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Emerging Microbes & Infections|August 9, 2018
Adaptive mutation F772S-enhanced p7-NS4A cooperation facilitates the assembly and release of hepatitis C virus and is associated with lipid droplet enlargementXiaobing Duan, Muhammad Ikram Anwar, Zhanxue Xu, et al.European Journal of Medicinal Chemistry|July 23, 2013
Synthesis and anticancer activity evaluation of a series of [1,2,4]triazolo[1,5-a]pyridinylpyridines in vitro and in vivoXiao-Meng Wang, Jing Xu, Yi-Ping Li, et al.Oncotarget|March 31, 2016
p21-activated kinase 1 (PAK1) expression correlates with prognosis in solid tumors: A systematic review and meta-analysisFang Fang, Jian Pan, Yi-Ping Li, et al.Molecular Medicine Reports|March 22, 2019
Serum‑derived hepatitis C virus can infect human glioblastoma cell line SF268 and activate the PI3K‑Akt pathwayGuosheng Yuan, Liang Rong, Junwei Liu, et al.STAR Protocols|September 1, 2024
Protocol for establishing and evaluating a cancer cachexia mouse modelZhijun Zhou, Jingxuan Yang, Mingyang Liu, et al.The Science of the Total Environment|September 6, 2023
Clarification of the phosphorus release mechanism for recovering phosphorus from biofilm sludge in alternating aerobic/anaerobic biofilm systemHao Zhang, Shuang-Shuang Zhang, Wei Zhang, et al.The Biochemical Journal|May 12, 2020
Runx1 up-regulates chondrocyte to osteoblast lineage commitment and promotes bone formation by enhancing both chondrogenesis and osteogenesisChen-Yi Tang, Wei Chen, Yuan Luo, et al.FEBS Letters|January 3, 2012
Splice blocking of zygotic sox31 leads to developmental arrest shortly after Mid-Blastula Transition and induces apoptosis in zebrafishSheng-Nan Hu, Hui Yu, Yun-Bin Zhang, et al.Proceedings of the National Academy of Sciences of the United States of America|May 23, 2014
Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal developmentWei Chen, Junqing Ma, Guochun Zhu, et al.Journal of Virology|December 24, 2010
Efficient culture adaptation of hepatitis C virus recombinants with genotype-specific core-NS2 by using previously identified mutationsTroels K H Scheel, Judith M Gottwein, Thomas H R Carlsen, et al.Pageof 32