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A cell's response to damaged DNA is triggered when two proteins leave the nucleus and converge upon a signaling complex in the cytoplasm. This activates a key transcription factor that then moves into the nucleus to promote cell survival.
The authors are at the Institute of Cancer Biology and Centre for Genotoxic Stress Research, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark. E-mail: jb{at}cancer.dk
The Spindle Positioning Protein Kar9p Interacts With the Sumoylation Machinery in Saccharomyces cerevisiae.
N. Meednu, H. Hoops, S. D'Silva, L. Pogorzala, S. Wood, D. Farkas, M. Sorrentino, E. Sia, P. Meluh, and R. K. Miller (2008)
Genetics
180, 2033-2055
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Novel Mechanism whereby Nuclear Factor {kappa}B Mediates DNA Damage Repair through Regulation of O6-Methylguanine-DNA-Methyltransferase.
I. Lavon, D. Fuchs, D. Zrihan, G. Efroni, B. Zelikovitch, Y. Fellig, and T. Siegal (2007)
Cancer Res.
67, 8952-8959
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Review: Ubiquitination and de-ubiquitination: role in regulation of signaling by Toll-like receptors.
E. L. Lowe, T. M. Doherty, H. Karahashi, and M. Arditi (2006)
Innate Immunity
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