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Ming-Yang Deng

Showing results (1-10 of 11) with videos related to

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Light, Science & Applications|June 25, 2020
Mini-LED, Micro-LED and OLED displays: present status and future perspectivesYuge Huang, En-Lin Hsiang, Ming-Yang Deng, et al.
HLA|December 8, 2022
The novel HLA-B*48:01:11 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individualShan Xu, Zhong-Zheng Zheng, Ke-Ming Du, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|June 11, 2005
[The dynamic analysis and the clinical significance of vascular endothelial cell markers and hemolysis parameters in thrombotic thrombocytopenic purpura]Ming-yang Deng, Guang-sen Zhang, Bin Li, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|December 3, 2009
[The frequency of JAK2 V617F mutation, expression level of phosphorylated JAK/STATs proteins and their clinical significance in myeloproliferative disorders patients]Guo-Yu Hu, Ming-Yang Deng, Guang-Sen Zhang, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|October 15, 2019
[Relationship between TET2 Gene SNP rs3733609 C/T and JAK2V617F Allele Burden in Patients with Myeloproliferative Neoplasms]Xiang Xiao, Xiao-Liu Liu, Xiao-Hui Shen, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 2010
Antithrombin Cambridge II(A384S) mutation frequency and antithrombin activity levels in 120 of deep venous thrombosis and 150 of cerebral infarction patients in a single center in Southern ChinaGuang-sen Zhang, Yang-ming Tang, Mei-qing Tang, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|August 27, 2013
Analysis of clinical and laboratory characteristics in 42 patients with thrombotic thrombocytopenic purpura from a single center in ChinaMing-yang Deng, Guang-sen Zhang, Yang Zhang, et al.
Thrombosis Research|August 13, 2016
Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypesMing-Yang Deng, Zi-Xian Liu, Hai-Fan Huang, et al.
Plos One|March 6, 2013
An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasiaQian Yu, Xiao-Hui Shen, Ying Li, et al.
Oncotarget|February 5, 2016
A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineagesXiao-hui Shen, Nan-nan Sun, Ya-fei Yin, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Light, Science & Applications|June 25, 2020
Mini-LED, Micro-LED and OLED displays: present status and future perspectivesYuge Huang, En-Lin Hsiang, Ming-Yang Deng, et al.
HLA|December 8, 2022
The novel HLA-B*48:01:11 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individualShan Xu, Zhong-Zheng Zheng, Ke-Ming Du, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|June 11, 2005
[The dynamic analysis and the clinical significance of vascular endothelial cell markers and hemolysis parameters in thrombotic thrombocytopenic purpura]Ming-yang Deng, Guang-sen Zhang, Bin Li, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|December 3, 2009
[The frequency of JAK2 V617F mutation, expression level of phosphorylated JAK/STATs proteins and their clinical significance in myeloproliferative disorders patients]Guo-Yu Hu, Ming-Yang Deng, Guang-Sen Zhang, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|October 15, 2019
[Relationship between TET2 Gene SNP rs3733609 C/T and JAK2V617F Allele Burden in Patients with Myeloproliferative Neoplasms]Xiang Xiao, Xiao-Liu Liu, Xiao-Hui Shen, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 2010
Antithrombin Cambridge II(A384S) mutation frequency and antithrombin activity levels in 120 of deep venous thrombosis and 150 of cerebral infarction patients in a single center in Southern ChinaGuang-sen Zhang, Yang-ming Tang, Mei-qing Tang, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|August 27, 2013
Analysis of clinical and laboratory characteristics in 42 patients with thrombotic thrombocytopenic purpura from a single center in ChinaMing-yang Deng, Guang-sen Zhang, Yang Zhang, et al.
Thrombosis Research|August 13, 2016
Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypesMing-Yang Deng, Zi-Xian Liu, Hai-Fan Huang, et al.
Plos One|March 6, 2013
An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasiaQian Yu, Xiao-Hui Shen, Ying Li, et al.
Oncotarget|February 5, 2016
A TET2 rs3733609 C/T genotype is associated with predisposition to the myeloproliferative neoplasms harboring JAK2(V617F) and confers a proliferative potential on erythroid lineagesXiao-hui Shen, Nan-nan Sun, Ya-fei Yin, et al.
Pageof 2