Yuta Imai

Kanazawa, 9200942, Japan

Last Updated: 09/26/2026

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Found 11 publications

Functional characterization of two protein C variants causing type I deficiency via cellular degradation or retention.

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

Real-time imaging of blood coagulation and angiogenesis during development in a zebrafish model of type I antithrombin deficiency.

Real-time imaging of blood coagulation and angiogenesis during development in a zebrafish model of type I antithrombin deficiency.

Journal: Scientific reports

Published: December 17, 2024

Mechanism of antithrombin deficiency due to the novel variant C32W in the C-terminus of the signal peptide.

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

Large-scale purification of mitochondrial protein complexes in yeast expression system for structural analyses.

Large-scale purification of mitochondrial protein complexes in yeast expression system for structural analyses.

Journal: Methods in enzymology

Published: November 02, 2024

Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles.

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.

Functional analysis of two abnormal antithrombin proteins with different intracellular kinetics.

Journal: Thrombosis research

Published: April 04, 2023

Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency.

Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency.

Journal: International journal of hematology

Published: July 08, 2022

First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.

First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.

Journal: Haematologica

Published: June 23, 2021

Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.

Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.

Journal: Thrombosis research

Published: November 13, 2019

Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.

Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.

Journal: International journal of hematology

Published: May 08, 2019

Showing 1-11 of 11

Last Updated: 09/26/2026