Satomi Nagaya
Kanazawa, Japan
Last Updated: 09/26/2026
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Found 22 publications
Recurrent miscarriage and thrombosis in Asian antiphospholipid syndrome: a systematic review.
Journal: Journal of reproductive immunology
Published: April 23, 2026
Functional characterization of two protein C variants causing type I deficiency via cellular degradation or retention.
Journal: International journal of hematology
Published: May 13, 2025
Tissue Factor Pathway-Driven Initial Thrombin Generation is Associated with Hypercoagulability in Obesity.
Journal: Thrombosis and haemostasis
Published: March 06, 2025
Molecular Mechanism Underlying Functional Defects in the Prothrombin Variant Segovia that Cause a Bleeding Tendency.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: December 09, 2024
Effect of Antithrombin Leakage From Hemodialysis Therapy on Antithrombin Hemodynamics.
Journal: Cureus
Published: December 04, 2024
Mechanism of antithrombin deficiency due to the novel variant C32W in the C-terminus of the signal peptide.
Journal: International journal of hematology
Published: November 25, 2024
The novel protein C variant p.C101F results in early intracellular degradation that drives type I protein C deficiency.
Journal: International journal of hematology
Published: November 07, 2024
Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles.
Journal: Thrombosis research
Published: October 16, 2023
Protein S deficiency caused by cryptic splicing due to the novel intron variant c.346+5G>C in PROS1.
Protein S deficiency caused by cryptic splicing due to the novel intron variant c.346+5G>C in PROS1.
Journal: Thrombosis research
Published: April 21, 2023
Functional analysis of two abnormal antithrombin proteins with different intracellular kinetics.
Journal: Thrombosis research
Published: April 04, 2023
Last Updated: 09/26/2026