Associated Papers
[Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis].
Lu YF et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2026
Novel compound heterozygous mutations in plasminogen (p.Gly568Arg/p.Ala620Thr) impair protein structure and function in type II deficiency: mechanistic insights into a hereditary thrombogenic disorder.
Lu Y et al.
Orphanet Journal of Rare Diseases, 2025
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
Plasminogen missense variants and their involvement in cardiovascular and inflammatory disease.
Brito-Robinson T et al.
Frontiers in Cardiovascular Medicine, 2024
Ligneous periodontitis exacerbated by Behçet's disease in a patient with plasminogen deficiency and a stop-gained variant PLG c.1468C > T: a case report.
Shinoda-Ito Y et al.
Bmc Oral Health, 2023
Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.
Huang YC et al.
Journal of Personalized Medicine, 2023
Screening for thrombophilia in patients with thromboangitis obliterans using whole-exome sequencing.
Chen F et al.
Thrombosis Research, 2023
Analysis of cerebral infarction caused by dysplasminogenemia in three pedigrees.
Chen X et al.
Frontiers in Genetics, 2023
Severe dysplasminogenemia due to homozygous PLG Ala620Thr variant in a Korean woman without a history of venous thromboembolism: A case report and literature review.
Lee B et al.
Medicine, 2022
Non-cancer-related pathogenic germline variants and expression consequences in ten-thousand cancer genomes.
Wang Z et al.
Genome Medicine, 2021
Novel homozygous mutation of plasminogen in ligneous conjunctivitis: a case report and literature review.
Xu L et al.
Ophthalmic Genetics, 2021
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
Plasminogen Tochigi mice exhibit phenotypes similar to wild-type mice under experimental thrombotic conditions.
Tashima Y et al.
Plos One, 2017
No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
Miyata T et al.
International Journal of Hematology, 2016
Asynchronous Bilateral Renal Infarction and Thrombophilia With Associated Gene Mutations in a 43-Year-Old Man: A Case Report.
Zhou XJ et al.
Medicine, 2016
Protein S K196E mutation, a genetic risk factor for venous thromboembolism, is limited to Japanese.
Liu W et al.
Thrombosis Research, 2013
Plasma protein S activity correlates with protein S genotype but is not sensitive to identify K196E mutant carriers.
Kimura R et al.
Journal of Thrombosis and Haemostasis : Jth, 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-K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients.
Kimura R et al.
Blood, 2006
Plasma transfusion combined with chelating therapy alleviates fulminant Wilson's disease with a single Arg778Leu heterozygote mutation.
Liu L et al.
Annals of Hepatology, 0