257 related articles for article (PubMed ID: 24441149)
21. Identification of novel fusion genes with 28S ribosomal DNA in hematologic malignancies.
Kobayashi S; Taki T; Nagoshi H; Chinen Y; Yokokawa Y; Kanegane H; Matsumoto Y; Kuroda J; Horiike S; Nishida K; Taniwaki M
Int J Oncol; 2014 Apr; 44(4):1193-8. PubMed ID: 24504345
[TBL] [Abstract][Full Text] [Related]
22. HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32).
Su XY; Della-Valle V; Andre-Schmutz I; Lemercier C; Radford-Weiss I; Ballerini P; Lessard M; Lafage-Pochitaloff M; Mugneret F; Berger R; Romana SP; Bernard OA; Penard-Lacronique V
Blood; 2006 Dec; 108(13):4198-201. PubMed ID: 16926283
[TBL] [Abstract][Full Text] [Related]
23. Low expression of T-cell transcription factor BCL11b predicts inferior survival in adult standard risk T-cell acute lymphoblastic leukemia patients.
Bartram I; Gökbuget N; Schlee C; Heesch S; Fransecky L; Schwartz S; Stuhlmann R; Schäfer-Eckhart K; Starck M; Reichle A; Hoelzer D; Baldus CD; Neumann M
J Hematol Oncol; 2014 Jul; 7():51. PubMed ID: 25023966
[TBL] [Abstract][Full Text] [Related]
24. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
[TBL] [Abstract][Full Text] [Related]
25. Diagnostic challenge of identifying cases with recurrent t(8;14)(q24.21;q32.2) Involving
Bendig S; Stengel A; Walter W; Meggendorfer M; Baer C; Müller ML; Haferlach T; Kern W; Haferlach C
Leuk Lymphoma; 2022 Mar; 63(3):747-750. PubMed ID: 34738838
[No Abstract] [Full Text] [Related]
26. Novel and Rare Fusion Transcripts Involving Transcription Factors and Tumor Suppressor Genes in Acute Myeloid Leukemia.
Padella A; Simonetti G; Paciello G; Giotopoulos G; Baldazzi C; Righi S; Ghetti M; Stengel A; Guadagnuolo V; De Tommaso R; Papayannidis C; Robustelli V; Franchini E; Rorà AGLD; Ferrari A; Fontana MC; Bruno S; Ottaviani E; Soverini S; Storlazzi CT; Haferlach C; Sabattini E; Testoni N; Iacobucci I; Huntly BJP; Ficarra E; Martinelli G
Cancers (Basel); 2019 Dec; 11(12):. PubMed ID: 31817495
[TBL] [Abstract][Full Text] [Related]
27. A new complex rearrangement involving the ETV6, LOC115548, and MN1 genes in a case of acute myeloid leukemia.
Belloni E; Trubia M; Mancini M; Derme V; Nanni M; Lahortiga I; Riccioni R; Confalonieri S; Lo-Coco F; Di Fiore PP; Pelicci PG
Genes Chromosomes Cancer; 2004 Nov; 41(3):272-7. PubMed ID: 15334551
[TBL] [Abstract][Full Text] [Related]
28. Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.
Ma ESK; Wan TSK; Au CH; Ho DN; Ma SY; Ng MHL; Chan TL
Cancer Genet; 2017 Dec; 218-219():15-19. PubMed ID: 29153093
[TBL] [Abstract][Full Text] [Related]
29. Characterization of oncogene dysregulation in multiple myeloma by combined FISH and DNA microarray analyses.
Fabris S; Agnelli L; Mattioli M; Baldini L; Ronchetti D; Morabito F; Verdelli D; Nobili L; Intini D; Callea V; Stelitano C; Lombardi L; Neri A
Genes Chromosomes Cancer; 2005 Feb; 42(2):117-27. PubMed ID: 15543617
[TBL] [Abstract][Full Text] [Related]
30. Recurrent breakpoints in 14q32.13/TCL1A region in mature B-cell neoplasms with villous lymphocytes.
Urbankova H; Baens M; Michaux L; Tousseyn T; Rack K; Katrincsakova B; Ferreiro JF; van Loo P; de Kelver W; Dierickx D; Demuynck H; Delannoy A; Verschuere J; Jarošová M; de Wolf-Peeters C; Vandenberghe P; Wlodarska I
Leuk Lymphoma; 2012 Dec; 53(12):2449-55. PubMed ID: 22553924
[TBL] [Abstract][Full Text] [Related]
31. TCL1 oncogene activation in preleukemic T cells from a case of ataxia-telangiectasia.
Narducci MG; Virgilio L; Isobe M; Stoppacciaro A; Elli R; Fiorilli M; Carbonari M; Antonelli A; Chessa L; Croce CM; Russo G
Blood; 1995 Sep; 86(6):2358-64. PubMed ID: 7662982
[TBL] [Abstract][Full Text] [Related]
32. ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events.
Haferlach C; Bacher U; Schnittger S; Alpermann T; Zenger M; Kern W; Haferlach T
Genes Chromosomes Cancer; 2012 Apr; 51(4):328-37. PubMed ID: 22162288
[TBL] [Abstract][Full Text] [Related]
33. Cytogenetic findings in acute biphenotypic leukaemia.
Carbonell F; Swansbury J; Min T; Matutes E; Farahat N; Buccheri V; Morilla R; Secker-Walker L; Catovsky D
Leukemia; 1996 Aug; 10(8):1283-7. PubMed ID: 8709632
[TBL] [Abstract][Full Text] [Related]
34. Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings.
Watanabe N; Kobayashi H; Ichiji O; Yoshida MA; Kikuta A; Komada Y; Sekine I; Ishida Y; Horiukoshi Y; Tsunematsu Y; Yano M; Nakadate H; Kaneko Y
Leukemia; 2003 May; 17(5):876-82. PubMed ID: 12750700
[TBL] [Abstract][Full Text] [Related]
35. Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations.
Kühn MW; Bullinger L; Gröschel S; Krönke J; Edelmann J; Rücker FG; Eiwen K; Paschka P; Gaidzik VI; Holzmann K; Schlenk RF; Döhner H; Döhner K
Haematologica; 2014 Aug; 99(8):e133-5. PubMed ID: 24859875
[No Abstract] [Full Text] [Related]
36. Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases.
Haferlach C; Bacher U; Grossmann V; Schindela S; Zenger M; Kohlmann A; Kern W; Haferlach T; Schnittger S
Genes Chromosomes Cancer; 2012 Dec; 51(12):1079-85. PubMed ID: 22887804
[TBL] [Abstract][Full Text] [Related]
37. Down regulation of BCL11B expression inhibits proliferation and induces apoptosis in malignant T cells by BCL11B-935-siRNA.
Huang X; Chen S; Shen Q; Chen S; Yang L; Grabarczyk P; Przybylski GK; Schmidt CA; Li Y
Hematology; 2011 Jul; 16(4):236-42. PubMed ID: 21756541
[TBL] [Abstract][Full Text] [Related]
38. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
[TBL] [Abstract][Full Text] [Related]
39. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
De Braekeleer E; Douet-Guilbert N; Le Bris MJ; Morel F; Férec C; De Braekeleer M
Cancer Genet Cytogenet; 2008 Aug; 185(1):47-50. PubMed ID: 18656694
[TBL] [Abstract][Full Text] [Related]
40. t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH).
Berger R; Dastugue N; Busson M; Van Den Akker J; Pérot C; Ballerini P; Hagemeijer A; Michaux L; Charrin C; Pages MP; Mugneret F; Andrieux J; Talmant P; Hélias C; Mauvieux L; Lafage-Pochitaloff M; Mozziconacci MJ; Cornillet-Lefebvre P; Radford I; Asnafi V; Bilhou-Nabera C; Nguyen Khac F; Léonard C; Speleman F; Poppe B; Bastard C; Taviaux S; Quilichini B; Herens C; Grégoire MJ; Cavé H; Bernard OA;
Leukemia; 2003 Sep; 17(9):1851-7. PubMed ID: 12970786
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]