Detalhe da pesquisa
1.
Constitutional and acquired genetic variants in ARID5B in pediatric B-cell precursor acute lymphoblastic leukemia.
Genes Chromosomes Cancer
; 63(5): e23242, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38738968
2.
Postnatal origin of the chromosomal gains in older patients with high hyperdiploid acute lymphoblastic leukemia.
Haematologica
; 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38356456
3.
Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multi-center study.
Haematologica
; 106(1): 87-97, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31974198
4.
NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients.
BMC Cancer
; 13: 274, 2013 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23734977
5.
Short telomere length is associated with NOTCH1/SF3B1/TP53 aberrations and poor outcome in newly diagnosed chronic lymphocytic leukemia patients.
Am J Hematol
; 88(8): 647-51, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23620080
6.
Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia.
Nat Commun
; 14(1): 1658, 2023 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36966135
7.
Next generation RNA-sequencing in prognostic subsets of chronic lymphocytic leukemia.
Am J Hematol
; 87(7): 737-40, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22674506
8.
LPL is the strongest prognostic factor in a comparative analysis of RNA-based markers in early chronic lymphocytic leukemia.
Haematologica
; 96(8): 1153-60, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21508119
9.
Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia.
Haematologica
; 96(8): 1161-9, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21546498
10.
High-density screening reveals a different spectrum of genomic aberrations in chronic lymphocytic leukemia patients with 'stereotyped' IGHV3-21 and IGHV4-34 B-cell receptors.
Haematologica
; 95(9): 1519-25, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20421269
11.
Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.
Genes Chromosomes Cancer
; 47(8): 697-711, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18484635
12.
Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.
Leukemia
; 32(10): 2117-2125, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29626196
13.
Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia.
Leukemia
; 36(6): 1681-1684, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35365774
14.
Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing.
Leukemia
; 35(5): 1485-1489, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864028
15.
Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic lymphocytic leukemia.
J Exp Med
; 212(6): 833-43, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25987724
16.
Exploring the genetic landscape in chronic lymphocytic leukemia using high-resolution technologies.
Leuk Lymphoma
; 54(8): 1583-90, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23167608
17.
Prognostic markers and their clinical applicability in chronic lymphocytic leukemia: where do we stand?
Leuk Lymphoma
; 54(11): 2351-64, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23480493
18.
IGHV3-21 gene frequency in a Swedish cohort of patients with newly diagnosed chronic lymphocytic leukemia.
Clin Lymphoma Myeloma Leuk
; 12(3): 201-6, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22464020
19.
TP53 Mutations are infrequent in newly diagnosed chronic lymphocytic leukemia.
Leuk Res
; 35(2): 272-4, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20870288
20.
Lack of association between the MDM2 promoter polymorphism SNP309 and clinical outcome in chronic lymphocytic leukemia.
Leuk Res
; 34(3): 335-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19573916