Shindoh N - Search Results

1

Mutations in G protein β subunits promote transformation and kinase inhibitor resistance.

Yoda A, Adelmant G, Tamburini J, Chapuy B, Shindoh N, Yoda Y, Weigert O, Kopp N, Wu SC, Kim SS, Liu H, Tivey T, Christie AL, Elpek KG, Card J, Gritsman K, Gotlib J, Deininger MW, Makishima H, Turley SJ, Javidi-Sharifi N, Maciejewski JP, Jaiswal S, Ebert BL, Rodig SJ, Tyner JW, Marto JA, Weinstock DM, Lane AA. Yoda A, et al. Among authors: shindoh n. Nat Med. 2015 Jan;21(1):71-5. doi: 10.1038/nm.3751. Epub 2014 Dec 8. Nat Med. 2015. PMID: 25485910 Free PMC article.

2

Next-generation cDNA screening for oncogene and resistance phenotypes.

Shindoh N, Yoda A, Yoda Y, Sullivan TJ, Weigert O, Lane AA, Kopp N, Bird L, Rodig SJ, Fox EA, Weinstock DM. Shindoh N, et al. PLoS One. 2012;7(11):e49201. doi: 10.1371/journal.pone.0049201. Epub 2012 Nov 7. PLoS One. 2012. PMID: 23145123 Free PMC article.

3

ASP5878, a selective FGFR inhibitor, to treat FGFR3-dependent urothelial cancer with or without chemoresistance.

Kikuchi A, Suzuki T, Nakazawa T, Iizuka M, Nakayama A, Ozawa T, Kameda M, Shindoh N, Terasaka T, Hirano M, Kuromitsu S. Kikuchi A, et al. Among authors: shindoh n. Cancer Sci. 2017 Feb;108(2):236-242. doi: 10.1111/cas.13124. Cancer Sci. 2017. PMID: 27885740 Free PMC article.

4

ASP5878, a Novel Inhibitor of FGFR1, 2, 3, and 4, Inhibits the Growth of FGF19-Expressing Hepatocellular Carcinoma.

Futami T, Okada H, Kihara R, Kawase T, Nakayama A, Suzuki T, Kameda M, Shindoh N, Terasaka T, Hirano M, Kuromitsu S. Futami T, et al. Among authors: shindoh n. Mol Cancer Ther. 2017 Jan;16(1):68-75. doi: 10.1158/1535-7163.MCT-16-0188. Epub 2016 Nov 11. Mol Cancer Ther. 2017. PMID: 27837028

5

Identification of a novel oncogenic mutation of FGFR4 in gastric cancer.

Futami T, Kawase T, Mori K, Asaumi M, Kihara R, Shindoh N, Kuromitsu S. Futami T, et al. Among authors: shindoh n. Sci Rep. 2019 Oct 10;9(1):14627. doi: 10.1038/s41598-019-51217-6. Sci Rep. 2019. PMID: 31601997 Free PMC article.

6

YM753, a novel histone deacetylase inhibitor, exhibits antitumor activity with selective, sustained accumulation of acetylated histones in tumors in the WiDr xenograft model.

Shindoh N, Mori M, Terada Y, Oda K, Amino N, Kita A, Taniguchi M, Sohda KY, Nagai K, Sowa Y, Masuoka Y, Orita M, Sasamata M, Matsushime H, Furuichi K, Sakai T. Shindoh N, et al. Int J Oncol. 2008 Mar;32(3):545-55. Int J Oncol. 2008. PMID: 18292931

7

Histone deacetylase inhibitors from microorganisms: the Astellas experience.

Masuoka Y, Shindoh N, Inamura N. Masuoka Y, et al. Among authors: shindoh n. Prog Drug Res. 2008;66:335, 337-59. doi: 10.1007/978-3-7643-8595-8_7. Prog Drug Res. 2008. PMID: 18416310 Review.

8

Three new cyclostellettamines, which inhibit histone deacetylase, from a marine sponge of the genus Xestospongia.

Oku N, Nagai K, Shindoh N, Terada Y, van Soest RW, Matsunaga S, Fusetani N. Oku N, et al. Among authors: shindoh n. Bioorg Med Chem Lett. 2004 May 17;14(10):2617-20. doi: 10.1016/j.bmcl.2004.02.062. Bioorg Med Chem Lett. 2004. PMID: 15109664

9

Azumamides A-E: histone deacetylase inhibitory cyclic tetrapeptides from the marine sponge Mycale izuensis.

Nakao Y, Yoshida S, Matsunaga S, Shindoh N, Terada Y, Nagai K, Yamashita JK, Ganesan A, van Soest RW, Fusetani N. Nakao Y, et al. Among authors: shindoh n. Angew Chem Int Ed Engl. 2006 Nov 20;45(45):7553-7. doi: 10.1002/anie.200602047. Angew Chem Int Ed Engl. 2006. PMID: 16981208 No abstract available.

10

Catalyst-controlled torquoselectivity switch in the 4π ring-opening reaction of 2-amino-2-azetines giving β-substituted α,β-unsaturated amidines.

Shindoh N, Kitaura K, Takemoto Y, Takasu K. Shindoh N, et al. J Am Chem Soc. 2011 Jun 8;133(22):8470-3. doi: 10.1021/ja202576e. Epub 2011 May 16. J Am Chem Soc. 2011. PMID: 21557577

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