Showing results (1-10 of 2,251) with videos related to

Sort By:
Pageof 226
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 1998
Characterization of cDNA encoding full-length mouse platelet glycoprotein IXT Kitaguchi, M Murata, H Ambo, et al.
Thrombosis Research|July 15, 1997
Characterization of the gene encoding mouse platelet glycoprotien Ib betaT Kitaguchi, M Murata, H Anbo, et al.
Biochemical and Biophysical Research Communications|August 12, 1999
Characterization of liposomes carrying von Willebrand factor-binding domain of platelet glycoprotein Ibalpha: a potential substitute for platelet transfusionT Kitaguchi, M Murata, K Iijima, et al.
British Journal of Haematology|August 29, 1998
Novel point mutations in the alphaIIb subunit (Phe289-->Ser, Glu324-->Lys and Gln747-->Pro) causing thrombasthenic phenotypes in four Japanese patientsH Ambo, T Kamata, M Handa, et al.
Blood|July 15, 1997
Expression and functional characterization of an abnormal platelet membrane glycoprotein Ib alpha (Met239 --> Val) reported in patients with platelet-type von Willebrand diseaseT Moriki, M Murata, T Kitaguchi, et al.
British Journal of Haematology|September 1, 1999
A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo)T Zama, M Murata, R Watanabe, et al.
Biochemical and Biophysical Research Communications|April 28, 1997
High shear stress attenuates agonist-induced, glycoprotein IIb/IIIa-mediated platelet aggregation when von Willebrand factor binding to glycoprotein Ib/IX is blockedK Iijima, M Murata, K Nakamura, et al.
Biochemical and Biophysical Research Communications|October 29, 1998
Three novel integrin beta3 subunit missense mutations (H280P, C560F, and G579S) in thrombasthenia, including one (H280P) prevalent in Japanese patientsH Ambo, T Kamata, M Handa, et al.
British Journal of Haematology|August 1, 1993
Soluble P-selectin is present in normal circulation and its plasma level is elevated in patients with thrombotic thrombocytopenic purpura and haemolytic uraemic syndromeM Katayama, M Handa, Y Araki, et al.
Biochemical and Biophysical Research Communications|April 25, 2000
Targeting of liposomes carrying recombinant fragments of platelet membrane glycoprotein Ibalpha to immobilized von Willebrand factor under flow conditionsT Nishiya, M Murata, M Handa, et al.
Pageof 226