14 results for author:"Kuraoka I." in Literature citations
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| Identification of small molecule proliferating cell nuclear antigen (PCNA) inhibitor that disrupts interactions with PIP-box proteins and inhibits DNA replication. Punchihewa C., Inoue A., Hishiki A., Fujikawa Y., Connelly M., Evison B., Shao Y., Heath R., Kuraoka I., Rodrigues P. et al. J. Biol. Chem. 287:14289-14300(2012) · Mapped (8) |
| Xeroderma pigmentosum group F protein binds to Eg5 and is required for proper mitosis: implications for XP-F and XFE. Tan L.J., Saijo M., Kuraoka I., Narita T., Takahata C., Iwai S., Tanaka K. Genes Cells 17:173-185(2012) · Mapped (4) |
| MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation. Ito S., Tan L.J., Andoh D., Narita T., Seki M., Hirano Y., Narita K., Kuraoka I., Hiraoka Y., Tanaka K. |
| DNA conformation-dependent activities of human mitochondrial RNA polymerase. Fukuoh A., Ohgaki K., Hatae H., Kuraoka I., Aoki Y., Uchiumi T., Jacobs H.T., Kang D. Genes Cells 14:1029-1042(2009) · Mapped (7) |
| Isolation of XAB2 complex involved in pre-mRNA splicing, transcription, and transcription-coupled repair. Kuraoka I., Ito S., Wada T., Hayashida M., Lee L., Saijo M., Nakatsu Y., Matsumoto M., Matsunaga T., Handa H. et al. J. Biol. Chem. 283:940-950(2008) · Mapped (3) |
| DNA damage-dependent acetylation and ubiquitination of H2AX enhances chromatin dynamics. Ikura T., Tashiro S., Kakino A., Shima H., Jacob N., Amunugama R., Yoder K., Izumi S., Kuraoka I., Tanaka K. et al. Mol. Cell. Biol. 27:7028-7040(2007) · Mapped (4) |
| XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients. Ito S., Kuraoka I., Chymkowitch P., Compe E., Takedachi A., Ishigami C., Coin F., Egly J.M., Tanaka K. Mol. Cell 26:231-243(2007) · Mapped (10) |
| RNA polymerase II bypasses 8-oxoguanine in the presence of transcription elongation factor TFIIS. Kuraoka I., Suzuki K., Ito S., Hayashida M., Kwei J.S., Ikegami T., Handa H., Nakabeppu Y., Tanaka K. DNA Repair (Amst.) 6:841-851(2007) · Mapped (9) |
| CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome. Groisman R., Kuraoka I., Chevallier O., Gaye N., Magnaldo T., Tanaka K., Kisselev A.F., Harel-Bellan A., Nakatani Y. |
| Disruption of mouse XAB2 gene involved in pre-mRNA splicing, transcription and transcription-coupled DNA repair results in preimplantation lethality. Yonemasu R., Minami M., Nakatsu Y., Takeuchi M., Kuraoka I., Matsuda Y., Higashi Y., Kondoh H., Tanaka K. DNA Repair (Amst.) 4:479-491(2005) · Mapped (4) |
| Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome. Horibata K., Iwamoto Y., Kuraoka I., Jaspers N.G.J., Kurimasa A., Oshimura M., Ichihashi M., Tanaka K. Proc. Natl. Acad. Sci. U.S.A. 101:15410-15415(2004) · UniProtKB (1) · Mapped (4) |
| The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage. Groisman R., Polanowska J., Kuraoka I., Sawada J., Saijo M., Drapkin R., Kisselev A.F., Tanaka K., Nakatani Y. |
| Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA. Ikegami T., Kuraoka I., Saijo M., Kodo N., Kyogoku Y., Morikawa K., Tanaka K., Shirakawa M. Nat. Struct. Biol. 5:701-706(1998) · UniProtKB (2) |
| Mutations in the XPD gene leading to Xeroderma pigmentosum symptoms. Kobayashi T., Kuraoka I., Saijo M., Nakatsu Y., Tanaka A., Someda Y., Fukuro S., Tanaka K. Hum. Mutat. 9:322-331(1997) · UniProtKB (1) |