): 231-2, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24245784
18.
No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21-21q22.
Leuk Res
; 37(6): 721-3, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23498976
19.
Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization.
Clin Gastroenterol Hepatol
; 4(10): 1283-91, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16979954