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108 related items for PubMed ID: 15770670

  • 1. Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis.
    Seng TJ, Ichimura K, Liu L, Tingby O, Pearson DM, Collins VP.
    Genes Chromosomes Cancer; 2005 Jun; 43(2):181-93. PubMed ID: 15770670
    [Abstract] [Full Text] [Related]

  • 2. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
    Selzer RR, Richmond TA, Pofahl NJ, Green RD, Eis PS, Nair P, Brothman AR, Stallings RL.
    Genes Chromosomes Cancer; 2005 Nov; 44(3):305-19. PubMed ID: 16075461
    [Abstract] [Full Text] [Related]

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  • 4. Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH.
    Ichimura K, Mungall AJ, Fiegler H, Pearson DM, Dunham I, Carter NP, Collins VP.
    Oncogene; 2006 Feb 23; 25(8):1261-71. PubMed ID: 16205629
    [Abstract] [Full Text] [Related]

  • 5. Loss of heterozygosity on chromosome 10q associated with malignancy and prognosis in astrocytic tumors, and discovery of novel loss regions.
    Daido S, Takao S, Tamiya T, Ono Y, Terada K, Ito S, Ouchida M, Date I, Ohmoto T, Shimizu K.
    Oncol Rep; 2004 Oct 23; 12(4):789-95. PubMed ID: 15375501
    [Abstract] [Full Text] [Related]

  • 6. Chromosome 8 BAC array comparative genomic hybridization and expression analysis identify amplification and overexpression of TRMT12 in breast cancer.
    Rodriguez V, Chen Y, Elkahloun A, Dutra A, Pak E, Chandrasekharappa S.
    Genes Chromosomes Cancer; 2007 Jul 23; 46(7):694-707. PubMed ID: 17440925
    [Abstract] [Full Text] [Related]

  • 7. Molecular pathogenesis of pediatric astrocytic tumors.
    Nakamura M, Shimada K, Ishida E, Higuchi T, Nakase H, Sakaki T, Konishi N.
    Neuro Oncol; 2007 Apr 23; 9(2):113-23. PubMed ID: 17327574
    [Abstract] [Full Text] [Related]

  • 8. Gene expression analysis of chromosomal regions with gain or loss of genetic material detected by comparative genomic hybridization.
    Meléndez B, Díaz-Uriarte R, Cuadros M, Martínez-Ramírez A, Fernández-Piqueras J, Dopazo A, Cigudosa JC, Rivas C, Dopazo J, Martínez-Delgado B, Benítez J.
    Genes Chromosomes Cancer; 2004 Dec 23; 41(4):353-65. PubMed ID: 15382261
    [Abstract] [Full Text] [Related]

  • 9. Fine mapping of chromosome 22q tumor suppressor gene candidate regions in astrocytoma.
    Hartmann C, Nümann A, Mueller W, Holtkamp N, Simon M, von Deimling A.
    Int J Cancer; 2004 Mar 01; 108(6):839-44. PubMed ID: 14712485
    [Abstract] [Full Text] [Related]

  • 10. Array comparative genomic hybridization identifies genetic subgroups in grade 4 human astrocytoma.
    Misra A, Pellarin M, Nigro J, Smirnov I, Moore D, Lamborn KR, Pinkel D, Albertson DG, Feuerstein BG.
    Clin Cancer Res; 2005 Apr 15; 11(8):2907-18. PubMed ID: 15837741
    [Abstract] [Full Text] [Related]

  • 11. Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.
    Díaz de Ståhl T, Hartmann C, de Bustos C, Piotrowski A, Benetkiewicz M, Mantripragada KK, Tykwinski T, von Deimling A, Dumanski JP.
    Genes Chromosomes Cancer; 2005 Oct 15; 44(2):161-9. PubMed ID: 15945096
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 8():53. PubMed ID: 17311676
    [Abstract] [Full Text] [Related]

  • 13. Genomewide screening of DNA copy number changes in chronic myelogenous leukemia with the use of high-resolution array-based comparative genomic hybridization.
    Hosoya N, Sanada M, Nannya Y, Nakazaki K, Wang L, Hangaishi A, Kurokawa M, Chiba S, Ogawa S.
    Genes Chromosomes Cancer; 2006 May 20; 45(5):482-94. PubMed ID: 16425296
    [Abstract] [Full Text] [Related]

  • 14. Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
    Gratias S, Rieder H, Ullmann R, Klein-Hitpass L, Schneider S, Bölöni R, Kappler M, Lohmann DR.
    Cancer Res; 2007 Jan 01; 67(1):408-16. PubMed ID: 17210724
    [Abstract] [Full Text] [Related]

  • 15. Pediatric supratentorial ependymomas show more frequent deletions on chromosome 9 than infratentorial ependymomas: a microsatellite analysis.
    Schneider D, Monoranu CM, Huang B, Rutkowski S, Gerber NU, Krauss J, Puppe B, Roggendorf W.
    Cancer Genet Cytogenet; 2009 Jun 01; 191(2):90-6. PubMed ID: 19446744
    [Abstract] [Full Text] [Related]

  • 16. Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer.
    Bergamaschi A, Kim YH, Wang P, Sørlie T, Hernandez-Boussard T, Lonning PE, Tibshirani R, Børresen-Dale AL, Pollack JR.
    Genes Chromosomes Cancer; 2006 Nov 01; 45(11):1033-40. PubMed ID: 16897746
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 11(23):8265-72. PubMed ID: 16322284
    [Abstract] [Full Text] [Related]

  • 18. Microsatellite instability analysis of primary human brain tumors.
    Zhu J, Guo SZ, Beggs AH, Maruyama T, Santarius T, Dashner K, Olsen N, Wu JK, Black P.
    Oncogene; 1996 Apr 04; 12(7):1417-23. PubMed ID: 8622857
    [Abstract] [Full Text] [Related]

  • 19. DNA copy number alterations in prostate cancers: a combined analysis of published CGH studies.
    Sun J, Liu W, Adams TS, Sun J, Li X, Turner AR, Chang B, Kim JW, Zheng SL, Isaacs WB, Xu J.
    Prostate; 2007 May 15; 67(7):692-700. PubMed ID: 17342750
    [Abstract] [Full Text] [Related]

  • 20. Co-amplification of 8p12 and 11q13 in breast cancers is not the result of a single genomic event.
    Paterson AL, Pole JC, Blood KA, Garcia MJ, Cooke SL, Teschendorff AE, Wang Y, Chin SF, Ylstra B, Caldas C, Edwards PA.
    Genes Chromosomes Cancer; 2007 May 15; 46(5):427-39. PubMed ID: 17285574
    [Abstract] [Full Text] [Related]

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