Tomio Yamazaki (Former)

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2010
Mark The D2194G mutation is responsible for increased levels of FV1 in carriers of the factor V R2 haplotype
Yamazaki, Tomio ^LU ; Okada, Hiromi ; Balling, Kristoffer ; Dahlbäck, Björn ^LU and Nicolaes, Gerry (2010) In Thrombosis and Haemostasis 104(4). p.860-861
- Contribution to journal › Letter
2004
Mark Functional properties of recombinant factor V mutated in a potential calcium-binding site.
Sørensen, Kristoffer ^LU ; Nicolaes, Gerry A F ; Villoutreix, Bruno O ; Yamazaki, Tomio ^LU ; Tans, Guido ; Rosing, Jan and Dahlbäck, Björn ^LU (2004) In Biochemistry 43(19). p.5803-5810
- Contribution to journal › Article
2003
Mark Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized.
Steen, Mårten ^LU ; Miteva, Maria ; Villoutreix, Bruno O ; Yamazaki, Tomio ^LU and Dahlbäck, Björn ^LU (2003) In Blood 102(4). p.1316-1322
- Contribution to journal › Article
2002
Mark Defining the factor Xa-binding site on factor Va by site-directed glycosylation.
Steen, Mårten ^LU ; Villoutreix, Bruno O. ; Norström, Eva ^LU ; Yamazaki, Tomio ^LU and Dahlbäck, Björn ^LU (2002) In Journal of Biological Chemistry 277(51). p.50022-50029
- Contribution to journal › Article
Mark Structural requirements of anticoagulant protein S for its binding to the complement regulator c4b-binding protein
Giri, TK ; Linse, Sara ^LU ; Garcia de Frutos, Pablo ^LU ; Yamazaki, Tomio ^LU ; Villoutreix, BO and Dahlbäck, Björn ^LU (2002) In Journal of Biological Chemistry 277(17). p.15099-15106
- Contribution to journal › Article
Mark Molecular basis of quantitative factor V deficiency associated with factor V R2 haplotype.
Yamazaki, Tomio ^LU ; Nicolaes, Gerry A F ; Sørensen, Kristoffer ^LU and Dahlbäck, Björn ^LU (2002) In Blood 100(7). p.2515-2521
- Contribution to journal › Article
Mark Rapid intracellular degradation of a truncated mutant protein S (Q522X)
Yamazaki, Tomio ^LU ; Saito, H and Dahlbäck, Björn ^LU (2002) In Thrombosis and Haemostasis 87(1). p.171-172
- Contribution to journal › Letter