@article{oai:nagasaki-u.repo.nii.ac.jp:00014591,
 author = {Kobayashi, Junya and Iwabuchi, Kuniyoshi and Miyagawa, Kiyoshi and Sonoda, Eiichiro and Suzuki, Keiji and Takata, Minoru and Tauchi, Hiroshi},
 issue = {2},
 journal = {Journal of radiation research},
 month = {Mar},
 note = {DNA double strand break (DSB) is one of the most critical types of damage which is induced by ionizing radiation. In this review, we summarize current progress in investigations on the function of DSB repair-related proteins. We focused on recent findings in the analysis of the function of proteins such as 53BP1, histone H2AX, Mus81-Eme1, Fanc complex, and UBC13, which are found to be related to homologous recombination repair or to non-homologous end joining. In addition to the function of these proteins in DSB repair, the biological function of nuclear foci formation following DSB induction is discussed., Journal of radiation research, 49(2), pp.93-103; 2008},
 pages = {93--103},
 title = {Current Topics in DNA Double-Strand Break Repair},
 volume = {49},
 year = {2008}
}