Moriki T - Search Results

1

Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain.

Moriki T, Maruyama H, Maruyama IN. Moriki T, et al. J Mol Biol. 2001 Aug 31;311(5):1011-26. doi: 10.1006/jmbi.2001.4923. J Mol Biol. 2001. PMID: 11531336

2

Protein domain mapping by lambda phage display: the minimal lactose-binding domain of galectin-3.

Moriki T, Kuwabara I, Liu FT, Maruyama IN. Moriki T, et al. Biochem Biophys Res Commun. 1999 Nov 19;265(2):291-6. doi: 10.1006/bbrc.1999.1666. Biochem Biophys Res Commun. 1999. PMID: 10558859

3

Identification of ADAMTS13 peptide sequences binding to von Willebrand factor.

Moriki T, Maruyama IN, Igari A, Ikeda Y, Murata M. Moriki T, et al. Biochem Biophys Res Commun. 2010 Jan 1;391(1):783-8. doi: 10.1016/j.bbrc.2009.11.138. Epub 2009 Nov 26. Biochem Biophys Res Commun. 2010. PMID: 19944670

4

Epitope analysis of autoantibodies to ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura.

Yamaguchi Y, Moriki T, Igari A, Nakagawa T, Wada H, Matsumoto M, Fujimura Y, Murata M. Yamaguchi Y, et al. Among authors: moriki t. Thromb Res. 2011 Aug;128(2):169-73. doi: 10.1016/j.thromres.2011.03.010. Epub 2011 Apr 14. Thromb Res. 2011. PMID: 21496883

5

Identification of epitopes on ADAMTS13 recognized by a panel of monoclonal antibodies with functional or non-functional effects on catalytic activity.

Igari A, Nakagawa T, Moriki T, Yamaguchi Y, Matsumoto M, Fujimura Y, Soejima K, Murata M. Igari A, et al. Among authors: moriki t. Thromb Res. 2012 Sep;130(3):e79-83. doi: 10.1016/j.thromres.2012.06.006. Epub 2012 Jun 20. Thromb Res. 2012. PMID: 22721582

6

Expression and functional characterization of an abnormal platelet membrane glycoprotein Ib alpha (Met239 --> Val) reported in patients with platelet-type von Willebrand disease.

Moriki T, Murata M, Kitaguchi T, Anbo H, Handa M, Watanabe K, Takahashi H, Ikeda Y. Moriki T, et al. Blood. 1997 Jul 15;90(2):698-705. Blood. 1997. PMID: 9226170 Free article.

7

A novel polymorphism, 70Leu/Phe, disrupts a consensus Leu residue within the leucine-rich repeat sequence of platelet glycoprotein Ibalpha.

Matsubara Y, Murata M, Moriki T, Yokoyama K, Watanabe N, Nakajima H, Handa M, Kawano K, Aoki N, Yoshino H, Ikeda Y. Matsubara Y, et al. Among authors: moriki t. Thromb Haemost. 2002 May;87(5):867-72. Thromb Haemost. 2002. PMID: 12038791

8

Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency.

Ishii K, Oguchi S, Moriki T, Yatabe Y, Takeshita E, Murata M, Ikeda Y, Watanabe K. Ishii K, et al. Among authors: moriki t. Blood Coagul Fibrinolysis. 2004 Jul;15(5):367-73. doi: 10.1097/01.mbc.0000114447.59147.d1. Blood Coagul Fibrinolysis. 2004. PMID: 15205584

9

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency.

Oguchi S, Ishii K, Moriki T, Takeshita E, Murata M, Ikeda Y, Watanabe K. Oguchi S, et al. Among authors: moriki t. Thromb Res. 2005;115(3):191-7. doi: 10.1016/j.thromres.2004.08.027. Thromb Res. 2005. PMID: 15617741

10

Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X.

Isshiki I, Favier R, Moriki T, Uchida T, Ishihara H, Van Dreden P, Murata M, Ikeda Y. Isshiki I, et al. Among authors: moriki t. Blood Coagul Fibrinolysis. 2005 Jan;16(1):9-16. doi: 10.1097/00001721-200501000-00002. Blood Coagul Fibrinolysis. 2005. PMID: 15650540

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