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Monoallelic BUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome.
Matsuura S, Matsumoto Y, Morishima K, Izumi H, Matsumoto H, Ito E, Tsutsui K, Kobayashi J, Tauchi H, Kajiwara Y, Hama S, Kurisu K, Tahara H, Oshimura M, Komatsu K, Ikeuchi T, Kajii T. Matsuura S, et al. Among authors: morishima k. Am J Med Genet A. 2006 Feb 15;140(4):358-67. doi: 10.1002/ajmg.a.31069. Am J Med Genet A. 2006. PMID: 16411201
NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain.
Kobayashi J, Tauchi H, Sakamoto S, Nakamura A, Morishima K, Matsuura S, Kobayashi T, Tamai K, Tanimoto K, Komatsu K. Kobayashi J, et al. Among authors: morishima k. Curr Biol. 2002 Oct 29;12(21):1846-51. doi: 10.1016/s0960-9822(02)01259-9. Curr Biol. 2002. PMID: 12419185 Free article.
The forkhead-associated domain of NBS1 is essential for nuclear foci formation after irradiation but not essential for hRAD50[middle dot]hMRE11[middle dot]NBS1 complex DNA repair activity.
Tauchi H, Kobayashi J, Morishima K, Matsuura S, Nakamura A, Shiraishi T, Ito E, Masnada D, Delia D, Komatsu K. Tauchi H, et al. Among authors: morishima k. J Biol Chem. 2001 Jan 5;276(1):12-5. doi: 10.1074/jbc.C000578200. J Biol Chem. 2001. PMID: 11062235 Free article.
Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination.
Yamamoto K, Hirano S, Ishiai M, Morishima K, Kitao H, Namikoshi K, Kimura M, Matsushita N, Arakawa H, Buerstedde JM, Komatsu K, Thompson LH, Takata M. Yamamoto K, et al. Among authors: morishima k. Mol Cell Biol. 2005 Jan;25(1):34-43. doi: 10.1128/MCB.25.1.34-43.2005. Mol Cell Biol. 2005. PMID: 15601828 Free PMC article.
175 results