[HTML][HTML] IRF4 gene rearrangements define a subgroup of CD30-positive cutaneous T-cell lymphoma: a study of 54 cases

A Pham-Ledard, M Prochazkova-Carlotti… - Journal of investigative …, 2010 - Elsevier
The identification of IFN regulatory factor 4 gene (IRF4) translocation in 8 out of 14 cases of
cutaneous anaplastic large cell lymphomas (C-ALCLs)(Leukemia, 2009; 23 (3): 574–80) …

Haploinsufficiency of the IKZF1 (IKAROS) tumor suppressor gene cooperates with BCR-ABL in a transgenic model of acute lymphoblastic leukemia

C Virely, S Moulin, C Cobaleda, C Lasgi, A Alberdi… - Leukemia, 2010 - nature.com
2 Bullrich F, Morris SW, Hummel M, Pileri S, Stein H, Croce CM. Nucleophosmin (NPM)
gene rearrangements in Ki-1-positive lymphomas. Cancer Res 1994; 54: 2873–2877. 3 …

Nodal marginal zone lymphoma: gene expression and miRNA profiling identify diagnostic markers and potential therapeutic targets

AJ Arribas, Y Campos-Martín… - Blood, The Journal …, 2012 - ashpublications.org
Nodal marginal zone lymphoma (NMZL) is a small B-cell neoplasm whose molecular
pathogenesis is still essentially unknown and whose differentiation from other small B-cell …

Finding recurrent copy number alteration regions: a review of methods

OM Rueda, R Diaz-Uriarte - Current Bioinformatics, 2010 - ingentaconnect.com
Copy number alterations (CNA) in genomic DNA are linked to a variety of human diseases.
Although many methods have been developed to analyze data from a single subject …

Characterization of breast cancer by array comparative genomic hybridization

J Climent, JL Garcia, JH Mao, J Arsuaga… - … and Cell Biology, 2007 - cdnsciencepub.com
Cancer progression is due to the accumulation of recurrent genomic alterations that induce
growth advantage and clonal expansion. Most of these genomic changes can be detected …

Genomic changes in progression of low-grade gliomas

A Idbaih, R Carvalho Silva, E Crinière, Y Marie… - Journal of neuro …, 2008 - Springer
Using a one-megabase BAC-based array comparative genomic hybridization technique
(aCGH), we have investigated a series of 16 low-grade gliomas (LGGs) and their …

Spatial normalization of array-CGH data

P Neuvial, P Hupé, I Brito, S Liva, É Manié… - BMC …, 2006 - Springer
Background Array-based comparative genomic hybridization (array-CGH) is a recently
developed technique for analyzing changes in DNA copy number. As in all microarray …

Clonal analysis of deletions on chromosome 20q and JAK2-V617F in MPD suggests that del20q acts independently and is not one of the predisposing mutations for …

FX Schaub, R Jäger, R Looser… - Blood, The Journal …, 2009 - ashpublications.org
We developed a real-time copy number polymerase chain reaction assay for deletions on
chromosome 20q (del20q), screened peripheral blood granulocytes from 664 patients with …

High-resolution array comparative genomic hybridization of single micrometastatic tumor cells

C Fuhrmann, O Schmidt-Kittler… - Nucleic acids …, 2008 - academic.oup.com
Only few selected cancer cells drive tumor progression and are responsible for therapy
resistance. Their specific genomic characteristics, however, are largely unknown because …

CGHweb: a tool for comparing DNA copy number segmentations from multiple algorithms

W Lai, V Choudhary, PJ Park - Bioinformatics, 2008 - academic.oup.com
Accurate estimation of DNA copy numbers from array comparative genomic hybridization
(CGH) data is important for characterizing the cancer genome. An important part of this …