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Scientific Reports
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July 16, 2015
Corrigendum: Meta-Analysis of the Relationship between XRCC1-Arg399Gln and Arg280His Polymorphisms and the Risk of Prostate Cancer
Jie 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 images
Huiyu 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 pathway
Chaoyu Huang, Chen Qian, Zongxian Li, et al.
Cell Proliferation
|
October 15, 2025
Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future Directions
Qianyue 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 hypofibrinogenemia
Jie 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 carcinoma
Xiaohong 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 spleen
Hongkun 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 release
Jie Yan, Meiling Luo, Peng Cheng, et al.
Hematology (Amsterdam, Netherlands)
|
March 5, 2021
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
Aiqiu 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 China
Liqiu Pan, Yuling Qiu, Lihua Ye, et al.
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Search research articles
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Showing results (31-40 of 82) with videos related to
Sort By:
Page
of 9
Scientific Reports
|
July 16, 2015
Corrigendum: Meta-Analysis of the Relationship between XRCC1-Arg399Gln and Arg280His Polymorphisms and the Risk of Prostate Cancer
Jie 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 images
Huiyu 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 pathway
Chaoyu Huang, Chen Qian, Zongxian Li, et al.
Cell Proliferation
|
October 15, 2025
Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future Directions
Qianyue 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 hypofibrinogenemia
Jie 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 carcinoma
Xiaohong 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 spleen
Hongkun 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 release
Jie Yan, Meiling Luo, Peng Cheng, et al.
Hematology (Amsterdam, Netherlands)
|
March 5, 2021
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D region
Aiqiu 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 China
Liqiu Pan, Yuling Qiu, Lihua Ye, et al.
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of 9