Population-based distribution of plasminogen activity and estimated prevalence and relevance to thrombotic diseases of plasminogen deficiency in Japanese: the Suita Study
Open Access
- 1 November 2003
- journal article
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 1 (11), 2397-2403
- https://doi.org/10.1046/j.1538-7836.2003.00419.x
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Common Mutation of Plasminogen Detected in Three Asian Populations by an Amplification Refractory Mutation System and Rapid Automated Capillary ElectrophoresisThrombosis and Haemostasis, 1999
- Elucidation of the cause for reduced activity of abnormal human plasmin containing an Ala55‐Thr mutation: importance of highly conserved Ala55 in serine proteasesFEBS Letters, 1998
- Homozygous Mutations in the Plasminogen Gene of Two Unrelated Girls With Ligneous ConjunctivitisBlood, 1997
- Plasminogen with type-I mutation in the Chinese Han populationClinical Genetics, 1994
- Congenital plasminogen deficiency caused by a Ser572 to Pro mutationBlood, 1993
- Plasminogen with type-I mutation is polymorphic in the Japanese populationHuman Genetics, 1992
- Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.Proceedings of the National Academy of Sciences, 1991
- Differences of frequency distributions of plasminogen phenotypes between Japanese and American populations: New methods for the detection of plasminogen variantsBiochemical Genetics, 1984
- Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site.Proceedings of the National Academy of Sciences, 1982
- Abnormal PlasminogenJournal of Clinical Investigation, 1978