316 related articles for article (PubMed ID: 17363583)
1. Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.
Stark M; Hayward N
Cancer Res; 2007 Mar; 67(6):2632-42. PubMed ID: 17363583
[TBL] [Abstract][Full Text] [Related]
2. Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis.
Gorringe KL; Ramakrishna M; Williams LH; Sridhar A; Boyle SE; Bearfoot JL; Li J; Anglesio MS; Campbell IG
Genes Chromosomes Cancer; 2009 Oct; 48(10):931-42. PubMed ID: 19603523
[TBL] [Abstract][Full Text] [Related]
3. Somatic alterations in the melanoma genome: a high-resolution array-based comparative genomic hybridization study.
Gast A; Scherer D; Chen B; Bloethner S; Melchert S; Sucker A; Hemminki K; Schadendorf D; Kumar R
Genes Chromosomes Cancer; 2010 Aug; 49(8):733-45. PubMed ID: 20544847
[TBL] [Abstract][Full Text] [Related]
4. Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development.
Pollock PM; Welch J; Hayward NK
Cancer Res; 2001 Feb; 61(3):1154-61. PubMed ID: 11221846
[TBL] [Abstract][Full Text] [Related]
5. Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.
Jönsson G; Dahl C; Staaf J; Sandberg T; Bendahl PO; Ringnér M; Guldberg P; Borg A
Oncogene; 2007 Jul; 26(32):4738-48. PubMed ID: 17260012
[TBL] [Abstract][Full Text] [Related]
6. Integrated analysis of copy number alterations and loss of heterozygosity in human pancreatic cancer using a high-resolution, single nucleotide polymorphism array.
Lin LJ; Asaoka Y; Tada M; Sanada M; Nannya Y; Tanaka Y; Tateishi K; Ohta M; Seto M; Sasahira N; Tada M; Kawabe T; Zheng CQ; Kanai F; Ogawa S; Omata M
Oncology; 2008; 75(1-2):102-12. PubMed ID: 18787345
[TBL] [Abstract][Full Text] [Related]
7. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
8. "Lineage addiction" in human cancer: lessons from integrated genomics.
Garraway LA; Weir BA; Zhao X; Widlund H; Beroukhim R; Berger A; Rimm D; Rubin MA; Fisher DE; Meyerson ML; Sellers WR
Cold Spring Harb Symp Quant Biol; 2005; 70():25-34. PubMed ID: 16869735
[TBL] [Abstract][Full Text] [Related]
9. Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis.
Ross CW; Ouillette PD; Saddler CM; Shedden KA; Malek SN
Clin Cancer Res; 2007 Aug; 13(16):4777-85. PubMed ID: 17699855
[TBL] [Abstract][Full Text] [Related]
10. Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9.
Kumar R; Angelini S; Hemminki K
Oncogene; 2003 Dec; 22(58):9217-24. PubMed ID: 14681681
[TBL] [Abstract][Full Text] [Related]
11. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
[TBL] [Abstract][Full Text] [Related]
12. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.
Gaasenbeek M; Howarth K; Rowan AJ; Gorman PA; Jones A; Chaplin T; Liu Y; Bicknell D; Davison EJ; Fiegler H; Carter NP; Roylance RR; Tomlinson IP
Cancer Res; 2006 Apr; 66(7):3471-9. PubMed ID: 16585170
[TBL] [Abstract][Full Text] [Related]
13. Single nucleotide polymorphism array analysis of cancer.
Dutt A; Beroukhim R
Curr Opin Oncol; 2007 Jan; 19(1):43-9. PubMed ID: 17133111
[TBL] [Abstract][Full Text] [Related]
14. Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
Calhoun ES; Hucl T; Gallmeier E; West KM; Arking DE; Maitra A; Iacobuzio-Donahue CA; Chakravarti A; Hruban RH; Kern SE
Cancer Res; 2006 Aug; 66(16):7920-8. PubMed ID: 16912165
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide allelotype study of primary glioblastoma multiforme.
Hu J; Jiang C; Ng HK; Pang JC; Tong CY; Chen S
Chin Med J (Engl); 2003 Apr; 116(4):577-83. PubMed ID: 12875726
[TBL] [Abstract][Full Text] [Related]
16. Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.
Langdon JA; Lamont JM; Scott DK; Dyer S; Prebble E; Bown N; Grundy RG; Ellison DW; Clifford SC
Genes Chromosomes Cancer; 2006 Jan; 45(1):47-60. PubMed ID: 16149064
[TBL] [Abstract][Full Text] [Related]
17. High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines.
Jänne PA; Li C; Zhao X; Girard L; Chen TH; Minna J; Christiani DC; Johnson BE; Meyerson M
Oncogene; 2004 Apr; 23(15):2716-26. PubMed ID: 15048096
[TBL] [Abstract][Full Text] [Related]
18. Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.
Gunnarsson R; Staaf J; Jansson M; Ottesen AM; Göransson H; Liljedahl U; Ralfkiaer U; Mansouri M; Buhl AM; Smedby KE; Hjalgrim H; Syvänen AC; Borg A; Isaksson A; Jurlander J; Juliusson G; Rosenquist R
Genes Chromosomes Cancer; 2008 Aug; 47(8):697-711. PubMed ID: 18484635
[TBL] [Abstract][Full Text] [Related]
19. Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays.
Zhou X; Rao NP; Cole SW; Mok SC; Chen Z; Wong DT
Cancer Genet Cytogenet; 2005 May; 159(1):53-7. PubMed ID: 15860358
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide amplification and allelotyping of sporadic pituitary adenomas identify novel regions of genetic loss.
Simpson DJ; Bicknell EJ; Buch HN; Cutty SJ; Clayton RN; Farrell WE
Genes Chromosomes Cancer; 2003 Jul; 37(3):225-36. PubMed ID: 12759921
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
