Xi Wu

No. 197 Ruijin Second Road
Shanghai, 200025, China

Last Updated: 09/26/2026

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Found 23 publications

Thrombomodulin Gly430Ser mutation attenuates the affinity with thrombin and contributes to thrombosis development.

Thrombomodulin Gly430Ser mutation attenuates the affinity with thrombin and contributes to thrombosis development.

Journal: Journal of thrombosis and thrombolysis

Published: May 02, 2026

SERPINC1 p.M313T Variant Induces Aberrant O-Glycosylation and Leads to Conformational Instability-Related Transient Antithrombin Deficiency.

SERPINC1 p.M313T Variant Induces Aberrant O-Glycosylation and Leads to Conformational Instability-Related Transient Antithrombin Deficiency.

Journal: Thrombosis and haemostasis

Published: March 20, 2026

Molecular basis of the E69Q and R383W heterozygous F2 variants identified in the proband associated with severe hemostatic defects.

Molecular basis of the E69Q and R383W heterozygous F2 variants identified in the proband associated with severe hemostatic defects.

Journal: Thrombosis research

Published: February 26, 2026

Trp83 is vital to the interaction with phospholipids in γ-carboxyglutamic acid domain of protein C.

Trp83 is vital to the interaction with phospholipids in γ-carboxyglutamic acid domain of protein C.

Journal: Journal of thrombosis and haemostasis : JTH

Published: February 06, 2026

Thrombosis Caused by Factor XI Gly397Ser Mutation with Enhanced Procoagulant Activity.

Thrombosis Caused by Factor XI Gly397Ser Mutation with Enhanced Procoagulant Activity.

Journal: Thrombosis and haemostasis

Published: December 08, 2025

Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous Male.

Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous Male.

Journal: Thrombosis and haemostasis

Published: April 18, 2025

Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis risk.

Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis risk.

Journal: Thrombosis research

Published: April 18, 2025

A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities.

A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities.

Journal: Journal of thrombosis and haemostasis : JTH

Published: November 18, 2024

Heterozygous Prothrombin Mutation-Associated Thrombophilia.

Heterozygous Prothrombin Mutation-Associated Thrombophilia.

Journal: Thrombosis and haemostasis

Published: June 24, 2024

Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosis.

Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosis.

Journal: Thrombosis research

Published: March 28, 2024

Met343Val mutation disrupts the shuttling of Trp380 leading to a low-activity conformer of activated protein C and causes thrombosis.

Met343Val mutation disrupts the shuttling of Trp380 leading to a low-activity conformer of activated protein C and causes thrombosis.

Journal: Journal of thrombosis and haemostasis : JTH

Published: February 18, 2024

Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency.

Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency.

Journal: Thrombosis and haemostasis

Published: November 27, 2023

Showing 1-12 of 23

Last Updated: 09/26/2026