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Journal Abstract Search


170 related items for PubMed ID: 3274085

  • 1. A rearranged transforming gene, tre, is made up of human sequences derived from chromosome regions 5q, 17q and 18q.
    Huebner K, Cannizzaro LA, Nakamura T, Hillova J, Mariage-Samson R, Hecht F, Hill M, Croce CM.
    Oncogene; 1988 Oct; 3(4):449-55. PubMed ID: 3274085
    [Abstract] [Full Text] [Related]

  • 2. The human tropomyosin gene involved in the generation of the TRK oncogene maps to chromosome 1q31.
    Radice P, Sozzi G, Miozzo M, De Benedetti V, Cariani T, Bongarzone I, Spurr NK, Pierotti MA, Della Porta G.
    Oncogene; 1991 Nov; 6(11):2145-8. PubMed ID: 1834975
    [Abstract] [Full Text] [Related]

  • 3. The FGF-related oncogene, K-FGF, maps to human chromosome region 11q13, possibly near int-2.
    Huebner K, Ferrari AC, Delli Bovi P, Croce CM, Basilico C.
    Oncogene Res; 1988 Nov; 3(3):263-70. PubMed ID: 3060803
    [Abstract] [Full Text] [Related]

  • 4. The human erg gene maps to chromosome 21, band q22: relationship to the 8; 21 translocation of acute myelogenous leukemia.
    Rao VN, Modi WS, Drabkin HD, Patterson D, O'Brien SJ, Papas TS, Reddy ES.
    Oncogene; 1988 Nov; 3(5):497-500. PubMed ID: 3274086
    [Abstract] [Full Text] [Related]

  • 5. Rearrangement of the human tre oncogene by homologous recombination between Alu repeats of nucleotide sequences from two different chromosomes.
    Onno M, Nakamura T, Hillova J, Hill M.
    Oncogene; 1992 Dec; 7(12):2519-23. PubMed ID: 1461655
    [Abstract] [Full Text] [Related]

  • 6. Isolation and fluorescence in situ hybridization mapping of 60 cosmid clones on human chromosome 18.
    Nakashima H, Sakai M, Inaba R, Imamura T.
    Genomics; 1994 Feb; 19(3):577-80. PubMed ID: 8188303
    [Abstract] [Full Text] [Related]

  • 7. Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes.
    Johnson CV, Cool DE, Glaccum MB, Green N, Fischer EH, Bruskin A, Hill DE, Lawrence JB.
    Genomics; 1993 Jun; 16(3):619-29. PubMed ID: 8325634
    [Abstract] [Full Text] [Related]

  • 8. An oncogenic chromosome 8-9 gene fusion isolated following transfection of human ovarian carcinoma cell line DNA.
    Halverson D, Modi W, Dean M, Gelmann EP, Dunn KJ, Clanton D, Oskarsson M, O'Brien SJ, Blair DG.
    Oncogene; 1990 Jul; 5(7):1085-9. PubMed ID: 1973829
    [Abstract] [Full Text] [Related]

  • 9. Loss of the chromosomal region 5q11-q31 in the myeloid cell line HL-60: characterization by comparative genomic hybridization and fluorescence in situ hybridization.
    Shipley J, Weber-Hall S, Birdsall S.
    Genes Chromosomes Cancer; 1996 Mar; 15(3):182-6. PubMed ID: 8721684
    [Abstract] [Full Text] [Related]

  • 10. Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes.
    Van Keuren ML, Stewart GD, Bradley CM, Kurnit DM, Neve RL, Watkins PC, Tanzi RE, Gusella JF, Patterson D.
    Am J Med Genet; 1989 Jul; 33(3):369-75. PubMed ID: 2529766
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  • 15. Human ros1 and mas1 oncogenes located in regions of chromosome 6 associated with tumor-specific rearrangements.
    Rabin M, Birnbaum D, Young D, Birchmeier C, Wigler M, Ruddle FH.
    Oncogene Res; 1987 Jul; 1(2):169-78. PubMed ID: 3329713
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  • 16. Regional mapping panels for chromosomes 3, 4, 5, 11, 15, 17, 18, and X.
    Leonard JC, Drwinga HL, Kim CH, Toji LH, Bender PK, Mulivor RA, Beck JC.
    Genomics; 1997 Dec 15; 46(3):530-4. PubMed ID: 9441767
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  • 17. Regional localization of 32 NotI-HindIII fragments from a human chromosome 13 library by a somatic cell hybrid panel and in situ hybridization.
    Warburton D, Yu MT, Tantravahi U, Lee C, Cayanis E, Russo J, Fischer SG.
    Genomics; 1993 May 15; 16(2):355-60. PubMed ID: 8314575
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  • 19. Molecular evolution of ets genes from avians to mammals and their cytogenetic localization to regions involved in leukemia.
    Papas TS, Watson DK, Sacchi N, O'Brien SJ, Ascione R.
    Gene Amplif Anal; 1986 May 15; 4():207-38. PubMed ID: 3333359
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  • 20. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
    Lau CC, Harris CP, Lu XY, Perlaky L, Gogineni S, Chintagumpala M, Hicks J, Johnson ME, Davino NA, Huvos AG, Meyers PA, Healy JH, Gorlick R, Rao PH.
    Genes Chromosomes Cancer; 2004 Jan 15; 39(1):11-21. PubMed ID: 14603437
    [Abstract] [Full Text] [Related]


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