Protein S down-regulates factor Xase activity independent of activated protein C: specific binding of factor VIII(a) to protein S inhibits interactions with factor IXa
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2008.07366.x/fullpdf
Reference42 articles.
1. Recurrent venous thromboembolism in patients with a partial deficiency of protein S;Comp;The New England Journal of Medicine,1984
2. Familial protein S deficiency is associated with recurrent thrombosis;Comp;The Journal of Clinical Investigation,1984
3. Inhibition of protein Ca cofactor function of human and bovine protein S by C4b-binding protein;Dahlbäck;The Journal of Biological Chemistry,1986
4. High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein;Dahlbäck;Proceedings of the National Academy of Sciences of the United States of America,1981
5. Characterization of protein S, a gamma-carboxyglutamic acid containing protein from bovine and human plasma;DiScipio;Biochemistry,1980
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1. Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events;International Journal of Laboratory Hematology;2024-01-18
2. Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency;Annals of Hematology;2024-01-04
3. A Case of Type 2 Protein S Deficiency Presenting as Cerebral Venous Thrombosis (CVT) in an 18-Year-Old Female;Cureus;2022-08-20
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