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Chehab, N. H., Malikzay, A., Stavridi, E. S., Halazonetis, T. D. (1999) Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage. Proceedings of the National Academy of Sciences, 96 (24) 13777-13782 doi:10.1073/pnas.96.24.13777

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Reference TypeJournal (article/letter/editorial)
TitlePhosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage
JournalProceedings of the National Academy of Sciences
AuthorsChehab, N. H.Author
Malikzay, A.Author
Stavridi, E. S.Author
Halazonetis, T. D.Author
Year1999 (November 23)Volume96
Issue24
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.96.24.13777Search in ResearchGate
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Mindat Ref. ID1632087Long-form Identifiermindat:1:5:1632087:5
GUID0
Full ReferenceChehab, N. H., Malikzay, A., Stavridi, E. S., Halazonetis, T. D. (1999) Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage. Proceedings of the National Academy of Sciences, 96 (24) 13777-13782 doi:10.1073/pnas.96.24.13777
Plain TextChehab, N. H., Malikzay, A., Stavridi, E. S., Halazonetis, T. D. (1999) Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage. Proceedings of the National Academy of Sciences, 96 (24) 13777-13782 doi:10.1073/pnas.96.24.13777
In(1999, November) Proceedings of the National Academy of Sciences Vol. 96 (24) Proceedings of the National Academy of Sciences

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Duckett, D. R., Bronstein, S. M., Taya, Y., Modrich, P. (1999) hMutSalpha - and hMutLalpha -dependent phosphorylation of p53 in response to DNA methylator damage. Proceedings of the National Academy of Sciences, 96 (22) 12384-12388 doi:10.1073/pnas.96.22.12384
Khosravi, R., Maya, R., Gottlieb, T., Oren, M., Shiloh, Y., Shkedy, D. (1999) Rapid ATM-dependent phosphorylation of MDM2 precedes p53 accumulation in response to DNA damage. Proceedings of the National Academy of Sciences, 96 (26) 14973-14977 doi:10.1073/pnas.96.26.14973
Chao, C., Saito, S.'i., Anderson, C. W., Appella, E., Xu, Y. (2000) Phosphorylation of murine p53 at Ser-18 regulates the p53 responses to DNA damage. Proceedings of the National Academy of Sciences, 97 (22) 11936-11941 doi:10.1073/pnas.220252297
Boehme, K. A., Kulikov, R., Blattner, C. (2008) p53 stabilization in response to DNA damage requires Akt/PKB and DNA-PK. Proceedings of the National Academy of Sciences, 105 (22) 7785-7790 doi:10.1073/pnas.0703423105
Brown, A. L., Lee, C.-H., Schwarz, J. K., Mitiku, N., Piwnica-Worms, H., Chung, J. H. (1999) A human Cds1-related kinase that functions downstream of ATM protein in the cellular response to DNA damage. Proceedings of the National Academy of Sciences, 96 (7) 3745-3750 doi:10.1073/pnas.96.7.3745
Ullrich, S. J., Sakaguchi, K., Lees-Miller, S. P., Fiscella, M., Mercer, W. E., Anderson, C. W., Appella, E. (1993) Phosphorylation at Ser-15 and Ser-392 in mutant p53 molecules from human tumors is altered compared to wild-type p53. Proceedings of the National Academy of Sciences, 90 (13) 5954-5958 doi:10.1073/pnas.90.13.5954
Halazonetis, T. D., Kandil, A. N. (1991) Determination of the c-MYC DNA-binding site. Proceedings of the National Academy of Sciences, 88 (14) 6162-6166 doi:10.1073/pnas.88.14.6162
Anantha, R. W., Sokolova, E., Borowiec, J. A. (2008) RPA phosphorylation facilitates mitotic exit in response to mitotic DNA damage. Proceedings of the National Academy of Sciences, 105 (35) 12903-12908 doi:10.1073/pnas.0803001105
Aguda, B. D. (1999) A quantitative analysis of the kinetics of the G2 DNA damage checkpoint system. Proceedings of the National Academy of Sciences, 96 (20) 11352-11357 doi:10.1073/pnas.96.20.11352
Pereg, Y., Shkedy, D., de Graaf, P., Meulmeester, E., Edelson-Averbukh, M., Salek, M., Biton, S., Teunisse, A. F. A. S., Lehmann, W. D., Jochemsen, A. G., Shiloh, Y. (2005) Phosphorylation of Hdmx mediates its Hdm2- and ATM-dependent degradation in response to DNA damage. Proceedings of the National Academy of Sciences, 102 (14) 5056-5061 doi:10.1073/pnas.0408595102
Cai, X., Liu, X. (2008) Inhibition of Thr-55 phosphorylation restores p53 nuclear localization and sensitizes cancer cells to DNA damage. Proceedings of the National Academy of Sciences, 105 (44) 16958-16963 doi:10.1073/pnas.0804608105
 
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