Detalhe da pesquisa
1.
Cryptic aberrations may allow more accurate prognostic classification of patients with myelodysplastic syndromes and clonal evolution.
Genes Chromosomes Cancer
; 59(7): 396-405, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170980
2.
International cooperative study identifies treatment strategy in childhood ambiguous lineage leukemia.
Blood
; 132(3): 264-276, 2018 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29720486
3.
Implication of cytogenetic and molecular cytogenetic analysis in diagnosis of hematological malignancies in the era of the new sequencing techniques.
Cas Lek Cesk
; 158(1): 22-27, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31046388
4.
Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly.
Hum Mutat
; 39(5): 709-716, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29405539
5.
Association of unbalanced translocation der(1;7) with germline GATA2 mutations.
Blood
; 138(23): 2441-2445, 2021 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469508
6.
Differential expression of homologous recombination DNA repair genes in the early and advanced stages of myelodysplastic syndrome.
Eur J Haematol
; 99(4): 323-331, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28681469
7.
Mantle cell lymphoma-variant Richter syndrome: Detailed molecular-cytogenetic and backtracking analysis reveals slow evolution of a pre-MCL clone in parallel with CLL over several years.
Int J Cancer
; 139(10): 2252-60, 2016 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27407063
8.
Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups.
Cancer
; 122(24): 3821-3830, 2016 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27529519
9.
Fibroblast activation protein alpha is expressed by transformed and stromal cells and is associated with mesenchymal features in glioblastoma.
Tumour Biol
; 37(10): 13961-13971, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27492457
10.
Loss of B cells and their precursors is the most constant feature of GATA-2 deficiency in childhood myelodysplastic syndrome.
Haematologica
; 101(6): 707-16, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27013649
11.
Genetic and epigenetic characterization of low-grade gliomas reveals frequent methylation of the MLH3 gene.
Genes Chromosomes Cancer
; 54(11): 655-67, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26303387
12.
A high TP53 mutation burden is a strong predictor of primary refractory mantle cell lymphoma.
Br J Haematol
; 191(5): e103-e106, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32862455
13.
Genome-wide miRNA profiling in myelodysplastic syndrome with del(5q) treated with lenalidomide.
Eur J Haematol
; 95(1): 35-43, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25287904
14.
Rapidly progressing acute myeloid leukemia with KAT6A-LEUTX fusion in a newborn.
Pediatr Blood Cancer
; 67(10): e28663, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32779858
15.
[The prospects for children with acute lymphoblastic leukemia of being cured has increased in the Czech Republic in the 21st century to 90% - outcome of the ALL-IC BFM 2002 trial]. / Sance na vylécení detí s akutní lymfoblastickou leukémií stoupla v Ceské republicev 21. století na 90 % - výsledky studie ALL IC-BFM 2002.
Cas Lek Cesk
; 154(2): 79-89, 2015.
Artigo
em Cs
| MEDLINE | ID: mdl-25994910
16.
Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia.
Genes Chromosomes Cancer
; 52(7): 619-35, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23580398
17.
Single-dose cefixime 800 mg plus doxycycline 100 mg twice a day for 7 days compared with single-dose ceftriaxone 1 g plus single-dose azithromycin 2 g for treatment of urogenital, rectal, and pharyngeal gonorrhoea: a randomised clinical trial.
Clin Microbiol Infect
; 30(2): 211-215, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981059
18.
Cytogenomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals TCR rearrangements as predictive factors for exceptional prognosis.
Mol Cytogenet
; 17(1): 14, 2024 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38783324
19.
Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study.
Blood
; 117(26): 7102-11, 2011 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-21551233
20.
From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype.
Genes Chromosomes Cancer
; 51(5): 419-28, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22250017