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Wenman Wu

Showing results (21-30 of 57) with videos related to

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Blood|June 8, 2012
The kunitz protease inhibitor domain of protease nexin-2 inhibits factor XIa and murine carotid artery and middle cerebral artery thrombosisWenman Wu, Hongbo Li, Duraiswamy Navaneetham, 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.
Blood Cells, Molecules & Diseases|July 20, 2024
Accelerated phase development in a late-onset adolescent Chediak-Higashi syndrome patient caused by compound novel LYST mutations in the setting of SARS-CoV-2 infectionPing Guo, Xi Wu, Mingkang Yang, 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.
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.
The Biochemical Journal|December 5, 2015
Determination of sites of U50,488H-promoted phosphorylation of the mouse κ opioid receptor (KOPR): disconnect between KOPR phosphorylation and internalizationChongguang Chen, Yi-Ting Chiu, Wenman Wu, 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.
Thrombosis Research|February 22, 2024
A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand diseaseQian Liang, Ziqi Zhang, Biying Ding, et al.
Human Genomics|July 27, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disordersWenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Blood|June 8, 2012
The kunitz protease inhibitor domain of protease nexin-2 inhibits factor XIa and murine carotid artery and middle cerebral artery thrombosisWenman Wu, Hongbo Li, Duraiswamy Navaneetham, 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.
Blood Cells, Molecules & Diseases|July 20, 2024
Accelerated phase development in a late-onset adolescent Chediak-Higashi syndrome patient caused by compound novel LYST mutations in the setting of SARS-CoV-2 infectionPing Guo, Xi Wu, Mingkang Yang, 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.
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.
The Biochemical Journal|December 5, 2015
Determination of sites of U50,488H-promoted phosphorylation of the mouse κ opioid receptor (KOPR): disconnect between KOPR phosphorylation and internalizationChongguang Chen, Yi-Ting Chiu, Wenman Wu, 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.
Thrombosis Research|February 22, 2024
A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand diseaseQian Liang, Ziqi Zhang, Biying Ding, et al.
Human Genomics|July 27, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disordersWenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
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