Associated Papers
Whole genome sequencing identifies pathogenic genetic variants in Han Chinese patients with familial venous thromboembolism.
Zhang Z et al.
Communications Biology, 2025
40221599 (PubMed )
Supplement: 42003_2025_7935_MOESM1_ESM.pdf
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.5
Molecular profiling of TAM tyrosine kinase receptors and ligands in endometrial carcinoma: An in silico-study.
Dilara Fatma Akin et al.
Taiwanese Journal of Obstetrics & Gynecology, 2023
Case Report: PROS1 (p.Leu584Arg) pathogenic mutation causes portal and superior mesenteric venous thromboembolism.
Ding P et al.
Frontiers in Cardiovascular Medicine, 2023
Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments.
Maruyama K et al.
Research and Practice in Thrombosis and Haemostasis, 2021
Molecular basis of protein S deficiency in China.
Tang L et al.
American Journal of Hematology, 2013
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