147 related articles for article (PubMed ID: 14580769)
1. High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia.
Costa D; Queralt R; Aymerich M; Carrió A; Rozman M; Vallespí T; Colomer D; Nomdedeu B; Montserrat E; Campo E
Cancer Genet Cytogenet; 2003 Nov; 147(1):36-43. PubMed ID: 14580769
[TBL] [Abstract][Full Text] [Related]
2. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
Soulier J; Pierron G; Vecchione D; Garand R; Brizard F; Sigaux F; Stern MH; Aurias A
Genes Chromosomes Cancer; 2001 Jul; 31(3):248-54. PubMed ID: 11391795
[TBL] [Abstract][Full Text] [Related]
3. 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).
Dürig J; Bug S; Klein-Hitpass L; Boes T; Jöns T; Martin-Subero JI; Harder L; Baudis M; Dührsen U; Siebert R
Leukemia; 2007 Oct; 21(10):2153-63. PubMed ID: 17713554
[TBL] [Abstract][Full Text] [Related]
4. Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia.
Espinet B; Solé F; Salido M; Lloveras E; Abella E; Besses C; Serrano S; Woessner S; Florensa L
Haematologica; 2000 Jun; 85(6):607-12. PubMed ID: 10870117
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature.
Mossafa H; Brizard A; Huret JL; Brizard F; Lessard M; Guilhot F; Tanzer J
Br J Haematol; 1994 Apr; 86(4):780-5. PubMed ID: 7918072
[TBL] [Abstract][Full Text] [Related]
6. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.
Maljaei SH; Brito-Babapulle V; Hiorns LR; Catovsky D
Cancer Genet Cytogenet; 1998 Jun; 103(2):110-6. PubMed ID: 9614908
[TBL] [Abstract][Full Text] [Related]
7. T-cell prolymphocytic leukemia with hemorrhagic gastrointestinal involvement and a new chromosomal abnormality.
Toyota S; Nakamura N; Dan K
Int J Hematol; 2002 Apr; 75(3):314-7. PubMed ID: 11999363
[TBL] [Abstract][Full Text] [Related]
8. 14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia.
Kojima K; Kobayashi H; Imoto S; Nakagawa T; Matsui T; Kawachi Y; Oda K; Yano T; Kobayashi H; Noguchi M; Hara M; Oshimi K
Int J Hematol; 1998 Oct; 68(3):291-6. PubMed ID: 9846013
[TBL] [Abstract][Full Text] [Related]
9. Identification of two subgroups of mantle cell leukemia with distinct clinical and biological features.
Vizcarra E; Martínez-Climent JA; Benet I; Marugan I; Terol MJ; Prosper F; Marco J; Sanchez D; Ferrandez A; Tormo M; Sarsotti E; Ferrer R; García M; Ortuño F; Montagud M; García-Conde J
Hematol J; 2001; 2(4):234-41. PubMed ID: 11920255
[TBL] [Abstract][Full Text] [Related]
10. [Detection of chromosomal DNA imbalance in medulloblastoma by comparative genomic hybridization].
Sun YJ; Yu SZ; Sun CY; Wang Q; Jin SM; Wu WX; An TL
Zhonghua Bing Li Xue Za Zhi; 2010 Sep; 39(9):606-10. PubMed ID: 21092588
[TBL] [Abstract][Full Text] [Related]
11. Comparative genomic hybridization analysis of natural killer cell lymphoma/leukemia. Recognition of consistent patterns of genetic alterations.
Siu LL; Wong KF; Chan JK; Kwong YL
Am J Pathol; 1999 Nov; 155(5):1419-25. PubMed ID: 10550295
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetic aberrations in primary and recurrent fibrolamellar hepatocellular carcinoma detected by comparative genomic hybridization.
Wilkens L; Bredt M; Flemming P; Kubicka S; Klempnauer J; Kreipe H
Am J Clin Pathol; 2000 Dec; 114(6):867-74. PubMed ID: 11338475
[TBL] [Abstract][Full Text] [Related]
13. Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses.
Bentz M; Huck K; du Manoir S; Joos S; Werner CA; Fischer K; Döhner H; Lichter P
Blood; 1995 Jun; 85(12):3610-8. PubMed ID: 7780145
[TBL] [Abstract][Full Text] [Related]
14. Biallelic mutations in the ATM gene in T-prolymphocytic leukemia.
Stilgenbauer S; Schaffner C; Litterst A; Liebisch P; Gilad S; Bar-Shira A; James MR; Lichter P; Döhner H
Nat Med; 1997 Oct; 3(10):1155-9. PubMed ID: 9334731
[TBL] [Abstract][Full Text] [Related]
15. Complex karyotype in one patient with small cell variant of T-prolymphocytic leukemia. Analysis by G-banding and comparative genomic hybridization.
Odero MD; Matutes E; Valgañón M; Cigudosa JC; Bengoechea E; Calasanz MJ
Haematologica; 2001 Mar; 86(3):324-5. PubMed ID: 11255284
[No Abstract] [Full Text] [Related]
16. Multiple karyotypic abnormalities in three cases of small cell variant of T-cell prolymphocytic leukemia.
Heinonen K; Mahlamäki E; Hämäläinen E; Nousiainen T; Mononen I
Cancer Genet Cytogenet; 1994 Nov; 78(1):28-35. PubMed ID: 7987802
[TBL] [Abstract][Full Text] [Related]
17. Genomic aberrations in carcinomas of the uterine corpus.
Micci F; Teixeira MR; Haugom L; Kristensen G; Abeler VM; Heim S
Genes Chromosomes Cancer; 2004 Jul; 40(3):229-46. PubMed ID: 15139002
[TBL] [Abstract][Full Text] [Related]
18. Comparative genomic hybridization shows complex genomic changes of plasmacytoid urothelial carcinoma.
Keck B; Ellmann C; Stoehr R; Weigelt K; Goebell PJ; Kunath F; Taubert H; Hartmann A; Wullich B; Wach S
Urol Oncol; 2014 Nov; 32(8):1234-9. PubMed ID: 25087089
[TBL] [Abstract][Full Text] [Related]
19. Genotypic analysis of esophageal squamous cell carcinoma by molecular cytogenetics and real-time quantitative polymerase chain reaction.
Yen CC; Chen YJ; Lu KH; Hsia JY; Chen JT; Hu CP; Chen PM; Liu JH; Chiou TJ; Wang WS; Yang MH; Chao TC; Lin CH
Int J Oncol; 2003 Oct; 23(4):871-81. PubMed ID: 12963965
[TBL] [Abstract][Full Text] [Related]
20. Distinct chromosomal aberrations of ampulla of Vater and pancreatic head cancers detected by laser capture microdissection and comparative genomic hybridization.
Chang MC; Chang YT; Tien YW; Sun CT; Wu MS; Lin JT
Oncol Rep; 2005 Oct; 14(4):867-72. PubMed ID: 16142344
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]