Shima M - Search Results

1

Assessing the clinical severity of type 1 von Willebrand disease patients with a microchip flow-chamber system.

Nogami K, Ogiwara K, Yada K, Shida Y, Takeyama M, Yaoi H, Minami H, Furukawa S, Hosokawa K, Shima M. Nogami K, et al. Among authors: shima m. J Thromb Haemost. 2016 Apr;14(4):667-74. doi: 10.1111/jth.13273. Epub 2016 Mar 15. J Thromb Haemost. 2016. PMID: 27061057 Free article.

2

ABO blood group genotype and plasma von Willebrand factor in normal individuals.

Shima M, Fujimura Y, Nishiyama T, Tsujiuchi T, Narita N, Matsui T, Titani K, Katayama M, Yamamoto F, Yoshioka A. Shima M, et al. Vox Sang. 1995;68(4):236-40. doi: 10.1111/j.1423-0410.1995.tb02579.x. Vox Sang. 1995. PMID: 7660643

3

A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine.

Shima M, Scandella D, Yoshioka A, Nakai H, Tanaka I, Kamisue S, Terada S, Fukui H. Shima M, et al. Thromb Haemost. 1993 Mar 1;69(3):240-6. Thromb Haemost. 1993. PMID: 7682339

4

Factor VIII Ise (R2159C) in a patient with mild hemophilia A, an abnormal factor VIII with retention of function but modification of C2 epitopes.

Suzuki H, Shima M, Arai M, Kagawa K, Fukutake K, Kamisue S, Nakai H, Morichika S, Tanaka I, Inoue M, Gale K, Tuddenham EG, Yoshioka A. Suzuki H, et al. Among authors: shima m. Thromb Haemost. 1997 May;77(5):862-7. Thromb Haemost. 1997. PMID: 9184393

5

The role of platelet von Willebrand factor in the binding of factor VIII to activated platelets.

Suzuki H, Shima M, Kamisue S, Nakai H, Nogami K, Shibata M, Morichika S, Tanaka I, Giddings JC, Yoshioka A. Suzuki H, et al. Among authors: shima m. Thromb Res. 1998 Jun 1;90(5):207-14. doi: 10.1016/s0049-3848(98)00034-6. Thromb Res. 1998. PMID: 9694242

6

Identification of the binding site for an alloantibody to von Willebrand factor which inhibits binding to glycoprotein Ib within the amino-terminal region flanking the A1 domain.

Shibata M, Shima M, Fujimura Y, Takahashi Y, Nakai H, Sakurai Y, Asatani M, Nomura A, Take H, Giddings JC, Yoshioka A. Shibata M, et al. Among authors: shima m. Thromb Haemost. 1999 May;81(5):793-8. Thromb Haemost. 1999. PMID: 10365755

7

Identification of a factor VIII peptide, residues 2315-2330, which neutralizes human factor VIII C2 inhibitor alloantibodies: requirement of Cys2326 and Glu2327 for maximum effect.

Nogami K, Shima M, Nakai H, Tanaka I, Suzuki H, Morichika S, Shibata M, Saenko EL, Scandella D, Giddings JC, Yoshioka A. Nogami K, et al. Among authors: shima m. Br J Haematol. 1999 Oct;107(1):196-203. doi: 10.1046/j.1365-2141.1999.01673.x. Br J Haematol. 1999. PMID: 10520041 Free article.

8

Role of factor VIII C2 domain in factor VIII binding to factor Xa.

Nogami K, Shima M, Hosokawa K, Suzuki T, Koide T, Saenko EL, Scandella D, Shibata M, Kamisue S, Tanaka I, Yoshioka A. Nogami K, et al. Among authors: shima m. J Biol Chem. 1999 Oct 22;274(43):31000-7. doi: 10.1074/jbc.274.43.31000. J Biol Chem. 1999. PMID: 10521497 Free article.

9

Factor VIII C2 domain contains the thrombin-binding site responsible for thrombin-catalyzed cleavage at Arg1689.

Nogami K, Shima M, Hosokawa K, Nagata M, Koide T, Saenko EL, Tanaka I, Shibata M, Yoshioka A. Nogami K, et al. Among authors: shima m. J Biol Chem. 2000 Aug 18;275(33):25774-80. doi: 10.1074/jbc.M002007200. J Biol Chem. 2000. PMID: 10831589 Free article.

10

An alloantibody recognizing the FVIII A1 domain in a patient with CRM reduced haemophilia A due to deletion of a large portion of the A1 domain DNA sequence.

Shibata M, Shima M, Morichika S, McVey J, Tuddenham EG, Tanaka I, Suzuki H, Nogami K, Minamoto Y, Hato T, Saenko EL, Scandella D, Yoshioka A. Shibata M, et al. Among authors: shima m. Thromb Haemost. 2000 Sep;84(3):442-8. Thromb Haemost. 2000. PMID: 11019969

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