225 related articles for article (PubMed ID: 17182545)
1. Regulation of reactive oxygen species by Atm is essential for proper response to DNA double-strand breaks in lymphocytes.
Ito K; Takubo K; Arai F; Satoh H; Matsuoka S; Ohmura M; Naka K; Azuma M; Miyamoto K; Hosokawa K; Ikeda Y; Mak TW; Suda T; Hirao A
J Immunol; 2007 Jan; 178(1):103-10. PubMed ID: 17182545
[TBL] [Abstract][Full Text] [Related]
2. Endogenously induced DNA double strand breaks arise in heterochromatic DNA regions and require ataxia telangiectasia mutated and Artemis for their repair.
Woodbine L; Brunton H; Goodarzi AA; Shibata A; Jeggo PA
Nucleic Acids Res; 2011 Sep; 39(16):6986-97. PubMed ID: 21596788
[TBL] [Abstract][Full Text] [Related]
3. ATM deficiency impairs thymocyte maturation because of defective resolution of T cell receptor alpha locus coding end breaks.
Vacchio MS; Olaru A; Livak F; Hodes RJ
Proc Natl Acad Sci U S A; 2007 Apr; 104(15):6323-8. PubMed ID: 17405860
[TBL] [Abstract][Full Text] [Related]
4. ATM prevents unattended DNA double strand breaks on site and in generations to come.
Yin B; Savic V; Bassing CH
Cancer Biol Ther; 2007 Dec; 6(12):1837-9. PubMed ID: 18087222
[TBL] [Abstract][Full Text] [Related]
5. Aberrant V(D)J recombination in ataxia telangiectasia mutated-deficient lymphocytes is dependent on nonhomologous DNA end joining.
Bredemeyer AL; Huang CY; Walker LM; Bassing CH; Sleckman BP
J Immunol; 2008 Aug; 181(4):2620-5. PubMed ID: 18684952
[TBL] [Abstract][Full Text] [Related]
6. Antioxidant N-acetyl cysteine reduces incidence and multiplicity of lymphoma in Atm deficient mice.
Reliene R; Schiestl RH
DNA Repair (Amst); 2006 Jul; 5(7):852-9. PubMed ID: 16781197
[TBL] [Abstract][Full Text] [Related]
7. Concurrent V(D)J recombination and DNA end instability increase interchromosomal trans-rearrangements in ATM-deficient thymocytes.
Bowen S; Wangsa D; Ried T; Livak F; Hodes RJ
Nucleic Acids Res; 2013 Apr; 41(8):4535-48. PubMed ID: 23470994
[TBL] [Abstract][Full Text] [Related]
8. Regulation of oxidative stress responses by ataxia-telangiectasia mutated is required for T cell proliferation.
Bagley J; Singh G; Iacomini J
J Immunol; 2007 Apr; 178(8):4757-63. PubMed ID: 17404255
[TBL] [Abstract][Full Text] [Related]
9. Deregulation of mTOR signaling is involved in thymic lymphoma development in Atm-/- mice.
Kuang X; Shen J; Wong PK; Yan M
Biochem Biophys Res Commun; 2009 Jun; 383(3):368-72. PubMed ID: 19364503
[TBL] [Abstract][Full Text] [Related]
10. Redundant and nonredundant functions of ATM and H2AX in αβ T-lineage lymphocytes.
Yin B; Lee BS; Yang-Iott KS; Sleckman BP; Bassing CH
J Immunol; 2012 Aug; 189(3):1372-9. PubMed ID: 22730535
[TBL] [Abstract][Full Text] [Related]
11. ATM and p53 are essential in the cell-cycle containment of DNA breaks during V(D)J recombination in vivo.
Dujka ME; Puebla-Osorio N; Tavana O; Sang M; Zhu C
Oncogene; 2010 Feb; 29(7):957-65. PubMed ID: 19915617
[TBL] [Abstract][Full Text] [Related]
12. Pathological neoangiogenesis depends on oxidative stress regulation by ATM.
Okuno Y; Nakamura-Ishizu A; Otsu K; Suda T; Kubota Y
Nat Med; 2012 Aug; 18(8):1208-16. PubMed ID: 22797809
[TBL] [Abstract][Full Text] [Related]
13. Process for immune defect and chromosomal translocation during early thymocyte development lacking ATM.
Isoda T; Takagi M; Piao J; Nakagama S; Sato M; Masuda K; Ikawa T; Azuma M; Morio T; Kawamoto H; Mizutani S
Blood; 2012 Jul; 120(4):789-99. PubMed ID: 22709691
[TBL] [Abstract][Full Text] [Related]
14. Kinase-dead ATM protein causes genomic instability and early embryonic lethality in mice.
Yamamoto K; Wang Y; Jiang W; Liu X; Dubois RL; Lin CS; Ludwig T; Bakkenist CJ; Zha S
J Cell Biol; 2012 Aug; 198(3):305-13. PubMed ID: 22869596
[TBL] [Abstract][Full Text] [Related]
15. Immunoglobulin class switch recombination is impaired in Atm-deficient mice.
Lumsden JM; McCarty T; Petiniot LK; Shen R; Barlow C; Wynn TA; Morse HC; Gearhart PJ; Wynshaw-Boris A; Max EE; Hodes RJ
J Exp Med; 2004 Nov; 200(9):1111-21. PubMed ID: 15504820
[TBL] [Abstract][Full Text] [Related]
16. Ataxia-telangiectasia-mutated-dependent activation of Ku in human fibroblasts exposed to hydrogen peroxide.
Lee JH; Kim KH; Morio T; Kim H
Ann N Y Acad Sci; 2006 Dec; 1091():76-82. PubMed ID: 17341604
[TBL] [Abstract][Full Text] [Related]
17. The RAG2 C terminus suppresses genomic instability and lymphomagenesis.
Deriano L; Chaumeil J; Coussens M; Multani A; Chou Y; Alekseyenko AV; Chang S; Skok JA; Roth DB
Nature; 2011 Mar; 471(7336):119-23. PubMed ID: 21368836
[TBL] [Abstract][Full Text] [Related]
18. Rag-dependent and Rag-independent mechanisms of Notch1 rearrangement in thymic lymphomas of Atm(-/-) and scid mice.
Tsuji H; Ishii-Ohba H; Noda Y; Kubo E; Furuse T; Tatsumi K
Mutat Res; 2009 Jan; 660(1-2):22-32. PubMed ID: 19000702
[TBL] [Abstract][Full Text] [Related]
19. ATM-dependent DNA damage surveillance in T-cell development and leukemogenesis: the DSB connection.
Matei IR; Guidos CJ; Danska JS
Immunol Rev; 2006 Feb; 209():142-58. PubMed ID: 16448540
[TBL] [Abstract][Full Text] [Related]
20. DNA double-strand breaks and ATM activation by transcription-blocking DNA lesions.
Sordet O; Nakamura AJ; Redon CE; Pommier Y
Cell Cycle; 2010 Jan; 9(2):274-8. PubMed ID: 20023421
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
