Pages that link to "Q36718712"
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The following pages link to The prion strain phenomenon: molecular basis and unprecedented features (Q36718712):
Displaying 50 items.
- Pruritus is a common feature in sheep infected with the BSE agent (Q21203575) (← links)
- Prion hypothesis: the end of the controversy? (Q24599702) (← links)
- Molecular cross talk between misfolded proteins in animal models of Alzheimer's and prion diseases (Q24633202) (← links)
- Structural classification of toxic amyloid oligomers (Q30484255) (← links)
- Function of SSA subfamily of Hsp70 within and across species varies widely in complementing Saccharomyces cerevisiae cell growth and prion propagation (Q33493419) (← links)
- Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate (Q34023019) (← links)
- Lack of prion transmission by sexual or parental routes in experimentally infected hamsters (Q34051195) (← links)
- The prion hypothesis: from biological anomaly to basic regulatory mechanism (Q34412881) (← links)
- The intricate mechanisms of neurodegeneration in prion diseases. (Q34664576) (← links)
- The glycosylation status of PrPC is a key factor in determining transmissible spongiform encephalopathy transmission between species (Q35488786) (← links)
- Striatal pathology underlies prion infection-mediated hyperactivity in mice (Q35714160) (← links)
- Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic features (Q35887756) (← links)
- Molecular pathogenesis of sporadic prion diseases in man. (Q36005158) (← links)
- Strain conformation, primary structure and the propagation of the yeast prion [PSI+]. (Q36375495) (← links)
- Strain-dependent profile of misfolded prion protein aggregates (Q36579439) (← links)
- Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties (Q36664699) (← links)
- Cell-specific susceptibility to prion strains is a property of the intact cell (Q36719055) (← links)
- Identity determinants of infectious proteins. (Q36869740) (← links)
- Cell-free propagation of prion strains. (Q36936923) (← links)
- REST alleviates neurotoxic prion peptide-induced synaptic abnormalities, neurofibrillary degeneration and neuronal death partially via LRP6-mediated Wnt-β-catenin signaling (Q37022098) (← links)
- Reduction of prion infectivity in packed red blood cells. (Q37022481) (← links)
- Role of Prion Replication in the Strain-dependent Brain Regional Distribution of Prions (Q37066538) (← links)
- Evidence for prion-like mechanisms in several neurodegenerative diseases: potential implications for immunotherapy (Q37280507) (← links)
- Crossing the species barrier by PrP(Sc) replication in vitro generates unique infectious prions. (Q37339448) (← links)
- A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP. (Q37359955) (← links)
- Similarities between forms of sheep scrapie and Creutzfeldt-Jakob disease are encoded by distinct prion types (Q37462678) (← links)
- Could avian scavengers translocate infectious prions to disease-free areas initiating new foci of chronic wasting disease? (Q37523060) (← links)
- Laboratory activities involving transmissible spongiform encephalopathy causing agents: risk assessment and biosafety recommendations in Belgium (Q37523329) (← links)
- Cross currents in protein misfolding disorders: interactions and therapy (Q37585420) (← links)
- Polymorphism at 129 dictates metastable conformations of the human prion protein N-terminal β-sheet. (Q37725033) (← links)
- Nanoimaging for prion related diseases (Q37781245) (← links)
- Fate of prions in soil: a review (Q37869096) (← links)
- Prion seeded conversion and amplification assays. (Q37890298) (← links)
- Biochemical and strain properties of CJD prions: complexity versus simplicity (Q37905853) (← links)
- Nanopore analysis: An emerging technique for studying the folding and misfolding of proteins (Q37993988) (← links)
- The role of genetics in chronic wasting disease of North American cervids (Q37998389) (← links)
- A closer look at prion strains: characterization and important implications. (Q38077404) (← links)
- Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases. (Q38176721) (← links)
- Prion-like features of misfolded Aβ and tau aggregates (Q38313208) (← links)
- Subcellular distribution of the prion protein in sickness and in health (Q38356292) (← links)
- The transmissible spongiform encephalopathies of livestock (Q38492754) (← links)
- Treatment with a non-toxic, self-replicating anti-prion delays or prevents prion disease in vivo. (Q38718288) (← links)
- Pathogenic mechanisms of prion protein, amyloid-β and α-synuclein misfolding: the prion concept and neurotoxicity of protein oligomers. (Q38928728) (← links)
- Potential mechanisms and implications for the formation of tau oligomeric strains (Q38960046) (← links)
- Looking at the recent advances in understanding α-synuclein and its aggregation through the proteoform prism. (Q39297100) (← links)
- Exploring Anti-Prion Glyco-Based and Aromatic Scaffolds: A Chemical Strategy for the Quality of Life. (Q39326827) (← links)
- The relevance of contact-independent cell-to-cell transfer of TDP-43 and SOD1 in amyotrophic lateral sclerosis (Q39437151) (← links)
- Strain conformation controls the specificity of cross-species prion transmission in the yeast model (Q40561872) (← links)
- Prion strains in mammals: Different conformations leading to disease (Q40953633) (← links)
- N-terminal Prion Protein Peptides (PrP(120-144)) Form Parallel In-register β-Sheets via Multiple Nucleation-dependent Pathways (Q42383183) (← links)