Detalhe da pesquisa
1.
Single-cell analysis identifies CRLF2 rearrangements as both early and late events in Down syndrome and non-Down syndrome acute lymphoblastic leukaemia.
Leukemia
; 33(4): 893-904, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30487598
2.
High-resolution analysis of DNA replication domain organization across an R/G-band boundary.
Mol Cell Biol
; 17(10): 6157-66, 1997 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-9315676
3.
The MLL recombinome of acute leukemias.
Leukemia
; 20(5): 777-84, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16511515
4.
Overexpression of the pseudoautosomal gene MIC2 in Ewing's sarcoma and peripheral primitive neuroectodermal tumor.
Oncogene
; 5(7): 1067-70, 1990 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-1695726
5.
A novel putative tyrosine kinase receptor with oncogenic potential.
Oncogene
; 6(11): 2113-20, 1991 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-1834974
6.
Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL.
Oncogene
; 20(23): 2900-7, 2001 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-11420702
7.
PAX5/ETV6 fusion defines cytogenetic entity dic(9;12)(p13;p13).
Leukemia
; 17(6): 1121-3, 2003 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-12764378
8.
RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications.
Leukemia
; 18(6): 1115-21, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15085163
9.
Regression and progression in neuroblastoma. Does genetics predict tumour behaviour?
Eur J Cancer
; 31A(4): 510-5, 1995.
Artigo
em Inglês
| MEDLINE | ID: mdl-7576955
10.
Neuroblastoma cells can actively eliminate supernumerary MYCN gene copies by micronucleus formation--sign of tumour cell revertance?
Eur J Cancer
; 33(12): 2043-9, 1997 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-9516850
11.
Diagnostic value of the molecular genetic detection of the t(11;22) translocation in Ewing's tumours.
Virchows Arch
; 425(2): 107-12, 1994.
Artigo
em Inglês
| MEDLINE | ID: mdl-7524975
12.
Translocation (12;13) in a case of infantile fibrosarcoma.
Cancer Genet Cytogenet
; 71(1): 94-6, 1993 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-8275459
13.
Isochromosome 12p and maternal loss of 1p36 in a pediatric testicular germ cell tumor.
Cancer Genet Cytogenet
; 91(2): 95-100, 1996 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-8944752
14.
An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome.
Leukemia
; 28(5): 1015-21, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24166298
15.
Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia.
Leukemia
; 21(3): 584-6, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17215856
16.
Spliced MLL fusions: a novel mechanism to generate functional chimeric MLL-MLLT1 transcripts in t(11;19)(q23;p13.3) leukemia.
Leukemia
; 21(3): 588-90, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17252016
17.
Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia.
Leukemia
; 23(1): 134-43, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19020546
18.
New insights to the MLL recombinome of acute leukemias.
Leukemia
; 23(8): 1490-9, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19262598
19.
All-trans retinoic acid and arsenic trioxide resistance of acute promyelocytic leukemia with the variant STAT5B-RARA fusion gene.
Leukemia
; 27(7): 1606-10, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23271512
20.
Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma.
Cytogenet Cell Genet
; 63(1): 24-8, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8449033