Suzuki T - Search Results

1

Identification and characterization of flavonoids as sialyltransferase inhibitors.

Hidari KI, Oyama K, Ito G, Nakayama M, Inai M, Goto S, Kanai Y, Watanabe K, Yoshida K, Furuta T, Kan T, Suzuki T. Hidari KI, et al. Among authors: suzuki t. Biochem Biophys Res Commun. 2009 May 8;382(3):609-13. doi: 10.1016/j.bbrc.2009.03.082. Epub 2009 Mar 19. Biochem Biophys Res Commun. 2009. PMID: 19303395

2

2beta,3beta-Difluorosialic acid derivatives structurally modified at the C-4 position: synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1.

Ikeda K, Kitani S, Sato K, Suzuki T, Hosokawa C, Suzuki Y, Tanaka K, Sato M. Ikeda K, et al. Among authors: suzuki y, suzuki t. Carbohydr Res. 2004 May 17;339(7):1367-72. doi: 10.1016/j.carres.2004.02.029. Carbohydr Res. 2004. PMID: 15113676

3

In vitro and in vivo inhibitory effects of disodium cromoglycate on influenza virus infection.

Hidari KI, Tsujii E, Hiroi J, Mano E, Miyatake A, Miyamoto D, Suzuki T, Suzuki Y. Hidari KI, et al. Among authors: suzuki y, suzuki t. Biol Pharm Bull. 2004 Jun;27(6):825-30. doi: 10.1248/bpb.27.825. Biol Pharm Bull. 2004. PMID: 15187427 Free article.

4

Purification and characterization of a soluble recombinant human ST6Gal I functionally expressed in Escherichia coli.

Hidari KI, Horie N, Murata T, Miyamoto D, Suzuki T, Usui T, Suzuki Y. Hidari KI, et al. Among authors: suzuki y, suzuki t. Glycoconj J. 2005 Feb;22(1-2):1-11. doi: 10.1007/s10719-005-0845-9. Glycoconj J. 2005. PMID: 15864429

5

Design and synthesis of artificial phospholipid for selective cleavage of integral membrane protein.

Furuta T, Sakai M, Hayashi H, Asakawa T, Kataoka F, Fujii S, Suzuki T, Suzuki Y, Tanaka K, Fishkin N, Nakanishi K. Furuta T, et al. Among authors: suzuki y, suzuki t. Chem Commun (Camb). 2005 Sep 28;(36):4575-7. doi: 10.1039/b507917a. Epub 2005 Aug 17. Chem Commun (Camb). 2005. PMID: 16158119

6

Identification and characterization of carbohydrate molecules in mammalian cells recognized by dengue virus type 2.

Aoki C, Hidari KI, Itonori S, Yamada A, Takahashi N, Kasama T, Hasebe F, Islam MA, Hatano K, Matsuoka K, Taki T, Guo CT, Takahashi T, Sakano Y, Suzuki T, Miyamoto D, Sugita M, Terunuma D, Morita K, Suzuki Y. Aoki C, et al. Among authors: suzuki y, suzuki t. J Biochem. 2006 Mar;139(3):607-14. doi: 10.1093/jb/mvj067. J Biochem. 2006. PMID: 16567427

7

Human trachea primary epithelial cells express both sialyl(alpha2-3)Gal receptor for human parainfluenza virus type 1 and avian influenza viruses, and sialyl(alpha2-6)Gal receptor for human influenza viruses.

Kogure T, Suzuki T, Takahashi T, Miyamoto D, Hidari KI, Guo CT, Ito T, Kawaoka Y, Suzuki Y. Kogure T, et al. Among authors: suzuki y, suzuki t. Glycoconj J. 2006 Feb;23(1-2):101-6. doi: 10.1007/s10719-006-5442-z. Glycoconj J. 2006. PMID: 16575527

In addition, the Siaalpha2-3Gal linkage was predominantly recognized by avian and horse influenza viruses, and human parainfluenza virus type 1 (hPIV-1), whereas the Siaalpha2-6Gal linkage was mainly recognized by human influenza viruses (Paulson JC in "The Receptors'' [Conn M Ed …

In addition, the Siaalpha2-3Gal linkage was predominantly recognized by avian and horse influenza viruses, and human parainfluenza virus typ …

8

Suppression of the biosynthesis of cellular sphingolipids results in the inhibition of the maturation of influenza virus particles in MDCK cells.

Hidari KI, Suzuki Y, Suzuki T. Hidari KI, et al. Among authors: suzuki y, suzuki t. Biol Pharm Bull. 2006 Aug;29(8):1575-9. doi: 10.1248/bpb.29.1575. Biol Pharm Bull. 2006. PMID: 16880607 Free article.

9

2-Deoxy-2,3-didehydro-N-acetylneuraminic acid analogues structurally modified at the C-4 position: synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1.

Ikeda K, Sato K, Kitani S, Suzuki T, Maki N, Suzuki Y, Sato M. Ikeda K, et al. Among authors: suzuki y, suzuki t. Bioorg Med Chem. 2006 Dec 1;14(23):7893-7. doi: 10.1016/j.bmc.2006.07.045. Bioorg Med Chem. 2006. PMID: 16908163

10

Thiosialoside clusters using carbosilane dendrimer core scaffolds as a new class of influenza neuraminidase inhibitors.

Sakamoto J, Koyama T, Miyamoto D, Yingsakmongkon S, Hidari KI, Jampangern W, Suzuki T, Suzuki Y, Esumi Y, Hatano K, Terunuma D, Matsuoka K. Sakamoto J, et al. Among authors: suzuki y, suzuki t. Bioorg Med Chem Lett. 2007 Feb 1;17(3):717-21. doi: 10.1016/j.bmcl.2006.10.085. Epub 2006 Nov 1. Bioorg Med Chem Lett. 2007. PMID: 17095224

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