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Journal of Cellular Physiology|July 24, 2019
Rac3, but not Rac1, promotes ox-LDL induced endothelial dysfunction by downregulating autophagyDan He, Ling Xu, Yuhang Wu, et al.Plos One|November 22, 2022
A pyridinesulfonamide derivative FD268 suppresses cell proliferation and induces apoptosis via inhibiting PI3K pathway in acute myeloid leukemiaYi Chen, Tianze Wu, Chengbin Yang, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|September 9, 2020
DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathwayLingling Liu, Weiqi Liu, Yan Shi, et al.Cell Reports|September 16, 2020
The Natural Compound Notopterol Binds and Targets JAK2/3 to Ameliorate Inflammation and ArthritisQiong Wang, Xin Zhou, Long Yang, et al.BMC Medical Genomics|January 9, 2016
Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han populationYu An, Wenyuan Duan, Guoying Huang, et al.International Journal of Nanomedicine|April 29, 2026
Inhibitory Effect of Allium cepa L.-Derived Extracellular Vesicles Loaded with Celecoxib on Osteoclast Differentiation in PeriodontitisHanyu Gao, Shoucheng Yin, Yuanzheng Yan, et al.Molecular Biology and Evolution|October 22, 2010
A genome-wide search for signals of high-altitude adaptation in TibetansShuhua Xu, Shilin Li, Yajun Yang, et al.The European Journal of Neuroscience|August 10, 2007
Nortriptyline delays disease onset in models of chronic neurodegenerationHongyan Wang, Yingjun Guan, Xin Wang, et al.Frontiers in Psychology|May 21, 2021
The Prevalence of Psychological Status During the COVID-19 Epidemic in China: A Systemic Review and Meta-AnalysisWei Li, Huijuan Zhang, Caidi Zhang, et al.Human Mutation|April 26, 2020
Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defectsJianhong Ye, Youli Tong, Jiashun Lv, et al.Pageof 125