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Qiulan Ding

Showing results (1-10 of 98) with videos related to

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Thrombosis Research|July 19, 2022
Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature reviewYang Li, Biying Ding, Xuefeng Wang, et al.
Thrombosis and Haemostasis|February 8, 2013
Expression and functional characterisation of natural R147W and K150del variants of protein C in the Chinese populationQiulan Ding, Likui Yang, Seyed Mahdi Hassanian, et al.
Thrombosis and Haemostasis|November 26, 2011
Impact of polymorphisms in genes involved in autoimmune disease on inhibitor development in Chinese patients with haemophilia AYeling Lu, Qiulan Ding, Jing Dai, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|March 27, 2014
[The functional study of antithrombin L99 mutation]Tingting Yu, Jing Dai, Qiulan Ding, et al.
Blood|September 28, 2019
Low factor V level ameliorates bleeding diathesis in patients with combined deficiency of factor V and factor VIIIYanyan Shao, Wenman Wu, Guanqun Xu, et al.
BMC Medical Genetics|March 29, 2018
The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosisXi Wu, Qiulan Ding, Xuefeng Wang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 31, 2010
Genetic analysis of a pedigree with combined factor XII and factor XI deficiencyXu Ye, Ying Feng, Qiulan Ding, et al.
Thrombosis Journal|May 4, 2023
A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiencyLei Li, Xi Wu, Wenman Wu, et al.
Blood|February 6, 2015
Protein C Thr315Ala variant results in gain of function but manifests as type II deficiency in diagnostic assaysQiulan Ding, Likui Yang, Peyman Dinarvand, et al.
Thrombosis and Haemostasis|May 17, 2013
The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascadeQiulan Ding, Yiping Shen, Likui Yang, et al.
Pageof 10

Showing results (1-10 of 98) with videos related to

Sort By:
Pageof 10
Thrombosis Research|July 19, 2022
Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature reviewYang Li, Biying Ding, Xuefeng Wang, et al.
Thrombosis and Haemostasis|February 8, 2013
Expression and functional characterisation of natural R147W and K150del variants of protein C in the Chinese populationQiulan Ding, Likui Yang, Seyed Mahdi Hassanian, et al.
Thrombosis and Haemostasis|November 26, 2011
Impact of polymorphisms in genes involved in autoimmune disease on inhibitor development in Chinese patients with haemophilia AYeling Lu, Qiulan Ding, Jing Dai, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|March 27, 2014
[The functional study of antithrombin L99 mutation]Tingting Yu, Jing Dai, Qiulan Ding, et al.
Blood|September 28, 2019
Low factor V level ameliorates bleeding diathesis in patients with combined deficiency of factor V and factor VIIIYanyan Shao, Wenman Wu, Guanqun Xu, et al.
BMC Medical Genetics|March 29, 2018
The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosisXi Wu, Qiulan Ding, Xuefeng Wang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 31, 2010
Genetic analysis of a pedigree with combined factor XII and factor XI deficiencyXu Ye, Ying Feng, Qiulan Ding, et al.
Thrombosis Journal|May 4, 2023
A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiencyLei Li, Xi Wu, Wenman Wu, et al.
Blood|February 6, 2015
Protein C Thr315Ala variant results in gain of function but manifests as type II deficiency in diagnostic assaysQiulan Ding, Likui Yang, Peyman Dinarvand, et al.
Thrombosis and Haemostasis|May 17, 2013
The missense Thr211Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascadeQiulan Ding, Yiping Shen, Likui Yang, et al.
Pageof 10