Associated Papers
Plasminogen missense variants and their involvement in cardiovascular and inflammatory disease.
Brito-Robinson T et al.
Frontiers in Cardiovascular Medicine, 2024
Plasminogen Tochigi mice exhibit phenotypes similar to wild-type mice under experimental thrombotic conditions.
Tashima Y et al.
Plos One, 2017
Plasminogen deficiency.
Schuster V et al.
Journal of Thrombosis and Haemostasis : Jth, 2007
Molecular and clinical spectrum of type I plasminogen deficiency: A series of 50 patients.
Tefs K et al.
Blood, 2006
Genetic risk factors for deep vein thrombosis among Japanese: importance of protein S K196E mutation.
Miyata T et al.
International Journal of Hematology, 2006
Protein S and protein C gene mutations in Japanese deep vein thrombosis patients.
Kinoshita S et al.
Clinical Biochemistry, 2005
A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia.
Tefs K et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2003
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
Higuchi Y et al.
British Journal of Haematology, 1998
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