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Showing results (121-130 of 236) with videos related to

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British Journal of Haematology|June 1, 1990
Clinical and biochemical characterization of antithrombin III Franconville, a variant with Pro 41 Leu mutationN de Roux, G Chadeuf, P Molho-Sabatier, et al.
The Journal of Biological Chemistry|February 13, 1999
Topology of the stable serpin-protease complexes revealed by an autoantibody that fails to react with the monomeric conformers of antithrombinV Picard, P E Marque, F Paolucci, et al.
British Journal of Haematology|March 1, 1988
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated familiesS Gandrille, P Priollet, L Capron, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 1998
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to ThrS Kemahli, M Alhenc-Gelas, S Gandrille, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 13, 2003
Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutationsC Boinot, D Borgel, A Kitzis, et al.
Thrombosis and Haemostasis|June 3, 1987
Antithrombin III and heparin cofactor II in patients with chronic renal failure undergoing regular hemodialysisP Toulon, C Jacquot, L Capron, et al.
Thrombosis and Haemostasis|December 29, 2000
A study of platelet functions with a new analyzer using high shear stress (PFA 100) in patients undergoing coronary artery bypass graftD Lasne, A Fiemeyer, G Chatellier, et al.
Circulation Research|April 17, 2001
Thrombomodulin prolongs thrombin-induced extracellular signal-regulated kinase phosphorylation and nuclear retention in endothelial cellsJ M Olivot, E Estebanell, M Lafay, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1996
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S DeficienciesD Borgel, J Duchemin, M Alhenc-Gelas, et al.
Nephron|January 1, 1992
Significance of high levels of heparin cofactor II in the plasma and urine of adult patients with nephrotic syndromeP Toulon, S Gandrille, P Remy, et al.
Pageof 24

Showing results (121-130 of 236) with videos related to

Sort By:
Pageof 24
British Journal of Haematology|June 1, 1990
Clinical and biochemical characterization of antithrombin III Franconville, a variant with Pro 41 Leu mutationN de Roux, G Chadeuf, P Molho-Sabatier, et al.
The Journal of Biological Chemistry|February 13, 1999
Topology of the stable serpin-protease complexes revealed by an autoantibody that fails to react with the monomeric conformers of antithrombinV Picard, P E Marque, F Paolucci, et al.
British Journal of Haematology|March 1, 1988
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated familiesS Gandrille, P Priollet, L Capron, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 1998
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to ThrS Kemahli, M Alhenc-Gelas, S Gandrille, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 13, 2003
Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutationsC Boinot, D Borgel, A Kitzis, et al.
Thrombosis and Haemostasis|June 3, 1987
Antithrombin III and heparin cofactor II in patients with chronic renal failure undergoing regular hemodialysisP Toulon, C Jacquot, L Capron, et al.
Thrombosis and Haemostasis|December 29, 2000
A study of platelet functions with a new analyzer using high shear stress (PFA 100) in patients undergoing coronary artery bypass graftD Lasne, A Fiemeyer, G Chatellier, et al.
Circulation Research|April 17, 2001
Thrombomodulin prolongs thrombin-induced extracellular signal-regulated kinase phosphorylation and nuclear retention in endothelial cellsJ M Olivot, E Estebanell, M Lafay, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1996
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S DeficienciesD Borgel, J Duchemin, M Alhenc-Gelas, et al.
Nephron|January 1, 1992
Significance of high levels of heparin cofactor II in the plasma and urine of adult patients with nephrotic syndromeP Toulon, S Gandrille, P Remy, et al.
Pageof 24