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Qiulan Ding

Showing results (41-50 of 98) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|February 21, 2020
Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrierYeling Lu, Hemant Giri, Bruno O Villoutreix, et al.
Pathology|February 15, 2017
Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutationTingting Yu, Jing Dai, Hongjing Liu, et al.
Thrombosis and Haemostasis|May 12, 2017
Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesisChangming Chen, Xiaoling Xie, Xi Wu, et al.
Pathology|May 1, 2012
Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutationsTingting Yu, Jing Dai, Hongjing Liu, et al.
Pathology|April 26, 2012
Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutationTingting Yu, Jing Dai, Hongjing Liu, et al.
Transfusion|June 28, 2017
An exonic missense mutation c.28G>A is associated with weak B blood group by affecting RNA splicing of the ABO geneXiaohong Cai, Chengrui Qian, Wenman Wu, et al.
Human Mutation|April 7, 2022
Effects of 14 F9 synonymous codon variants on hemophilia B expression: Alteration of splicing along with protein expressionHuayang Zhang, Changming Chen, Xi Wu, et al.
Orphanet Journal of Rare Diseases|July 26, 2019
Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangementSiyu Ma, Changming Chen, Qian Liang, et al.
Journal of Clinical Pathology|January 12, 2017
A pericentric inversion of chromosome X disrupting <i>F8</i> and resulting in haemophilia AYu Xin, Jingyi Zhou, Qiulan Ding, et al.
Thrombosis and Haemostasis|May 25, 2017
Molecular and clinical profile of VWD in a large cohort of Chinese population: application of next generation sequencing and CNVplex<sup>®</sup> techniqueQian Liang, Huanhuan Qin, Qiulan Ding, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Journal of Thrombosis and Haemostasis : JTH|February 21, 2020
Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrierYeling Lu, Hemant Giri, Bruno O Villoutreix, et al.
Pathology|February 15, 2017
Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutationTingting Yu, Jing Dai, Hongjing Liu, et al.
Thrombosis and Haemostasis|May 12, 2017
Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesisChangming Chen, Xiaoling Xie, Xi Wu, et al.
Pathology|May 1, 2012
Spectrum of F9 mutations in Chinese haemophilia B patients: identification of 20 novel mutationsTingting Yu, Jing Dai, Hongjing Liu, et al.
Pathology|April 26, 2012
Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutationTingting Yu, Jing Dai, Hongjing Liu, et al.
Transfusion|June 28, 2017
An exonic missense mutation c.28G>A is associated with weak B blood group by affecting RNA splicing of the ABO geneXiaohong Cai, Chengrui Qian, Wenman Wu, et al.
Human Mutation|April 7, 2022
Effects of 14 F9 synonymous codon variants on hemophilia B expression: Alteration of splicing along with protein expressionHuayang Zhang, Changming Chen, Xi Wu, et al.
Orphanet Journal of Rare Diseases|July 26, 2019
Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangementSiyu Ma, Changming Chen, Qian Liang, et al.
Journal of Clinical Pathology|January 12, 2017
A pericentric inversion of chromosome X disrupting <i>F8</i> and resulting in haemophilia AYu Xin, Jingyi Zhou, Qiulan Ding, et al.
Thrombosis and Haemostasis|May 25, 2017
Molecular and clinical profile of VWD in a large cohort of Chinese population: application of next generation sequencing and CNVplex<sup>®</sup> techniqueQian Liang, Huanhuan Qin, Qiulan Ding, et al.
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