Pages that link to "Q81632888"
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The following pages link to Fibril conformation as the basis of species- and strain-dependent seeding specificity of mammalian prion amyloids (Q81632888):
Displaying 50 items.
- Leu138 in bovine prion peptide fibrils is involved in seeding discrimination related to codon 129 M/V polymorphism in the prion peptide seeding experiment (Q24337989) (← links)
- Selective incorporation of polyanionic molecules into hamster prions (Q24596538) (← links)
- Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles (Q25257725) (← links)
- Atomic structures of amyloid cross-beta spines reveal varied steric zippers (Q27644644) (← links)
- Molecular mechanisms for protein-encoded inheritance (Q27657037) (← links)
- Atomic Structures Suggest Determinants of Transmission Barriers in Mammalian Prion Disease (Q27666974) (← links)
- The effect of β2-α2 loop mutation on amyloidogenic properties of the prion protein (Q28511581) (← links)
- Heterologous cross-seeding mimics cross-species prion conversion in a yeast model. (Q30377551) (← links)
- Toward the treatment and prevention of Alzheimer's disease: rational strategies and recent progress (Q30419992) (← links)
- Polymorphism of β2-microglobulin amyloid fibrils manifested by ultrasonication-enhanced fibril formation in trifluoroethanol (Q30453082) (← links)
- The expanding universe of prion diseases (Q33239695) (← links)
- Observation of intermediate states of the human prion protein by high pressure NMR spectroscopy (Q33250429) (← links)
- Nanomechanical properties of human prion protein amyloid as probed by force spectroscopy (Q33341391) (← links)
- Investigating the conformational stability of prion strains through a kinetic replication model (Q33478386) (← links)
- Dissecting the potential molecular mechanisms underlying alpha-synuclein cell-to-cell transfer in Parkinson's disease (Q33524953) (← links)
- Mutation-dependent polymorphism of Cu,Zn-superoxide dismutase aggregates in the familial form of amyotrophic lateral sclerosis (Q33559556) (← links)
- Prion diseases and their biochemical mechanisms (Q33584925) (← links)
- Enhanced neuroinvasion by smaller, soluble prions (Q33588967) (← links)
- Conformational flexibility of Y145Stop human prion protein amyloid fibrils probed by solid-state nuclear magnetic resonance spectroscopy (Q33727311) (← links)
- A molecular switch controls interspecies prion disease transmission in mice (Q33968102) (← links)
- Interaction between human prion protein and amyloid-beta (Abeta) oligomers: role OF N-terminal residues (Q34074414) (← links)
- Structure of core domain of fibril-forming PHF/Tau fragments. (Q34354306) (← links)
- The prion hypothesis: from biological anomaly to basic regulatory mechanism (Q34412881) (← links)
- Physical and structural basis for polymorphism in amyloid fibrils (Q34559641) (← links)
- Relationship between prion propensity and the rates of individual molecular steps of fibril assembly (Q34752080) (← links)
- Molecular biology and pathology of prion strains in sporadic human prion diseases. (Q34802620) (← links)
- Prion strain-dependent differences in conversion of mutant prion proteins in cell culture (Q35023923) (← links)
- Cyclin-dependent kinase 5 phosphorylation of familial prion protein mutants exacerbates conversion into amyloid structure (Q35126695) (← links)
- Intermolecular alignment in Y145Stop human prion protein amyloid fibrils probed by solid-state NMR spectroscopy (Q35190046) (← links)
- Segmental polymorphism in a functional amyloid (Q35512684) (← links)
- Amyloid polymorphism: structural basis and neurobiological relevance (Q35586308) (← links)
- Structural polymorphism in amyloids: new insights from studies with Y145Stop prion protein fibrils. (Q35604887) (← links)
- Beta-sheet core of human prion protein amyloid fibrils as determined by hydrogen/deuterium exchange (Q35616300) (← links)
- Aβ(1-42) fibril structure illuminates self-recognition and replication of amyloid in Alzheimer's disease (Q35766611) (← links)
- Local unfolding of Cu, Zn superoxide dismutase monomer determines the morphology of fibrillar aggregates (Q35873804) (← links)
- Specific soluble oligomers of amyloid-β peptide undergo replication and form non-fibrillar aggregates in interfacial environments (Q36033240) (← links)
- Conformational basis for asymmetric seeding barrier in filaments of three- and four-repeat tau. (Q36051973) (← links)
- Distinct C9orf72-Associated Dipeptide Repeat Structures Correlate with Neuronal Toxicity. (Q36173153) (← links)
- Molecular architecture of human prion protein amyloid: a parallel, in-register beta-structure (Q36277140) (← links)
- Promiscuous cross-seeding between bacterial amyloids promotes interspecies biofilms (Q36318763) (← links)
- Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation (Q36474016) (← links)
- Molecular conformation and dynamics of the Y145Stop variant of human prion protein in amyloid fibrils (Q36608983) (← links)
- Fecal transmission of AA amyloidosis in the cheetah contributes to high incidence of disease. (Q36649384) (← links)
- Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties (Q36664699) (← links)
- X-Ray fiber and powder diffraction of PrP prion peptides. (Q36693073) (← links)
- From the polymorphism of amyloid fibrils to their assembly mechanism and cytotoxicity (Q36693078) (← links)
- The same primary structure of the prion protein yields two distinct self-propagating states (Q36701859) (← links)
- The prion strain phenomenon: molecular basis and unprecedented features (Q36718712) (← links)
- A common beta-sheet architecture underlies in vitro and in vivo beta2-microglobulin amyloid fibrils (Q36719294) (← links)
- Soluble prion protein and its N-terminal fragment prevent impairment of synaptic plasticity by Aβ oligomers: Implications for novel therapeutic strategy in Alzheimer's disease (Q36880081) (← links)