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Biochimie
|
January 1, 1974
Preparation of iodo derivatives and high specific activity 3H synthetic human gastrin I
J P Girma, J L Morgat, P Fromageot, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 11, 2004
Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)
A Veyradier, J-M Lavergne, A-S Ribba, et al.
The New England Journal of Medicine
|
February 11, 1982
Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers
H J Weiss, D Meyer, R Rabinowitz, et al.
FEBS Letters
|
July 15, 1976
Interaction of 3H-labelled synthetic human gastrin I with rat gastric plasma membranes. Evidence for the existence of biologically reactive gastrin receptor sites
M Lewin, A Soumarmon, J P Bali, et al.
Blood
|
May 1, 1986
Mapping of distinct von Willebrand factor domains interacting with platelet GPIb and GPIIb/IIIa and with collagen using monoclonal antibodies
J P Girma, M Kalafatis, G Piétu, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 8, 2006
Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13
J Rayes, A Hommais, P Legendre, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
April 1, 1994
Interaction of von Willebrand factor with platelets activated by thrombin or a synthetic 7-amino acid peptide derived from the cleaved thrombin receptor
O Minckes, J M Freyssinet, C Rouault, et al.
Thrombosis and Haemostasis
|
January 1, 1997
Abnormal proteolytic processing of von Willebrand factor Arg611 Cys and Arg611His
T Nishikubo, O Christophe, J M Lavergne, et al.
Thrombosis and Haemostasis
|
October 5, 2001
Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen
A S Ribba, I Loisel, J M Lavergne, et al.
Blood
|
June 15, 1994
Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor
O Christophe, A S Ribba, D Baruch, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
Biochimie
|
January 1, 1974
Preparation of iodo derivatives and high specific activity 3H synthetic human gastrin I
J P Girma, J L Morgat, P Fromageot, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 11, 2004
Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)
A Veyradier, J-M Lavergne, A-S Ribba, et al.
The New England Journal of Medicine
|
February 11, 1982
Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers
H J Weiss, D Meyer, R Rabinowitz, et al.
FEBS Letters
|
July 15, 1976
Interaction of 3H-labelled synthetic human gastrin I with rat gastric plasma membranes. Evidence for the existence of biologically reactive gastrin receptor sites
M Lewin, A Soumarmon, J P Bali, et al.
Blood
|
May 1, 1986
Mapping of distinct von Willebrand factor domains interacting with platelet GPIb and GPIIb/IIIa and with collagen using monoclonal antibodies
J P Girma, M Kalafatis, G Piétu, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 8, 2006
Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS-13
J Rayes, A Hommais, P Legendre, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
April 1, 1994
Interaction of von Willebrand factor with platelets activated by thrombin or a synthetic 7-amino acid peptide derived from the cleaved thrombin receptor
O Minckes, J M Freyssinet, C Rouault, et al.
Thrombosis and Haemostasis
|
January 1, 1997
Abnormal proteolytic processing of von Willebrand factor Arg611 Cys and Arg611His
T Nishikubo, O Christophe, J M Lavergne, et al.
Thrombosis and Haemostasis
|
October 5, 2001
Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen
A S Ribba, I Loisel, J M Lavergne, et al.
Blood
|
June 15, 1994
Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor
O Christophe, A S Ribba, D Baruch, et al.
Page
of 7