Showing results (2271-2280 of 2,911) with videos related to
Sort By:
Pageof 292
Frontiers in Neurology|April 9, 2025
Rituximab treatment in Chinese patients with primary angiitis of the central nervous systemYu-Zhen Wei, Hua-Bing Wang, Lin-Lin Yin, et al.Nature|October 25, 2002
The prolyl isomerase Pin1 is a regulator of p53 in genotoxic responseHongwu Zheng, Han You, Xiao Zhen Zhou, et al.British Journal of Pharmacology|June 6, 2006
The PPARalpha/gamma dual agonist chiglitazar improves insulin resistance and dyslipidemia in MSG obese ratsPing-Ping Li, Song Shan, Yue-Teng Chen, et al.Nature Communications|October 9, 2015
Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite filmsSang Mo Yang, Shinbuhm Lee, Jie Jian, et al.Scientific Reports|June 16, 2019
Traumatic Brain Injury-related voiding dysfunction in mice is caused by damage to rostral pathways, altering inputs to the reflex pathwaysOnder Albayram, Bryce MacIver, John Mathai, et al.Briefings in Bioinformatics|May 3, 2021
Systematic comparison of ligand-based and structure-based virtual screening methods on poly (ADP-ribose) polymerase-1 inhibitorsYue Zhao, Xiang-Gui Wang, Zhong-Ye Ma, et al.International Journal of Molecular Sciences|January 10, 2026
NGR1 Pretreatment Enhances the Therapeutic Efficacy of Transplanting Cardiomyocytes Derived from Human Induced Pluripotent Stem Cells for Myocardial InfarctionHao Cai, Meng-Ying Huang, Fang-Fang Mou, et al.Stem Cell Research & Therapy|November 13, 2024
Pretreatment with Notoginsenoside R1 enhances the efficacy of neonatal rat mesenchymal stem cell transplantation in model of myocardial infarction through regulating PI3K/Akt/FoxO1 signaling pathwaysHao Cai, Xiao-Jing Han, Zhi-Rong Luo, et al.Guang Pu Xue Yu Guang Pu Fen Xi = Guang Pu|April 14, 2012
[Study on the automatic recognition method of elemental spectra in laser induced breakdown spetroscopy]Li-tuo Liu, Jian-guo Liu, Nan-jing Zhao, et al.European Journal of Medical Genetics|October 12, 2021
Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing lossSha Yu, Wen-Xia Chen, Yun-Fei Zhang, et al.Pageof 292