Published in Sci Rep on August 08, 2014
Ubiquitin-specific protease 14 modulates degradation of cellular prion protein. Sci Rep (2015) 0.87
Structure-Based Drug Discovery for Prion Disease Using a Novel Binding Simulation. EBioMedicine (2016) 0.83
Prions. Proc Natl Acad Sci U S A (1998) 27.80
IRFs: master regulators of signalling by Toll-like receptors and cytosolic pattern-recognition receptors. Nat Rev Immunol (2006) 7.98
Sustained translational repression by eIF2α-P mediates prion neurodegeneration. Nature (2012) 3.54
Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells. J Virol (1993) 3.07
A systems approach to prion disease. Mol Syst Biol (2009) 2.49
Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein. J Virol (2000) 2.18
Regulation of IRF-3-dependent innate immunity by the papain-like protease domain of the severe acute respiratory syndrome coronavirus. J Biol Chem (2007) 2.07
Human immunodeficiency virus type 1 mediates global disruption of innate antiviral signaling and immune defenses within infected cells. J Virol (2009) 1.53
Classical swine fever virus Npro interacts with interferon regulatory factor 3 and induces its proteasomal degradation. J Virol (2007) 1.34
Ubiquitination and proteasomal degradation of interferon regulatory factor-3 induced by Npro from a cytopathic bovine viral diarrhea virus. Virology (2007) 1.28
Loss of interferon regulatory factor 3 in cells infected with classical swine fever virus involves the N-terminal protease, Npro. J Virol (2005) 1.23
Prion strain-dependent differences in conversion of mutant prion proteins in cell culture. J Virol (2006) 1.14
Biological and biochemical characteristics of prion strains conserved in persistently infected cell cultures. J Virol (2005) 1.11
Prion protein interaction with stress-inducible protein 1 enhances neuronal protein synthesis via mTOR. Proc Natl Acad Sci U S A (2010) 1.06
Cloning and functional analysis of the human IRF-3 promoter. DNA Cell Biol (1999) 0.98
Protective role of interferon regulatory factor 3-mediated signaling against prion infection. J Virol (2012) 0.91
The Small RNA gene activator protein, SphI postoctamer homology-binding factor/selenocysteine tRNA gene transcription activating factor, stimulates transcription of the human interferon regulatory factor-3 gene. J Biol Chem (2001) 0.90
Characterization of the human IRF-3 promoter and its regulation by the transcription factor E2F1. Mol Biol Rep (2009) 0.84
Protective role of MyD88-independent innate immune responses against prion infection. Prion (2012) 0.79
Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay. PLoS One (2013) 1.30
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study. Ann Neurol (2016) 0.93
Rapid and Quantitative Assay of Amyloid-Seeding Activity in Human Brains Affected with Prion Diseases. PLoS One (2015) 0.93
Ubiquitin-specific protease 14 modulates degradation of cellular prion protein. Sci Rep (2015) 0.87
Conformational properties of prion strains can be transmitted to recombinant prion protein fibrils in real-time quaking-induced conversion. J Virol (2014) 0.86
Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. BMJ Open (2014) 0.85
The real-time quaking-induced conversion assay for detection of human prion disease and study of other protein misfolding diseases. Nat Protoc (2016) 0.78
Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma. Dig Liver Dis (2015) 0.77
Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients. EBioMedicine (2016) 0.76
Strain-Dependent Effect of Macroautophagy on Abnormally Folded Prion Protein Degradation in Infected Neuronal Cells. PLoS One (2015) 0.76