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Qiulan Ding

Showing results (21-30 of 98) with videos related to

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Thrombosis and Haemostasis|September 8, 2012
Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemiaQiulan Ding, Qi Ouyang, Xiaodong Xi, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|September 4, 2020
Changes in Biomarkers of Coagulation, Fibrinolytic, and Endothelial Functions for Evaluating the Predisposition to Venous Thromboembolism in Patients With Hereditary ThrombophiliaLei Li, Lixia Gao, Xi Wu, et al.
Biochemistry|May 1, 2012
Characterization of the heparin-binding site of the protein z-dependent protease inhibitorLikui Yang, Qiulan Ding, Xin Huang, et al.
Blood Cells, Molecules & Diseases|September 7, 2012
Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patientsQiulan Ding, Wei Shen, Xu Ye, et al.
Thrombosis Research|March 7, 2015
Identification of anti-moesin antibodies in the serums of patients with antiphospholipid syndromeXiaoyi Lin, Qian Liang, Lin Lin, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University|February 28, 2012
[A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C]Xu Ye, Xiaoli Liu, Ying Feng, et al.
Frontiers in Molecular Biosciences|May 23, 2022
Unexpected Dynamic Binding May Rescue the Binding Affinity of Rivaroxaban in a Mutant of Coagulation Factor XZhi-Li Zhang, Changming Chen, Si-Ying Qu, et al.
Thrombosis and Haemostasis|December 16, 2016
Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutationQiulan Ding, Likui Yang, Xiaoqing Zhao, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|October 20, 2015
[Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review]Guanqun Xu, Qian Liang, Liwei Zhang, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|March 26, 2016
[Genetic diagnosis of a Chinese pedigree with X-Linked sideroblastic anemia: a case report and literature review]Changming Chen, Qiulan Ding, Yeling Lu, et al.
Pageof 10

Showing results (21-30 of 98) with videos related to

Sort By:
Pageof 10
Thrombosis and Haemostasis|September 8, 2012
Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemiaQiulan Ding, Qi Ouyang, Xiaodong Xi, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|September 4, 2020
Changes in Biomarkers of Coagulation, Fibrinolytic, and Endothelial Functions for Evaluating the Predisposition to Venous Thromboembolism in Patients With Hereditary ThrombophiliaLei Li, Lixia Gao, Xi Wu, et al.
Biochemistry|May 1, 2012
Characterization of the heparin-binding site of the protein z-dependent protease inhibitorLikui Yang, Qiulan Ding, Xin Huang, et al.
Blood Cells, Molecules & Diseases|September 7, 2012
Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patientsQiulan Ding, Wei Shen, Xu Ye, et al.
Thrombosis Research|March 7, 2015
Identification of anti-moesin antibodies in the serums of patients with antiphospholipid syndromeXiaoyi Lin, Qian Liang, Lin Lin, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University|February 28, 2012
[A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C]Xu Ye, Xiaoli Liu, Ying Feng, et al.
Frontiers in Molecular Biosciences|May 23, 2022
Unexpected Dynamic Binding May Rescue the Binding Affinity of Rivaroxaban in a Mutant of Coagulation Factor XZhi-Li Zhang, Changming Chen, Si-Ying Qu, et al.
Thrombosis and Haemostasis|December 16, 2016
Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutationQiulan Ding, Likui Yang, Xiaoqing Zhao, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|October 20, 2015
[Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review]Guanqun Xu, Qian Liang, Liwei Zhang, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|March 26, 2016
[Genetic diagnosis of a Chinese pedigree with X-Linked sideroblastic anemia: a case report and literature review]Changming Chen, Qiulan Ding, Yeling Lu, et al.
Pageof 10