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Faquan Lin

Showing results (31-40 of 82) with videos related to

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Scientific Reports|July 16, 2015
Corrigendum: Meta-Analysis of the Relationship between XRCC1-Arg399Gln and Arg280His Polymorphisms and the Risk of Prostate CancerJie Yan, Xiantao Wang, Hui Tao, et al.
Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|March 28, 2007
Towards efficient registration of medical imagesHuiyu Zhou, Tangwei Liu, Faquan Lin, et al.
Journal of Ethnopharmacology|April 4, 2025
Rosa roxburghii juice alleviates DEHP-induced reproductive system damage in male mice via the PI3K/AKT signaling pathwayChaoyu Huang, Chen Qian, Zongxian Li, et al.
Cell Proliferation|October 15, 2025
Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future DirectionsQianyue Liu, Hongshuai Zheng, Jing Liu, et al.
International Journal of Laboratory Hematology|June 29, 2021
The β-chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemiaJie Yan, Yangyang Wu, Lin Liao, et al.
Translational Cancer Research|January 9, 2026
Multivesicular body subunit 12B (MVB12B) overexpression represses proliferation and migration in bladder urothelial carcinomaXiaohong Li, Caize Cen, Rongxin Li, et al.
Molecular Biology Reports|April 24, 2026
Tunicamycin-induced endoplasmic reticulum stress triggers ZBP1-Mediated PANoptosis in macrophages and mouse spleenHongkun Jiang, Chen Qian, Xiaoting Lin, et al.
International Journal of Hematology|December 10, 2016
A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A releaseJie Yan, Meiling Luo, Peng Cheng, et al.
Hematology (Amsterdam, Netherlands)|March 5, 2021
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D regionAiqiu Wei, Yangyang Wu, Liqun Xiang, et al.
Laboratory Medicine|April 6, 2024
A clinical update of compound heterozygosity for hemoglobin Hekinan II [a27(B8)Glu-Asp; HBA1: c.84G>T] variant in ChinaLiqiu Pan, Yuling Qiu, Lihua Ye, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Scientific Reports|July 16, 2015
Corrigendum: Meta-Analysis of the Relationship between XRCC1-Arg399Gln and Arg280His Polymorphisms and the Risk of Prostate CancerJie Yan, Xiantao Wang, Hui Tao, et al.
Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|March 28, 2007
Towards efficient registration of medical imagesHuiyu Zhou, Tangwei Liu, Faquan Lin, et al.
Journal of Ethnopharmacology|April 4, 2025
Rosa roxburghii juice alleviates DEHP-induced reproductive system damage in male mice via the PI3K/AKT signaling pathwayChaoyu Huang, Chen Qian, Zongxian Li, et al.
Cell Proliferation|October 15, 2025
Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future DirectionsQianyue Liu, Hongshuai Zheng, Jing Liu, et al.
International Journal of Laboratory Hematology|June 29, 2021
The β-chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemiaJie Yan, Yangyang Wu, Lin Liao, et al.
Translational Cancer Research|January 9, 2026
Multivesicular body subunit 12B (MVB12B) overexpression represses proliferation and migration in bladder urothelial carcinomaXiaohong Li, Caize Cen, Rongxin Li, et al.
Molecular Biology Reports|April 24, 2026
Tunicamycin-induced endoplasmic reticulum stress triggers ZBP1-Mediated PANoptosis in macrophages and mouse spleenHongkun Jiang, Chen Qian, Xiaoting Lin, et al.
International Journal of Hematology|December 10, 2016
A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A releaseJie Yan, Meiling Luo, Peng Cheng, et al.
Hematology (Amsterdam, Netherlands)|March 5, 2021
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D regionAiqiu Wei, Yangyang Wu, Liqun Xiang, et al.
Laboratory Medicine|April 6, 2024
A clinical update of compound heterozygosity for hemoglobin Hekinan II [a27(B8)Glu-Asp; HBA1: c.84G>T] variant in ChinaLiqiu Pan, Yuling Qiu, Lihua Ye, et al.
Pageof 9