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Blood|November 5, 1997
An in vitro analysis of the combination of hemophilia A and factor V(LEIDEN)C van 't Veer, N J Golden, M Kalafatis, et al.Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.Blood|June 1, 1989
Partial gene deletion in a family with factor X deficiencyF Bernardi, G Marchetti, P Patracchini, et al.The Journal of Biological Chemistry|May 9, 1998
Identification and partial characterization of factor Va heavy chain kinase from human plateletsM KalafatisThrombosis Research|March 15, 2001
A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian familyP Simioni, F Vianello, M Kalafatis, et al.Bailliere'S Best Practice & Research. Clinical Haematology|June 17, 2000
The molecular genetics of familial venous thrombosisP SimioniJournal of Thrombosis and Haemostasis : JTH|December 20, 2005
Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutationJ M Brugge, P Simioni, F Bernardi, et al.Advances in Experimental Medicine and Biology|September 14, 2001
Factor V: Dr. Jeckyll and Mr. HydeM Kalafatis, K G MannThe Journal of Biological Chemistry|December 25, 1993
Role of the membrane in the inactivation of factor Va by activated protein CM Kalafatis, K G MannThe Journal of Biological Chemistry|March 30, 2001
The role of the membrane in the inactivation of factor va by plasmin. Amino acid region 307-348 of factor V plays a critical role in factor Va cofactor functionM Kalafatis, K G MannPageof 44