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Journal Abstract Search

67 related items for PubMed ID: 8222756

  • 1. Detection of amplified sequences at 5q11-->q13 in a homogenously staining region found by fluorescent in situ hybridization in a case of B-cell non-Hodgkin's lymphoma.
    Wlodarska I, De Wolf-Peeters C, Dierick H, Hilliker C, Thomas J, Mecucci C, Cassiman JJ, Van den Berghe H.
    Cytogenet Cell Genet; 1994; 65(3):179-83. PubMed ID: 8222756
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  • 3. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
    Dierlamm J, Wlodarska I, Michaux L, Vermeesch JR, Meeus P, Stul M, Criel A, Verhoef G, Thomas J, Delannoy A, Louwagie A, Cassiman JJ, Mecucci C, Hagemeijer A, Van den Berghe H.
    Genes Chromosomes Cancer; 1997 Oct; 20(2):155-66. PubMed ID: 9331566
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  • 4. Rapid detection, cloning and molecular cytogenetic characterisation of sequences from an MRP-encoding amplicon by chromosome microdissection.
    Ray ME, Guan XY, Slovak ML, Trent JM, Meltzer PS.
    Br J Cancer; 1994 Jul; 70(1):85-90. PubMed ID: 8018546
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  • 7. Hybrid selection of transcribed sequences from microdissected DNA: isolation of genes within amplified region at 20q11-q13.2 in breast cancer.
    Guan XY, Xu J, Anzick SL, Zhang H, Trent JM, Meltzer PS.
    Cancer Res; 1996 Aug 01; 56(15):3446-50. PubMed ID: 8758910
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  • 9. Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization.
    Gisselsson D, Höglund M, Mertens F, Mitelman F, Mandahl N.
    Genes Chromosomes Cancer; 1998 Nov 01; 23(3):203-12. PubMed ID: 9790500
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  • 10. Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes.
    Kanda N, Schreck R, Alt F, Bruns G, Baltimore D, Latt S.
    Proc Natl Acad Sci U S A; 1983 Jul 01; 80(13):4069-73. PubMed ID: 6575396
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  • 11. DNA amplification at 11q13.5-q14 in human breast cancer.
    Szepetowski P, Ollendorff V, Grosgeorge J, Courseaux A, Birnbaum D, Theillet C, Gaudray P.
    Oncogene; 1992 Dec 01; 7(12):2513-7. PubMed ID: 1461654
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  • 12. DNA sequence amplification in human prostate cancer identified by chromosome microdissection: potential prognostic implications.
    Van Den Berg C, Guan XY, Von Hoff D, Jenkins R, Bittner, Griffin C, Kallioniemi O, Visakorpi, McGill, Herath J.
    Clin Cancer Res; 1995 Jan 01; 1(1):11-8. PubMed ID: 9815882
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  • 13. Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions.
    Muleris M, Almeida A, Gerbault-Seureau M, Malfoy B, Dutrillaux B.
    Genes Chromosomes Cancer; 1995 Nov 01; 14(3):155-63. PubMed ID: 8589031
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  • 14. Amplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaks.
    Singer MJ, Mesner LD, Friedman CL, Trask BJ, Hamlin JL.
    Proc Natl Acad Sci U S A; 2000 Jul 05; 97(14):7921-6. PubMed ID: 10859355
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  • 18. A YAC contig of the region containing the spinal muscular atrophy gene (SMA): identification of an unstable region.
    Carpten JD, DiDonato CJ, Ingraham SE, Wagner-McPherson C, Nieuwenhuijsen BW, Wasmuth JJ, Burghes AH.
    Genomics; 1994 Nov 15; 24(2):351-6. PubMed ID: 7698758
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  • 19. 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
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  • 20. Detection of 11q13 amplification as the origin of a homogeneously staining region in small cell lung cancer by chromosome microdissection.
    Xu J, Tyan T, Cedrone E, Savaraj N, Wang N.
    Genes Chromosomes Cancer; 1996 Nov 01; 17(3):172-8. PubMed ID: 8946196
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