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Journal Abstract Search

180 related items for PubMed ID: 14983023

  • 1. Artemis and p53 cooperate to suppress oncogenic N-myc amplification in progenitor B cells.
    Rooney S, Sekiguchi J, Whitlow S, Eckersdorff M, Manis JP, Lee C, Ferguson DO, Alt FW.
    Proc Natl Acad Sci U S A; 2004 Feb 24; 101(8):2410-5. PubMed ID: 14983023
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  • 4. Amplification of IGH/MYC fusion in clinically aggressive IGH/BCL2-positive germinal center B-cell lymphomas.
    Martín-Subero JI, Odero MD, Hernandez R, Cigudosa JC, Agirre X, Saez B, Sanz-García E, Ardanaz MT, Novo FJ, Gascoyne RD, Calasanz MJ, Siebert R.
    Genes Chromosomes Cancer; 2005 Aug 24; 43(4):414-23. PubMed ID: 15852472
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  • 7. DNA-PKcs and Artemis function in the end-joining phase of immunoglobulin heavy chain class switch recombination.
    Franco S, Murphy MM, Li G, Borjeson T, Boboila C, Alt FW.
    J Exp Med; 2008 Mar 17; 205(3):557-64. PubMed ID: 18316419
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  • 8. Genetic pathway to recurrent chromosome translocations in murine lymphoma involves V(D)J recombinase.
    Vanasse GJ, Halbrook J, Thomas S, Burgess A, Hoekstra MF, Disteche CM, Willerford DM.
    J Clin Invest; 1999 Jun 17; 103(12):1669-75. PubMed ID: 10377173
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  • 12. A p53 defect sensitizes various stages of B cell development to lymphomagenesis in mice carrying an IgH 3' regulatory region-driven c-myc transgene.
    Fiancette R, Rouaud P, Vincent-Fabert C, Laffleur B, Magnone V, Cogné M, Denizot Y.
    J Immunol; 2011 Dec 01; 187(11):5772-82. PubMed ID: 22039300
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  • 14. Mechanisms that can promote peripheral B-cell lymphoma in ATM-deficient mice.
    Tepsuporn S, Hu J, Gostissa M, Alt FW.
    Cancer Immunol Res; 2014 Sep 01; 2(9):857-66. PubMed ID: 24913718
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  • 15. Chromosomal location targets different MYC family gene members for oncogenic translocations.
    Gostissa M, Ranganath S, Bianco JM, Alt FW.
    Proc Natl Acad Sci U S A; 2009 Feb 17; 106(7):2265-70. PubMed ID: 19174520
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  • 16. H2AX prevents DNA breaks from progressing to chromosome breaks and translocations.
    Franco S, Gostissa M, Zha S, Lombard DB, Murphy MM, Zarrin AA, Yan C, Tepsuporn S, Morales JC, Adams MM, Lou Z, Bassing CH, Manis JP, Chen J, Carpenter PB, Alt FW.
    Mol Cell; 2006 Jan 20; 21(2):201-14. PubMed ID: 16427010
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  • 17. A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.
    Jacobs C, Huang Y, Masud T, Lu W, Westfield G, Giblin W, Sekiguchi JM.
    Hum Mol Genet; 2011 Feb 15; 20(4):806-19. PubMed ID: 21147755
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  • 18. The RAG-1/2 endonuclease causes genomic instability and controls CNS complications of lymphoblastic leukemia in p53/Prkdc-deficient mice.
    Gladdy RA, Taylor MD, Williams CJ, Grandal I, Karaskova J, Squire JA, Rutka JT, Guidos CJ, Danska JS.
    Cancer Cell; 2003 Jan 15; 3(1):37-50. PubMed ID: 12559174
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  • 19. Role of genomic instability and p53 in AID-induced c-myc-Igh translocations.
    Ramiro AR, Jankovic M, Callen E, Difilippantonio S, Chen HT, McBride KM, Eisenreich TR, Chen J, Dickins RA, Lowe SW, Nussenzweig A, Nussenzweig MC.
    Nature; 2006 Mar 02; 440(7080):105-9. PubMed ID: 16400328
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  • 20. Molecular and clinical features of non-Burkitt's, diffuse large-cell lymphoma of B-cell type associated with the c-MYC/immunoglobulin heavy-chain fusion gene.
    Akasaka T, Akasaka H, Ueda C, Yonetani N, Maesako Y, Shimizu A, Yamabe H, Fukuhara S, Uchiyama T, Ohno H.
    J Clin Oncol; 2000 Feb 02; 18(3):510-18. PubMed ID: 10653866
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