Pages that link to "Q36211122"

The following pages link to Birth of a prion: spontaneous generation revisited (Q36211122):

Displaying 34 items.

• Generating a prion with bacterially expressed recombinant prion protein (Q24626352) (← links)
• Proteins behaving badly. Substoichiometric molecular control and amplification of the initiation and nature of amyloid fibril formation: lessons from and for blood clotting (Q26739684) (← links)
• Cellular aspects of prion replication in vitro (Q27014940) (← links)
• NMR structures of two designed proteins with high sequence identity but different fold and function (Q27652181) (← links)
• Mutational Tipping Points for Switching Protein Folds and Functions (Q27677203) (← links)
• Quantitative recovery of scrapie agent with minimal protein from highly infectious cultures (Q34186004) (← links)
• Propagation of RML prions in mice expressing PrP devoid of GPI anchor leads to formation of a novel, stable prion strain (Q34299382) (← links)
• Cell-free formation of misfolded prion protein with authentic prion infectivity (Q35127478) (← links)
• Effects of the Pathogenic Mutation A117V and the Protective Mutation H111S on the Folding and Aggregation of PrP106-126: Insights from Replica Exchange Molecular Dynamics Simulations (Q35629014) (← links)
• Opinion: What is the role of protein aggregation in neurodegeneration? (Q36259086) (← links)
• GroEL-mediated protein folding: making the impossible, possible (Q36539816) (← links)
• Structure, function, and amyloidogenesis of fungal prions: filament polymorphism and prion variants (Q36693068) (← links)
• Gene and protein patterns of potential prion-related markers in the central nervous system of clinical and preclinical infected sheep (Q36716041) (← links)
• Cell-specific susceptibility to prion strains is a property of the intact cell (Q36719055) (← links)
• Small-ruminant lentivirus enhances PrPSc accumulation in cultured sheep microglial cells (Q36933940) (← links)
• Structural basis of infectious and non-infectious amyloids (Q36944974) (← links)
• Anti-LRP/LR antibody W3 hampers peripheral PrPSc propagation in scrapie infected mice (Q37080701) (← links)
• Therapies for human prion diseases (Q37199225) (← links)
• Serum amyloid A and protein AA: molecular mechanisms of a transmissible amyloidosis (Q37459593) (← links)
• Biology of Amyloid: Structure, Function, and Regulation (Q37800223) (← links)
• α-Secretase-derived cleavage of cellular prion yields biologically active catabolites with distinct functions (Q37977276) (← links)
• Protein misfolding cyclic amplification (PMCA): Current status and future directions. (Q38274835) (← links)
• The activities of amyloids from a structural perspective (Q39004351) (← links)
• Mammalian prion protein (PrP) forms conformationally different amyloid intracellular aggregates in bacteria. (Q40923016) (← links)
• Prion protein amyloid formation under native-like conditions involves refolding of the C-terminal alpha-helical domain (Q41176371) (← links)
• Limited transcriptional response of ovine microglia to prion accumulation (Q42155809) (← links)
• What makes a good prion? Conference on Prion Biology. (Q42704096) (← links)
• Transmissible encephalopathy agents: virulence, geography and clockwork (Q42713213) (← links)
• Ultrastructural characteristics (or evaluation) of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseases (Q42821914) (← links)
• Do prion protein gene polymorphisms induce apoptosis in non-mammals? (Q46584144) (← links)
• Role of N-terminal familial mutations in prion protein fibrillization and prion amyloid propagation in vitro (Q46916908) (← links)
• Dynamic Meso-Scale Anchorage of GPI-Anchored Receptors in the Plasma Membrane: Prion Protein vs. Thy1. (Q47153809) (← links)
• Clinical and therapeutic aspects of prion disease (Q49076335) (← links)
• Constant-pH Molecular Dynamics Simulations Reveal a β-Rich Form of the Human Prion Protein (Q85033594) (← links)