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Wenman Wu

Showing results (41-50 of 57) with videos related to

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Plos One|February 6, 2014
Proteomics analysis of co-purifying cellular proteins associated with rAAV vectorsBiao Dong, Xunbao Duan, Hoi Yee Chow, et al.
Human Gene Therapy|January 18, 2006
Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophiliaBernd Hauck, Ray Ruian Xu, Jing Xie, et al.
Thrombosis and Haemostasis|March 20, 2026
SERPINC1 p.M313T variant induces aberrant O-Glycosylation and leads to conformational instability-related transient antithrombin deficiencyChangming Chen, Yinqi Mao, Liya Lin, et al.
Blood|March 18, 2004
Dominant factor XI deficiency caused by mutations in the factor XI catalytic domainDmitri V Kravtsov, Wenman Wu, Joost C M Meijers, et al.
Thrombosis and Haemostasis|April 18, 2025
Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous MaleJunwei Yuan, Shijie Zhou, Xi Wu, et al.
Thrombosis and Haemostasis|November 27, 2023
Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C DeficiencyShijie Zhou, Xi Wu, Ying Song, et al.
Journal of Clinical Pathology|August 25, 2016
Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerizationJingyi Zhou, Qiulan Ding, Wenman Wu, et al.
Thrombosis Research|June 2, 2024
Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosisZhe Lai, Jiaming Li, Shijie Zhou, et al.
Thrombosis and Haemostasis|June 24, 2024
Heterozygous Prothrombin Mutation-Associated ThrombophiliaXi Wu, Lei Li, Zhengjing Lu, et al.
Thrombosis Research|June 10, 2025
Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis riskZhe Lai, Junwei Yuan, Fang Li, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Plos One|February 6, 2014
Proteomics analysis of co-purifying cellular proteins associated with rAAV vectorsBiao Dong, Xunbao Duan, Hoi Yee Chow, et al.
Human Gene Therapy|January 18, 2006
Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophiliaBernd Hauck, Ray Ruian Xu, Jing Xie, et al.
Thrombosis and Haemostasis|March 20, 2026
SERPINC1 p.M313T variant induces aberrant O-Glycosylation and leads to conformational instability-related transient antithrombin deficiencyChangming Chen, Yinqi Mao, Liya Lin, et al.
Blood|March 18, 2004
Dominant factor XI deficiency caused by mutations in the factor XI catalytic domainDmitri V Kravtsov, Wenman Wu, Joost C M Meijers, et al.
Thrombosis and Haemostasis|April 18, 2025
Asn384Ser Mutation in Protein C is Associated with Multiple-Site Thrombosis in a Young Heterozygous MaleJunwei Yuan, Shijie Zhou, Xi Wu, et al.
Thrombosis and Haemostasis|November 27, 2023
Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C DeficiencyShijie Zhou, Xi Wu, Ying Song, et al.
Journal of Clinical Pathology|August 25, 2016
Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerizationJingyi Zhou, Qiulan Ding, Wenman Wu, et al.
Thrombosis Research|June 2, 2024
Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosisZhe Lai, Jiaming Li, Shijie Zhou, et al.
Thrombosis and Haemostasis|June 24, 2024
Heterozygous Prothrombin Mutation-Associated ThrombophiliaXi Wu, Lei Li, Zhengjing Lu, et al.
Thrombosis Research|June 10, 2025
Thrombomodulin Arg403Lys mutation impairs protein C activation and increases thrombosis riskZhe Lai, Junwei Yuan, Fang Li, et al.
Pageof 6