Detalhe da pesquisa
1.
Correction: Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups.
Leukemia
; 33(9): 2342, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31316144
2.
Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
Leukemia
; 21(10): 2153-63, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17713554
3.
High expression of several tyrosine kinases and activation of the PI3K/AKT pathway in mediastinal large B cell lymphoma reveals further similarities to Hodgkin lymphoma.
Leukemia
; 21(4): 780-7, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17375124
4.
A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation.
Leukemia
; 21(7): 1532-44, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17495977
5.
Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups.
Leukemia
; 32(2): 573, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29160863
6.
Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups.
Leukemia
; 32(2): 332-342, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28584254
7.
Differentiation stage of myeloma plasma cells: biological and clinical significance.
Leukemia
; 31(2): 382-392, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27479184
8.
Disruption of the BCL11B gene through inv(14)(q11.2q32.31) results in the expression of BCL11B-TRDC fusion transcripts and is associated with the absence of wild-type BCL11B transcripts in T-ALL.
Leukemia
; 19(2): 201-8, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15668700
9.
Expression pattern of intracellular leukocyte-associated proteins in primary mediastinal B cell lymphoma.
Leukemia
; 19(5): 856-61, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15744341
10.
Detection of secondary genetic aberrations in follicle center cell derived lymphomas: assessment of the reliability of comparative genomic hybridization and standard chromosome analysis.
Leukemia
; 15(1): 177-83, 2001 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11243387
11.
Molecular cytogenetic detection of chromosomal breakpoints in T-cell receptor gene loci.
Leukemia
; 17(4): 738-45, 2003 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12682631
12.
Segmental chromosomal aberrations and centrosome amplifications: pathogenetic mechanisms in Hodgkin and Reed-Sternberg cells of classical Hodgkin's lymphoma?
Leukemia
; 17(11): 2214-9, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14523479
13.
A B-cell epigenetic signature defines three biologic subgroups of chronic lymphocytic leukemia with clinical impact.
Leukemia
; 29(3): 598-605, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25151957
14.
Molecular cytogenetic analysis of chromosomal breakpoints in the IGH, MYC, BCL6, and MALT1 gene loci in primary cutaneous B-cell lymphomas.
J Invest Dermatol
; 123(1): 213-9, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15191563
15.
Cytogenetic and molecular characterization of simultaneous chronic and acute myelocytic leukemia.
Cancer Genet Cytogenet
; 142(1): 80-2, 2003 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12660040
16.
Amplification of ERBB2, RARA, and TOP2A genes in a myelodysplastic syndrome transforming to acute myeloid leukemia.
Cancer Genet Cytogenet
; 127(2): 174-6, 2001 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-11425459
17.
Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL.
Cancer Genet Cytogenet
; 130(1): 8-13, 2001 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11672767
18.
Insertion (22;9)(q11;q34q21) in a patient with chronic myeloid leukemia characterized by fluorescence in situ hybridization.
Cancer Genet Cytogenet
; 125(2): 167-70, 2001 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11369063
19.
Towards defining the lymphoma methylome.
Leukemia
; 20(10): 1658-60, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17041636
20.
Partial uniparental disomy: a recurrent genetic mechanism alternative to chromosomal deletion in malignant lymphoma.
Leukemia
; 20(5): 904-5, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16511509