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Journal Abstract Search

224 related items for PubMed ID: 11238951

  • 1. Distinct functional domains of nibrin mediate Mre11 binding, focus formation, and nuclear localization.
    Desai-Mehta A, Cerosaletti KM, Concannon P.
    Mol Cell Biol; 2001 Mar; 21(6):2184-91. PubMed ID: 11238951
    [Abstract] [Full Text] [Related]

  • 2. Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation.
    Cerosaletti KM, Desai-Mehta A, Yeo TC, Kraakman-Van Der Zwet M, Zdzienicka MZ, Concannon P.
    Mutagenesis; 2000 May; 15(3):281-6. PubMed ID: 10792024
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  • 3. Active role for nibrin in the kinetics of atm activation.
    Cerosaletti K, Wright J, Concannon P.
    Mol Cell Biol; 2006 Mar; 26(5):1691-9. PubMed ID: 16478990
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  • 4. Independent roles for nibrin and Mre11-Rad50 in the activation and function of Atm.
    Cerosaletti K, Concannon P.
    J Biol Chem; 2004 Sep 10; 279(37):38813-9. PubMed ID: 15234984
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  • 5. Nibrin forkhead-associated domain and breast cancer C-terminal domain are both required for nuclear focus formation and phosphorylation.
    Cerosaletti KM, Concannon P.
    J Biol Chem; 2003 Jun 13; 278(24):21944-51. PubMed ID: 12679336
    [Abstract] [Full Text] [Related]

  • 6. The Nijmegen breakage syndrome protein is essential for Mre11 phosphorylation upon DNA damage.
    Dong Z, Zhong Q, Chen PL.
    J Biol Chem; 1999 Jul 09; 274(28):19513-6. PubMed ID: 10391882
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  • 12. Arsenic-induced Mre11 phosphorylation is cell cycle-dependent and defective in NBS cells.
    Yuan SS, Su JH, Hou MF, Yang FW, Zhao S, Lee EY.
    DNA Repair (Amst); 2002 Feb 28; 1(2):137-42. PubMed ID: 12509260
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  • 13. Defective signal joint recombination in fanconi anemia fibroblasts reveals a role for Rad50 in V(D)J recombination.
    Donahue SL, Tabah AA, Schmitz K, Aaron A, Campbell C.
    J Mol Biol; 2007 Jul 13; 370(3):449-58. PubMed ID: 17524422
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  • 14. A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
    Berardinelli F, di Masi A, Salvatore M, Banerjee S, Myung K, De Villartay JP, Revy P, Plebani A, Soresina A, Taruscio D, Tanzarella C, Antoccia A.
    Eur J Med Genet; 2007 Jul 13; 50(3):176-87. PubMed ID: 17395558
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  • 15. V(D)J rearrangement in Nijmegen breakage syndrome.
    Yeo TC, Xia D, Hassouneh S, Yang XO, Sabath DE, Sperling K, Gatti RA, Concannon P, Willerford DM.
    Mol Immunol; 2000 Dec 13; 37(18):1131-9. PubMed ID: 11451418
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  • 16. Adenovirus oncoproteins inactivate the Mre11-Rad50-NBS1 DNA repair complex.
    Stracker TH, Carson CT, Weitzman MD.
    Nature; 2002 Jul 18; 418(6895):348-52. PubMed ID: 12124628
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  • 17. The Aspergillus nidulans sldI(RAD50) gene interacts with bimE(APC1), a homologue of an anaphase-promoting complex subunit.
    Malavazi I, Lima JF, von Zeska Kress Fagundes MR, Efimov VP, de Souza Goldman MH, Goldman GH.
    Mol Microbiol; 2005 Jul 18; 57(1):222-37. PubMed ID: 15948962
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  • 18. Nijmegen breakage syndrome disease protein and MRE11 at PML nuclear bodies and meiotic telomeres.
    Lombard DB, Guarente L.
    Cancer Res; 2000 May 01; 60(9):2331-4. PubMed ID: 10811102
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  • 19. Characterization of CDKN1A (p21) binding to sites of heavy-ion-induced damage: colocalization with proteins involved in DNA repair.
    Jakob B, Scholz M, Taucher-Scholz G.
    Int J Radiat Biol; 2002 Feb 01; 78(2):75-88. PubMed ID: 11779358
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  • 20. Human RAD50 deficiency: Confirmation of a distinctive phenotype.
    Ragamin A, Yigit G, Bousset K, Beleggia F, Verheijen FW, de Wit MY, Strom TM, Dörk T, Wollnik B, Mancini GMS.
    Am J Med Genet A; 2020 Jun 01; 182(6):1378-1386. PubMed ID: 32212377
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