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Qiulan Ding

Showing results (51-60 of 98) with videos related to

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Thrombosis Research|August 13, 2013
Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patientsQiulan Ding, Min Wang, Guanqun Xu, et al.
Thrombosis and Haemostasis|December 16, 2014
Characterisation and quantification of F8 transcripts of ten putative splice site mutationsQian Liang, Mingjie Xiang, Yeling Lu, et al.
Thrombosis Research|August 16, 2024
Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasiaJunwei Yuan, Xi Wu, Jialu Zhao, et al.
Thrombosis and Haemostasis|February 23, 2010
Occurence of haemophilia A and B in a Chinese family with mosaicism of the F9 gene mutation in the HB index's maternal grandfatherYeling Lu, Bingshou Xie, Qiulan Ding, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 7, 2009
A case of factor XI deficiency caused by compound heterozygous F11 gene mutationJing Wang, Xuefeng Wang, Jing Dai, et al.
Blood Cells, Molecules & Diseases|April 13, 2016
Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in ChinaYanyan Shao, Yanan Cao, Yeling Lu, et al.
Pathology|February 15, 2017
Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutationsTingting Yu, Jing Dai, Hongjing Liu, et al.
Haematologica|August 11, 2019
Ile73Asn mutation in protein C introduces a new N-linked glycosylation site on the first EGF-domain of protein C and causes thrombosisYeling Lu, Padmaja Mehta-D'souza, Indranil Biswas, et al.
Human Genetics|July 2, 2005
Gene symbol: F2. Disease: HypoprothrombinemiaHongli Wang, Wenbin Wang, Qihua Fu, et al.
Thrombosis Research|June 26, 2026
Molecular basis of the E69Q and R383W heterozygous F2 variants identified in the proband associated with severe hemostatic defectsLiya Lin, Yang Li, Changming Chen, et al.
Pageof 10

Showing results (51-60 of 98) with videos related to

Sort By:
Pageof 10
Thrombosis Research|August 13, 2013
Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patientsQiulan Ding, Min Wang, Guanqun Xu, et al.
Thrombosis and Haemostasis|December 16, 2014
Characterisation and quantification of F8 transcripts of ten putative splice site mutationsQian Liang, Mingjie Xiang, Yeling Lu, et al.
Thrombosis Research|August 16, 2024
Molecular mechanisms and clinical manifestations of hereditary hemorrhagic telangiectasiaJunwei Yuan, Xi Wu, Jialu Zhao, et al.
Thrombosis and Haemostasis|February 23, 2010
Occurence of haemophilia A and B in a Chinese family with mosaicism of the F9 gene mutation in the HB index's maternal grandfatherYeling Lu, Bingshou Xie, Qiulan Ding, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 7, 2009
A case of factor XI deficiency caused by compound heterozygous F11 gene mutationJing Wang, Xuefeng Wang, Jing Dai, et al.
Blood Cells, Molecules & Diseases|April 13, 2016
Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in ChinaYanyan Shao, Yanan Cao, Yeling Lu, et al.
Pathology|February 15, 2017
Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutationsTingting Yu, Jing Dai, Hongjing Liu, et al.
Haematologica|August 11, 2019
Ile73Asn mutation in protein C introduces a new N-linked glycosylation site on the first EGF-domain of protein C and causes thrombosisYeling Lu, Padmaja Mehta-D'souza, Indranil Biswas, et al.
Human Genetics|July 2, 2005
Gene symbol: F2. Disease: HypoprothrombinemiaHongli Wang, Wenbin Wang, Qihua Fu, et al.
Thrombosis Research|June 26, 2026
Molecular basis of the E69Q and R383W heterozygous F2 variants identified in the proband associated with severe hemostatic defectsLiya Lin, Yang Li, Changming Chen, et al.
Pageof 10