The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population
- 27 April 2004
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 125 (5) , 647-654
- https://doi.org/10.1111/j.1365-2141.2004.04961.x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- A study of Protein S antigen levels in 3788 healthy volunteers: influence of age, sex and hormone use, and estimate for prevalence of deficiency stateBritish Journal of Haematology, 2001
- Deficient APC-cofactor activity of protein S Heerlen in degradation of factor Va Leiden: a possible mechanism of synergism between thrombophilic risk factorsBlood, 2000
- Homozygosity for the Protein S Heerlen Allele Is Associated with Type I PS Deficiency in a Thrombophilic Pedigree with Multiple Risk FactorsThrombosis and Haemostasis, 2000
- A Novel Mutation in Intron K of the PROS1 Gene Causes Aberrant RNA Splicing and Is a Common Cause of Protein S Deficiency in a UK Thrombophilia CohortThrombosis and Haemostasis, 1998
- Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategyBlood, 1995
- Differential regulation of alpha and beta chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein SBlood, 1994
- A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PSα (PROS1)Nucleic Acids Research, 1991
- Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460Blood, 1990
- The Regulation of Natural Anticoagulant PathwaysScience, 1987
- High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein.Proceedings of the National Academy of Sciences, 1981