Man-Sun Sy
Affiliations: | Case Western Reserve University School of Medicine, Cleveland, OH, United States |
Area:
Molecular Biology, Pathology, Neuroscience BiologyGoogle:
"Man-Sun Sy"Mean distance: 53433
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Publications
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Ke J, Wu G, Zhang J, et al. (2019) Melanoma migration is promoted by prion protein via Akt-hsp27 signaling axis. Biochemical and Biophysical Research Communications |
Gao Z, Shi J, Cai L, et al. (2018) Prion dimer is heterogenous and is modulated by multiple negative and positive motifs. Biochemical and Biophysical Research Communications |
Wu GR, Mu TC, Gao ZX, et al. (2017) Prion protein is required for tumor necrosis factor alpha (TNFα)-triggered nuclear factor kappa B (NF-κB) signaling and cytokine production. The Journal of Biological Chemistry |
Ni CL, Seth D, Fonseca FV, et al. (2016) Polyglutamine Tract Expansion Increases S-Nitrosylation of Huntingtin and Ataxin-1. Plos One. 11: e0163359 |
Wang Y, Yu S, Huang D, et al. (2016) Cellular Prion Protein Mediates Pancreatic Cancer Cell Survival and Invasion through Association with and Enhanced Signaling of Notch1. The American Journal of Pathology |
Yang L, Gao Z, Hu L, et al. (2016) Glycosylphosphatidylinositol anchor modification machinery deficiency is responsible for the formation of pro-prion protein (PrP) in BxPC-3 cells and increases cancer cell motility. The Journal of Biological Chemistry. 291: 6785 |
Yang L, Gao Z, Hu L, et al. (2015) GPI Anchor Modification Machinery Deficiency is Responsible for the Formation of Pro-PrP in BxPC-3 and Increases Cancer Cell Motility. The Journal of Biological Chemistry |
Kim C, Haldiman T, Surewicz K, et al. (2012) Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C). Plos Pathogens. 8: e1002835 |
Kim C, Haldiman T, Cohen Y, et al. (2011) Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate. Plos Pathogens. 7: e1002242 |
Wang F, Yin S, Wang X, et al. (2010) Role of the highly conserved middle region of prion protein (PrP) in PrP-lipid interaction. Biochemistry. 49: 8169-76 |