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Thrombosis Research
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February 22, 2024
A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand disease
Qian Liang, Ziqi Zhang, Biying Ding, et al.
International Journal of Clinical and Experimental Medicine
|
August 27, 2015
A novel factor X gene mutation Val (GTC) 384Ala (GCC) in a Chinese family resulting in congenital factor X deficiency
Yanming Wang, Junjie Ma, Xinguang Liu, et al.
Thrombosis Research
|
December 30, 2023
A novel GATA1 variant p.G229D causing the defect of procoagulant platelet formation
Biying Ding, Yinqi Mao, Yang Li, et al.
Thrombosis Research
|
April 17, 2026
Pseudoexon inclusion induced by three deep intronic variants in hemophilia B and correction achieved through an antisense oligonucleotide-based strategy
Guangming Chen, Jialu Zhang, Liya Lin, et al.
Chemical Biology & Drug Design
|
May 21, 2019
An unexpected dynamic binding mode between coagulation factor X and Rivaroxaban reveals importance of flexibility in drug binding
Si-Ying Qu, Qin Xu, Wenman Wu, et al.
Human Mutation
|
December 9, 2021
Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor
Qian Liang, Xiaoyi Lin, Xi Wu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 17, 2025
Correction of VWF multimerization in type 2A/IIC von Willebrand disease by exogenous VWF propeptide supplementation
Ziqi Zhang, Qian Liang, Xiaoqian Xu, et al.
Haematologica
|
July 10, 2025
Perioperative management of total hip arthroplasty in hemophilia A following gene therapy
Yanyan Shao, Chuanlong Wu, Wei Liu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 27, 2019
Prothrombin Arg541Trp Mutation Leads to Defective PC (Protein C) Pathway Activation and Constitutes a Novel Genetic Risk Factor for Venous Thrombosis
Xi Wu, Jing Dai, Xiaoqian Xu, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 8, 2025
A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities
Changming Chen, Xi Wu, Lei Li, et al.
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Search research articles
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Showing results (61-70 of 98) with videos related to
Sort By:
Page
of 10
Thrombosis Research
|
February 22, 2024
A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand disease
Qian Liang, Ziqi Zhang, Biying Ding, et al.
International Journal of Clinical and Experimental Medicine
|
August 27, 2015
A novel factor X gene mutation Val (GTC) 384Ala (GCC) in a Chinese family resulting in congenital factor X deficiency
Yanming Wang, Junjie Ma, Xinguang Liu, et al.
Thrombosis Research
|
December 30, 2023
A novel GATA1 variant p.G229D causing the defect of procoagulant platelet formation
Biying Ding, Yinqi Mao, Yang Li, et al.
Thrombosis Research
|
April 17, 2026
Pseudoexon inclusion induced by three deep intronic variants in hemophilia B and correction achieved through an antisense oligonucleotide-based strategy
Guangming Chen, Jialu Zhang, Liya Lin, et al.
Chemical Biology & Drug Design
|
May 21, 2019
An unexpected dynamic binding mode between coagulation factor X and Rivaroxaban reveals importance of flexibility in drug binding
Si-Ying Qu, Qin Xu, Wenman Wu, et al.
Human Mutation
|
December 9, 2021
Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor
Qian Liang, Xiaoyi Lin, Xi Wu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 17, 2025
Correction of VWF multimerization in type 2A/IIC von Willebrand disease by exogenous VWF propeptide supplementation
Ziqi Zhang, Qian Liang, Xiaoqian Xu, et al.
Haematologica
|
July 10, 2025
Perioperative management of total hip arthroplasty in hemophilia A following gene therapy
Yanyan Shao, Chuanlong Wu, Wei Liu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 27, 2019
Prothrombin Arg541Trp Mutation Leads to Defective PC (Protein C) Pathway Activation and Constitutes a Novel Genetic Risk Factor for Venous Thrombosis
Xi Wu, Jing Dai, Xiaoqian Xu, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 8, 2025
A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities
Changming Chen, Xi Wu, Lei Li, et al.
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