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M Aiach

Showing results (221-230 of 236) with videos related to

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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) deficiencyJ 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 glutamineS 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 thrombosisM 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 thrombosisG 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 deficiencyA 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 domainD 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 HaemostasisD 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 substrateR 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 StudyE 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 geneV Picard, A Bura, J Emmerich, et al.
Pageof 24

Showing results (221-230 of 236) with videos related to

Sort By:
Pageof 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) deficiencyJ 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 glutamineS 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 thrombosisM 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 thrombosisG 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 deficiencyA 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 domainD 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 HaemostasisD 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 substrateR 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 StudyE 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 geneV Picard, A Bura, J Emmerich, et al.
Pageof 24