770 related articles for article (PubMed ID: 9312059)
1. ATM-dependent telomere loss in aging human diploid fibroblasts and DNA damage lead to the post-translational activation of p53 protein involving poly(ADP-ribose) polymerase.
Vaziri H; West MD; Allsopp RC; Davison TS; Wu YS; Arrowsmith CH; Poirier GG; Benchimol S
EMBO J; 1997 Oct; 16(19):6018-33. PubMed ID: 9312059
[TBL] [Abstract][Full Text] [Related]
2. Critical telomere shortening regulated by the ataxia-telangiectasia gene acts as a DNA damage signal leading to activation of p53 protein and limited life-span of human diploid fibroblasts. A review.
Vaziri H
Biochemistry (Mosc); 1997 Nov; 62(11):1306-10. PubMed ID: 9467855
[TBL] [Abstract][Full Text] [Related]
3. Functional interplay between p53 and E2F through co-activator p300.
Lee CW; Sørensen TS; Shikama N; La Thangue NB
Oncogene; 1998 May; 16(21):2695-710. PubMed ID: 9652736
[TBL] [Abstract][Full Text] [Related]
4. Regulation of the IRF-1 tumour modifier during the response to genotoxic stress involves an ATM-dependent signalling pathway.
Pamment J; Ramsay E; Kelleher M; Dornan D; Ball KL
Oncogene; 2002 Nov; 21(51):7776-85. PubMed ID: 12420214
[TBL] [Abstract][Full Text] [Related]
5. The apoptotic and transcriptional transactivation activities of p53 can be dissociated.
Bissonnette N; Wasylyk B; Hunting DJ
Biochem Cell Biol; 1997; 75(4):351-8. PubMed ID: 9493957
[TBL] [Abstract][Full Text] [Related]
6. p53 is preferentially recruited to the promoters of growth arrest genes p21 and GADD45 during replicative senescence of normal human fibroblasts.
Jackson JG; Pereira-Smith OM
Cancer Res; 2006 Sep; 66(17):8356-60. PubMed ID: 16951143
[TBL] [Abstract][Full Text] [Related]
7. Poly(ADP-ribosyl)ation affects stabilization of Che-1 protein in response to DNA damage.
Bacalini MG; Di Lonardo D; Catizone A; Ciccarone F; Bruno T; Zampieri M; Guastafierro T; Calabrese R; Fanciulli M; Passananti C; Caiafa P; Reale A
DNA Repair (Amst); 2011 Apr; 10(4):380-9. PubMed ID: 21317046
[TBL] [Abstract][Full Text] [Related]
8. DNA-dependent protein kinase is not required for accumulation of p53 or cell cycle arrest after DNA damage.
Rathmell WK; Kaufmann WK; Hurt JC; Byrd LL; Chu G
Cancer Res; 1997 Jan; 57(1):68-74. PubMed ID: 8988043
[TBL] [Abstract][Full Text] [Related]
9. Irreversible cellular senescence induced by prolonged exposure to H2O2 involves DNA-damage-and-repair genes and telomere shortening.
Duan J; Duan J; Zhang Z; Tong T
Int J Biochem Cell Biol; 2005 Jul; 37(7):1407-20. PubMed ID: 15833273
[TBL] [Abstract][Full Text] [Related]
10. Cardiac stem cell and myocyte aging, heart failure, and insulin-like growth factor-1 overexpression.
Torella D; Rota M; Nurzynska D; Musso E; Monsen A; Shiraishi I; Zias E; Walsh K; Rosenzweig A; Sussman MA; Urbanek K; Nadal-Ginard B; Kajstura J; Anversa P; Leri A
Circ Res; 2004 Mar; 94(4):514-24. PubMed ID: 14726476
[TBL] [Abstract][Full Text] [Related]
11. Myc suppression of the p21(Cip1) Cdk inhibitor influences the outcome of the p53 response to DNA damage.
Seoane J; Le HV; Massagué J
Nature; 2002 Oct; 419(6908):729-34. PubMed ID: 12384701
[TBL] [Abstract][Full Text] [Related]
12. Poly(ADP-ribose) polymerase-1 regulates the stability of the wild-type p53 protein.
Wesierska-Gadek J; Schmid G
Cell Mol Biol Lett; 2001; 6(2):117-40. PubMed ID: 11544635
[TBL] [Abstract][Full Text] [Related]
13. Arecoline-induced phosphorylated p53 and p21(WAF1) protein expression is dependent on ATM/ATR and phosphatidylinositol-3-kinase in clone-9 cells.
Chou WW; Guh JY; Tsai JF; Hwang CC; Chiou SJ; Chuang LY
J Cell Biochem; 2009 Jun; 107(3):408-17. PubMed ID: 19343784
[TBL] [Abstract][Full Text] [Related]
14. Proinflammatory cytokine-induced cellular senescence of biliary epithelial cells is mediated via oxidative stress and activation of ATM pathway: a culture study.
Sasaki M; Ikeda H; Sato Y; Nakanuma Y
Free Radic Res; 2008 Jul; 42(7):625-32. PubMed ID: 18608517
[TBL] [Abstract][Full Text] [Related]
15. c-Jun-deficient cells undergo premature senescence as a result of spontaneous DNA damage accumulation.
MacLaren A; Black EJ; Clark W; Gillespie DA
Mol Cell Biol; 2004 Oct; 24(20):9006-18. PubMed ID: 15456874
[TBL] [Abstract][Full Text] [Related]
16. Cooperation between ARID3A and p53 in the transcriptional activation of p21WAF1 in response to DNA damage.
Lestari W; Ichwan SJ; Otsu M; Yamada S; Iseki S; Shimizu S; Ikeda MA
Biochem Biophys Res Commun; 2012 Jan; 417(2):710-6. PubMed ID: 22172947
[TBL] [Abstract][Full Text] [Related]
17. p53 protein accumulation in addition to the transactivation activity is required for p53-dependent cell cycle arrest after treatment of cells with camptothecin.
Jaks V; Jõers A; Kristjuhan A; Maimets T
Oncogene; 2001 Mar; 20(10):1212-9. PubMed ID: 11313865
[TBL] [Abstract][Full Text] [Related]
18. Decrease of p400 ATPase complex and loss of H2A.Z within the p21 promoter occur in senescent IMR-90 human fibroblasts.
Lee K; Lau ZZ; Meredith C; Park JH
Mech Ageing Dev; 2012; 133(11-12):686-94. PubMed ID: 23146670
[TBL] [Abstract][Full Text] [Related]
19. ING1 represses transcription by direct DNA binding and through effects on p53.
Kataoka H; Bonnefin P; Vieyra D; Feng X; Hara Y; Miura Y; Joh T; Nakabayashi H; Vaziri H; Harris CC; Riabowol K
Cancer Res; 2003 Sep; 63(18):5785-92. PubMed ID: 14522900
[TBL] [Abstract][Full Text] [Related]
20. HIPK2 contributes to PCAF-mediated p53 acetylation and selective transactivation of p21Waf1 after nonapoptotic DNA damage.
Di Stefano V; Soddu S; Sacchi A; D'Orazi G
Oncogene; 2005 Aug; 24(35):5431-42. PubMed ID: 15897882
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
