Search research articles
Contact Us
Filters
Showing results (221-230 of 236) with videos related to
Page
of 24
Sort By:
Blood
|
November 1, 1995
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency
J Duchemin, S Gandrille, D Borgel, et al.
The Journal of Biological Chemistry
|
November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine
S Gandrille, M Aiach, D A Lane, et al.
Thrombosis and Haemostasis
|
March 4, 1999
The factor V gene A4070G mutation and the risk of venous thrombosis
M Alhenc-Gelas, V Nicaud, S Gandrille, et al.
The American Journal of Medicine
|
January 12, 2001
Factors V leiden and II 20210A in patients with symptomatic pulmonary embolism and deep vein thrombosis
G Meyer, J Emmerich, D Helley, et al.
Thrombosis and Haemostasis
|
June 1, 1997
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiency
A Inbal, G Kenet, A Zivelin, et al.
The Biochemical Journal
|
November 22, 2001
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain
D Borgel, P Gaussem, C Garbay, et al.
Thrombosis and Haemostasis
|
August 2, 1993
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
D A Lane, R J Olds, M Boisclair, et al.
British Journal of Haematology
|
January 1, 1991
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrate
R Caso, D A Lane, E A Thompson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 11, 2000
Polymorphisms in the 5' regulatory region of the tissue factor gene and the risk of myocardial infarction and venous thromboembolism: the ECTIM and PATHROS studies. Etude Cas-Témoins de l'Infarctus du Myocarde. Paris Thrombosis case-control Study
E Arnaud, V Barbalat, V Nicaud, et al.
British Journal of Haematology
|
September 21, 2000
Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene
V Picard, A Bura, J Emmerich, et al.
Page
of 24
Search research articles
Search
Showing results (221-230 of 236) with videos related to
Sort By:
Page
of 24
Blood
|
November 1, 1995
The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency
J Duchemin, S Gandrille, D Borgel, et al.
The Journal of Biological Chemistry
|
November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine
S Gandrille, M Aiach, D A Lane, et al.
Thrombosis and Haemostasis
|
March 4, 1999
The factor V gene A4070G mutation and the risk of venous thrombosis
M Alhenc-Gelas, V Nicaud, S Gandrille, et al.
The American Journal of Medicine
|
January 12, 2001
Factors V leiden and II 20210A in patients with symptomatic pulmonary embolism and deep vein thrombosis
G Meyer, J Emmerich, D Helley, et al.
Thrombosis and Haemostasis
|
June 1, 1997
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiency
A Inbal, G Kenet, A Zivelin, et al.
The Biochemical Journal
|
November 22, 2001
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain
D Borgel, P Gaussem, C Garbay, et al.
Thrombosis and Haemostasis
|
August 2, 1993
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
D A Lane, R J Olds, M Boisclair, et al.
British Journal of Haematology
|
January 1, 1991
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrate
R Caso, D A Lane, E A Thompson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 11, 2000
Polymorphisms in the 5' regulatory region of the tissue factor gene and the risk of myocardial infarction and venous thromboembolism: the ECTIM and PATHROS studies. Etude Cas-Témoins de l'Infarctus du Myocarde. Paris Thrombosis case-control Study
E Arnaud, V Barbalat, V Nicaud, et al.
British Journal of Haematology
|
September 21, 2000
Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene
V Picard, A Bura, J Emmerich, et al.
Page
of 24