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]