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121 related items for PubMed ID: 11063795

  • 1. Unusual breakpoint distribution of 8p abnormalities in T-prolymphocytic leukemia: a study with YACS mapping to 8p11-p12.
    Sorour A, Brito-Babapulle V, Smedley D, Yuille M, Catovsky D.
    Cancer Genet Cytogenet; 2000 Sep; 121(2):128-32. PubMed ID: 11063795
    [Abstract] [Full Text] [Related]

  • 2. Abnormalities of chromosome band 8p11 in leukemia: two clinical syndromes can be distinguished on the basis of MOZ involvement.
    Aguiar RC, Chase A, Coulthard S, Macdonald DH, Carapeti M, Reiter A, Sohal J, Lennard A, Goldman JM, Cross NC.
    Blood; 1997 Oct 15; 90(8):3130-5. PubMed ID: 9376594
    [Abstract] [Full Text] [Related]

  • 3. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.
    Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D.
    Cancer Genet Cytogenet; 1998 Jun 15; 103(2):110-6. PubMed ID: 9614908
    [Abstract] [Full Text] [Related]

  • 4. Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia.
    Salomon-Nguyen F, Brizard F, Le Coniat M, Radford I, Berger R, Brizard A.
    Leukemia; 1998 Jun 15; 12(6):972-5. PubMed ID: 9639428
    [Abstract] [Full Text] [Related]

  • 5. Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome.
    Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Gonçalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC.
    Blood; 1998 Sep 01; 92(5):1735-42. PubMed ID: 9716603
    [Abstract] [Full Text] [Related]

  • 6. Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization.
    Chernova O, Still I, Kalaycio M, Hoeltge G, Cowell JK.
    Genes Chromosomes Cancer; 1998 Feb 01; 21(2):160-5. PubMed ID: 9491328
    [Abstract] [Full Text] [Related]

  • 7. Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 Mbp region of chromosome 13.
    Kempski H, MacDonald D, Michalski AJ, Roberts T, Goldman JM, Cross NC, Cowell JK.
    Genes Chromosomes Cancer; 1995 Apr 01; 12(4):283-7. PubMed ID: 7539283
    [Abstract] [Full Text] [Related]

  • 8. Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
    Dürig J, Bug S, Klein-Hitpass L, Boes T, Jöns T, Martin-Subero JI, Harder L, Baudis M, Dührsen U, Siebert R.
    Leukemia; 2007 Oct 01; 21(10):2153-63. PubMed ID: 17713554
    [Abstract] [Full Text] [Related]

  • 9. Identification of four new translocations involving FGFR1 in myeloid disorders.
    Sohal J, Chase A, Mould S, Corcoran M, Oscier D, Iqbal S, Parker S, Welborn J, Harris RI, Martinelli G, Montefusco V, Sinclair P, Wilkins BS, van den Berg H, Vanstraelen D, Goldman JM, Cross NC.
    Genes Chromosomes Cancer; 2001 Oct 01; 32(2):155-63. PubMed ID: 11550283
    [Abstract] [Full Text] [Related]

  • 10. Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature.
    Mossafa H, Brizard A, Huret JL, Brizard F, Lessard M, Guilhot F, Tanzer J.
    Br J Haematol; 1994 Apr 01; 86(4):780-5. PubMed ID: 7918072
    [Abstract] [Full Text] [Related]

  • 11. Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder.
    Smedley D, Somers G, Venter D, Chow CW, Cooper C, Shipley J.
    Genes Chromosomes Cancer; 1998 Jan 01; 21(1):70-3. PubMed ID: 9443043
    [Abstract] [Full Text] [Related]

  • 12. t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.
    Chaffanet M, Popovici C, Leroux D, Jacrot M, Adélaïde J, Dastugue N, Grégoire MJ, Hagemeijer A, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ.
    Oncogene; 1998 Feb 19; 16(7):945-9. PubMed ID: 9484786
    [Abstract] [Full Text] [Related]

  • 13. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.
    Wilke CM, Guo SW, Hall BK, Boldog F, Gemmill RM, Chandrasekharappa SC, Barcroft CL, Drabkin HA, Glover TW.
    Genomics; 1994 Jul 15; 22(2):319-26. PubMed ID: 7806217
    [Abstract] [Full Text] [Related]

  • 14. Identification of a yeast artificial chromosome spanning the 8q12 translocation breakpoint in pleomorphic adenomas with t(3;8)(p21;q12).
    Röijer E, Kas K, Klawitz I, Bullerdiek J, Van de Ven W, Stenman G.
    Genes Chromosomes Cancer; 1996 Nov 15; 17(3):166-71. PubMed ID: 8946195
    [Abstract] [Full Text] [Related]

  • 15. Loss of heterozygosity analysis and DNA copy number measurement on 8p in bladder cancer reveals two mechanisms of allelic loss.
    Adams J, Williams SV, Aveyard JS, Knowles MA.
    Cancer Res; 2005 Jan 01; 65(1):66-75. PubMed ID: 15665280
    [Abstract] [Full Text] [Related]

  • 16. Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11.
    Still IH, Chernova O, Hurd D, Stone RM, Cowell JK.
    Blood; 1997 Oct 15; 90(8):3136-41. PubMed ID: 9376595
    [Abstract] [Full Text] [Related]

  • 17. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J, Pierron G, Vecchione D, Garand R, Brizard F, Sigaux F, Stern MH, Aurias A.
    Genes Chromosomes Cancer; 2001 Jul 15; 31(3):248-54. PubMed ID: 11391795
    [Abstract] [Full Text] [Related]

  • 18. p53 allele deletion and protein accumulation occurs in the absence of p53 gene mutation in T-prolymphocytic leukaemia and Sezary syndrome.
    Brito-Babapulle V, Hamoudi R, Matutes E, Watson S, Kaczmarek P, Maljaie H, Catovsky D.
    Br J Haematol; 2000 Jul 15; 110(1):180-7. PubMed ID: 10930996
    [Abstract] [Full Text] [Related]

  • 19. A 2-Mb YAC contig and physical map covering the chromosome 8q12 breakpoint cluster region in pleomorphic adenomas of the salivary glands.
    Kas K, Röijer E, Voz M, Meyen E, Stenman G, Van de Ven WJ.
    Genomics; 1997 Aug 01; 43(3):349-58. PubMed ID: 9268638
    [Abstract] [Full Text] [Related]

  • 20. Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
    Scott SA, Cohen N, Brandt T, Warburton PE, Edelmann L.
    Hum Mol Genet; 2010 Sep 01; 19(17):3383-93. PubMed ID: 20570968
    [Abstract] [Full Text] [Related]

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