BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 9881706)

  • 21. Molecular cloning and analysis of chromosome band 11q23 involved in leukaemia-associated translocations.
    Das S; Kearney L; Bower M; Chaplin T; Riley JH; Anand R; Young BD
    Genes Chromosomes Cancer; 1992 Oct; 5(3):244-51. PubMed ID: 1384678
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular characterization of the genomic breakpoint junction in a t(11;22) translocation in Ewing sarcoma.
    Obata K; Hiraga H; Nojima T; Yoshida MC; Abe S
    Genes Chromosomes Cancer; 1999 May; 25(1):6-15. PubMed ID: 10221334
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The rhombotin family of cysteine-rich LIM-domain oncogenes: distinct members are involved in T-cell translocations to human chromosomes 11p15 and 11p13.
    Boehm T; Foroni L; Kaneko Y; Perutz MF; Rabbitts TH
    Proc Natl Acad Sci U S A; 1991 May; 88(10):4367-71. PubMed ID: 2034676
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Consistent breakage between consensus recombinase heptamers of chromosome 9 DNA in a recurrent chromosomal translocation of human T cell leukemia.
    Tycko B; Reynolds TC; Smith SD; Sklar J
    J Exp Med; 1989 Feb; 169(2):369-77. PubMed ID: 2536065
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sequence analysis of the breakpoint cluster region in the ALL-1 gene involved in acute leukemia.
    Gu Y; Alder H; Nakamura T; Schichman SA; Prasad R; Canaani O; Saito H; Croce CM; Canaani E
    Cancer Res; 1994 May; 54(9):2327-30. PubMed ID: 8162575
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of translocational breakpoints within the intron region before the last coding exon (exon 12) of the EVI1 gene in two cases of CML-BC with inv(3)(q21q26).
    Suzukawa K; Taki T; Abe T; Asoh H; Kamada N; Yokota J; Morishita K
    Genomics; 1997 Jun; 42(2):356-60. PubMed ID: 9192861
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clustering of genomic breakpoints at the MLL locus in therapy-related acute leukemia with t(4;11)(q21;q23).
    Hasan SK; Barba G; Metzler M; Divona M; Ottone T; Cicconi L; Falini B; Mecucci C; Lo-Coco F
    Genes Chromosomes Cancer; 2014 Mar; 53(3):248-54. PubMed ID: 24310817
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rearrangement of the MLL gene in acute lymphoblastic and acute myeloid leukemias with 11q23 chromosomal translocations.
    Thirman MJ; Gill HJ; Burnett RC; Mbangkollo D; McCabe NR; Kobayashi H; Ziemin-van der Poel S; Kaneko Y; Morgan R; Sandberg AA
    N Engl J Med; 1993 Sep; 329(13):909-14. PubMed ID: 8361504
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Re: G. Cimino et al., Cloning of ALL-1, the locus involved in leukemias with the t(4;11)(q21;q23), t(9;11)(p22;q23), and t(11;19)(q23;p13) chromosome translocations. Cancer Res., 51: 6712-6714, 1991.
    Rowley JD; Diaz MO
    Cancer Res; 1992 May; 52(10):2999. PubMed ID: 1581914
    [No Abstract]   [Full Text] [Related]  

  • 31. Centromeric alpha-satellite DNA break in reciprocal translocations.
    Wang JC; Hajianpour A; Habibian R
    Cytogenet Genome Res; 2009; 125(4):329-33. PubMed ID: 19864896
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gene mapping by microdissection and enzymatic amplification: heterogeneity in leukaemia associated breakpoints on chromosome 11.
    Cotter FE; Lillington D; Hampton G; Riddle P; Nasipuri S; Gibbons B; Young BD
    Genes Chromosomes Cancer; 1991 Jan; 3(1):8-15. PubMed ID: 2069910
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Chromosome translocation based on illegitimate recombination in human tumors.
    Zucman-Rossi J; Legoix P; Victor JM; Lopez B; Thomas G
    Proc Natl Acad Sci U S A; 1998 Sep; 95(20):11786-91. PubMed ID: 9751743
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13).
    Gajecka M; Gentles AJ; Tsai A; Chitayat D; Mackay KL; Glotzbach CD; Lieber MR; Shaffer LG
    Genome Res; 2008 Nov; 18(11):1733-42. PubMed ID: 18765821
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.
    Gajecka M; Pavlicek A; Glotzbach CD; Ballif BC; Jarmuz M; Jurka J; Shaffer LG
    Hum Genet; 2006 Nov; 120(4):519-26. PubMed ID: 16847692
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Long AT-rich palindromes and the constitutional t(11;22) breakpoint.
    Kurahashi H; Emanuel BS
    Hum Mol Genet; 2001 Nov; 10(23):2605-17. PubMed ID: 11726547
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of DNA surrounding the breakpoints of chromosomal translocations involving the beta T cell receptor gene in human lymphoblastic neoplasms.
    Reynolds TC; Smith SD; Sklar J
    Cell; 1987 Jul; 50(1):107-17. PubMed ID: 3036364
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosomal translocations induced at specified loci in human stem cells.
    Brunet E; Simsek D; Tomishima M; DeKelver R; Choi VM; Gregory P; Urnov F; Weinstock DM; Jasin M
    Proc Natl Acad Sci U S A; 2009 Jun; 106(26):10620-5. PubMed ID: 19549848
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination.
    Hill AS; Foot NJ; Chaplin TL; Young BD
    Hum Mol Genet; 2000 Jun; 9(10):1525-32. PubMed ID: 10888603
    [TBL] [Abstract][Full Text] [Related]  

  • 40. hREC2, a RAD51-like gene, is disrupted by t(12;14) (q15;q24.1) in a uterine leiomyoma.
    Ingraham SE; Lynch RA; Kathiresan S; Buckler AJ; Menon AG
    Cancer Genet Cytogenet; 1999 Nov; 115(1):56-61. PubMed ID: 10565301
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.