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Journal Abstract Search

114 related items for PubMed ID: 10557049

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  • 4. Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene.
    Berger R, Le Coniat M, Lacronique V, Daniel MT, Lessard M, Berthou C, Marynen P, Bernard O.
    Leukemia; 1997 Sep; 11(9):1400-3. PubMed ID: 9305591
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  • 5. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
    Tosi S, Hughes J, Scherer SW, Nakabayashi K, Harbott J, Haas OA, Cazzaniga G, Biondi A, Kempski H, Kearney L.
    Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
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  • 6. Analysis of the V(D)J recombination efficiency at lymphoid chromosomal translocation breakpoints.
    Raghavan SC, Kirsch IR, Lieber MR.
    J Biol Chem; 2001 Aug 03; 276(31):29126-33. PubMed ID: 11390401
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  • 7. An atypical myelodysplastic syndrome with t(9;12)(q22;p12) and TEL gene rearrangement.
    Kuno Y, Abe A, Emi N, Iida M, Yamamori T, Tanimoto M, Saito H.
    Br J Haematol; 1999 Aug 03; 106(2):570-1. PubMed ID: 10460625
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  • 8. A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia.
    Le Coniat M, Della Valle V, Marynen P, Berger R.
    Leukemia; 1997 Aug 03; 11(8):1360-3. PubMed ID: 9264392
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  • 9. Evidence for position effects as a variant ETV6-mediated leukemogenic mechanism in myeloid leukemias with a t(4;12)(q11-q12;p13) or t(5;12)(q31;p13).
    Cools J, Mentens N, Odero MD, Peeters P, Wlodarska I, Delforge M, Hagemeijer A, Marynen P.
    Blood; 2002 Mar 01; 99(5):1776-84. PubMed ID: 11861295
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  • 10. t(7;12)(q36;p13) and t(7;12)(q32;p13)--translocations involving ETV6 in children 18 months of age or younger with myeloid disorders.
    Slater RM, von Drunen E, Kroes WG, Weghuis DO, van den Berg E, Smit EM, van der Does-van den Berg A, van Wering E, Hählen K, Carroll AJ, Raimondi SC, Beverloo HB.
    Leukemia; 2001 Jun 01; 15(6):915-20. PubMed ID: 11417477
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  • 11. Mapping of MYC breakpoints in 8q24 rearrangements involving non-immunoglobulin partners in B-cell lymphomas.
    Bertrand P, Bastard C, Maingonnat C, Jardin F, Maisonneuve C, Courel MN, Ruminy P, Picquenot JM, Tilly H.
    Leukemia; 2007 Mar 01; 21(3):515-23. PubMed ID: 17230227
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  • 12. 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 01; 169(2):369-77. PubMed ID: 2536065
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  • 13. Differential expression of TCL1 during pre-B-cell acute lymphoblastic leukemia progression.
    Fears S, Chakrabarti SR, Nucifora G, Rowley JD.
    Cancer Genet Cytogenet; 2002 Jun 01; 135(2):110-9. PubMed ID: 12127395
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  • 14. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia.
    Romana SP, Poirel H, Leconiat M, Flexor MA, Mauchauffé M, Jonveaux P, Macintyre EA, Berger R, Bernard OA.
    Blood; 1995 Dec 01; 86(11):4263-9. PubMed ID: 7492786
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  • 15. TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia.
    Takeuchi S, Seriu T, Bartram CR, Golub TR, Reiter A, Miyoshi I, Gilliland DG, Koeffler HP.
    Leukemia; 1997 Aug 01; 11(8):1220-3. PubMed ID: 9264373
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  • 16. The t(8; 14) chromosomal translocation occurring in B-cell malignancies results from mistakes in V-D-J joining.
    Haluska FG, Finver S, Tsujimoto Y, Croce CM.
    Nature; 1997 Aug 01; 324(6093):158-61. PubMed ID: 3097550
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  • 17. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
    Super HG, Strissel PL, Sobulo OM, Burian D, Reshmi SC, Roe B, Zeleznik-Le NJ, Diaz MO, Rowley JD.
    Genes Chromosomes Cancer; 1997 Oct 01; 20(2):185-95. PubMed ID: 9331569
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  • 18. t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia.
    Tosi S, Harbott J, Teigler-Schlegel A, Haas OA, Pirc-Danoewinata H, Harrison CJ, Biondi A, Cazzaniga G, Kempski H, Scherer SW, Kearney L.
    Genes Chromosomes Cancer; 2000 Dec 01; 29(4):325-32. PubMed ID: 11066076
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  • 19. Loss of the TEL/ETV6 gene by a second translocation in ALL patients with t(12;21).
    Coniat MB, Poirel H, Leblanc T, Bernard OA, Berger R.
    Leuk Res; 1999 Oct 01; 23(10):895-9. PubMed ID: 10573134
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  • 20. Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies.
    Tosi S, Giudici G, Mosna G, Harbott J, Specchia G, Grosveld G, Privitera E, Kearney L, Biondi A, Cazzaniga G.
    Genes Chromosomes Cancer; 1998 Mar 01; 21(3):223-9. PubMed ID: 9523197
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