Pages that link to "Q36624152"
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The following pages link to Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cells (Q36624152):
Displaying 50 items.
- Yeast prions: structure, biology, and prion-handling systems (Q27007482) (← links)
- Treatment of Prion Disease with Heterologous Prion Proteins (Q27303161) (← links)
- Trans-dominant inhibition of prion propagation in vitro is not mediated by an accessory cofactor (Q27316451) (← links)
- N-Terminal Helix-Cap in α-Helix 2 Modulates β-State Misfolding in Rabbit and Hamster Prion Proteins (Q27678150) (← links)
- Glycosylation influences cross-species formation of protease-resistant prion protein (Q28365495) (← links)
- The comprehensive native interactome of a fully functional tagged prion protein (Q33408170) (← links)
- Cellular biology of prion diseases (Q33558398) (← links)
- Species-independent inhibition of abnormal prion protein (PrP) formation by a peptide containing a conserved PrP sequence (Q33816387) (← links)
- Identification of two prion protein regions that modify scrapie incubation time (Q33836445) (← links)
- Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155. (Q33840809) (← links)
- Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform (Q33847297) (← links)
- Pregnancy status and fetal prion genetics determine PrPSc accumulation in placentomes of scrapie-infected sheep (Q34029006) (← links)
- Strain Specific Resistance to Murine Scrapie Associated with a Naturally Occurring Human Prion Protein Polymorphism at Residue 171 (Q34042693) (← links)
- Overexpression of Nonconvertible PrP c Δ114–121 in Scrapie-Infected Mouse Neuroblastoma Cells Leads to trans -Dominant Inhibition of Wild-Type PrP Sc Accumulation (Q34069408) (← links)
- Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie (Q34250173) (← links)
- Antagonistic interactions between yeast [PSI(+)] and [URE3] prions and curing of [URE3] by Hsp70 protein chaperone Ssa1p but not by Ssa2p (Q34280090) (← links)
- Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier (Q34393434) (← links)
- Multiple amino acid residues within the rabbit prion protein inhibit formation of its abnormal isoform (Q34467477) (← links)
- Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line (Q34580839) (← links)
- Glycoform-selective prion formation in sporadic and familial forms of prion disease (Q34634279) (← links)
- Protein inheritance (prions) based on parallel in-register beta-sheet amyloid structures (Q34911325) (← links)
- Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene (Q34960558) (← links)
- Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein (Q35053001) (← links)
- Prion diseases of yeast: Amyloid structure and biology (Q35053520) (← links)
- Insights into prion biology: integrating a protein misfolding pathway with its cellular environment (Q35194908) (← links)
- Proteinase K-resistant material in ARR/VRQ sheep brain affected with classical scrapie is composed mainly of VRQ prion protein. (Q35531568) (← links)
- Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers (Q35750568) (← links)
- A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells. (Q35852143) (← links)
- Prion infection of muscle cells in vitro (Q35857376) (← links)
- Late virus replication events in microglia are required for neurovirulent retrovirus-induced spongiform neurodegeneration: evidence from neural progenitor-derived chimeric mouse brains (Q35874088) (← links)
- Discovering protein-based inheritance through yeast genetics (Q35922438) (← links)
- The N-terminal, polybasic region of PrP(C) dictates the efficiency of prion propagation by binding to PrP(Sc). (Q36208488) (← links)
- Characterization of conformation-dependent prion protein epitopes (Q36347803) (← links)
- Prions of fungi: inherited structures and biological roles (Q36647771) (← links)
- Recombinant scrapie-like prion protein of 106 amino acids is soluble (Q37096971) (← links)
- Cells expressing anchorless prion protein are resistant to scrapie infection (Q37157117) (← links)
- Recombinant human prion protein inhibits prion propagation in vitro (Q37221670) (← links)
- A specific population of abnormal prion protein aggregates is preferentially taken up by cells and disaggregated in a strain-dependent manner (Q37252741) (← links)
- Prion propagation: the role of protein dynamics (Q37375827) (← links)
- PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection (Q37560815) (← links)
- Enhanced virulence of sheep-passaged bovine spongiform encephalopathy agent is revealed by decreased polymorphism barriers in prion protein conversion studies (Q37644096) (← links)
- Rapid cell-surface prion protein conversion revealed using a novel cell system (Q39556052) (← links)
- Prion Propagation in Cells Expressing PrP Glycosylation Mutants (Q39605681) (← links)
- Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein (Q39673524) (← links)
- Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease (Q40370560) (← links)
- Potential approaches for heterologous prion protein treatment of prion diseases (Q40883026) (← links)
- Ovine recombinant PrP as an inhibitor of ruminant prion propagation in vitro. (Q41358656) (← links)
- Mechanism of inhibition of Psi+ prion determinant propagation by a mutation of the N-terminus of the yeast Sup35 protein (Q41989863) (← links)
- Prion protein dynamics before aggregation. (Q42183733) (← links)
- Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state (Q42675291) (← links)