Pages that link to "Q27014940"
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The following pages link to Cellular aspects of prion replication in vitro (Q27014940):
Displaying 29 items.
- Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells (Q33821808) (← links)
- Prion protein-specific antibodies-development, modes of action and therapeutics application (Q34423386) (← links)
- Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA. (Q34458035) (← links)
- Modulation of Glycosaminoglycans Affects PrPSc Metabolism but Does Not Block PrPSc Uptake. (Q36080838) (← links)
- Susceptibility of GT1-7 cells to mouse-passaged field scrapie isolates with a long incubation (Q36147951) (← links)
- Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells (Q36569559) (← links)
- Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin-proteasome system (Q36578308) (← links)
- Cell-to-cell propagation of infectious cytosolic protein aggregates (Q36762492) (← links)
- A specific population of abnormal prion protein aggregates is preferentially taken up by cells and disaggregated in a strain-dependent manner (Q37252741) (← links)
- Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes (Q37415409) (← links)
- Life cycle of cytosolic prions (Q38136055) (← links)
- Prions Ex Vivo: What Cell Culture Models Tell Us about Infectious Proteins (Q38166717) (← links)
- The standard scrapie cell assay: development, utility and prospects (Q38324712) (← links)
- Prion strains depend on different endocytic routes for productive infection. (Q38650733) (← links)
- Generation of Infectious Prions and Detection with the Prion-Infected Cell Assay (Q38693596) (← links)
- Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells (Q38734782) (← links)
- Prions on the run: How extracellular vesicles serve as delivery vehicles for self-templating protein aggregates (Q39237605) (← links)
- The relevance of contact-independent cell-to-cell transfer of TDP-43 and SOD1 in amyotrophic lateral sclerosis (Q39437151) (← links)
- Cell Biology Approaches to Studying Prion Diseases (Q40061707) (← links)
- Correlation of cellular factors and differential scrapie prion permissiveness in ovine microglia (Q40103519) (← links)
- Chronic wasting disease prion infection of differentiated neurospheres (Q40111506) (← links)
- Dual MicroRNA to Cellular Prion Protein Inhibits Propagation of Pathogenic Prion Protein in Cultured Cells. (Q40267284) (← links)
- Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner (Q46174770) (← links)
- Cellular mechanisms responsible for cell-to-cell spreading of prions (Q88673114) (← links)
- Quantifying Nucleation In Vivo Reveals the Physical Basis of Prion-like Phase Behavior (Q89446379) (← links)
- Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments (Q89893387) (← links)
- Gene-edited murine cell lines for propagation of chronic wasting disease prions (Q92353432) (← links)
- Transient multimers modulate conformer abundances of prion protein monomer through conformational selection (Q92757387) (← links)
- All the Same? The Secret Life of Prion Strains within Their Target Cells (Q93005212) (← links)