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British Journal of Haematology
|
May 1, 1994
Fine epitope mapping of monoclonal antibodies to the NH2-terminal part of von Willebrand factor (vWF) by using recombinant and synthetic peptides: interest for the localization of the factor VIII binding domain
S Jorieux, C Gaucher, G Piétu, et al.
Blood
|
February 1, 1992
The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor
S Jorieux, E A Tuley, C Gaucher, et al.
Thrombosis and Haemostasis
|
August 1, 1996
Combined hereditary disorders of haemophilia B Leyden (-6 G-->A) and type 1 von Willebrand disease
G Pernod, C Vinciguerra, C Gaucher, et al.
British Journal of Haematology
|
March 1, 1997
Rapid mutation screening in type 2A von Willebrand's disease using universal heteroduplex generators
D Culpan, G Standen, N Wood, et al.
Clinical Hemorheology and Microcirculation
|
July 21, 2007
In vitro impact of physiological shear stress on endothelial cells gene expression profile
C Gaucher, C Devaux, C Boura, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 27, 2015
[Diseases revealed by the mouth]
S Opsahl-Vital, C Gaucher, C Bardet, et al.
British Journal of Haematology
|
December 19, 1998
Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu
L Hilbert, C Gaucher, J F Abgrall, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
October 1, 1990
Expression in Escherichia coli of a recombinant fragment (Ile 914-Leu 1364) of human von Willebrand factor containing a collagen binding domain
S Jorieux, G Piétu, C Gaucher, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 4, 2022
Natural gas of radiolytic origin: An overlooked component of shale gas
Maria Naumenko-Dèzes, Wolfram Kloppmann, Michaela Blessing, et al.
Thrombosis and Haemostasis
|
April 1, 1995
Diagnosis of subtype 2B von Willebrand disease in a patient with 2A phenotype of plasma von Willebrand factor
C Gaucher, C de Romeuf, M Rauïs-Morret, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 58) with videos related to
Sort By:
Page
of 6
British Journal of Haematology
|
May 1, 1994
Fine epitope mapping of monoclonal antibodies to the NH2-terminal part of von Willebrand factor (vWF) by using recombinant and synthetic peptides: interest for the localization of the factor VIII binding domain
S Jorieux, C Gaucher, G Piétu, et al.
Blood
|
February 1, 1992
The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor
S Jorieux, E A Tuley, C Gaucher, et al.
Thrombosis and Haemostasis
|
August 1, 1996
Combined hereditary disorders of haemophilia B Leyden (-6 G-->A) and type 1 von Willebrand disease
G Pernod, C Vinciguerra, C Gaucher, et al.
British Journal of Haematology
|
March 1, 1997
Rapid mutation screening in type 2A von Willebrand's disease using universal heteroduplex generators
D Culpan, G Standen, N Wood, et al.
Clinical Hemorheology and Microcirculation
|
July 21, 2007
In vitro impact of physiological shear stress on endothelial cells gene expression profile
C Gaucher, C Devaux, C Boura, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 27, 2015
[Diseases revealed by the mouth]
S Opsahl-Vital, C Gaucher, C Bardet, et al.
British Journal of Haematology
|
December 19, 1998
Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu
L Hilbert, C Gaucher, J F Abgrall, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
October 1, 1990
Expression in Escherichia coli of a recombinant fragment (Ile 914-Leu 1364) of human von Willebrand factor containing a collagen binding domain
S Jorieux, G Piétu, C Gaucher, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 4, 2022
Natural gas of radiolytic origin: An overlooked component of shale gas
Maria Naumenko-Dèzes, Wolfram Kloppmann, Michaela Blessing, et al.
Thrombosis and Haemostasis
|
April 1, 1995
Diagnosis of subtype 2B von Willebrand disease in a patient with 2A phenotype of plasma von Willebrand factor
C Gaucher, C de Romeuf, M Rauïs-Morret, et al.
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of 6