Keiko Maruyama
Suita, Japan
Last Updated: 09/26/2026
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Found 13 publications
A long first intron of PROS1 modulates protein S expression across tissues in mice and humans.
Journal: Blood advances
Published: January 16, 2026
Development of an assay using a modified coagulation factor V to measure protein S activity.
Journal: Journal of thrombosis and haemostasis : JTH
Published: May 29, 2024
Alpha-HIT assay: A new assay for heparin-induced thrombocytopenia antibody detection using FcγRIIa-coated beads and Alpha technology.
Journal: Research and practice in thrombosis and haemostasis
Published: July 13, 2022
First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.
Journal: Haematologica
Published: June 23, 2021
A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder.
Journal: Blood advances
Published: November 13, 2020
Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments.
Journal: Research and practice in thrombosis and haemostasis
Published: June 29, 2020
Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report.
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: September 03, 2019
Protein S K196E mutation reduces its cofactor activity for APC but not for TFPI.
Journal: Research and practice in thrombosis and haemostasis
Published: February 21, 2018
Thrombophilia in East Asian countries: are there any genetic differences in these countries?
Journal: Thrombosis journal
Published: October 22, 2016
Congenital thrombophilia in Japanese, comparison to Caucasian
Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology
Published: September 05, 2014
Last Updated: 09/26/2026