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Qiulan Ding

Showing results (31-40 of 98) with videos related to

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Thrombosis Journal|October 3, 2023
Evaluation of prothrombotic risk of two PROC hotspot mutations (Arg189Trp and Lys193del) in Chinese population: a retrospective studyLei Li, Jian Li, Xi Wu, et al.
Thrombosis and Haemostasis|April 14, 2017
Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant functionChangming Chen, Likui Yang, Bruno O Villoutreix, et al.
Thrombosis and Haemostasis|June 22, 2005
Novel aberrant splicings caused by a splice site mutation (IVS1a+5g>a) in F7 geneQiulan Ding, Wenman Wu, Qihua Fu, et al.
Thrombosis Research|May 14, 2013
Six novel missense mutations causing factor X deficiency and application of thrombin generation testQian Liang, Qiong Chen, Qiulan Ding, et al.
Research and Practice in Thrombosis and Haemostasis|August 21, 2023
Fibrinogen BOE II: dysfibrinogenemia with bleeding and defective thrombin bindingYang Li, Qian Liang, Wenman Wu, et al.
Thrombosis and Haemostasis|November 27, 2023
Complete F9 Gene Deletion, Duplication, and Triplication Rearrangements: Implications for Factor IX Expression and Clinical PhenotypesYuXin Ma, Yang Li, Jie Sun, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2019
Characterization of two large duplications of F9 associated with mild and severe haemophilia B, respectivelyXiaoling Xie, Changming Chen, Qian Liang, et al.
Thrombosis and Haemostasis|July 13, 2021
Antithrombin Resistance Rescues Clotting Defect of Homozygous Prothrombin-Y510N DysprothrombinemiaYeling Lu, Bruno O Villoutreix, Indranil Biswas, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|November 25, 2014
[Study on the impact of Trp1707Ser mutation on the binding mechanism of rF VIII light chain with VWF]Kun Chi, Yanyan Shao, Yeling Lu, et al.
Thrombosis and Haemostasis|May 19, 2020
Thr90Ser Mutation in Antithrombin is Associated with Recurrent Thrombosis in a Heterozygous CarrierYeling Lu, Bruno O Villoutreix, Indranil Biswas, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
Thrombosis Journal|October 3, 2023
Evaluation of prothrombotic risk of two PROC hotspot mutations (Arg189Trp and Lys193del) in Chinese population: a retrospective studyLei Li, Jian Li, Xi Wu, et al.
Thrombosis and Haemostasis|April 14, 2017
Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant functionChangming Chen, Likui Yang, Bruno O Villoutreix, et al.
Thrombosis and Haemostasis|June 22, 2005
Novel aberrant splicings caused by a splice site mutation (IVS1a+5g>a) in F7 geneQiulan Ding, Wenman Wu, Qihua Fu, et al.
Thrombosis Research|May 14, 2013
Six novel missense mutations causing factor X deficiency and application of thrombin generation testQian Liang, Qiong Chen, Qiulan Ding, et al.
Research and Practice in Thrombosis and Haemostasis|August 21, 2023
Fibrinogen BOE II: dysfibrinogenemia with bleeding and defective thrombin bindingYang Li, Qian Liang, Wenman Wu, et al.
Thrombosis and Haemostasis|November 27, 2023
Complete F9 Gene Deletion, Duplication, and Triplication Rearrangements: Implications for Factor IX Expression and Clinical PhenotypesYuXin Ma, Yang Li, Jie Sun, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2019
Characterization of two large duplications of F9 associated with mild and severe haemophilia B, respectivelyXiaoling Xie, Changming Chen, Qian Liang, et al.
Thrombosis and Haemostasis|July 13, 2021
Antithrombin Resistance Rescues Clotting Defect of Homozygous Prothrombin-Y510N DysprothrombinemiaYeling Lu, Bruno O Villoutreix, Indranil Biswas, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|November 25, 2014
[Study on the impact of Trp1707Ser mutation on the binding mechanism of rF VIII light chain with VWF]Kun Chi, Yanyan Shao, Yeling Lu, et al.
Thrombosis and Haemostasis|May 19, 2020
Thr90Ser Mutation in Antithrombin is Associated with Recurrent Thrombosis in a Heterozygous CarrierYeling Lu, Bruno O Villoutreix, Indranil Biswas, et al.
Pageof 10