512 related articles for article (PubMed ID: 15298715)
21. Increased number of chromosomal imbalances and high-level DNA amplifications in mantle cell lymphoma are associated with blastoid variants.
Beà S; Ribas M; Hernández JM; Bosch F; Pinyol M; Hernández L; García JL; Flores T; González M; López-Guillermo A; Piris MA; Cardesa A; Montserrat E; Miró R; Campo E
Blood; 1999 Jun; 93(12):4365-74. PubMed ID: 10361135
[TBL] [Abstract][Full Text] [Related]
22. Identification of novel candidate target genes in amplicons of Glioblastoma multiforme tumors detected by expression and CGH microarray profiling.
Ruano Y; Mollejo M; Ribalta T; Fiaño C; Camacho FI; Gómez E; de Lope AR; Hernández-Moneo JL; Martínez P; Meléndez B
Mol Cancer; 2006 Sep; 5():39. PubMed ID: 17002787
[TBL] [Abstract][Full Text] [Related]
23. Ring chromosomes in parosteal osteosarcoma contain sequences from 12q13-15: a combined cytogenetic and comparative genomic hybridization study.
Szymanska J; Mandahl N; Mertens F; Tarkkanen M; Karaharju E; Knuutila S
Genes Chromosomes Cancer; 1996 May; 16(1):31-4. PubMed ID: 9162194
[TBL] [Abstract][Full Text] [Related]
24. Identification of CCND3 and BYSL as candidate targets for the 6p21 amplification in diffuse large B-cell lymphoma.
Kasugai Y; Tagawa H; Kameoka Y; Morishima Y; Nakamura S; Seto M
Clin Cancer Res; 2005 Dec; 11(23):8265-72. PubMed ID: 16322284
[TBL] [Abstract][Full Text] [Related]
25. Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.
Heidenblad M; Jonson T; Mahlamäki EH; Gorunova L; Karhu R; Johansson B; Höglund M
Genes Chromosomes Cancer; 2002 Jun; 34(2):211-23. PubMed ID: 11979555
[TBL] [Abstract][Full Text] [Related]
26. Genomic DNA-chip hybridization reveals a higher incidence of genomic amplifications in pancreatic cancer than conventional comparative genomic hybridization and leads to the identification of novel candidate genes.
Holzmann K; Kohlhammer H; Schwaenen C; Wessendorf S; Kestler HA; Schwoerer A; Rau B; Radlwimmer B; Döhner H; Lichter P; Gress T; Bentz M
Cancer Res; 2004 Jul; 64(13):4428-33. PubMed ID: 15231651
[TBL] [Abstract][Full Text] [Related]
27. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
Weiss MM; Snijders AM; Kuipers EJ; Ylstra B; Pinkel D; Meuwissen SG; van Diest PJ; Albertson DG; Meijer GA
J Pathol; 2003 Jul; 200(3):320-6. PubMed ID: 12845628
[TBL] [Abstract][Full Text] [Related]
28. Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal- and microsatellite-unstable sporadic colorectal carcinomas.
Lassmann S; Weis R; Makowiec F; Roth J; Danciu M; Hopt U; Werner M
J Mol Med (Berl); 2007 Mar; 85(3):293-304. PubMed ID: 17143621
[TBL] [Abstract][Full Text] [Related]
29. Detection of oncogene amplifications in medulloblastomas by comparative genomic hybridization and array-based comparative genomic hybridization.
Tong CY; Hui AB; Yin XL; Pang JC; Zhu XL; Poon WS; Ng HK
J Neurosurg; 2004 Feb; 100(2 Suppl Pediatrics):187-93. PubMed ID: 14758948
[TBL] [Abstract][Full Text] [Related]
30. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
[TBL] [Abstract][Full Text] [Related]
31. Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization.
van Duin M; van Marion R; Watson JE; Paris PL; Lapuk A; Brown N; Oseroff VV; Albertson DG; Pinkel D; de Jong P; Nacheva EP; Dinjens W; van Dekken H; Collins C
Cytometry A; 2005; 63(1):10-9. PubMed ID: 15619731
[TBL] [Abstract][Full Text] [Related]
32. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.
Bayani J; Zielenska M; Pandita A; Al-Romaih K; Karaskova J; Harrison K; Bridge JA; Sorensen P; Thorner P; Squire JA
Genes Chromosomes Cancer; 2003 Jan; 36(1):7-16. PubMed ID: 12461745
[TBL] [Abstract][Full Text] [Related]
33. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D
Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
[TBL] [Abstract][Full Text] [Related]
34. Molecular classification of human gliomas using matrix-based comparative genomic hybridization.
Roerig P; Nessling M; Radlwimmer B; Joos S; Wrobel G; Schwaenen C; Reifenberger G; Lichter P
Int J Cancer; 2005 Oct; 117(1):95-103. PubMed ID: 15880582
[TBL] [Abstract][Full Text] [Related]
35. Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
Heidenblad M; Schoenmakers EF; Jonson T; Gorunova L; Veltman JA; van Kessel AG; Höglund M
Cancer Res; 2004 May; 64(9):3052-9. PubMed ID: 15126341
[TBL] [Abstract][Full Text] [Related]
36. Analysis of segmental duplications, mouse genome synteny and recurrent cancer-associated amplicons in human chromosome 6p21-p12.
Martin JW; Yoshimoto M; Ludkovski O; Thorner PS; Zielenska M; Squire JA; Nuin PA
Cytogenet Genome Res; 2010 Jun; 128(4):199-213. PubMed ID: 20453501
[TBL] [Abstract][Full Text] [Related]
37. Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.
Veltman JA; Fridlyand J; Pejavar S; Olshen AB; Korkola JE; DeVries S; Carroll P; Kuo WL; Pinkel D; Albertson D; Cordon-Cardo C; Jain AN; Waldman FM
Cancer Res; 2003 Jun; 63(11):2872-80. PubMed ID: 12782593
[TBL] [Abstract][Full Text] [Related]
38. High-resolution analysis of DNA copy number alterations in colorectal cancer by array-based comparative genomic hybridization.
Nakao K; Mehta KR; Fridlyand J; Moore DH; Jain AN; Lafuente A; Wiencke JW; Terdiman JP; Waldman FM
Carcinogenesis; 2004 Aug; 25(8):1345-57. PubMed ID: 15001537
[TBL] [Abstract][Full Text] [Related]
39. Identification of chromosomal aberrations associated with disease progression and a novel 3q13.31 deletion involving LSAMP gene in osteosarcoma.
Yen CC; Chen WM; Chen TH; Chen WY; Chen PC; Chiou HJ; Hung GY; Wu HT; Wei CJ; Shiau CY; Wu YC; Chao TC; Tzeng CH; Chen PM; Lin CH; Chen YJ; Fletcher JA
Int J Oncol; 2009 Oct; 35(4):775-88. PubMed ID: 19724913
[TBL] [Abstract][Full Text] [Related]
40. DNA copy number changes in alveolar soft part sarcoma: a comparative genomic hybridization study.
Kiuru-Kuhlefelt S; El-Rifai W; Sarlomo-Rikala M; Knuutila S; Miettinen M
Mod Pathol; 1998 Mar; 11(3):227-31. PubMed ID: 9521467
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]