Nakatsuru Y - Search Results

1

MK-5108, a highly selective Aurora-A kinase inhibitor, shows antitumor activity alone and in combination with docetaxel.

Shimomura T, Hasako S, Nakatsuru Y, Mita T, Ichikawa K, Kodera T, Sakai T, Nambu T, Miyamoto M, Takahashi I, Miki S, Kawanishi N, Ohkubo M, Kotani H, Iwasawa Y. Shimomura T, et al. Among authors: nakatsuru y. Mol Cancer Ther. 2010 Jan;9(1):157-66. doi: 10.1158/1535-7163.MCT-09-0609. Epub 2010 Jan 6. Mol Cancer Ther. 2010. PMID: 20053775

2

Potent anti-tumor activity of a macrocycle-quinoxalinone class pan-Cdk inhibitor in vitro and in vivo.

Hirai H, Takahashi-Suziki I, Shimomura T, Fukasawa K, Machida T, Takaki T, Kobayashi M, Eguchi T, Oki H, Arai T, Ichikawa K, Hasako S, Kodera T, Kawanishi N, Nakatsuru Y, Kotani H, Iwasawa Y. Hirai H, et al. Among authors: nakatsuru y. Invest New Drugs. 2011 Aug;29(4):534-43. doi: 10.1007/s10637-009-9384-8. Epub 2010 Jan 19. Invest New Drugs. 2011. PMID: 20084424

3

Biological characterization of 2-aminothiazole-derived Cdk4/6 selective inhibitor in vitro and in vivo.

Hirai H, Shimomura T, Kobayashi M, Eguchi T, Taniguchi E, Fukasawa K, Machida T, Oki H, Arai T, Ichikawa K, Hasako S, Haze K, Kodera T, Kawanishi N, Takahashi-Suziki I, Nakatsuru Y, Kotani H, Iwasawa Y. Hirai H, et al. Among authors: nakatsuru y. Cell Cycle. 2010 Apr 15;9(8):1590-600. doi: 10.4161/cc.9.8.11306. Epub 2010 Apr 15. Cell Cycle. 2010. PMID: 20372067

4

MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo.

Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, Tsujioka K, Ueno Y, Hatch H, Majumder PK, Pan BS, Kotani H. Hirai H, et al. Among authors: nakatsuru y. Mol Cancer Ther. 2010 Jul;9(7):1956-67. doi: 10.1158/1535-7163.MCT-09-1012. Epub 2010 Jun 22. Mol Cancer Ther. 2010. PMID: 20571069

5

Imidazopyridine derivatives as potent and selective Polo-like kinase (PLK) inhibitors.

Sato Y, Onozaki Y, Sugimoto T, Kurihara H, Kamijo K, Kadowaki C, Tsujino T, Watanabe A, Otsuki S, Mitsuya M, Iida M, Haze K, Machida T, Nakatsuru Y, Komatani H, Kotani H, Iwasawa Y. Sato Y, et al. Among authors: nakatsuru y. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4673-8. doi: 10.1016/j.bmcl.2009.06.084. Epub 2009 Jun 25. Bioorg Med Chem Lett. 2009. PMID: 19589677

6

Evaluating Chemical CDK Inhibitors as Cell Death Inducers.

Hirai H, Nakatsuru Y. Hirai H, et al. Among authors: nakatsuru y. Methods Mol Biol. 2016;1336:167-78. doi: 10.1007/978-1-4939-2926-9_14. Methods Mol Biol. 2016. PMID: 26231716

7

cDNA cloning and developmental expression of the porcine homologue of WT1.

Tsurutani N, Oda H, Nakatsuru Y, Imai Y, Zhang S, Ueno Y, Ishikawa T. Tsurutani N, et al. Among authors: nakatsuru y. Gene. 1998 May 12;211(2):215-20. doi: 10.1016/s0378-1119(98)00112-7. Gene. 1998. PMID: 9602131

8

Dibenzo[A,L]pyrene-induced genotoxic and carcinogenic responses are dramatically suppressed in aryl hydrocarbon receptor-deficient mice.

Nakatsuru Y, Wakabayashi K, Fujii-Kuriyama Y, Ishikawa T, Kusama K, Ide F. Nakatsuru Y, et al. Int J Cancer. 2004 Nov 1;112(2):179-83. doi: 10.1002/ijc.20365. Int J Cancer. 2004. PMID: 15352028

9

Base excision repair as a therapeutic target in colon cancer.

Liu L, Nakatsuru Y, Gerson SL. Liu L, et al. Among authors: nakatsuru y. Clin Cancer Res. 2002 Sep;8(9):2985-91. Clin Cancer Res. 2002. PMID: 12231545

10

O6-methylguanine DNA methyltransferase activity in liver from various fish species.

Nakatsuru Y, Nemoto N, Nakagawa K, Masahito P, Ishikawa T. Nakatsuru Y, et al. Carcinogenesis. 1987 Aug;8(8):1123-7. doi: 10.1093/carcin/8.8.1123. Carcinogenesis. 1987. PMID: 3608094

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