Congratulations to Toshiyuki Miyata, PhD
Author:
Affiliation:
1. Emeritus Professor and Director, University Clinic of Hematology, University of Bern, Bern
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/33/6/33_2022_JJTH_33_6_722-724/_pdf
Reference10 articles.
1. 1) Miyata T, Kawabata S-I, Iwanaga S, Takahashi I, Alving B, Saito H: Coagulation factor XII (Hageman factor) Washington D.C.: Inactive factor XIIa results from Cys-571 → Ser substitution. Proc Natl Acad Sci U S A 86: 8319–8322, 1989.
2. 2) Wuillemin WA et al.: Functional characterization of an abnormal factor XII molecule (FXII Bern). Blood 78: 997–1004, 1991.
3. 3) Wuillemin WA et al.: Functional characterization of a variant factor XII (FXII Locarno) in a cross reacting material positive FXII deficient plasma. J Thromb Haemost 67: 219–225, 1992.
4. 4) Kremer Hovinga J et al.: Coagulation factor XII Locarno: The functional defect is caused by the amino acid substitution Arg 353 → Pro leading to loss of a kallikrein cleavage site.
5. 5) Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, Tamai H, Konno M, Kamide K, Kawano Y, Miyata T, Fujimura Y: Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci U S A 99: 11902–11907, 2002.
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