Akira Takagi

Nagoya, Japan

Last Updated: 09/26/2026

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Found 39 publications

Antithrombotic Therapy on Antithrombin Resistance in a Mouse Model.

Antithrombotic Therapy on Antithrombin Resistance in a Mouse Model.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: January 08, 2026

Polyester Adhesives via One-Pot, One-Step Copolymerization of Cyclic Anhydride, Epoxide, and Lactide.

Polyester Adhesives via One-Pot, One-Step Copolymerization of Cyclic Anhydride, Epoxide, and Lactide.

Journal: Polymers

Published: August 23, 2024

Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development.

Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development.

Journal: The Journal of biological chemistry

Published: August 06, 2021

F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B.

F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B.

Journal: Thrombosis research

Published: March 02, 2021

Essential role of a carboxyl-terminal α-helix motif in the secretion of coagulation factor XI.

Essential role of a carboxyl-terminal α-helix motif in the secretion of coagulation factor XI.

Journal: Journal of thrombosis and haemostasis : JTH

Published: June 12, 2020

Aberrant X chromosomal rearrangement through multi-step template switching during sister chromatid formation in a patient with severe hemophilia A.

Aberrant X chromosomal rearrangement through multi-step template switching during sister chromatid formation in a patient with severe hemophilia A.

Journal: Molecular genetics & genomic medicine

Published: January 15, 2020

Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing.

Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing.

Journal: Thrombosis research

Published: March 01, 2019

Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency.

Molecular basis of SERPINC1 mutations in Japanese patients with antithrombin deficiency.

Journal: Thrombosis research

Published: December 13, 2018

Vwf K1362A resulted in failure of protein synthesis in mice.

Vwf K1362A resulted in failure of protein synthesis in mice.

Journal: International journal of hematology

Published: December 08, 2017

Optimisation of antithrombin resistance assay as a practical clinical laboratory test: Development of prothrombin activator using factors Xa/Va and automation of assay.

Optimisation of antithrombin resistance assay as a practical clinical laboratory test: Development of prothrombin activator using factors Xa/Va and automation of assay.

Journal: International journal of laboratory hematology

Published: October 08, 2017

Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese family.

Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese family.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: September 19, 2017

Familial pulmonary thromboembolism with a prothrombin mutation and antithrombin resistance.

Familial pulmonary thromboembolism with a prothrombin mutation and antithrombin resistance.

Journal: Journal of cardiology cases

Published: September 07, 2017

Showing 1-12 of 39

Last Updated: 09/26/2026